healthcare workers, volunteers and...
TRANSCRIPT
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Mandatory Seasonal Flu Shot Vaccination for
Healthcare Workers,
Volunteers and Students TABLE 1
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Multidisciplinary Team Members• Ambulatory services: Michael Koller, Bridgid Steele, Cheryl White• Emergency Medicine: Chris Chaput, Katherine Martens • Human Resources: Vicky Piper• Infection Control: Jaime Belmares, Bridget Gaughan, Jorge Parada• IT: Roger Russel• Legal: Jill Koppell• Media Services: Anne Dillon• Nursing Administration: Paula Hindle, Carol Schleffendorf• Occupational Health: Sandra Brehm, Mary Capelli-Schellpfeffer• Pharmacy: Brian Hardy• Safety & Security: Jen Carlson• Stritch School of Medicine: Mike Lambesis
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Project Aim Statement• 1984 - CDC recommends yearly flu shot for all health care workers
(HCW)• 2009 Infectious Disease Society of America recommends mandatory
flu vaccination for HCW• 2009 Nursing Magnet Forces align with vaccination
• Despite best efforts, LUHS flu HCW flu shot rate is 73% in 2008- 2009
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Target
100% HCW, volunteer and student participation in mandatory influenza vaccination program
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Solutions Implemented• HR policy includes flu shot as condition of employment• Widespread publicity in local media and throughout health system
(including “Safety Dance”video) • 3 ply consent form and portal based tracking system created to
measure compliance• HR implements exemption process• EMS coordinates mass vaccination drill Oct 15 & 16• Student affairs office coordinates medical school efforts• Nursing administration coordinates times and locations for vaccination
up to December 1 deadline
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Analysis: Target achieved!100% participation 99.3% vaccinated
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Next Steps• Utilize ID card swipe tracking system• Consider earlier deadline if vaccine supply permits• Encourage vaccination at large scale events• Avoid perceived resource competition between immunization delivery
to employees and patients• Align policies at Loyola and Gottlieb campuses • Incorporate messaging that includes compliance with immunization
policy into broader education emphasizing the holistic relationship between patients and employee safety actions
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Team Membership Emergency Department Nursing Staff and Physicians
Bypassing the Bypass:Elimination of Emergency Department
and Hospital Bypass Time
TABLE 2
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Goal
Develop and implement strategies to decrease Emergency Department and Hospital bypass time to zero hours immediately without compromising patient safety and quality care.
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• February 2009 – commitment from hospital and ED to avoid bypass as tool to manage ED overcrowding
• March 2009 – instituted the use of an ED physician in triage with second triage nurse to expedite evaluations and work-ups during peak census (1pm-9pm)
• Reallocation of physician and nursing staff hours to accommodate expanded use of ED triage and Patient Care Annex (PCA)-previously Fast Track area
• Expanded ED triage from one to four rooms and Patient Care Annex from five to six treatment rooms
• Work-up of patients directly from waiting room and evaluation of higher acuity patients in PCA
Solutions Implemented
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Num
ber o
f ED
Vis
itsED Volume
Confidential for Quality Improvement Purposes Only
2005
Q120
05Q2
2005
Q320
05Q4
2006
Q120
06Q2
2006
Q320
06Q4
2007
Q120
07Q2
2007
Q320
07Q4
2008
Q120
08Q2
2008
Q320
08Q4
2009
Q120
09Q2
2009
Q320
09Q4
2010
Q120
10Q2
2010
Q3
12000
12500
13000
13500
14000
14500
UCL = 14238.30
Mean = 12956.26
LCL = 11674.23
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Bypa
ss H
ours
Confidential for Quality Improvement Purposes OnlyQuarter (FY)
2005
Q120
05Q2
2005
Q320
05Q4
2006
Q120
06Q2
2006
Q320
06Q4
2007
Q120
07Q2
2007
Q320
07Q4
2008
Q120
08Q2
2008
Q320
08Q4
2009
Q120
09Q2
2009
Q320
09Q4
2010
Q120
10Q2
2010
Q3
0
50
100
150
200
250
300
350
UCL = 242.62
Mean = 80.31
ED Bypass Hours per Quarter
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Per
cent
age
of E
D p
atie
nts
LWBS
Confidential for Quality Improvement Purposes OnlyFY Quarter
2005
Q120
05Q2
2005
Q320
05Q4
2006
Q120
06Q2
2006
Q320
06Q4
2007
Q120
07Q2
2007
Q320
07Q4
2008
Q120
08Q2
2008
Q320
08Q4
2009
Q120
09Q2
2009
Q320
09Q4
2010
Q120
10Q2
2010
Q3
1
2
3
4
5
6
UCL = 6.62
Mean = 3.84
LCL = 1.07
Zero Bypass Instituted
Left Without Being Seen (LWBS)
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Per
cent
age
LWBS
Emergency Department LWBS RateJune 2009 - Feb 2010
Confidential for Quality Improvement Purposes Only
6/28-7
/047/0
5-7/11
7/12-7
/187/1
9-7/25
7/26-8
/018/0
2-8/08
8/09-8
/158/1
6-8/22
8/23-8
/298/3
0-9/05
9/06-9
/129/1
3-9/19
9/20-9
/269/2
7-10/0
3
10/04
-10/10
10/11
-10/17
10/18
-10/24
10/25
-10/31
11/1-
11/07
11/8-
11/14
11/18
-11/21
11/22
-11/28
11/29
-12/05
12/06
-12/12
12/13
-12/19
12/20
-12/26
12/27
-1/02
1/03-1
/091/1
0-1/16
1/17-1
/231/2
4-1/30
1/31-2
/62/7
-2/13
2/14-2
/202/2
1-2/27
2/28-3
/63/7
-3/13
3/14-3
/203/2
1-3/27
0
1
2
3
4
5
6UCL = 6.24
Mean = 3.06
UCL = 3.55
LUMC Mean = 1.77
(since Nov 2009)
UHC Mean= 3.9%
Mean = 1.77
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ED Volume and LWBS
0
20004000
6000
8000
1000012000
14000
16000
2005
Q120
05Q2
2005
Q320
05Q4
2006
Q120
06Q2
2006
Q320
06Q4
2007
Q120
07Q2
2007
Q320
07Q4
2008
Q120
08Q2
2008
Q320
08Q4
2009
Q120
09Q2
2009
Q320
09Q4
2010
Q120
10Q2
2010
Q3
ED V
olum
e
0
1
2
3
4
5
6
7
Perc
ent L
WB
S
Visits LWBS Percentage
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Tim
e in
Min
utes
1/8/20
082/8
/2008
3/8/20
084/8
/2008
5/8/20
086/8
/2008
7/8/20
088/8
/2008
9/8/20
0810
/8/20
0811
/8/20
0812
/8/20
081/8
/2009
2/8/20
093/8
/2009
4/8/20
095/8
/2009
6/8/20
097/8
/2009
8/8/20
099/8
/2009
10/8/
2009
11/8/
2009
12/8/
2009
1/8/20
102/8
/2010
5
10
15
20UCL = 19.12
Mean = 11.04
LCL = 2.95
No Bypass 2/09
ED Time to Evaluate by Acuity Level 1(lowest level of care)
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No Bypass 2/09
Tim
e in
Min
utes
1/8/20
082/8
/2008
3/8/20
084/8
/2008
5/8/20
086/8
/2008
7/8/20
088/8
/2008
9/8/20
0810
/8/20
0811
/8/20
0812
/8/20
081/8
/2009
2/8/20
093/8
/2009
4/8/20
095/8
/2009
6/8/20
097/8
/2009
8/8/20
099/8
/2009
10/8/
2009
11/8/
2009
12/8/
2009
1/8/20
102/8
/2010
10
12
14
16
18
20
UCL = 21.18
Mean = 15.54
LCL = 9.90
ED Time to Evaluate by Acuity Level 2 (Simple – lower level of care)
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Tim
e in
Min
utes
1/8/20
082/8
/2008
3/8/20
084/8
/2008
5/8/20
086/8
/2008
7/8/20
088/8
/2008
9/8/20
0810
/8/20
0811
/8/20
0812
/8/20
081/8
/2009
2/8/20
093/8
/2009
4/8/20
095/8
/2009
6/8/20
097/8
/2009
8/8/20
099/8
/2009
10/8/
2009
11/8/
2009
12/8/
2009
1/8/20
102/8
/2010
16
18
20
22
24
26 UCL = 25.95
Mean = 20.42
LCL = 14.89
No Bypass 2/09
ED Time to Evaluate by Acuity Level 3 (Urgent)
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Tim
e in
Min
utes
1/8/20
082/8
/2008
3/8/20
084/8
/2008
5/8/20
086/8
/2008
7/8/20
088/8
/2008
9/8/20
0810
/8/20
0811
/8/20
0812
/8/20
081/8
/2009
2/8/20
093/8
/2009
4/8/20
095/8
/2009
6/8/20
097/8
/2009
8/8/20
099/8
/2009
10/8/
2009
11/8/
2009
12/8/
2009
1/8/20
102/8
/2010
13
14
15
16
17
18
19
20
21
UCL = 20.37
Mean = 16.54
LCL = 12.71
No Bypass 2/09
ED Time to Evaluate by Acuity Level 4(Urgent-requiring higher level of care)
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Tim
e in
Min
utes
1/8/20
082/8
/2008
3/8/20
084/8
/2008
5/8/20
086/8
/2008
7/8/20
088/8
/2008
9/8/20
0810
/8/20
0811
/8/20
0812
/8/20
081/8
/2009
2/8/20
093/8
/2009
4/8/20
095/8
/2009
6/8/20
097/8
/2009
8/8/20
099/8
/2009
10/8/
2009
11/8/
2009
12/8/
2009
1/8/20
102/8
/2010
8
10
12
14
16
18
20
22UCL = 21.52
Mean = 14.08
LCL = 6.63
No Bypass 2/09
ED Time to Evaluate by Acuity Level 5(Critical – highest level of care)
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Analysis
• The ED has maintained ZERO Bypass since February 2009. In addition, despite an increase in ED volume, patients Left Without Being Seen (LWBS) has decreased below UHC average for academic medical centers.
• The time-to-evaluate for acuity levels 3-5 has shown a statistically significant decrease in minutes in the last several months.
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Projected Gross Charges Resulting from Decreased LWBS Rate
• PROJECTED reduction of LWBS patients = 306 patients for FY10– FY09 = 1752 LWBS patients (actual)– FY10 = 1446 LWBS patients (projected based
on current trend and annualized rate of 3.96 pts/day)
• PROJECTED FY10 Gross Charges = $334,759*
* Based upon average charge per patient of $1093.98
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Next Steps
• Continue to utilize the strategies implemented• Continue to monitor LWBS rate and identify and
implement solutions to further decrease rate• Work with Lean Team to optimize flow
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Pediatric Assessment of Rapid Treatment Needs and the Emergency Response System
Department of PediatricsPediatric and Pediatric Critical Care
Kathleen Webster M.D.Jenny Wang MDDina Calamur MDCindi La Porte BSN, RN
TABLE 3
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When your patient needs help, call on your
Pediatric Assessment of Rapid Treatment Needs and Emergency Response System
AIM STATEMENT•Reduce mortality of internal pediatric transfer patients below the overall pediatric ICU mortality rate of 1.7%.
GOAL•To provide multidisciplinary team assistance for an acutely ill or decompensating patient prior to an arrest state.
MAGNET• Force 7: Quality Improvement
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BACKGROUND Mortality Risk of Ward Patients
Transferred to ICU
• Michigan: Patients transferred from the ward to the ICU have a higher risk of mortality than pt admitted from the emergency room1
• Not statistically significant– Small numbers
• ? Target group for intervention
1Odetola PCCM 2008
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Mor
talit
y of
Ped
iatri
c Pa
tient
s
Pediatr ic Mortality RateLoy ola University Health Sy stem
For quality improvement purposes only
W ard Tran sfersIC U P atien ts
20 03
20 05
20 07
2
3
4
5
6
7
Prior to “PARTNERS” implementation, patients admitted to ward or ICU prior to transfer to PICU experienced a mortality rate
as high as 7% exceeding the overall ICU mortality rate of 1.7%
Telemedicine Implemented
Target 1.7%
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Solutions Implemented
• Creation of PARTNERS: Pediatric Assessment of Rapid Treatment Needs and Emergency Response System
• Defined team members roles• Developed criteria for contacting rapid response team• In-service to all RN staff in PICU, IMC, and floor• In-service to respiratory therapists• In-service to intensivists• Weekly review of team calls and transfers • Feedback to staff regarding appropriateness of calls, missed
opportunities
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Team Composition and Roles• Bedside Nurse
– Activates team– Keeps record
• Critical Care Nurse– Brings telemedicine cart– Initial assessment and
intervention– Updates family
• Respiratory Care Practitioner– Brings respiratory box– Provides airway/breathing
interventions• Intensivist
– Team leader– Updates primary team
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PARTNERS: Phase 1 June 2008-December 2008
• Implemented June 2008– 12 evaluations
• Reason– Respiratory: 7– Neurological: 3– Cardiovascular: 2
• Change in management: 83%– Transferred to PICU: 75%– Intubation: 17%, NIV: 17%– Imaging: 8%– Urgent surgical intervention: 8%
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PARTNERS: Phase 2 January-December 2009
• 6 change in management • Transferred to Peds ICU 9 • Stayed in Peds IMC 5• Transferred to Peds IMC 1
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Mor
talit
y of
ped
iatri
c pa
tient
s
P ed ia tr ic M or ta lity RateLoy o la Un ive rsity Hea lth S y stem
Fo r q u a l i ty im p ro ve m e n t p u rp o s e s o n ly
W a rd T ran s fe rsIC U P a t ie n ts
20 03
20 04
20 05
20 06
20 07
20 08
20 09
0
1
2
3
4
5
6
7
Phase 2 of “PARTNERS” implementation outcomes: patients admitted to ward or ICU prior to transfer to PICU: a mortality rate of 0.0% which demonstrates a decrease below the overall ICU
mortality rate of 1.7% in 2009.
Telemedicine Implemented PARTNERS implemented
Target 1.7%
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July2006June 2007
July2007June 2008
July 2008June 2009
July 2009March 2010
Percent of ward admits transferred to PICU
2.7 2.1 2.4 2.3
Actual mortality 2.4% 4.6% 0% 0%
Impact of Rapid Response TeamImpact of Rapid Response Team
In FY 09 there were no deaths of patients transferred from ward/IMC to PICU.
Predicted mortality (Pediatric Index of Mortality Score) for this time period is 9.1%
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Validating our Conclusions
• Telemedicine facilitates intensivist led RRT.• Helps achieve goal of evaluation of high risk
patients quickly.• Increased evaluation of patients prior
to transfer. • Decrease in mortality rate for internal transfer
patients to 0%.
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Next Steps• PARTNERS : Pediatric Rapid Response Team
will continue• Utilize the Epic document flow sheet to document when a
rapid response occurred• Develop a clarity report to monitor PARTNERS activity• Develop a tracking mechanism to monitor PARTNERS calls• Practice mock rapid responses and mock codes: identify
areas for improvement• Investigate outliers• Report to key stakeholders• Celebrate Successes
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Reduction of Reduction of Calcium Bolus Infusions Calcium Bolus Infusions
in the Neonatal ICUin the Neonatal ICU
TABLE 4
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Team MembershipTeam MembershipPamela Pamela NicoskiNicoski PharmDPharmDLawrence Bennett MD Lawrence Bennett MD
Barb Barb HeringHering RN RN Lisa Lisa FestleFestle RNRNMarc Weiss MDMarc Weiss MD
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BackgroundBackground•• Identified inconsistent use of calcium Identified inconsistent use of calcium
bolus infusions to treat bolus infusions to treat hypocalcemia in neonatal patients.hypocalcemia in neonatal patients.
•• Inherent risks are associated with the Inherent risks are associated with the administration of intravenous administration of intravenous calcium (i.e. severe bradycardia, calcium (i.e. severe bradycardia, tissue necrosis).tissue necrosis).
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Improve the utilization of calcium Improve the utilization of calcium bolus infusions in Neonatal ICU bolus infusions in Neonatal ICU patients by establishing and patients by establishing and adhering to guidelines for the adhering to guidelines for the treatment of hypocalcemia.treatment of hypocalcemia.
Project Aim StatementProject Aim Statement
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Nursing Magnet ForcesNursing Magnet Forces
Forces 6: Quality of CareForces 6: Quality of CareForce 7: Quality ImprovementForce 7: Quality ImprovementForce 11: Nurses as Teachers Force 11: Nurses as Teachers Force 12: Image of NursingForce 12: Image of NursingForce 13: Interdisciplinary RelationshipsForce 13: Interdisciplinary Relationships
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Phase 1Phase 1•• Evaluated 1 year data on IV calcium Evaluated 1 year data on IV calcium
orders. orders. –– June 2007June 2007––May 2008May 2008
•• Identified avoidable administration of Identified avoidable administration of calcium bolus infusions. calcium bolus infusions.
•• Created departmental guidelines for the Created departmental guidelines for the treatment of hypocalcemia:treatment of hypocalcemia:–– Increase calcium in continuous IV fluids / TPN Increase calcium in continuous IV fluids / TPN –– Calcium bolus infusions:Calcium bolus infusions:
•• Symptomatic (neuromuscular irritability, cardiac Symptomatic (neuromuscular irritability, cardiac effects) effects)
•• Asymptomatic (Ca: <0.85 Asymptomatic (Ca: <0.85 mmolmmol/L)/L)
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•• Recommended laboratory values to Recommended laboratory values to help elucidate cause:help elucidate cause:–– Magnesium, Phosphorus, pHMagnesium, Phosphorus, pH
•• Determined how many calcium bolus Determined how many calcium bolus infusions may have been avoided with infusions may have been avoided with guidelines in place.guidelines in place.
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•• NICU physicians and nurses inNICU physicians and nurses in-- serviced on new recommendations.serviced on new recommendations.–– Changes presented at Neonatal Division Changes presented at Neonatal Division
meeting, QA meeting and daily nursing meeting, QA meeting and daily nursing report. report.
–– ““NICU NewsflashNICU Newsflash”” ee--mailed to all NICU mailed to all NICU nurses.nurses.
–– Guidelines reinforced monthly during resident Guidelines reinforced monthly during resident neonatal TPN lecture.neonatal TPN lecture.
–– Guidelines added to LUMC Neonatal Guidelines added to LUMC Neonatal Resident Physician Manual .Resident Physician Manual .
Phase 2Phase 2
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•• Reinforced that administration for Reinforced that administration for calcium bolus infusions should be calcium bolus infusions should be through a central line, if possible.through a central line, if possible.–– If no central line, nurses are instructed to verify If no central line, nurses are instructed to verify
with another nurse that the peripheral IV is with another nurse that the peripheral IV is patent. patent.
•• EPIC medication order pathway EPIC medication order pathway updated to include new updated to include new recommendations.recommendations.
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* Given for low calcium.
*
Guidelines implemented
Number of Calcium Bolus Infusions*
ResultsResults
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* Given for low calcium.
*
81% decrease
Number of Calcium Bolus Infusions*
One year Prior to Guideline Implementation
One year After Guideline Implementation
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Calcium Bolus Infusions Given for Asymptomatic Hypocalcemia Relative to Ionized Calcium
<0.85 0.85 - 0.89 0.9 - 0.94 0.95 - 0.99 > 1
One year Prior to Guideline Implementation (n=170)
One year After Guideline Implementation (n=33)
11%
14%
25%27%
23%
53%
16%
13%
9%9%
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AnalysisAnalysis•• Development of departmental Development of departmental
guidelines along with staff guidelines along with staff education improved judicious use of education improved judicious use of calcium bolus infusions in the calcium bolus infusions in the Neonatal ICU:Neonatal ICU:–– 81% reduction in the number of calcium 81% reduction in the number of calcium
bolus infusions given to patients in the bolus infusions given to patients in the NICU. NICU.
–– Avoided 137 calcium bolus infusions over a one Avoided 137 calcium bolus infusions over a one year period based on historical data.year period based on historical data.
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–– Reduction of potential harm to our neonatal Reduction of potential harm to our neonatal patients (severe bradycardia, patients (severe bradycardia, extravasationextravasation risk).risk).
–– Cost savings to the Medical Center.Cost savings to the Medical Center.–– Room for improvement:Room for improvement:
•• Only 17/32 (53%) of calcium bolus infusions Only 17/32 (53%) of calcium bolus infusions administered for hypocalcemia (not documented as administered for hypocalcemia (not documented as symptomatic) met guideline criteriasymptomatic) met guideline criteria..
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Next StepsNext Steps•• Increase compliance of current Increase compliance of current
guidelines, focusing on management guidelines, focusing on management of asymptomatic patientsof asymptomatic patients::–– Continue to reinforce guidelines to incoming Continue to reinforce guidelines to incoming
medical teams.medical teams.–– If calcium given for symptomatic If calcium given for symptomatic
hypocalcemia, reinforce need for comment hypocalcemia, reinforce need for comment in patient care note.in patient care note.
–– ReRe--evaluate in one year.evaluate in one year.
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•• Positive results from these guidelines Positive results from these guidelines have prompted the goal of reviewing have prompted the goal of reviewing other electrolyte bolus infusions other electrolyte bolus infusions includingincluding::–– Potassium chloride Potassium chloride –– Sodium bicarbonateSodium bicarbonate
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Team Membership
Oversight Team: Sharon Englert, Dr. John Gianopoulos, Mark Cerkvanik, Karen Pickney, Anne Porter, LuAnn Vis, Sandy Swanson, Barb Pudelek, Elaine Trulis, Maureen Davey
Multidisciplinary Change Team: Dr. Marc Weiss, Dr. Paula White, Pat Hester-Lund, Laurie Brennan, Carolanne Bartosiewicz, Linda Juretschke, Chris Besler, Julie Kramer, Rita Risatti, Dr. Ku-mie Kim, Dr. Renata Wilczek, Dr. John Gianopoulos, LuAnn Vis, Sandy Swanson, Barb Pudelek, Elaine Trulis, Maureen Davey
Teaming Up for Patient Safety: Implementation of a Team
Training Program
TABLE 5
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Team STEPPS is an evidence-based team training system developed by the Department of Defense (DOD) in collaboration with the Agency for Healthcare Research and Quality (AHRQ)
Team training provides methods to empower all members of the healthcare team, creates a shared mental framework to organize communication, and provides a structured communication process
Background
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• The purpose of Team Training is to reduce medical errors by teaching human-factors concepts to interdisciplinary teams of medical professionals
• This requires a culture change form a focus on individual performance to one that values team performance and encourages effective communication
• Team Training focuses on leadership, workload performance, situation monitoring, policy/regulations, mutual support, available resources, communication, and operating strategy
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Aim
Improve patient safety and eliminate adverse events by implementing AHRQ Team STEPPS (Team Training) for the all team members in Labor & Delivery, Women’s Health and the NICU
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• Developed a multidisciplinary change team
• September, 2009: Change team trained, planned for tool implantation for whole staff when training implemented
• Implemented Perinatal Briefs, unit huddles and NICU Evening Rounds from change team training
• Oct/Nov 2009: Introductory training completed for whole multidisciplinary team in 2 week burst of training (10-27-09 to 11-05-09)
• November 2009: Grand rounds with Team Training expert MD presented to broad Loyola Audience
• Change team evaluated training and planned next steps
• January 5, 2010: Change team implemented SBAR train- the trainer-education as second “dose” of team training
Solutions Implemented
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00.5
11.5
22.5
33.5
44.5
5
Mean Score
Key Principles Team Tools Apply Strategies
Measure
Team Training Evaluations (Range 0= Strongly disagree, 5=Strongly agree)
StaffMD
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Evaluation Comments
•Identify change you plan to make:
•“Better handoffs and feedback”
•“Will use SBAR for communication/ use SBAR more frequently”
•“Daily multi-team meetings with NICU, L&D, and Women’s Health”
•“Be more assertive”
•“Implement debriefings and huddles”
•“This was better than I thought it would be!”
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Percent of time Perinatal Briegs and NICU Evening Rounds are Occuring
0
20
40
60
80
100
120
Sept Oct Nov Dec Jan Feb
Perinatal Briefs NICU Evening Rounds
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Adverse Outcome Indicator and Weighted AO Score
0
0.5
1
1.5
2
2.5
3
3.5
4
Q1, 2008 Q2, 2008 Q3, 2008 Q4, 2008 Q1, 2009 Q2, 2009
AOI/W
AO
S
Adverse Outcome Index Weighted AO score
Low risk OB to Gottlieb
Adverse Outcome Index (AOI): the # of deliveries with 1 or more of the perinatal adverse events as a proportion of total deliveries
Weighted AO Score (WAOS): the total weights of all the adverse events divided by the total number of deliveries
From the National Perinatal Information Center/Quality Analytic Services (NPIC/QAS) www.npic.org
These scores represent the Loyola experience pre-implementation of Team Training. One measure we will follow is whether these scores increase or decrease.
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Perinatal Adverse Outcomes
•Maternal death
•Intrapartum and Neonatal Death
•Uterine Rupture
•Maternal Admission to ICU
•Birth Trauma
•Return to OR/L&D
•Admission to NICU
•APGAR 5 <7
•Blood Transfusions
•3rd and 4th degree perineal laceration
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Analysis– Staff driven strategies- Briefs, huddles,
evening rounds- were implemented and continue to occur regularly
– The Change Team is actively engaged in determining next steps
– SBAR training was developed and implemented by Change Team as a second training initiative
– Consultant scheduled to return to coach Change Team and complete education for those on LOA during previous training sessions
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Next Steps• Change Team to receive additional coaching education• Change Team to review “Magic Wand list” and prioritize plans for
future activities• Completion of team training for those who were unable to
participate• Regular new inservices related to AHRQ Team Training tools
implemented• AOI measures reviewed• Team behavior observation by external consultant during visit to
assess implementation progress
• Long term – observe incidents of significant adverse outcomes and dollars spent in malpractice settlements
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Keep it in Neutral … Let’s Get Off to a Good Head Start
Preventing IVH in the Very Low Birth Weight Infant
The Outstanding NICU Nursing StaffLisa Festle, MSN, RNC-NIC, APRN/CNS & Barb Hering, MSN, RNC-NIC, APRN/CNS
NICU Education, Co-chairsMarianne Chybik, MSN, RNC-NIC, APN/CNS, NICU Case Manager
Elaine Trulis, BSN, NE-BC, Nurse ManagerMarc Weiss, MD, Director of Neonatology
TABLE 6
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BackgroundCurrent rates of Intraventricular Hemorrhage (IVH)
range between 10 –
15%; for the very low birth weight (VLBW) infant, this risk is highest during the
first week of life.
The severity of IVH is classified Grade 1 – 4
Grades 3 & 4 are the most severe and associated with poor long term outcomes
Magnet Forces 5,6,7,8,9
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Background
The negative impact of IVH on long term outcomes includes:
Impaired cognitive skills/learning disabilities
motor deficits, including fine or gross motor delay and cerebral palsy
sensory impairment, including hearing or vision loss
behavioral and psychological problems
Current evidence suggests that maintaining the head and body in neutral alignment may
prevent functional obstruction of cerebral venous drainage
prevent elevation of central venous pressure...and thus IVH
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Aim Statement
1. Reduce the incidence of severe IVH in VLBW infants at LUMC to less than the national average (9.4%) as benchmarked against the Vermont Oxford Network (VON)
*VON - international collaborative group of NICU’s who report quality data
2. All infants < 32 weeks gestational age will be maintained in a neutral head position for the first week of life
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Solutions Implemented
For all infants <32 weeks gestational age during the first week of life:Only supine or side-lying positioning with the
head midline in a neutral position; when turning, do so slowly and make sure that the head and body are turned as a unitNo prone positioningElevate Head of Bed 30°No routine suctioningMinimal handlingMaintain normal body temperature
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Results – All NICU PatientsIncidence of severe IVH (grades 3 & 4)
decreased from ~28% to ~17% in the NICU (VON benchmark)
Severe IVH (Grades 3 & 4)
2006 2007 2008 2009
VON 9.7% 9.3% 9.3% 9.3%
Loyola NICU
28% 25.7% 16.2% 17%
* LUMC is less than the national average for Grades 1 & 2 IVH
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Results Inborn Infants with Severe IVH
* LUMC is less than the national average for Grade 1 & 2 IVH
25.0%23.9%
14.3%
16.5%
8.1% 8.0% 7.8% 7.8%
0.0%
5.0%
10.0%
15.0%
20.0%
25.0%
30.0%
2006 2007 2008 2009Year
Seve
re IV
H ra
tes
LUMCVON
Neutral Head Positioning initated
4/08
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Analysis
Decreased incidence of severe IVH by almost 50% since instituting neutral midline head positioning
Potentially better long term developmental outcomes for VLBW infants in the NICU
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Next Steps• Incorporating IVH prevention guidelines as part of a
multidisciplinary VLBW protocol• Develop a standard admission order set in EPIC
integrating best practices for care of the VLBW infant on admission and during the first weeks of life as these infants transition to extra-uterine life
• Focus on “the Golden Hour”…the first hour of life:consistent care beginning in the delivery room through admission to the NICU
• Neutral midline positioning• Hypothermia prevention• Minimal handling
• Incorporate guidelines into inter hospital transports and provide education to network hospitals
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References• Bada H, et al. Frequent handling in the neonatal intensive care unit
and intraventricular hemorrhage. J of Pediatrics, July 1990; 117 (1): 126-131.
• Carteaux P, et al. Evaluation and development of potentially better practices for the prevention of brain hemorrhage and ischemia in the very low birth weight infants. Pediatrics, April 2003, 111 (4): e489- 496.
• Cowan F. Thoresen M. Changes in superior sagittal sinus blood velocities due to postural alterations and pressure on the head of the newborn infant. Pediatrics, 75 (6): 1038-1047.
• Emery J. Peabody J. Head position affects intracranial pressure in newborn infants. J of Pediatrics., 1983, 103 (6): 950-953.
• Kenner C. McFrath J. Developmental care of newborns and infants guide for health professionals. St. Louis: Elsevier; 2004: 309-311.
• McLendon D et al. Implementation of potentially better practices for the prevention of brain hemorrhage and ischemic brain injury in very low birth weight infants. Pediatrics, April 2003; 111 (4): e497-503.
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PNEUMONIATeam Membership:
Mary Altier, MS, RNRose Lach, Administrative Director
Clinical Departments: Emergency Medical Services, General Medicine, Cardiac Services
Hospital Departments: 6 Northeast, 3NESW, 2 NE, Emergency Department, Medical Records, Quality & Resource Management, Center for Clinical Effectiveness
Confidential: For Quality Improvement Purposes Only
Force 6:Quality of CareForce 7: Quality ImprovementForce 9: Autonomy
TABLE 7
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Room for Improvement
To increase the rates for those quality measures specific to the Pneumonia Core measure:
•
Antibiotic timing•
Appropriate Antibiotic Administered
•
Adult Smoking Cessation Counseling•
Blood Culture Collection
•
Pneumococcal Vaccination: > 65 years of age•
Influenza Vaccination: > 50 years of age
Confidential: For Quality Improvement Purposes Only
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Goals
•
Initial antibiotics administered within 6 hours of arrival at hospital
•
Appropriate antibiotic administered
•
Blood cultures collected prior to initial antibiotic dose
•
Pneumococcal Vaccine administered to patients > 65 years old prior to discharge
•
Influenza Vaccine administered to patients > 50 years old prior to discharge
•
Smoking Cessation Counseling completed prior to discharge
Confidential: For Quality Improvement Purposes Only
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Plan
•
System-wide influenza campaign Oct-Feb with posters placed in general population and all in-patient rooms.
•
Pneumovax/ Influenza in-services to inpatient units.
•
SAC and 5Tower now completing Pneumonia/Influenza screens.
•
Monthly ED “dashboard” reports with
timing/outliers provided.•
Provide performance data to Senior Management, Leapfrog Committee, Pneumonia Task Force &all nursing units.
•
EPIC pneumonia & influenza vaccine screening on patient data base. If screen positive, vaccination orders placed by nurse.
Confidential: For Quality Improvement Purposes Only
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Next Steps•
Continue to provide in-services for inpatient units to increase compliance of Pneumococcal and Influenza vaccination screening and administration
•
Continue to monitor effectiveness of vaccination screening on admission data base.
•
Continue individual nurse specific reports for vaccine screening and administration on a bi-weekly basis.
•
Identify physician champion.
Confidential: For Quality Improvement Purposes Only
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HEART FAILURE
TEAM MEMBERSHIPDEPARTMENTS OF CARDIOLOGY, CARDIOVASCULAR SURGERY, MEDICINE, NURSING, QUALITY AND RESOURCE MANAGEMENT,
THE CENTER FOR CLINICAL EFFECTIVENESS, MEDICAL RECORDS, INFORMATION TECHNOLOGIES/EPIC
PROJECT COORDINATORCARMEN BARC, RN TABLE 8
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AIM STATEMENT
Improve the quality of care for heart failure patients by providing evidence- based treatment as outlined in the Heart Failure Core Measures 100% of the time
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Heart failure accounts for more hospital admissions than any other Medicare diagnosis. Research shows that the following care processes decrease morbidity and mortality rates for heart failure patients*:
Left ventricular systolic function (LVSF) assessment
Angiotensin converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) prescribed for left ventricular systolic dysfunction (LVSD). Ejection fraction (EF) <40% or description of moderate/severe dysfunction.
Written discharge instructions regarding activity, diet, follow-up, medications, what to do if heart failure symptoms worsen, and weight monitoring
Smoking cessation counseling for patients who have smoked within the last twelve months
*Heart Failure Society of America. HFSA 2006 Comprehensive Heart Failure Practice Guideline
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FORCES OF MAGNETISM
Force 6: Quality of CareForce 7: Quality ImprovementForce 9: AutonomyForce 11: Nurses as TeachersForce 13: Interdisciplinary
Relationships
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2009 INTERVENTIONSUpdated the EPIC discharge navigator to include the new discharge instructions requirement for what to do if heart failure symptoms worsen
Revised the discharge appointment element to be required and prechecked in the EPIC Medicine and CV discharge order sets
Smoking cessation counseling removed from the discharge order set and incorporated into the EPIC discharge instructions report.
Nursing developed “smart text” for documentation of heart failure patient education
Provided practitioner specific feedback
Heart failure patient lists made available on the portal
Inservices to nursing units and internal medicine residents
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NEXT STEPSRemove discharge instructions regarding weight monitoring and what to do if symptoms worsen from the discharge order set and incorporate them into the EPIC discharge instruction report.
Standardize nursing “smart text” for documentation of heart failure patient education
Provide midyear follow-up to internal medicine residents as a group
Add patient diagnosis to physician feedback reports
Ongoing nursing and physician education
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Hospital Outpatient Quality Data Reporting Program
(HOP QDRP)
Team Members:Anesthesia
Same Day SurgeryMain Operating Room
Labor & DeliveryNursing Education
Electrophysiology
LabUrology Outpatient DepartmentCenter for Clinical Effectiveness
National Hospital Quality Measures
TABLE 9
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FORCES OF MAGNETISM
Force 6: Quality of Care
Force 7: Quality Improvement
Force 8: Consultation and Resources
Force 11: Nurses as Teachers
Force 13: Interdisciplinary Relationships
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AIM STATEMENT
Surgical site infections (SSI) are one of the most common causes
of postoperative morbidity and mortality in surgical patients.1
The HOP QDRP is modeled after the established Surgical Care Improvement Project that focuses on surgical in-patients. This project’s guiding principles aimed at preventing surgical site infections are timely administration of
prophylactic antibiotics within one hour of incision and the proper use of recommended prophylactic antibiotics.
Nguyen, N., Yegiyants, S., Kaloostian, C., et al. The surgical care improvement project (SCIP) initiative to reduce infection in elective colorectal surgery: which performance measures affect outcome? The American Surgeon 2008; 74:1012-1016.
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QUALITY MEASURES
Timing of Antibiotic ProphylaxisAntibiotic administration within one hour prior to surgical incision
Selection of Prophylactic AntibioticOver 200 Procedure Codes Types of Surgeries:
Cardiac: Pacemaker revisions, battery change-outsVascular: graftsGenitourinary: Transrectal prostate biopsyGastric biliary: peg placements, laparoscopic appendectomy Gynecology: Vaginal hysterectomy, synthetic pubovaginal slingHead and Neck: Treatment of jaw fractures
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2009 INTERVENTIONS
Partnered with Nursing Education to abstract charts
Educated nurse abstractors on project specifications and data abstraction
Provided inservices
to Outpatient Urology, Same Day Surgery and EP Lab regarding the project and identification of opportunities for improvement
Placement of EPIC smart text in the outpatient urology nursing note to document antibiotics taken the morning of procedures
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Definition: Correct antibiotic selection for procedure Data Source: Data abstracted from LUMC charts by RNs
Analysis: Significant improvement realized after implementation
of smart text in urology nursing note documenting antibiotics taken morning of procedure.
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Definition: Documentation that an antibiotic was initiated within 60 minutes (120 minutes for Vancomycin
or Quinolones) prior to surgical incision/procedure start timeData Source: Data abstracted from LUMC charts by RNs
Analysis: Performance remains consistent at 84%. Improvement anticipated with planned 2010 interventions
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NEXT STEPS
Creation of physician-specific reports
Follow-up with departments and physicians regarding outliers, opportunities for improvement and celebrate successes
Report to key stakeholders
Re-education of data abstractors to changing specifications
Team meetings to review results
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Making Surgery Safer:Making Surgery Safer: Surgical Infection Prevention
Team Members:Dr. W. Jellish, Dr. P. O’Keefe, Dr. J. Parada, M. Altier, C. Barc, J. Bredemeyer, M. Fitzgerald, M. Kawka, J. Keane, D. Marra, C. Schriever, D. Serwa, S. Swanson, A. Tomich, L. Vis, M. Wall:Magnet Forces: 6 - Quality of Care7 - Quality Improvement13 - Interdisciplinary Relationships
Confidential: For Quality Improvement Purposes Only
TABLE 10
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Aim StatementAim StatementThe Surgical Care Improvement Project (SCIP) is a national quality partnership of organizations interested in improving surgical care by significantly reducing surgical complications, specifically surgical site infection, venous thrombo-embolism, and acute myocardial infarction. Loyola’s performance for these measures is publicly reported at:– CMS: www.hospitalcompare.hhs.gov– JOINT COMMISION: www.qualitycheck.org– IDPH: www.healthcarereportcard.illinois.gov
Confidential: For Quality Improvement Purposes Only
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Project GoalsProject GoalsTO ACHIEVE TOP DECILE PERFORMANCE NATIONALLY FOR THE FOLLOWING
MEASURES:
• SSI Measures:• Antibiotic within 60 minutes of surgical incision• Appropriate antibiotic selection• Discontinuation of antibiotics within 24 hours after surgery• Post-operative Glucose control for cardiac surgery patients• Appropriate hair removal• (new) Postoperative temperature control for all surgeries lasting greater than 60 minutes• (new) Removal of urinary catheter by the end of post-op Day 2
• VTE Measures: • VTE prophylaxis ordered• VTE prophylaxis received
• AMI Measures:• Perioperative beta-blocker administration
•Confidential: For Quality Improvement Purposes Only
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Solutions Implemented in 2009Solutions Implemented in 20092009 Overall Improvement Activities Included:
1. Comprehensive review/analysis of all outliers
2. Physician-specific reports sent to MD’S
3. Evaluated impact of 2 new measures
4. Antibiotic selection• MRSA screen results added to Anesthesia Record
5. Beta-Blocker Documentation• Prompt added to Pre-Op Checklist• “Last Taken” prompt added with New Epic Medication Reconciliation Tools• Staff Education• Created SAC Manager Portal Report to track compliance
6. SSI is now a National Patient Safety Goal• E-learning module created for staff• Infection Control Practitioner’s monitor post-op SSI rates
Confidential: For Quality Improvement Purposes Only
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Confidential: For Quality Improvement Purposes Only
Definition: Surgical patients receiving 100% of indicated antibiotic prophylaxis, glucose control, hair removal, temperature control, beta-blocker continuation, and venous thromboembolism therapy / Patients undergoing CABG, cardiac surgery, hip / knee arthroplasty, colon surgery, hysterectomy, or vascular surgery.Data source: LUMC medical records abstracted by RNs. Analysis: Recent results are consistent with eighty-four percent of selected surgical patients are receiving all indicated care to prevent surgical infections. This performance has recently decreased due to performance on the perioperative beta-blocker medication measure. Education regarding documentation has been provided to improve this performance.
Per
cent
Core MeasuresSurgical Care Improvement Project Composite Performance
Month (number of patients)
UCL = 99.7
Mean = 83.5
LCL = 67.4
Apr 2
008 (
n=54
)May
2008
(n=5
0)Ju
n 200
8 (n=
51)
Jul 2
008 (
n=50
)Au
g 20
08 (n
=54)
Sep
2008
(n=4
8)Oct
2008
(n=5
1)Nov
2008
(n=5
1)Dec
2008
(n=4
5)Ja
n 200
9 (n=
52)
Feb 2
009
(n=48
)Mar
2009
(n=4
8)Ap
r 200
9 (n=
45)
May 20
09 (n
=51)
Jun 2
009 (
n=47
)Ju
l 200
9 (n=
51)
Aug
2009
(n=5
1)Se
p 20
09 (n
=45)
Oct 20
09 (n
=51)
Nov 20
09 (n
=49)
Dec 20
09 (n
=51)
Jan 2
010 (
n=46
)Fe
b 201
0 (n=
5)
0
20
40
60
80
100
120
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Confidential: For Quality Improvement Purposes Only
Definition: Surgical patients who received prophylactic antibiotics within 60 minutes prior to surgical incision / Patients undergoing CABG, cardiac surgery, hip / knee arthroplasty, colon surgery, hysterectomy, or vascular surgery. Vancomycin and fluoroquinolonestimeframe is extended to 120 minutes prior to incision.Data source: LUMC medical records abstracted by RNs. Analysis: Ninety-seven percent of LUMC patients receive prophylactic antibiotics within the recommended timeframe prior to surgical incision. August 2009 shows an significant change (more) outlier cases have been actively review by clinicians.
Per
cent
Surgical patients receiving prophylactic antibioticswithin one hour prior to surgical incision
Month (number of patients)
UCL = 106.5
Mean = 96.9
LCL = 87.2
Apr 2
008 (
n=29
)May
2008
(n=2
5)Ju
n 200
8 (n=
32)
Jul 2
008 (
n=25
)Au
g 20
08 (n
=33)
Sep
2008
(n=3
4)Oct
2008
(n=3
3)Nov
2008
(n=2
9)Dec
2008
(n=2
5)Ja
n 200
9 (n=
34)
Feb 2
009
(n=35
)Mar
2009
(n=2
9)Ap
r 200
9 (n=
29)
May 20
09 (n
=30)
Jun 2
009 (
n=33
)Ju
l 200
9 (n=
28)
Aug
2009
(n=3
0)Se
p 20
09 (n
=28)
Oct 20
09 (n
=27)
Nov 20
09 (n
=34)
Dec 20
09 (n
=35)
Jan 2
010 (
n=32
)Fe
b 201
0 (n=
3)
0
20
40
60
80
100
120
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Confidential: For Quality Improvement Purposes Only
Definition: Surgical patients receiving prophylactic antibiotics consistent with current guidelines / Patients undergoing CABG, cardiac surgery, hip / knee arthroplasty, colon surgery, hysterectomy, or vascular surgery.
Data source: LUMC medical records abstracted by RNs.
Analysis: Ninety-seven percent of LUMC patients receive prophylactic antibiotics consistent with current guidelines.
Per
cent
Surgical patients receiving prophylactic antibioticsconsistent with current guidelines
Month (number of patients)
UCL = 106.3
Mean = 97.2
LCL = 88.2
Apr 2
008 (
n=30
)May
2008
(n=2
5)Ju
n 200
8 (n=
32)
Jul 2
008 (
n=28
)Au
g 20
08 (n
=35)
Sep
2008
(n=3
4)Oct
2008
(n=3
2)Nov
2008
(n=2
8)Dec
2008
(n=2
4)Ja
n 200
9 (n=
32)
Feb 2
009
(n=33
)Mar
2009
(n=2
8)Ap
r 200
9 (n=
28)
May 20
09 (n
=27)
Jun 2
009 (
n=33
)Ju
l 200
9 (n=
28)
Aug
2009
(n=2
8)Se
p 20
09 (n
=27)
Oct 20
09 (n
=25)
Nov 20
09 (n
=33)
Dec 20
09 (n
=35)
Jan 2
010 (
n=32
)Fe
b 201
0 (n=
3)
0
20
40
60
80
100
120
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Confidential: For Quality Improvement Purposes Only
Definition: Surgical patients with prophylactic antibiotics discontinued within twenty-four hours after surgery end time / Patients undergoing hip / knee arthroplasty, colon surgery, hysterectomy, or vascular surgery. CABG and other cardiac surgeries are allowed 48 hours.
Data source: LUMC medical records abstracted by RNs.
Analysis: Performance is consistently above 90%.
Per
cent
Surgical patients with prophylactic antibioticsdiscontinued within the recommended timeframe
Month (number of patients)
UCL = 106.6
Mean = 96.9
LCL = 87.2
Apr 2
008 (
n=29
)May
2008
(n=2
4)Ju
n 200
8 (n=
32)
Jul 2
008 (
n=25
)Au
g 20
08 (n
=33)
Sep
2008
(n=3
4)Oct
2008
(n=3
2)Nov
2008
(n=2
8)Dec
2008
(n=2
4)Ja
n 200
9 (n=
32)
Feb 2
009
(n=33
)Mar
2009
(n=2
8)Ap
r 200
9 (n=
28)
May 20
09 (n
=27)
Jun 2
009 (
n=33
)Ju
l 200
9 (n=
28)
Aug
2009
(n=2
8)Se
p 20
09 (n
=27)
Oct 20
09 (n
=25)
Nov 20
09 (n
=33)
Dec 20
09 (n
=35)
Jan 2
010 (
n=32
)Fe
b 201
0 (n=
3)
0
20
40
60
80
100
120
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Confidential: For Quality Improvement Purposes Only
Per
cent
of C
ardi
ac S
urge
ry P
atie
nts
with
Con
trol
led
Pos
tope
rativ
e G
luco
se Controlled Postoperative Serum Glucose - Cardiac Surgery Patients
Month (number of patients)
UCL = 116.0
Mean = 93.5
LCL = 71.1
Apr 2
008
(n=1
2)M
ay 20
08 (n
=11)
Jun
2008
(n=1
3)Ju
l 200
8 (n
=11)
Aug 2
008
(n=1
1)Se
p 200
8 (n
=12)
Oct 20
08 (n
=12)
Nov 2
008
(n=1
0)Dec
200
8 (n
=12)
Jan
2009
(n=1
3)Fe
b 20
09 (n
=11)
Mar
2009
(n=1
0)Ap
r 200
9 (n
=9)
May
2009
(n=1
3)Ju
n 20
09 (n
=12)
Jul 2
009
(n=1
1)Au
g 200
9 (n
=11)
Sep 2
009
(n=1
1)Oct
2009
(n=9
)Nov
200
9 (n
=11)
Dec 2
009
(n=1
2)Ja
n 20
10 (n
=10)
Feb
2010
(n=1
)
0
20
40
60
80
100
120
140
160
Definition: Percent of cardiac surgery patients with controlled 6AM post-operative glucose. Control is defined as serum glucose reading of 200mg/dL or less on both post-operative day 1 and day 2. Results show cardiac surgery patients with the presence of post-operative day 1 and day 2 glucose measurements, readings closest to 6AM were selected for inclusion.
Data Source: LUMC medical records abstracted by RNs.
Analysis: 6AM postoperative glucose control on both postoperative days 1 and 2 has been consistent at 94%. All outlier cases are shared with clinicians.
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Confidential: For Quality Improvement Purposes Only
Per
cent
of S
urge
ry P
atie
nts
with
App
ropr
iate
Hai
r R
emov
al
Surgical Patients with Appropriate Hair Removal - (Not Razors)
Month (number of patients)
UCL = 102.3Mean = 99.6LCL = 97.0
Apr 2
008
(n=5
4)M
ay 20
08 (n
=50)
Jun
2008
(n=5
1)Ju
l 200
8 (n
=50)
Aug 2
008
(n=5
4)Se
p 200
8 (n
=48)
Oct 20
08 (n
=51)
Nov 2
008
(n=5
1)Dec
200
8 (n
=45)
Jan
2009
(n=5
2)Fe
b 20
09 (n
=48)
Mar
2009
(n=4
8)Ap
r 200
9 (n
=45)
May
2009
(n=5
1)Ju
n 20
09 (n
=47)
Jul 2
009
(n=5
1)Au
g 200
9 (n
=51)
Sep 2
009
(n=4
5)Oct
2009
(n=4
4)Nov
200
9 (n
=48)
Dec 2
009
(n=4
6)Ja
n 20
10 (n
=43)
Feb
2010
(n=5
)
0
20
40
60
80
100
Definition: Number of Surgical cases abstracted without the use of razors for hair removal / Number of Surgical Cases Sampled. Appropriate hair removal includes: use of clippers, use of depilatory, or no hair removal.
Data source: LUMC medical records abstracted by RNs.
Analysis: Performance is consistently near 100%.
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Confidential: For Quality Improvement Purposes Only
Per
cent
of S
urge
ry P
atie
nts
with
Per
iope
rativ
e Tem
pera
ture
Man
agem
ent Surgery Patients with Perioperative Temperature Management
Month (number of patients)
Oct
200
9 (n
=38)
Nov 2
009
(n=33
)
Dec 2
009
(n=38
)
Jan
2010
(n=3
6)
Feb 2
010
(n=4
)
0
20
40
60
80
100
Definition: The percent of patients who had either active warming applied intraoperatively, or who had at least one body temperature equal to or greater than 36 degrees Celsius (recorded within 30 before or 15 minutes after anesthesia end time).
Data source: LUMC medical records abstracted by RNs.
Analysis: This is a new measure. Performance has been in the high 90%’s.
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Confidential: For Quality Improvement Purposes Only
Per
cent
of S
urge
ry P
atie
nts
with
VTE
Pro
phyl
axis
Ord
ered
Surgery Patients with Recommended Venous Thromboembolism Prophylaxis Ordered
Month (number of patients)
UCL = 109.4
Mean = 96.8
LCL = 84.2
Apr 2
008
(n=3
3)M
ay 20
08 (n
=30)
Jun
2008
(n=3
0)Ju
l 200
8 (n
=29)
Aug 2
008
(n=3
2)Se
p 200
8 (n
=28)
Oct 20
08 (n
=16)
Nov 2
008
(n=1
3)Dec
200
8 (n
=12)
Jan
2009
(n=1
3)Fe
b 20
09 (n
=15)
Mar
2009
(n=1
5)Ap
r 200
9 (n
=14)
May
2009
(n=1
7)Ju
n 20
09 (n
=14)
Jul 2
009
(n=1
4)Au
g 200
9 (n
=14)
Sep 2
009
(n=1
4)Oct
2009
(n=1
3)Nov
200
9 (n
=14)
Dec 2
009
(n=1
3)Ja
n 20
10 (n
=10)
Feb
2010
(n=2
)
60
70
80
90
100
110
120
130
Definition: Number of surgery cases in which orders were placed for appropriate measure to prevent venous thromboembolism(VTE; blood clots in legs or lungs) / Patient undergoing intracranial neurosurgery, elective spinal surgery, general surgery, gynecologic surgery, urologic surgery, elective total hip or knee replacement, or hip fracture surgery.
Data source: LUMC medical records abstracted by RNs.
Analysis: The rate of ordering recommended measures to prevent VTE averages 97%. Feedback has been provided to physicians on an ongoing basis.
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Confidential: For Quality Improvement Purposes Only
Per
cent
of S
urge
ry P
atie
nts
with
VT
E P
roph
ylax
is R
ecei
ved
Surgery Patients with Recommended Venous Thromboembolism Prophylaxis Received
Month (number of patients)
UCL = 111.0
Mean = 94.0
LCL = 77.1
Apr 2
008
(n=33
)May
2008
(n=3
0)Ju
n 20
08 (n
=30)
Jul 2
008
(n=29
)Au
g 20
08 (n
=32)
Sep
2008
(n=2
8)Oct
2008
(n=1
6)Nov
200
8 (n=
13)
Dec 2
008
(n=10
)Ja
n 20
09 (n
=13)
Feb
2009
(n=1
5)M
ar 20
09 (n
=15)
Apr 2
009
(n=14
)May
2009
(n=1
7)Ju
n 20
09 (n
=14)
Jul 2
009
(n=14
)Au
g 20
09 (n
=14)
Sep
2009
(n=1
4)Oct
2009
(n=1
3)Nov
200
9 (n=
14)
Dec 2
009
(n=13
)Ja
n 20
10 (n
=10)
Feb
2010
(n=2
)
40
60
80
100
120
140
Definition: Number of surgery cases receiving recommended measures to prevent venous thromboembolism (VTE) / Patient undergoing intracranial neurosurgery, elective spinal surgery, general surgery, gynecologic surgery, urologic surgery, elective total hip or knee replacement, or hip fracture surgery.
Data source: LUMC medical records abstracted by RNs.
Analysis: The rate of administering recommended VTE preventive measures (prophylaxis) is consistent at 95%.
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Confidential: For Quality Improvement Purposes Only
Per
cent
of S
urge
ry P
atie
nts
Con
tinui
ng B
eta-
Blo
cker
s P
erio
pera
tivel
y
Continuing Beta-Blockers Perioperatively to Prevent Myocardial Infarction
Month (number of patients)
UCL = 109.4
Mean = 84.9
LCL = 60.5
Apr 2
008
(n=2
5)M
ay 20
08 (n
=22)
Jun
2008
(n=2
0)Ju
l 200
8 (n
=18)
Aug
2008
(n=2
5)Se
p 20
08 (n
=22)
Oct 20
08 (n
=16)
Nov 2
008
(n=1
4)Dec
200
8 (n
=19)
Jan
2009
(n=2
7)Fe
b 20
09 (n
=22)
Mar
200
9 (n=
18)
Apr 2
009
(n=2
3)M
ay 20
09 (n
=13)
Jun
2009
(n=1
5)Ju
l 200
9 (n
=19)
Aug
2009
(n=1
9)Se
p 20
09 (n
=22)
Oct 20
09 (n
=15)
Nov 2
009
(n=2
7)Dec
200
9 (n
=21)
Jan
2010
(n=2
0)Fe
b 20
10 (n
=2)
20
40
60
80
100
120
140
160
Definition: Number of surgery cases receiving beta-blocker (medication to slow heart rate) during the peri-operative period / Patient undergoing major surgery who received beta-blocker therapy prior to admission. This treatment is designed to reduce the risk of myocardial infarction (heart attack) following surgery.
Data source: LUMC medical records abstracted by RNs.
Analysis: LUMC performance decreased significantly due to lack of documentation of pre-operative beta-blocker dose information (time taken). Education has been provided regarding complete documentation of medications taken before admission and improvement have begun in July 2009.
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Confidential: For Quality Improvement Purposes Only
Per
cent
of S
urge
ry P
atie
nts
with
Cat
hete
rs R
emov
ed P
OD
1 or
PO
D2
Urinary Catheter Removed on POD1 or POD2
Month (number of patients)
Oct
200
9 (n
=25)
Nov 2
009
(n=23
)
Dec 2
009
(n=24
)
Jan
2010
(n=2
5)
Feb 2
010
(n=3
)
0
20
40
60
80
100
Definition: Number of surgery cases where the urinary catheter is removed by the end of post-operative day 2 out of all eligible patients. Patients are excluded from this measure automatically if they are in the ICU with diuretics, or if the procedure was urological, gynecological or perineal .
Data source: LUMC medical records abstracted by RNs.
Analysis: This is a new measure. Performance is recently in the high 90%’s.
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Next StepsNext Steps
• Outlier review and analysis• Identify improvement opportunities for
the two new measures based on initial results
• Foley removal• Peri-Op Temperature
• Implement staff, physician, and patient education on SSI reduction
Confidential: For Quality Improvement Purposes Only
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Departments: Pediatrics, Pediatric Critical Care,Medical Center Information Systems and
Center for Clinical Effectiveness
Lindy Champa, BSN, RNKathleen Webster, MD Matthew Leischner, MDMichael Wall, PharmD, MBAConnie Giere, BSN, RNSandra Swanson, BSN, RN, MSOD Jacqulene Camerino, BSN, RN Cindi La Porte, BSN RN
Confidential: For quality improvement purposes only.
ChildrenChildren’’s Asthma Care s Asthma Care Core MeasureCore Measure
TABLE 11
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Project AimsTo provide quality and effective care to children with asthmaTo provide education for all pediatric patients and their families with the primary diagnosis of asthmaTo utilize evidence based medicineTo meet the Joint Commission Association Core Measure for Children’s Asthma with 100% compliance
.
Children’s Asthma Care Core Measure
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Children’s Asthma Care Core Measure
The Joint Commission launched project activities to examine Children’s Asthma performance measures for
inclusion in theORYX® performance measurement initiative. This work was conducted in collaboration with national children’s health care organizations, particularly, the National Association of Children’s Hospitals and Related Institutions (NACHRI), Child
Health Corporation of America (CHCA), and Medical Management Planning, Inc. (MMP)
Magnet Forces of MagnetismForce 7: Quality Improvement
Confidential: For quality improvement purposes only.
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Children’s Asthma Care Core Measure• JCA introduced three measures for implementation effective April 1, 2007:
CAC - 1 Use of Relievers for Inpatient Asthma CAC - 2 Use of Systemic Corticosteroids for Inpatient Asthma CAC - 3 Home Management Plan of Care Given to Patient/Caregiver
• Data collection for the measure set began with April 2007 discharges. CAC-3 was implemented as a test measure pending National Quality Forum (NQF) endorsement. Although included on the hospital’s ORYX Performance Measure Report, data analysis for CAC-3 was not used in the accreditation process or publicly reported on Quality Check.
• The CAC-3 measure has now been endorsed by the NQF and was implemented as a production measure effective with July 1, 2008 discharges. (JCA)
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Children’s Asthma Care Core Measure
• Percent of pediatric inpatients who: – are given Reliever Medication – are given Systemic Corticosteroids– receive a Home Management Plan of Care that is a separate
document and includes identification of asthma triggers and use of rescue, controller and reliever medication
Confidential: For quality improvement purposes only.
What are we measuring
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• A Pediatric Asthma education board was placed in residents work area in May that showed:• How to find a “Pediatric” Asthma Action Plan• Identified the 3 components of the pediatric asthma care core measure that should be included.• Also included the 6 components for the Pediatric Asthma Home Management Plan of Care• Incoming residents would have this board to refer too for each months rotation.• Identified in Epic that the Asthma Action Plan (adult) comes up before the
Pediatric AAP in the EPIC listing.• This led to a concern that the Adult Asthma Action Plan came under the listing Asthma Action
Plan so the Peds Core Measurement team asked if the Pediatric Asthma Action Plan could come before the Asthma Action Plan and Indicate it as:
• Asthma Action Plan (Pediatric) then Asthma Action Plan ( Adult) respectively• Confidential: For quality improvement purposes only.
Children’s Asthma Care Core Measure Changes that we made:
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• Now the residents will have first access to the Pediatric Asthma Action Plan in EPIC
• Also upon reviewing the data the Asthma Action Plan Adult did not have a page break so the Peds Core Measure team asked Connie Giere’s team to do the same for the adult asthma action plan with a page break. 12/2/09
• Lindy spoke with the Chief Resident Rajiv Kumar about next steps with education and the resident impact on the Pediatric Asthma Action Plan.
• After data collected and the discharge MD’s (residents) were noted Not to have a asthma action plan pediatric they were sent a letter with copies to Dr. Leischner, Dr. Kumar and Dr. Webster to share the importance of selection of the AAP Pediatric for their patients.
Audited records of discharge MD, RN and attending for those without AAP.
• All RN staff educated not to discharge Asthmatic patients or Reactive Airway patients without a AAP-Pediatric
• Confidential: For quality improvement purposes only.
Children’s Asthma Care Core Measure Changes that we made:
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• We continue to see 100% compliance with the use of relievers and the use of corticosteroids during hospitalization.
• 100% of those patients received Relievers and Systemic Corticosteroids during their hospitalization.
• Number of cases that met all 6 requirements: 59/80= 74% compliance • (pediatric and adult AAPs)• The monthly breakdown below that • October: 15/25= 60%• November: 17/19=89%• December: 12/16=75%• January: 5/9 = 56%• February: 10/11= 90%• Number of cases that were not separate: • Peds: (AAP-Pediatric before 8/10/09) = 0 cases• Adult: (AAP-Adult not separate until 12/2/09) =5/60 = 8.3%• Number of cases that did not have an AAP: 11/60= 18.3%
Confidential: For quality improvement purposes only.
Children’s Asthma Care Core Measure Results:
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Children’s Asthma Care Core Measure Data Tool
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Children’s Asthma Care Core Measure Data Tool
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Per
cent
Core MeasuresChildren's Asthma Care - Composite Score
Month
UCL = 83.9
Mean = 41.6
LCL = 0.0
Apr 20
08 (n=1
2)May
2008
(n=12
)Ju
n 200
8 (n=
3)Ju
l 200
8 (n=5
)Aug
2008
(n=1
2)Sep
2008
(n=2
8)Oct
2008 (
n=22)
Nov 20
08 (n
=13)
Dec 20
08 (n
=3)
Jan 2
009 (
n=6)
Feb 20
09 (n
=7)Mar
2009
(n=12
)Apr
2009 (
n=7)
May 20
09 (n
=15)
Jun 2
009 (
n=5)
Jul 2
009 (
n=5)
Aug 20
09 (n
=13)
Sep 20
09 (n
=26)
Oct 20
09 (n=2
4)Nov
2009
(n=1
8)Dec
2009
(n=1
6)Ja
n 201
0 (n=
5)
0
20
40
60
80
100
120
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Per
cent
Children's Asthma Care - Home Management Plan of Care
Month
UCL = 83.2
Mean = 41.1
LCL = 0.0
Apr 20
08 (n=1
3)May
2008
(n=12
)Ju
n 200
8 (n=
4)Ju
l 200
8 (n=5
)Aug
2008
(n=1
2)Sep
2008
(n=2
8)Oct
2008 (
n=22)
Nov 20
08 (n
=13)
Dec 20
08 (n
=3)
Jan 2
009 (
n=6)
Feb 20
09 (n
=7)Mar
2009
(n=12
)Apr
2009 (
n=7)
May 20
09 (n
=15)
Jun 2
009 (
n=5)
Jul 2
009 (
n=5)
Aug 20
09 (n
=13)
Sep 20
09 (n
=26)
Oct 20
09 (n=2
4)Nov
2009
(n=1
8)Dec
2009
(n=1
6)Ja
n 201
0 (n=
4)
0
20
40
60
80
100
Peds RN data collectors
MD’s / RN education
CAC Asthma Home plan separat
CAC Asthma plan moved aboveadult Asthma plan in EPIC
Adult Asthma plan separated too
RN’s checking problem list
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Per
cent
Children's Asthma Care - Use of Relievers
Month
Apr 20
08 (n=1
3)May
2008
(n=12
)Ju
n 200
8 (n=
4)Ju
l 200
8 (n=5
)Aug
2008
(n=1
2)Sep
2008
(n=2
8)Oct
2008 (
n=22)
Nov 20
08 (n
=13)
Dec 20
08 (n
=3)
Jan 2
009 (
n=6)
Feb 20
09 (n
=7)Mar
2009
(n=12
)Apr
2009 (
n=7)
May 20
09 (n
=15)
Jun 2
009 (
n=5)
Jul 2
009 (
n=5)
Aug 20
09 (n
=13)
Sep 20
09 (n
=26)
Oct 20
09 (n=2
4)Nov
2009
(n=1
8)Dec
2009
(n=1
6)Ja
n 201
0 (n=
5)
0
20
40
60
80
100
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Per
cent
Children's Asthma Care - Use of Systemic Corticosteroids
Month
Apr 20
08 (n=1
2)May
2008
(n=12
)Ju
n 200
8 (n=
3)Ju
l 200
8 (n=5
)Aug
2008
(n=1
2)Sep
2008
(n=2
8)Oct
2008 (
n=22)
Nov 20
08 (n
=13)
Dec 20
08 (n
=3)
Jan 2
009 (
n=6)
Feb 20
09 (n
=7)Mar
2009
(n=12
)Apr
2009 (
n=7)
May 20
09 (n
=15)
Jun 2
009 (
n=5)
Jul 2
009 (
n=5)
Aug 20
09 (n
=13)
Sep 20
09 (n
=26)
Oct 20
09 (n=2
4)Nov
2009
(n=1
8)Dec
2009
(n=1
6)Ja
n 201
0 (n=
5)
0
20
40
60
80
100
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Next Steps• Continue to monitor LUMC records for meeting the core measure.• Continue to monitor asthma core measure compliance.• Continue to provide asthma education to patients, families and staff.• Discuss with the physicians the changes that have been made in EPIC to ensure the
correct AAP-Pediatric is chosen and to make sure the AAP-Pediatric includes the 6 components of the home management plan of care and the 3 other components of the Pediatric Asthma Core Measure.
• Talk with Connie Giere in Epic to see if the discharge instructions could pull the discharge diagnosis of “Asthma” so the staff RN would know to ensure that an Asthma Action plan was completed and given to the patient
• Have the RN’s look at the problem list concurrently with the discharge instructions to see if a discharge diagnosis was asthma or reactive airway disease which would result in needing a Home Asthma Action Plan
Confidential: For quality improvement purposes only.
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Acute Myocardial Infarction (AMI)
• Team Members: – B. Majcher, MSN, CV, CNS, C. Mulhall, MSN, CV, CNS – M. Jarotkiewicz, MBA, – Director of Cardiovascular Line - D. Wilber, MD, K. McLean, MD, – Director of Emergency Medicine - M. Cichon, MD, – Director of Cardiac Cath Lab - F. Leya, MD, – Director of Interventional Cardiology Research - J. Lopez, MD,
Michelle Fennessy, Adult Nurse Practitioner – Nursing Staff of 3 NEWS, 5 Tower, CCU, HTU, Emergency
Department, Cardiac Cath Lab, Medical Records Department, Information Technology Department, and Center for Clinical Effectiveness.
Force of Magnetism Force 1: Quality ImprovementForce 13: Interdisciplinary Relationships
TABLE 12
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• Optimal treatment of ST elevated Myocardial Infarction (STEMI) or left bundle branch block (LBBB) patients withPercutaneous Coronary Intervention (PCI) within 90 minutes door-to- balloon inflation.
• Since May 2002 LUMC has been reporting performance on Acute Myocardial Infarction (AMI) patients for Core Measures.
• These Core Measures, developed by the Joint Commission and the Center for Medicare and Medicaid Services (CMS), examine the care of all Acute Myocardial Infarction patients.
• The Core Measures are based on guidelines established by the American Heart Association (AHA) and the American College of Cardiology (ACC).
Project Aim Statement
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• In March 2009, LUMC announced, Heart Attack Rapid Response Team (HARRT)
• Nurse Practitioner evaluates the process and timing of the patient’s arrival in the Emergency Department and provides timely feedback to the departments and municipalities involved in the care of the ST elevated Myocardial Infarction (STEMI) patient
• Monthly STEMI committee meetings review all ST elevated Myocardial Infarction (STEMI) cases, a process to find ways to improve the care of the AMI patient; and to use this review process to acknowledge when things are done well.
Solutions Implemented
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Solutions Continued
• The ED has ongoing training with local municipalities to help interpret ST elevated Myocardial Infarction (STEMI) cases in the field.
• Annually educate all physicians on the components of Acute Myocardial Infarction Core Measures data.
• In January 2007 stage 2 triage initiated in the Emergency Department to expedite Electrocardiogram (ECG) process.
• In June 2007 coordinated accuracy of clock times with Emergency Department, Cardiac Catheterization Laboratory and Call Connection Center. In addition the concept of Code STEMI was discussed.
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Solutions Continued• On a daily basis every newly admitted ST elevated Myocardial
Infarction (STEMI)/ Left Bundle Branch Block (LBBB) case is reviewed by Cardiovascular Clinical Nurse Specialist. This involves looking at time arrival, initial Electrocardiogram, Aspirin in 24 hours, cardiac cath report, changes in patient’s severity and planned discharge date.
• Developed outlier reports in order to improve and inform each physician on corrections to be made.
• January 2009 met with Information Technology Department representative to generate bi-weekly reports of ST elevated Myocardial Infarction (STEMI)/ Left Bundle Branch Block (LBBB) patients that would allow expediting care in a more timely manner.
• September 2009 began a daily review of all inpatient elevated troponin levels within the LUMC system.
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Solutions Continued
• On discharge each Acute Myocardial Infarction patient’s chart and discharge summary has been reviewed and assessed by Cardiovascular Clinical Nurse Specialist for accurate documentation of Acute Myocardial Infarction information and discharge medications.
• Physician review is included on all expired patients or when documentation is unclear.
• Report quarterly to the Nursing Quality & Safety Council on Acute Myocardial Infarction (AMI) core measure outcomes.
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ResultsP
erce
nt
Core MeasuresAcute Myocardial Infarction Composite Score
Month
UCL = 114.1
Mean = 93.4
LCL = 72.8
Oct 20
07 (n=1
2)
Nov 20
07 (n
=14)
Dec 20
07 (n
=18)
Jan 2
008 (
n=11
)
Feb 20
08 (n
=10)
Mar 20
08 (n
=7)
Apr 20
08 (n=1
0)
May 20
08 (n
=6)Ju
n 200
8 (n=
8)
Jul 2
008 (
n=20)
Aug 20
08 (n
=14)
Sep 20
08 (n
=11)
Oct 20
08 (n=1
4)
Nov 20
08 (n
=11)
Dec 20
08 (n
=18)
Jan 2
009 (
n=14
)
Feb 20
09 (n
=9)
Mar 20
09 (n
=12)
Apr 20
09 (n=1
2)
May 20
09 (n
=15)
Jun 2
009 (
n=16
)
Jul 2
009 (
n=16)
Aug 20
09 (n
=14)
Sep 20
09 (n
=12)
Oct 20
09 (n=1
9)
Nov 20
09 (n
=12)
Dec 20
09 (n
=13)
Jan 2
010 (
n=9)
60
70
80
90
100
110
120
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ResultsP
erce
nt
Percutaneous Coronary Intervention Within 90 Minutes
Month
UCL = 159.2
Mean = 71.0
LCL = 0.0
Oct 20
07 (n=2
)Nov
2007
(n=4
)Dec
2007
(n=3
)Ja
n 200
8 (n=
2)Feb
2008
(n=2)
Mar 20
08 (n
=3)Apr
2008 (
n=2)
May 20
08 (n
=1)Ju
n 200
8 (n=
2)Ju
l 200
8 (n=2
)Aug
2008
(n=2
)Oct
2008 (
n=4)
Nov 20
08 (n
=3)
Dec 20
08 (n
=5)
Jan 2
009 (
n=1)
Feb 20
09 (n
=1)Mar
2009
(n=1)
Apr 20
09 (n=2
)Ju
n 200
9 (n=
1)Ju
l 200
9 (n=4
)Aug
2009
(n=4
)Sep
2009
(n=3
)Oct
2009 (
n=5)
Nov 20
09 (n
=1)
Dec 20
09 (n
=1)
Jan 2
010 (
n=1)
0
50
100
150
200
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Analysis
– In 2008, the Acute Myocardial Infarction composite score was 89.4%(a composite of all Acute Myocardial Infarction arrival and discharge measures)
– 2009 showed improvements with a composite score to date of 92.6%. The above control chart displays an improvement in outcomes;
– Since January of 2009 we have been at 100% in all months except for April & December 2009.
– Since January 2009 we have been at 100% of Percutaneous Coronary Intervention door to balloon time.
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Next Steps• Recommendations for Further Study or Action:
– Continue monthly ST elevated Myocardial Infarction (STEMI) committee meetings to evaluate the processes and address areas where delays occur.
– Continue Annual meetings with the physicians to educate them on Core Measure data points and proper documentation to see that these data points are met
– Educate nursing staff: schedule Bi-annual meetings to educate the Nursing Staff on 5 Tower and 3 NEWS on Core Measure Data points for the Acute Myocardial Infarction (AMI) patient’s.
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STROKE PERFORMANCE
MEASURES
TABLE 13
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Multidisciplinary Stroke TeamCORE STROKE TEAM
Jose Biller, MDJurate M. Platakis, RN, MSN
Neurologists Neurosurgeons Advance Practice NursesRima Dafer, MD Hazem Ahmed, MD Karen Potocki, APRN – BCMichael Schneck, MD Douglas Anderson, MD Stephen Roberts, APRN – BCJohn Whapham, MD Thomas Origitano, MD
Vikram Prabhu, MDNeurology Residents Neurosurgery Residents Ancillary Team MembersYeeshu Arora, MD John Braca, MD Matthew Eaton, ChaplainFarrukh Chaudhry, MD Ronald Hammers, MD Heather Morris, RD, LDNChandril Chugh, MD Dustin Hayward, MD Elizabeth Fries, MS, OTRLSara Hocker, MD Ahmad Khaldi, MD Martina Novotny, PharmacistAlejandro Hornik, MD Dawid Liniewski, MD Erin Mitchell, DPTRagasri Kumar, MD Nikhil Patel, MD Jenifer Belacastro, DPTSarkis Morales, MD Edward Perry, MD Stacy Scarpetti, MS, CCC-SLPChristopher Morgan, MD Phillip Toussaint, MD Nina Hossa, Social WorkerEva Pilcher, MD Diane Broadley, RNHussam Seif-Eddeine, MD Martha Martin, RNRajinder Singh, MD Michael Jarotkiewicz, ADAlexander Venizelos, MD CCEShawn Wallery, MD Lab, Cardiographics, Radiology
»
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• To “harmonize”/blend the AHA/ASA stroke guidelines into specificpatient care for all ischemic and hemorrhagic stroke patients toimprove quality of patient care and outcomes.
• To maintain Primary Stroke Center (PSC) Disease Specific Care (DSC)Certification through the Joint Commission.
• To sustain The Gold Plus Performance Achievement Award delegated by the AHA for achieving 85% or higher adherence to allharmonized measures for consecutive 12 month intervals.
Project Aim Statement
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Stroke, Guidelines for the Early Management of Patients With Ischemic Stroke: A Scientific Statement From the Stroke Council of the American Stroke Association. 2003:34;1056-1083Stroke, Guidelines for the Management of Aneurysmal Subarachnoid Hemorrhage: AStatement for Healthcare Professionals from a Special Writing Group of the Stroke Council, American Heart Association. 2009:40;994-1025
Magnet Forces of MagnetismForce 7: Quality Improvement
The organization has structures and processes for the measurement of quality and programs for improving the
quality of care and services within the organization.
To establish best practice from these guidelines through the collection, analysis and review of identified data elements via the AHA/ASA dataregistry and collection tool Get With the Guidelines (GWTG) of Outcome Sciences, Inc.
Aim Statement Continued
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ALL STROKE/TIA PATIENTS SHOULD HAVE IMAGING STUDIES AND EKG DONE ON ADMISSION IF NOT CURRENTLY AVAILABLE
Disease-specific care stroke performance measure set follows harmonization with data elements of the Paul Coverdell National Acute Stroke Registry and American Heart Association/American Stroke Association Get With The GuidelinesSM .
Disease-Specific Care Certification requirements for Primary Stroke Centers require data collection and reporting for all 8 measures in this set except for STK-7 and STK-9. Loyola’s stroke program will continue to monitor all 10.
January 2010
Set No.
Stroke Measure Ischemic
Stroke/TIA Hemorrhagic
Stroke STK-1 DVT Prophylaxis
▪ UF Heparin ▪ LMW Heparin ▪ SCD ▪ Other X X
STK-2 Discharged on Antithrombotic Therapy ▪ Antiplatelet ▪ Anticoagulant
X STK-3 Patients with Atrial Fibrillation Receiving Anticoagulation
Therapy ▪ UF Heparin ▪ Enoxaparin ▪ Warfarin ▪ Other
X
STK-4 Thrombolytic Therapy Administered ▪ Did the patient receive t-PA?
X STK-5 Antithrombotic Therapy by the end of Day 2
▪ Antiplatelet ▪ Anticoagulant X
Discharged on Cholesterol Reducing Medication ▪ Lipid Profile ▪ HA1C ▪ Statin ▪ Fibrate ▪ Niacin ▪ Other
X STK-6
▪ Nutrition consult ▪ Record anthropometric measurements Height, Weight and Abdominal Circumference
X X
STK-7 Dysphasia Screening ▪ Swallow screening and/or evaluation completed and documented
X X STK-8 Stroke Education
▪ Stroke Patient Education Form ▪ Stroke Education Packet ▪ Documentation in IP neuroscience nursing note ▪ Stroke Documentation Checklist
X X
STK-9 Smoking Cessation/Advice/Counseling ▪ Smoking Cessation Consult ▪ Noted on discharge order set
X X STK-10 Assessed for Rehabilitation
▪ Rehab service screening and/or consult noted and documented ▪PM&R X X
STROKE PERFORMANCE MEASURES(STK)
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– Revised and implemented Clinical Guidelines and Order Sets– Revised and implemented Neuroscience resident and nursing notes
to include critical documentation components– Revised Stroke Educational Materials and their distribution process
for staff, patients, families and the community
– Standardized swallow screening process– Maintain GWTG data base and analyze results – Enhanced Rapid Response to Acute Stroke Alerts– Increased collaboration between departments and disciplines to
enhance, support and standardize stroke care delivery– Facilitate multidisciplinary team rounding – Support participation in Acute and Preventative Stroke Trials– Engage professional and community activities to promote stroke
awareness
Solutions Implemented
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Perc
enta
ge c
ompl
iant
Deep Vein Thrombosis (DVT) ProphylaxisTJC Stroke Measure 1
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=1
)Mar-
08 (n
=2)
Apr-08
(n=7
)May
-08 (n
=6)
June
-08 (n
=3)Ju
ly-08
(n=3)
Aug-08
(n=8)
Sep-08
(n=6)
Oct-08
(n=6
)Nov
-08 (n
=8)Dec
-08 (n
=7)Ja
n-09 (
n=10
)Feb
-09 (n
=5)
Mar-09
(n=1
3)Apr-
09 (n
=9)
May-09
(n=6
)Ju
ne-09
(n=12
)Ju
ly-09
(n=10
)Aug
-09 (n
=7)Sep
-09 (n
=19)
Oct-09
(n=2
8)Nov
-09 (n
=17)
Dec-09
(n=17
)Ja
n-10 (
n=22
)Feb
-10 (n
=17)
99.990
99.995
100.000
100.005
100.010
Mean = 100.0
Definition: Patients with an ischemic stroke or a hemorrhagic stroke and who are non-ambulatory who receive DVT prophylaxis by end of hospital day two/All patients with ischemic stroke.Source: Nurse chart reviewAnalysis: Performance has been at 100% since February of 2008.
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Perc
enta
ge C
ompl
iant
Discharged on Antithrombotic TherapyTJC Stroke Measure 2
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=5
)Mar-
08 (n
=9)
Apr-08
(n=1
8)May
-08 (n
=13)
June
-08 (n
=22)
July-
08 (n
=15)
Aug-08
(n=16
)Sep
-08 (n
=19)
Oct-08
(n=1
6)Nov
-08 (n
=17)
Dec-08
(n=13
)Ja
n-09 (
n=16
)Feb
-09 (n
=19)
Mar-09
(n=1
2)Apr-
09 (n
=23)
May-09
(n=1
5)Ju
ne-09
(n=22
)Ju
ly-09
(n=21
)Aug
-09 (n
=12)
Sep-09
(n=19
)Oct-
09 (n
=17)
Nov-09
(n=15
)Dec
-09 (n
=12)
Jan-1
0 (n=
19 )
Feb-10
(n=1
9)
99.990
99.995
100.000
100.005
100.010
Mean = 100.0
Definition: Patients with an ischemic stroke prescribed antithrombotic therapy at discharge/All patients with ischemic stroke.Source: Nurse chart reviewAnalysis: Performance has been at 100% since February of 2008.
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Perc
enta
ge C
ompl
iant
Patients with Atrial Fibrillation Receiving Anticoagulation TherapyTJC Stroke Measure 3
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=1
)Mar-
08 (n
=2)
Apr-08
(n=5
)May
-08 (n
=1)
June
-08 (n
=2)Ju
ly-08
(n=1)
Aug-08
(n=5)
Sep-08
(n=3)
Oct-08
(n=3
)Nov
-08 (n
=2)Ja
n-09 (
n=5)
Feb-09
(n=3
)Mar-
09 (n
=1)
Apr-09
(n=3
)May
-09 (n
=2)
June
-09 (n
=2)Ju
ly-09
(n=2)
Aug-09
(n=1)
Sep-09
(n=2)
Oct-09
(n=1
)Nov
-09 (n
=2)Dec
-09 (n
=2)Feb
-10 (n
=2)
99.990
99.995
100.000
100.005
100.010
Mean = 100.0
Definition: Patients with an ischemic stroke prescribed antithrombotic therapy at discharge/All patients with ischemic stroke.Source: Nurse chart reviewAnalysis: Performance has been at 100% since February 2008.
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Perc
enta
ge C
ompl
iant
Thrombolytic Therapy AdministeredTJC Stroke Measure 4
This information is confidential and to be used for quality improvement purposes onlyMonth
Apr-08
(n=1
)May
-08 (n
=1)
June
-08 (n
=1)Ju
ly-08
(n=1)
Aug-08
(n=2)
Sep-08
(n=2)
Dec-09
(n=2)
Jan-0
9 (n=
1)Mar-
09 (n
=1)
Apr-09
(n=1
)May
-09 (n
=3)
July-
09 (n
=1)Aug
-09 (n
=1)Sep
-09 (n
=1)Oct-
09 (n
=2)
Nov-09
(n=1)
Jan-1
0 (n=
2 )
0
20
40
60
80
100
120
Mean = 94.2
Definition: Acute ischemic stroke patients who arrive at the hospital within 120 minutes (2 hours) of time last known well and for whom intravenous tissue plasminogen activator (IV t-PA) was initiated at this hospital within 180 minutes (3 hours) of time last known well/All patients with acute ischemic stroke whose arrival is within 2 hours (120 minutes) of time known well.Source: Nurse chart reviewAnalysis: Performance has been at 100% since April 2008. In July 2009, there was one patient who received IV t-PA per the new expanded time frame of up to 4.5 hours and so did not meet criteria for the under 3 hour window.
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Perc
enta
ge C
ompl
iant
Antithrombotic Therapy By End of Hospital Day TwoTJC Stroke Measure 5
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=5
)Mar-
08 (n
=8)
Apr-08
(n=1
6)May
-08 (n
=13)
June
-08 (n
=20)
July-
08 (n
=11)
Aug-08
(n=15
)Sep
-08 (n
=19)
Oct-08
(n=1
5)Nov
-08 (n
=17)
Dec-08
(n=11
)Ja
n-09 (
n=12
)Feb
-09 (n
=18)
Mar-09
(n=1
2)Apr-
09 (n
=18)
May-09
(n=1
0)Ju
ne-09
(n=19
)Ju
ly-09
(n=17
)Aug
-09 (n
=6)Sep
-09 (n
=18)
Oct-09
(n=1
8)Nov
-09 (n
=11)
Dec-09
(n=11
)Ja
n-10 (
n=14
)Feb
-10 (n
=20)
99.990
99.995
100.000
100.005
100.010
Mean = 100.0
Definition: Patients with ischemic stroke who receive antithrombotic therapy by the end of hospital day two/All patients with ischemic stroke.Source: Nurse chart reviewAnalysis: Performance has been at 100% since February of 2008
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Perc
enta
ge C
ompl
iant
Discharged on Cholesterol Reducing MedicationTJC Stroke Measure 6
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=4
)Mar-
08 (n
=6)
Apr-08
(n=1
3)May
-08 (n
=10)
June
-08 (n
=19)
July-
08 (n
=11)
Aug-08
(n=10
)Sep
-08 (n
=15)
Oct-08
(n=1
5)Nov
-08 (n
=13)
Dec-08
(n=9)
Jan-0
9 (n=
12)
Feb-09
(n=1
5)Mar-
09 (n
=12)
Apr-09
(n=1
8)May
-09 (n
=10)
June
-09 (n
=17)
July-
09 (n
=18)
Aug-09
(n=8)
Sep-09
(n=16
)Oct-
09 (n
=12)
Nov-09
(n=11
)Dec
-09 (n
=13)
Jan-1
0 (n=
14 )
Feb-10
(n=1
8)
92
94
96
98
100
Mean = 99.7
Definition: Ischemic stroke patients with low density lipoprotein level (LDL) >100, or LDL not measured, or on cholesterol-reducer prior to admission, who are discharged on cholesterol reducing drugs/All ischemic patients with an LDL>100mg/dL or who were on cholesterol reducing therapy prior to hospitalization or LDL not measured.Source: Nurse chart reviewAnalysis: Reinforced resident education about this measure. Performance at 100% since February 2008 except July 2008.
Consult Service Patient Recommendation for Labs/Meds overlooked
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Perc
enta
ge c
ompl
iant
Discharged on StatinTJC Stroke Measure 6
This information is confidential and to be used for quality improvement purposes onlyMonth
Jan -
09 (n
=3)
Feb-09
(n=1
1)
Mar-09
(n=1
0)
Apr-09
(n=1
5)
May-09
(n=6
)
June
-09 (n
=7)Ju
ly-09
(n=10
)
Aug-09
(n=4)
Sep-09
(n=13
)
Oct-09
(n=1
0)
Nov-09
(n=9)
Dec-09
(n=13
)Ja
n-10 (
n=12
)
Feb-10
(n=1
7)
99.990
99.995
100.000
100.005
100.010
Mean = 100.0
Definition: All ischemic stroke patients diagnosed with ischemic stroke due to atherosclerosis who are discharged with Intensive Statin Therapy/All ischemic patients with a low density lipoprotein level (LDL) >100mg/dL or who were on cholesterol reducing therapy prior to hospitalization or LDL not measured.Source: Nurse chart reviewAnalysis: Performance at 100% since January 2009 when tracking of this measure was initiated.
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Perc
enta
ge C
ompl
iant
Dysphagia ScreeningTJC Stroke Measure 7
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=5
)Mar-
08 (n
=13)
Apr-08
(n=2
4)May
-08 (n
=20)
June
-08 (n
=24)
July-
8 (n=
16)
Aug-08
(n=20
)Sep
-08 (n
=23)
Oct-08
(n=2
0)Nov
-08 (n
=19)
Dec-08
(n=20
)Ja
n-09 (
n=19
)Feb
-09 (n
=24)
Mar-09
(n=1
6)Apr-
09 (n
=30)
May-09
(n=2
0)Ju
ne-09
(n=29
)Ju
ly-09
(n=24
)Aug
-09 (n
=15)
Sep-09
(n=24
)Oct-
09 (n
=33)
Nov-09
(n=19
)Dec
-09 (n
=17)
Jan-1
0 (n=
27 )
Feb-10
(n=2
5)
99.990
99.995
100.000
100.005
100.010
Mean = 100.0
Definition: Patients with ischemic or hemorrhagic stroke with a dysphagia screen before being given anything by mouth/All patients with an acute ischemic or hemorrhagic stroke.Source: Nurse chart review.Analysis: Performance has been at 100% since February 2008. A swallow screening evaluation tool was developed and implemented after successful completion of in-servicing to the neurology residents.
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Perc
enta
ge C
ompl
iant
Stroke EducationTJC Stroke Measure 8
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=5
)Mar-
08 (n
=14)
Apr-08
(n=2
3)May
-08 (n
=20)
June
-08 (n
=24)
July-
08 (n
=16)
Aug-08
(n=20
)Sep
-08 (n
=21)
Oct-08
(n=2
1)Nov
-08 (n
=20)
Dec -0
8 (n=
22)
Jan -
09 (n
=21)
Feb-09
(n=2
4)Mar-
09 (n
=19)
Apr-09
(n=3
3)May
-09 (n
=20)
June
-09 (n
=31)
July-
09 (n
=26)
Aug-09
(n=17
)Sep
-09 (n
=26)
Oct-09
(n=2
0)Nov
-09 (n
=22)
Dec-09
(n=20
)Ja
n-10 (
n=30
)Feb
-10 (n
=24)
90
92
94
96
98
100
102
104
Mean = 98.9
Definition: Patients with ischemic or hemorrhagic stroke or their caregivers who were given education or educational materials during the hospital stay addressing all of the following: personal risk factors for stroke, warning signs for stroke, activation of emergency medical system, need for follow-up after discharge, and medications prescribed/All patients with ischemic or hemorrhagic stroke.Source: Nurse chart reviewAnalysis: Performance at 100% since February 2008 thru November 2008. Staff re-education done Dec’08 on neuroscience note documentation, stroke education packet and available teaching resources. Stroke documentation audit tool initiated in March’09. Staff re-education re stroke education resources done Oct’09. In November ’09, stroke specific educational materials made available in the Electronic Medical Record (EMR).
Staff re -education
Staff re -education
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Perc
enta
ge C
ompl
iant
Smoking Cessation/ Advice/ CounselingTJC Stroke Measure 9
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=1
)Apr-
08 (n
=2)
May-08
(n=1
)Ju
ne-08
(n=5)
July-
08 (n
=2)Aug
-08 (n
=5)Sep
-08 (n
=3)Oct-
08 (n
=2)
Nov -0
8 (n=
5)Dec
-08 (
n=6)
Jan-0
9 (n=
2)Feb
-09 (n
=5)
Mar-09
(n=4
)Apr-
09 (n
=5)
May-09
(n=4
)Ju
ne-09
(n=9)
July-
09 (n
=4)Aug
-09 (n
=5)Sep
-09 (n
=6)Oct-
09 (n
=4)
Nov-09
(n=4)
Dec-09
(n=3)
Jan-1
0 (n=
5 )Feb
-10 (n
=5)
99.990
99.995
100.000
100.005
100.010
.
Mean = 100.0
Definition: Patients with ischemic or hemorrhagic stroke with a history of smoking cigarettes, who are, or whose caregivers are, given smoking cessation advice or counseling during hospital stay/All ischemic or hemorrhagic patients with a history of smoking cigarettes any time during the year prior to hospital arrival.Source: Nurse chart reviewAnalysis: Performance has been at 100% since February 2008.
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Perc
enta
ge C
ompl
iant
Assessed for RehabilitationTJC Stroke Measure 10
This information is confidential and to be used for quality improvement purposes onlyMonth
Feb-08
(n=5
)Mar-
08 (n
=14)
Apr-08
(n=2
3)May
-08 (n
=20)
June
-08 (n
=24)
July-
08 (n
=16)
Aug-08
(n=20
)Sep
-08 (n
=21)
Oct -08
(n=2
1)Nov
-08 (
n=20
)Dec
-08 (
n=22
)Ja
n-09 (
n=21
)Feb
-09 (n
=24)
Mar-09
(n=1
9)Apr-
09 (n
=34)
May-09
(n=2
0)Ju
ne-09
(n=31
)Ju
ly-09
(n=26
)Aug
-09 (n
=17)
Sep-09
(n=26
)Oct-
09 (n
=20)
Nov-09
(n=22
)Dec
-09 (n
=20)
Jan-1
0 (n=
30 )
Feb-10
(n=2
4)
99.990
99.995
100.000
100.005
100.010
Mean = 100.0
Definition: Patients with an ischemic stroke or hemorrhagic stroke who were assessed for rehabilitation services/All patients with ischemic or hemorrhagic stroke.Source: Nurse chart reviewAnalysis: Neurology note edited previously and residents in-serviced. Performance has been at 100% since February 2008.
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Next Steps• Continue to actively monitor all stroke performance measures• Support collaborative efforts of the multidisciplinary team to
maximize patient outcomes • Enhance stroke educational efforts professionally and for the
community• Support the Loyola Stroke Network
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Susan Finn, MSN; Glynis Adams, MSN; Sandra Swanson, MSOD; Karen Judy, MD;
Linda Rush, PCT; Geri Augustine, BS, MT(ASCP)
COMMUNITY COMMUNITY LEAD SCREENINGLEAD SCREENING
TABLE 14
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Lead exposure is a problem which impacts the growth and development of the young child. Early diagnosis and management are critical in preventing damage.
A multidisciplinary team, with nursing as a key stake- holder, implemented a CLIA-waived lead testing method in September 2007. (CLIA: Clinical Laboratory Improvement Amendment 1988)
This new testing method requires less blood for the sample and provides results within three minutes.
Background
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Aim Statement/Goals
• To streamline the process for screening at-risk children for lead exposure.
• To optimize time spent with parent and school health staff so appropriate education and intervention may occur.
• To increase the number of children screened for lead exposure by 20% in the first two years of using the CLIA-waived testing method.
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Aim Statement Continued
Forces of Magnetism:
Force 7: This process improves quality of care in our organization.Decreased waiting time for test results leads to better and more timely follow up.
Force 10: Community presence through this ongoing, long-term outreach strengthens our position as a productive corporate citizen.
Force 13: Interdisciplinary collaboration and mutual respect contribute to positive relationships within our organization and enhanced outcomes.
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• Implementation of a CLIA-waived testing method for lead screening - A collaborative effort with our clinical laboratory facilitated the introduction of a CLIA-waived testing method for lead screening. After careful testing of the instrument and correlation with our core laboratory, the instrument was introduced on our pediatric mobile health unit for screening at-risk children for lead exposure.
SolutionsSolutions ImplementedImplemented
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ResultsResults
Community Lead Screening
0
10
20
30
40
50
60
70
80
90
FY06Q2
FY06Q3
FY06Q4
FY07Q1
FY07Q2
FY07Q3
FY07Q4
FY08Q1
FY08Q2
FY08Q3
FY08Q4
FY09Q1
FY09Q2
FY09Q3
FY09Q4
FY10Q1
FY10Q2
Lead Care II(CLIA waived testing)Core laboratory testing
Num
ber
of sc
reen
ings
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ResultsResultsN
umbe
r of s
cree
ning
s
Community Lead Screening
FY06 Q
2FY06
Q3
FY06 Q
4FY07
Q1
FY07 Q
2FY07
Q3
FY07 Q
4FY08
Q1
FY08 Q
2FY08
Q3
FY08 Q
4FY09
Q1
FY09 Q
2FY09
Q3
FY09 Q
4FY10
Q1
FY10 Q
2
0
20
40
60
80
100
Mean = 25.63
Mean = 34.56
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Results/Analysis
• The number of children screened for lead exposure increased by 50% in the first two years of utilizing the CLIA-waived testing method.
• Ongoing education of school health personnel and parents about the risk of lead exposure has facilitated the implementation of this program.
• Shorter time for results (three minutes as compared to an average of five days) improved dissemination of results to parents and school health staff. The result was more timely education and intervention.
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Next Steps
• To continue screening for lead exposure within the Chicago metropolitan area.
• To increase the number of children screened through our pediatric mobile health unit by another 10% over the next year.
• To continue to provide outreach education to schools and community centers about the risk for lead exposure to children and need for screening and environmental modifications.
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MEDICATION RECONCILIATION
It Only Helps If You Get It Right
TABLE 15
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TEAM MEMBERSHIP
Garry Sigman MD
Ramzan Shahid MD
Olivia Mittel MD
Ami Giardina RN MHA
Annette Jenero RN,ADN
Laura Belling RN BSN
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PROJECT AIM STATEMENT
Develop a process whereby every patient’s medical record is an accurate reflection of currently prescribed medications.
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SOLUTIONS IMPLEMENTED
Multidisciplinary committee formed to improve medication reconciliation practice. Committee’s Decision: Physicians are accountable for medication reconciliation.
Baseline chart audits were conducted for medication accuracy and shared with each physician.
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SOLUTIONS IMPLEMENTED
Education provided to all physicians on agreed upon method of medication reconciliation.
Post-implementation audit conducted and shared with each physician.
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RESULTS
Percentage of Reconciled Charts
0.00%
10.00%
20.00%
30.00%
40.00%
50.00%
60.00%
70.00%
80.00%
90.00%
Attending Physicians Resident Physicians
Baseline DataPost Implementaion
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ANALYSIS
There was significant improvement, especially among the resident physicians.
The medical staff has accepted accountability for medication reconciliation.
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NEXT STEPS
It is our intention to perform chart review on a quarterly basis and share the data with the physicians. We will continue to educate as needed.
Although there has been improvement, our goal is to have medications reconciled at every patient encounter.
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CT RADIATION DOSE: A BALANCE BETWEEN
IMAGE QUALITY AND DOSE
Dr. Kevin Corrigan Ph.D., Dr. Harold Posniak M.D.,Loren Eade BSRT, Lorraine Dean BSRT,
James Ryva BSRTTABLE 16
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BACKGOUND & PROJECT GOALS• While pursuing the American College of Radiology (ACR)
accreditation & becoming part of the Image Gently Campaign the issue of radiation dose & image quality surfaced.
• We elected to look at CT exams that offered the greatest opportunity to reduce dose & the most frequently ordered exams which totaled 48% of all our exams.
• Utilizing a team approach, ionization chambers, and anatomical phantoms we measured & calculated patient radiation dose from all of our CT scanners.
• We looked at all the CT technical factors that influence dose & image quality.
• We evaluated CT image quality looking at image sharpness, resolution, contrast, and noise.
• Our project goal was two fold: 1) to reduce CT radiation dose by at least 10%, and 2) to achieve an optimal balance between acceptable CT patient dose and high image quality.
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CT SCANNER EVALUATION, ACR TEST PHANTOM
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CT PATIENT RADIATION DOSE MEASUREMENT
Use ACR endorsed phantoms which simulateaverage adult body, head.
Scan technique for average adult, child mustproduce < established dose limits.
Adult AbAdult Head
Ion Chamber Dosimeter
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SOLUTIONS IMPLEMENTED• Implemented ALARA (as low as reasonably achievable)
with respect to using only the amount of radiation necessary to obtain optimal images.
• Developed CT technical scanning protocols for the selected exams in which we wanted to reduce radiation dose.
• Developed weight based, procedural based, & body part specific scanning protocols.
• Implemented the use of new breast protective shields to reduce radiation dose.
• Utilized prospective gating & ECG Automatic Dose Modulation to reduce radiation dose for our CT Cardiac Angiographic patients.
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RESULTS
AVERAGE PERCENT RADIATION DOSE REDUCTION
0%
5%
10%
15%
20%
25%
30%
35%
40%
45%
50%
Adult Head AdultAbdomen
AdultC ardiac
P ediatricHead
P ediatricAbdomen
S eries 1
20% 33% 45% 23% 40%
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RESULTS• ACHIEVED A THREE YEAR ACCREDITATION FROM THE
AMERICAN COLLEGE OF RADIOLOGY (ACR) FOR ALL CT SCANNERS.
• RECEIVED RECOGNITION FROM THE AMERICAN ACADEMY OF PEDIATRICS, ACR, & AMERICAN ASSOCIATION OF PHYSICISTS IN MEDICINE FOR OUR PARTICIPATION IN THE IMAGE GENTLY CAMPAIGN.
• OUR DOSE REDUCTIONS CORRELATED WITH NATIONALLY PUBLISHED DATA FROM THE NATIONAL COUNCIL ON RADIATION PROTECTION & MEASEAUREMENTS & VALIDATED BY THE ACR.
Loyola University Health System
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ANALYSIS
• We well exceeded our target of 10% radiation dose reduction in all exam categories.
• By using the reconstructive algorithms we realized that we were able to reduce noise in CT cardiac images and still maintain the ability to visualize small structures.
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NEXT STEPS
• Look at all remaining CT protocols to evaluate dose reduction.
• Look at other areas of Radiology such as Interventional Radiology with respect to radiation dose & fluoroscopy time.
• Assess radiopharmaceutical dose in the pediatric population in Nuclear Medicine.
• Work with Radiology equipment vendors to standardize dose assessment & dose reporting.
• When looking at future CT equipment purchases, select vendors that address radiation dose reduction.
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Hospital Acquired Pressure Ulcer
TABLE 17
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Reduction Project
Jodi Blaszczyk RN, BSN, CWOCN, Kathy Thiesse RN, BSN, CWOCN
Skin Care Liaison Committee, Judy McHugh RN, MSN
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Impact of Hospital Acquired Pressure Ulcers
• Annual estimate of treatment costs in US hospitals is $11 Billion with a mean length of stay of 13 days.
• Estimated cost of a stage 3 or 4 pressure ulcer is $9,900.
• Loyola experience- 2007 LUMC Hospital Acquired Cases found =78- 2009 LUMC Hospital Acquired Cases found =39- Cost avoidance ($9,900 x 39) =$386,100
Institute for Healthcare Improvement. Five million lives campaign. Getting started kit: prevent pressure ulcers. IHI, 2008Xakellis, G.C., Frantz, R., (1996). The cost of healing pressure ulcers across multiple health care settings.. Adv Wound Care, 9 (6) 6: 18-22
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• Reduce Hospital Acquired “Pressure Ulcers” (PU) Rate– Goal: 0%
• Prevent Hospital Acquired “Heel” Pressure Ulcers– Goal: 0%
• Increase daily Braden Scale Compliance– Goal: 100%
• Documentation of skin assessment on admission– Goal: 100%
• LUMC participates in quarterly National Database of Nursing Quality Indicators (NDNQI) Studies – Point prevalence performed
consists of a one day study in which head to toe skin assessments for pressure ulcers, documentation, Braden Scale, & chart audits.
• Braden Scale Daily* Compliance is monitored monthly*as a proxy Braden Scale daily compliance consists of random audit done 2 times a month.
Aim Statement / Goals PLAN
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Policy & Practice:
• Implemented evidenced based Decision Tree for heel pressure relief – MF 6, 7, 8.
• Updated Braden Scale P&P – MF 7, 9.
Staff Education:• Developed 2009 Resources Available Manual &
Skin Care Liaisons provided individual unit education – MF 8,11.
• Initiated additional Night Shift Skin Care Liaison Committee meet 4th Friday of month MF 6, 9.
• Began monthly education for new employee RN/PCT orientation on skin & ostomy care MF 1, 8, 11, 14.
Documentation Improvements:
• Relocated Braden Scale documentation in EPIC to improve compliance – MF 7, 9.
• Added ED documentation on admission POA in ED Admission Navigator – MF 12.
Compliance Monitoring:
• Continue stage I inter-rater reliability of skin surveyor - Magnet Force (MF) 7.
• Created weekly Inpatient Pressure Ulcer report for managers on portal MF 3, 7.
Solutions Implemented to Reduce PU
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HW Noso Skin Ulcer Rate
Conf idential f or Quality Improvement Purposes Only
2 Q 06 Jun10.3
3 Q 06 Sep12.1
4 Q 06 Nov13.9
1 Q 07 Mar7.3
2 Q 07 May7.3
3 Q 07 Sep7.8
4 Q 07 Nov5.6
1 Q 08 Feb6.8
2 Q 08 Jun8.1
3 Q 08 Sep5.1
4 Q 08 Dec4.5
1 Q 09 Mar4.1
2 Q 09 Jun3.3
3 Q 09 Sep3.7
4 Q 09 Nov3.0
Quarter1
IndividualsTemporary: UCL=10.91, Mean=6.86, LCL=2.81 (mR=2)
2 Q 06
Jun
3 Q 06
Sep4 Q
06 N
ov1 Q
07 M
ar2 Q
07 M
ay3 Q
07 Sep
4 Q 07
Nov
1 Q 08
Feb
2 Q 08
Jun
3 Q 08
Sep4 Q
08 D
ec1 Q
09 M
ar2 Q
09 Ju
n3 Q
09 Sep
4 Q 09
Nov
4
6
8
10
12
14
UCL = 10.91
Mean = 6.86
LCL = 2.81
NDNQI SurveyTeam Training& Staging
Acute Rehab & ICUAdmission Ulcer DocumentationGreater than 4 Linen Layers
Inter-Rater ReliabilityStage 1
Skin SurveyRe Education
New EPICRN Documentation
Back to BedSave Our Skin
Daily BradenScoring
Manager Meeting Agenda Item
Reduced Linen LayerNon Plastic Adult Briefs
Criticaid Clear Ointment
Prevalon Boots
HW Order Set Education
ED POA doc
HW Hospital Acquired Pressure Ulcer Rate
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Bra
den
Sca
le R
ate
HOSPITAL WIDE BRADEN SCALE COMPLIANCE44
DEC 0850451199
45JAN 09
56958098
46FEB 09
55757198
47MAR 09
568568100
48APR 09
58959599
49MAY 09
28529796
50JUN 09
57157699
51Jul 09
492521100
52Sep 09
266270100
53Oct 09
580583100
54Nov 09
517518100
55Dec 09
269270100
NUMBERDATE
ASSESSCENSUS
1Individuals
Temporary: UCL=101.74, Mean=99.08, LCL=96.42 (mR=2)
DEC 08
JAN 09
FEB
09
MAR 09
APR 09
MAY 09
JUN 09
Jul 0
9
Sep 0
9
Oct 09
Nov 09
Dec 09
96
97
98
99
100
101
UCL = 101.74
Mean = 99.08
LCL = 96.42
Goal = 100%
Bra
den
Sca
le R
ate
HOSPITAL WIDE BRADEN SCALE COMPLIANCE44
DEC 0850451199
45JAN 09
56958098
46FEB 09
55757198
47MAR 09
568568100
48APR 09
58959599
49MAY 09
28529796
50JUN 09
57157699
51Jul 09
492521100
52Sep 09
266270100
53Oct 09
580583100
54Nov 09
517518100
55Dec 09
269270100
NUMBERDATE
ASSESSCENSUS
1Individuals
Temporary: UCL=101.74, Mean=99.08, LCL=96.42 (mR=2)
DEC 08
JAN 09
FEB
09
MAR 09
APR 09
MAY 09
JUN 09
Jul 0
9
Sep 0
9
Oct 09
Nov 09
Dec 09
96
97
98
99
100
101
UCL = 101.74
Mean = 99.08
LCL = 96.42
Goal = 100%
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Combined Analysis of Data
• Nosocomial PU rate has decreased with implementation of Inter-Rater Reliability on Stage 1 ulcers.
• New ED RN Documentation is assisting in capturing Pressure Ulcers Present on Admission (POA).
• Implementation of Decision Tree for heel pressure relief and low, mod, high risk Braden order sets has reduced nosocomial heel ulcers. Met Zero Heel Pressure ulcers past 2 quarters.
• Met Braden Scale 100% compliance – Identifying who is at risk allows for earlier implementation of a pressure
ulcer action plan.
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Next StepsCompliance Monitoring:• Maintain stage 1 inter-rater reliability of skin
surveyor – MF 7.• Evaluate , with clarity report, ED documentation
on admission POA – MF 12.• Utilize weekly Inpatient hospital acquired PU
report to identify and target nursing units with high rates – MF 7.
Policy & Practice:
• Evaluate Wound Care Product line with Med/Surg Value Analysis Team (VAT) –MF 7.
• Adding hyper links to references available to EPIC Braden Scale Order Sets – MF 7.
Documentation Improvements:
• Formulate plan for house wide education on wound documentation – MF 7.
• Submit improvements in EPIC for documentation on wounds – MF 7.
Staff Education:• Night shift Skin Care Liaisons to complete
NDNQI PU training modules with 1.5 CEUs –MF 6, 7, 8.
• Educate managers/skin care liaisons onInterpreting/utilizing weekly inpatient PUreport &NDNQI reports on report channel totarget individual units areas of improvements– MF 3,7,11.
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Meet the Skin Care Liaison TeamDay
Jodi Blaszczyk ET, ChairKathy Thiesse ETGail Klotz 7SW Debbie Terrell 2NESusie Irving 7BICUPaula Ferrel 6E Soo Howell 2ICUIsabel Orona 6EMelody Cibock 6WBMT Charlene Wiegland 5RehabMark Beluga 5RehabSandy Carmargo HTUBarb Brower 2ICU Barbara Rumik MICUMary Montevecchi MICUJennifer Data 2WLindsey Keeler PAR
Night
Kathy Thiesse, ET ChairJane Williams MICU Co-ChairSally Ciukaj EDJessica Ray 2WJessica Amundsen 2WJohnson Vachachira HTUTracy Frazzini HTUJamise Gant 3NEWSJason Morandi 4ICUKimberly Simons 4TAnitha Saravanan 5TBobbie Halikowska 5TPaula Farrell 6ESandra Dominguez BICU
Karen Thomas 5TDebra Callender ERMaria Poblete GIMichelle Regasa 3NEWSDivine Tongol GITheresa Pavone 3NEWSMarybeth Jabeguero GIJudy King 4ICULindsey Buckman 4TMegan Pugh PEDSMelinda Mars PEDSGinger Lewis UrologyTheresa Schwenkel 2NEEva Grabala 2WEli Ayala HTURenee Pach PEDSAlona Gomez-Ricar OR
Lori Black MICUDeborah Zatecka 6WPaula Farrell 6EBrianna Piet 6E
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Pharmacist Epic Medication Order Verification Training and
the Impact on Order Verification Time.
TABLE 18
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Committee Members• George Krempel MBA
ASQ Certified Six Sigma Green Belt
• Richard Ricker RPh MBA• Greg Horner ASQ Certified
Six Sigma Black Belt • Gayle Thompson PharmD• John Ilic PharmD
• Andrea Quinn PharmD BCPS
• Nancy Doulas PharmD• Martina Novotny PharmD• Dan Govoni RPh• Allison Schriever PharmD
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Background• TJC requires pharmacist review of medication orders
prior to administration.• Epic medication order verification is one piece of efficient
and appropriate medication delivery to patients.• Order verification directly impacts patient care and
nursing workflow.• Time delays for pharmacotherapeutically correct orders
can occur if pharmacists are unfamiliar with Epic’s full capabilities or specific patient information location.
• Inappropriate verification can occur if patient information is researched inappropriately.
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Project Objective & Goal
Assess the impact of pharmacist Epic medication order verification
training on order cycle time.
– Cycle time reflects the time difference between time of order entry and pharmacist verification.
– Goal: Decrease cycle time through training.
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Pilot Training• Eight (8) pharmacists from different areas
working 1st and 2nd shifts were included in the pilot assessment. – Four (4) pharmacists underwent verification
training. – Four (4) pharmacists matched for area and
shift served as controls.• Baseline cycle time was measured for select
nursing units(2E, 6N, 6S, 7S, 7W) pre-training (all staff) and post training (select pharmacists).
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Results from the Pilot Training
• Average baseline medication order cycle time approximated 24.69 minutes (N=1653 orders)
• Average order cycle time post training initiative approximated 23.61 minutes (N=1304 orders)– Untrained pharmacist average 29.45 minutes
(N= 309 orders)– Trained pharmacist average 21.79 minutes
(N=995 orders)
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Expansion of Training Initiative• The results of the pilot training led our team to
provide mandatory pharmacist Epic medication order verification training.– Inpatient and outpatient pharmacists (n=72) were
provided an Epic medication verification training guide, were required to attend small group didactic training which utilized ‘live’ Epic functions and successfully complete an E-learning module.
– Training occurred for 2 weeks in November 2009.• Cycle times were assessed pre and post global
training.
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Expanded Training Results
Month Average cycle time (minutes)
Number of medication orders
October 2009 (pre- training)
17.24 48055
December 2009 (post training)
16.8 44801
January 2010 12.2 13741
February 2010 * 15.19 46741
* February data had ~4 times the number of orders and pharmacists were short-staffed!
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Expanded Training Results
0
5
10
15
20
October 2009(Pre-training)
December2009 (PostTraining)
January 2010 February 2010
Min
utes Global Verification
times
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Conclusions
• Formal Epic medication order verification training impacted overall verification cycle time, resulting in an overall decrease in cycle time from baseline assessment.
• The variations between January and February cycle times may be associated with the increased order volume, pharmacy staffing shortages and potential reporting error.
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Limitations• Cycle time analysis does not differentiate
between pharmacotherapeutically appropriate orders and those requiring clarification. Orders requiring clarification may result in longer verification times.
• Cycle time reflects the time the order is entered until it is verified. At this time, Epic is unable to quantify time for pharmacist verification activities.
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Next Steps• Epic medication order
verification cycle times will be sporadically monitored.
• Pharmacists will undergo periodic training updates and E-learning assessments.
• The verification guide will be updated with system updates, as deemed necessary.
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Implementation of a Pediatric Pressure Ulcer Prevention Tool
Promoting Directed Interventions and Alleviating Risk
POSTER 19
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PUPPI-C Team Members
Marsi Appleby BSN, RN (PICU), Team LeaderRenee Pach BSN, RN (PEDS), Co-Team LeaderJudy McHugh MSN, RN, FacilitatorJodi Blaszczyk BSN, RN, CWOCN, Skin ConsultantMelinda Mars BSN, RN (PICU), Data CollectorCindi LaPorte, BSN, RN, Pediatric ManagerKatie Hollish MSN, RN, EducatorSamatha Sage BSN, RN (PEDS)Christine Lewkowicz BSN, RN (PEDS)Kathy Thesse BSN, RN, CWOCN, Skin ConsultantJeanne Sadlik, LUHS LibrarianAda Koch, PharmacistDana Fortado, Occupational TherapistCarly Houston, Registered Dietician
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Problem focused triggers Knowledge focused triggerspatient safety & risk management data new research or other literatureprocess improvement data national agencies or organizationalinternal/external benchmarking data standards & guidelinesfinancial data philosophies of careidentification of clinical problem questions from institutional councils & committeesidentification of system problempatient/family concerns
Is this topic apriority for theorganization?
Bring topic to the NsgExecutive Council toevaluate priority inlight of other pendingprojects.
Include input from allrelevent stakeholders.
Consider othertriggers
Form a team
Interdisciplinary whenappropriate
Consider non-clinicalmembers (e.g.,support depts)
Include member w/research competencyIdentify desired outcome(s)
Assesmble relevent research andrelated literature
Critique, weigh evidence, andsynthesize research for use in practice
Pilot the change in practice Implement Rapid-Cycle Improvement
Process Select outcomes to be achieved Collect baseline data Design EBP guideline(s) Implement EBP on pilot units Evaluate process and outcomes Modify the practice guideline
Is there asufficient research
base?
Base practice on other types of evidence: case reports expert opinion scientific principles theory best practice guidelines patient preferences
Conductresearch
Assess feasibility, benefits, and risk ofpractice change
Is changeappropriate for
adoption inpractice?
Continue to evaluate quality ofcare and new knowledge Institute the change in practice
Monitor & analyze structure, process, and outcome data environment staff cost patient & family
Disseminate results
Assess need forchange; identify the
problem to becorrected (may
occur at Unit-Basedor System-wide
level)
No
Yes
Yes No
YesNo
Refer recommendatins for system-wide practicechanges to Nursing Executive Council
Iowa Model of Evidence-Based PracticeAdapted for Use at Loyola University He(Copyright of University of Iowa Hospitals and Marita Titler. Reproduced with permission from Marita Titler, PhD, RN, FAAN; for permission to use or reproduce the model, please contact Dr. Titler at [email protected].)
Quality Pathway
Purpose:To implement an evidenced-based Pediatric Skin Assessment tool to prevent pressure ulcers
Significance/Priority:
Decrease Risk of Pressure Ulcers Reduce pressure ulcers to 0
Clinical PICO Question:
P: Pediatric Hospitalized Patients with Limited or No
Mobility
I: What are the current Skin Care Assessment
Tools/Interventions to prevent pressure ulcers
C: No pediatric evidenced-based skin care
assessment vs an evidenced- based skin care
assessment
O: Decrease Risk of Pressure Ulcers Decrease Pressure Ulcers to Zero
Key StakeholdersPUPPI Committee:•Pediatric Nursing Staff•Pediatric Nurse Manager•ET Skin Care Nurse WOCN•Nursing Performance Improvement•PT/Occupational Therapy•Pharmacist•Registered Dietician•APN •Pediatric Medical Staff
Approvals Obtained: EBP•Nurse Executive Council•Nursing Quality and Safety Council•Nurse Skin Care Committee•Pediatric Nursing Staff Education CommitteeBaseline Date:
Problem FocusedOccipital Pressure Ulcers seen more frequently in PEDS •Potential Pressure Ulcer -12 hrs post adm to PICU•Hospital Acquired Pressure Ulcers-Harm, Increase LOS/Cost
Knowledge-Focus Triggers•Pediatric Skin Assessment Tool- Braden Q or other tools•What are the principal components for early interventions •CMS New Ruling-Hospital Acquired- Discount Hospital Bill or Negative effect
Synthesis of Evidence:
•30 articles, 12 years of research•Adaptation of the Braden Scale for pediatrics iscalled Braden Q by Quigley &
Curley(1996)
Body of Evidence–Multisite prospective cohort descriptive study–Retrospective Cohort–Case Control Study–Systematic Review
Synthesis of Evidence–During committee meetings–Unit Huddles–Through collaboration with ET RN Therapist
EBP InterferencesEvidence Supports:–Utilization of Braden Q no adaptations–Skin Care Assessments every days
Length of intubation
Pilot the Change in Practice
•Did Braden Q Capture Skin Care Risk Level•Evaluated current Pressure Ulcers on Pediatric Units•Evaluated and determine High, Moderate, Low Risk Interventions •Developed LUHS Pediatric Skin Interventions on Paper Form
•Pilot on PICU•Implemented EBP on pilot units•Evaluated Skin Assessment Process and Outcomes•Incorporated into EMR (EPIC)- Braden Q Skin Assessment and LUHS Pediatric Skin Intervention (Order Sets)
Plan, Do, Study, Act (PDSA)
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PLAN:
Project Aim Statement:
Prevent and minimize risk for hospital- acquired pediatric pressure ulcers by creating an interdisciplinary team to analyze past pressure ulcer patterns, evaluate current trends, and implement an evidence-based pediatric pressure ulcer prevention.
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PLAN:
Measurement Goal & Target:
Reduce hospital-acquired pediatric pressure ulcers to zero
Complete Braden Q assessment upon admission and once a day, and provide skin care interventions when appropriate
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PLAN:
Evidence-Base:
An extensive literature review conducted by the committee identified the Modified Braden Q Pressure Ulcer Risk Assessment Scale (Braden Q), which is an evidence- based pediatric assessment tool that modifies the original Braden Scale largely through the inclusion of a subscale addressing tissue perfusion and oxygenation. Approval for the use of this instrument was obtained from Sandy Quigley, RN, CWOCN, CPNP, one of its principal authors.
Through the PUPPI-C literature review, it was also revealed that no evidence-based intervention system for addressing pediatric pressure ulcers existed. So, a pilot pediatric intervention tool was created. This was based upon an adult intervention protocol already in use at Loyola, but was modified based upon a review of the relevant research literature, to render it appropriate for the treatment of pediatric patients. In September of 2009, a pilot study of this intervention protocol was initiated. In March, 2010, the Loyola Pediatric Skin Interventions were introduced into Epic.
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PLAN:
Magnet Force:
Quality Improvement # 7
Quality is the systematic driving force for nursing and the organization. Nurses serving in leadership positions are responsible for providing an environment that positively influences patient outcomes. There is a pervasive perception among nurses that they provide high-quality care to patients.
Interdisciplinary Relationships # 13
Collaborative working relationships within and among the disciplines are valued. Mutual respect is based on the premise that all members of the healthcare team make essential and meaningful contributions to the achievement of clinical outcomes. Conflict management strategies are in place and are used effectively, when indicated.
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DO:
Solutions Implemented:
Adopted and applied the Iowa Model of Evidence-based Practice to examine current best practices
Developed an interdisciplinary committee derived from the Nursing Quality and Safety Council to evaluate pediatric skin care assessment
Named committee “PUPPI-C”: Pressure Ulcer Prevention Pediatric Interdisciplinary-Committee
Reviewed and discussed relevant literature identifying best practices in pediatric skin assessment
Assessed feasibility of the Modified Braden Q Pressure Ulcer Risk Assessment Scale-a comprehensive tool that has 7 subscales with an additional scale specifically for pediatric population - tissue perfusion and oxygenation
Piloted and adopted the Braden Q Pressure Ulcer Risk Assessment Scale
Built a skin assessment screen for pediatrics in EPIC
Confidential: For Quality Improvement Purpose Only
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DO:
Developed and piloted evidence-based interventions through a literature search to help indicate: Low/Moderate/High risk pediatric groups (Loyola Pediatric Skin Interventions)
Developed and implemented an E-Learning education tool for the Braden Q and the Interventions for High/Moderate/Low risk pediatric patients
Developed and educated PEDS and PICU nurses on resource binder and unit education boards
Educated PEDS and PICU nurses on assessment and interventions for pressure ulcer prevention
Created and incorporated the Loyola Pediatric Skin Interventions into EPIC
Created a hyperlink from the intervention order sets to reference material in EPIC about skin protection for pediatric families
Incorporated lessons learned from hospital-acquired pressure ulcers post implementation: Nursing owns each hospital-acquired pressure ulcer and actively investigates solutions and educates nurse on trends if appropriate
Confidential: For Quality Improvement Purpose Only
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DO:
Presentations:
March 2009 LUHS Evidenced-based Practice Day and Shared Governance Day - PUPPI-C
March 2009 LUHS Women and Children’s Conference - PUPPI-C
April 2010 LUHS Patient Safety and Quality Fair - PUPPI-C
April 2010 Sigma Theta Tau - PUPPI-C
April 2010 Poster presentation at University of Iowa Evidenced-Based Practice Conference - PUPPI-C
Applied:
October 2010 Poster Magnet Conference - PUPPI-C
Confidential: For Quality Improvement Purpose Only
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STUDY:
Analysis:
Baseline data was retrieved from the EPIC doc flowsheet for skin integrity
An EPIC clarity report revealed six pressure ulcers that were identified as hospital-acquired from January through August 2008
All six cases were reviewed by the interdisciplinary team:
4 cases were incorrectly classified as pressure ulcers in the EPIC documentation by the staff RN
2 cases were correctly identified:
1. Occipital pressure ulcer where alopecia occurred once the pressure ulcer was healed
2. Gluteal fold, stage two pressure ulcer in PICU
Confidential: For Quality Improvement Purpose Only
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STUDY:
Analysis:
Since the implementation in May 2009 of the Pediatric Pressure Ulcer program:
PICU
100% compliance for Braden Q performed upon patient admission
100% compliance for Braden Q assessment daily
PEDS
99.38% compliance for Braden Q performed upon patient admission
99.38% compliance for Braden Q assessment daily
Confidential: For Quality Improvement Purpose Only
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STUDY:
Analysis:
Total Number of Hospital-Acquired Pressure Ulcer for 2009:
PEDS: 0 Hospital-Acquired Pressure ulcers
PICU: 7 Hospital-Acquired Pressure ulcers
3 of those 7 occurred post implementation (May 2009)
There were no hospital-acquired pressure ulcers since August 2009
Confidential: For Quality Improvement Purpose Only
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Braden Q Assessment Upon AdmissionPEDS and PICU
July 2009 - February 2010
92
94
96
98
100
102
Jul 09 N=17
Aug 09 N=39
Sep 09 N=32
Oct 09 N=32
Nov 09 N=28
Dec 09 N=34
Jan 09 N=34
Feb 09 N=26
Months
Perc
ent C
ompl
ianc
e
Random Braden Q Monthly
Confidential: For Quality Improvement Purpose Only
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Braden Q Assessment DailyPEDS and PICU
July 2009 - February 2010
92
94
96
98
100
102
Jul 09 N=17
Aug 09 N=39
Sep 09 N=32
Oct 09 N=32
Nov 09 N=28
Dec 09 N=34
Jan 09 N=34
Feb 09 N=26
Months
Perc
ent C
ompl
ianc
e
Random Braden Q Monthly
Confidential: For Quality Improvement Purpose Only
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Confidential: For Quality Improvement Purpose Only
Current
number of
days ‘ulcer
free’PUPPI –C
Project
Implemente
d
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ACT:
Continue to:
Evaluate for pressure ulcers on PEDS and PICU
Analyze each case in the PICU to determine what triggered the “skin breakdown” (e.g. paralytics, medications, acuity, diagnosis, LOS, and location of ulcer)
Audit and educate for correct use of tools
Evaluate the Loyola Pediatric Skin Interventions utilizing the High, Moderate, and Low Risk Categories
Educate on Braden Q Scoring, Documentation, and Prevention through data collection and analysis
Develop:
Pediatric Skin Intervention Principles to be incorporated into the patient care policy
Inservice for proper turning of “at-risk” pediatric patients and identify other educational topics arising from the data collection and analysis process
Pediatric Occipital Preservation Program
Confidential: For Quality Improvement Purpose Only
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LESSONS LEARNED:
Post implementation of the PUPPI-C protocol to eliminate hospital-acquired pressure ulcers:
Nurses own each hospital-acquired pressure ulcer
Nurses investigate solutions and educate each other and parents on trends when appropriate
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M.Parthasarathy, S.Wojtowicz, C.Delsarto, K.Kiley, N.Porter, M.Volle, M.Payan, M Brush; T.Rodriguez, S.Smith, S.Lichtenstein, P.Mumby ; B.Emami; P.Stiff BMT Clinical Team, Department of Radiation Oncology
M.Parthasarathy, S.Wojtowicz, C.Delsarto, K.Kiley, N.Porter, M.Volle, M.Payan, M Brush; T.Rodriguez, S.Smith, S.Lichtenstein, P.Mumby ; B.Emami; P.Stiff BMT Clinical Team, Department of Radiation Oncology
Can Total Body Irradiation (TBI) for Allogeneic BMT Patients be Administeredin Out-patient Setting Safely?
OPPORTUNITY STATEMENT
• To evaluate administration of Total Body Irradiation (TBI) treatment prior to Allogeneic Stem Cell Transplants in the out-patient setting instead of the traditional in- patient setting.
• This will reduce the number of inpatient days for transplant admission and free up beds in BMT unit for new admissions
• To avoid any delay in admissions due to lack of bed availability for patients to proceed with stem cell transplant
• To be able to administer TBI in out-patient setting to all
eligible Allogeneic transplant patients
• Reduction in hospital length of stay for transplant admission.
• A positive impact on patient satisfaction and quality of life
measures due to decrease in in-patient length of stay
• To increase the capacity and avoid delays to perform more
allogeneic transplants in the transplant unit.
• To analyze data for any cost savings due to change of practice.
RESULTS
• Initiating transplant prep regimen with out patient TBI is safe and not associated with any increased risk of complications during transplant.
• This allows us to maximize our bed utilization on the inpatient unit as we are facing an ever increasing number of transplant procedures at Loyola
• This also leads to substantial cost savings for both patients and the institution.
• The is an ongoing project to evaluate a large number of patients. Comparative Statistical analysis will be performed including quality of life issues on a larger sample size in future. Going forward, all eligible allogeneic transplant patients will receive TBI in out- patient setting.
CONCLUSIONS
REASONS FOR CURRENT OPPORTUNITY
OVERALL SURVIVAL
RESULTS
• Gradual increase in the number of Allogeneic transplants performed over the last 5 years is resulting in a need to asses a change of practice.
• A need To extend our experience (published data) in performing autologous transplants with TBI regimen in the out-patient setting to the Allogeneic transplant population.
• A need to assess the feasibility and safety of administering TBI in out-patient setting for all eligible Allogeneic Stem Cell Transplant Patients.
SOLUTIONS IMPLEMENTED
• Change patients transplant schedule and calendar for Prep Regimen to accommodate out patient TBI
• Train / educate care givers to manage / help patients at home during this treatment
• Coordinate schedule with Radiation Oncology
• Plan in-patient admissions to have a smooth transition to BMTU unit post TBI
• All eligible patients were received outpatient TBI
• A considerable decrease in planned length of stay of 4 days per patient in the OP TBI Group was expected. However we observed a 6 day shortening of hospital stay. The reasons for this are not clear, but could be due to sample size or better acceptance of out patient therapy in our study group.
• No difference in Engraftment time between the two groups.
• No difference in treatment related complications between two groups.
• No difference in Day 100 survival between the two groups
• Cost savings were: $1000 Ambulance charges per patient$20,000 per patient difference for inpatient chargeTotal projected savings per year: $525,000
METHODS
• Change patients transplant schedule and calendar for Prep Regimen to accommodate out patient TBI
• Train / educate care givers to manage / help patients at home during this treatment
• Coordinate schedule with Radiation Oncology
• Plan in-patient admissions to have a smooth transition to BMTU unit post TBI
• All eligible patients were received outpatient TBI
• A total of 15 eligible patients (based on patient performance and payor requirements) out of 25 who received TBI for regimen were given Out Patient TBI.
• Transplant outcome data for this group was compared to the historic control group of 82 patients from 2 prior years who received TBI as In Patient
• Engraftment and In patient length of Stay data was compared
• Data was also collected and analyzed for complications related to this treatment viz. Mucositis, Infections and GI toxicity
• Day 100 survival data was collected for both groups and compared
• Data was analyzed for cost savings
RESULTS
N M/FMedia nAge
Median Days to Engraftment
Median Length of Inpatient Stay
DESIRED OUTCOME
POSTER 20
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3 NEWS Cardiac Telemetry
Chart Smart: A plan to improve patient
education nursing documentation
•Confidential: Quality Improvement Material
TABLE 21
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Nursing Magnet Forces: Nursing Excellence
Force 1-
Quality of Nursing LeadershipForce 3-
Management Style
Force 6-
Quality of CareForce 7-
Quality Improvement
Force 8-
Consultation and ResourcesForce 11-
Nurses as Teachers
Force 12-
Image of NursingForce 13-
Interdisciplinary Relationships
Force 14-
Professional Development•Confidential: Quality Improvement Material
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Aim
To improve patient education nursing documentation
Patient education nursing documentation will increase to achieve 100% compliance
•Confidential: Quality Improvement Material
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Nursing Documentation Compliance After Cycle 1
•Confidential: Quality Improvement Material
Patient Education Documentation Compliance3 NEWS Cardiac Telemetry
0%10%20%30%40%50%60%70%80%90%
May
June Ju
ly
Aug Sep Nov Dec Jan
FebMarc
h
Audit Month
% C
ompl
ianc
e
Focused efforts to document
Data collected without focused efforts
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Cycle 1 Plan and Do
•
May and June 09–
Patient Education sheets located at bedside for nursing documentation
•
July 09–
Compliance continued to improve with focus efforts–
RNs voiced concern about created burden of documentation that was not supported by EPIC
•
Aug 2009–
Work collaboratively with IT to develop a teaching sheet that works with the EPIC system
•
Improving systems already in place•
Providing smooth transition to standardized note•
Placing Pt education sheets into EPIC•
Educating RNs about initiative
•Confidential: Quality Improvement Material
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Cycle 2 Plan and Do
•
September 2009–
EPIC documentation revised with staff input
–
Educated documentation process to RNs•
November 2009–
Further EPIC documentation revision
–
Pt education record documentation simplified–
Continued education efforts
•
January 2010–
EPIC documentation includes plan of care flowsheet
•Confidential: Quality Improvement Material
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•Confidential: Quality Improvement Material
Nursing Documentation Compliance Progress
Patient Education Documentation Compliance3 NEWS Cardiac Telemetry
0%10%20%30%40%50%60%70%80%90%
100%
May
June Ju
ly
Aug Sep Nov Dec Jan
FebMarc
h
Audit Month
% C
ompl
ianc
e
Data collected without focused efforts
Improving systems already in placePlacing Pt education sheets into EPICEducating RNs about initiative
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Analysis
•
Manage for daily improvement resulting in greater than 85% compliance
•
Provide a culture for continuous improvement while standardizing a nursing note
•
Create intra departmental process and add value to process
•Confidential: Quality Improvement Material
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Next Steps
•
Continue to educate staff and work with patient education liaison to improve compliance
•
Monitor sustained compliance•
Share documentation process with other inpatient nursing units
•
Celebrate success
•Confidential: Quality Improvement Material
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You too can be… TCABLE
Team Members
•
TCAB Team•
3 NESW Cardiac Telemetry Nursing Staff
•
Julia Havey
RN, Sr. Systems Analyst Medical Information System
•Confidential: Quality Improvement Material
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Radiation Oncology IT Integration
IMAGES, DATA & PAPER CHARTS TO E-RECORDS
Committee Members:
John Roeske, Ph.D., Committee ChairmanTeresita F. McCoo, RT(NM), MS, MBAKevin Albuquerque, MD, Dolores Franco, RN, Angela McCrum, RT(T)Michelle Reynolds, RT(T), Faisal Vali, MD, Douglas Michels, System Analyst, Mohammed Siddiqui, RT(T), CMD
TABLE 22
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RADIATION ONCOLOGY E-CHART TEAM MEMBERS
• John Roeske, Ph.D., Committee Chairman• Kevin Albuquerque, MD• Dolores Franco, RN• Teresita F. McCoo, RT(NM), MS, MBA• Angela McCrum, RT(T)• Douglas Michels, System Analyst• Michelle Reynolds, RT(T)• Mohammed Siddiqui, RT(T), CMD• Faisal Vali, MD
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Project Goals• Be Compliant with the 2014 government
mandate to have an electronic record • Design & Implement an electronic version of
the Radiation Oncology paper chart within the IMPAC-MOSAIC environment.
• Create an integrated infrastructure that support workflow and safe, high quality care.
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Measurement of Success
– Percent Completion of the Project– Access to the record from multiple sites– Implementation of E-environment
Policies
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Project Scope & Management• There were multiple sections of the paper chart that had
to be converted into the electronic environment. These sections were used to break the project development /implementation into modules.
TheOrder
The Treatment
Plan
new
Com-munication
Tools
Treatment Delivery Records
Nursing &MD
Patient TXMngt.
Documents
PhysicsRecords Audits
& Reports
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DO- Integrate Systems LINAC,CT Scanner, Physics Systems, Data Storage, Treatment PLANS,
End Users….
MOSAIQ
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Measurement of Success-Project Completion
Chart Conversion to E-Format: % Completion of Conversion
020406080
100
3rd QTR 4th QTR 1st QTR 2ndQTR
3rd QTR 4th QTR 1st QTR
2008 2009 2010
Period
%Completion ofConversion
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Implementation of e-Chart
0
20
40
60
80
100
Mar-09 Jun-09 Sep-09 Dec-09 Mar-10
Perc
ent I
mpl
emen
ted
PrescriptionTreatment PlanTreatment Fields
Various phasesof e-chartimplementedover time
STATUS OF THE IMPLEMENTATION
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Measurement of Success
• Policies were developed & implemented• Records are now accessible from all
practice sites • Cancer Center Clinics• LOC Clinics• Offices• Hines Clinic
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Result- Better Integration of Care• Created a System of Communicating
Treatment flow
Contours Needed
Contours MD Done
CT SimScheduled
ChartChecked
Spec Proc. Notes
PT Educ.
GOAL
Chart to beChecked
Therapist
Schedulers
DosimetristCT Sim
Billing
MD
Physics
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Result- Capture Ancillary Documentation
Example: TimeExample: Time--Out Documentation Out Documentation & IV Contrast Safety Questionnaire & IV Contrast Safety Questionnaire
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Example e-Prescription Report
Physicianintent
MD Approval
Dosing andTreatment fields
The prescription & treatment field specifications are now in e-form
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Result- Simultaneous Viewing from Multiple sites
Multiple staff are able to work on different parts of the record at the same time.
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Comprehensive checklist prior to treatment
Each group completestheir portion of theChecklist prior tohand-off to the next group.
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Results-Ease of Auditing Process
• A by-product of the project is the ability to generate a list of pending tasks. It helps in ensuring complete documentation, timely billing, efficient turnaround times.
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Result- Standardization of Practice
• Policies and procedures were developed to address how the operation should be conducted in the electronic world.
• Naming of treatment fields• Where documents should go.• How daily treatments and adjustments will be
documented• Approval of plans for treatment
……And more
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Other benefits-• Going to a paperless environment has
created a more robust database that could be used for looking at patient mix, frequency of diagnosis, research etc.
• Improved the ease of getting information needed by insurance companies for reimbursement.
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Conclusion
• The department achieved its goal of creating an electronic environment to replace the paper chart. It is supported by an infrastructure and by procedural policies that makes it work well.
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Hematopoietic Cell Transplantation- Specific Comorbidity Index (HCT-CI) and Karnofsky Performance Scale
IS THERE A CORRELATION WITH SURVIVAL?
TEAM MEMBERS:M. Brush, APN, AOCN; C. DelSarto, RN; K. Kiley, ANP-BC, AOCN; M. Payan, ANP-BC; N. Porter, APN, AOCN; M. Volle, ACNP, OCN; S. Wojtowicz, BSN, OCN; P. Stiff, MD; T. Rodriguez, MD; and S. Smith, MD
TABLE 23
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BACKGROUND• The HCT-CI was developed to identify relevant
comorbidities in the allogeneic stem cell transplantation population and to enable risk assessment prior to allogeneic stem cell transplantation.
• The HCT-CI is able to classify patients into three risk groups (low, intermediate and high) which are predictive of 2 year non-relapse mortality post- transplantation.
• The HCT-CI was derived and validated by investigators at the Fred Hutchinson Cancer Research Center[Sorror et al. Hematopoietic cell transplantation (HCT)-specific co-morbidity index: A new tool for risk assessment before allogeneic HCT. Blood 2005: 106 (2912-2919)]
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PROJECT AIM• To increase documentation of the HCT-CI
score and Karnofsky score on all patients undergoing hematopoietic stem cell transplantation within one week of transplant admission.
• To determine whether there is a correlation between HCT-CI scores and two year non-relapse survival at LUMC
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Solutions Implemented
• All Bone Marrow Transplant (BMT) Advanced Practice Nurses (APN’s) were educated on the HCT-CI form (which included the Karnofsky score) and the expectations for completion of the form.
• A smart set was developed for EPIC to facilitate the use of the HCT-CI form.
• Written and verbal reminders were given to the APN’s on a frequent basis to encourage timely completion of the HCT-CI.
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Compliance with Completing HCT-CI Forms
0102030405060708090
100
Per
cent
Com
plia
nce
Jul-09 Aug-09 Sep-09 Oct-09 Nov-09 Dec-09 Jan-10 Feb-10
Month
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0
10203040506070
8090
100
0 (n=5) 1-2 (n=4) > 2 (n=8)HCT-CI Score
100 Day Survival Autologous Stem Cell Transplants
100 Day Survival Autologous Stem Cell Transplants
(Note: The HCT-CI is predictive of non-relapse mortality 2 years post allogeneic transplant)
100% 100% 100%
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100 Day Survival Allogeneic Stem Cell Transplants
(Note: The HCT-CI is predictive of non-relapse mortality 2 years post allogeneic transplant)
0102030405060708090
100
0 (n=5 1-2 (n=9 >2 (n=10)HCT-CI Score
100 Day Survival Allogeneic Stem Cell Transplants
100%
80% 80%
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ANALYSIS• For the first 8 months of data collection, there was a
compliance rate of 89% which is below the target of 95%.
• As mentioned earlier, the HCT-CI is designed to be predictive of non-relapse mortality 2 years post allogeneic stem cell transplant. Given that we have been collecting data for only 8 months, it is too early to determine whether it is predictive of non-relapse mortality for transplants performed here at Loyola University Medical Center.
• Because the ultimate goal of collecting this data is to determine whether the HCT-CI tool can be used to predict non-relapse mortality here at Loyola, further education will be required regarding the importance of collecting this data.
• Because the HCT-CI purportedly predicts 2 year non- relapse mortality, survival statistics will need to be collected on all patients for a period of 2 years post transplant.
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Next Steps
• Continuing education on importance of completion of HCT-CI tool
• Identify barriers to completion of tool• Post monthly audit results • Continue to monitor and post
correlation of HCT-CI tool with 2 year non-relapse mortality rates
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the Safety and Efficacy the Safety and Efficacy of a Patientof a Patient’’s Treatment s Treatment on a Clinical Trialon a Clinical Trial
Team Members: Team Members: Chemotherapy QI Committee , BEACON Core Team, Cancer Chemotherapy QI Committee , BEACON Core Team, Cancer Clinical Trials Office, Pharmacy (Clinical and Investigational),Clinical Trials Office, Pharmacy (Clinical and Investigational), Clinical Nurses, and Cancer Center Physicians Clinical Nurses, and Cancer Center Physicians
A Multidisciplinary A Multidisciplinary Approach to EnsuringApproach to Ensuring
TABLE 24
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Project AimsProject Aims
•• Identify potential for error in current Identify potential for error in current processes for building, reviewing and processes for building, reviewing and approving BEACON treatment plans approving BEACON treatment plans for Clinical Trials for Clinical Trials
•• Achieve an efficient standardized Achieve an efficient standardized process process
•• Achieve 100% Accuracy of BEACON Achieve 100% Accuracy of BEACON treatment plans for Clinical Trials treatment plans for Clinical Trials
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ProblemProblem•• Number of new Cancer Clinical Trials processed a year Number of new Cancer Clinical Trials processed a year
increased by 42% over the past two years increased by 42% over the past two years •• Complexity and variety of trials has increased over the past Complexity and variety of trials has increased over the past
few years.few years.•• Many sources for trials to include access to eleven NCI Many sources for trials to include access to eleven NCI
(National Cancer Institute) Cooperative Groups, Academic (National Cancer Institute) Cooperative Groups, Academic Consortiums, Investigator initiated and Pharmaceutical Consortiums, Investigator initiated and Pharmaceutical companiescompanies
•• Twenty Twenty ––three investigators with varying frequency with three investigators with varying frequency with submitting new trials submitting new trials
•• Process unclear and has potential for error Process unclear and has potential for error •• Process cannot be auditedProcess cannot be audited•• Timeline too narrow to adequately process new BEACON Timeline too narrow to adequately process new BEACON
treatment plans (BEACON is the EPIC oncology module)treatment plans (BEACON is the EPIC oncology module)
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Approach to the ProblemApproach to the Problem
•• Used a modified Failure Modes and Effects Analysis Used a modified Failure Modes and Effects Analysis Process (FMEA)Process (FMEA)
•• Flow charted the current processFlow charted the current process•• Identified potential problem steps and processesIdentified potential problem steps and processes•• Determined which steps and processes needed to be revised Determined which steps and processes needed to be revised
based on team discussion and analysisbased on team discussion and analysis•• Revised the processes to reduce potential for errorRevised the processes to reduce potential for error•• Flow charted the new process at a high level and with Flow charted the new process at a high level and with
detaildetail•• Continue to monitor performanceContinue to monitor performance
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Research RN notifies
BEACON team
when firstpatient is screened
Previous ProcessPrevious Process
Potential Communication
Error
Potential Communication
error Timeline too narrow
for BEACON to build treatment plan… potential
for excessive workload
Difficult for RN to
manage within short time frame
Individual research RN’s send data to Beacon team, with
no centralized control of what’s
being sent
PI review timeframe too short
Possible Problems
Research RN receives
notice from IRB that study is approved
Potential for inaccurate BEACON
orders
Research RN routes orders
to PI to review
and approved
BEACON team builds
plan and informs
Research RN when ready to review
Orders approved
and released for use
Research RN notifies
Investigationalpharmacist who Processes ERX
BEACON= EPIC Oncology moduleIRB = Institutional Review BoardPI= Principle InvestigatorERX= Electronic drug record
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SolutionsSolutions•• Clearly defined workflow for building BEACON Clearly defined workflow for building BEACON
treatment plans between the Information treatment plans between the Information Technology dept, Investigational Pharmacy and Technology dept, Investigational Pharmacy and BEACON TeamBEACON Team
•• Determined earlier submission timeline to Determined earlier submission timeline to BEACON teamBEACON team
•• Formalized the multidisciplinary review processFormalized the multidisciplinary review process•• Centralized coordination and documentation of Centralized coordination and documentation of
the review processthe review process•• Centralized the information about the status of Centralized the information about the status of
the BEACON treatment planthe BEACON treatment plan•• New process initiated in September, 2009New process initiated in September, 2009
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Research Nurse reviews
and edits Treatment Plan
Revised ProcessRevised Process High Level Flow ChartHigh Level Flow Chart
Beacon Team has more time to build treatment
plan
Process is centralized
through CCTO
Research nurse has more time to review and edit
plan
PI has more time for review and has a formal sign off
Process begins earlier – when
protocol is submitted to the
IRB
Process allows for a final review
by all
New Changes
CCTO sends protocols to
Beacon Team & Investigational
Pharmacistwhen sent
to IRB
Status of Active Treatment Plans
are posted on CCTO website.
Completed routing form filed.
Beacon Team revises plan followed by final review
by pharmacy, nurses and PI
PI reviews and edits Treatment Plan and
signs off on routing form
Beacon treatment plan released and notification takes place
Beacon Team builds
Treatment Plans and notifies CCTO when
ready forreview
CCTO = Cancer Clinical Trials Office Manager
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BEACON Treatment Plans for NEW and Amended Clinical Trials Process for submission of research protocols to BEACON Build team. Process for review and approval of Treatment plans for Clinical Trials
CCTO (Manager) sends all protocols reviewed at Protocol Review Committee (PRC) to
Investigational Pharmacist. Include the order of priority for building
ERX records.PRC meeting 3rd Tues of Month
Investigational pharmacistcreates ERX record for study-supplied and investigational drugs and sets up study in
Investigational Pharmacy Management System
Timeline Cooperative Group Studies
4-6 weeks from PRC
BEACON team builds treatment plan and notifies CCTO manager that treatment plan is ready to
review, returning routing form
Research Nurse Reviews and edits as needed
PI Reviews and edits
BEACON Team revises treatment plan
BEACON treatment plan released and pharmacist notifies CCTO Manager
PI forwards to research nurse or manager and signs off on routing form
Timeline Pharma and PI Initiated
Studies 2-4 months from PRC
Manager notifies the research nurse and PI that the Treatment plan is ready to review
Final review of treatment plan Pharmacy , Research Nurse and PI
Manager notifies PI and nurse, then posts on CCTO Website that the BEACON treatment plan is active.
Completed Routing form will be stored in central file.
RN coordinates with PI for review-Sends routing form to PI
Note:Knowing at what point the treatment plan is in the process is dependent on communication between
pharmacy and the CCTO due to inability to differentiate in BEACON
CCTO (Manager) Sends NEW protocols and routing form to BEACON TEAM at time of IRB Submission
(LU # included)
BEACON TeamTina Cabala 72710Donna Fletcher-Gonzalez 63702Germika Collier 72085Janine Marschalk 72006
Protocol Amendments
Clinical Regulatory Coordinator sends notice to PI, staff and
BEACON builder when the IRB approves an amendment
CRC distributes amendment routing
form for review
Investigational Pharmacist Bushra Muneer 66225
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ResultsResults
Goal: 100% Accuracy of BEACON Treatment Plans Built for Clinical Trials June 2009- Feb 2010
75%
80%
85%
90%
95%
100%
June July
Aug
Sept
Oct Nov
Dec
Jan
Feb
Percentage of Protocols with Accurate BEACON Orders
BEACON is the EPIC Oncology ModuleBEACON is the EPIC Oncology Module
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Next StepsNext Steps
•• Determine best approach to utilize BEACON with ensuring Determine best approach to utilize BEACON with ensuring study parameters and dose modifications are met.study parameters and dose modifications are met.
•• Elicit end user feedbackElicit end user feedback-- the physicians entering the orders the physicians entering the orders and nurses executing the ordersand nurses executing the orders
•• Define categories within BEACON and the type of Define categories within BEACON and the type of information to include in these categoriesinformation to include in these categories
•• Improve readability for end usersImprove readability for end users•• Differentiate in treatment plan what is standard vs. nonDifferentiate in treatment plan what is standard vs. non--
standard or study relatedstandard or study related•• Develop guidelines for reviewing treatment plans Develop guidelines for reviewing treatment plans •• Determine best method to measure medication errors Determine best method to measure medication errors
associated with treatment plans for clinical trialsassociated with treatment plans for clinical trials
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Understanding each otherUnderstanding each other’’s view and role s view and role improves the processimproves the process
EveryoneEveryone’’s view in BEACON is differents view in BEACON is different
Lessons LearnedLessons Learned
Together we all ensure the safety Together we all ensure the safety of the patientof the patient
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Team Membership
Sandra M. Weszelits APNNurse Practitioner, Pediatric Surgery
Loretto A. Glynn, MDMedical Director, Pediatric Surgery
Preventing Complications in Preventing Complications in Gastrostomy/JejunostomyGastrostomy/Jejunostomy
Tubes in Tubes in
Pediatric PatientsPediatric Patients
TABLE 25
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This project was introduced as a method to identify the best manner to secure Gastrostomy/Jejunostomy
Tubes in place so that
dislodgement is prevented. When discussing various prevention methods, skin care became a prevalent factor to evaluate. If tubes are dislodged or if skin integrity is breached the patient is at risk for serious complication and there is an increased healthcare cost to the patient and hospital
Background
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Goal
Reduce the incidence of Gastrostomy/Jejunostomy tube displacement within the initial 30 day post-operative period to 0% and maintain skin integrity around stoma site.
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• Standardized suturing protocol by both pediatric surgeons who place Gastrostomy/Jejunostomy Tubes
• Education for nursing and residents on site care and dressings
• Standardized clinical protocol and ordersets for Gastrostomy care
• Standardized teaching material for parents• APN run Gastrostomy Tube Clinic
Solutions Implemented
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Results
SUTURING of the Gastrostomy/ Jejunostomy
tube provided the most
stability and prevent dislodgement and skin breakdown in 100% of our patients
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Number of Complications by Method of Securing Tube
05
101520253035404550
Number of tubes placed 44 17 25# Complications 5 10 0
Tape Sutured Disk Sutured Tube
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010
2030405060
7080
2007 (n=3/26) 2008 (n=12/27) 2009 (n=0/23)
Percentage of Complication by Method and Year
Tape Sutured Disk Sutured Tube
Per
cent
Com
plic
atio
n
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DISK
Skin
Stomach
Catheter Tip
Gastrostomy Tube
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Analysis
• Tape and suturing of the disk were standard practice for stabilizing the gastrostomy/jejunostomy tube.
• These methods resulted in higher complication rates from tube dislodgment, potential for peritonitis, and skin breakdown
• Current literature supported suturing the tube as the standard method for stabilizing the tubes and resulted in ZERO tube dislodgments and skin breakdown.
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Next Steps
• Continue to monitor for complications• Utilize suturing of tube as the standard
method for securing Gastrostomy/Jejunostomy tubes
• Work with other services to standardize their method of securing tube to suturing of tube
• Evaluate PEG tubes and the potential for conversion to open procedure as compared to Laparascopic Assisted PEG placement
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APN Gastrostomy Clinic
• Provides– Gastrostomy Tube changes– Maintenance of Gastrostomy Tubes– Skin assessment and treatment– Patient Education– Family Support– Daily Clinic Availability
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Magnet Forces• Force 6 Quality of Care
Quality is the systemic driving force for nursing and the organization. Nurses serving in leadership positions are responsible for providing and environment that positively influences patient outcomes and is a pervasive perception among nurses that they provide high quality care to patients.
• Force 12 Image of NursingThe services provided by nurses are characterized as essential by other members of the healthcare team. Nurses are viewed as integral to the healthcare organization’s ability to provide patient care. Nursing effectively influences system-wide processes.
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Improving Compliance with Positioning, Splinting & Activity of the Burn Patient
Melissa Drews-Lane, MS, OTR/LKathy Supple, ACNP
Adam Young, PT
TABLE 26
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Activity and positioning of the burn patient are key to the patient’s functional outcome. Splints are given to most patients to assure maximal functional outcome. The consequences of immobility should be avoided by this activity. A patient needs to be up out of bed throughout the day to regain strength and maintain functional independence. The multidisciplinary team on the burn unit strives to provide excellence with patient care. We identified an inconsistency among staff with compliance regarding activity, splinting, and positioning of the burn patient. Specifically, we identified a problem with compliance of application and documentation of splints and the activity level of patients.
Background
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Goal
1. Improve compliance with patient splinting and activity orders 100% of the time
2. Improve documentation of splinting and activity level in EPIC to 100%
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• Staff education on the importance of documentation and compliance
• Implementation of binder for self-education and permanent resource. Available to staff at all times
• Implementation of visual pictures in patient’s room of splints/positioning/activity
• Resident education on activity orders for burn patients
Solutions Implemented
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0%
20%
40%
60%
80%
100%
Pre Post
87%
59%
Documentation of OOB
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Patients OOB within 24 hours period
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
Pre Post
65%
84%
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Splint wear schedule provided for patients
0%
20%
40%
60%
80%
100%
Pre Post
100%100%
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Splint wear schedule posted in room
100% 100%
0%
20%
40%
60%
80%
100%
Pre Post
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Splint wear documented in EPIC
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
Pre Post
14%
86%
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0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
Pre Post
Documentation of splints worn correctly and on schedule
86%
7%
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Analysis– Documentation of splint wear and activity has
improved– Compliance with activity orders has increased
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Next Steps• Revise Burn ordersets to include splinting orders• Revise Burn ordersets to include specific activity orders• Revise resident education manual• Continue to provide education to RN’s, PCT’s, and
residents• Provide education to all OT staff and extend education
hospital-wide to all RN’s, PCT’s and residents• Continue to monitor progress
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Organizational Initiatives to Optimize Organ Donation
Rose Lach, PhD Kim Reeks, RNFred Luchette, MD Cindi Laporte, RNMichael Schneck, MD A. Mostofi, MSNThomas Esposito, MD Megan Kuck, RNHoward Sankary, MD Kathryn Ichniowski, RNDavid Holt, MD Mary McGillicuddy, MSWCharles Alex, MD Marie Coglianese, MPSNandine Calamur, MD Katherine Abhalter, GOHJessica Wanger, GOH
For Quality Improvement PurposesTABLE 27
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Background
Over 105,000 persons are waiting for organs yet only 19,000 have been transplanted in 2009.
To narrow the gap between organ need and organ donation, the US Department of Health & Human Services (HHS) has set a goal for each hospital to achieve a 75% organ donation rate or 3.65 organs/person.Since 2003, HHS has promoted a national collaborative to increase organ donation.
For Quality Improvement Purposes
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Aim Statement
TargetsLUMC will achieve a 75% organ conversion rate.Timely referrals for organ donation to the Gift of Hope (GOH) will be greater than 90%.
Applicable Magnet ForcesForce 6: Quality of CareForce 13: Interdisciplinary Relationships
LUMC’s Organ Donation Committee launched several initiatives to raise awareness and outlined procedures to increase organ donation.
For Quality Improvement Purposes
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Solutions Implemented
A multidisciplinary organ donation committee was initiated including ICU physician directors, managers, an ethicist, a chaplian, a social worker, and GOH representatives.
GOH provided bi-monthly data on LUMC’s conversion rate and barriers discussed.
A policy outlining the process for brain death and “donation after cardiac death” was implemented.
For Quality Improvement Purposes
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Solutions Implemented
GOH given “read only” access to EPIC to review potential donors.
Brain death protocol orders established by the GOH implemented.
A GOH representative exclusive to LUMC assigned.
Organ donation education provided at nurses and physicians orientation and annual continuing education programs.
For Quality Improvement Purposes
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Per
cent
LUMC Organ Conversion Rate
Quarter
UCL = 97
Mean = 41
1Q 2007
2Q 2007
3Q 2007
4Q 2007
1Q 2008
2Q 2008
3Q 2008
4Q 2008
1Q 2009
2Q 2009
3Q 2009
4Q 2009
0
20
40
60
80
100
For Quality Improvement Purposes
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Per
cent
LUMC Timely Notification of Potential Donors
Quarter
UCL = 130
Mean = 80
LCL = 31
1Q 2007
2Q 2007
3Q 2007
4Q 2007
1Q 2008
2Q 2008
3Q 2008
4Q 2008
1Q 2009
2Q 2009
3Q 2009
4Q 2009
0
20
40
60
80
100
120
For Quality Improvement Purposes
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Analysis
Organ Donation conversion rate increased from 41% in January, 2007 to 100% in Dec., 2009
Timely referral rate to the GOH increased from 83% in January, 2007 to 100% in Dec., 2009.
For Quality Improvement Purposes
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Next Steps
Continue with quarterly analysis of organ conversion rate, however, move report to ICU Committee.
Hold regular “huddles” after organ donation to discuss success and failures.
Provide regular report to senior leadership.
Continue to thank staff for their involvement and report on “lives saved”.
For Quality Improvement Purposes
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Achieving and Maintaining 80% Compliance with the Use of
Intravenous Pump Safety Software
Dorothy Bourgeois, RN; Joan Howard, RN; Gwen Loes, RN; Richard Mattis, MD; Tom Busse, Pharm
D; Connie Clark, RN
TABLE 28
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Project Aim Statement
•
Improve patient safety through the use of “smart pumps”
•
Achieve and maintain at least 80% compliance on all inpatient units
Pertinent Magnet Forces1. Quality of Nursing Leadership2. Management Style6. Quality of Care7. Quality Improvement
13. Interdisciplinary RelationshipsConfidential – for quality improvement purposes only
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Solutions ImplementedDepartment Actions and Communications
-
communication of expectations-
achievement standard on performance reviews
Unit Actions and Communications-
Nurse Manager/charge nurse rounds-
identification of super-users on all shifts
Nursing-Pharmacy-Medical Staff Collaboration-
drug library customized for each unitmost frequently used drugs come up first on the screen
-
ease of accessing Code 88 drugs-
patient weight entry calculates weight based medications-
achievement reported at medical Executive and Pharmacy and Therapeutics Committees
Confidential – for quality improvement purposes only
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Compliance with Safety Software for MednNet IV Pumps April 2006-February 2010
Perc
ent C
ompl
ianc
e
For Quality Improvement Purposes Only
4/ 1/ 2
0065/ 1
/2006
6/ 1/ 2
0067/1
/2006
8/ 1/ 2
0069/1
/ 2006
10 /1/2
0 06
11 /1/2
0 06
12 /1/2
0 061/ 1
/ 200 7
2/ 1/2
0073/ 1
/ 2007
4/1/2
0075/ 1
/ 2007
6/ 1/2
0077/ 1
/ 2007
8/1/2
0079/ 1
/ 2007
10 /1/2
0 07
11 /1/2
0 07
12 /1/2
0 071/ 1
/ 2008
2/ 1/ 2
00 83/ 1
/2008
4/ 1/ 2
00 85/ 1
/ 2008
6/ 1/ 2
0087/ 1
/2008
8/ 1/ 2
0089/ 1
/2008
10 /1/2
0 08
11 /1/2
0 08
12 /1/2
0 081/1
/ 2009
2/ 1/ 2
0093/1
/ 2009
4/ 1/ 2
0095/ 1
/ 200 9
6/ 1/ 2
0097/ 1
/ 2009
8/ 1/ 2
0099/ 1
/ 2009
10 /1/2
0 09
11 /1/2
0 09
12 /1/2
0 091/ 1
/ 2010
2/1/2
010
20
30
40
50
60
70
80 T a r g e t
Drug library revision and educational in-services
Drug library revision and educational in-services
Drug library revision and educational in-services
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Per
cent
Com
plia
nce
For Quality Improvement Purposes Only
8/2008 (n
=6597)
9/2008 (n
=5711)
10/2008 (n
=6700)
11/2008 (n
=8486)
12/2008 (n
=7155)
1/2009 (n
=7319)
2/2009 (n
=8361)
3/2009 (n
=7944)
4/2009 (n
=7942)
5/2009 (n
=8211)
6/2009 (n
=7468)
7/2009 (n
=7161)
8/2009 (n
=7353)
9/2009 (n
=8551)
10/2009 (n
=7432)
11/2009 (n
=7074)
12/2009 (n
=8364)
1/2010 (n
=8580)
2/2010 (n
=7230)
79
80
81
82
83
84
85
Target
M ean
UCL
M ean
LCL
19
Compliance with Safety Software for MedNet IV Pumps August 2008-February 2010
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AnalysisThe safety software has prevented infusion
rate errors* on
224 occasionsIn the past 12 months (0.23% of 95,994
programming events)
*This means that a rate limit warning was displayed and the nurse changed the rate on the pump prior to starting the infusion
Confidential – for quality improvement purposes only
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Next Steps•
Ensure compliance and consistency in outpatient areas
•
Learn for the future when purchasing programmable equipment
Confidential – for quality improvement purposes only
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Improve Quality of Care by Instituting Clinical Protocols
in the Gottlieb Wound Healing & Hyperbaric
Medicine Center
TABLE 29
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Team Membership
Richard Viglione, M.D. Medical Director
Sung Kim, M.D. Leslie Phillips, Program DirectorLinda Dent, HBO Safety DirectorSari Cairo, R.N. Clinical CoordinatorAndy Cerna, R. N.
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Background• An estimated eight million Americans suffer from
chronic wounds. Wounds come from a variety of different medical conditions, and they don't heal for many different reasons. Typically, a wound that does not respond to normal medical care within 30 days is considered a problem or chronic wound.
• Hard to heal wounds such as diabetic ulcers, surgical wound or venous stasis ulcers require specialized treatment with specialized dressings, pressure relieving casts, and hyperbaric oxygen chambers.
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Problem Statement
The Wound Healing & Hyperbaric Medicine Center identified two key quality of care indicators that were outside acceptable limits of the national benchmark
• Days to heal
• Healing percentage
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Goals:• Reduce the rate of “Days to
heal” to less than 35 days
• Increase the healing percentage of wounds to 88%
Project Aim Statement
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Definitions:
Days to heal is defined as the number of days from the wound admission until the wound is healed and measured at 0x0x0 cm.
Healing percentage is defined as the percentage of wounds that are discharged as healed versus an unfavorable outcome (e.g. amputation, etc.).
Aim Statement Continued
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Aim Statement Continued
Magnet Forces of Magnetism
Force 6: Quality of CareForce 7: Quality Improvement Force 8: Consultation & ResourcesForce 13: Interdisciplinary
Relationships
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– Formed a multidisciplinary team to investigate best practices.
– Implementation of evidenced-based Clinical Practice Guidelines in July 2007.
– Wound Healing Society Guidelines for the Best Care of Chronic Wounds 2006
– Wound Ostomy Continence Nurses Society Clinical Practice Guidelines 2002-2005
– Oxygen therapy Committee Report of the Undersea and Hyperbaric Medicine Society 2003
– All staff and physicians were educated on the new Clinical Practice Guidelines.
Solutions Implemented
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– The Clinical Practice Guidelines include: • Diagnostic criteria• Key therapeutic objectives• Common pathways to non healing• Assessment and intervention recommendations• Timely and appropriate utilization of adjunct therapies
including Hyperbaric Oxygen Therapy and Bioengineered Skin Substitutes.
• Time references for wound progress and interventions
• References
Solutions Implemented
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Day
s to
Hea
l
Fo r Q u a lity Imp ro v e me n t Pu r p o s e s O n ly
Jul- S
e p 06
Oct
-Dec
06
Jan -M
a r 07
Ap r-
Jun 0
7
Jul- S
ep 07
Oct
-Dec
07
Jan -M
a r 08
Ap r-
Jun 0
8
Jul- S
e p 08
Oct -D
ec 0
8
Jan -M
a r 09
Ap r-
Jun 0
9
Jul- S
ep 09
Oct
-Dec
09
Jan -M
a r 10
2 0
3 0
4 0
5 0
6 0
7 0
T a r g e t
M e a n
U C L
M e a n
L C L
The Wound Healing & Hyperbaric Medicine Center’s days to heal decreased by 12.4 days from 49.2 to 30 days after project
implementation in July 2007.
Number of days to heal below mean of 40 days for last year.
CPG Implementation 3Q07
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Per
cent
age
of W
ound
s H
eale
d
Fo r Q u a lity Imp ro v e me n t Pu r p o s e s O n ly
Jul- S
e p 06
Oct
-Dec
06
Jan -M
a r 07
Ap r-
Jun 0
7
Jul- S
ep 07
Oct
-Dec
07
Jan -M
a r 08
Ap r-
Jun 0
8
Jul- S
e p 08
Oct -D
ec 0
8
Jan -M
a r 09
Ap r-
Jun 0
9
Jul- S
ep 09
Oct
-Dec
09
Jan -M
a r 10
8 5
9 0
9 5
1 0 0
1 0 5
T a r g e t
M e a n
U C L
M e a n
L C L
The Wound Healing & Hyperbaric Medicine Center’s healing percentage consistently remains above the target of 88%
after project implementation in 2007.
The mean average of wounds healed is 95%
CPG Implementation 3Q07
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Award Winning Performance
The Wound Healing & Hyperbaric Medicine Center at Gottlieb Memorial Hospital has been recognized as a Center of Distinction in both 2008 and 2009 by it’s parent company, Diversified Clinical Services, Inc. The Center also earned the company’s Robert A. Warriner, M.D., Center of Excellence award in recognition of earning its second consecutive Center of Distinction Award.
These awards recognize the Center's delivery of outstanding results for twelve consecutive months in both 2008 and 2009, through the meeting or exceeding of company benchmarks in Healing Outcomes, Patient Satisfaction, Outlier Management and Days to Heal.
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Next Steps
•Increase healing percentage target to 96% •Analyze outliers for common trends•Share results with key stakeholders•Celebrate successes
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LEAN Transformation: The GI Lab Journey to Enhance Patient Flow & Volumes
Team Leadership:Claus Fimmel, MDRose Lach, RN, PhDDeb Kull, MBA John Zinkel, MS, BBA, RRT, RCP Lynn Heicher, RN, MS, CGRN, CLNCCarmen Acevedo
Team Membership: The GI Lab Staff and Physicians
Magnet Forces:Force 6: Quality of CareForce 7: Quality ImprovementForce 11:Nurses as teachers
TABLE 30
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Project Aim Statement
To utilize LEAN concepts to increase and sustain operational efficiencies in the GI Lab.
Goals:
Increase volume from 35 to 60 average cases per day
Increase gross revenues
Eliminate registry personnel
Sustain transformed areas by using a standard work format
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The Value Stream Map November 2-5, 2009
To determine capacity and overall efficiencies of the GI Lab, a Value Stream Map was developed.
Comprehensive time studies to measure patient flow pre, intra, and post procedure.
Baseline 5S (Sort, Straighten, Shine, Standardize, Sustain) scores collected for the nurses station, pre op, post op and procedure rooms.
Baseline data collected for 1 week.
Value stream map created and problem burst areas clearly defined.
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The Value Stream Map (VSM)
The VSM is ground zero and drives our GI Kaizens!
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A “Road Map” was created to highlight key improvement opportunities. Several Kaizen events
were planned and executed
Date EventNovember 9-13, 2009 5S Pre procedure, Post Procedure and
Procedure RoomsDecember 14-18, 2009 Kaizen - Appointment Scheduling
January 28, 2010 Visual Management Board
February 8-12, 2010 5S Nurse Station
February 8-12, 2010 Room 1, Motility, Capsule Studies,Breath Tests
February 15-19, 2010 Kaizen – Physician Scheduling
March 22-26, 2010 5S Endoscope Reprocessing Room
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5S - Sort, Straighten, Shine, Standardize, Sustain
Evaluated the pre-procedure & post-procedure areas
Set standard work flow
Established standard supply par levels
A Standard Work Survey is done daily to sustain what was improved
BEFORE AFTER
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Steady improvement in 5S scores demonstrate staff compliance with sustaining the changes made
Target = 5.0 Score
TARGET: 5.0GI Laboratory 5S Scorecard
0.2
1.8
4.2
4.64.8
3
3.63.8
0
0.5
1
1.5
2
2.5
3
3.5
4
4.5
5
11/9/09 11/16/2009 11/25/09 12/4/2009 1/28/2010 2/12/2010 3/19/10 3/26/10
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Appointment & Physician Scheduling December 14-18, 2009; February 15-19, 2010
Initiated “first contact” script for schedulers.
Initiated HACC in-basket messaging.
Mirrored scheduling set up for appointments.
Implemented use of the Daily Appointment screens.
Developed and implemented phone tree.
Developed a physician block schedule.
Established an ‘Add On Room’ for in-patients.
Adjusted staffing plan to meet provider and patient care needs.
Time A B C D E F A B C D E F A B C D E F Time A B C D E F A B C D E F700 700730 730800 800830 830900 900930 9301000 10001030 10301100 11001130 11301200 1200 Break1230 12301300 13001330 13301400 14001430 14301500 15001530 15301600 16001630 16301700 17001730 17301800 18001830 18301900 1900
* Schnell may use Add On Rm first thing in morning.
Peds
?
Levi
s
Add
-Ons
/Con
sult
Phys
Add
-Ons
/Con
sult
Phys
A P
illai
Fim
mel
(2nd
& 4
th)
Isla
m
Dor
fmei
ster
?
Levi
s
Leya
Affr
onti
Levi
sLe
vis
Add
-Ons
/Con
sult
Phys
Add
-Ons
/Con
sult
Phys
Leya
Leya
Levi
s
Add
-Ons
/Con
sult
Phys
Add
-Ons
/Con
sult
Phys
Losa
vio
Kla
mut
Leya
Slog
off
Levi
s
Losa
vio
Lap
Ban
d(s
urge
on)
Affr
onti
TBD
BreakBreak
Add
-Ons
/Con
sult
Phys
Add
-Ons
/Con
sult
Phys
Affr
onti
Losa
vio
Ahn
Gha
zanf
ari
Dor
fmei
ster
TBD
Kla
mut
Kla
mut
Dor
fmei
ster
Break Break
Affr
onti
Losa
vio
Add
-Ons
/Con
sult
Phys
Add
-Ons
/Con
sult
Phys
Slog
off
Monday Tuesday Wednesday Thursday Friday
Affr
onti
Kla
mut
Isla
m
Lecture Lecture
Time A B C D E F A B C D E F A B C D E F A B C D E F A B C D E F700730800830900930
1000103011001130120012301300133014001430150015301600163017001730180018301900
LectureLecture
Affr
onti
Kla
mut Is
lam
Kla
mut
Gha
zanf
ari
R.P
illai
Levi
sLe
vis
Slog
off
Isla
m
Losa
vio
Levi
s
Affr
onti
Affr
onti
R. P
illai
Losa
vio
Losa
vio
Dor
fmei
ster
Kla
mut
Affr
onti
Ahn
Losa
vio
A. P
illai
Dor
fmei
ster
Leya
Leya
Isla
m
Affr
onti
R.P
illai
Levi
sLe
vis
Fim
mel
(2
nd &
4th
)
Monday Tuesday Wednesday Thursday Friday
Old
New
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Visual Management January 28, 2010
Re-formatted existing white board in the GI Lab Nurses Station – divided by rooms to create 60 slots
Use board to track patient flow through the system - arrival time, location, and discharge time
Staff and physicians now have a “visual cue” for patient tracking and space utilization
Reduced congestion in the charge nurse area
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Average Case Volume per Day
41.15
32.7532.77
37.68
39.837.38
36
41.4239.42
37.8 37.72
15
20
25
30
35
40
45
May-09 Jun-09 Jul-09 Aug-09 Sep-09 Oct-09 Nov-09 Dec-09 Jan-10 Feb-10 Mar-10
Appointment & Physician scheduling changes have increased capacity
The LEAN journey begins
Target: 60 cases/day
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Next Steps: Roll out and Implementation
Physician scheduling plan April 15, 2010
Staff scheduling plan April 15, 2010
Mini-Kaizen Events: materials, supply and pharmaceutical ordering processes, endoscope reprocessing room
March 2010
Continue to develop subject matter experts; Divine Grace Tongol and Michalene Facenda will be Loyola’s 1st certified subject matter experts.
March 2010
Build and grow volume. OngoingSustain all areas. Ongoing
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Enhancing Quality In Patient Care by Implementing a Lean
Culture
Picture
For Quality Improvement Purposes
TABLE 31
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Goals and Objectives
• Transform Loyola to a culture of continuous improvement using lean methodology
• Educate 100% of management on lean methodology by July, 2010
• Measure performance of operational initiatives
For Quality Improvement Purposes
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What is Lean Transformation?
For Quality Improvement Purposes
• A change in thinking• Individual optimization to process optimization• Questioning “what we’ve always done”
• A change in behavior• Defining the critical few metrics and opportunities• Measuring performance at all levels
• A change in culture• Engages all employees• Enables daily improvement
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Phases of a Transformation
N/10 pace and 1–3% dedicated to Continuous Improvement
ChangingActions
Apply
tools
Borrowing th
en
Develo
ping Technique Developing
New Beliefs Fore
ver I
mprov
e
Cultur
e Cha
nge
Impr
ovem
ents
in H
D, Q
, C, D
Introduction Year 1-2
IntenseYear 3-5
Development Year 5 - 10
ChangingHabits
ChangingValues
Understanding &
EmbeddingPrinciples
Loyola’s Transformation
More People – Improving Faster
Impr
ovem
ents
in S
QDPC
Changing
Culture
For Quality Improvement Purposes
We are here
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Transferring Knowledge• 100 % of Management
– 35 Trained– 225 Total
Subject Matter Expert Development
For Quality Improvement Purposes
Voice of the Customer
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“How We Do It” Kaizen Event Week
DAY 1 DAY 5DAY 4DAY 3DAY 2
Tool Specific Training
Observe & Analyze Current
Process / Begin
Improvements
Continued Improvements
Refinement And Finalize
Improvements Final Presentation
Leader Meeting
Leader Meeting
Leader Meeting
For Quality Improvement Purposes
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GI Lab Nurse to Patient Contact Time
Before Kaizen 60% of the Nurse’s time was
spent hunting and gathering
After Kaizen 87% of the Nurse’s time was spent in direct
patient contact
For Quality Improvement Purposes
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Sustainment
For Quality Improvement Purposes
3.64.2 4.0
5.0
5.9
0
1
2
3
4
5
6
Nov-09 Dec-09 Jan-10 Feb-10 Mar-10
SRP Technician Productivity: Average Trays Per Hour
Average Case Volume per Day
41.15
32.7532.77
37.68
39.837.38
36
41.4239.42
37.8 37.72
15
20
25
30
35
40
45
May-09 Jun-09 Jul-09 Aug-09 Sep-09 Oct-09 Nov-09 Dec-09 Jan-10 Feb-10 Mar-10
Target 60 cases/ per day
GI Lab
The LEAN Journey Begins
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Next Steps
For Quality Improvement Purposes
• Develop Subject Matter Experts
• Patient Throughput
• Scheduling Access
• Supply Chain Management
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Team MembersGreg Horner Brad Helfand Jon Brickman Jose Gonzalez Josephine Servano Jill Anderson Dwayne Walton James Vondra Linda Flemm Gilberto Carnalla Lori Mohito Matt Gimble
Operational Excellence TeamSurgical Reprocessing Staff
Operating Room StaffPP&G, IT, & House Keeping Staff
The Lean Journey: The Lean Journey: Operational Improvement of Operational Improvement of
Surgical ReprocessingSurgical Reprocessing
For Quality Improvement PurposesTABLE 32
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Project AimProject AimTo maximize the production capacity of the tray assembly area in order to better align with the demand of the Operating Room.
A misalignment of output vs. demand causes:• OR inefficiencies• Increased flash sterilization rates• Limits the time practitioners have to focus
on our patients• Inflated staffing to keep up with demand
For Quality Improvement Purposes
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To improve department workflow, production, and quality by reducing process waste and increasing technician productivity.
Our Key Process Indicator: Assembly Technician Productivity
Our Goal:5.0 trays per hour per Assembly Technician
Project GoalProject Goal
For Quality Improvement Purposes
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Solutions Implemented Solutions Implemented Date Project Description Waste
ReductionNovember 20th, 2009
-Assembly Lane/Decontam Workflow Reconstruction-Standard Work Instructions
56 Steps
November 30th, 2009
Sonic Lane Workflow Reconstruction-Standard Work Instructions
28 Steps
December 22nd, 2009
Picture Catalog Construction N/AFebruary 5th, 2010 Instrument Supply
Reorganization36 Steps
March 5th, 2010 -Missing Instrument Root Cause Analysis-Standard Work Instructions
Results not yet realized
For Quality Improvement Purposes
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Station 3
Station 4
Station 5
Station 6
Station 7
Station 8
Sonics 2
Station 1
Printers
OnSite
Station
Implant Table &Drawers
Peel Pack and Battery Charger Station
Sterilizers
Cart 1
Cart 3
Cart 4
Cart 5
Cart 6
Cart 2
Priority Cart
Washers
Drill Cart
Inc. Cart
Sterrad
Units
ORIGINAL DEPARTMENT LAYOUT/WORKFLOWORIGINAL DEPARTMENT LAYOUT/WORKFLOW
For Quality Improvement Purposes
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NEW DEPARTMENT LAYOUT/WORKFLOWNEW DEPARTMENT LAYOUT/WORKFLOW
For Quality Improvement Purposes
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DO NOT SUBSTITUTE
WITH THE REGULAR VERSION
DO NOT SUBSTITUTE
WITH THE REGULAR VERSION
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Project Data AnalysisProject Data Analysis• Available Data indicates a 2.3 tray per hour
average increase from November 2009 to March 2010 – 3.6 to 5.9 trays per hour
• The 2.3 tray per hour increase equates to:– 16.1 additional trays per technician over a
7 hour shift– Or 161 additional trays per ten assemblers
––NO ADDITIONAL NO ADDITIONAL MANPOWER NEEDEDMANPOWER NEEDED
For Quality Improvement Purposes
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Next Steps & Lessons LearnedNext Steps & Lessons Learned
• Stabilize productivity on a day to day basis– Consistently hitting 5 trays per hour will allow us
to surpass the original goal– Staff accordingly to the OR demand based on the
average tray demand of 400 per day
What we are learning:• The basis of LEAN is to put a structure in place that
promotes “Continuous Improvement”…….• This project has only scratched the surface of
improving the department…several more in the planning stageFor Quality Improvement Purposes
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THE ROADMAP FOR IMPROVEMENTTHE ROADMAP FOR IMPROVEMENT
For Quality Improvement Purposes
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Monitoring Use of Flash Sterilization: Systems approach to documentation and management of
short-cycle steam sterilization
2010 LUHS Quality & Safety FairTeam Members:
Brad Helfand, Surgical Services Debbie Marra, OR Nursing
Alex Tomich, Infection Control Debbie Serwa, ASC
Lu Ann Vis, CCE Jon Brickman, OR Support
For Quality Improvement Purposes
TABLE 33
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Flash Sterilization = steam sterilization as defined by 3 minute cycle at 270 degree Fahrenheit at 27 to 28 pounds of pressure.
Definition of Flash Sterilization
For Quality Improvement Purposes
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• Inconsistent flash logs to capture data between Russo and ASC• Internal audits of Russo flash sterilization logs found missing information
such as instrument or tray processed and reason for use of flash cycle• LUMC cited by the Joint Commission in 2007 for instances of flash
sterilization• The Joint Commission released new guidance on flash sterilization in July
2009 announcement to hospitals. This guidance focused on three key elements:
• Cleaning and decontamination: all visible soil must be removed prior to sterilization
• Sterilization: cycle must conform to instrument manufacturer recommendations for proper time, temperature, and pressure
• Storage and return to the sterile field: the sterilized instrument must be protected to ensure that it does not get contaminated prior to placing it on the sterile field
Key Challenges
For Quality Improvement Purposes
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• Develop consistent methods for documenting the 5 W’s (Who, What, Where, When, and Why) related to flash cycles
• Establish on-going measurement and tracking of flash cycles• Provide education to caregivers on recommended steps for safe use of flash
sterilization equipment• Acquire new tools (e.g., covered flash pans) to meet regulatory guidance• Establish easy access to manufacturer guidelines on sterilization parameters• Monitor and report on flash sterilization trends to key stakeholders
Project Objectives & Goals
Correct ToolsProper Documentation
On-going Tracking
For Quality Improvement Purposes
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• Formed Flash Committee (July 2009)• Reviewed Literature of Best Practices (July 2009)• Developed Process for Nursing-SRP Collaboration on Decontamination of
Instruments to be Flash Sterilized (July 2009)• Educated Staff on Proper Protocols for Flash Sterilization (August 2009)• Initiated On-Going Data Collection (August 2009)• Launched Revised Flash Sterilization Log (September 2009)• Requested Covered Flash Pans (October 2009)• Assessed Instrument Capital and Inventory Needs (November 2009)• Requested One Source Document Management System for Manufacturer
Guidelines on Sterilization (December 2009)• Implemented Spot Audits of Flash Log Documentation and Clear
Accountability Standards (January 2010)• Conducted Tracer Audits of the End-to-End Process (January 2010)• Implemented Flash Pans and One Source System (March 2010)
Tactics to Improve Monitoring of Flash Sterilization
For Quality Improvement Purposes
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New Flash Sterilization Log
Sterilizer Location
Receipt with Cycle ID
Name of Instrument
Reason for Flash Cycle
Limit of Two Records Per Page
For Quality Improvement Purposes
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Flash Sterilization Trends as a Percentage of Overall Steam Sterilization
Flash cycles seen as a percentage of overall sterilization cycles in a given month. Calculation based on number of flash cycles divided by total steam sterilization cycles. Steam sterilization cycles taken from the Horizon Tray Tracking System.
For Quality Improvement Purposes
Flash Percentage Trend
8.87%
11.39%
9.46%
10.73%
9.31%
7.96%8.36%
0.00%
2.00%
4.00%
6.00%
8.00%
10.00%
12.00%
Base
line
Octo
ber 2
009
Nove
mber
2009
Dece
mbe
r 200
9Jan
uary
2010
Febr
uary
2010
Mar
ch 20
10
Percentage
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Analysis of Reasons for Flash Sterilization
Source: Russo and ASC OR Flash Logs, Average December 2009 – February 2009, excludes test cycles and cycles with missing documentation
Contaminated in OR, 34.8%
Sterile Processing Sent Unsterile to OR,
41.9%
Back-to-back procedures, 2.7%
One-of-a-kind instrumentation,
14.2%
Package Integrity, 0.3%
Not for patient use-decontam only,
6.2%
For Quality Improvement Purposes
Contaminated in OR, 4%Sterile Processing Sent to
OR Unsterile, 19%
Back to back procedures, 51%
One-of-a-kind instrumentation, 15%
Package integrity, 1%
Not for patient use - decontam only, 11%
RUSSO ASC
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• ENHANCED KNOWLEDGE OF STERILIZATION TECHNIQUES
• IMPROVED QUALITY AND SAFETY FOR PATIENTS
• GREATER COOPERATION BETWEEN SRP TECHNICIANS AND OR NURSES
Project Results
For Quality Improvement Purposes
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• On-going data analysis and tracking of key trends
• Implementation of flash pans and new web-based system to manage manufacturer guidelines for sterilization parameters
• Daily rounding by OR management to monitor staff compliance with documentation standards on flash sterilization
• Continuous process improvement (“kaizen” events) in SRP to improve production capabilities and reduce dependence on flash sterilization
Next Steps
For Quality Improvement Purposes