pamela richtmyer, mgh research compliance€¦ · study report – on epic dashboard must be done...
TRANSCRIPT
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Pamela Richtmyer, MGH Research Compliance
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September 27 - Session 1 Basic overview
October 4 - Session 2 Tracking patient care charges
Insight Patient Care Corrections
Invoices to sponsor
October 11 - Session 3 Inpatient studies
Medicare Coverage Analysis (MCA
Device study requirements
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Improve ability to assess study costs
Develop study budget that will cover all costs
Determine what is billable to insurance
Appropriate charge direction
Maintain financial health of study
Understand relevant regulations and requirements
Available resources
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Link the admission in Epic PHS ADT Expected Admissions (Preadmissions) to Link to
Study Report – on Epic Dashboard Must be done in advance of scheduled admission
PHS ADT Inpatient Admission, HOV, or ED to Link to Study Report - on Epic Dashboard Must be linked prior to day of discharge
Research Orders for inpatients Research staff cannot enter orders for inpatients Licensed provider must enter and sign order Coordinate with inpatient clinical Blood specimens collected by inpatient nursing staff
Separate process for Emergency Department
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Technical charges post to Research Billing Review report once discharged All charges from admission will route to the report for
review Helpful hints:
Select All option available
Sort charges by date of service or charge description
Professional fees can post daily Be aware of 72 hour rule Late charges an issue Entire account appears Green check marks indicate charges already reviewed
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Any research protocols involving the ED must be reviewed and approved by the ED Includes recruiting participants in ED
Contact Blair Parry
ED approved studies Meet with ED prior to study start to verify process
Research coordinators can enter orders
Research coordinators can perform phlebotomy in ED
Certification required
Use ED Track Board to identify potential subjects
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FDA regulations – types of device studies Significant risk (SR) Implant Sustains/supports life Has importance in diagnosing, curing, or treating disease Potential for serious risk to health, safety, or welfare Investigational Device Exemption number assigned by FDA
Non-significant risk (NSR) Does not meet any of the criteria for SR devices
General Controls Companies must register establishments and list
medical devices they market Adhere to Good Manufacturing Practices Label devices as required by labeling regulations
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Non-significant Risk (NSR) Class I Subject to general controls only
Elastic bandages, exam gloves
Class II General controls plus special controls identified by FDA
(special labeling requirements, post-market surveillance, performance standards)
Infusion pumps, surgical drapes, powered wheelchairs
Significant Risk (SR) Class III Insufficient information exists for safety and efficacy
Implants, heart valves
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To assist Centers for Medicare and Medicaid Services (CMS) in determining coverage FDA categorizes all IDE devices Category A (Experimental):
absolute risk has not been established
Initial questions of safety and efficacy not determined
Category B (Non-experimental/investigational):
Initial questions of safety and efficacy determined OR
Manufacturer has FDA premarket approval or clearance
FDA notifies CMS when sponsor is notified about category
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Category A and B Medicare covers “routine care items and services”
furnished in FDA-approved Category A IDE studies if CMS ( or its designated entity) determines that the Medicare coverage IDE study criteria are met Sponsor submits a request to CMS for review and
approval Outline scope and nature of the IDE study
FDA approval letter of the IDE
IDE protocol
IRB approval letter
NCT number
Supporting materials
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“Routine care and services refers to items and services that are otherwise generally available to Medicare beneficiaries (that is, a benefit category exists, it is not statutorily excluded, and there is not a national non-coverage decision) that are furnished in a clinical study and that would be otherwise furnished if the beneficiary were not enrolled in a clinical study”
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Investigational Devices need charge code assigned CTO/Department notify PHS Revenue integrity Device information: model #, description, price
Clinical Trial information: IDE #, IRB protocol #, study title, PI
If later approved a new charge code must be assigned
If CMS approves coverage petition, complete MGH IDE PMA Notification form each time device is utilized
Documentation must support services provided and reference the clinical trial and device
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Prior authorization/Pre-approval required for “research-related” procedures MGH FAU Expedited Authorization Request
Form available in Clinical Trial Billing Guidelines
“Pre-Auth Request - Clinical Letter Attached”
Attach PI letter explaining study
If request approved a “pre-auth” number will be provided (not guarantee of payment)
If request denied or not obtained procedure may be cancelled
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Medicare revised policy regarding coverage of patient care costs in clinical trials – Medicare Clinical Trial Policy (effective 2000, revised
2007) Medicare covers routine costs of qualifying clinical trials Includes items and services that are otherwise available to
Medicare beneficiaries
MCA - Partners requirement since January 2008 (MGH, BWH, Spaulding, Faulkner)
MCA determination required prior to IRB approval/activation 2 categories Qualifying Clinical Trial (QCT) Non-qualifying Clinical Trial
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Qualifying Full MCA required 3 criteria mandatory Study must have therapeutic intent Enroll individuals with diagnosed disease
Healthy individuals only as controls
Evaluate item or service that Medicare covers Study-specific billing grid/calendar created PI notified of determination and receives copy of MCA billing
grid (see handout) Guides charge direction Template for Timeline in Epic Medicare covers:
Usual and customary care, Detection/prevention/treatment of complications, Administration of investigational drug/device
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CTO gets input from PI especially about “usual and customary” care
Not a reimbursement analysis Qualitative assessment only
Identifies what is and is not billable to Medicare Does not apply to other payers Obtain Prior Authorization for study procedures as
needed
Template for Clinical Trial Budget and Epic Patient Timeline
Amendments to study may have an impact on MCA Contact CTO as necessary
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Documentation required in medical record to support billing to Medicare or other payers Same requirement for services outside clinical trial
Must also support the service provided is usual care for patient’s condition
“Patient is a participant in a qualifying clinical trial, PI name, title of study” Helpful if protocol # referenced
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1. Billing Grid
a) Lists items and services included in study and appropriate charge direction
2. Investigational item or service analysis a) IND # or IDE #
b) QCT criteria
c) Sponsor provided items
d) Informed consent statement regarding costs
3. List of study identifying information and documents received
4. NCT and CMS billing information
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MCA Billing Grid used as reference for Epic Timeline
PI receives email notification when Epic Timeline created
Process Enroll patient in study and add Timeline
Enter “From Date”
Choose whether to set subsequent dates automatically or not
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Non-qualifying MCA billing grid/calendar not required
PI receives notification of non-qualifying status
Majority of studies
Study pays for all patient care charges OR
No patient care charges in study
Usual and customary services provided outside of study covered as usual
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Make certain fund is set up for patient care charges
Make certain fund is appropriate to cover research and patient care charges
Contact CTO if: You disagree with determination OR
Your study is revised to include usual and customary care that will be billed to insurance
Confirm your budget will cover all costs including patient care professional fees
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Device Research Policies https://partnershealthcare-
public.sharepoint.com/ClinicalResearch/Requirements_for_an_IDE_for_Human-Subjects_Research.pdf
https://partnershealthcare-public.sharepoint.com/ClinicalResearch/HUD_Checklist.pdf
https://partnershealthcare-public.sharepoint.com/ClinicalResearch/Emergency_Use_of_an_Drug_Biological_Device.pdf
QI Device Accountability Log https://partnershealthcare-
public.sharepoint.com/_layouts/15/WopiFrame.aspx?sourcedoc=%7bD2D55D04-3CCA-49AF-917E-112798F4648A%7d&file=device-accountability-log.dot&action=default
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Partners Clinical Trials Office (CTO) Agreements and Clinical Trial Budgets https://partnershealthcare.sharepoint.com/sites/phrmInitiate
/iian/Pages/Industry-Sponsored-Basic-Research-Agreements.aspx
MCA https://partnershealthcare.sharepoint.com/sites/phrmInitiate
/iian/Pages/Medicare-Coverage-Analysis.aspx
Research Management – Research Finance https://partnershealthcare.sharepoint.com/sites/phrmDepartm
ents/prd/rf
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Partners IRB Policies https://partnershealthcare.sharepoint.com/sites/phr
mApply/aieipa/irb/Pages/PHRC-Policy-and-Guidance.aspx#9
Partners Quality Improvement https://partnershealthcare.sharepoint.com/sites/phr
mdepartments/poc/qi Medicare National Coverage Decision https://www.cms.gov/Medicare/Coverage/ClinicalTri
alPolicies/downloads/finalnationalcoverage.pdf
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MGH Research Compliance Clinical Trial Billing Guidelines http://mghresearch.partners.org/Research_Compliance/HumanS
ubsResearch.aspx
Microstrategy Procedure Picker Email the Help Desk: [email protected]
Department of Clinical Research (formerly CRP) Epic FAQs Tip Sheets Step by step research billing review slides https://hub.partners.org/ecare/ Sign on with Partners username and password
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