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Discharge Readiness in Heart Failure A Thesis Submitted to the Faculty of Drexel University By Linda M. Celia in partial fulfillment of the requirements for the degree of Doctor of Nursing Practice November 2015

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Page 1: Discharge Readiness in Heart Failure6571/datastream/OBJ/download...Discharge Readiness in Heart Failure Linda M. Celia Patients with heart failure (HF) face the challenge of living

Discharge Readiness in Heart Failure

A Thesis

Submitted to the Faculty

of

Drexel University

By

Linda M. Celia

in partial fulfillment of the

requirements for the degree

of

Doctor of Nursing Practice

November 2015

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© Copyright 2015

Linda M. Celia. All Rights Reserved

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Dedication

This is dedicated to my mother Rose, who has taught me to strive to do your best at all

times. She has been my support through the years at each stage of my life and advancing

my education. She is the architect who taught me to be a good person and respect

everyone I have the privilege to meet along life’s journey.

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Acknowledgements

I would like to acknowledge the following that have supported my educational journey.

Dr. Albert Rundio for your advice and insight in completing my doctoral studies and

your guidance through all renditions of my study. I appreciate the meetings and

suggestions to strengthen my research. I am grateful to you for taking the time and

imparting your knowledge to me.

Dr. Marylou McHugh for your guidance and suggestions through the dissertation writing

process.

Dr. Ruth Wittman Price for providing the encouragement to start me on the journey

toward doctoral education.

My brother Jim, sister-in-law Barbara and niece Sarah, for your support and constant

encouragement throughout the doctoral journey.

Members of Staff Education and Professional Development (my Hahnemann Family) for

supporting me through the classroom times, practicum experiences and offering me

encouragement.

Dulcine Dinsmore aka”Stella Two”, my rock during good and challenging days. The

phone calls were a continuous source of friendship and support. Your emotional boosts

are deeply appreciated.

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Brian Hall, Palaka Levey, Dulcine Dinsmore, Alison Lesniak, Scott Alcott, Barbara Celia

and Sarah Gallagher for proofreading all my drafts of papers and offering constructive

suggestions.

Dr. Kathy Anselmi, Dr. Rose Ann DiMaria-Ghalili, Dr. Ellen Giarelli and Dr. Joanne

Serembus for being my professional Drexel support team.

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Table of Contents

LIST OF TABLES……………………………………………………………………….vii

ABSTRACT…………………………………………………………………………….viii

1. CHAPTER 1 - Problem Identification

1.1 Problem Identification………………………………………………………..1

1.2 Heart Failure and Readmissions…….………………………………………...2

1.3 Heart Failure and Discharge…………………………………………………..4

1.4 Theoretical Framework………………………………………………………..8

1.5 Purpose……………………………………………………………………….10

2. CHAPTER 2 - Methods/Implementation

2.1 Components………………………………………………………………….11

2.2 Sample Participants………………………………………………………….11

2.3 Instrument……………………………………………………………………12

2.4 Resources and Personnel……………………………………………………..14

2.5 Procedures and Protocol……………………………………………………..14

3. CHAPTER 3 - Results

3.1 Results………………………………………………………………………..16

3.2 Limitations…………………………………………………………………...21

4. CHAPTER 4 – Conclusions and Recommendations

4.1 Discussion……………………………………………………………………22

4.2 Summary……………………………………………………………………..23

List of References……………………………………………………………………24

APPENDIX A – Transition Theory………………………………………………….28

APPENDIX B – Nurse Script for Recruiting Patients………………………………29

APPENDIX C – Demographic Questionnaire……………………………………… 30

APPENDIX D- Readiness for Hospital Discharge – Adult Form…………………...32

APPENDIX E – Permission for Use Agreement……………………………………35

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LIST OF TABLES

Table 1 – Demographic Characteristics of Heart Failure Patients…………………..19

Table 2 – Demographics of Hospital Stay…………………………...........................20

Table 3 - Other Medical Conditions Reported byPatient………………………….…20

Table 4 – Readiness for Hospital Discharge Scores………………………………....21

Table 5 – Readmitted Heart Failure Patients……………………………..………….22

Table 6 – RHDS Results for Readmitted Patients…………………………………..23

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Abstract

Discharge Readiness in Heart Failure

Linda M. Celia

Patients with heart failure (HF) face the challenge of living with a chronic condition. The

transition from the hospital environment to home requires diligent attention to ensure that

the patient is ready for discharge. Being ready to go home or “discharge readiness” is

vital to the successful transition of HF patients. Discharge readiness is related to the

discharge outcomes for the hospital and is an indicator of the need for additional

discharge transition support interventions in the home setting. The purpose of this study

was to evaluate the level of readiness for discharge in the HF patient and examine if

further patient education prevents readmission within thirty days. Readiness for

discharge encompasses personal status, coping, knowledge, and expected support prior to

the hospital discharge.

A descriptive comparative study was conducted with patients divided into two groups,

one receiving the Readiness for Hospital Discharge Scale (RHDS) and additional

education on HF and the other group standard nursing care with no intervention. The

RHDS captured the patient’s perception of discharge readiness. The study was conducted

in an urban academic medical center. Patients (N=50) with a diagnosis of HF were

recruited.

Six patients from both study groups were readmitted to the hospital within the thirty day

period post discharge. Over sixty percent of the patients had income levels below

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$20,000 and had a previous hospital stay within the last six months. Arthritis and

respiratory problems were the most frequently reported co-morbid conditions.

With the emphasis on reducing HF readmissions, it is imperative that nurses are

cognizant of the patient’s discharge readiness prior to discharge. Nurses need to examine

approaches in preparing the patient for a successful transition to the home environment

that takes into consideration recent hospitalizations, income levels and co-morbid

conditions.

Keywords: discharge, discharge planning, readiness, heart failure

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Chapter 1: Problem Identification

Current procedures for discharging patients from the hospital setting utilize a

discharge process that does not consider patient preferences related to the information

that the patient receives. Overlooking patient preferences may not satisfy the patient’s

needs and may lead to non-compliance or unwillingness to adhere to discharge plans

(Huber & McClelland, 2003). Another concern is the passive role often taken by patients

not willing to voice their concerns with health care professionals regarding discharge

needs (Corser, 2006).

Patient perceptions of life at home following discharge from the hospital reveal

multiple difficulties in coping. Frustrations arise as patients try to deal with complex

health care systems while not being involved in decisions for discharge care (Corser,

2006). Patients reveal that health care providers do not recognize their needs regarding

activities of daily living (Grimmer, Moss, Falco & Kindness, 2006; LeClerc, Wells,

Craig, & Wilson, 2002; McKeown, 2007; Miller, Piacentine, & Weiss, 2008), their

decreased mobility to get around their home which leaves the patient with a fear of

falling (Corser, 2006; Heine, Koch, & Goldie, 2004; LeClerc et al., 2002; Miller et al.,

2008), and fatigue which puts the patient at risk for not performing household tasks

(LeClerc et al., 2002). Patients need social and emotional support to get them through

the anxious and fearful period as they transition back to the home environment (Corser,

2006; Grimmer et al., 2006; LeClerc et al., 2002; McKeown, 2007; Miller et al., 2008).

Being a burden to others and uncertainty about recovery are concerns for patients who are

preparing for discharge (Miller et al., 2008).

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Weiss, Yakusheva, & Bobay, (2010) conducted a study on discharge readiness at

four Midwestern hospitals and analyzed the data on nurses’ (N = 162) perceptions of

patient readiness that was drawn from a larger study (readiness for hospital discharge,

quality of discharge teaching, post hospital utilization, emergency department utilization

and relationship of nurse staffing) with adult medical-surgical patients. Patients

completed the Readiness for Hospital Discharge Scale (RHDS). Registered nurses were

administered a nurse version of the RHDS in the parent study for their assessment of the

patients readiness for discharge. Nurses reported significantly greater patient readiness

than the individual patients reported for the total scale, personal status and knowledge

scale regarding patients’ readiness for discharge (Weiss et al., 2010).

A secondary analysis of data collected on the Quality of Discharge Teaching

Scale (QDTS) revealed the amount of informational content perceived by the patient was

less (M = 6.2; SD = 15.6) than the amount of discharge teaching they received (M = 37.5;

SD = 15.5). Non-white patients required more patient education for discharge. Patients

with a previous hospitalization received more discharge content than patients with no

prior hospitalization. This study revealed that there was a lack of congruence between the

patient's perceptions of needs for discharge and the nurses’ perceptions (Maloney &

Weiss, 2008).

Heart Failure and Readmissions

Heart failure (HF) is one of the most common reasons for hospitalization in

patients over the age of 65. The incidence of HF has increased as the population has aged

(Hunt et al., 2009) and will increase 46% from 2012 to 2030 (Heidenreich et al., 2013).

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People are surviving longer with HF and other chronic conditions due to advances in

healthcare (Hunt et al., 2009). The number of patients diagnosed and hospitalized with

HF has trended upward since the 1970s and currently over one million HF patients are

admitted annually to hospitals (Institute, 2011). In the United States in 2010, over

5,800,000 people have the diagnosis of HF with direct and indirect costs of $39.2 billion

to treat the condition (Lloyd-Jones et al., 2010); these costs are projected to rise to $53.1

billion by 2030 (Heidenreich et al., 2013). More Medicare dollars are spent for HF than

any other condition (Hunt et al., 2009).

HF is one of the ten most common diagnoses for hospitalized patients and impacts

Medicare costs. The Centers for Medicare and Medicaid Services (CMS) have put in

place a method to track readmissions of patients with HF within thirty days of discharge.

Readmissions cost the CMS program over $15 billion annually (CMS, 2009). The aim of

CMS reporting measures is to encourage hospitals to have quality care programs and

vigilant discharge practices to reduce readmissions. Since 2012, hospitals have lost

reimbursement when HF patients are readmitted prior to thirty days post discharge (CMS,

2009). Hospitals are engaged in examining HF readmission rates and developing

programs to reduce readmissions in order to stay competitive and adjust to payment

changes related to CMS and health care reform (Hines, Yu, & Randall, 2010).

Hospital readmissions increase when patients with HF do not comply with

discharge instructions and care plans related to their diagnosis, or clinicians fail to

adequately treat the symptoms of HF (Hunt et al., 2009). With decreases in length of

hospital stay (LOS), patients may feel unprepared or that they are being pressured into

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going home (Bauer, Fitzgerald, Haesler, & Manfrin, 2009; Clarke, Sohanpal, Wilson, &

Taylor, 2010). Patients' perceived unmet needs, as well as lack of preparation for

discharge, may result in hospital readmissions, emergency room visits following

discharge, or additional unscheduled visits to their health care provider (Corser, 2006).

As patients prepare for discharge, non-congruency may exist between the patient

and health care team concerning the patient's perception of discharge readiness as well as

the nurses' perceptions of the patient's discharge readiness (Anthony & Hudson-Barr,

2004). Bull (1994) notes that readmission can be related to the nurse not adequately

assessing what an older individual may require in the home setting or not coordinating

appropriate resources to use in the home environment. The discharge process can be

confusing and complicated for the patient. Discharge plans that do not take into

consideration the patient's perspective, are poorly prepared and/or not adequately

assessed, may lead to hospital readmission (Wong et al., 2008). Readmissions may be

related to the lack of assessment and coordination of the home care needs of the patient.

This study examined the readiness for discharge among hospitalized patients diagnosed

with HF and receiving additional HF education and the impact on readmission.

Heart Failure and Discharge

HF patients face many challenges once they are discharged to the home

environment. A secondary analysis of HF readmissions in California, Massachusetts and

New York was conducted using data from the American Hospital Association, CMS and

Hospital Consumer Assessment of Health Care Providers System (HCAHPS). The

sample included 577 non-federated hospitals. Three factors were found to be related to an

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increased HF readmission ratio: poor nursing communication to patients regarding

discharge instructions, increased admissions per beds and admission to a teaching

hospital. A decreased HF readmission ratio was related to California hospitals; higher

average of nursing hours per patient day and the patients reporting they received

sufficient education regarding their care at home (Stamp, Flanagan, Gregas & Shindul-

Rothschild, 2014). Howie-Esquivel and Spicer (2012) in a retrospective chart review

found that lack of support from a partner was significantly associated with readmission

for all patients (p=.02) regardless of age for hospital readmission. Most of the older

patients studied did not have a partner. Older patients with HF that were admitted to a

skilled nursing facility had a lower readmission rate. The authors concluded that lack of a

partner in the older HF patient could be a powerful predictor of readmission.

A study of US Veterans with HF in urban and rural settings from October 2005

through September 2007 revealed that veterans over the age of 80 were most likely

(p<.002 ) to be readmitted for HF within a thirty day period post discharge; low income,

disabilities and a length of stay (LOS) greater than one week can also increase the

incidence of readmission to the hospital (p<.001) (Muus, Klug, Gokun, Sarrazin &

Kaboli, 2010).

Russell, Rosati, Sobolewski, Marien and Rosenfeld (2011) explored the

implementation of a transitional care program for high risk HF patients. The

retrospective, observational study looked at patients with transitional care services

(N=223) and patients receiving usual home services (N=224) post discharge. Average

age of the participants was 79.7. The transitional group received an assessment of the

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home environment, phone calls, home visits and collaboration with their primary care

provider. The odds ratio for the 30 day hospitalization in the transitional interventional

group was 0.57 (p <.01) and this group was 43% less likely to be readmitted. This study

noted that in the interventional group there was more comorbidities and great utilization

of physical therapy services than the control group.

The use of advanced practice nurses (APN’s) to follow HF patients at home has

been shown to have a beneficial effect. Naylor et al., (2004) performed a randomized

control trial with elders diagnosed with HF using an APN intervention. The APN met

with the patients to discuss preventing functional decline in the home setting, helping the

patient and caregiver learn to manage care at home and planning for follow-up care post

discharge. The APN had a flexible protocol to manage the patient’s HF needs at home.

Using the transition of care program lengthened the time for hospital readmission and

improved quality of life for the interventional group. The intervention group had a lower

rehospitalization (47.5% versus 61.2%) and the study revealed a decrease in healthcare

costs related to hospitalization and LOS with the utilization of APN’s. Stauffer et al.,

(2011) found similar results when APN’s met with patients in the hospital and performed

home visits post discharge. The thirty day readmission rate was reduced for HF but there

was low impact on LOS and the sixty day direct cost for care. Brandon, Schuessler,

Ellison and Lazenby (2009) used an APN led telephone intervention for patients with HF,

the intervention group reported a higher score on self-care behaviors post intervention

from 95.9 to 128 and an improved quality of life on the Minnesota Living with HF

Questionnaire. Heart failure readmissions were lower (f=7.63, p=.013) in the control

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group. A limitation of this study was small sample size of twenty and one APN who

performed the interventions.

Paimjariyaku, Smith, Wekowitch & Elyachar, (2012) performed a qualitative

study examining the perspectives of the HF patients, health care professionals and the

caregivers. Patient themes that emerged from the study were the need for family

involvement, the need for ongoing HF education, feeling too rushed at discharge to learn

properly, coping with the diagnosis of HF, lifestyle adjustments, and financial needs

related to treatment and being able to learn from patients that have HF. Caregivers

expressed a knowledge deficit regarding the care required once the patient was home.

Many caregivers expressed that they were not present when discharge instructions were

given to the patient. Caregivers expressed concern over their uncertainty about symptom

management and diet management for the patient at home. Healthcare professionals felt

at times that the patients were too ill to comprehend education about disease management

at home and reported that financial issues as well depression and situational grief over the

diagnosis of HF impacted treatment (Paimjariyaku et al., 2012).

Helleso, Eines and Faermoen (2011) elicited themes regarding variation in

involvement for the HF patients and caregivers, information ambivalence related to

managing their care while ill, feeling overwhelmed, feelings of fatigue, and difficulty

remembering what they were taught. Patients expressed struggles with remaining

independent and having control of their lives. Caregivers expressed frustration with not

being present when information for discharge instructions was given. Caregivers with a

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medical background expressed an advantage since they were able to help the patient with

discharge information and terminology they did not understand.

Heart failure admissions within a thirty day window of discharge can lead to

penalties in reimbursement for hospitals. Finding solutions to reduce thirty day

readmissions is a financial benefit for the hospital and allows the patient to remain in

their current environment.

Theoretical Framework

Meleis' (1991) middle-range theory on transitions was used as a conceptual

framework for this study. Transition as defined by Meleis denotes a change in health

status, abilities, expectations, and/or role relationships. Transitions for the patient occur

over time and are not static events (Meleis & Trangenstein, 1994). A patient may

experience multiple transitions associated with an illness and may be challenged to cope

and adapt as a result of the illness (Meleis, 1991; Meleis, Sawyer, Im, Messias, &

Schumacher, 2000). Transitions may be associated with health problems such as the

passage into late adulthood that may be affected by chronic illness, retirement and loss of

relationships. Situational transitions involve role changes for the patient such as the loss

of a spouse/partner or becoming a parent. Health/illness transitions may occur as the

patient moves from a state of wellness to an acute illness or to a chronic illness, at which

time coping and adapting may occur with a positive or negative outcome (Meleis, 1991).

A patient, who transitions successfully from hospital to home environment feels

connected, develops confidence and copes with their illness effectively. Outcome

indicators of a positive transition will focus on the patient’s mastery of being able to

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accomplish new skills, attain an adequate level of knowledge, and exhibit behaviors to

enable changes (Meleis et al., 2000; Meleis & Trangenstein, 1994). Nurses interact with

patients who are undergoing the transitional process and are therefore in a unique

position to assess readiness for discharge. Nurses can assist patients as they find their

comfort level and achieve mastery of changes that are occurring in their life (Meleis,

1991; Meleis et al., 2000). As nurses facilitate the patient’s discharge transition, nurses

demonstrate their expertise in supporting discharge preparation and education (Meleis &

Trangenstein, 1994). A patient who does not receive adequate care and education as they

transition to the home environment may experience complications and be at risk for

hospital readmission (Meleis, 2010).

In this study, a transition was conceptualized as the patient’s discharge to home

(Appendix A). The perception of readiness for discharge was perceived preparedness for

transition or readiness for transition to the home. Discharge readiness is a “multifaceted

concept that provides an estimate of a patient’s ability to leave an acute care facility”

(Steele & Sterling, 1992, p. 80). Discharge readiness assessment consists of the

individual’s physiological status, competency to care for self at home, self-efficacy to

carry out self-care, amount of social support, access to community healthcare services,

knowledge of care after discharge and skills to care for self at home (Titler & Pettit,

1995). Including the family and caregivers in the discharge process with discharge

instructions such as the patient’s functional status, social support, and teach back

(ensuring comprehension of taught material) will ensure a safe transition to home

(Nielsen, G.A., et al., 2008). The patient is experiencing a transition from the hospital

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experience to home. This study examined the transition conditions of one group of

patients’ perceptions of discharge readiness related to discharge versus a group of

patients receiving standard nursing care. The premise of the transition theory is how the

interaction of the patient’s pattern of response during a transition will be affected by their

transition conditions, the nature of the transition, as well as nursing discharge

interventions (Weiss et al., 2007).

Purpose

The purpose of this project is to evaluate if assessing the patient’s readiness for

discharge and if providing HF education will reduce the thirty day readmission rate for

HF patients.

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Chapter 2: Methods/Implementation

Components

This research study utilized a descriptive comparative design. Fifty patients were

divided into Group A, demographics only and Group B, demographics, RHDS and

additional HF patient education. The study was approved by the institutional review

board (IRB) from Drexel University, the research committee of the hospital and Parent

Corporation. The site for the study was a large urban teaching hospital located in center

city Philadelphia. The hospital is licensed as a 600 bed, tertiary care medical center and

was chosen because of its large inpatient HF population.

Sample Participants

The sample population (N=50) consisted of hospitalized patients diagnosed with

HF. Patients were selected from inpatient units that admit patients diagnosed with HF.

Inclusion criteria included:

1. Diagnosis of HF upon admission

2. Ages 18 to 99 years

Exclusion criteria included:

1. Being discharged to a long-term care facility, rehabilitation facility or hospice,

transfer to another acute care facility and leaving the hospital against medical

advice.

2. Patients with any diagnosis of cognitive impairment were not recruited.

Eligible participants were approached by their nurse after admission to determine their

willingness to participate in the study. The nurses used a standard script for consistency

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(Appendix B). The participants were informed that their participation would involve

completing a demographic survey, potentially a questionnaire and receiving additional

HF education. The patient’s nurse informed the investigator if the patient was willing to

participate in the study. The investigator provided respondents with a verbal and written

description of the study and obtained written informed consent.

An investigator-developed patient demographic collection sheet (Appendix C)

was utilized. Racial categories were defined by the 2010 U.S. Census Bureau as: White;

Black or African American; Asian, American Indian or Alaska Native; Native Hawaiian

or Other Pacific Islander and additional categories entitled "Some other race," And “Two

or More Races” (US Census 2010, 2010). The data for education allowed the participant

to fill in the years of formal education. Marital status, support for living arrangements,

yearly income, and occupation were part of the demographic collection. Data regarding

the subject’s medical status included: the first hospital stay, date of last hospital stay and

other medical conditions.

Instrument

The readiness for hospital discharge for patients in Group B was measured using

the RHDS (Weiss & Piancentine, 2006) (Appendix D). This 21-item instrument

measures the patient's perceptions of readiness for discharge from the hospital

environment that includes four attributes related to the patient's readiness for discharge:

personal status, knowledge, coping ability and expected support (Weiss & Piacentine,

2006). Personal status is defined as how the patient is feeling at the time of discharge.

Knowledge is defined as a measure of how much they think they know about discharge

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content related to self-management at home (for example: restrictions, medications,

medical treatments and communication with a health care provider). Perceived coping

status is defined as how well the patient will be able to handle care needs at home.

Expected support is defined as the amount of assistance and emotional support that will

be available to the patient in the home (Weiss et al., 2010). The respondent indicated

how much of each item is experienced by indicating on an 11 point Likert-type scale

from 0 (not ready, no pain/discomfort, weak, low energy, none, not able, know nothing at

all, not at all) to 10 (totally ready, severe pain/discomfort, strong, high energy, a great

deal, totally able, know all, extremely well). Higher scores indicate greater readiness for

discharge (Weiss et al., 2007).

Reliability and validity were established for the 21 item RHDS on three patient

samples (medical-surgical patients, post-partum mothers and parents of hospitalized

children). Following reliability and confirmatory factor analysis, the scale was reduced

to 21 items. Cronbach's coefficient for the total sample (N=356) for the 21 items was

0.90. The personal status subscale had a Cronbach's coefficient of 0.80; knowledge

subscale had a Cronbach’s coefficient of 0.87; coping ability subscale had a Cronbach's

coefficient of 0.85 and expected support subscale had a Cronbach's coefficient of 0.85

(Weiss & Piacentine, 2006).

The RHDS psychometric properties were confirmed with "construct validity,

using confirmatory factor analysis and contrasted group comparisons and predictive

validity have been established for the 21-item scale" (Weiss et al., 2007, p. 35). The

Chronbach’s alpha reliability estimate for the 22-item RHDS - adult form was 93 (Weiss,

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et al., 2007). On the adult RHDS, content validity testing of the instrument resulted in

"Content Validity Index composite score across all items and raters for the total scale of

0.89" (Weiss, 2006, p.167). The 21 items were common to the three populations studied

and an additional item was added to the adult measure for 22 items.

Resources and Personnel

The investigator is an experienced registered nurse with thirty-eight years of

clinical experience with adult patients as well as teaching practicing nurses. The

investigator was responsible for all data collection and consenting of patients for the

study. The investigator had access to office space within the hospital to store research

materials. A password protected computer in a locked office was available to run

statistical software and enter data.

Procedure and Protocol

The investigator utilized nursing care units that cared for HF patients and were

approved by the IRB. Data collection was conducted in person by the investigator. The

investigator consulted daily with the registered nurses to find out if HF patients were

interested in participating in the study. The registered nurse used the approved script to

ask the patient if they were interested in participating in the study. Having the patient’s

registered nurse ask the patient if they were interested in participating in the study

lessened the chance that the patient felt pressure from the investigator to participate.

The investigator spoke with interested patients who had a diagnosis of HF and

explained the purpose of the study. The investigator obtained the patient’s written

consent. Patients were randomly placed into Group A with the demographic sheet or

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Group B with demographics, RHDS and additional HF patient education. The first patient

consented was placed into Group A and the next patient was assigned to Group B, this

process continued until the fiftieth patient was recruited.

Patients in Group B who agreed to participate were given the demographic sheet

and RHDS to fill out at their bedside. The investigator provided additional education to

the patient on HF. All patients were given the option to opt out of the study at any time.

Descriptive statistics were run through SPSS to analyze demographic data and

readmission statistics. Patient data was coded to protect anonymity and confidentiality

and entered into an Excel© file. The investigator has access to a computer that is

password protected for all computer files. Raw data is stored in a locked office for three

years from the completion of the study. The investigator had access to the electronic

medical record in order to track if the patient was readmitted prior to thirty days from

discharge.

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Chapter 3: Results

Fifty patients with HF were recruited for the study. Males (N=38) represented

fifty-six percent of the participants. The average age of the participants was 60.38 years

of age. Ninety-six percent of the participants were non-Hispanic. Seventy-four percent of

the patients were African-American and twenty-four percent were Caucasian. The

average year of education as reported by the participants was 12.06 years. Forty-four

percent of the participants reported they were single and sixty-six percent reported that

they lived with a spouse or friend for support. Sixty-eight percent of the participants

reported an annual income of less than $20,000. Forty-six percent of the participants were

retired. Demographic data is presented in Table 1. Regarding hospital stays, ninety-two

percent of the participants stated that this was not their first hospital stay related to HF.

Thirty percent of the participants stated they had been hospitalized within the last four to

six months. Demographics of hospital stay are presented in Table 2.

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Table 1 – Demographic Characteristics of Sample

Demographics Characteristics of Sample (N=50)

Variable N Percent of Total Total A B A B

Gender Male 28 14 14 56 56 56

Female 22 11 11 44 44 44

Age 30-39 2 1 1 4 4 4

40-49 11 5 6 22 20 24

50-59 10 5 5 20 20 20

60-69 17 10 7 34 40 28

70-79 6 2 4 12 8 16

80-89 3 2 1 6 8 4

90-99 1 0 1 2 0 4

Ethnic Status Non-Hispanic 48 24 24 96 96 96

Hispanic 2 1 1 4 4 4

Race White 12 7 5 24 28 20

Black or African

American

38 18 20 76 72 80

Asian 0 0 0 0 0 0

American Indian or

Alaska Native

0 0 0 0 0 0

Some Other Race 0 0 0 0 0 0

Two or More Races 0 0 0 0 0 0

Years of Education 0-8 3 2 1 6 8 4

9-12 32 18 14 64 72 56

13-16 13 4 9 26 16 36

17 and > 2 1 1 4 4 4

Marital Status Single 22 10 12 44 24 36

Married 15 6 9 30 24 36

Divorced 5 4 1 10 16 4

Widow/Widower 8 5 3 16 20 12

Support Live with Spouse 13 5 8 26 20 32

Live with

Relative/Friend

20 9 11 40 36 44

Live Alone 17 11 6 34 44 24

Yearly Income * Less than 10,000 17 13 4 34 52 16

10,000 to 20, 000 17 7 10 34 28 40

21,000 to 30, 000 4 0 4 8 0 16

31,000 to 40,000 4 1 3 8 4 12

*One subject

declined to answer

Greater than 40,000 7 4 3 14 16 12

Occupation Disabled 18 11 7 36 44 28

Working 6 3 3 12 12 12

Retired 23 9 14 46 36 56

Unemployed 3 2 1 6 8 4

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Table 2 – Demographics of Hospital Stay

Demographics of Hospital Stay

Variable N Percent of Total

A B A B

First Hospital

Stay

Yes 2 1 1 8 4 4

No 47 23 24 92 96 96

Date of Last

Hospitalization

0-3 Months 14 6 8 28 24 32

4-6 Months 15 9 6 30 36 24

7-9 Months 5 1 4 10 4 16

10-12 Months 1 0 1 2 0 4

During 2014 4 1 3 8 4 12

Earlier than

2014

10 7 3 20 28 142

No

Hospitalization

1 0 1 2 2 0

Participants were asked to self-report other medical conditions. Fifty percent of the

participants reported respiratory problems and forty-four percent reported problems with

arthritis. Thirty-eight percent of the patients reported that they were diabetic.

Demographics of other medical conditions are presented in Table 3.

Table 3 – Other Medical Conditions Reported by Patient

Other Medical Conditions Reported by Patient

Variable N Percent of Total

Total A B Total A B

Asthma/Respiratory Problems 25 14 11 50 56 44

Arthritis 22 11 11 44 44 44

Diabetes 19 10 9 38 40 36

Stomach Problems 10 3 7 14 12 28

Vision Problems 6 4 2 12 16 8

Kidney Disease 6 4 2 12 16 8

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Hearing Problems 5 3 2 10 12 8

Neurological Problems 5 3 2 10 12 8

Cancer 4 2 2 8 8 8

Men’s Health Problems 4 1 3 8 4 12

Skin Problems 3 2 1 6 8 4

Mental Disorder 3 3 0 6 12 0

Women’s Health Problems 2 1 1 4 4 4

Thyroid Disease 1 1 0 2 4 0

Liver Disease 1 1 0 2 4 0

Table 3 continued

Patients in Group B were asked to complete the Readiness for Hospital Discharge Survey

(RHDS). In the four sub-sections of the survey, the average score was 42.92 for

Personal, 72.28 for Knowledge, 25.44 for Coping and 30.12 for Expected Support. The

overall average score for the RHDS was 170.76. The score for the Readiness for

Hospital Discharge are listed in Table 4.

Table 4 – Readiness for Hospital Discharge Scores

Readiness for Hospital Discharge Scores

Subject Personal Knowledge Coping Expected

Support

Total Score

1 49 88 29 38 204

2 40 81 29 39 189

3 38 57 19 22 136

4 48 73 24 28 173

5 38 64 21 28 151

6 57 81 22 38 198

7 44 71 26 40 181

8 38 90 30 0 158

9 41 64 25 25 155

10 41 39 30 30 140

11 30 53 11 26 120

12 41 68 29 15 153

13 46 83 27 40 196

14 36 77 30 30 173

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15 59 77 29 40 205

16 24 78 27 38 167

17 52 64 30 40 186

18 39 89 30 40 198

19 49 59 20 23 151

20 34 74 26 28 162

21 41 62 20 26 149

22 49 85 28 36 198

23 48 85 30 30 193

24 39 82 26 35 182

25 52 63 18 18 151

Average Score 42.92 72.28 25.44 30.12 170.76

Table 4 continued

Six patients were readmitted from both study groups within thirty days of discharge for a

HF readmission. Table 5 lists the patients with readmissions. Eighty-three percent of the

readmitted patients were male. Two patients were from Group A, demographics only and

four patients from Group B, demographics, RHDS and extra HF education were

readmitted. All readmitted patients had a hospital stay within six months of the most

recent admission to the hospital. The RHDS scores for the four readmitted patients are

displayed in Table 6. The scores for the readmitted patients are within the average

reported range of 170.76. In the category of Personal Status, all readmitted patients

scored below the average of 42.

Table 5 – Readmitted Patients

Readmitted Patients

Patient Age Race Support Education Income Last

Admission

Reason

17A 46

M

Black Married

with

spouse

12 $0-9,999 4-6

months

Chest pain

18A 53

M

Black Single

with

friend

0 $0-9,999 0-3

months

Heart failure

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2B 45

M

Black Single

with

friend

12 $10,000-

19,999

4-6

months

Heart failure

14B 63

M

White Married

with

spouse

18 >$40,000 4-6

months

Cardiomyopathy

16B 66

F

Black Married

with

spouse

11 $10,000-

19,999

4-6

months

Chest Pain

20B 62

M

Black Single

with

friend

12 $30,000-

39,999

0-3

months

Non ST

Elevation

Myocardial

Infarction

Table 5 continued

Table 6 – RHDS for Readmitted Patients

RHDS Results for Readmitted Patients

RHDS 2B 14B 16B 20B Average

Score

Personal Status 40 36 24 34 42.92

Knowledge 81 77 78 74 72.28

Coping 29 30 27 26 25.44

Expected Support 39 30 38 28 30.12

Total 189 173 167 162 170.16

Limitations

A limitation of the study is the use of a single healthcare institution to perform the

study and a small sample size. Readmissions were only tracked to the one hospital and

not to any other hospital. The RHDS questionnaire was not administered to both groups

of patients and as such a comparison T-test could not be completed.

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Chapter 4 – Conclusions and Recommendations

Discussion

For this study, providing additional HF education did not reduce or lessen hospital

readmissions within the thirty day window of discharge. For the six patients readmitted,

eighty-three percent were African-American. A closer look at the relationship of race to

readmission needs to be explored. For the four readmitted patients in Group B, the

patients scored below the average score on the sub section for Personal Status. These

questions focused on ready to go home, pain, energy and pain levels and emotionally

ready to go home. Further investigation is needed to determine if this is specifically

related to HF or the patient’s classification of HF. Sixty-eight percent of the patients

reported incomes of $20,000 or less. The impact of income needs to be investigated to

determine how much this impacts their ability to obtain medications, food and maintain

their home.

Demographic data not captured by this study such as HF classification, smoking

status, medication adherence and adherence to follow up may have an impact on

readmissions within the thirty day window of discharge.

Future studies by the investigator will expand the demographics to include zip

code, HF classification, number of medications prescribed, smoking status, transportation

availability, adherence to follow-up appointments, food accessibility, and the use of

devices such as left ventricular assist device or life vest. Future research studies may

focus on the impact of financial status on ability to obtain medications and purchase food.

Since arthritis and breathing problems were noted as high co-morbidities for this group of

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patients, a further analysis of this impact is needed on the HF population. Future

qualitative studies can focus on patients’ perceptions regarding the impact of

rehospitalization on the transition to home, their ability to comply with strict fluid

restrictions and HF instructions in the home environment.

Summary

This study gave the investigator added insight into HF patients’ perceptions of discharge

readiness. These results can potentially provide clinical applications for preventing

readmission within thirty days. The investigator will team with members of the hospital

to examine if changes are needed to the approach that nurses take regarding discharge

preparations for patients.

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Appendix A

Transitions Theory

(Conceptualized by Investigator)

Patient

Transitions Health

Personal Status Health

Role Relationships

Knowledge

Nurse Facilitating

Patient Transitions

Expected Support

Abilities

Coping

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Appendix B

Nurse Script for Recruiting Patients

Good (morning or afternoon)

One of our nurses at Hahnemann is doing a study on the patient’s

feelings about going home at discharge. There is a short survey

that you will be asked to fill out. The only information that can

identify you as participating will be your medical record number

that will be used to track if you are readmitted in thirty days. All

information is kept in a secure office that is locked. The survey

should take about fifteen minutes. If you would like to participate,

I will call the nurse to come and visit you.

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Appendix C

Demographic Questionnaire

Demographic Information ID Medical Record Number:__________

Gender: □ Male □ Female

Age: ___________

Ethnic Status

□ Non Hispanic

□ Hispanic

Race: □ White

□ Black or African American

□ Asian

□American Indian or Alaska Native

□ Native Hawaiian or Other Pacific Islander

□ Some Other Race

□ Two or More Races

Years of Education: ___________________________________________

Marital Status:

□ Single

□ Married

□Divorced

□Widow/Widower

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Support

□ Live with spouse

□ Live with relative/friend

□ Live alone

Yearly Income:

□ Less than $9,999

□ $10,000 to $19,999

□ $20,000 to $29,999

□ $30,000 to $39,999

□ Greater than $40,000

Occupation:________________________________

Is this your first hospital stay?

No

If you answered no, what was the date of your last hospitalization?

_____________________

Do you have any other medical conditions? Check all that apply

Arthritis Cancer

Kidney Disease Liver Disease Respiratory

Problems

Stomach Problems Vision Problems Hearing Problems

Skin Problems

Problems

Women's Health Problems Other (please list)________________

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Appendix D

ID#

READINESS FOR HOSPITAL DISCHARGE - ADULT FORM

Please check or circle our answer. Most of the responses are on a scale from 0 to 10 the

words below the number indicate what the 0 or the 10 means. Pick the number

between 0 and 10 that best describes how you feel. For example, circling number

7 means you feel more like the description of number 10 than number 0 but not

completely.

1 As you think about your

discharge from the hospital, do

you believe you are ready to go

home as planned?

[ ] No [ ] Yes

2. How physically ready are you

to go home?

0 1 2 3 4 5 6 7 8 9 10

Not Totally

ready ready

3. How would you describe your

pain or discomfort today?

0 1 2 3 4 5 6 7 8 9 10

No pain Severe pain/

discomfort discomfort

4. How would you describe your

strength today?

0 1 2 3 4 5 6 7 8 9 10

Weak Strong

5. How would you describe your

energy today?

0 1 2 3 4 5 6 7 8 9 10

Low energy High energy

6. How much stress do you feel

today?

0 1 2 3 4 5 6 7 8 9 10

None A great deal

7. How emotionally ready are you

to go home today?

0 1 2 3 4 5 6 7 8 9 10

Not Totally

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ready ready

8. How would you describe your

physical ability to care for yourself

today (for example, hygiene,

walking, toileting)

0 1 2 3 4 5 6 7 8 9 10

Not able Totally able

9. How much do you know about

caring for yourself after you go

home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

10. How much do you know about

taking care of your personal

needs (for example, hygiene,

bathing, toileting, eating) after you

go home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

11. How much do you know about

taking care of our medical needs

(treatments, medications) after you

go home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

12. How much do you know

about problems to watch out for

after you go home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

13. How much do you know

about who and when to call if

you have problems to watch for

after you go home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

14. How much to you know about

restrictions (what you are allowed

and not allowed to do) after you go

home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

15. How much do you know

about what happens next in your

follow-up medical treatment plan

after you go home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

16. How much do you know

about services and information

available to you in your

community after you go home?

0 1 2 3 4 5 6 7 8 9 10

No nothing at all Know all

17. How well will you be able to

handle the demands of life at

home?

0 1 2 3 4 5 6 7 8 9 10

Not at all Extremely well

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18. How well will you be able to

perform your personal care (for

example, hygiene, bathing,

toileting, eating) at home?

0 1 2 3 4 5 6 7 8 9 10

Not at all Extremely well

19. How well will you be able to

perform your medical

treatments (for example, caring

for a surgical incision, respiratory

treatments, exercise, rehabilitation,

taking your medications in the

correct amounts and at the correct

times) at home?

0 1 2 3 4 5 6 7 8 9 10

Not at all Extremely well

20. How much emotional

support will you have after you go

home?

0 1 2 3 4 5 6 7 8 9 10

None A great deal

21. How much help will you have

with your personal care after you

go home?

0 1 2 3 4 5 6 7 8 9 10

None A great deal

22. How much help will you have

with household activities (for

example, cooking, cleaning,

shopping, babysitting) after you go

home?

0 1 2 3 4 5 6 7 8 9 10

None A great deal

23. How much help- will you have

with your medical care needs

(treatments, medications)?

0 1 2 3 4 5 6 7 8 9 10

None A great deal

Comments:

Thank you for participating in our study.

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Appendix E

PERMISSION FOR USE AGREEMENT

READINESS FOR HOSPITAL DISCHARGE SCALE (RHDS)

QUALITY OF DISCHARGE TEACHING SCALE (QDTS)

POST-DISCHARGE COPING DIFFICULTY SCALE (PDCDS)

Marianne Weiss, DNSC, RN, author

You may use the RHDS/QDTS/PDCDS for clinical practice or research purposes under

the following conditions: You agree to provide me with

1. a brief description of the study and/or clinical population for which it is used

2. a summary of any results from use of the instrument; for example, reliability

coefficients, differences among groups, correlations, predictors, and/or outcomes

3.. where possible, a copy of RHDS/QDTS AND/OR PDCDS data for inclusion in an

instrument database for further analysis of psychometric properties (not required for

permission to use)

Please complete the following questions:

1. Your name:_____Linda M. Celia______________________________________

2. Your organization:___Drexel University___________________________________

3. Your address:_42 North Wycombe Avenue, Lansdowne, PA 19050__

4. Your telephone number:_215-762-7283_________________________________

5. Your e-mail address:[email protected] and

[email protected]_________

6. Purposes(s) for using the instrument(s):

[ ] clinical practice

[x ] research, If yes, will you use the instrument(s)for [ ]master’s thesis

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[x ] PhD dissertation/DNP

Project

7. Which Iinstrument(s) do you plan to use in your research?

[x ] RHDS [ ] QDTS [ ] PDCDS

Which version of the instrument(s) do you plan to use?

[ ] New mothers form(s) [x ] Adult medical-surgical form(s) [ ] Parent of

hospitalized

child form(s)

8. Describe how you plan to use the instrument? (If research, please briefly describe the

research

questions and methods)

Examining discharge readiness in heart failure patients with additional education and the

RHDS compared to a group just completing the demographic information and receiving

standard nursing care.

9. Describe the patients who will complete the instrument(s).

Adult patients on medical surgical units at a large urban tertiary medical center

Signature:___Linda M. Celia_______________Date:_6/10/2011________________

Please e-mail this form to Dr Marianne Weiss at [email protected] or mail

to:

Dr Marianne Weiss, Marquette University College of Nursing,PO Box 1881,Milwaukee

WI, 53201-1881