SUSTAIN-IT: Sustaining Quality of Life of the Aged: Heart Transplant or Mechanical Support?
Study Details
Study Description
Brief Summary
The purpose of this study is to compare health-related quality of life (HRQOL) outcomes in older (60-80 years) advanced heart failure (HF) patients who undergo heart transplantation (HT) or mechanical circulatory support (MCS) as a permanent implant (i.e., destination therapy [DT]) and their caregivers. Our study will contribute to better patient-centered care of older advanced HF patients and their caregivers, by informing decision making and guiding strategies to enhance post-operative HRQOL.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
The purpose of this study is to compare health-related quality of life (HRQOL) outcomes in older (60-80 years) advanced heart failure (HF) patients who undergo heart transplantation (HT) or mechanical circulatory support (MCS) as a permanent implant (i.e., destination therapy [DT]) and their caregivers, risk factors for poor HRQOL, adverse event and symptom burden, and quality-adjusted life years (QALYs). Advanced HF patients, 60-80 years of age, are an appropriate target group for this study because they are receiving HTs and MCS devices more frequently, and despite a greater risk for poor clinical outcomes, they have acceptable rates of survival. Using a prospective, longitudinal design, our multi-site comparative effectiveness research will compare HRQOL outcomes in patients who receive HT or DT MCS and their caregivers, from baseline to 2 years post-operatively. The primary aim of this proposed study is to determine whether older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT, experience non-inferior change in overall HRQOL (primary), and domains of HRQOL (physical, mental, and social) from baseline through 2 years after surgery. Secondary Aims are (1.) to determine whether caregivers of older advanced HF patients who undergo DT MCS, compared to caregivers of older advanced HF patients who undergo HT, experience non-inferior change in overall HRQOL and domains from baseline through 2 years after surgery; (2.-3.) to identify risk factors related to poorer overall HRQOL in older DT MCS patients and their caregivers, as compared to older HT patients and their caregivers, at 2 years after surgery; (4.) to determine whether older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT, have non-inferior rates of freedom from adverse events & symptoms at 1 and 2 years after surgery; and (5) to evaluate the distribution of QALYs in older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT at 2 years after surgery. Our proposed study will contribute to better patient-centered care of older advanced HF patients and their caregivers, by informing decision making and guiding strategies to enhance post-operative HRQOL.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Heart Transplantation (HT) The cohort includes advanced heart failure patients (60-80 years of age) listed for HT and their caregivers. |
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| Mechanical Circulatory Support (MCS) The cohort includes advanced heart failure patients (60-80 years of age) scheduled for DT MCS and their caregivers. |
Outcome Measures
Primary Outcome Measures
- Non-inferior change in patient HRQOL [baseline through 2 years after surgery]
To determine whether older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT, experience non-inferior change in overall HRQOL (primary outcome) and HRQOL domains (physical, mental, and social [secondary outcomes]) from baseline through 2 years after surgery.
Secondary Outcome Measures
- Non-inferior change in caregiver HRQOL [baseline through 2 years after surgery]
To determine whether caregivers of older advanced HF patients who undergo DT MCS, as compared to caregivers of older advanced HF patients who undergo HT, experience non-inferior change in overall HRQOL and HRQOL domains from baseline through 2 years after surgery.
- Risk factors related to poorer patient overall HRQOL [2 years after surgery]
To identify risk factors related to poorer overall HRQOL in older DT MCS patients, as compared to older HT patients, at 2 years after surgery.
- Risk factors related to poorer caregiver overall HRQOL [2 years after surgery]
To identify risk factors related to poorer overall HRQOL in caregivers of older DT MCS patients, as compared to caregivers of older HT patients, at 2 years after surgery.
- Non-inferior rates of freedom from adverse events & symptoms [1 and 2 years after surgery]
To determine whether older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT, have non-inferior rates of freedom from adverse events & symptoms at 1 & 2 years after surgery.
- Distribution of QALYs [2 years after surgery]
To evaluate the distribution of QALYs in older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT at 2 years after surgery.
Eligibility Criteria
Criteria
Patient Inclusion Criteria:
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Advanced HF and listed with the United Network for Organ Sharing (UNOS) for a "primary" HT or scheduled to receive a "primary" DT LVAD;
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Ages 60-80 years and able to speak, read, and understand English;
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Willing to participate and ability to provide informed consent.
Caregiver Inclusion criteria:
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Primary caregiver, identified by the patient, prior to DT MCS or while a candidate for HT;
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Unpaid family member or friend who helps the patient with self-care;
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Age > 21 years and able to speak, read, and write English;
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Willing to participate and ability to provide informed consent.
Patient Exclusion criteria
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Patient has a prior HT or MCS device
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Patient is listed for multiple organ transplantation (i.e., heart/lung, heart/kidney, etc.)
Caregiver Exclusion criterion:
- Patient refusal to participate.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Alabama at Birmingham (UAB) | Birmingham | Alabama | United States | 35294 |
| 2 | Florida Hospital | Orlando | Florida | United States | 32803-1248 |
| 3 | Northwestern University | Chicago | Illinois | United States | 60611 |
| 4 | Advocate Christ Medical Center | Oak Lawn | Illinois | United States | 60453 |
| 5 | University of Michigan | Ann Arbor | Michigan | United States | 48109 |
| 6 | University of Minnesota Medical Center-Fairview Health Services | Minneapolis | Minnesota | United States | 55454 |
| 7 | Saint Luke's Hospital | Kansas City | Missouri | United States | 64111 |
| 8 | Washington University | Saint Louis | Missouri | United States | 63110 |
| 9 | Columbia University | New York | New York | United States | 10032-3702 |
| 10 | Cleveland Clinic | Cleveland | Ohio | United States | 44195 |
| 11 | The Ohio State University (OSU) | Columbus | Ohio | United States | 43210 |
| 12 | University of Pittsburgh Medical Center (UPMC) | Pittsburgh | Pennsylvania | United States | 15213 |
| 13 | University of Wisconsin-Madison | Madison | Wisconsin | United States | 53706-1490 |
Sponsors and Collaborators
- Northwestern University
- National Institute on Aging (NIA)
Investigators
- Principal Investigator: Kathleen Grady, RN, PhD, Northwestern University
Study Documents (Full-Text)
More Information
Publications
None provided.- STU00200851
- 1R01AG047416