Background. Heart transplantation (HT) in the United States continues to be increasingly performed in the setting of expanding Medicare and Medicaid public insurance coverage. We analyze the impact of recipient insurance trajectories on long-term graft and recipient survival following the 2018 United Network for Organ Sharing (UNOS) heart allocation change. Methods. Adults aged 18-64 undergoing first-time HT between 10/2018 and 3/2024 were identified in the UNOS database. Patients surviving ≥1 year were stratified by insurance trajectory (private vs. public, including Medicare, Medicaid, and VA) at waitlist, transplantation, and 1-year follow-up. Kaplan-Meier and Cox regression models were used to assess survival and graft failure risk. Results. Among 15,864 patients, 42.5% had continuous private insurance, 33.9% had continuous public insurance, 12.6% transitioned from private to public, 4.8% transitioned from public to private, and 6.3% experienced multiple transitions. Five-year survival (p<0.0001) and graft survival (p=0.03) were poorer in patients with continuous public insurance or who transitioned from private to public insurance. Primary graft dysfunction rates were highest among recipients with continuous public insurance (1.4%; p<0.0001). Continuous public insurance (HR 1.27, p<0.0001) and multiple transitions (HR 1.19, p=0.04) increased mortality risk compared to continuous private insurance. Continuous public insurance (HR 1.29, p=0.01), private-to-public transition (HR 1.32, p=0.03), and multiple transitions (HR 1.09, p=0.02) were linked to higher graft failure risk. Public-to-private transition was associated with lower graft failure risk (HR 0.73, p=0.02). Residence in distressed communities increased mortality (HR 1.21, p=0.003) and graft failure risk (HR 1.31, p=0.001). Conclusions. Public insurance and insurance instability are associated with worse HT outcomes, while gaining private insurance was associated with improved outcomes, highlighting disparities in post-transplant care.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialN/A
Funding StatementNone.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
This study was reviewed by the Virginia Commonwealth University Institutional Review Board and determined to be exempt from review because it used de-identified, publicly available data from the Organ Procurement and Transplantation Network/United Network for Organ Sharing Standard Transplant Analysis and Research files. All data use complied with relevant federal and institutional guidelines and regulations.
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityThe data that support the findings of this study are available from the Organ Procurement and Transplantation Network (OPTN) and the United Network for Organ Sharing (UNOS) Standard Transplant Analysis and Research (STAR) files. Restrictions apply to the availability of these data, which were used under license for this study. Researchers may request access to the STAR files through the OPTN/UNOS data request process (https://optn.transplant.hrsa.gov/data/request-data/). No additional, unpublished data are available.
Comments (0)