Clinical Outcomes With Normothermic Pulsatile Organ Perfusion in Heart Transplantation: A Report From the OCS Heart Perfusion Registry
Abstract
BACKGROUND: A preservation system, the Organ Care System (OCS; TransMedics) uses normothermic pulsatile perfusion during organ transport for heart transplantation. This system has demonstrated favorable outcomes in hearts recovered from extended-criteria donors after brain death (DBD) and donors after circulatory death (DCD). METHODS: The OCS Heart Perfusion Registry collects data on US heart transplantations using the OCS, static cold storage (SCS), or thoracoabdominal normothermic regional perfusion (NRP) and donor hearts recovered from DBD or DCD donors. We analyzed donor and recipient characteristics and posttransplantation outcomes in patients transplanted with OCS donor hearts (either DBD or DCD) compared with SCS hearts, and with OCS hearts from DCD donors compared with those recovered with NRP followed by SCS. Propensity score matching was used in survival analyses to adjust for differences among recipient characteristics. RESULTS: Between 2021 and 2023, 3225 consecutive heart transplantations enrolled from 56 centers were analyzed in the Heart Perfusion Registry. The OCS was used in 854 of 3225 heart transplantations (26.4%), among which 340 (39.8%) were DBD and 514 (60.2%) were DCD donors, whereas 2174 DBD donors were recovered with SCS and another 197 DCD donors with NRP techniques. The OCS-DBD group experienced a greater number of organ offer refusals before final acceptance (13 versus 6; Wilcoxon rank sum, P <0.001) and a longer transport distance (667 miles versus 232 miles; Wilcoxon rank sum, P <0.001) compared with SCS-DBD. Survival at 12 months was similar between the 2 groups (89.9% for OCS-DBD versus 90.6% for SCS-DBD; marginal Cox model, P =0.54). Among the OCS-DCD and SCS-DBD groups, survival at 12 months was also similar (91.0% versus 92.5%, respectively; marginal Cox model, P =0.32). The OCS-DCD and NRP-DCD groups demonstrated similar survival (91.0% versus 91.7%, respectively; log rank, P =0.63), although the transport distance was longer in OCS-DCD compared with DCD with NRP followed by SCS (400 miles versus 223 miles; Wilcoxon rank sum, P <0.001). By 2023, 90% of all OCS donor management and recovery was performed with dedicated organ recovery teams. CONCLUSIONS: We demonstrate that real-world implementation of the OCS for DBD donors (using predominantly a dedicated recovery team) is associated with expanded donor criteria, longer transport distance, and excellent posttransplantation outcomes. In OCS-DCD donors, outcomes parallel those of donors recovered with NRP-DCD and compare favorably with DBD donor organs.
Article Details
Authors (42)
Josef Stehlik
University of Utah School of Medicine, Salt Lake City, Utah, United States
Maryjane A. Farr
UT Southwestern Medical Center, Dallas, TX (M.A.F.).
Mandeep R. Mehra
Brigham and Women’s Hospital, Boston, MA (M.R.M., A.I.).
Jacob N. Schroder
Duke University Hospital, Durham, NC (J.N.S., C.A.M.).
David A. D’Alessandro
Massachusetts General Hospital, Boston (D.A.D.).
Jay D. Pal
Mauricio A. Villavicencio
Mayo Clinic Hospital Minnesota, Rochester (M.A.V.).
Peter J. Gruber
Department of Surgery, Yale University School of Medicine
Gregory S. Couper
Tufts Medical Center, Boston, MA (G.S.C.).
Yasuhiro Shudo
Stanford Health Care, Palo Alto, CA (Y.S.).
Parag C. Patel
Mayo Clinic Hospital Florida, Jacksonville (P.C.P.).
Mani A. Daneshmand
Emory University Hospital, Atlanta, GA (M.A.D.).
Liviu Klein
UNIVERSITY OF CALIFORNIA, San Francisco, California, United States
Ashish S. Shah
Department of Cardiac Surgery, Vanderbilt University Medical Center, Nashville
Eric R. Skipper
Carolinas Medical Center, Charlotte, NC (E.R.S.).
Fardad Esmailian
Cedars-Sinai Medical Center, Los Angeles, CA (F.E.).
Daniel Goldstein
Montefiore Medical Center, Bronx, NY (D.G.).
Suguru Ohira
Westchester Medical Center, Valhalla, NY (S.O.).
Lucian Lozonschi
University of South Florida, Tampa General Hospital, Tampa, Florida, United States
David J. Kaczorowski
University of Pittsburgh Medical Center, PA (D.J.K.).
Koji Takeda
Rajasekhar S.R. Malyala
University of Kentucky Medical Center, Lexington (R.S.R.M.).
Jonathan W. Haft
University of Michigan Medical Center, Ann Arbor (J.W.H.)
Dan M. Meyer
Baylor University Medical Center, Dallas, TX (D.M.M.).
Benjamin C. Sun
Abbott Northwestern Hospital, Minneapolis, MN (B.C.S.).
Victor Pretorius
UCSD, Sleepy Hollow, New York, United States
Arman Kilic
MUSC, Charleston, South Carolina, United States
Anelechi C. Anyanwu
Mount Sinai Medical Center, New York, NY (A.C.A., S.P.P.).
Celeste T. Williams
Henry Ford Hospital, Detroit, MI (C.T.W.).
Duc T. Pham
Northwestern Memorial Hospital, Chicago, IL (D.T.P.).
Masashi Kai
Beth Israel Deaconess Medical Center, Brookline, Massachusetts, United States
Nasir Z. Sulemanjee
Aurora St. Luke’s Medical Center, Milwaukee, WI (N.Z.S.).
Akinobu Itoh
Brigham and Women’s Hospital, Boston, MA (M.R.M., A.I.).
Masaki Funamoto
Methodist Specialty and Transplant Hospital, San Antonio, TX (M.F.).
Christopher T. Salerno
University of Chicago Medical Center, IL (C.T.S.).
John S. Ikonomidis
University of North Carolina Hospitals, Chapel Hill (J.S.I.).
Lucian A. Durham
Froedtert Memorial Lutheran Hospital, Milwaukee, WI (L.A.D.).
Andrew Shaffer
University of Minnesota Medical Center, Fairview, Minneapolis (A.S.).
Xiang Zhou
Farhan Zafar
Sean P. Pinney
Mount Sinai Medical Center, New York, NY (A.C.A., S.P.P.).
Carmelo A. Milano