Bridge-to-transplant temporary mechanical circulatory support and risk of allosensitization.


Journal

Clinical transplantation
ISSN: 1399-0012
Titre abrégé: Clin Transplant
Pays: Denmark
ID NLM: 8710240

Informations de publication

Date de publication:
May 2024
Historique:
revised: 07 04 2024
received: 13 12 2023
accepted: 22 04 2024
medline: 8 5 2024
pubmed: 8 5 2024
entrez: 8 5 2024
Statut: ppublish

Résumé

Since the 2018 change in the US adult heart allocation policy, more patients are bridged-to-transplant on temporary mechanical circulatory support (tMCS). Previous studies indicate that durable left ventricular assist devices (LVAD) may lead to allosensitization. The goal of this study was to assess whether tMCS implantation is associated with changes in sensitization. We included patients evaluated for heart transplants between 2015 and 2022 who had alloantibody measured before and after MCS implantation. Allosensitization was defined as development of new alloantibodies after tMCS implant. A total of 41 patients received tMCS before transplant. Nine (22.0%) patients developed alloantibodies following tMCS implantation: 3 (12.0%) in the intra-aortic balloon pump group (n = 25), 2 (28.6%) in the microaxial percutaneous LVAD group (n = 7), and 4 (44.4%) in the veno-arterial extra-corporeal membrane oxygenation group (n = 9)-p = .039. Sensitized patients were younger (44.7 ± 11.6 years vs. 54.3 ± 12.5 years, p = .044), were more likely to be sensitized at baseline - 3 of 9 (33.3%) compared to 2 out of 32 (6.3%) (p = .028) and received more transfusions with red blood cells (6 (66.6%) vs. 8 (25%), p = .02) and platelets (6 (66.6%) vs. 5 (15.6%), p = .002). There was no significant difference in tMCS median duration of support (4 [3,15] days vs. 8.5 [5,14.5] days, p = .57). Importantly, out of the 11 patients who received a durable LVAD after tMCS, 5 (45.5%) became sensitized, compared to 4 out of 30 patients (13.3%) who only had tMCS-p = .028. Our findings suggest that patients bridged-to-transplant with tMCS, without significant blood product transfusions and a subsequent durable LVAD implant, have a low risk of allosensitization. Further studies are needed to confirm our findings and determine whether risk of sensitization varies by type of tMCS and duration of support.

Identifiants

pubmed: 38716787
doi: 10.1111/ctr.15330
doi:

Substances chimiques

Isoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e15330

Subventions

Organisme : NHLBI NIH HHS
Pays : United States

Informations de copyright

© 2024 The Authors. Clinical Transplantation published by John Wiley & Sons Ltd.

Références

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Drakos SG, Kfoury AG, Kotter JR, et al. Prior human leukocyte antigen‐allosensitization and left ventricular assist device type affect degree of post‐implantation human leukocyte antigen‐allosensitization. J Heart Lung Transplant. 2009;28(8):838‐842.
Tsau PH, Arabia FA, Toporoff B, Paramesh V, Sethi GK, Copeland JG. Positive panel reactive antibody titers in patients bridged to transplantation with a mechanical assist device: risk factors and treatment. ASAIO J. 1998;44(5):M634‐637.
De Mattos AM, Head MA, Everett J, et al. HLA‐DR mismatching correlates with early cardiac allograft rejection, incidence, and graft survival when high‐confidence‐level serological DR typing is used. Transplantation. 1994;57(4):626‐630.
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Zerbe TR, Arena VC, Kormos RL, Griffith BP, Hardesty RL, Duquesnoy RJ. Histocompatibility and other risk factors for histological rejection of human cardiac allografts during the first three months following transplantation. Transplantation. 1991;52(3):485‐490.
Frazier OH, Rose EA, Oz MC, et al. Multicenter clinical evaluation of the HeartMate vented electric left ventricular assist system in patients awaiting heart transplantation. J Thorac Cardiovasc Surg. 2001;122(6):1186‐1195.
Cole R, Moriguchi J, Kittleson M, et al. Do temporary mechanical circulatory support devices activate sensitization pathways in patients awaiting heart transplantation? J Heart Lung Transplant. 2022;41(4):S469. Supplement.
Goetz RL, Kaleekal TS, Wille KM, et al. HLA sensitization in patients bridged to lung transplantation with extracorporeal membrane oxygenation. Transplant Direct. 2023;9(7):e1497.
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Auteurs

Konstantinos Sideris (K)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Eszter Lázár-Molnár (E)

Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Christos P Kyriakopoulos (CP)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Iosif Taleb (I)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Denise Hurst (D)

Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Sharon Ugolini (S)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Craig H Selzman (CH)

Division of Cardiothoracic Surgery, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Lina Brinker (L)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Stavros G Drakos (SG)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Joseph E Tonna (JE)

Division of Cardiothoracic Surgery, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Laura Geer (L)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Matthew L Goodwin (ML)

Division of Cardiothoracic Surgery, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Omar Wever-Pinzon (O)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Thomas C Hanff (TC)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

James C Fang (JC)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Spencer Carter (S)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

Josef Stehlik (J)

Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

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