Heart waitlist survival in adults with an intra-aortic balloon pump relative to other Status 2, Status 1, and inotrope Status 3 patients.


Journal

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
ISSN: 1557-3117
Titre abrégé: J Heart Lung Transplant
Pays: United States
ID NLM: 9102703

Informations de publication

Date de publication:
03 2023
Historique:
received: 11 08 2022
revised: 03 10 2022
accepted: 09 10 2022
pmc-release: 01 03 2024
pubmed: 12 11 2022
medline: 25 2 2023
entrez: 11 11 2022
Statut: ppublish

Résumé

Intra-aortic balloon pump (IABP) utilization has significantly outpaced other Status 2 eligibility criteria for heart transplant. The risk of waitlist mortality of IABP-supported patients relative to other Status 2 listed patients has not been described. We performed a retrospective analysis of all adult patients listed Status 2 for heart transplantation under the current U.S. allocation policy, using data from the United Network for Organ Sharing. Patients listed status 1 and status 3 for high-dose inotropes were included for reference. Mortality and waitlist decompensation were modeled as a function of time-varying status in cause-specific Cox survival models. We identified 3638 Status 2 listings, of whom 1676 (46%) were Status 2 due to IABP. Relative to patients supported with IABP, status 2 patients with ventricular tachycardia/fibrillation [VT/VF] (HR 4.0, p < .001), right-or-biventricular assist device configurations (HR 2.3, p = .002), or temporary surgical left ventricular assist devices [LVAD] (HR 2.6, p = .003) had greater risk of waitlist mortality and decompensation. Other Status 2 subgroups had mortality comparable to IABP Status 2. Risk of waitlist mortality and decompensation for IABP Status 2 was similar to Status 3 patients listed for high-dose inotropes (HR 1.2, p = .27) and lower than Status 1 patients (HR 0.7, p = .002). Waitlist mortality varies significantly by Status 2 eligibility criteria and is highest among patients listed for VT/VF, right-or-biVAD configurations, or temporary surgical LVADs. IABP-supported patients were among those with the lowest Status 2 waitlist mortality risk and comparable to Status 3 inotrope-supported patients.

Sections du résumé

BACKGROUND
Intra-aortic balloon pump (IABP) utilization has significantly outpaced other Status 2 eligibility criteria for heart transplant. The risk of waitlist mortality of IABP-supported patients relative to other Status 2 listed patients has not been described.
METHODS
We performed a retrospective analysis of all adult patients listed Status 2 for heart transplantation under the current U.S. allocation policy, using data from the United Network for Organ Sharing. Patients listed status 1 and status 3 for high-dose inotropes were included for reference. Mortality and waitlist decompensation were modeled as a function of time-varying status in cause-specific Cox survival models.
RESULTS
We identified 3638 Status 2 listings, of whom 1676 (46%) were Status 2 due to IABP. Relative to patients supported with IABP, status 2 patients with ventricular tachycardia/fibrillation [VT/VF] (HR 4.0, p < .001), right-or-biventricular assist device configurations (HR 2.3, p = .002), or temporary surgical left ventricular assist devices [LVAD] (HR 2.6, p = .003) had greater risk of waitlist mortality and decompensation. Other Status 2 subgroups had mortality comparable to IABP Status 2. Risk of waitlist mortality and decompensation for IABP Status 2 was similar to Status 3 patients listed for high-dose inotropes (HR 1.2, p = .27) and lower than Status 1 patients (HR 0.7, p = .002).
CONCLUSIONS
Waitlist mortality varies significantly by Status 2 eligibility criteria and is highest among patients listed for VT/VF, right-or-biVAD configurations, or temporary surgical LVADs. IABP-supported patients were among those with the lowest Status 2 waitlist mortality risk and comparable to Status 3 inotrope-supported patients.

Identifiants

pubmed: 36369224
pii: S1053-2498(22)02179-9
doi: 10.1016/j.healun.2022.10.010
pmc: PMC9974555
mid: NIHMS1850686
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

368-376

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL135121
Pays : United States
Organisme : HSRD VA
ID : I01 HX002922
Pays : United States
Organisme : CSRD VA
ID : I01 CX000710
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL132067
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL156667
Pays : United States
Organisme : CSRD VA
ID : I01 CX002291
Pays : United States

Informations de copyright

Copyright © 2022 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.

Références

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pubmed: 26858290
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pubmed: 29307954
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pubmed: 35184091
J Thorac Cardiovasc Surg. 2016 Dec;152(6):1484-1486
pubmed: 27692950
BMJ. 2007 Oct 20;335(7624):806-8
pubmed: 17947786
J Heart Lung Transplant. 2020 Jul;39(7):725-726
pubmed: 32307250
JAMA Cardiol. 2020 Jun 1;5(6):728-729
pubmed: 32293645
J Heart Lung Transplant. 2020 Nov;39(11):1191-1194
pubmed: 32950380
Circ Heart Fail. 2021 Nov;14(11):e008764
pubmed: 34689572
J Am Coll Cardiol. 2020 Jun 16;75(23):2906-2916
pubmed: 32527399
Clin Transplant. 2022 Feb;36(2):e14533
pubmed: 34786769

Auteurs

Thomas C Hanff (TC)

Division of Cardiovascular Medicine, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah. Electronic address: thomas.hanff@hsc.utah.edu.

Adeline Browne (A)

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

Jacqueline Dickey (J)

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

Holly Gaines (H)

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

Michael O Harhay (MO)

Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Matt Goodwin (M)

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

Craig H Selzman (CH)

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

James C Fang (JC)

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

Stavros G Drakos (SG)

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

Josef Stehlik (J)

Division of Cardiovascular Medicine, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah; Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

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Classifications MeSH