Evidence map›Paper›PMID 38716787›Full record

ArticleClinical transplantation2024

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

Konstantinos Sideris, Eszter Lázár-Molnár, Christos P Kyriakopoulos, Iosif Taleb, Denise Hurst, Sharon Ugolini, Craig H Selzman, Lina Brinker, Stavros G Drakos, Joseph E Tonna and 7 more

Abstract read
In one paragraph

Article in Clinical transplantation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Konstantinos SiderisDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.ORCID 0009-0007-9369-0782
Eszter Lázár-MolnárDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.ORCID 0000-0003-0802-9409
Christos P KyriakopoulosDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.ORCID 0000-0001-9415-1245
Iosif TalebDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Denise HurstDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Sharon UgoliniDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Craig H SelzmanDivision of Cardiothoracic Surgery, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Lina BrinkerDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Stavros G DrakosDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Joseph E TonnaDivision of Cardiothoracic Surgery, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Laura GeerDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Matthew L GoodwinDivision of Cardiothoracic Surgery, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Omar Wever-PinzonDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Thomas C HanffDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
James C FangDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Spencer CarterDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Josef StehlikDivision of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.ORCID 0000-0002-7362-0513

Funding

TRAINING IN CARDIOVASCULAR RESEARCHT32HL007576 · NHLBI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Stavros George Drakos, Robin M Shaw · 1985 to 2026
$10.6M
NHLBI NIH HHS L30 HL170339NHLBI NIH HHS T32 HL007576
6 · The paper itself

Abstract

introductionSince 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.

methodsWe 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.

resultsA 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.

conclusionsOur 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.

Indexed as

Heart-Assist DevicesHeart TransplantationIsoantibodiesAdultFemaleFollow-Up StudiesGraft RejectionHeart FailureHumansMaleMiddle AgedPrognosisRetrospective StudiesRisk FactorsIsoantibodiesallosensitizationheart transplanttemporary mechanical circulatory support

Identifiers

PMID38716787
PMCPMC11283677

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