The impact of pre-existing hematologic disorders on morbidity and mortality following heart transplantation: Focus on early graft dysfunction
- PMID: 36938656
- PMCID: PMC11877356
- DOI: 10.1111/ctr.14974
The impact of pre-existing hematologic disorders on morbidity and mortality following heart transplantation: Focus on early graft dysfunction
Abstract
Background: Heart transplantation (HT) is the gold standard therapy for advanced heart failure, providing excellent long-term outcomes. However, postoperative outcomes are limited by bleeding, infections, and primary graft dysfunction (PGD) that contribute to early mortality after HT. HT candidates with pre-existing hematologic disorders, bleeding, and clotting, may represent a higher risk population. We assessed the short- and long-term outcomes of patients with pre-existing hematologic disorders undergoing HT.
Methods and results: Medical records of all adult patients who received HT from January 2010 to December 2019 at our institution were retrospectively reviewed. Hematologic disorders were identified via chart review and adjudicated by a board-certified hematologist. Inverse probability weighting and multivariable models were used to adjust for potential pretransplant confounders. Four hundred and ninety HT recipients were included, of whom 29 (5.9%) had a hematologic disorder. Hematologic disorders were associated with severe PGD requiring mechanical circulatory support (aOR 3.15 [1.01-9.86]; p = .049), postoperative infections (aOR 2.93 [1.38-6.23]; p = .01), and 3-year acute cellular rejection (ACR) (≥1R/1B) (aSHR 2.06 [1.09-3.87]; p = .03). There was no difference in in-hospital mortality (aOR 1.23 [.20-7.58], p = .82) or 3-year mortality (aHR 1.58 [.49-5.12], p = .44).
Conclusions: Patients with hematologic disorders undergoing HT are at increased risk of severe PGD, postoperative infections, and ACR, while in-hospital and 3-year mortality remain unaffected.
Keywords: coagulopathy; heart transplantation; hematologic disorders; primary graft dysfunction.
© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Conflict of interest statement
CONFLICT OF INTEREST STATEMENT
Ms. Molinsky is supported by an NHLBI training grant (T32HL007779). Dr. Clerkin is supported in part by an NIH grant (K23HL148528). Dr. Sayer reports consulting fees from Abbott and serving on the advisory board of CareDx. Dr. Uriel reports serving on the medical advisory board of LiveMetric, Leviticus Cardio, and Revamp Medical as well as institutional grant support from Abbott, Abiomed, and FIRE1 and meeting support from Abbott. Dr. Colombo reports personal fees from Roche and Abbott. All other authors have nothing to disclose.
Figures
References
-
- Khush KK, Hsich E, Potena L, et al. The International Thoracic Organ Transplant Registry of the International Society for Heart and Lung Transplantation: thirty-eighth adult heart transplantation report - 2021; focus on recipient characteristics. J Heart Lung Transplant. 2021;40(10):1035–1049. - PMC - PubMed
-
- Kobashigawa J, Zuckermann A, Macdonald P, et al. Report from a consensus conference on primary graft dysfunction after cardiac transplantation. J Heart Lung Transplant. 2014;33(4):327–340. - PubMed
-
- Buchan TA, Moayedi Y, Truby LK, et al. Incidence and impact of primary graft dysfunction in adult heart transplant recipients: a systematic review and meta-analysis. J Heart Lung Transplant. 2021;40(7):642–651. - PubMed
-
- Delvaeye M, Conway EM. Coagulation and innate immune responses: can we view them separately. Blood. 2009;114(12):2367–2374. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
