Literature DB >> 30049365

Invasive Hemodynamics and Rejection Rates in Patients With Cardiac Sarcoidosis After Heart Transplantation.

David G Rosenthal1, Molly E Anderson2, Bradley J Petek3, Daniel M Arnett4, Paco E Bravo5, Ganesh Raghu6, Zachary D Goldberger4, Kristen K Patton4, Richard K Cheng4.   

Abstract

BACKGROUND: Orthotopic heart transplant (OHT) is increasingly used for end-stage heart failure due to cardiac sarcoidosis (CS). However, concern regarding long-term outcomes in patients with CS after OHT persists because of multiorgan involvement.
METHODS: Baseline demographics and invasive hemodynamics were measured in 12 patients with CS and 28 patients with nonischemic cardiomyopathy requiring OHT at the time of transplantation, 1 week after OHT, and in routine follow-up. Primary endpoints included changes in pulmonary artery pressure, right ventricular stroke work index, and pulmonary compliance. Secondary endpoints included degree of allograft rejection and death.
RESULTS: During a mean follow-up of 73.8 months, no differences in pulmonary artery pressures, right ventricular stroke work index, or cardiac index were observed in patient with CS (n = 12) compared with those without CS (n = 28) between 1 week after OHT and the most recent follow-up. Long-term follow-up showed that pulmonary hemodynamics remained normal in the CS group. International Society for Heart and Lung Transplantation (ISHLT) 1990 grade ≥ 1a rejection occurred less frequently in the CS group (17% vs 68%, P = 0.006), and 0 of 12 patients in the CS group experienced histologic or clinical recurrence of sarcoidosis or ≥2 rejection. Patients with CS had excellent survival after OHT, with 0 deaths or significant rejection.
CONCLUSIONS: Patients with CS have similar post-transplant hemodynamics as patients without CS, without evidence of right ventricular dysfunction or pulmonary hypertension. Neither significant rejection nor recurrence of sarcoid in the allograft was observed in this cohort of patients with CS. Survival is similar between patients with CS and those without CS. Heart transplant is a viable strategy in selected patients with CS with excellent outcomes.
Copyright © 2018 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 30049365     DOI: 10.1016/j.cjca.2018.03.021

Source DB:  PubMed          Journal:  Can J Cardiol        ISSN: 0828-282X            Impact factor:   5.223


  3 in total

1.  Recurrent cardiac sarcoidosis after heart transplantation.

Authors:  Giacomo Veronese; Manlio Cipriani; Duccio Petrella; Stefano Geniere Nigra; Patrizia Pedrotti; Andrea Garascia; Gabriella Masciocco; Manuela A Bramerio; Karin Klingel; Maria Frigerio; Enrico Ammirati
Journal:  Clin Res Cardiol       Date:  2019-05-09       Impact factor: 5.460

2.  Short- and long-term outcomes after heart transplantation in cardiac sarcoidosis and giant-cell myocarditis: a systematic review and meta-analysis.

Authors:  Emanuele Bobbio; Marie Björkenstam; Bright I Nwaru; Francesco Giallauria; Eva Hessman; Niklas Bergh; Christian L Polte; Jukka Lehtonen; Kristjan Karason; Entela Bollano
Journal:  Clin Res Cardiol       Date:  2021-08-17       Impact factor: 5.460

3.  Outcomes after heart transplantation in patients with cardiac sarcoidosis.

Authors:  Rabea Asleh; Alexandros Briasoulis; Ilias Doulamis; Hilmi Alnsasra; Aspasia Tzani; Paulino Alvarez; Toshiki Kuno; Polydoros Kampaktsis; Sudhir Kushwaha
Journal:  ESC Heart Fail       Date:  2022-01-15
  3 in total

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