Clinical course of arrhythmogenic right ventricular cardiomyopathy with end-stage heart failure and outcome after heart transplantation

被引:0
|
作者
Petruescu, Laura [1 ,3 ]
Lebreton, Guillaume [2 ,4 ]
Coutance, Guillaume [2 ,4 ]
Maupain, Carole [1 ]
Fressart, Veronique [5 ]
Badenco, Nicolas [1 ]
Waintraub, Xavier [1 ]
Duthoit, Guillaume [1 ]
Laredo, Mikael [1 ]
Himbert, Caroline [1 ]
Hidden-Lucet, Francoise [1 ]
Leprince, Pascal [2 ,4 ]
Varnous, Shaida [4 ]
Gandjbakhch, Estelle [1 ,2 ,6 ]
机构
[1] Ctr Hosp Univ Pitie Salpetriere, APHP, Dept Cardiol, Fdn ICAN, F-75013 Paris, France
[2] Sorbonne Univ, F-75013 Paris, France
[3] Univ Paris, Hop Hotel Dieu, AP HP, Diag & Therapeut Ctr, F-75004 Paris, France
[4] Ctr Hosp Univ Pitie Salpetriere, APHP, Dept Chirurg Cardiaque, F-75013 Paris, France
[5] Ctr Hosp Univ Pitie Salpetriere, APHP, Serv Biochim Metab, UF Cardiogenet & Myogenet Mol & Cellulaire, F-75013 Paris, France
[6] Grp Hosp Pitie Salpetriere Charles Foix, Inst Cardiol, 47-83 Blvd Hop, F-75013 Paris, France
关键词
Arrhythmogenic right ventricular; cardiomyopathy; Arrhythmogenic right ventricular dysplasia; ARVC; Heart transplantation; Heart failure; CARDIAC TRANSPLANTATION; RISK; DIAGNOSIS;
D O I
10.1016/j.acvd.2022.10.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Few data exist on the characteristics and outcomes of patients with arrhythmogenic right ventricular cardiomyopathy and advanced heart failure who undergo heart transplantation. Aim: To explore the pretransplant course and outcomes of patients with arrhythmogenic right ventricular cardiomyopathy after heart transplantation.Methods: This observational retrospective monocentric study included all consecutive patients with arrhythmogenic right ventricular cardiomyopathy who underwent heart transplantation during a 13-year period (2006-2019) at Pitie-Salpetriere University Hospital (Paris).Results: A total of 23 patients with arrhythmogenic right ventricular cardiomyopathy underwent heart transplantation between 2006 and 2019. The median time from diagnosis to heart transplantation was 9 years, and the median age at transplantation was 50 years. At diagnosis, half of the patients had left ven-tricular dysfunction, 59% had extensive T-wave inversion and 43% had a history of sustained ventricular tachycardia. Only five patients were involved in intensive sport activity. Indications for heart transplan-tation were end-stage biventricular dysfunction in 13 patients, end-stage right ventricular heart failure in seven and electrical storm in three. Only three patients had pulmonary hypertension, and half of the patients had atrial arrhythmias. The survival rate 1 year after heart transplantation was 74% (95% con-fidence interval 53-88%). Eight patients experienced primary graft dysfunction needing extracorporeal membrane oxygenation.Conclusions: Patients with arrhythmogenic right ventricular cardiomyopathy who eventually needed heart transplantation mostly exhibited extended disease with biventricular dysfunction at diagnosis. Intensive sport activity did not seem to be a major determinant. Advanced heart failure usually occurred late in the course of the disease. Primary graft dysfunction after heart transplantation was frequent, and should be anticipated. Additional data are needed to identify the optimal timing for heart trans-plantation and predictors of end-stage heart failure in patients with arrhythmogenic right ventricular cardiomyopathy.(c) 2022 Elsevier Masson SAS. All rights reserved.
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页码:9 / 17
页数:9
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