Should Advanced Friedreich's Ataxia Be a Contraindication for Heart Transplantation? A Case Report of a Successful Procedure in a 58-Year-Old Patient.
Friedreich’s ataxia
ethics
heart transplantation
neuromuscular disease
prognosis
Journal
Journal of cardiovascular development and disease
ISSN: 2308-3425
Titre abrégé: J Cardiovasc Dev Dis
Pays: Switzerland
ID NLM: 101651414
Informations de publication
Date de publication:
09 Mar 2022
09 Mar 2022
Historique:
received:
10
02
2022
revised:
03
03
2022
accepted:
07
03
2022
entrez:
24
3
2022
pubmed:
25
3
2022
medline:
25
3
2022
Statut:
epublish
Résumé
The information on heart transplantation (HT) in patients with Friedreich's Ataxia (FA) is scarce, and the few published case reports are limited to young patients with mild neurological manifestations. We present the case of a 58-year-old patient with advanced FA (Scale for the Assessment and Rating of Ataxia [SARA] score 30/40), wheelchair-bound for the last 16 years and had urinary incontinence, dysarthria, and neurosensorial deafness. The patient was admitted for a refractory arrhythmic storm and had previous hypertrophic cardiomyopathy that evolved to dilated cardiomyopathy with severely reduced left ventricular ejection fraction and recurrent ventricular arrhythmias. A multidisciplinary team discussed the HT option. The patient was aware of the risks and benefits and considered worthy of the intervention, so he was listed for HT. After a successful surgical intervention, the patient had a long postoperative stay in ICU. He required a high dose of vasopressors, underwent hemofiltration for one month, suffered critical illness myopathy, had several respiratory infections and delayed tracheal extubation. Two and a half months after HT and almost five months at the hospital, the patient was successfully discharged. FA patients with severe heart conditions should be carefully evaluated by a multidisciplinary team to decide the candidacy for HT.
Identifiants
pubmed: 35323628
pii: jcdd9030080
doi: 10.3390/jcdd9030080
pmc: PMC8952784
pii:
doi:
Types de publication
Case Reports
Langues
eng
Références
Arch Dis Child. 2001 Feb;84(2):167-8
pubmed: 11159298
Neurology. 2006 Jun 13;66(11):1717-20
pubmed: 16769946
Lancet Neurol. 2015 Feb;14(2):174-82
pubmed: 25566998
JAMA Neurol. 2015 Nov;72(11):1334-41
pubmed: 26414159
Ir J Med Sci. 2011 Dec;180(4):799-805
pubmed: 21822977
J Neurol Sci. 2017 Apr 15;375:471-473
pubmed: 28109580
J Child Neurol. 2012 Sep;27(9):1193-6
pubmed: 22752490
Lancet Neurol. 2021 May;20(5):362-372
pubmed: 33770527
Nat Med. 2014 May;20(5):542-7
pubmed: 24705334
J Heart Lung Transplant. 2001 Feb;20(2):169
pubmed: 11250265
J Heart Lung Transplant. 2004 Nov;23(11):1304-6
pubmed: 15539131
J Neurochem. 2013 Aug;126 Suppl 1:103-17
pubmed: 23859346
Br Med Bull. 2017 Dec 01;124(1):19-30
pubmed: 29053830
Qual Life Res. 2020 Feb;29(2):413-420
pubmed: 31564022
J Neurol Sci. 2011 Aug 15;307(1-2):46-9
pubmed: 21652007
J Heart Lung Transplant. 2016 Sep;35(9):1144-5
pubmed: 27469014