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一名患有丙酸血症且由左心室辅助装置(LVAD)支持的患者接受心脏和肝脏联合移植。

Combined heart and liver transplantation in a patient supported by left ventricular assist device (LVAD) with propionic acidemia.

作者信息

Lotan Dor, DeFilippis Ersilia M, Oren Daniel, Vinogradsky Alice, Rubinstein Gal, Mathur Abhishek, Takeda Koji, Hua May, Gaglio Paul J, Szabolcs Matthias J, Sayer Gabriel, Uriel Nir, Iglesias Alejandro Daniel, Latif Farhana

机构信息

Division of Cardiology, Columbia University Irving Medical Center/New York-Presbyterian Hospital New York, NY, USA.

Division of Cardiology, Columbia University Irving Medical Center/New York-Presbyterian Hospital New York, NY, USA.

出版信息

Nutr Metab Cardiovasc Dis. 2023 Mar;33(3):667-670. doi: 10.1016/j.numecd.2022.12.022. Epub 2023 Jan 3.

Abstract

Propionic acidemia (PA) is a rare inherited metabolic disease due to inborn errors of metabolism. PA results in the accumulation of abnormal organic acid metabolites in multiple systems, mainly the central nervous system and the heart. Cardiac complications include dilated cardiomyopathy (DCM) and carry a 40-50% increased mortality risk. Liver transplantation (LT) is required in PA patients when medical treatment fails and may prevent or slow down the cardiomyopathy progression. However, severe heart disease may be a serious contraindication to LT. We present a complicated case of a PA patient, supported with a Left Ventricular Assist Device, who underwent a heart and Liver transplant. PA patients are at increased risk for metabolic acidosis during surgery, with increased anion gap and hyperammonemia. A strict multi-disciplinary approach is needed to prevent and treat metabolic decompensation. The patient had a successful heart and liver transplant after a strict treatment protocol in the pre, intra, and post-operative periods. His case highlights the complexity of PA patients and the increased risk for metabolic decompensation during surgery and provides an insight into how to manage such complicated patients.

摘要

丙酸血症(PA)是一种由于先天性代谢缺陷引起的罕见遗传性代谢疾病。PA导致多种系统中异常有机酸代谢产物的积累,主要是中枢神经系统和心脏。心脏并发症包括扩张型心肌病(DCM),死亡风险增加40%-50%。当药物治疗无效时,PA患者需要进行肝移植(LT),这可能会预防或减缓心肌病的进展。然而,严重的心脏病可能是LT的严重禁忌症。我们报告了一例复杂的PA患者,该患者在左心室辅助装置的支持下接受了心脏和肝脏移植。PA患者在手术期间发生代谢性酸中毒的风险增加,伴有阴离子间隙增加和高氨血症。需要采取严格的多学科方法来预防和治疗代谢失代偿。该患者在术前、术中和术后严格遵循治疗方案,成功进行了心脏和肝脏移植。他的病例突出了PA患者的复杂性以及手术期间代谢失代偿风险的增加,并为如何管理此类复杂患者提供了见解。

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