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亚洲背景下转甲状腺素蛋白淀粉样变性肝移植麻醉管理中的困境与挑战:一例报告

Dilemmas and Challenges in the Anesthetic Management of Liver Transplantation for Transthyretin Amyloidosis in the Asian Context: A Case Report.

作者信息

Yek Jacklyn, Chan Steffi, Tay Sook Muay, Tan Selene

机构信息

Division of Anaesthesiology and Perioperative Medicine, Singapore General Hospital, Singapore, SGP.

出版信息

Cureus. 2025 Apr 22;17(4):e82784. doi: 10.7759/cureus.82784. eCollection 2025 Apr.

Abstract

Transthyretin (TTR) amyloidosis is a progressive, debilitating, and eventually fatal disease that is under-recognized and underdiagnosed in Asian patients. Liver transplantation is performed in patients with hereditary transthyretin amyloidosis to remove the source of abnormal transthyretin production to slow disease progression. There is uncertainty about the risk-benefit ratio due to the less favourable five-year survival of liver transplantation for Asian patients with non-Val30Met transthyretin amyloidosis, as the heterogeneity of non-Val30Met mutations and the potential for disease progression despite transplantation can make transplant outcomes unpredictable. Additionally, limited access and the prohibitive costs of disease-modifying therapies may influence the decision-making process with regard to liver transplantation. We present a case of a 57-year-old male with Ala117Ser TTR amyloidosis and clinical manifestations of polyneuropathy, cardiac amyloidosis, and autonomic neuropathy. He received a living-related liver transplant. We describe the dilemmas and challenges in the anesthetic planning and management of this patient. Along with limited scientific data on liver transplantation for non-Val30Met TTR amyloidosis patients, we faced challenges in the management of intraoperative tachyarrhythmias, which eventually necessitated the use of a relatively contraindicated drug, verapamil, to achieve rate control. The lack of specific data meant that we had to base some decisions on practical wisdom.

摘要

转甲状腺素蛋白(TTR)淀粉样变性是一种进行性、使人衰弱并最终致命的疾病,在亚洲患者中未得到充分认识和诊断。对于遗传性转甲状腺素蛋白淀粉样变性患者,会进行肝移植以去除异常转甲状腺素蛋白产生的源头,从而减缓疾病进展。对于亚洲非Val30Met转甲状腺素蛋白淀粉样变性患者,肝移植的五年生存率较低,由于非Val30Met突变的异质性以及尽管进行了移植仍有疾病进展的可能性,使得移植结果难以预测,因此风险效益比存在不确定性。此外,疾病修饰疗法的可及性有限且成本高昂,可能会影响肝移植的决策过程。我们报告一例57岁男性患者,患有Ala117Ser TTR淀粉样变性,临床表现为多发性神经病、心脏淀粉样变性和自主神经病变。他接受了活体亲属肝移植。我们描述了该患者麻醉计划和管理中的困境与挑战。除了关于非Val30Met TTR淀粉样变性患者肝移植的科学数据有限外,我们在术中快速性心律失常的管理上面临挑战,最终不得不使用一种相对禁忌的药物维拉帕米来控制心率。缺乏具体数据意味着我们不得不基于实际经验做出一些决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/458c/12097723/5b3502be6814/cureus-0017-00000082784-i01.jpg

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