2023 Expert Consensus of the Taiwan Society of Cardiology on the Diagnosis and Treatment of Cardiac Amyloidosis.

IF 1.8 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Chun-Chieh Wang, Wei-Ting Chang, Yen-Hung Lin, Bing-Hsiean Tzeng, Ting-Hsing Chao, Chung-Lieh Hung, Yen-Wen Wu, Cheng-Hsuan Tsai, Wei-Wen Lin, Kuan-Cheng Chang, Hung-Yu Chang, Wen-Chung Yu, Wen-Hwa Wang, Cheng-I Cheng, Tzung-Dau Wang, Charles Jia-Yin Hou, Wen-Jone Chen
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引用次数: 0

Abstract

Cardiac amyloidosis is one form of systemic amyloidosis caused by abnormal amyloid fibrils deposited in the extracellular space of the myocardium causing heart failure because of restrictive cardiomyopathy and conduction disturbances. The incidence and prevalence of cardiac amyloidosis are higher than previously noted, particularly among special populations. The most common forms of cardiac amyloidosis are light chain and transthyretin amyloid cardiomyopathy. Even though more than 70% of patients with systemic amyloidosis have cardiac amyloidosis, the diagnosis is often delayed, suggesting significant gaps in the knowledge of cardiac amyloidosis and a lack of multidisciplinary teamwork in our daily practice. The Taiwan Society of Cardiology Heart Failure Committee organized experts to draft the "Expert Consensus on the diagnosis and treatment of cardiac amyloidosis." This statement aims to help clinicians and healthcare professionals improve early diagnosis and management of cardiac amyloidosis in Taiwan. The expert panel met virtually to review the data and discuss the consensus statements. Our review provided practical information about diagnostic methods and algorithms, clinical clues and red-flag signs, cardiac amyloidosis per se and its comorbidities treatment modalities, and follow-up plans for asymptomatic transthyretin gene carriers. We especially innovate two acronyms, "HFpEF MUTED CALL" and "HFmrEF MUST COUNT", to help in the early diagnosis and screening of transthyretin amyloid cardiomyopathy as shown in the Central Illustration.

2023台湾心脏病学会《心脏淀粉样变性诊断与治疗专家共识》
心脏淀粉样变性是由异常淀粉样原纤维沉积在心肌细胞外间隙引起的系统性淀粉样变性的一种形式,由于限制性心肌病和传导障碍导致心力衰竭。心脏淀粉样变的发病率和流行率比以前注意到的要高,特别是在特殊人群中。心脏淀粉样变最常见的形式是轻链和转甲状腺素淀粉样心肌病。尽管超过70%的系统性淀粉样变性患者患有心脏淀粉样变性,但诊断往往被延迟,这表明我们对心脏淀粉样变性的认识存在重大差距,并且在日常实践中缺乏多学科合作。台湾心脏病学会心衰专业委员会组织专家起草《心脏淀粉样变性诊断与治疗专家共识》。本声明旨在帮助台湾临床医师和医疗保健专业人员改善心脏淀粉样变的早期诊断和管理。专家小组举行了虚拟会议,审查数据并讨论共识声明。我们的综述提供了关于无症状转甲状腺素基因携带者的诊断方法和算法、临床线索和危险信号、心脏淀粉样变本身及其合并症的治疗方式以及随访计划的实用信息。我们特别创新了两个首字母缩略词,“HFpEF沉默呼叫”和“HFmrEF必须计数”,以帮助早期诊断和筛查甲状腺素淀粉样心肌病,如图所示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Cardiologica Sinica
Acta Cardiologica Sinica 医学-心血管系统
CiteScore
2.90
自引率
15.80%
发文量
144
审稿时长
>12 weeks
期刊介绍: Acta Cardiologica Sinica welcomes all the papers in the fields related to cardiovascular medicine including basic research, vascular biology, clinical pharmacology, clinical trial, critical care medicine, coronary artery disease, interventional cardiology, arrythmia and electrophysiology, atherosclerosis, hypertension, cardiomyopathy and heart failure, valvular and structure cardiac disease, pediatric cardiology, cardiovascular surgery, and so on. We received papers from more than 20 countries and areas of the world. Currently, 40% of the papers were submitted to Acta Cardiologica Sinica from Taiwan, 20% from China, and 20% from the other countries and areas in the world. The acceptance rate for publication was around 50% in general.
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