在三级医疗中心使用PYP扫描评估ATTR心脏淀粉样变性。

The British journal of cardiology Pub Date : 2022-05-31 eCollection Date: 2022-01-01 DOI:10.5837/bjc.2022.019
Joshua Dower, Danai Dima, Mumtu Lalla, Ayan R Patel, Raymond L Comenzo, Cindy Varga
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引用次数: 2

摘要

心脏转甲状腺蛋白淀粉样变性(ATTR)是一种常被误诊的疾病,可导致患者显著的发病率和死亡率。近年来,锝-99m焦磷酸盐闪烁成像(PYP)已成为一种标准的护理诊断工具,帮助临床医生识别这种疾病。随着ATTR心肌病的新疗法的出现,尽早确定有资格接受治疗的患者是至关重要的。在我们的机构,我们试图描述PYP扫描的频率,以及它如何影响怀疑患有淀粉样蛋白心肌病的患者的管理。在2017年1月1日至2020年12月31日期间,我们确定了273名在塔夫茨医疗中心(一家三级医疗中心)完成PYP扫描以评估心脏淀粉样变性的患者。我们回顾了所有研究对象的相关临床资料。当心脏与对侧肺的比值大于或等于1.5,视觉分级为2或3,并通过单光子发射计算机断层扫描(SPECT)成像证实时,PYP扫描被认为是阳性的。总共有55例阳性,202例阴性,16例模棱两可的PYP扫描。在PYP结果后很少进行心内膜活检。在接受活检的7例PYP扫描阳性患者中,5例ATTR淀粉样蛋白阳性;在活检阴性的扫描患者中,无一例为ATTR淀粉样变性阳性,2例为淀粉样蛋白轻链(AL)淀粉样变性阳性。采用Mann-Whitney U统计分析发现,PYP阳性组的生物标志物肌钙蛋白I、b型自然肽(BNP)和n端原BNP (NT-proBNP)以及超声心动图上的室间隔舒张末期厚度(IVSd)均高于PYP阴性组。总的来说,55例PYP扫描阳性的患者中有27例接受了针对心脏淀粉样蛋白的特异性治疗。总之,本研究加强了PYP扫描在心脏淀粉样变性诊断和治疗中的临床意义。阳性的扫描结果允许医生实施早期淀粉样蛋白定向治疗,而阴性的扫描结果鼓励医生寻求替代诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The use of PYP scan for evaluation of ATTR cardiac amyloidosis at a tertiary medical centre.

Cardiac transthyretin amyloidosis (ATTR) is an often underdiagnosed disease that can lead to significant morbidity and mortality for patients. In recent years, technetium-99m pyrophosphate scintigraphy (PYP) imaging has become a standard of care diagnostic tool to help clinicians identify this disease. With newly emerging therapies for ATTR cardiomyopathy, it is critical to identify patients who are eligible for therapy as early as possible. At our institution, we sought to describe the frequency of PYP scanning and how it has impacted the management of a patient suspected to have amyloid cardiomyopathy. Between 1 January 2017 and 31 December 2020, we identified 273 patients who completed PYP scanning for evaluation of cardiac amyloidosis at Tufts Medical Center, a tertiary care centre. We reviewed pertinent clinical data for all study subjects. A PYP scan was considered positive when the heart to contralateral lung ratio was greater than or equal to 1.5, with a visual grade of 2 or 3, and confirmation with single-photon emission computerised tomography (SPECT) imaging. In total there were 55 positive, 202 negative, and 16 equivocal PYP scans. Endomyocardial biopsies were rarely performed following PYP results. Of the seven patients with a positive PYP scan who underwent biopsy, five were positive for ATTR amyloid; of the patients with a negative scan who were biopsied, none were positive for ATTR amyloidosis and two were positive for amyloid light-chain (AL) amyloidosis. The biomarkers troponin I, B-type naturietic peptide (BNP), and N-terminal pro-BNP (NT-proBNP), as well as the interventricular septal end-diastolic thickness (IVSd) seen on echocardiogram, were all found to be statistically higher in the PYP positive cohort than in the PYP negative cohort using Mann-Whitney U statistical analysis. In total, 27 out of the 55 patients with a positive PYP scan underwent therapy specific for cardiac amyloid. In conclusion, this study reinforces the clinical significance of the PYP scan in the diagnosis and management of cardiac amyloidosis. A positive scan allowed physicians to implement early amyloid-directed treatment while a negative scan encouraged physicians to pursue an alternative diagnosis.

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