影响淀粉样变性鉴定和转诊到专科中心准确性的因素。

IF 5.2 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Andrew Staron, Lisa M Mendelson, Tracy Joshi, Frederick L Ruberg, Vaishali Sanchorawala
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引用次数: 0

摘要

目的:淀粉样变性的诊断算法在过去的十年中不断发展,特别是结合了基于成像的技术来检测淀粉样心肌病。我们试图确定社区中淀粉样变性误诊的主要来源,这导致了三级中心的假阳性转诊。方法:我们对2010年至2021年所有转介到淀粉样变性中心的病例进行了回顾性分析,并在中心广泛评估后确定了最终裁决缺乏淀粉样病变的病例。检查假阳性转诊的因素。结果:2409例疑似淀粉样变的转诊患者中,147例(6%)没有淀粉样病变。这一比例从2010年的4%上升到2021年的13%。假阳性的推荐包括更多的有色人种。最常见的不准确来源是组织标本用刚果红染色错误,其次是心脏成像的暗示性发现。近年来,对99mtechnetium-焦磷酸盐闪烁成像的误解成为假阳性转诊的主要来源。结论:在淀粉样变的检查中认识到这些潜在的诊断错误来源可以改善患者的护理。转介到卓越的中心淀粉样变性有助于确认准确的诊断和避免虐待。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors affecting the accuracy of amyloidosis identification and referral to a specialty centre.

Objective: Diagnostic algorithms for amyloidosis have evolved over the past decade, particularly with the incorporation of imaging-based techniques to detect amyloid cardiomyopathy. We sought to identify the key sources of amyloidosis misidentification in the community, which lead to false positive referrals to a tertiary centre.

Methods: We conducted a retrospective review of all referrals to the Amyloidosis Centre from 2010 to 2021 and identified cases lacking amyloid pathology upon final adjudication after extensive assessment at the centre. Factors for false positive referrals were examined.

Results: Among 2409 referrals of suspected amyloidosis, 147 (6%) demonstrated an absence of amyloid pathology. This percentage increased over time from 4% in 2010 to 13% in 2021. False positive referrals consisted of more people of colour. The most frequent source of inaccuracy was the erroneous staining of tissue specimens with Congo red, followed by suggestive findings on cardiac imaging. In recent years, misinterpretation of 99mtechnetium- pyrophosphate scintigraphy emerged as a major source of false positive referrals.

Conclusion: Recognising these potential sources of diagnostic error in the workup of amyloidosis can improve patient care. Referral to a centre of excellence for amyloidosis helps confirm an accurate diagnosis and avoid mistreatment.

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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
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