Investigation of Bleeding Disorders: When and How Should We Test Platelet Functions?

IF 2.7 4区 医学 Q2 HEMATOLOGY
Paolo Gresele, Emanuela Falcinelli, Loredana Bury
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引用次数: 0

Abstract

Inherited platelet disorders (IPDs) are rare conditions with diverse underlying pathophysiology which should be suspected in patients presenting with mucocutaneous bleeding or hemorrhages upon hemostatic challenges, in the presence or not of thrombocytopenia. Identifying IPDs is critical for providing appropriate care, preventing misdiagnosis, and avoiding unnecessary interventions, such as splenectomy. Syndromic IPDs, which may be associated with severe complications like kidney failure, infection, and malignancies, underscore the importance of accurate diagnosis and tailored management.Diagnosing IPDs remains challenging, requiring a comprehensive approach that integrates clinical assessment, evaluation of the bleeding history using standardized tools, like the ISTH-BAT, and first-line laboratory tests, such as light transmission aggregometry and flow cytometry. Second-line and specialized tests, including transmission electron microscopy, genetic analysis, and biochemical studies, may provide further insight in complex cases. Technological advancements, including multicolor flow cytometry and microfluidic tools, may in perspective improve IPD diagnostics by providing high-throughput and precise laboratory assays. In particular, mass cytometry and multi-omics may contribute to unraveling IPD pathophysiology, identifying novel markers, and refining disease classification. The application of artificial intelligence shows potential for improving diagnostic accuracy through the automated analysis of platelet morphology and function, from flow cytometry and digital microscopy assays, and for improving the understanding of pathogenic mechanisms of IPD through the examination of big data.This review summarizes current IPD platelet function testing strategies, emphasizing the need for a structured, tiered approach and examining emerging technologies and AI applications that could revolutionize diagnostic workflows, leading to personalized care and to an expanded understanding of IPDs.

出血性疾病的调查:何时以及如何检测血小板功能?
遗传性血小板疾病(IPDs)是一种罕见的疾病,具有多种潜在的病理生理,在出现粘膜皮肤出血或止血困难出血的患者中,无论是否存在血小板减少症,都应怀疑其存在。确定ipd对于提供适当的护理、防止误诊和避免不必要的干预(如脾切除术)至关重要。综合征性ipd可能与肾功能衰竭、感染和恶性肿瘤等严重并发症相关,因此强调了准确诊断和量身定制治疗的重要性。诊断ipd仍然具有挑战性,需要一种综合的方法,包括临床评估,使用标准化工具(如ISTH-BAT)评估出血史,以及一线实验室测试(如光透射聚集术和流式细胞术)。二线和专门的测试,包括透射电子显微镜、遗传分析和生化研究,可以为复杂病例提供进一步的了解。技术的进步,包括多色流式细胞术和微流体工具,可能会通过提供高通量和精确的实验室分析来改善IPD的诊断。特别是,大量细胞术和多组学可能有助于揭示IPD的病理生理,识别新的标记物,并完善疾病分类。人工智能的应用显示出通过流式细胞术和数字显微镜分析自动分析血小板形态和功能来提高诊断准确性的潜力,并通过检查大数据来提高对IPD致病机制的理解。本综述总结了目前IPD血小板功能检测策略,强调需要一种结构化、分层的方法,并研究了新兴技术和人工智能应用,这些技术和人工智能应用可以彻底改变诊断工作流程,从而实现个性化护理并扩大对IPD的理解。
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
Hamostaseologie
Hamostaseologie HEMATOLOGY-
CiteScore
5.50
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Hämostaseologie is an interdisciplinary specialist journal on the complex topics of haemorrhages and thromboembolism and is aimed not only at haematologists, but also at a wide range of specialists from clinic and practice. The readership consequently includes both specialists for internal medicine as well as for surgical diseases.
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