如何调查轻中度出血性疾病和原因不明的出血性疾病。

IF 2.2 4区 医学 Q3 HEMATOLOGY
Alessandro Casini, Johanna Gebhart
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引用次数: 0

摘要

出血倾向是血液科医生最常见的主诉之一。将临床症状不明显的出血与需要止血评估和医疗干预的出血表型区分开来具有挑战性。全面回顾个人和家族病史、使用出血评估工具客观评估出血严重程度以及进行重点体格检查对于正确识别轻度至中度出血性疾病(MBD)疑似患者至关重要。所有因出血倾向转诊的患者都应进行基本的实验室检查。如果发现止血异常,如冯-威廉氏病、血小板功能紊乱或凝血因子缺乏,则应进行更广泛的检查以进一步确定出血性疾病的特征。相反,如果所有结果都正常,则认为患者患有原因不明的出血性疾病(BDUC)。对于原因不明的出血性疾病患者,进一步的评估可能包括非常规检查,以寻找常规止血检查未发现的罕见出血性疾病,如血栓调节蛋白相关性凝血病、组织因子通路抑制剂相关性出血性疾病、高纤溶性出血性疾病或组织因子生成障碍。在这篇综述中,我们总结了 MBD 的逐步诊断程序,并对 BDUC 的生物学特征提出了一些见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

How to investigate mild to moderate bleeding disorders and bleeding disorder of unknown cause

How to investigate mild to moderate bleeding disorders and bleeding disorder of unknown cause

A bleeding tendency is one of the most common complaints observed by hematologists. It is challenging to differentiate a clinically insignificant bleeding from a bleeding phenotype that requires hemostatic evaluation and medical intervention. A thorough review of personal and familial history, objective assessment of bleeding severity using a bleeding assessment tool, and a focused physical examination are critical to correctly identifying suspected patients with mild to moderate bleeding disorders (MBDs). A basic laboratory work-up should be performed in all patients referred for a bleeding tendency. If a hemostatic abnormality is found such as evidence of von Willebrand disease, a platelet function disorder, or a coagulation factor deficiency, more extensive testing should be performed to further characterize the bleeding disorder. Conversely, if all results are normal the patient is considered to have bleeding disorder of unknown cause (BDUC). For patients with BDUC, further evaluation may include non-routine testing to look for rare bleeding disorders not detected by routine hemostasis tests, such as thrombomodulin-associated coagulopathy, tissue factor pathway inhibitor-related bleeding disorder, hyperfibrinolytic-bleeding disorders or impaired tissue factor production. In this review, we summarize the stepwise diagnostic procedure in MBDs and provide some insights into the biological features of BDUC.

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来源期刊
CiteScore
4.50
自引率
6.70%
发文量
211
审稿时长
6-12 weeks
期刊介绍: The International Journal of Laboratory Hematology provides a forum for the communication of new developments, research topics and the practice of laboratory haematology. The journal publishes invited reviews, full length original articles, and correspondence. The International Journal of Laboratory Hematology is the official journal of the International Society for Laboratory Hematology, which addresses the following sub-disciplines: cellular analysis, flow cytometry, haemostasis and thrombosis, molecular diagnostics, haematology informatics, haemoglobinopathies, point of care testing, standards and guidelines. The journal was launched in 2006 as the successor to Clinical and Laboratory Hematology, which was first published in 1979. An active and positive editorial policy ensures that work of a high scientific standard is reported, in order to bridge the gap between practical and academic aspects of laboratory haematology.
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