Clinical Division of Hematology and Hemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Institute of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Hamostaseologie. 2024 Oct;44(5):358-367. doi: 10.1055/a-2330-9112. Epub 2024 Jul 1.
Bleeding disorder of unknown cause (BDUC) is a diagnosis of exclusion after exhaustive evaluation of plasmatic coagulation and platelet function. This review explores the utility of global hemostatic assays as confirmatory tests and in elucidating the pathophysiology of BDUC. Unlike traditional hemostatic tests that focus on coagulation factors, global assays are conducted both in plasma and also whole blood. These assays provide a more comprehensive understanding of the cell-based model of coagulation, aid in the identification of plasmatic factor abnormalities that may reduce hemostatic capacity, and allow for the assessment of impaired platelet-endothelial interactions under shear stress, as well as hyperfibrinolytic states. While clinical tests such as skin bleeding time and global assays such as PFA-100 exhibit limited diagnostic capacity, the role of viscoelastic testing in identifying hemostatic dysfunction in patients with BDUC remains unclear. Thrombin generation assays have shown variable results in BDUC patients; some studies demonstrate differences compared with healthy controls or reference values, whereas others question its clinical utility. Fibrinolysis assessment in vitro remains challenging, with studies employing euglobulin clot lysis time, plasma clot lysis time, and fluorogenic plasmin generation yielding inconclusive or conflicting results. Notably, recent studies suggest that microfluidic analysis unveils shear-dependent platelet function defects in BDUC patients, undetected by conventional platelet function assays. Overall, global assays might be helpful for exploring underlying hemostatic impairments, when conventional hemostatic laboratory tests yield no results. However, due to limited data and/or discrepant results, further research is needed to evaluate the utility of global assays as screening tools.
不明原因出血性疾病(BDUC)是在详尽评估血浆凝血和血小板功能后排除其他原因的诊断。本综述探讨了全止血检测作为确认试验和阐明 BDUC 病理生理学的效用。与专注于凝血因子的传统止血检测不同,全止血检测在血浆和全血中进行。这些检测提供了对基于细胞的凝血模型的更全面了解,有助于识别可能降低止血能力的血浆因子异常,并允许评估在切变应力下受损的血小板-内皮相互作用以及高纤维蛋白溶解状态。虽然临床检测(如皮肤出血时间)和全止血检测(如 PFA-100)的诊断能力有限,但粘弹性检测在识别 BDUC 患者止血功能障碍方面的作用仍不清楚。凝血酶生成检测在 BDUC 患者中的结果存在差异;一些研究与健康对照组或参考值相比显示出差异,而其他研究则质疑其临床实用性。体外纤溶评估仍然具有挑战性,使用全血纤维蛋白溶解时间、血浆纤维蛋白溶解时间和荧光生成纤溶酶原检测的研究得出的结果不一致或相互矛盾。值得注意的是,最近的研究表明,微流控分析揭示了 BDUC 患者中剪切依赖性血小板功能缺陷,这在常规血小板功能检测中无法检测到。总体而言,当传统的止血实验室检测没有结果时,全止血检测可能有助于探索潜在的止血障碍。然而,由于数据有限和/或结果不一致,需要进一步研究来评估全止血检测作为筛选工具的效用。