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首页> 外文期刊>Journal of thrombosis and haemostasis: JTH >Diagnostic utility of light transmission platelet aggregometry: results from a prospective study of individuals referred for bleeding disorder assessments.
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Diagnostic utility of light transmission platelet aggregometry: results from a prospective study of individuals referred for bleeding disorder assessments.

机译:透光血小板凝集测定法的诊断实用性:对涉及出血性疾病评估的个体进行的前瞻性研究结果。

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摘要

BACKGROUND: Light transmission aggregometry (LTA) is commonly performed to assess individuals for bleeding disorders. OBJECTIVES: The goal was to evaluate the incidence and spectrum of platelet function abnormalities in a prospective cohort of individuals referred for bleeding disorder assessments after exclusion of thrombocytopenia and von Willebrand disease. PATIENTS/METHODS: Subjects were healthy controls and patients from a prospective cohort of individuals referred for bleeding disorder assessments after exclusion of thrombocytopenia and von Willebrand disease. LTA was performed by standardized methods using platelet-rich plasma adjusted to 250x10(9) platelets L(-1). Maximal aggregation data were analyzed to determine the likelihood of detecting a platelet function disorder by LTA, and the sensitivity and specificity of LTA for platelet disorders. RESULTS: The incidence of false positive LTA among subjects excluded of having bleeding disorders was similar to healthy controls. Abnormal LTA was morecommon in subjects with bleeding disorders and the likelihood of a bleeding disorder was significantly increased (odds ratio 32) when maximal aggregation was reduced with two or more agonists. Receiver operator curve analyses indicated that LTA had high specificity and moderate sensitivity for detecting inherited defects in platelet function and that the LTA agonists 1.25 microg mL(-1) collagen, 6 microM epinephrine, 1.6 mM arachidonic acid and 1.0 microM thromboxane analogue U44619 detected most inherited disorders with abnormal LTA. CONCLUSIONS: LTA is valuable for detecting platelet function abnormalities among individuals referred for bleeding problems, particularly when the test indicates abnormal responses to multiple agonists.
机译:背景:通常采用光透射聚集法(LTA)来评估个体的出血性疾病。目的:目的是评估排除血小板减少症和von Willebrand病后进行出血性疾病评估的预期人群的血小板功能异常的发生率和范围。患者/方法:受试者为健康对照组,是排除血小板减少症和von Willebrand病后接受出血性疾病评估的预期人群的患者。通过标准方法使用富含血小板的血浆将LTA调整为250x10(9)血小板L(-1)。分析最大聚集数据以确定通过LTA检测血小板功能障碍的可能性,以及LTA对血小板疾病的敏感性和特异性。结果:在排除出血性疾病的受试者中,假阳性LTA的发生率与健康对照组相似。在患有出血性疾病的受试者中,LTA异常更为常见,并且当使用两种或多种激动剂使最大聚集减少时,出血性疾病的可能性显着增加(优势比32)。接收者操作曲线分析表明,LTA对检测血小板功能的遗传缺陷具有高特异性和中等灵敏度,而LTA激动剂1.25 microg mL(-1)胶原蛋白,6 microM肾上腺素,1.6 mM花生四烯酸和1.0 microM血栓烷类似物U44619检测到最多LTA异常的遗传性疾病。结论:LTA对于在因出血问题而被转诊的个体中检测血小板功能异常非常有价值,特别是当测试表明对多种激动剂的反应异常时。

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