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缺血性脑卒中患者凝血功能障碍的诊断检测

Diagnostic testing for coagulopathies in patients with ischemic stroke.

作者信息

Bushnell C D, Goldstein L B

机构信息

Department of Medicine (Neurology), Duke Center for Cerebrovascular Disease, Center for Clinical Health Policy Research, Duke University, and Durham VA Medical Center, Durham, NC 27710, USA.

出版信息

Stroke. 2000 Dec;31(12):3067-78. doi: 10.1161/01.str.31.12.3067.

Abstract

BACKGROUND

Hypercoagulable states are a recognized, albeit uncommon, etiology of ischemic stroke. It is unclear how often the results of specialized coagulation tests affect management. Using data compiled from a systematic review of available studies, we employed quantitative methodology to assess the diagnostic yield of coagulation tests for identification of coagulopathies in ischemic stroke patients.

SUMMARY OF REVIEW

We performed a MEDLINE search to identify controlled studies published during 1966-1999 that reported the prevalence of deficiencies of protein C, protein S, antithrombin III, plasminogen, activated protein C resistance (APCR)/factor V Leiden mutation (FVL), anticardiolipin antibodies (ACL), or lupus anticoagulant (LA) in patients with ischemic stroke. The cumulative prevalence rates (pretest probabilities) and positive likelihood ratios for all studies and for those including only patients aged </=50 years were used to calculate posttest probabilities for each coagulopathy, reflecting diagnostic yield. The cumulative pretest probabilities of coagulation defects in ischemic stroke patients are as follows: LA, 3% (8% for those aged </=50 years); ACL, 17% (21% for those aged </=50 years); APCR/FVL, 7% (11% for those aged </=50 years); and prothrombin mutation, 4.5% (5.7% for those aged </=50 years). The posttest probabilities of ACL, LA, and APCR increased with increasing pretest probability, the specificity of the tests, and features of the patients' history and clinical presentation.

CONCLUSIONS

The pretest probabilities of coagulation defects in ischemic stroke patients are low. The diagnostic yield of coagulation tests may be increased by using tests with the highest specificities and by targeting patients with clinical or historical features that increase pretest probability. Consideration of these data might lead to more rational ordering of tests and an associated cost savings.

摘要

背景

高凝状态是缺血性卒中一种已被认识到的病因,尽管并不常见。目前尚不清楚专门的凝血检查结果对治疗管理的影响频率如何。我们利用从现有研究的系统评价中收集的数据,采用定量方法评估凝血检查在识别缺血性卒中患者凝血障碍方面的诊断收益。

综述总结

我们进行了一项MEDLINE检索,以识别1966年至1999年期间发表的对照研究,这些研究报告了缺血性卒中患者中蛋白C、蛋白S、抗凝血酶III、纤溶酶原、活化蛋白C抵抗(APCR)/因子V莱顿突变(FVL)、抗心磷脂抗体(ACL)或狼疮抗凝物(LA)缺乏的患病率。所有研究以及仅纳入年龄≤50岁患者的研究的累积患病率(验前概率)和阳性似然比,用于计算每种凝血障碍的验后概率,反映诊断收益。缺血性卒中患者凝血缺陷的累积验前概率如下:LA为3%(年龄≤50岁者为8%);ACL为17%(年龄≤50岁者为21%);APCR/FVL为7%(年龄≤50岁者为11%);凝血酶原突变率为4.5%(年龄≤50岁者为5.7%)。ACL、LA和APCR的验后概率随着验前概率、检查的特异性以及患者病史和临床表现特征的增加而升高。

结论

缺血性卒中患者凝血缺陷的验前概率较低。通过使用特异性最高的检查,并针对具有增加验前概率的临床或病史特征的患者,可以提高凝血检查的诊断收益。考虑这些数据可能会使检查的安排更加合理,并节省相关费用。

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