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应用决策规则和 D-二聚体检测对肺栓塞的诊断。

Application of a decision rule and a D-dimer assay in the diagnosis of pulmonary embolism.

机构信息

Department of Vascular Medicine, Academical Medical Center, Amsterdam, The Netherlands.

出版信息

Thromb Haemost. 2010 Apr;103(4):849-54. doi: 10.1160/TH08-09-0564. Epub 2010 Feb 19.

DOI:10.1160/TH08-09-0564
PMID:20174752
Abstract

Current strategies for diagnosing pulmonary embolism (PE) include a clinical decision rule (CDR), followed by a D-dimer assay in patients with an unlikely clinical probability. We assessed the implementation of the current guidelines for the diagnosis of PE. A first questionnaire was sent to internists and pulmonologists to assess the proportion of physicians that adequately applied the guidelines. Two versions of a second questionnaire were sent presenting five hypothetical cases of which in two cases with an intermediate clinical probability an abnormal D-dimer test result was added to one version. We assessed the variation of the CDR and compared the proportions of a likely clinical probability between the two versions. A total of 65 physicians responded to the first questionnaire (response rate 75%). Half of the physicians (N=29; 46%) indicated that they use a CDR in all patients and 22 physicians (45%) indicated that they review the D-dimer result after they examined patients. Sixty-two physicians responded on the second questionnaire (response rate 36%). A shift was observed from an unlikely to a likely probability when an abnormal D-dimer test result was added to the clinical information (22% to 41%; p=0.22 and 26% to 50%; p<0.05). Our findings indicate that physicians do not use the guidelines for diagnosis of PE consistently. Furthermore, the knowledge of an abnormal D-dimer test result before seeing the patient leads to a higher CDR score. Physicians should therefore first examine patients before taking note of the D-dimer test result.

摘要

目前,诊断肺栓塞(PE)的策略包括临床决策规则(CDR),然后对临床可能性较低的患者进行 D-二聚体检测。我们评估了当前用于诊断 PE 的指南的实施情况。首先向内科医生和肺科医生发送了一份调查问卷,以评估充分应用指南的医生比例。随后发送了两种版本的第二个调查问卷,提出了五个假设病例,其中两个病例的临床可能性中等,在一个版本中增加了异常 D-二聚体检测结果。我们评估了 CDR 的变化,并比较了两种版本之间可能的临床概率比例。共有 65 名医生对第一个调查问卷做出了回应(回应率为 75%)。一半的医生(N=29;46%)表示他们在所有患者中使用 CDR,22 名医生(45%)表示他们在检查患者后会查看 D-二聚体结果。62 名医生对第二个调查问卷做出了回应(回应率为 36%)。当将异常 D-二聚体检测结果添加到临床信息中时,从不太可能到更有可能的概率发生了转变(22%至 41%;p=0.22 和 26%至 50%;p<0.05)。我们的研究结果表明,医生并没有一致地使用指南来诊断 PE。此外,在见到患者之前了解异常 D-二聚体检测结果会导致更高的 CDR 评分。因此,医生在记录 D-二聚体检测结果之前,应首先检查患者。

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