Carrier Marc, Wells Philip S, Rodger Marc A
Department of Medicine, University of Ottawa, ON, Canada.
Thromb Res. 2006;117(4):469-74. doi: 10.1016/j.thromres.2005.04.005.
Less than 35% of patients suspected of having pulmonary embolism (PE) actually have PE. Safe bedside methods to exclude PE could save scarce health care resources if they exclude large proportions of patients with suspected PE and are widely applicable. Non-Elisa D-dimer in combination with pre-test probability of suspected PE can safely exclude PE at the bedside. Pre-test probability can be assigned by gestalt or by using clinical models (Wells, Wicki, Rodger).
We combined two databases from studies of patients with suspected PE and retrospectively compared the diagnostic test characteristics of the different methods of assigning pre-test probability.
535 patients were studied. PE was confirmed in 20.8% of study patients. Two clinical predictive models (Rodger and Wells) and overall diagnostic impression have similar sensitivities ranging from 96% (95% confidence interval (CI) 89-99%) to 99% (93-100%). Wicki's model has a sensitivity of 89% (77-96%). The Wells' model with a cutoff of less than 2 points in association with semi-quantitative D-dimer has a specificity of 11% (CI 7-15%). The specificities for the other clinical predictive model are ranging from 21% (17-25%) to 49% (CI 42-55%).
Semi-quantitative D-dimer must be combined with safe clinical probability assessment to safely exclude PE in a significant proportion of patients. Wicki's model in association with semi-quantitative D-dimer has the lowest sensitivity and should be used carefully to exclude PE at the bedside. The Wells' model with a cutoff of less than 2 points when combined with semi-quantitative D-dimer excluded very few patients and therefore limits its clinical utility.
疑似肺栓塞(PE)的患者中实际患有PE的比例不到35%。如果能排除大部分疑似PE患者且广泛适用,那么安全的床旁检查方法可节省稀缺的医疗资源。非酶联免疫吸附测定D-二聚体结合疑似PE的预检概率可在床旁安全排除PE。预检概率可通过整体判断或使用临床模型(Wells、Wicki、Rodger)来确定。
我们合并了两项关于疑似PE患者研究的数据库,并回顾性比较了不同预检概率确定方法的诊断测试特征。
共研究了535例患者。20.8%的研究患者确诊为PE。两种临床预测模型(Rodger和Wells)以及总体诊断印象的敏感性相似,范围从96%(95%置信区间(CI)89 - 99%)到99%(93 - 100%)。Wicki模型的敏感性为89%(77 - 96%)。截断值小于2分的Wells模型与半定量D-二聚体联合使用时,特异性为11%(CI 7 - 15%)。其他临床预测模型的特异性范围为21%(17 - 25%)至49%(CI 42 - 55%)。
半定量D-二聚体必须与安全的临床概率评估相结合,才能在相当一部分患者中安全排除PE。Wicki模型与半定量D-二聚体联合使用时敏感性最低,在床旁排除PE时应谨慎使用。截断值小于2分的Wells模型与半定量D-二聚体联合使用时排除的患者极少,因此其临床实用性有限。