Stein Paul D, Hull Russell D, Patel Kalpesh C, Olson Ronald E, Ghali William A, Brant Rollin, Biel Rita K, Bharadia Vinay, Kalra Neeraj K
Saint Joseph Mercy-Oakland, Pontiac, Michigan 48341, USA.
Ann Intern Med. 2004 Apr 20;140(8):589-602. doi: 10.7326/0003-4819-140-8-200404200-00005.
Despite extensive literature, the diagnostic role of d-dimer for deep venous thrombosis (DVT) or pulmonary embolism (PE) remains unclear, reflecting multiple d-dimer assays and concerns about differing sensitivities and variability.
To systematically review trials that assessed sensitivity, specificity, likelihood ratios, and variability among d-dimer assays.
Studies in all languages were identified by searching PubMed from 1983 to January 2003 and EMBASE from 1988 to January 2003.
The researchers selected prospective studies that compared d-dimer with a reference standard. Studies of high methodologic quality were included in the primary analyses; sensitivity analysis included additional weaker studies.
Two authors collected data on study-level factors: d-dimer assay used, cutoff value, and whether patients had suspected DVT or PE.
For DVT, the enzyme-linked immunosorbent assay (ELISA) and quantitative rapid ELISA dominate the rank order for these values: sensitivity, 0.96 (95% confidence limit [CL], 0.91 to 1.00), and negative likelihood ratio, 0.12 (CL, 0.04 to 0.33); and sensitivity, 0.96 (CL, 0.90 to 1.00), and negative likelihood ratio, 0.09 (CL, 0.02 to 0.41), respectively. For PE, the ELISA and quantitative rapid ELISA also dominate the rank order for these values: sensitivity, 0.95 (CL, 0.85 to 1.00), and negative likelihood ratio, 0.13 (CL, 0.03 to 0.58); and sensitivity, 0.95 (CL, 0.83 to 1.00), and negative likelihood ratio, 0.13 (CL, 0.02 to 0.84), respectively. The ELISA and quantitative rapid ELISA have negative likelihood ratios that yield a high certainty for excluding DVT or PE. The positive likelihood values, which are in the general range of 1.5 to 2.5, do not greatly increase the certainty of diagnosis. Sensitivity analyses do not affect these findings.
Although many studies evaluated multiple d-dimer assays, findings are based largely on indirect comparisons of test performance characteristics across studies.
The ELISAs in general dominate the comparative ranking among the d-dimer assays for sensitivity and negative likelihood ratio. For excluding PE or DVT, a negative result on quantitative rapid ELISA is as diagnostically useful as a normal lung scan or negative duplex ultrasonography finding.
尽管有大量文献,但D-二聚体对深静脉血栓形成(DVT)或肺栓塞(PE)的诊断作用仍不明确,这反映出有多种D-二聚体检测方法,且人们担心其敏感性和变异性存在差异。
系统评价评估D-二聚体检测方法的敏感性、特异性、似然比和变异性的试验。
通过检索1983年至2003年1月的PubMed以及1988年至2003年1月的EMBASE来识别所有语言的研究。
研究人员选择了将D-二聚体与参考标准进行比较的前瞻性研究。主要分析纳入了方法学质量高的研究;敏感性分析纳入了其他质量稍差的研究。
两位作者收集了关于研究水平因素的数据:使用的D-二聚体检测方法、临界值以及患者是否疑似患有DVT或PE。
对于DVT,酶联免疫吸附测定(ELISA)和定量快速ELISA在这些值的排序中占主导地位:敏感性为0.96(95%置信区间[CL],0.91至1.00),阴性似然比为0.12(CL,0.04至0.33);以及敏感性为0.96(CL,0.90至1.00),阴性似然比为0.09(CL,0.02至0.41)。对于PE,ELISA和定量快速ELISA在这些值的排序中也占主导地位:敏感性为0.95(CL,0.85至1.00),阴性似然比为0.13(CL,0.03至0.58);以及敏感性为0.95(CL,0.83至1.00),阴性似然比为0.13(CL,0.02至0.84)。ELISA和定量快速ELISA的阴性似然比在排除DVT或PE方面具有很高的确定性。阳性似然值一般在1.5至2.5范围内,对诊断确定性的提高不大。敏感性分析不影响这些结果。
尽管许多研究评估了多种D-二聚体检测方法,但研究结果很大程度上基于不同研究间检测性能特征的间接比较。
一般来说,ELISA在D-二聚体检测方法的敏感性和阴性似然比的比较排名中占主导地位。对于排除PE或DVT,定量快速ELISA的阴性结果在诊断上与正常肺部扫描或双功超声检查阴性结果同样有用。