Maria V A, Victorino R M
Faculty of Medicine of Lisbon, Department of Medicine 2, Clinical Immunology, Portugal.
Hepatology. 1997 Sep;26(3):664-9. doi: 10.1002/hep.510260319.
The objective of this study is to present and validate a clinical scale for the diagnosis of drug-induced liver injury (DILI). Five components were selected to be included in the scale: temporal relationship between drug intake and the onset of clinical picture, exclusion of alternative causes, extrahepatic manifestations, rechallenge or accidental re-exposure, and previous report in medical literature. The relative importance of each component was weighed, and arbitrary scores were attributed. The probability of the diagnosis of DILI was expressed as a final score, which could vary from -6 to 20. Content validity, criterion validity, construct validity, and inter-rater reliability were studied. To analyze validity and reliability, a random sample of 50 cases of suspected DILI was drawn from a series of 120 cases reported to our unit. The classification of the 50 cases by three experts in DILI was used as the external standard in the study of criterion validity. Agreement between the scale and the standard, and agreement between two independent raters (inter-rater reliability) was analyzed by weighted kappa coefficient. There was agreement between the scale and the standard in 42 cases (84%) with a weighted kappa coefficient of 0.90. A good discriminatory capacity of the scale was found when construct validity was studied. Agreement between raters was observed in 86% of the cases, corresponding to the weighted kappa of 0.93. In conclusion, the clinical scale was shown to have a high-level of validity and inter-rater reliability as well as a good discriminatory capacity between different levels of probability. These data suggest that the scale is suitable for use in clinical practice and may contribute to overcome the difficulties in the process of causality assessment in DILI.
本研究的目的是提出并验证一种用于诊断药物性肝损伤(DILI)的临床量表。该量表选取了五个组成部分:药物摄入与临床表现发作之间的时间关系、排除其他病因、肝外表现、再激发或意外再次接触以及医学文献中的既往报道。对每个组成部分的相对重要性进行了权衡,并赋予了任意分数。DILI诊断的概率以最终得分表示,范围从-6到20。研究了内容效度、标准效度、结构效度和评分者间信度。为分析效度和信度,从向本单位报告的120例疑似DILI病例中随机抽取50例作为样本。在标准效度研究中,将50例病例由三位DILI专家进行的分类用作外部标准。通过加权kappa系数分析量表与标准之间的一致性以及两位独立评分者之间的一致性(评分者间信度)。量表与标准在42例病例(84%)中达成一致,加权kappa系数为0.90。在研究结构效度时发现该量表具有良好的区分能力。86%的病例观察到评分者之间达成一致,对应加权kappa为0.93。总之,该临床量表显示出高水平的效度、评分者间信度以及在不同概率水平之间的良好区分能力。这些数据表明该量表适用于临床实践,并可能有助于克服DILI因果关系评估过程中的困难。