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Drug induced liver injury with analysis of alternative causes as confounding variables

机译:药物诱导肝损伤随着替代原因的分析为混杂的变量

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Aims Drug‐induced liver injury (DILI) is rare compared to the worldwide frequent acute or chronic liver diseases. Therefore, patients included in series of suspected DILI are at high risk of not having DILI, whereby alternative causes may confound the DILI diagnosis. The aim of this review is to evaluate published case series of DILI for alternative causes. Methods Relevant studies were identified using a computerized search of the Medline database for publications from 1993 through 30 October 2017. We used the following terms: drug hepatotoxicity, drug induced liver injury, hepatotoxic drugs combined with diagnosis, causality assessment and alternative causes. Results Alternative causes as variables confounding the DILI diagnosis emerged in 22 published DILI case series, ranging from 4 to 47%. Among 13?335 cases of suspected DILI, alternative causes were found to be more likely in 4555 patients (34.2%), suggesting that the suspected DILI was probably not DILI. Biliary diseases such as biliary obstruction, cholangitis, choledocholithiasis, primary biliary cholangitis and primary sclerosing cholangitis were among the most missed diagnoses. Alternative causes included hepatitis B, C and E, cytomegalovirus, Epstein–Barr virus, ischemic hepatitis, cardiac hepatopathy, autoimmune hepatitis, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, and alcoholic liver disease. Conclusions In more than one‐third of published global DILI case series, alternative causes as published in these reports confounded the DILI diagnosis. In the future, published DILI case series should include only patients with secured DILI diagnosis, preferentially established by prospective use of scored items provided by robust diagnostic algorithms such as the updated Roussel Uclaf causality assessment method.
机译:目的,与全球常见的急性或慢性肝病相比,药物诱导的肝损伤(Dili)是罕见的。因此,包括在一系列疑似帝力的患者的患者处于高风险,不具有帝力的风险,从而替代原因可能会混淆DILI诊断。本次审查的目的是评估发布的案例系列DILI以获得替代原因。方法采用1993年10月30日至30日至10月30日,使用电脑搜索相关研究的相关研究。我们使用以下条款:药物肝毒性,药物诱导的肝损伤,肝毒性药物联合诊断,因果关系评估和替代原因。结果替代原因随着变量混杂于22种出版的Diri案例系列中出现的Dili诊断,范围为4%至47%。在13岁?335例怀疑帝力病例中,发现替代原因在4555名患者中更有可能更容易出现(34.2%),这表明疑似的帝力可能不是Dili。胆道障碍如胆管梗阻,胆管炎,胆总管胆管,原代胆管炎和原发性硬化性胆管炎是最遗漏的诊断。替代原因包括乙型肝炎,C和E,塞细胞病毒,EpstemGalovirus,缺血性肝炎,心脏肝病,自身免疫性肝炎,非酒精性脂肪肝疾病,非酒精性脱脂性肝炎和酒精性肝病。结论出版的全球帝力案系列的三分之一以上,这些报告中发表的替代原因涉及帝力诊断。未来,已发布的Diri案例系列仅包括患有可靠的Dili诊断患者,优先通过预期使用由强大的诊断算法提供的较新的ROOSSEL UCLAF因果关系评估方法提供的较新的诊断算法提供。

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