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Herbalife hepatotoxicity: Evaluation of cases with positive reexposure tests

机译:康宝莱肝脏毒性:再暴露试验阳性的病例评估

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摘要

AIM: To analyze the validity of applied test criteria and causality assessment methods in assumed Herbalife hepatotoxicity with positive reexposure tests.METHODS: We searched the Medline database for suspected cases of Herbalife hepatotoxicity and retrieved 53 cases including eight cases with a positive unintentional reexposure and a high causality level for Herbalife. First, analysis of these eight cases focused on the data quality of the positive reexposure cases, requiring a baseline value of alanine aminotransferase (ALT) < 5 upper limit of normal (N) before reexposure, with N as the upper limit of normal, and a doubling of the ALT value at reexposure as compared to the ALT value at baseline prior to reexposure. Second, reported methods to assess causality in the eight cases were evaluated, and then the liver specific Council for International Organizations of Medical Sciences (CIOMS) scale validated for hepatotoxicity cases was used for quantitative causality reevaluation. This scale consists of various specific elements with scores provided through the respective case data, and the sum of the scores yields a causality grading for each individual case of initially suspected hepatotoxicity.RESULTS: Details of positive reexposure test conditions and their individual results were scattered in virtually all cases, since reexposures were unintentional and allowed only retrospective rather than prospective assessments. In 1/8 cases, criteria for a positive reexposure were fulfilled, whereas in the remaining cases the reexposure test was classified as negative (n = 1), or the data were considered as uninterpretable due to missing information to comply adequately with the criteria (n = 6). In virtually all assessed cases, liver unspecific causality assessment methods were applied rather than a liver specific method such as the CIOMS scale. Using this scale, causality gradings for Herbalife in these eight cases were probable (n = 1), unlikely (n = 4), and excluded (n = 3). Confounding variables included low data quality, alternative diagnoses, poor exclusion of important other causes, and comedication by drugs and herbs in 6/8 cases. More specifically, problems were evident in some cases regarding temporal association, daily doses, exact start and end dates of product use, actual data of laboratory parameters such as ALT, and exact dechallenge characteristics. Shortcomings included scattered exclusion of hepatitis A-C, cytomegalovirus and Epstein Barr virus infection with only globally presented or lacking parameters. Hepatitis E virus infection was considered in one single patient and found positive, infections by herpes simplex virus and varicella zoster virus were excluded in none.CONCLUSION: Only one case fulfilled positive reexposure test criteria in initially assumed Herbalife hepatotoxicity, with lower CIOMS based causality gradings for the other cases than hitherto proposed.
机译:目的:通过阳性暴露试验,分析假定的康宝莱肝毒性中适用的测试标准和因果关系评估方法的有效性。方法:我们在Medline数据库中搜索了怀疑的康宝莱肝毒性病例,并检索了53例病例,其中包括8例无意再暴露阳性和康宝莱的因果关系很高。首先,对这八例病例的分析重点在于阳性再暴露病例的数据质量,要求在再次暴露前丙氨酸转氨酶(ALT)的基线值<正常值上限(N)的5,以N为正常值上限,以及与再次暴露前的基线ALT值相比,再次暴露时的ALT值增加了一倍。其次,评估了八种病例的因果关系评估报告方法,然后使用针对肝毒性病例验证的肝特异性国际医学会国际医学委员会(CIOMS)量表对因果关系进行定量评估。该量表由各种具体要素组成,并通过各自的病例数据提供分数,分数的总和为每个最初怀疑具有肝毒性的个案提供因果关系评分。结果:阳性再暴露测试条件的详细信息及其各自的结果分散在几乎所有情况都是这样,因为再暴露是无意的,只能进行回顾性评估,而不是前瞻性评估。在1/8的情况下,满足了阳性再暴露的标准,而在其他情况下,再暴露测试被归为阴性(n = 1),或者由于缺少足够的信息以使数据充分符合标准而被认为是不可解释的( n = 6)。在几乎所有评估病例中,均采用了肝脏非特异性因果关系评估方法,而不是采用诸如CIOMS量表之类的肝脏特异性方法。使用此量表,这八种情况下康宝莱的因果关系等级很可能(n = 1),不太可能(n = 4)和被排除(n = 3)。令人困惑的变量包括数据质量低下,替代诊断,重要其他原因的排除不佳以及药物和草药的喜剧性治疗占6/8例。更具体地说,在某些情况下,有关时间关联,每日剂量,产品使用的确切开始和结束日期,实验室参数(例如ALT)的实际数据以及确切的脱毒特性等问题很明显。缺点包括仅在全球范围内提供或缺乏参数的A-C型肝炎,巨细胞病毒和爱泼斯坦巴尔病毒感染的分散排斥。仅一名患者考虑了戊型肝炎病毒感染,但发现为阳性,未排除单纯疱疹病毒和水痘带状疱疹病毒的感染。对于迄今为止尚未提出的其他情况。

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