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Assessment of drug-induced hepatotoxicity in clinical practice: A challenge for gastroenterologists 被引量:18
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作者 raúl j andrade Mercedes Robles +3 位作者 Alejandra Fernández-Castaer Susana lópez-Ortega M Carmen lópez-Vega M Isabel lucena 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第3期329-340,共12页
Currently, pharmaceutical preparations are serious contributors to liver disease; hepatotoxicity ranking as the most frequent cause for acute liver failure and post-commercialization regulatory decisions. The diagnosi... Currently, pharmaceutical preparations are serious contributors to liver disease; hepatotoxicity ranking as the most frequent cause for acute liver failure and post-commercialization regulatory decisions. The diagnosis of hepatotoxicity remains a difficult task because of the lack of reliable markers for use in general clinical practice. To incriminate any given drug in an episode of liver dysfunction is a step-by-step process that requires a high degree of suspicion, compatible chronology, awareness of the drug’s hepatotoxic potential, the exclusion of alternative causes of liver damage and the ability to detect the presence of subtle data that favors a toxic etiology. This process is time-consuming and the final result is frequently inaccurate. Diagnostic algorithms may add consistency to the diagnostic process by translating the suspicion into a quantitative score. Such scales are useful since they provide a framework that emphasizes the features that merit attention in cases of suspected hepatic adverse reaction as well. Current efforts in collecting bona fide cases of drug-induced hepatotoxicity will make refinements of existing scales feasible. It is now relatively easy to accommodate relevant data within the scoring system and to delete low-impact items. Efforts should also be directed toward the development of an abridged instrument for use in evaluating suspected drug-induced hepatotoxicity at the very beginning of the diagnosis and treatment process when clinical decisions need to be made. The instrument chosen would enable a confident diagnosis to be made on admission of the patient and treatment to be fine-tuned as further information is collected. 展开更多
关键词 肝病 肝中毒 诊断方法 药物治疗
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Adverse hepatic reactions associated with calcium carbimide and disulfiram therapy: Is there still a role for these drugs? 被引量:2
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作者 Carmen Verge M Isabel lucena +4 位作者 Enrique lópez-Torres M josé Puche-García Enrique Fraga Manuel Romero-Gomez raúl j andrade 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第31期5078-5080,共3页
四乙秋兰姆化二硫和钙 carbimide 是二白酒威慑然而,广泛地在那里在酒精中毒治疗使用的狂言存在对他们的安全的大担心。hepatotoxicity 上的报告主要与四乙秋兰姆化二硫治疗有关,被出版了。钙 carbimide 的肝毒素的潜力是很好描绘的... 四乙秋兰姆化二硫和钙 carbimide 是二白酒威慑然而,广泛地在那里在酒精中毒治疗使用的狂言存在对他们的安全的大担心。hepatotoxicity 上的报告主要与四乙秋兰姆化二硫治疗有关,被出版了。钙 carbimide 的肝毒素的潜力是很好描绘的更少。这里,我们描述与被提交到 hepatotoxicity 的一张注册表并且当规定这些混合物时,指出我们面对的限制的这个治疗学的组有关的肝损坏的四个案例。对在白酒依赖的管理的这些混合物的角色的重估清楚地被需要。 展开更多
关键词 异氰酸脂 肝中毒 戒酒硫 治疗
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Prolonged cholestasis after raloxifene and fenofibrate interaction: A case report
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作者 M Isabel lucena raúl j andrade +3 位作者 luis Vicioso F jesús González Ketevan Pachkoria Beatriz García-Mu(n|~)oz 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第32期5244-5246,共3页
当超过一药能是负责的时,在导致药的肝损伤分配诱发性特别地是挑战性的。我们与 raloxifen 在长期的治疗上报导一个女人立即在开始 fenofibrate 以后开发了尖锐胆汁郁积。图画演变为长期的胆汁郁积。我们假设了那在新陈代谢的水平的一... 当超过一药能是负责的时,在导致药的肝损伤分配诱发性特别地是挑战性的。我们与 raloxifen 在长期的治疗上报导一个女人立即在开始 fenofibrate 以后开发了尖锐胆汁郁积。图画演变为长期的胆汁郁积。我们假设了那在新陈代谢的水平的一个相互作用能在这个病人在 fenofibrate 的暴露的一很短的时间以后触发了 hepatotoxicity 的演讲。调查结果一过去在肝活体检视的脉管的内皮生长因素的表示建议血管生成可能在有毒的胆汁郁积的坚持起一个作用。 展开更多
关键词 慢性胆汁淤积 非诺贝特 肝中毒 病理机制
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drug-induced autoimmune liver disease:a diagnostic dilemma of an increasingly reported disease 被引量:13
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作者 Agustin Castiella Eva Zapata +1 位作者 M Isabel lucena raúl j andrade 《World Journal of Hepatology》 CAS 2014年第4期160-168,共9页
The aetiology of autoimmune hepatitis(AIH) is uncer-tain but the disease can be triggered in susceptible patients by external factors such as viruses or drugs.AIH usually develops in individuals with a genetic back-gr... The aetiology of autoimmune hepatitis(AIH) is uncer-tain but the disease can be triggered in susceptible patients by external factors such as viruses or drugs.AIH usually develops in individuals with a genetic back-ground mainly consisting of some risk alleles of the major histocompatibility complex(HLA).Many drugs have been linked to AIH phenotypes,which sometimes persist after drug discontinuation,suggesting that they awaken latent autoimmunity.At least three clini-cal scenarios have been proposed that refers to drug- induced autoimmune liver disease(DIAILD):AIH with drug-induced liver injury(DILI); drug induced-AIH(DI-AIH); and immune mediated DILI(IM-DILI).In addi-tion,there are instances showing mixed features of DI-AIH and IM-DILI,as well as DILI cases with positive autoantibodies.Histologically distinguishing DILI from AIH remains a challenge.Even more challenging is the differentiation of AIH from DI-AIH mainly relying in histological features; however,a detailed standard-ised histologic evaluation of large cohorts of AIH and DI-AIH patients would probably render more subtle features that could be of help in the differential diag-nosis between both entities.Growing information on the relationship of drugs and AIH is being available,being drugs like statins and biologic agents more fre-quently involved in cases of DIAILD.In addition,there is some evidence on the fact that patients diagnosed with DIAILD may have had a previous episode of hepa-totoxicity.Further collaborative studies in DIAILD will strengthen the knowledge and understanding of this intriguing and complex disorder which might represent different phenotypes across the spectrum of 展开更多
关键词 DRUG-INDUCED LIVER injury AUTOIMMUNE HEPATITIS DRUGS DRUG-INDUCED AUTOIMMUNE HEPATITIS DRUG-INDUCED AUTOIMMUNE LIVER DISEASE
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