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Azathioprine-Induced Rapid Hepatotoxicity

机译:硫唑嘌呤诱导的快速肝毒性

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摘要

>Objective: To report a case of rapid hepatotoxicity seen within days of initiating azathioprine therapy as a possible adverse reaction. >Case Summary: A 62-year-old female with Crohn’s disease was being maintained on occasional oral prednisone when more aggressive therapy became indicated. The patient was started on azathioprine and continued a prednisone taper. Liver enzymes became elevated by the third day of therapy. Peak liver enzyme values on day 10 of therapy were aspartate aminotransferase 119 U/L, alanine aminotransferase 210 U/L, and alkaline phosphatase 460 U/L. The patient did not develop any symptoms of hepatotoxicity. Azathioprine was discontinued and liver enzyme levels returned to baseline within 3 weeks. >Discussion: Azathioprine hepatotoxicity has been reported previously. A MEDLINE search (1966 to August 2013) found 39 articles related to various types of azathioprine hepatotoxicity. Previous literature predominately involves male patients and a general onset of 2 to 12 months after starting azathioprine therapy. Our case involves a female patient with an onset of days. According to the Naranjo probability scale, this reaction is considered possible, whereas the Council for International Organizations of Medical Sciences Probability Scale categorized this reaction as probable. The concurrent prednisone therapy may have increased the patient’s risk of azathioprine hepatotoxicity, but is not likely the sole cause as prior to and after discontinuing azathioprine the liver enzymes remained normal despite prednisone therapy. >Conclusions: Prescribers should be aware that monitoring liver enzymes when initiating azathioprine may be warranted within the first week, especially if the patient is taking corticosteroids or other high-risk medications that cause hepatotoxicity.
机译:>目的:报告一例在开始硫唑嘌呤治疗后几天内出现快速肝毒性的可能不良反应的案例。 >病例总结:当有迹象表明需要更积极的治疗时,一名62岁的患有克罗恩病的女性偶尔会接受口服泼尼松治疗。该患者开始接受硫唑嘌呤治疗,并继续使用泼尼松锥度。在治疗的第三天,肝酶升高。治疗第10天的肝酶峰值为天冬氨酸转氨酶119 U / L,丙氨酸转氨酶210 U / L和碱性磷酸酶460 U / L。该患者没有出现任何肝中毒症状。停用硫唑嘌呤,并且在3周内肝酶水平恢复至基线。 >讨论:硫唑嘌呤的肝毒性已有报道。 MEDLINE搜索(1966年至2013年8月)发现39篇与各种硫唑嘌呤肝毒性有关的文章。以前的文献主要涉及男性患者,开始硫唑嘌呤治疗后的一般发作为2至12个月。我们的病例涉及一名女性,发病几天。根据Naranjo概率量表,该反应被认为是可能的,而国际医学科学组织概率量表则将该反应归为可能。并用泼尼松治疗可能会增加患者硫唑嘌呤肝毒性的风险,但在停用硫唑嘌呤之前和之后,可能不是唯一的原因,尽管泼尼松治疗仍使肝酶保持正常。 >结论:开处方者应该意识到,在开始服用硫唑嘌呤时,有必要对肝酶进行监测,尤其是当患者服用皮质类固醇或其他引起肝毒性的高危药物时。

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