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首页> 外文期刊>The annals of pharmacotherapy >Fatal hepatitis after long-term pulse itraconazole treatment for onychomycosis.
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Fatal hepatitis after long-term pulse itraconazole treatment for onychomycosis.

机译:长期脉冲伊曲康唑治疗甲癣后可发生致命性肝炎。

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摘要

OBJECTIVE: To report the occurrence of acute cytolytic hepatitis in a patient exposed to pulse itraconazole therapy for 24 weeks and provide a concise review of the literature on cases of itraconazole-induced hepatitis. CASE SUMMARY: A 61-year-old woman with no apparent risk factors for liver injury developed acute hepatitis one week after the final dose of a long-term course of pulse itraconazole therapy (200 mg orally twice daily, 1 wk on, 3 wk off, for 24 wk) for onychomycosis. Monitoring of liver enzymes was not performed during the treatment period. Serologic evaluations on presentation ruled out infectious diseases or other etiological factors. Liver function tests showed alanine aminotransferase 3330 U/L, aspartate aminotransferase 3250 U/L, and bilirubin 21 mg/dL. Liver function continued to deteriorate, and the patient underwent liver transplantation 17 days after admission. Her liver displayed reduced volume and there was a mild accumulation of ascitic fluid in the retroperitoneal cavity. Histologic evaluation showed massive panlobular necrosis. Complications occurred after transplantation and a rejection crisis worsened the clinical picture until the patient died about 4 months later. Use of the Naranjo probability scale showed the relationship of itraconazole therapy and the occurrence of acute hepatitis as probable. DISCUSSION: Itraconazole pulse therapy for onychomycosis appears to be at least as effective as and safer than a continuous treatment regimen, particularly from the perspective of potential liver damage. Only one case of severe symptomatic hepatitis occurring after pulse therapy with itraconazole for onychomycosis and requiring transplantation has been reported previously. In that case, as well as the one reported here, hepatitis symptoms occurred after completion of long-term treatment in patients who were asymptomatic both before and during therapy. CONCLUSIONS: Prolonged exposure to itraconazole, administered either continuously or intermittently, may precipitate severe and irreversible hepatotoxic events. Accordingly, careful monitoring of liver function parameters should be performed both during and after treatment when onychomycosis requires prolonged itraconazole administration, even in asymptomatic patients lacking apparent risk factors of hepatic injury.
机译:目的:报告接受脉冲伊曲康唑治疗24周的患者发生急性细胞溶解性肝炎的情况,并简要回顾伊曲康唑诱发的肝炎病例的文献。病例摘要:一名无明显肝损伤危险因素的61岁妇女在长期服用伊曲康唑脉冲治疗的最终剂量(每天200 mg,每日两次,每周1周,每周3周)后一周出现急性肝炎关闭,持续24周)用于灰指甲。在治疗期间未进行肝酶的监测。表现的血清学评估排除了传染病或其他病因。肝功能测试显示丙氨酸氨基转移酶3330 U / L,天冬氨酸氨基转移酶3250 U / L和胆红素21 mg / dL。肝功能持续恶化,患者在入院后17天接受肝移植。她的肝脏体积缩小,腹膜后腔中有少量腹水积聚。组织学评价显示大量小叶坏死。移植后发生并发症,排斥反应恶化使患者的临床情况恶化,直到患者在约4个月后死亡。使用Naranjo概率量表显示可能存在伊曲康唑治疗与急性肝炎发生的关系。讨论:伊曲康唑脉冲疗法治疗甲癣似乎比连续治疗方案至少有效和安全,尤其是从潜在的肝损害的角度来看。先前仅报道了伊曲康唑用于甲癣的脉冲治疗后发生的一例严重症状性肝炎,需要移植。在这种情况下,以及在此报道的情况下,治疗前和治疗过程中无症状的患者经过长期治疗后均会出现肝炎症状。结论:连续或间断给药的伊曲康唑长时间接触可能会引发严重且不可逆的肝毒性事件。因此,当灰指甲病需要长期服用伊曲康唑时,即使在缺乏明显肝损伤危险因素的无症状患者中,也应在治疗期间和治疗后对肝功能参数进行仔细监测。

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