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Ciprofloxacin-lnduced Hepatotoxicity Resolved With Levofloxacin: A Case Report and a Reviewof the Literature

机译:左氧氟沙星解决环丙沙星诱导的肝毒性:病例报告和文献复习。

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Objective: To report a case of elevated hepatic transaminases in a patient receiving ciprofloxacin that resolved upon discontinuation and initiation of levofloxacin.Summary: A 45-year-old white woman was initiated on ciprofloxacin and gentamicin after a blood culture revealed gram-negative rods. On day 2 of antibiotic therapy, the patient's aspartate aminotransferase (AST) and ala-nine aminotransferase (ALT) increased to 2,352 units/L and 783 units/L, respectively, and remained elevated for the following 4 days. Baseline AST and ALT were within normal limits. On day 5 of therapy, ciprofloxacin was discontinued and levofloxacin was initiated. On the following day, the hepatic transaminases decreased (AST, 192 units/L; ALT, 582 units/L) and continued to normalize prior to hospital discharge. On a subsequent admission later in the month, levofloxacin was again administered for treatment of a gram-positive bacteremia, with no subsequent elevation of hepatic transaminases.Discussion: An objective causality assessment revealed that the adverse drug reaction (ADR) was probable. Although reports of this ADR have been noted, there is no previously documented occurrence of resolution of elevated hepatic transaminases on therapeutic modification to another fluor o quinolone.Conclusion: Ciprofloxacin may significantly elevate hepatic transaminases. The clinician should be aware of the unique ADR profiles of the different fluoroquinolones because hepatotoxicity may not be a class effect.
机译:目的:报道一例接受环丙沙星治疗的患者肝转氨酶升高的情况,该患者经左氧氟沙星停用和开始治疗后即可消解。摘要:一名45岁的白人妇女在血液培养显示革兰氏阴性杆菌感染后开始使用环丙沙星和庆大霉素治疗。在抗生素治疗的第2天,患者的天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)分别增至2,352单位/ L和783单位/ L,并在接下来的4天中保持升高。基线AST和ALT均在正常范围内。治疗第5天,停用环丙沙星并开始使用左氧氟沙星。第二天,肝转氨酶下降(AST,192单位/ L; ALT,582单位/ L),并在出院前继续恢复正常。在该月晚些时候的随后入院时,再次使用左氧氟沙星治疗革兰氏阳性菌血症,而随后的肝转氨酶水平没有升高。尽管已经注意到了该ADR的报道,但以前没有文献报道对另一种氟喹诺酮进行治疗性修饰后,肝转氨酶升高的解决方法。结论:环丙沙星可能会明显提高肝转氨酶的水平。临床医师应了解不同氟喹诺酮类药物的独特ADR资料,因为肝毒性可能不是一种类效应。

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