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头孢曲松与阿昔洛韦联用——肾毒性潜力是否被低估?

Combination of ceftriaxone and acyclovir - an underestimated nephrotoxic potential?

作者信息

Vomiero Gemma, Carpenter Blair, Robb Ian, Filler Guido

机构信息

Department of Pediatrics, Division of Nephrology, Children's Hospital of Eastern Ontario, University of Ottawa, 401 Smyth Road, Ottawa, Ontario, K1H 8L1, Canada.

出版信息

Pediatr Nephrol. 2002 Aug;17(8):633-7. doi: 10.1007/s00467-002-0867-5. Epub 2002 May 17.

Abstract

Management of meningo-encephalitis often involves the need for antibiotic and antiviral treatment. We report a retrospective analysis over a 6-month period of 17 patients (age range 1-14 years) who were treated with combination therapy of ceftriaxone and acyclovir. Mean acyclovir and ceftriaxone doses were 1,222+/-304 and 2,315+/-509 mg/m(2) per day, respectively. Three patients developed acute renal failure with a peak creatinine of up to 865% above baseline, occurring 2-3 days after starting combination therapy. Patients revealed a tubular proteinuria pattern. Renal biopsy of 1 patient showed a tubulotoxic picture but no evidence of crystals. In 12 of 17 patients (70%) there was a significant increase in serum creatinine. This was significantly greater than literature reports of 16% with acyclovir monotherapy. The degree of renal impairment in our patients correlated significantly with the acyclovir dose, while no correlation was found with the ceftriaxone dose. We conclude that the addition of a second nephrotoxic drug aggravated the extent of renal injury in our patients. The mechanism is tubulotoxicity. Caution should be exercised when using this potentially nephrotoxic cocktail, with clear criteria established for the initiation of combination therapy and close monitoring of serum creatinine.

摘要

脑膜脑炎的治疗通常需要使用抗生素和抗病毒药物。我们报告了一项为期6个月的回顾性分析,涉及17例年龄在1至14岁之间接受头孢曲松和阿昔洛韦联合治疗的患者。阿昔洛韦和头孢曲松的平均每日剂量分别为1222±304和2315±509mg/m²。3例患者出现急性肾衰竭,肌酐峰值比基线水平高出865%,在开始联合治疗后2至3天出现。患者表现为肾小管蛋白尿模式。1例患者的肾活检显示肾小管毒性表现,但无晶体证据。17例患者中有12例(70%)血清肌酐显著升高。这明显高于阿昔洛韦单药治疗文献报道的16%。我们患者的肾功能损害程度与阿昔洛韦剂量显著相关,而与头孢曲松剂量无相关性。我们得出结论,添加第二种肾毒性药物加重了我们患者的肾损伤程度。其机制为肾小管毒性。使用这种潜在的肾毒性联合用药时应谨慎,制定明确的联合治疗起始标准并密切监测血清肌酐。

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