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腹腔注射万古霉素后发生万古霉素冲洗反应:病例报告。

Vancomycin flushing reaction after intraperitoneal vancomycin: A case report.

机构信息

Department of Clinical Pharmacy, University Medical Centre Utrecht, University Utrecht, The Netherlands.

Department of Nephrology and Hypertension, University Medical Centre Utrecht, University Utrecht, The Netherlands.

出版信息

Perit Dial Int. 2024 Mar;44(2):145-148. doi: 10.1177/08968608231199735. Epub 2023 Sep 25.

Abstract

Vancomycin has been reported to cause vancomycin flushing reaction (VFR), a hypersensitivity reaction that mostly occurs after intravenous administration. The incidence of VFR in a patient receiving intraperitoneal vancomycin is rare. We report a case of a female peritoneal dialysis (PD) patient with a PD-related peritonitis who developed VFR after intraperitoneal administration of 2000 mg vancomycin. Seventy-five minutes after instillation, she developed flushing, a pruritic erythema on the upper body and swelling of the lips. Blood results revealed a vancomycin plasma concentration of 54.8 mg/L and a normal tryptase level. During a relapse of her PD-related peritonitis, vancomycin was successfully reintroduced in a 50% reduced dose. No symptoms of VFR developed, and the corresponding vancomycin plasma concentration was 33.6 mg/L. Intraperitoneal treatment was continued with 500 mg vancomycin every 2-3 days with frequently measured, adequate trough levels ranging from 15-22 mg/L. This case illustrates the risk factors for the development of VFR after intraperitoneal administration of vancomycin, namely a high and concentrated loading dose together with a low body weight, a fast peritoneal transport state and peritonitis. Reintroduction of vancomycin after occurrence of VFR is safe, but a lower loading dose or a slower instillation rate is recommended.

摘要

万古霉素曾被报道可引起万古霉素 flush 反应(VFR),这是一种主要在静脉给药后发生的过敏反应。腹腔内给予万古霉素的患者中 VFR 的发生率很少见。我们报告了一例女性腹膜透析(PD)患者,其 PD 相关性腹膜炎在给予 2000mg 万古霉素腹腔内给药后发生了 VFR。灌洗 75 分钟后,她出现了潮红、上半身瘙痒性红斑和嘴唇肿胀。血液检查结果显示万古霉素血药浓度为 54.8mg/L,血清胰蛋白酶正常。在 PD 相关性腹膜炎复发时,以 50%的减少剂量成功重新引入了万古霉素。未出现 VFR 症状,相应的万古霉素血药浓度为 33.6mg/L。继续给予 500mg 万古霉素,每 2-3 天腹腔内治疗一次,频繁测量的药物谷浓度维持在 15-22mg/L。该病例说明了腹腔内给予万古霉素后发生 VFR 的危险因素,即高浓度的负荷剂量、体重低、快速的腹膜转运状态和腹膜炎。发生 VFR 后重新引入万古霉素是安全的,但建议使用较低的负荷剂量或较慢的注入速度。

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