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肥胖时代静脉用泊沙康唑剂量的影响。

Implications for IV posaconazole dosing in the era of obesity.

机构信息

Department of Pharmacy, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

Center of Expertise in Mycology Radboudumc/CWZ, Nijmegen, The Netherlands.

出版信息

J Antimicrob Chemother. 2020 Apr 1;75(4):1006-1013. doi: 10.1093/jac/dkz546.

Abstract

BACKGROUND

The prevalence of obesity has shown a dramatic increase over recent decades. Obesity is associated with underdosing of antimicrobial drugs for prophylaxis and treatment. Posaconazole is a broad-spectrum triazole antifungal drug licensed for prophylaxis and treatment of invasive fungal infections. It is unclear how posaconazole should be dosed in obese patients.

METHODS

We performed a prospective study investigating the pharmacokinetics of posaconazole in morbidly obese (n = 16) and normal-weight (n = 8) subjects, with a weight ranging between 61.4 and 190 kg, after a 300 or 400 mg IV dose. Population pharmacokinetic modelling was used to assess the effect of body size on posaconazole pharmacokinetics. ClinicalTrials.gov Identifier: NCT03246386.

RESULTS

Total body weight best predicted changes in CL and V. Model-based simulations demonstrated that, for treatment of fungal infections, a daily IV dose of 300 mg will result in a PTA of ≥90% in individuals up to 140 kg, after which both twice daily loading and the daily maintenance dose should be increased to 400 mg. For prophylaxis, a 300 mg IV dose is adequate in patients up to 190 kg.

CONCLUSIONS

Body size has a significant impact on posaconazole CL and V, resulting in a lower exposure in obese subjects compared with normal-weight subjects. For therapeutic use of posaconazole, a dose increase is required in patients above 140 kg. For prophylaxis, a 300 mg IV dose is adequate. For oral treatment, these recommendations can act as a starting point followed by therapeutic drug monitoring.

摘要

背景

肥胖症的患病率在最近几十年呈显著上升趋势。肥胖与抗菌药物预防和治疗剂量不足有关。泊沙康唑是一种广谱三唑类抗真菌药物,用于预防和治疗侵袭性真菌感染。泊沙康唑在肥胖患者中的剂量应如何确定尚不清楚。

方法

我们进行了一项前瞻性研究,调查了体重在 61.4 至 190 公斤之间的病态肥胖(n=16)和正常体重(n=8)受试者在接受 300 或 400mg IV 剂量后泊沙康唑的药代动力学。采用群体药代动力学模型评估身体大小对泊沙康唑药代动力学的影响。临床试验.gov 标识符:NCT03246386。

结果

总身体重量最佳预测了 CL 和 V 的变化。基于模型的模拟表明,对于真菌感染的治疗,每天静脉注射 300mg 将导致 140kg 以下个体的 PTA≥90%,此后,每日两次负荷剂量和维持剂量均应增加至 400mg。对于预防,体重高达 190kg 的患者静脉注射 300mg 是足够的。

结论

身体大小对泊沙康唑 CL 和 V 有显著影响,导致肥胖受试者的暴露量低于正常体重受试者。对于泊沙康唑的治疗用途,140kg 以上的患者需要增加剂量。对于预防,静脉注射 300mg 是足够的。对于口服治疗,这些建议可以作为起始点,然后进行治疗药物监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c06/7069473/88792049d34e/dkz546f1.jpg

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