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阿奇霉素在囊性纤维化患者每周一次给药期间的药代动力学及痰液穿透情况。

Pharmacokinetics and sputum penetration of azithromycin during once weekly dosing in cystic fibrosis patients.

作者信息

Wilms E B, Touw D J, Heijerman H G M

机构信息

Central Hospital Pharmacy, Escamplaan 900, 2547EX The Hague, The Netherlands.

出版信息

J Cyst Fibros. 2008 Jan;7(1):79-84. doi: 10.1016/j.jcf.2007.05.005. Epub 2007 Jun 27.

Abstract

In this study we examined pharmacokinetics, systemic exposure and sputum penetration of azithromycin (AZM) in CF patients on chronic daily AZM therapy after changing to a once weekly dosing scheme. Eight adult CF patients using AZM 500 mg/day were changed to a once weekly dose of 1000 mg during 3 months. Once per month sputum and blood samples were collected. AZM was quantified in blood plasma and polymorphonuclear neutrophils. The cumulative weekly dose was reduced with a factor of 3.5 (7x500 mg vs. 1x1000 mg weekly). This led to a reduction in area under the curve (AUC+/-S.D.) with a factor of 2.5+/-0.8 in plasma, 2.8+/-0.9 in blood, 2.2+/-1.1 in PMNNs and to a reduction in average sputum concentration with a factor of 3.0 (+/-1.5). At 1000 mg once weekly reduced but still substantial concentrations were achieved in PMNNs and in sputum. Although not significant, a tendency towards less than linear reduction was found. In order to calculate and propose an optimal dosing scheme we need to establish a relation between exposure levels and clinical efficacy.

摘要

在本研究中,我们检测了囊性纤维化(CF)患者在从每日慢性服用阿奇霉素(AZM)治疗方案转换为每周一次给药方案后,阿奇霉素的药代动力学、全身暴露情况及痰液穿透性。8名成年CF患者,原本每日服用500mg AZM,在3个月期间转换为每周一次服用1000mg。每月采集一次痰液和血液样本。对血浆和多形核中性粒细胞中的AZM进行定量分析。每周累积剂量降低了3.5倍(7×500mg对比每周1×1000mg)。这导致血浆中曲线下面积(AUC+/-标准差)降低了2.5+/-0.8倍,血液中降低了2.8+/-0.9倍,多形核中性粒细胞中降低了2.2+/-1.1倍,痰液平均浓度降低了3.0(+/-1.5)倍。每周一次服用1000mg时,多形核中性粒细胞和痰液中的浓度降低但仍处于较高水平。虽然差异不显著,但发现存在小于线性降低的趋势。为了计算并提出最佳给药方案,我们需要确定暴露水平与临床疗效之间的关系。

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