Pharmacodynamics and tolerability of high-dose, prolonged infusion carbapenems in adults with cystic fibrosis – A review of 3 cases

Catharine C. Bulik , Richard Quintiliani Jr. , J. Samuel Pope , Joseph L. Kuti , David P. Nicolau
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引用次数: 19

Abstract

Cystic fibrosis (CF) is a disease marked by repeated acute pulmonary exacerbations of infections, often caused by Pseudomonas aeruginosa and Burkholderia cepacia. As antibiotic susceptibility declines, dose optimization must be considered to provide adequate pharmacodynamic exposure. We report three cases of CF exacerbations in adults caused by multi-drug resistant P. aeruginosa and B. cepacia. Each case required dosing strategies greater than currently recognized in package inserts: meropenem 3000 mg every 8 h (3-hour infusion) and doripenem 2000 mg every 8 h (4-hour infusion). Pharmacokinetic analyses demonstrated that targeted pharmacodynamic exposures were achieved against most of the organisms, resulting in clinical improvements despite laboratory reported resistance. The high-dose, prolonged infusion regimens were well tolerated demonstrating that pharmacodynamically optimized carbapenem regimens may be used safely and effectively in patients with limited conventional treatment options.

3例成人囊性纤维化患者大剂量、长时间输注碳青霉烯类药物的药效学和耐受性
囊性纤维化(CF)是一种以反复急性肺部感染为特征的疾病,通常由铜绿假单胞菌和洋葱伯克霍尔德菌引起。随着抗生素敏感性的下降,必须考虑剂量优化以提供足够的药效学暴露。我们报告三例CF恶化的成年人引起的多重耐药铜绿假单胞菌和洋葱芽胞杆菌。每个病例需要的剂量策略都大于目前包装说明书中认可的剂量策略:美罗培南每8小时3000毫克(3小时输注)和多利培南每8小时2000毫克(4小时输注)。药代动力学分析表明,针对大多数生物体的靶向药效学暴露得以实现,尽管实验室报告了耐药性,但仍导致临床改善。高剂量、长时间输注方案耐受性良好,表明药效学优化的碳青霉烯类方案可以安全有效地用于常规治疗方案有限的患者。
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