Zhou Qing-Tao, He Bei, Shen Ning, Liang Ying, Sun Li-Na
Department of Respiratory Medicine, Peking University Third Hospital, No. 49 North Garden Road., Haidian District, Beijing, 100191, China.
Drugs Aging. 2017 Feb;34(2):115-121. doi: 10.1007/s40266-016-0431-9.
Meropenem is used for the treatment of severe lower respiratory tract infections (LRTIs) caused by multidrug-resistant Gram-negative bacilli.
We evaluated the clinical benefits of a strategy of meropenem dosing based on a population pharmacokinetics/pharmacodynamics (PK/PD) model in elderly patients with an LRTI.
In this prospective single-center open-label randomized controlled trial, 79 elderly patients with an LRTI caused by Gram-negative bacilli were randomized to a study group (SG) or a control group (CG). The latter received meropenem according to a regimen decided by the attending physician. The SG received individualized meropenem therapy with a dosing strategy based on software developed from a meropenem population PK/PD model. The primary endpoint was clinical response to meropenem therapy. Secondary endpoints were the amount of antibiotics used and bacteriologic response.
Klebsiella pneumoniae was the most common pathogen (32.9%), followed by Pseudomonas aeruginosa (30.4%) and Escherichia coli (17.7%). A total of 63 (79.7%) patients achieved clinical success. Prevalence of clinical success was significantly higher in the SG than in the CG (89.7 vs. 70.0%; p = 0.029). The daily dose of meropenem was significantly lower in the SG than in the CG (1.5 vs. 2.0 g; p = 0.017). A total of 52 (65.8%) patients experienced bacteriologic success, the median duration of meropenem therapy was 9 days, and the median total dose of meropenem was 18.0 g. There were no significant differences between the groups in these parameters.
A strategy for meropenem dosing based on a population PK/PD model can improve clinical response and avoid overtreatment in elderly patients with an LRTI. ClinicalTrials.gov registration number NCT01944319.
美罗培南用于治疗由多重耐药革兰阴性杆菌引起的严重下呼吸道感染(LRTIs)。
我们评估了基于群体药代动力学/药效学(PK/PD)模型的美罗培南给药策略对老年LRTI患者的临床益处。
在这项前瞻性单中心开放标签随机对照试验中,79例由革兰阴性杆菌引起LRTI的老年患者被随机分为研究组(SG)和对照组(CG)。后者根据主治医师确定的方案接受美罗培南治疗。SG组采用基于美罗培南群体PK/PD模型开发的软件进行给药策略的个体化美罗培南治疗。主要终点是美罗培南治疗的临床反应。次要终点是抗生素使用量和细菌学反应。
肺炎克雷伯菌是最常见的病原体(32.9%),其次是铜绿假单胞菌(30.4%)和大肠埃希菌(17.7%)。共有63例(79.7%)患者取得临床成功。SG组的临床成功率显著高于CG组(89.7%对70.0%;p = 0.029)。SG组美罗培南的每日剂量显著低于CG组(1.5 g对2.0 g;p = 0.017)。共有52例(65.8%)患者取得细菌学成功,美罗培南治疗的中位持续时间为9天,美罗培南的中位总剂量为18.0 g。这些参数在两组之间无显著差异。
基于群体PK/PD模型的美罗培南给药策略可改善老年LRTI患者的临床反应并避免过度治疗。ClinicalTrials.gov注册号NCT01944319。