Zhao Hui-Ying, Gu Jian, Lyu Jie, Liu Dan, Wang Yi-Tong, Liu Fang, Zhu Feng-Xue, An You-Zhong
Department of Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
Department of Pharmacy, Peking University People's Hospital, Beijing 100044, China.
Chin Med J (Engl). 2017 May 20;130(10):1139-1145. doi: 10.4103/0366-6999.205859.
The antibiotic meropenem is commonly administered in patients with severe sepsis and septic shock. We compared the pharmacokinetic, clinical, and bacteriological efficacies of continuous infusion of meropenem versus intermittent administration in such patients.
Patients admitted to the Intensive Care Unit (ICU) with severe sepsis or septic shock who received meropenem were randomly assigned to either the continuous (n = 25) or intermittent groups (n = 25). The continuous group received a loading dose of 0.5 g of meropenem followed by a continuous infusion of 3 g/day; the intermittent group received an initial dose of 1.5 g followed by 1 g for every 8 h. Clinical success, microbiological eradication, superinfection, ICU mortality, length of ICU stay, and duration of meropenem treatment were assessed. Serial plasma meropenem concentrations for the first and third dosing periods (steady state) were also measured.
Clinical success was similar in both the continuous (64%) and intermittent (56%) groups (P = 0.564); the rates of microbiological eradication and superinfection (81.8% vs. 66.7% [ P = 0.255] and 4% vs. 16% [ P = 0.157], respectively) showed improvement in the continuous group. The duration of meropenem treatment was significantly shorter in the continuous group (7.6 vs. 9.4 days; P= 0.035), where a better steady-state concentration was also achieved. Peak and trough concentrations were significantly different between the continuous and intermittent groups both in the first (Cmax: 19.8 mg/L vs. 51.8 mg/L, P= 0.000; Cmin: 11.2 mg/L vs. 0.5 mg/L, P= 0.000) and third dosing periods (Cmax: 12.5 mg/L vs. 46.4 mg/L, P= 0.000; Cmin: 11.4 mg/L vs. 0.6 mg/L, P= 0.000). For medium-susceptibility pathogens, continuous infusion concentrations above the minimal inhibitory concentration were 100%, which was better than that in the intermittent group.
Continuous infusion of meropenem provides significantly shorter treatment duration and a tendency for superior bacteriological efficacy than intermittent administration. Continuous infusion may be more optimal against intermediate-susceptibility pathogens.
美罗培南抗生素常用于严重脓毒症和脓毒性休克患者。我们比较了此类患者中持续输注美罗培南与间歇性给药的药代动力学、临床和细菌学疗效。
入住重症监护病房(ICU)且接受美罗培南治疗的严重脓毒症或脓毒性休克患者被随机分为持续输注组(n = 25)和间歇性给药组(n = 25)。持续输注组先给予负荷剂量0.5 g美罗培南,随后以3 g/天的剂量持续输注;间歇性给药组初始剂量为1.5 g,随后每8小时给予1 g。评估临床疗效、微生物清除情况、二重感染、ICU死亡率、ICU住院时间和美罗培南治疗持续时间。并测量了首个给药期和第三个给药期(稳态)的系列血浆美罗培南浓度。
持续输注组(64%)和间歇性给药组(56%)的临床疗效相似(P = 0.564);持续输注组的微生物清除率和二重感染率(分别为81.8%对66.7%[P = 0.255]和4%对16%[P = 0.157])有所改善。持续输注组的美罗培南治疗持续时间显著更短(7.6天对9.4天;P =