Boselli Emmanuel, Breilh Dominique, Rimmelé Thomas, Guillaume Christian, Xuereb Fabien, Saux Marie-Claude, Bouvet Lionel, Chassard Dominique, Allaouchiche Bernard
Claude Bernard Lyon I University, Lyon, France.
Crit Care Med. 2008 May;36(5):1500-6. doi: 10.1097/CCM.0b013e318170ba21.
To determine the steady-state serum and alveolar concentrations of piperacillin/tazobactam administered in continuous infusion to critically ill patients with ventilator-associated pneumonia and various degrees of renal failure.
Prospective comparative study.
An intensive care unit and research ward in a university hospital.
Forty patients with microbiologically documented ventilator-associated pneumonia.
Patients were randomized to receive piperacillin/tazobactam daily continuous infusions of 12/1.5 g or 16/2 g after a loading dose of 4/0.5 g. The serum and alveolar piperacillin/tazobactam concentrations were determined at steady-state with high performance liquid chromatography.
The median (interquartile) serum and alveolar piperacillin concentrations were respectively 25.3 mg/L (23.1-32.6) and 12.7 mg/L (6.7-18.0) for 12/1.5 g/day, and 38.9 mg/L (32.9-59.6) and 19.1 mg/L (14.0-21.5), respectively, for 16/2 g/day in patients with no/mild renal failure. In patients with moderate/advance renal failure, the median (interquartile) serum and alveolar piperacillin concentrations were 102.4 mg/L (97.4-112.6) and 44.1 mg/L (33.4-48.3), respectively, for 12/1.5 g/day, and 135.3 mg/L (119.5-146.2) and 54.9 mg/L (45.2-110.3), respectively, for 16/2 g/day. Our results show great variability in piperacillin/tazobactam concentrations, with an alveolar percentage penetration of 40-50% for piperacillin and 65-85% for tazobactam and a negative association between serum or alveolar concentrations and creatinine clearance.
A target piperacillin serum concentration of at least 35-40 mg/L is probably required to provide alveolar concentrations exceeding the susceptibility breakpoint for gram-negative bacteria (16 mg/L) during ventilator-associated pneumonia. In patients with no/mild renal failure, a continuous daily dose of piperacillin/tazobactam 16/2 g allows reaching this target concentration, which might be not observed with 12/1.5 g/day. In patients with moderate/advanced renal failure, both dosages achieve serum concentrations far above the 35-40 mg/L threshold, suggesting that in that case, therapeutic drug monitoring should be performed in order to adjust the daily dose.
确定持续静脉输注哌拉西林/他唑巴坦后,患有呼吸机相关性肺炎及不同程度肾衰竭的重症患者的稳态血清和肺泡浓度。
前瞻性对照研究。
一所大学医院的重症监护病房和研究病房。
40例微生物学确诊的呼吸机相关性肺炎患者。
患者在给予4/0.5g负荷剂量后,随机接受每日持续静脉输注12/1.5g或16/2g哌拉西林/他唑巴坦。采用高效液相色谱法测定稳态时血清和肺泡中哌拉西林/他唑巴坦的浓度。
对于未合并/轻度肾衰竭的患者,每日12/1.5g剂量组的哌拉西林血清和肺泡浓度中位数(四分位间距)分别为25.3mg/L(23.1 - 32.6)和12.7mg/L(6.7 - 18.0),每日16/2g剂量组分别为38.9mg/L(32.9 - 59.6)和19.1mg/L(14.0 - 21.5)。对于中度/重度肾衰竭患者,每日12/1.5g剂量组的哌拉西林血清和肺泡浓度中位数(四分位间距)分别为102.4mg/L(97.4 - 112.6)和44.1mg/L(33.4 - 48.3),每日16/2g剂量组分别为135.3mg/L(119.5 - 146.2)和54.9mg/L(45.2 - 110.3)。我们的结果显示哌拉西林/他唑巴坦浓度存在很大变异性,哌拉西林的肺泡穿透率为40% - 50%,他唑巴坦为65% - 85%,血清或肺泡浓度与肌酐清除率呈负相关。
在呼吸机相关性肺炎期间,可能需要将哌拉西林血清浓度目标设定为至少35 - 40mg/L,以确保肺泡浓度超过革兰阴性菌的药敏折点(16mg/L)。对于未合并/轻度肾衰竭的患者,每日持续给予16/2g哌拉西林/他唑巴坦可达到该目标浓度,而每日12/1.5g可能无法达到。对于中度/重度肾衰竭患者,两种剂量的血清浓度均远高于35 - 40mg/L阈值,这表明在这种情况下,应进行治疗药物监测以调整每日剂量。