Division of Nephrology and Hypertension, Department of Internal Medicine, Hannover Medical School, Germany.
Clin J Am Soc Nephrol. 2012 Mar;7(3):385-90. doi: 10.2215/CJN.05690611. Epub 2012 Jan 5.
The fixed antibacterial combination of ampicillin and sulbactam is frequently used for various infections. Intact kidneys eliminate approximately 71% of ampicillin and 78% of sulbactam. Patients on thrice-weekly low-flux hemodialysis exhibit an ampicillin t(1/2) of 2.3 hours on and 17.4 hours off dialysis. Despite its frequent use in intensive care units, there are no available dosing recommendations for patients with AKI undergoing renal replacement therapy. The aims of this study were to evaluate the pharmacokinetics of ampicillin/sulbactam in critically ill patients with AKI undergoing extended dialysis (ED) and to establish a dosing recommendation for this treatment method.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Twelve critically ill patients with anuric AKI being treated with ED were enrolled in a prospective, open-label, observational pharmacokinetic study. Pharmacokinetics after a single dose of ampicillin/sulbactam (2 g/1 g) was obtained in 12 patients. Multiple-dose pharmacokinetics after 4 days of twice-daily ampicillin/sulbactam (2 g/1 g) was obtained in three patients.
The mean dialyzer clearance for ampicillin/sulbactam was 80.1 ± 7.7/83.3 ± 12.1 ml/min. The t(1/2) of ampicillin and sulbactam in patients with AKI undergoing ED were 2.8 ± 0.8 hours and 3.5 ± 1.5 hours, respectively. There was no significant accumulation using a twice-daily dosage of 2 g/1 g ampicillin/sulbactam.
Our data suggest that in patients treated with ED using a high-flux dialyzer (polysulphone, 1.3 m(2); blood and dialysate flow, 160 ml/min; treatment time, 480 minutes), a twice-daily dosing schedule of at least 2 g/1 g ampicillin/sulbactam, with one dose given after ED, should be used to avoid underdosing.
氨苄西林-舒巴坦固定抗菌合剂常用于各种感染。肾脏可清除约 71%的氨苄西林和 78%的舒巴坦。每周三次低通量血液透析的患者在透析时氨苄西林的半衰期为 2.3 小时,透析后为 17.4 小时。尽管氨苄西林-舒巴坦合剂在重症监护病房中频繁使用,但对于接受肾脏替代治疗的 AKI 患者,尚无可用的剂量推荐。本研究旨在评估接受延长透析(ED)的 AKI 危重症患者氨苄西林-舒巴坦的药代动力学,并为这种治疗方法建立剂量推荐。
设计、设置、参与者和测量:纳入了 12 例接受 ED 治疗的无尿性 AKI 危重症患者进行前瞻性、开放标签、观察性药代动力学研究。12 例患者单次给予氨苄西林-舒巴坦(2 g/1 g)后获得药代动力学数据。3 例患者在接受 4 天每天两次氨苄西林-舒巴坦(2 g/1 g)治疗后获得多次剂量药代动力学数据。
氨苄西林-舒巴坦的透析器清除率为 80.1±7.7/83.3±12.1 ml/min。ED 治疗的 AKI 患者氨苄西林和舒巴坦的半衰期分别为 2.8±0.8 小时和 3.5±1.5 小时。使用每天两次 2 g/1 g 氨苄西林-舒巴坦剂量无明显蓄积。
我们的数据表明,对于使用高通量透析器(聚砜,1.3 m2;血液和透析液流量 160 ml/min;治疗时间 480 分钟)进行 ED 治疗的患者,至少每天两次给予 2 g/1 g 氨苄西林-舒巴坦的剂量方案,在 ED 后给予一剂,应可避免剂量不足。