Department of Urology, Hôpital européen Georges-Pompidou (HEGP), Assistance Publique-Hôpitaux de Paris (AP-HP), 20-40 rue Leblanc, 75015 Paris, France; Université Paris Descartes, Sorbonne Paris Cité, Faculté de médecine, 15 rue de l'École de Médecine, 75006 Paris, France.
Clinical Pharmacy Department, HU Necker-Enfants malades, AP-HP, 149 rue de Sèvres, 75746 Paris, France.
Int J Antimicrob Agents. 2016 Aug;48(2):168-74. doi: 10.1016/j.ijantimicag.2016.04.027. Epub 2016 Jun 2.
The incidence of urinary tract infections caused by extended-spectrum β-lactamase (ESBL)-producing pathogens is increasing. These infections are associated with a long hospital stay in patients undergoing urological procedures. We aimed to demonstrate that significant intraprostatic diffusion of ertapenem is achieved after a single preoperative administration. A referred sample of 19 patients requiring surgery for benign prostatic hyperplasia was prospectively included. Patients received a 1 g intravenous (i.v.) dose of ertapenem 1 h (n = 10, group A) or 12 h (n = 9, group B) before blood and prostatic samples were collected. Plasma and intraprostatic concentrations of ertapenem were measured using LC-MS/MS. Intraprostatic concentrations were considered satisfactory when higher than the MIC90 value of urinary-targeted pathogens perioperatively and for 40% of the dosing interval. The Wilcoxon test and a pharmacokinetic predictive model were used. Median plasma concentrations of ertapenem were 144.3 mg/L (95% CI 126.5-157.9) in group A and 30.7 mg/L (95% CI 22.9-36.4) in group B (P < 0.001); median intraprostatic concentrations were 16.6 mg/L (95% CI 13.3-31.4 mg/L) and 4.2 mg/L (95% CI 3.1-4.9 mg/L), respectively (P < 0.001), which were above the MIC90 values of bacteria, including ESBL-producers, during surgery and for 40% of the dosing interval. The plasma-to-prostate concentration ratio was not significantly different between groups (P = 0.97). Single-dose i.v. ertapenem reached satisfactory intraprostatic concentrations, suggesting that it could be a relevant prophylactic strategy for carriers of ESBL-producing bacteria undergoing prostatic procedures, which needs to be confirmed by further prospective trials.
产超广谱β-内酰胺酶(ESBL)的病原体引起的尿路感染发病率正在上升。这些感染与接受泌尿科手术的患者住院时间延长有关。我们旨在证明单次术前给药后,厄他培南可在前列腺内实现显著扩散。前瞻性纳入了 19 名因良性前列腺增生症需要手术的患者。患者在手术前 1 小时(n=10,A 组)或 12 小时(n=9,B 组)静脉注射(i.v.)1 克厄他培南,然后采集血样和前列腺样本。采用 LC-MS/MS 测定厄他培南的血浆和前列腺内浓度。如果前列腺内浓度高于围手术期尿靶向病原体的 MIC90 值和 40%的给药间隔时间,则认为前列腺内浓度令人满意。采用 Wilcoxon 检验和药代动力学预测模型。A 组的厄他培南中位血浆浓度为 144.3mg/L(95%CI 126.5-157.9),B 组为 30.7mg/L(95%CI 22.9-36.4)(P<0.001);前列腺内浓度中位数分别为 16.6mg/L(95%CI 13.3-31.4mg/L)和 4.2mg/L(95%CI 3.1-4.9mg/L)(P<0.001),在手术期间和 40%的给药间隔时间内均高于细菌(包括产 ESBL 菌)的 MIC90 值。两组间的血浆与前列腺浓度比值无显著差异(P=0.97)。单次静脉注射厄他培南可达到满意的前列腺内浓度,提示其可能是前列腺手术中携带产 ESBL 菌患者的一种相关预防策略,需要进一步的前瞻性试验来证实。