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首页> 外文期刊>Antimicrobial agents and chemotherapy. >High-dose continuous oxacillin infusion results in achievement of pharmacokinetics targets in critically ill patients with deep sternal wound infections following cardiac surgery
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High-dose continuous oxacillin infusion results in achievement of pharmacokinetics targets in critically ill patients with deep sternal wound infections following cardiac surgery

机译:大剂量连续奥沙西林输注可在心脏手术后深胸骨深部感染的危重患者中实现药代动力学目标

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摘要

Knowledge regarding antimicrobial therapy strategies in deep sternal wound infections (DSWI) following cardiac surgery is limited. Therefore, we aimed to determine the steady-state plasma and mediastinal concentrations of oxacillin administered by continuous infusion in critically ill patients with DSWI and to compare these concentrations with the susceptibility of staphylococci recovered. A continuous infusion of oxacillin (150 to 200 mg/kg of body weight/24 h) was administered after a loading dose (50 mg/kg). Plasma and mediastinal concentrations of total and unbound oxacillin were determined 4 h after the loading dose (H4) and then at day 1 (H24) and day 2 (H48). Twelve patients were included. Nine patients exhibited bacteremia, 5 were in septic shock, 8 were positive for Staphylococcus aureus, and 4 were positive for coagulase-negative staphylococci. The median MIC (first to third interquartile range) was 0.25 (0.24 to 0.41) mg/liter. Median plasma concentrations of total and unbound oxacillin at H4, H24, and H48 were, respectively, 64.4 (41.4 to 78.5) and 20.4 (12.4 to 30.4) mg/liter, 56.9 (31.4 to 80.6) and 21.7 (6.5 to 27.3) mg/liter, and 57.5 (32.2 to 85.1) and 20 (14.3 to 35.7) mg/liter. The median mediastinal concentrations of total and unbound oxacillin at H4, H24, and H48 were, respectively, 2.3 (0.7 to 25.9) and 0.9 (<0.5 to 15) mg/liter, 29.1 (19.7 to 38.2) and 12.6 (5.9 to 19.8) mg/liter, and 31.6 (14.9 to 42.9) and 17.1 (6.7 to 26.7) mg/liter. High-dose oxacillin delivered by continuous infusion is a valuable strategy to achieve our pharmacokinetic target (4 x MIC) at the site of action at H24. But concerns remain in cases of higher MICs, emphasizing the need for clinicians to obtain the MICs for the bacteria and to monitor oxacillin concentrations, especially the unbound forms, at the target site.
机译:关于心脏手术后深胸骨伤口感染(DSWI)中抗菌治疗策略的知识有限。因此,我们的目的是确定危重病DSWI患者连续输注奥沙西林的稳态血浆和纵隔浓度,并比较这些浓度与恢复的葡萄球菌敏感性。负荷剂量(50 mg / kg)后连续输注奥沙西林(150至200 mg / kg体重/ 24 h)。在负荷剂量(H4)后4小时,然后在第1天(H24)和第2天(H48)确定总和未结合的奥沙西林的血浆和纵隔浓度。包括十二名患者。 9名患者出现菌血症,败血症性休克5例,金黄色葡萄球菌阳性8例,凝固酶阴性葡萄球菌阳性4例。中值MIC(第一至第三四分位数范围)为0.25(0.24至0.41)毫克/升。 H4,H24和H48时总和未结合的奥沙西林血浆中位数浓度分别为64.4(41.4至78.5)和20.4(12.4至30.4)mg / L,56.9(31.4至80.6)和21.7(6.5至27.3)mg / L /升,以及57.5(32.2至85.1)和20(14.3至35.7)毫克/升。 H4,H24和H48时总和未结合的奥沙西林的纵隔中位浓度分别为2.3(0.7至25.9)和0.9(<0.5至15)mg / L,29.1(19.7至38.2)和12.6(5.9至19.8)毫克/升,以及31.6(14.9至42.9)和17.1(6.7至26.7)毫克/升。连续输注大剂量奥沙西林是在H24的作用部位实现我们的药代动力学目标(4 x MIC)的重要策略。但是,对于MIC较高的情况,仍然存在担忧,强调临床医生需要获得细菌的MIC,并需要监测目标部位的奥沙西林浓度,尤其是未结合形式。

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