Intraperitoneal vancomycin concentrations during peritoneal dialysis-associated peritonitis: correlation with serum levels.

Richard Fish, Robert Nipah, Chris Jones, Hazel Finney, Stanley L S Fan
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引用次数: 25

Abstract

Background: For the treatment of peritoneal dialysis-associated peritonitis (PDP), it has been suggested that serum concentrations of vancomycin be kept above 12 mg/L-15 mg/L. However, studies correlating vancomycin concentrations in serum and peritoneal dialysate effluent (PDE) during active infection are sparse. We undertook the present study to investigate this issue and to determine whether achieving the recommended serum level of vancomycin results in therapeutic levels intraperitoneally.

Methods: We studied patients treated with intraperitoneal (i.p.) vancomycin for non-gram-negative PDP. We gave a single dose (approximately 30 mg/kg) at presentation, and we subsequently measured vancomycin levels in PDE on day 5; we wanted to determine if efflux of vancomycin from serum to PDE during a 4-hour dwell was consistent and resulted in therapeutic levels.

Results: Of the 48 episodes of PDP studied, serum vancomycin concentrations exceeding 12 mg/L were achieved in 98% of patients, but in 11 patients (23%), a PDE vancomycin level below 4 mg/L--the minimal inhibitory concentration (MIC) of many gram-positive organisms--was observed at the end of a 4-hour dwell on day 5. The correlation between the concentrations of vancomycin in serum and PDE (from efflux of antibiotic over 4 hours) was statistically significant, but poor (R(2) = 0.18).

Conclusions: Our data support the International Society for Peritoneal Dialysis statement that adequate serum vancomycin concentrations can be achieved with intermittent dosing (single dose every 5 days), but cannot guarantee therapeutic PDE levels in the treatment of PDP. Intermittent dosing of vancomycin may not consistently result in PDE concentrations markedly greater than MIC of many important pathogens. Although the clinical significance of this finding remains to be determined, it may be preferable to give smaller but more frequent doses of PDE vancomycin (continuous dosing) for adults with PDP (as is currently recommended for children).

腹膜透析相关性腹膜炎期间腹膜内万古霉素浓度:与血清水平的相关性。
背景:对于腹膜透析相关性腹膜炎(PDP)的治疗,建议血清万古霉素浓度保持在12mg /L- 15mg /L以上。然而,关于活动性感染期间血清和腹膜透析液流出物(PDE)中万古霉素浓度相关性的研究很少。我们进行本研究是为了调查这一问题,并确定达到推荐的血清万古霉素水平是否会导致腹腔内治疗水平的提高。方法:采用万古霉素腹腔注射治疗非革兰氏阴性PDP患者。我们在就诊时给予单剂量(约30 mg/kg),随后在第5天测量PDE中的万古霉素水平;我们想确定4小时内万古霉素从血清到PDE的外排是否一致并导致治疗水平。结果:在研究的48例PDP发作中,98%的患者血清万古霉素浓度超过12mg /L,但在11例患者(23%)中,PDE万古霉素水平低于4mg /L——许多革兰氏阳性生物的最小抑制浓度(MIC)——在第5天4小时的观察结束时被观察到。血清万古霉素浓度与PDE (4 h以上抗生素外排)的相关性有统计学意义,但较差(R(2) = 0.18)。结论:我们的数据支持国际腹膜透析学会的声明,即间歇给药(每5天给药一次)可以达到足够的血清万古霉素浓度,但不能保证PDP治疗中PDE的治疗水平。间歇性给药万古霉素可能不会始终导致PDE浓度显著高于许多重要病原体的MIC。虽然这一发现的临床意义仍有待确定,但对于患有PDP的成人(目前推荐用于儿童),可能更可取的是给予较小但更频繁的PDE万古霉素(连续给药)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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