首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Intraperitoneal vancomycin concentrations during peritoneal dialysis-associated peritonitis: Correlation with serum levels
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Intraperitoneal vancomycin concentrations during peritoneal dialysis-associated peritonitis: Correlation with serum levels

机译: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

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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 (IP) 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).
机译:背景:为治疗腹膜透析相关性腹膜炎(PDP),已建议万古霉素的血清浓度保持在12 mg / L-15 mg / L以上。但是,有关活动性感染期间血清和腹膜透析液流出物(PDE)中万古霉素浓度的研究很少。我们进行了本研究以调查此问题,并确定达到推荐的万古霉素血清水平是否会导致腹膜内治疗水平。方法:我们研究了接受腹膜内(IP)万古霉素治疗非革兰氏阴性PDP的患者。我们在演示时给予了单剂量(约30 mg / kg),随后在第5天测量了PDE中万古霉素的水平;我们想确定在4小时的停留时间内万古霉素从血清到PDE的流出是否一致并达到治疗水平。结果:在研究的48次PDP发作中,有98%的患者血清万古霉素浓度达到12 mg / L以上,但11例患者(23%)的PDE万古霉素水平低于4 mg / L-最低抑菌浓度(在第5天的4小时停留结束时观察到了许多革兰氏阳性生物的MIC。血清中万古霉素浓度与PDE的相关性(4小时以上的抗生素流出)具有统计学意义,但差(R 2 = 0.18)。结论:我们的数据支持国际腹膜透析协会的说法,即间歇给药(每5天一次)可达到足够的血清万古霉素浓度,但不能保证治疗PDP时的治疗性PDE水平。万古霉素的间歇给药可能不会始终导致PDE浓度明显高于许多重要病原体的MIC。尽管这一发现的临床意义尚待确定,但对于患有PDP的成人(目前建议用于儿童),更小剂量但更频繁的PDE万古霉素(连续给药)剂量可能更可取。

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