首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Comparison of vancomycin versus cefazolin as initial therapy for peritonitis in peritoneal dialysis patients.
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Comparison of vancomycin versus cefazolin as initial therapy for peritonitis in peritoneal dialysis patients.

机译:万古霉素与头孢唑林作为腹膜透析患者腹膜炎初始治疗的比较。

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The incidence of peritonitis ranges from 1 episode every 24 patient treatment months to 1 episode every 60 patient treatment months [Keane WF, et al. ISPD Guidelines/Recommendations. Adult peritoneal dialysis-related peritonitis treatment recommendations: 2000 update. Perit Dial Int 2000; 20:396-411.]. Gram-positive organisms account for over 80% of continuous ambulatory peritoneal dialysis (PD)-associated peritonitis. Recent fear of vancomycin-resistant enterococci (VRE) has prompted suggestions of limiting vancomycin use. Fifty-one episodes of peritonitis in 30 patients studied over 2 years were evaluated. Cloudiness of the PD fluid and/or abdominal pain were considered suggestive of peritonitis and were confirmed by cell count and culture. Baseline cell count, Gram stain, and cultures were obtained, with periodic follow-up. Patients were randomized to receive either vancomycin 1 g/L intraperitoneally (IP) as loading dose, repeated on day 5 or day 8, depending on residual renal function, for 2 weeks, or cefazolin 1 g in the first PD bag and continued with 125 mg/L every exchange for 2 or 3 weeks, depending on culture results. All patients also received gentamicin 40 mg IP every day until the culture results were available. A similar randomized trial comparing vancomycin and cefazolin in the past used a lower concentration of cefazolin 50 mg/L [Flanigan MJ, Lim VS. Initial treatment of dialysis associated peritonitis: a controlled trial of vancomycin versus cefazolin. Perit Dial t 1991; 11:31-7.]. Peritoneal dialysate fluid cultures revealed 31(60.7%) gram-positive organisms, 7(13.7%) gram-negative organisms, and 2 (3.9%) cultured yeast; 11 (21.5%) cultures yielded no growth. The incidence of peritonitis at our center was 1 episode every 42 patient treatment months. No case of VRE was noted. There was no statistical difference in clinical response or relapse rate for the two protocols. It was the authors' and nurses' observation that patient compliance and satisfaction was better with vancomycin, and the cost per treatment was 23% less than cefazolin. Based on these data we believe vancomycin should still be considered for first-line treatment of PD-associated peritonitis.
机译:腹膜炎的发生率范围为每24个患者治疗月1次发作至每60个患者治疗月1次发作[Keane WF等。 ISPD准则/建议。成人腹膜透析相关性腹膜炎的治疗建议:2000年更新。 Perit Dial Int 2000; 20:396-411。]。革兰氏阳性菌占持续性非卧床腹膜透析(PD)相关性腹膜炎的80%以上。最近对耐万古霉素的肠球菌(VRE)的恐惧提示了限制使用万古霉素的建议。评估了在2年中研究的30例患者中的51例腹膜炎发作。 PD液体混浊和/或腹痛被认为提示腹膜炎,并通过细胞计数和培养得到证实。获得基线细胞计数,革兰氏染色和培养物,并定期随访。患者随机接受腹膜内(IP)万古霉素(IP)负荷剂量,根据残余肾功能在第5天或第8天重复2周,或在第一个PD袋中接受头孢唑林1 g并继续125每次交换2 mg / L,持续2或3周,具体取决于培养结果。所有患者还每天接受庆大霉素40 mg IP腹腔注射,直到获得培养结果为止。过去类似的一项比较万古霉素和头孢唑林的随机试验使用的头孢唑林浓度较低,为50 mg / L [Flanigan MJ,Lim VS.透析相关腹膜炎的初始治疗:万古霉素与头孢唑林的对照试验。 Perit Dial / nt 1991; 11:31-7。]。腹膜透析液培养显示31(60.7%)革兰氏阳性菌,7(13.7%)革兰氏阴性菌和2(3.9%)酵母菌。 11(21.5%)个培养物未见生长。在我们中心,腹膜炎的发生率为每42个月患者治疗1次。没有记录到VRE的情况。两种方案的临床反应或复发率无统计学差异。作者和护士的观察表明,万古霉素可使患者的依从性和满意度更好,并且每次治疗的费用比头孢唑林少23%。基于这些数据,我们认为万古霉素仍应考虑用于PD相关性腹膜炎的一线治疗。

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