Australia and New Zealand Dialysis and Transplant Registry, Adelaide, Australia.
Clin J Am Soc Nephrol. 2013 Sep;8(9):1556-63. doi: 10.2215/CJN.12361212. Epub 2013 Aug 15.
The effect of biocompatible peritoneal dialysis (PD) solutions on PD-related peritonitis is unclear. This study sought to evaluate the relationship between use of biocompatible solutions and the probability of occurrence or clinical outcomes of peritonitis.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: The study included all incident Australian patients receiving PD between January 1, 2007, and December 31, 2010, using Australia and New Zealand Dialysis and Transplant Registry data. All multicompartment PD solutions of neutral pH were categorized as biocompatible solutions. The independent predictors of peritonitis and the use of biocompatible solutions were determined by multivariable, multilevel mixed-effects Poisson and logistic regression analysis, respectively. Sensitivity analyses, including propensity score matching, were performed.
Use of biocompatible solutions gradually declined (from 7.5% in 2007 to 4.2% in 2010), with preferential use among smaller units and among younger patients without diabetes mellitus. Treatment with biocompatible solution was associated with significantly greater overall rate of peritonitis (0.67 versus 0.47 episode per patient-year; incidence rate ratio, 1.49; 95% confidence interval [CI], 1.19 to 1.89) and with shorter time to first peritonitis (hazard ratio [HR], 1.48; 95% CI, 1.17 to 1.87), a finding replicated in propensity score-matched cohorts (HR, 1.36; 95% CI, 1.09 to 1.71).
In an observational registry study, use of biocompatible PD solutions was associated with higher overall peritonitis rates and shorter time to first peritonitis. Further randomized studies adequately powered for a primary peritonitis outcome are warranted.
生物相容性腹膜透析(PD)溶液对 PD 相关腹膜炎的影响尚不清楚。本研究旨在评估使用生物相容性溶液与腹膜炎发生或临床结局的概率之间的关系。
设计、设置、参与者和测量:该研究纳入了 2007 年 1 月 1 日至 2010 年 12 月 31 日期间使用澳大利亚和新西兰透析和移植登记处数据接受 PD 的所有新发病例澳大利亚患者。所有中性 pH 值的多腔 PD 溶液均归类为生物相容性溶液。通过多变量、多层次混合效应泊松和逻辑回归分析分别确定腹膜炎和生物相容性溶液使用的独立预测因素。进行了敏感性分析,包括倾向评分匹配。
生物相容性溶液的使用逐渐减少(从 2007 年的 7.5%降至 2010 年的 4.2%),在较小的单位和无糖尿病的年轻患者中更倾向于使用。使用生物相容性溶液与腹膜炎的总发生率显著增加相关(0.67 与 0.47 例/患者-年;发病率比,1.49;95%置信区间 [CI],1.19 至 1.89),且首次腹膜炎的时间更短(风险比 [HR],1.48;95%CI,1.17 至 1.87),这一发现在倾向评分匹配队列中得到了复制(HR,1.36;95%CI,1.09 至 1.71)。
在观察性登记研究中,使用生物相容性 PD 溶液与更高的总腹膜炎发生率和首次腹膜炎的时间更短相关。需要进一步进行充分针对原发性腹膜炎结局的随机研究。