Association of Biocompatible Peritoneal Dialysis Solutions with Peritonitis Risk, Treatment, and Outcomes

被引:23
作者
Cho, Yeoungjee [1 ,2 ]
Badve, Sunil V. [1 ,2 ]
Hawley, Carmel M. [1 ,2 ]
McDonald, Stephen P. [1 ,3 ]
Brown, Fiona G. [1 ,4 ]
Boudville, Neil [1 ,5 ]
Bannister, Kym M. [1 ,6 ]
Clayton, Philip A. [1 ,7 ,8 ]
Johnson, David W. [1 ,2 ]
机构
[1] Australia & New Zealand Dialysis & Transplant Reg, Adelaide, SA, Australia
[2] Univ Queensland, Princess Alexandra Hosp, Ctr Kidney Dis Res, Brisbane, Qld, Australia
[3] Univ Adelaide, Discipline Med, Adelaide, SA, Australia
[4] Monash Med Ctr, Dept Nephrol, Melbourne, Vic, Australia
[5] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6009, Australia
[6] Royal Adelaide Hosp, Dept Nephrol, Adelaide, SA 5000, Australia
[7] Royal Prince Alfred Hosp, Dept Renal Med, Sydney, NSW, Australia
[8] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2013年 / 8卷 / 09期
关键词
GLUCOSE-DEGRADATION PRODUCTS; RESIDUAL RENAL-FUNCTION; TO-MESENCHYMAL TRANSITION; MESOTHELIAL CELLS; LONG-TERM; CAPD PATIENTS; IN-VITRO; EX-VIVO; PATIENT SURVIVAL; STANDARD FLUID;
D O I
10.2215/CJN.12361212
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Background and objectivesThe 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, & measurementsThe 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.ResultsUse 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).ConclusionsIn 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.
引用
收藏
页码:1556 / 1563
页数:8
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