The association between peritoneal dialysis modality and peritonitis

Patrick G Lan, David W Johnson, Stephen P McDonald, Neil Boudville, Monique Borlace, Sunil V Badve, Kamal Sud, Philip A Clayton, Patrick G Lan, David W Johnson, Stephen P McDonald, Neil Boudville, Monique Borlace, Sunil V Badve, Kamal Sud, Philip A Clayton

Abstract

Background and objectives: There is conflicting evidence comparing peritonitis rates among patients treated with continuous ambulatory peritoneal dialysis (CAPD) or automated peritoneal dialysis (APD). This study aims to clarify the relationship between peritoneal dialysis (PD) modality (APD versus CAPD) and the risk of developing PD-associated peritonitis.

Design, setting, participants, & measurements: This study examined the association between PD modality (APD versus CAPD) and the risks, microbiology, and clinical outcomes of PD-associated peritonitis in 6959 incident Australian PD patients between October 1, 2003, and December 31, 2011, using data from the Australia and New Zealand Dialysis and Transplant Registry. Median follow-up time was 1.9 years.

Results: Patients receiving APD were younger (60 versus 64 years) and had fewer comorbidities. There was no association between PD modality and time to first peritonitis episode (adjusted hazard ratio [HR] for APD versus CAPD, 0.98; 95% confidence interval [95% CI], 0.91 to 1.07; P=0.71). However, there was a lower hazard of developing Gram-positive peritonitis with APD than CAPD, which reached borderline significance (HR, 0.90; 95% CI, 0.80 to 1.00; P=0.05). No statistically significant difference was found in the risk of hospitalizations (odds ratio, 1.12; 95% CI, 0.93 to 1.35; P=0.22), but there was a nonsignificant higher likelihood of 30-day mortality (odds ratio, 1.33; 95% CI, 0.93 to 1.88; P=0.11) at the time of the first episode of peritonitis for patients receiving APD. For all peritonitis episodes (including subsequent episodes of peritonitis), APD was associated with lower rates of culture-negative peritonitis (incidence rate ratio [IRR], 0.81; 95% CI, 0.69 to 0.94; P=0.002) and higher rates of gram-negative peritonitis (IRR, 1.28; 95% CI, 1.13 to 1.46; P=0.01).

Conclusions: PD modality was not associated with a higher likelihood of developing peritonitis. However, APD was associated with a borderline reduction in the likelihood of a first episode of Gram-positive peritonitis compared with CAPD, and with lower rates of culture-negative peritonitis and higher rates of Gram-negative peritonitis. Peritonitis outcomes were comparable between both modalities.

Keywords: peritoneal dialysis; peritonitis; registry study.

Copyright © 2014 by the American Society of Nephrology.

Figures

Figure 1.
Figure 1.
APD use over time: the proportion of incident Australian PD patients using APD according to time spent on PD during the period from 2003 to 2011. APD, automated peritoneal dialysis; CAPD, continuous ambulatory peritoneal dialysis; PD, peritoneal dialysis.
Figure 2.
Figure 2.
Association between APD (versus CAPD) and peritonitis-associated outcomes in incident Australian PD patients during the period from 2003 to 2011. All estimates are adjusted for previous RRT before PD, age, race, body mass index, diabetes mellitus, coronary artery disease, cigarette smoking, and cerebrovascular disease. Outcome of first infection also adjusted for organism. 95% CI, 95% confidence interval; HD, hemodialysis; HR, hazard ratio; IRR, incidence rate ratio; OR, odds ratio.

Source: PubMed

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