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Proton pump inhibitors and peritoneal dialysis-associated peritonitis: a cohort study in Newcastle, Australia
Kate Richards1, Eswari Vilayur1,2
1Nephrology and Transplantation Unit, John Hunter Hospital, Newcastle, New South Wales, Australia.
Insights
Proton pump inhibitors (PPIs) did not increase the risk of peritonitis in patients undergoing peritoneal dialysis (PD). This study found no association between PPI use and peritonitis rates in a local PD cohort.
Area of Science:
- Nephrology
- Gastroenterology
- Pharmacology
Background:
- Peritoneal dialysis (PD)-associated peritonitis leads to severe complications, including hospitalization, PD cessation, and mortality.
- Proton pump inhibitors (PPIs) are frequently prescribed to dialysis patients, despite previous studies suggesting a potential link to increased peritonitis risk.
Purpose of the Study:
- To investigate the association between PPI use and the risk of overall peritonitis in patients receiving PD.
- To evaluate if PPI exposure influences the incidence of peritonitis within a specific patient cohort.
Main Methods:
- A retrospective analysis of incident PD patients from 2012 to 2021 at a single Australian center.
- Patients were categorized based on PPI exposure, and multivariate Cox proportional hazard modeling was employed to assess the impact on time to first peritonitis.
- Peritonitis rates per patient-year were compared between PPI-exposed and unexposed groups.
Main Results:
- Out of 219 patients, 94 were exposed to PPIs. Peritonitis occurred in 42.6% of the PPI group versus 44.8% of the unexposed group.
- PPI use was not significantly associated with an increased risk of time to first peritonitis (HR 0.78; P=.2).
- Exploratory analysis indicated a potential association between atherosclerotic vascular disease and peritonitis.
Conclusions:
- In this cohort, PPI use was not found to be associated with an increased risk of peritonitis.
- Further research is warranted to reconcile conflicting findings across studies and explore potential organism-specific effects of PPIs on peritonitis risk.
Background:
Peritoneal dialysis (PD)-associated peritonitis results in poor outcomes, including hospitalisation, PD discontinuation and death. Proton pump inhibitors (PPIs) have been linked to an increased risk of organism-specific and/or overall peritonitis in prior studies, yet they are commonly prescribed in the dialysis population.
Aims:
To evaluate whether PPIs are associated with an increased risk of overall peritonitis in a local cohort.
Methods:
We retrospectively identified patients with incident PD at a single Australian centre between 2012 and 2021. Baseline comorbidities, medications and PD outcomes were recorded. Patients were stratified by PPI exposure. We assessed whether PPI use affected time to first peritonitis using multivariate Cox proportional hazard modelling. The overall rate of peritonitis per patient-year was compared between groups.
Results:
Of 219 patients, 94 were exposed to PPIs, of whom 40 of 94 (42.6%) developed peritonitis, compared to 56 of 125 (44.8%) of the unexposed group. PPI use was not associated with time to first peritonitis in a multivariate Cox analysis (hazard ratio 0.78 (95% confidence interval 0.51-1.18), P = 0.2). The peritonitis rate was marginally lower in the PPI group. Atherosclerotic vascular disease was associated with peritonitis in an exploratory analysis.
Conclusions:
PPI use was not associated with peritonitis risk in this cohort. Further work is needed to explain the discrepant findings between studies to date, including whether PPIs modulate the risk of peritonitis caused by specific organisms.
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