Gastric Acid Suppression Therapy and its Association with Peritoneal Dialysis-Associated Peritonitis in the Peritoneal Dialysis Outcomes and Practice Patterns Study (PDOPPS)

Author:

Goldman Shira123,Zhao Junhui4,Bieber Brian4,Pisoni Ronald L.4,Horowitz Laura5ORCID,Nessim Sharon J.6,Piraino Beth7ORCID,Lambie Mark8ORCID,Kanjanabuch Talerngsak9,Ito Yasuhiko10ORCID,Boudville Neil11ORCID,Teitelbaum Isaac12,Schreiber Martin13,Perl Jeffrey14,

Affiliation:

1. Division of Nephrology, St. Michael's Hospital, Toronto, Ontario, Canada

2. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

3. Department of Nephrology and Hypertension, Rabin Medical Center, Petach-Tikva, Israel

4. Arbor Research Collaborative for Health, Ann Arbor, MI, USA

5. Division of Nephrology, McGill University Health Center, Montreal, Quebec, Canada

6. Division of Nephrology, Jewish General Hospital, McGill University, Montreal, Quebec, Canada

7. Renal Electrolyte Division, University of Pittsburgh School of Medicine, Pittsburgh, PA

8. School of Medicine, Keele University, Keele, Staffordshire, United Kingdom.

9. Division of Nephrology, Department of Medicine, and Center of Excellence in Kidney Metabolic Disorders, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand

10. Department of Nephrology and Rheumatology, Aichi Medical University, Nagakute, Japan

11. Medical School, University of Western Australia, Perth, Australia

12. University of Colorado Hospital, Aurora, CO, USA

13. Davita Kidney Care, Denver, CO, USA

14. Department of Medicine, Division of Nephrology, St. Michael’s Hospital and the Keenan Research Center in the Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Ontario, Canada

Abstract

Background: Peritonitis is a major peritoneal dialysis (PD) related complication. We determined whether gastric acid suppression (GAS) (proton pump inhibitor (PPI) or histamine-2 receptor antagonists (H2RA)) use was associated with all-cause and organism-specific peritonitis in PD patients. Methods: In the Peritoneal Dialysis Outcomes and Practice Patterns Study (595 facilities, 8 countries, years 2014-2022), associations between GAS use and time to first episode of all-cause peritonitis were examined using Cox proportional hazards models. The primary exposure of interest was GAS, and secondarily PPI or H2RA use. Secondary outcomes were organism-specific peritonitis, peritonitis cure rates, and death. Results: Among patients (n=23 797) at study baseline, 6020 (25.3%) used PPIs, and 1382 (5.8%) used H2RAs. Overall risks of GAS use and peritonitis risk [adjusted hazard ratio (AHR)=1.05 (95% CI 0.98-1.13)], and use of PPI [AHR 1.06 (95% CI 0.99-1.14)] or H2RA [AHR 1.02 (95% CI 0.88-1.18)] did not reach statistical significance. In organism-specific analyses, GAS users displayed higher peritonitis risks for gram-negative (AHR 1.29, 95% CI 1.05-1.57), gram-positive (AHR 1.15, 95% CI 1.01-1.31), culture-negative (AHR 1.20, 95% CI 1.01-1.42), enteric (AHR 1.23, 95% CI 1.03-1.48), and particularly Streptococcal (AHR 1.47, 95% CI 1.15-1.89) peritonitis episodes. GAS was also associated with higher overall mortality [AHR 1.13 (95% CI 1.05-1.22)]. Conclusion: The association between GAS use and peritonitis risk was weaker (HR 1.05 [0.98-1.13]) than for streptococcal (HR 1.57 [1.15-1.89]) and gram-negative (HR 1.29 [1.05-1.57]) peritonitis. A better understanding of mechanisms surrounding the differential effects of GAS subtype on peritonitis risks is needed. Clinicians should be cautious when prescribing GAS. The impact of GAS deprescribing on peritonitis risk requires further evaluation.

Funder

AHRQ

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Psychiatry and Mental health,Neuropsychology and Physiological Psychology

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