Related Experiment Video
Updated: Apr 1, 2026

A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment
Published on: May 25, 2017
Comparative Safety of Potassium-Competitive Acid Blockers on the Risk of Clostridioides difficile Infection: A
Gyeongmin Lim1, Ju-Young Shin1,2,3, Da Eun Hyeon4
1Department of Biohealth Regulatory Science, Sungkyunkwan University, Suwon, Republic of Korea.
Introduction:
Proton pump inhibitors (PPIs) have been associated with an increased risk of Clostridioides difficile infection (CDI) in previous observational studies. However, real-world evidence on the CDI risk of potassium-competitive acid blockers (P-CABs), a newer class of acid suppressive agents, remains limited.
Methods:
We conducted a retrospective cohort study using electronic health record data from 15 hospitals standardized to the Observational Medical Outcomes Partnership Common Data Model and integrated through Federated E-Health Big Data for Evidence Renovation Network. Patients newly prescribed P-CABs, proton pump inhibitors (PPIs), or histamine 2 receptor antagonists (H2RAs) were included and the primary outcome was the occurrence of CDI. After 1:4 propensity score matching, pairwise comparisons were conducted using Cox proportional hazards models. Hazard ratios (HRs) and 95% confidence intervals (CIs) were then pooled across databases by meta-analysis.
Results:
In the 1:4 matched cohorts, we identified 61,596 P-CAB users (mean follow-up, 72.6 ± 29.9 days) and 132,683 PPI users (74.9 ± 28.6 days), 42,794 P-CAB users (69.5 ± 32.4 days) and 89,415 H2RA users (69.9 ± 33.1 days), and 85,686 PPI users (71.1 ± 31.2 days) and 159,178 H2RA users (68.0 ± 33.8 days) across the 3 pairwise comparisons. The pooled HRs were 0.87 (95% CI, 0.69-1.10) for P-CABs vs PPIs, 0.85 (0.64-1.12) for P-CABs vs H2RAs, and 1.13 (0.98-1.29) for PPIs vs H2RAs. Results were generally consistent across subgroup and sensitivity analyses.
Discussion:
In this cohort study, P-CAB use was not associated with a higher risk of CDI compared with PPIs or H2RAs.
More Related Videos
09:12A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection
Published on: June 15, 2018
06:51Cefoperazone-treated Mouse Model of Clinically-relevant Clostridium difficile Strain R20291
Published on: December 10, 2016
Related Concept Videos
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers
Acid Suppressive Drugs for Peptic Ulcer Disease: Proton Pump Inhibitors
Gastric acid, a potent cocktail of hydrogen and chloride ions, is produced in specialized parietal cells within the...
Acid Suppressive Drugs for Peptic Ulcer Disease: Antacids
However, this neutralization reaction between...
Antihypertensive Drugs: Potassium-Sparing Diuretics
Acid Suppressive Drugs for Peptic Ulcer Disease: Histamine H2-Receptor Antagonists