Use of proton pump inhibitors and the risk of community-acquired pneumonia: a population-based case-control study

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Abstract

BACKGROUND: Recently, the use of proton pump inhibitors (PPIs) has been associated with an increased risk of pneumonia. We aimed to confirm this association and to identify the risk factors. METHODS: We conducted a population-based case-control study using data from the County of Funen, Denmark. Cases (n=7642) were defined as all patients with a first-discharge diagnosis of community-acquired pneumonia from a hospital during 2000 through 2004. We also selected 34 176 control subjects, who were frequency matched to the cases by age and sex. Data on the use of PPIs and other drugs, on microbiological samples, on x-ray examination findings, and on comorbid conditions were extracted from local registries. Confounders were controlled by logistic regression. RESULTS: The adjusted odds ratio (OR) associating current use of PPIs with community-acquired pneumonia was 1.5 (95% confidence interval [CI], 1.3-1.7). No association was found with histamine(2)-receptor antagonists (OR, 1.10; 95% CI, 0.8-1.3) or with past use of PPIs (OR, 1.2; 95% CI, 0.9-1.6). Recent initiation of treatment with PPIs (0-7 days before index date) showed a particularly strong association with community-acquired pneumonia (OR, 5.0; 95% 2.1-11.7), while the risk decreased with treatment that was started a long time ago (OR, 1.3; 95% CI, 1.2-1.4). Subgroup analyses revealed high ORs for users younger than 40 years (OR, 2.3; 95% CI, 1.3-4.0). No dose-response effect could be demonstrated. CONCLUSION: The use of PPIs, especially when recently begun, is associated with an increased risk of community-acquired pneumonia.
Original languageEnglish
JournalArchives of Internal Medicine
Volume167
Issue number9
Pages (from-to)950-955
Number of pages5
ISSN0003-9926
DOIs
Publication statusPublished - 14. May 2007

Keywords

  • Adult
  • Anti-Ulcer Agents
  • Case-Control Studies
  • Community-Acquired Infections
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Female
  • H(+)-K(+)-Exchanging ATPase
  • Humans
  • Male
  • Middle Aged
  • Pneumonia
  • Registries
  • Risk Factors

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