Risk of Community-Acquired Pneumonia in Veteran Patients to Whom Proton Pump Inhibitors Were Dispensed

被引:47
作者
Hermos, John A. [1 ,2 ]
Young, Melissa M. [1 ]
Fonda, Jennifer R. [1 ]
Gagnon, David R. [1 ,3 ]
Fiore, Louis D. [1 ,2 ]
Lawler, Elizabeth V. [1 ,4 ]
机构
[1] VA Boston Healthcare Syst, VA Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Pharmacoepidemiol Grp, Boston, MA USA
[2] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA
[3] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
关键词
BACTERIAL OVERGROWTH; GASTROESOPHAGEAL-REFLUX; ACID SUPPRESSION; ASSOCIATION; INFECTIONS; DISEASE; ADULTS; OLDER; MANAGEMENT; THERAPY;
D O I
10.1093/cid/cir767
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Observational studies linking proton pump inhibitor (PPI) exposure with community-acquired pneumonia (CAP) have reported either modest or no associations. Accordingly, we studied PPI exposure and CAP in veteran patients, using a retrospective, nested case-control design. Methods. From linked pharmacy and administrative databases of the New England Veterans Healthcare System, we identified 71 985 outpatients newly prescribed PPIs between 1998 and 2007; 1544 patients met criteria for CAP subsequent to PPI initiation; 15 440 controls were matched through risk-set sampling by age and time under observation. Crude and adjusted odds ratios comparing current with past PPI exposures, as well as tests for interactions, were conducted for the entire and stratified samples. Results. Current PPI use associated with CAP (adjusted odds ratio [OR], 1.29 [95% confidence interval {CI}, 1.15-1.45]). Risks were not substantially altered by age or year of diagnosis. Dementia (n = 85; P = .062 for interaction) and sedative/tranquilizer use (n = 224; P = .049 for interaction) were likely effect modifiers increasing a PPI-CAP association; conversely, for some chronic medical conditions, PPI-associated CAP risks were reversed. PPI exposures between 1 and 15 days increased CAP risks, compared with longer exposures, but PPI initiation also frequently occurred shortly after CAP diagnoses. Prescribed PPI doses.1 dose/day also increased PPI-associated CAP risks. Conclusions. Among the veterans studied, current compared with past PPI exposures associated modestly with increased risks of CAP. However, our observations that recent treatment initiation and higher PPI doses were associated with greater risks, and the inconsistent PPI-CAP associations between patient subgroups, indicate that further inquiries are needed to separate out coincidental patterns of associations.
引用
收藏
页码:33 / 42
页数:10
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