PMID- 28085910 OWN - NLM STAT- MEDLINE DCOM- 20170808 LR - 20181113 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 12 IP - 1 DP - 2017 TI - Histamine H2-Blocker and Proton Pump Inhibitor Use and the Risk of Pneumonia in Acute Stroke: A Retrospective Analysis on Susceptible Patients. PG - e0169300 LID - 10.1371/journal.pone.0169300 [doi] LID - e0169300 AB - BACKGROUND: Although histamine H2-blockers (H2B) and proton pump inhibitors (PPI) are used commonly to prevent gastrointestinal bleeding in acute stroke, they are implicated in the increased risk of pneumonia in other disease populations. In acute stroke, the presence of distinctive risk factors of pneumonia, including dysphagia and impaired consciousness, makes inclusive analysis vulnerable to confounding. Our aim was to assess whether acid-suppressive drugs increase pneumonia in acute stroke in a population controlled for confounding. METHODS: We analyzed acute stroke patients admitted to a tertiary care hospital. To minimize confounding, we only included subjects who could not feed orally during 14 days of hospitalization. Exposure was defined as H2B or PPI, given in days; the outcome was development of pneumonia within this period. The incidence was calculated from the total number of pneumonias divided by the sum of person-days at risk. We additionally performed multivariate Poisson regression and propensity score analyses, although the restriction largely eliminated the need for multivariate adjustment. RESULTS: A total of 132 pneumonias occurred in 3582 person-days. The incidence was 3.69%/person-day (95% confidence interval (CI); 3.03-4.37%/day). All subjects had dysphagia. Stroke severity and consciousness disturbances were well-balanced between the groups exposed to H2B, PPI, or none. The relative risk (RR) compared with the unexposed was 1.22 in H2B (95%CI; 0.83-1.81) and 2.07 in PPI (95% CI; 1.13-3.62). The RR of PPI compared with H2B was 1.69 (95%CI; 0.95-2.89). In multivariate regression analysis, the RRs of H2B and PPI were 1.24 (95% CI; 0.85-1.81) and 2.00 (95% CI; 1.12-3.57), respectively; in propensity score analyses they were 1.17 (95% CI; 0.89-1.54) and 2.13 (95% CI; 1.60-2.84). CONCLUSIONS: The results of this study suggested that prophylactic acid-suppressive therapy with PPI may have to be avoided in acute stroke patients susceptible to pneumonia. FAU - Arai, Nobuhiko AU - Arai N AD - Department of Neurological Surgery, Hiratsuka City Hospital, Hiratsuka City, Kanagawa, Japan. FAU - Nakamizo, Tomoki AU - Nakamizo T AD - Department of Neurology, Hiratsuka City Hospital, Hiratsuka City, Kanagawa, Japan. FAU - Ihara, Hikaru AU - Ihara H AD - Department of Neurology, Hiratsuka City Hospital, Hiratsuka City, Kanagawa, Japan. FAU - Koide, Takashi AU - Koide T AD - Department of Neurology, Hiratsuka City Hospital, Hiratsuka City, Kanagawa, Japan. FAU - Nakamura, Akiyoshi AU - Nakamura A AD - Department of Neurological Surgery, Hiratsuka City Hospital, Hiratsuka City, Kanagawa, Japan. FAU - Tabuse, Masanao AU - Tabuse M AD - Department of Neurological Surgery, Hiratsuka City Hospital, Hiratsuka City, Kanagawa, Japan. FAU - Miyazaki, Hiromichi AU - Miyazaki H AD - Department of Neurological Surgery, Hiratsuka City Hospital, Hiratsuka City, Kanagawa, Japan. LA - eng PT - Journal Article PT - Observational Study DEP - 20170113 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Histamine H2 Antagonists) RN - 0 (Proton Pump Inhibitors) RN - 820484N8I3 (Histamine) SB - IM MH - Aged MH - Aged, 80 and over MH - Female MH - Histamine/*chemistry MH - Histamine H2 Antagonists/*adverse effects MH - Hospitalization MH - Humans MH - Incidence MH - Japan/epidemiology MH - Male MH - Pneumonia/chemically induced/*epidemiology MH - Propensity Score MH - Proton Pump Inhibitors/*adverse effects MH - Retrospective Studies MH - Risk Factors MH - Stroke/complications/*drug therapy PMC - PMC5234823 COIS- The authors have declared that no competing interests exist. EDAT- 2017/01/14 06:00 MHDA- 2017/08/09 06:00 PMCR- 2017/01/13 CRDT- 2017/01/14 06:00 PHST- 2016/07/18 00:00 [received] PHST- 2016/12/14 00:00 [accepted] PHST- 2017/01/14 06:00 [entrez] PHST- 2017/01/14 06:00 [pubmed] PHST- 2017/08/09 06:00 [medline] PHST- 2017/01/13 00:00 [pmc-release] AID - PONE-D-16-28755 [pii] AID - 10.1371/journal.pone.0169300 [doi] PST - epublish SO - PLoS One. 2017 Jan 13;12(1):e0169300. doi: 10.1371/journal.pone.0169300. eCollection 2017.