Department of Public Health Sciences, School of Public Health, University of Alberta, Edmonton, Alberta, Canada.
Am J Med. 2010 Jan;123(1):47-53. doi: 10.1016/j.amjmed.2009.05.032.
Several studies suggest that proton pump inhibitors (PPIs) and histamine 2-receptor antagonists (H2s) increase risk of community-acquired pneumonia. To test this hypothesis, we examined a prospective population-based cohort predisposed to pneumonia: elderly patients (> or =65 years) who had survived hospitalization for pneumonia.
This study featured a nested case-control design where cases were patients hospitalized for recurrent pneumonia (> or =30 days after initial episode) and controls were age, sex, and incidence-density sampling matched but never had recurrent pneumonia. PPI/H2 exposure was classified as never, past, or current use before recurrent pneumonia. The association between PPI/H2s and pneumonia was assessed using multivariable conditional logistic regression.
During 5.4 years of follow-up, 248 recurrent pneumonia cases were matched with 2476 controls. Overall, 71 of 608 (12%) current PPI/H2 users had recurrent pneumonia, compared with 130 of 1487 (8%) nonusers (adjusted odds ratio [aOR] 1.5; 95% confidence interval [CI], 1.1-2.1). Stratifying the 608 current users according to timing of PPI/H2 initiation revealed incident current-users (initiated PPI/H2 after initial pneumonia hospitalization, n=303) bore the entire increased risk of recurrent community-acquired pneumonia (15% vs 8% among nonusers, aOR 2.1; 95% CI, 1.4-3.0). The 305 prevalent current-users (PPI/H2 exposure before and after initial community-acquired pneumonia hospitalization) were equally likely to develop recurrent pneumonia as nonusers (aOR 0.99; 95% CI, 0.63-1.57).
Acid-suppressing drug use substantially increased the likelihood of recurrent pneumonia in high-risk elderly patients. The association was confined to patients initiating PPI/H2s after hospital discharge. Our findings should be considered when deciding to prescribe these drugs in patients with a recent history of pneumonia.
多项研究表明质子泵抑制剂(PPIs)和组胺 2 受体拮抗剂(H2s)会增加社区获得性肺炎的风险。为了验证这一假说,我们研究了一个易患肺炎的前瞻性基于人群的队列:曾因肺炎住院治疗后存活的老年患者(≥65 岁)。
本研究采用巢式病例对照设计,病例为因复发性肺炎(初次发作后≥30 天)再次住院的患者,对照为年龄、性别和发病率密度匹配但从未患过复发性肺炎的患者。PPI/H2 暴露情况分为从未、过去或当前使用,以前复发性肺炎为时间点。采用多变量条件逻辑回归评估 PPI/H2 与肺炎之间的关系。
在 5.4 年的随访期间,248 例复发性肺炎病例与 2476 例对照相匹配。总体而言,608 例当前 PPI/H2 使用者中有 71 例(12%)发生复发性肺炎,而 1487 例非使用者中有 130 例(8%)(校正比值比[aOR]1.5;95%置信区间[CI]1.1-2.1)。根据 PPI/H2 开始时间对 608 例当前使用者进行分层,发现新发当前使用者(初次肺炎住院后开始使用 PPI/H2,n=303)发生社区获得性复发性肺炎的风险增加(非使用者中为 15%,而使用者中为 8%,aOR 2.1;95%CI 1.4-3.0)。305 例现患当前使用者(初次社区获得性肺炎住院前后均使用 PPI/H2)与非使用者发生复发性肺炎的可能性相同(aOR 0.99;95%CI 0.63-1.57)。
在高危老年患者中,抑酸药物的使用显著增加了复发性肺炎的可能性。这种关联仅限于出院后开始使用 PPI/H2 的患者。在决定对近期有肺炎史的患者开这些药物时,应考虑到我们的发现。