Division of Gastroenterology, Massachusetts General Hospital, Boston, MA, USA.
Columbia Vagelos College of Physicians and Surgeons, New York, NY, USA.
Inflamm Bowel Dis. 2024 Jan 5;30(1):38-44. doi: 10.1093/ibd/izad035.
We tested whether proton pump inhibitors (PPIs) are associated with enteric infections among those with inflammatory bowel disease (IBD), after adequately accounting for baseline differences between PPI users and nonusers.
This was a self-controlled case series, with each patient serving as their own control. Ambulatory patients with IBD were included if they were tested for enteric infection by multiplex polymerase chain reaction testing panel (GIPCR) and/or Clostridoides difficile toxin PCR from 2015 to 2019 and received PPIs for some but not all of this period. Rates of enteric infections were compared between the PPI-exposed period vs pre- and post-PPI periods identical in duration to the exposed period. Conditional Poisson regression was used to adjust for time-varying factors.
Two hundred twenty-one IBD patients were included (49% ulcerative colitis, 46% Crohn's disease, and 5% indeterminate colitis). The median PPI duration was 7 months (interquartile range 4 to 11 months). A total of 25 (11%) patients had a positive GIPCR or C. difficile test in the PPI period, 9 (4%) in the pre-PPI period, and 8 (4%) in the post-PPI period. Observed incidence rates for enteric infections were 2.5, 7.4, and 2.2 per 100 person years for the pre-PPI, PPI, and post-PPI periods, respectively (adjusted incidence rate ratios, 2.8; 95% confidence interval [CI] 1.3-6.0) for PPI vs pre-PPI and 2.9 (95% CI, 1.3-6.4) for PPI vs post-PPI). The adjusted absolute excess risk associated with PPIs was 4.9 infections per 100 person years.
Proton pump inhibitors were associated with a 3-fold increased risk for enteric infection among those with IBD but had a modest absolute risk.
本研究旨在充分考虑使用质子泵抑制剂(PPIs)与未使用者之间的基线差异后,探究质子泵抑制剂是否与炎症性肠病(IBD)患者的肠内感染有关。
本研究采用自身对照病例系列研究,每位患者均作为自身对照。纳入 2015 年至 2019 年间因 IBD 接受多重聚合酶链反应检测面板(GIPCR)和/或艰难梭菌毒素 PCR 检测的门诊患者,这些患者在此期间曾使用过 PPI,但并非全部时期均使用。将 PPI 暴露期与与暴露期持续时间相同的 PPI 前和 PPI 后时期进行比较,以比较肠内感染的发生率。采用条件泊松回归来调整随时间变化的因素。
共纳入 221 例 IBD 患者(49%为溃疡性结肠炎,46%为克罗恩病,5%为不确定结肠炎)。PPI 中位使用时间为 7 个月(四分位间距 4-11 个月)。共有 25 例(11%)患者在 PPI 期间、9 例(4%)在 PPI 前期间和 8 例(4%)在 PPI 后期间的 GIPCR 或艰难梭菌检测呈阳性。PPI 前、PPI 和 PPI 后时期肠内感染的观察发生率分别为每 100 人年 2.5、7.4 和 2.2 例(PPI 与 PPI 前相比的调整发病率比,2.8;95%置信区间 [CI] 1.3-6.0),PPI 与 PPI 后相比的调整发病率比为 2.9(95% CI,1.3-6.4)。与 PPI 相关的绝对超额风险为每 100 人年 4.9 例感染。
质子泵抑制剂与 IBD 患者肠内感染的风险增加 3 倍相关,但绝对风险适中。