Center for Health Outcomes, Pharmacoinformatics, and Epidemiology, SUNY Buffalo School of Pharmacy and Pharmaceutical Sciences, Buffalo, NY, USA.
Pharmacoepidemiol Drug Saf. 2011 Oct;20(10):1035-42. doi: 10.1002/pds.2198. Epub 2011 Aug 10.
Clostridium difficile infection (CDI) is a major cause of hospital-acquired diarrhea worldwide. We examined the risk of CDI associated with the use of acid-suppressive agents (proton pump inhibitors [PPI] and histamine-2 receptor blockers) and determined whether this risk varied by number or type of antibiotic (high or low CDI risk) received during hospitalization.
We conducted a retrospective cohort study of hospitalizations among adult patients at an academic teaching hospital in Rochester, New York, during which two or more days of antibiotics were prescribed. Multivariable marginal Cox proportional hazards models with time-varying exposures were used to examine time to the development of CDI.
A total of 10 154 hospitalizations and 241 cases of CDI, defined as detection of C. difficile toxin in a diarrheal stool sample within 60 days of discharge, were identified. PPI use was independently associated with an increased risk of CDI (adjusted hazard ratio = 4.5; 95% confidence interval [CI] = 2.3-9.0). Among hospitalizations during which one, two, three or four, and five or more antibiotics were prescribed, the adjusted hazard ratios for PPI use were 15.7 (CI = 6.4-38.8), 4.9 (CI = 2.2-11.2), 4.3 (CI = 1.9-9.9), and 2.7 (CI = 1.2-5.9), respectively (p for interaction = .002).
The use of PPI is common among patients receiving antibiotics during hospitalization. The greater risk of CDI in relation to PPI among hospitalizations during which fewer or low-risk antibiotics were prescribed suggests a potentially clinically relevant interaction between antibiotics and PPI. Further study is needed to elucidate possible mechanisms for the observed effect.
艰难梭菌感染(CDI)是全球范围内医院获得性腹泻的主要原因。我们研究了使用抑酸剂(质子泵抑制剂[PPI]和 H2 受体阻滞剂)与 CDI 相关的风险,并确定了这种风险是否因住院期间使用的抗生素数量或类型(高或低 CDI 风险)而有所不同。
我们对纽约罗切斯特一家学术教学医院的成年住院患者进行了回顾性队列研究,在此期间,患者接受了两天或更长时间的抗生素治疗。使用时间依赖性暴露的多变量边际 Cox 比例风险模型来检查发生 CDI 的时间。
共确定了 10154 例住院治疗和 241 例 CDI,定义为在出院后 60 天内从腹泻粪便样本中检测到艰难梭菌毒素。PPI 的使用与 CDI 的风险增加独立相关(调整后的危险比=4.5;95%置信区间[CI]为 2.3-9.0)。在接受一种、两种、三种或四种以及五种或更多种抗生素治疗的住院期间,PPI 使用的调整后的危险比分别为 15.7(CI=6.4-38.8)、4.9(CI=2.2-11.2)、4.3(CI=1.9-9.9)和 2.7(CI=1.2-5.9)(p 交互作用=0.002)。
在接受抗生素治疗的住院患者中,PPI 的使用很常见。在接受抗生素治疗的住院期间,使用 PPI 与 CDI 的风险增加之间的相关性更强,而在接受低剂量或低风险抗生素治疗的住院期间,这一相关性更大,这表明抗生素和 PPI 之间可能存在潜在的临床相关相互作用。需要进一步研究阐明观察到的效应的可能机制。