Proton pump inhibitors and traditional nonsteroidal anti‐inflammatory drugs and the risk of acute interstitial nephritis and acute kidney injury

医学 急性肾损伤 优势比 内科学 间质性肾炎 药物流行病学 非甾体 肾炎 胃肠病学 药理学 药方
作者
Charles E. Leonard,Cristin P Freeman,Craig Newcomb,Peter P. Reese,Maximilian Herlim,Warren B. Bilker,Sean Hennessy,Brian L. Strom
出处
期刊:Pharmacoepidemiology and Drug Safety [Wiley]
卷期号:21 (11): 1155-1172 被引量:84
标识
DOI:10.1002/pds.3329
摘要

ABSTRACT Purpose This study aims to examine the associations between proton pump inhibitors (PPIs), traditional nonsteroidal anti‐inflammatory drugs (tNSAIDs), PPI + tNSAID co‐exposure, and the development of the following: (i) acute interstitial nephritis (AIN), a specific kidney injury often attributed to these drugs, and (ii) acute kidney injury (AKI), a general kidney injury encompassing AIN. Methods Two retrospective case–control studies were conducted, one for each outcome, within the General Practice Research Database. Cases were diagnostic‐coded AIN (primary outcome) or AKI (secondary outcome) events. Controls were matched on age, sex, and general practitioner practice. Exposures were defined by the presence/absence of the following mutually exclusive therapies on the index date: (i) PPI alone; (ii) tNSAID alone; (iii) PPI + tNSAID; or (iv) neither PPI nor tNSAID (referent). Results Sixty‐eight AIN cases and 3347 controls were identified. The adjusted odds ratios (ORs) for PPI and tNSAID exposures alone were 3.20 (0.80–12.79) and 1.90 (0.65–5.51), respectively. Numerous sensitivity analyses produced adjusted ORs for AIN between 3.0 and 7.7, and 1.6 and 1.9, respectively. We identified 27 982 AKI cases and 1 323 850 controls. The adjusted ORs for PPI alone, tNSAID alone, and PPI + tNSAID exposures were 1.05 (0.97–1.14), 1.31 (1.25–1.37), and 1.33 (1.07–1.64), respectively. Numerous sensitivity analyses produced adjusted ORs for AKI between 1.0 and 1.1, 1.1 and 1.3, and 1.3 and 1.4, respectively. Conclusions Proton pump inhibitor exposure may increase the odds of AIN, but this result was not definitive and should be confirmed in a dataset with more AIN cases to allow for increased statistical precision. tNSAIDs, yet not PPIs, were associated with a significantly increased odds of AKI. Copyright © 2012 John Wiley & Sons, Ltd.
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