Institute of Medicine, University of Bergen, Bergen, Norway.
Eur J Gastroenterol Hepatol. 2013 May;25(5):531-8. doi: 10.1097/MEG.0b013e32835d5acd.
Proton pump inhibitors (PPIs) play a well-documented role as a gastroprotective agent among NSAID users at an increased risk of peptic ulcer and bleeding. Observational studies have, however, suggested that the clinical efficacy of PPI therapy may be reduced because of poor adherence.
To study the association between adherence to concomitant PPI in current NSAID users and the risk of peptic ulcer and bleeding.
Case-control study linking nationwide data from the Swedish Patient Registry with the Swedish Drug Prescription Database. The study population included patients admitted for a first-time peptic ulcer or bleeding and who were incident users of NSAID. Each case was matched on age, sex, NSAID duration, and calendar month with five controls. PPI adherence was calculated as the proportion of NSAID days being covered by PPI therapy. Matched and adjusted odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using conditional logistic regression.
A total of 3649 cases were identified. Patients with poor adherence (<20% PPI coverage) had a significantly increased risk of upper gastrointestinal complications (OR=1.88, 95% CI 1.22-2.88) compared with fully adherent patients (≥80% PPI coverage). As a continuous variable, the risk of an event increased with 6% points for every 10% decrease in PPI adherence (OR=1.06, 95% CI 1.03-1.10).
The gastroprotective effect of PPI in NSAID users is highly dependent on adherence, with about twice the risk in patients with poor adherence. Efforts to increase adherence should be an integrated part of clinical practice.
质子泵抑制剂 (PPI) 在预防 NSAID 使用者发生消化性溃疡和出血方面具有良好的保护作用,这一点已被充分证实。然而,观察性研究表明,由于依从性差,PPI 治疗的临床疗效可能会降低。
研究当前 NSAID 使用者同时使用 PPI 的依从性与消化性溃疡和出血风险之间的关系。
本病例对照研究将来自瑞典患者登记处的全国性数据与瑞典药物处方数据库进行了关联。研究人群包括首次因消化性溃疡或出血住院且为 NSAID 新使用者的患者。每个病例都根据年龄、性别、NSAID 持续时间和日历月份与 5 名对照者相匹配。PPI 依从性计算为 NSAID 天数中 PPI 治疗覆盖的比例。使用条件逻辑回归计算匹配和调整后的比值比 (OR) 及其 95%置信区间 (CI)。
共确定了 3649 例病例。与完全依从的患者(PPI 覆盖率≥80%)相比,依从性差(<20% PPI 覆盖率)的患者上消化道并发症风险显著增加(OR=1.88,95% CI 1.22-2.88)。作为一个连续变量,事件风险随着 PPI 依从性每降低 10%而增加 6%点(OR=1.06,95% CI 1.03-1.10)。
PPI 在 NSAID 使用者中的胃保护作用高度依赖于依从性,依从性差的患者风险增加约两倍。提高依从性的努力应成为临床实践的一个组成部分。