Department of Pharmaceutical Care, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, Thailand.
Pharmacoepidemiology and Statistics Clinics, Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.
Nephrol Dial Transplant. 2018 Feb 1;33(2):331-342. doi: 10.1093/ndt/gfw470.
Existing epidemiological studies illustrate that proton pump inhibitors (PPIs) may be related to adverse kidney outcomes. To date, no comprehensive meta-analysis has been conducted to evaluate and quantify this association.
We performed a systematic review and meta-analysis of studies to assess the association between PPI use and the risk of adverse kidney outcomes. We searched MEDLINE, Embase, SCOPUS, Web of Science, CINAHL, Cochrane Library and grey literature with no language restrictions (through 31 October 2016). Adverse kidney outcomes were acute interstitial nephritis (AIN), acute kidney injury (AKI), chronic kidney disease (CKD) and end-stage renal disease (ESRD). The risk ratios (RRs) and confidence intervals (CIs) were pooled using a random effects model. The strength of evidence (SOE) for each outcome was assessed using the Grading of Recommended Assessment, Development and Evaluation system.
Of 2037 identified studies, four cohort and five case-control studies with ∼2.6 million patients were included. Of these, 534 003 (20.2%) were PPI users. Compared with non-PPI users, PPI users experienced a significantly higher risk of AKI [RR 1.44 (95% CI 1.08-1.91); P = 0.013; SOE, low] and CKD [RR 1.36 (95% CI 1.07-1.72); P = 0.012; SOE, low]. Moreover, PPIs increased the risk of AIN [RR 3.61 (95% CI 2.37-5.51); P < 0.001; SOE, insufficient] and ESRD [RR 1.42 (95% CI 1.28-1.58); P < 0.001; SOE, insufficient].
PPI usage was associated with adverse kidney outcomes; however, these findings were based on observational studies and low-quality evidence. Additional rigorous studies are needed for further clarification.
现有的流行病学研究表明质子泵抑制剂(PPIs)可能与肾脏不良结局有关。迄今为止,尚无综合的荟萃分析来评估和量化这种相关性。
我们对评估 PPI 使用与不良肾脏结局风险之间关系的研究进行了系统评价和荟萃分析。我们检索了 MEDLINE、Embase、SCOPUS、Web of Science、CINAHL、Cochrane 图书馆和无语言限制的灰色文献(截至 2016 年 10 月 31 日)。不良肾脏结局包括急性间质性肾炎(AIN)、急性肾损伤(AKI)、慢性肾脏病(CKD)和终末期肾病(ESRD)。使用随机效应模型汇总风险比(RR)和置信区间(CI)。使用推荐评估、制定和评价系统(Grading of Recommended Assessment, Development and Evaluation system)评估每个结局的证据强度(SOE)。
在 2037 项已确定的研究中,纳入了四项队列研究和五项病例对照研究,共涉及约 260 万名患者。其中,534003 例(20.2%)为 PPI 使用者。与非 PPI 使用者相比,PPI 使用者发生 AKI 的风险显著增加[RR 1.44(95%CI 1.08-1.91);P=0.013;SOE,低]和 CKD [RR 1.36(95%CI 1.07-1.72);P=0.012;SOE,低]。此外,PPIs 增加了 AIN 的风险[RR 3.61(95%CI 2.37-5.51);P<0.001;SOE,不充分]和 ESRD [RR 1.42(95%CI 1.28-1.58);P<0.001;SOE,不充分]的风险。
PPI 使用与肾脏不良结局相关;然而,这些发现基于观察性研究且证据质量低。需要进一步的严格研究来进一步澄清。