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The appropriate use of proton pump inhibitors (PPIs): Need for a reappraisal.质子泵抑制剂(PPIs)的合理使用:需要重新评估。
Eur J Intern Med. 2017 Jan;37:19-24. doi: 10.1016/j.ejim.2016.10.007. Epub 2016 Oct 23.
2
Trends in Prevalence of Chronic Kidney Disease in the United States.美国慢性肾脏病患病率的趋势
Ann Intern Med. 2016 Oct 4;165(7):473-481. doi: 10.7326/M16-0273. Epub 2016 Aug 2.
3
Global Prevalence of Chronic Kidney Disease - A Systematic Review and Meta-Analysis.全球慢性肾脏病患病率——一项系统评价与荟萃分析
PLoS One. 2016 Jul 6;11(7):e0158765. doi: 10.1371/journal.pone.0158765. eCollection 2016.
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Association Between the Use of Proton Pump Inhibitors and the Risk of ESRD in Renal Diseases: A Population-Based, Case-Control Study.质子泵抑制剂的使用与肾脏疾病中终末期肾病风险之间的关联:一项基于人群的病例对照研究。
Medicine (Baltimore). 2016 Apr;95(15):e3363. doi: 10.1097/MD.0000000000003363.
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Proton Pump Inhibitors and Risk of Incident CKD and Progression to ESRD.质子泵抑制剂与新发慢性肾脏病及进展至终末期肾病的风险
J Am Soc Nephrol. 2016 Oct;27(10):3153-3163. doi: 10.1681/ASN.2015121377. Epub 2016 Apr 14.
6
Association of Proton Pump Inhibitors With Risk of Dementia: A Pharmacoepidemiological Claims Data Analysis.质子泵抑制剂与痴呆风险的关联:基于药物流行病学索赔数据分析。
JAMA Neurol. 2016 Apr;73(4):410-6. doi: 10.1001/jamaneurol.2015.4791.
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Proton Pump Inhibitor Use and the Risk of Chronic Kidney Disease.质子泵抑制剂的使用与慢性肾脏病风险
JAMA Intern Med. 2016 Feb;176(2):238-46. doi: 10.1001/jamainternmed.2015.7193.
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Proton-pump inhibitors and risk of fractures: an update meta-analysis.质子泵抑制剂与骨折风险:一项更新的荟萃分析。
Osteoporos Int. 2016 Jan;27(1):339-47. doi: 10.1007/s00198-015-3365-x.
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Proton pump inhibitors and the risk of acute kidney injury in older patients: a population-based cohort study.质子泵抑制剂与老年患者急性肾损伤风险:一项基于人群的队列研究。
CMAJ Open. 2015 Apr 2;3(2):E166-71. doi: 10.9778/cmajo.20140074. eCollection 2015 Apr-Jun.
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Proton pump inhibitors linked to hypomagnesemia: a systematic review and meta-analysis of observational studies.质子泵抑制剂与低镁血症相关:一项观察性研究的系统评价和荟萃分析
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质子泵抑制剂与肾脏疾病——肾脏病医生面临的胃肠道不适问题?

Proton Pump Inhibitors and Kidney Disease - GI Upset for the Nephrologist?

作者信息

Toth-Manikowski Stephanie, Grams Morgan E

机构信息

Department of Medicine, Johns Hopkins University, Baltimore, Maryland.

Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore Maryland.

出版信息

Kidney Int Rep. 2017 May;2(3):297-301. doi: 10.1016/j.ekir.2017.01.005. Epub 2017 Jan 23.

DOI:10.1016/j.ekir.2017.01.005
PMID:28845467
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5568828/
Abstract

Widely regarded as safe and effective, proton pump inhibitors (PPIs) are among the most commonly used medications in the world today. However, a spate of observational studies suggest an association between PPI use and adverse events, including infection, bone fracture, and dementia. This review details evidence linking the use of PPI therapy to the development of kidney disease, including early case reports of acute interstitial nephritis and subsequent large observational studies of acute kidney injury (AKI), chronic kidney disease (CKD), and end-stage renal disease (ESRD). The majority of studies showed higher risk of kidney outcomes among persons prescribed PPI medications, with effect sizes that were slightly higher for AKI (∼2-3-fold) compared to CKD and ESRD (1.2-1.8-fold). Although observational pharmaco-epidemiology studies are limited by the possibility of residual confounding and confounding by indication, many of the described studies conducted rigorous sensitivity analyses aimed at minimizing these biases, including new-user design, comparison to similar agents (e.g., histamine receptor antagonists), and evaluation for a dose-response, with robust results. Given the widespread use of PPIs, even a small effect on kidney outcomes could result in large public health burden. Timely cessation of PPI therapy when there is no clear indication for use might reduce the population burden of kidney disease.

摘要

质子泵抑制剂(PPIs)被广泛认为是安全有效的,是当今世界上最常用的药物之一。然而,一系列观察性研究表明,使用PPIs与不良事件之间存在关联,包括感染、骨折和痴呆。这篇综述详细阐述了将PPI治疗的使用与肾脏疾病的发生联系起来的证据,包括急性间质性肾炎的早期病例报告以及随后对急性肾损伤(AKI)、慢性肾病(CKD)和终末期肾病(ESRD)的大型观察性研究。大多数研究表明,使用PPI药物的人群发生肾脏疾病的风险更高,与CKD和ESRD相比,AKI的效应大小略高(约2-3倍)(1.2-1.8倍)。尽管观察性药物流行病学研究受到残余混杂和指示性混杂可能性的限制,但许多上述研究进行了严格的敏感性分析,旨在尽量减少这些偏差,包括新用户设计、与类似药物(如组胺受体拮抗剂)比较以及剂量反应评估,结果可靠。鉴于PPIs的广泛使用,即使对肾脏疾病结果有微小影响也可能导致巨大的公共卫生负担。在没有明确使用指征时及时停止PPI治疗可能会减轻肾脏疾病的人群负担。