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中重度慢性肾脏病患者口服双膦酸盐类药物的安全性:一项跨国队列分析。

Safety of Oral Bisphosphonates in Moderate-to-Severe Chronic Kidney Disease: A Binational Cohort Analysis.

机构信息

Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford, Oxford, UK.

Faculty of Epidemiology and Population Health, Department of Non-communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, UK.

出版信息

J Bone Miner Res. 2021 May;36(5):820-832. doi: 10.1002/jbmr.4235. Epub 2021 Feb 8.

Abstract

Bisphosphonates are the first-line treatment for preventing fractures in osteoporosis patients. However, their use is contraindicated or to be used with caution in chronic kidney disease (CKD) patients, primarily because of a lack of information about their safety and effectiveness. We aimed to investigate the safety of oral bisphosphonates in patients with moderate to severe CKD, using primary-care electronic records from two cohorts, CPRD GOLD (1997-2016) and SIDIAP (2007-2015) in the UK and Catalonia, respectively. Both databases were linked to hospital records. SIDIAP was also linked to end-stage renal disease registry data. Patients with CKD stages 3b to 5, based on two or more estimated glomerular filtration rate measurements less than 45 mL/min/1.73 m , aged 40 years or older were identified. New bisphosphonate users were propensity score-matched with up to five non-users to minimize confounding within this population. Our primary outcome was CKD stage worsening (estimated glomerular filtration rate [eGFR] decline or renal replacement therapy). Secondary outcomes were acute kidney injury, gastrointestinal bleeding/ulcers, and severe hypocalcemia. Hazard ratios (HRs) were estimated using Cox regression and Fine and Gray sub-HRs were calculated for competing risks. We matched 2447 bisphosphonate users with 8931 non-users from CPRD and 1399 users with 6547 non-users from SIDIAP. Bisphosphonate use was associated with greater risk of CKD progression in CPRD (sub-HR [95% CI]: 1.14 [1.04, 1.26]) and SIDIAP (sub-HR: 1.15 [1.04, 1.27]). No risk differences were found for acute kidney injury, gastrointestinal bleeding/ulcers, or hypocalcemia. Hence, we can conclude a modest (15%) increased risk of CKD progression was identified in association with bisphosphonate use. No other safety concerns were identified. Our findings should be considered before prescribing bisphosphonates to patients with moderate to severe CKD. © 2020 American Society for Bone and Mineral Research (ASBMR).

摘要

双膦酸盐是预防骨质疏松症患者骨折的一线治疗药物。然而,由于缺乏关于其安全性和有效性的信息,在慢性肾脏病(CKD)患者中,其使用被禁忌或需谨慎使用。我们旨在使用来自英国 CPRD GOLD(1997-2016 年)和 SIDIAP(2007-2015 年)两个队列的初级保健电子记录以及加泰罗尼亚的医院记录,来研究中度至重度 CKD 患者口服双膦酸盐的安全性。SIDIAP 还与终末期肾病登记数据相关联。根据两次或两次以上估计肾小球滤过率测量值均小于 45 mL/min/1.73 m ,确定 CKD 分期为 3b 至 5 期,年龄在 40 岁或以上的患者为研究对象。新使用双膦酸盐的患者与最多 5 名未使用者进行倾向评分匹配,以最大限度地减少该人群内的混杂因素。我们的主要结局是 CKD 分期恶化(估计肾小球滤过率[eGFR]下降或肾脏替代治疗)。次要结局是急性肾损伤、胃肠道出血/溃疡和严重低钙血症。使用 Cox 回归估计风险比(HRs),并用 Fine 和 Gray 亚 HR 计算竞争风险。我们从 CPRD 匹配了 2447 名双膦酸盐使用者和 8931 名未使用者,从 SIDIAP 匹配了 1399 名使用者和 6547 名未使用者。在 CPRD(亚 HR [95%CI]:1.14 [1.04,1.26])和 SIDIAP(亚 HR:1.15 [1.04,1.27])中,双膦酸盐的使用与 CKD 进展的风险增加相关。在急性肾损伤、胃肠道出血/溃疡或低钙血症方面未发现风险差异。因此,我们可以得出结论,与双膦酸盐使用相关,发现 CKD 进展的风险略有增加(15%)。没有发现其他安全问题。在为中度至重度 CKD 患者开双膦酸盐处方之前,应该考虑到这些发现。© 2020 美国骨矿研究协会(ASBMR)。

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