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Estimating the risk of acute kidney injury associated with use of diuretics and renin angiotensin aldosterone system inhibitors: A population based cohort study using the clinical practice research datalink

机译:估算与利尿剂和肾素血管紧张素醛固酮系统抑制剂相关的急性肾损伤的风险:使用临床实践研究数据链接的基于群体的队列研究

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BACKGROUND:The risk of acute kidney injury (AKI) attributable to renin angiotensin aldosterone (RAAS) inhibitors and diuretics remains unclear.METHODS:We conducted a prospective cohort study using the Clinical Practice Research Datalink (2008-2015) linked to Hospital Episode Statistics - Admitted Patient Care and Office for National Statistics mortality data. Patients were included if they had one or more chronic diagnoses requiring medication. Exposed patients had a first ever prescription for RAAS inhibitors/diuretics during the study period. AKI risk associated with exposure was determined by multivariable Cox regression, propensity score-adjusted Cox regression and a prior event rate ratio (PERR) analysis.RESULTS:One hundred forty thousand nine hundred fifty-two individuals were included. Increased AKI risk in the exposed group was demonstrated in both the multivariable and propensity score-adjusted cox regressions (HR 1.23 (95% CI 1.04-1.45) and HR 1.24 (1.05-1.47) respectively). The PERR analysis provided a similar overall hazard ratio with a wider confidence interval (HR 1.29 (0.94-1.63)). The increased AKI risk in the exposed group was present only in those receiving two or more antihypertensives. Absolute AKI risk was small.CONCLUSIONS:RAAS inhibitors/diuretics result in an increased risk of AKI. The absolute increase in AKI risk is small, however, and needs to be considered in the context of any potential benefits.
机译:背景:急性肾损伤的风险(aki)归因于肾素血管紧张素醛酮(RAAs)抑制剂和利尿剂仍然尚未透明。方法:我们使用临床实践研究Datalink(2008-2015)与医院阶段统计相关的预期队列研究 - 承认患者护理和国家统计死亡率数据。如果患者有一个或多个需要药物的慢性诊断,则包括患者。暴露的患者在研究期间患有RAAS抑制剂/利尿剂的第一个处方。通过多变量的Cox回归,倾向评分调整的Cox回归和先前的事件率比(Perr)分析来确定与暴露相关的疾病风险。结果:包括一百四万九百五十二个人。在多变量和倾向分数调整的Cox回归中,在多变量和倾向分数调整的Cox回归中证明了暴露组中的AKI风险增加(HR 1.23(95%CI 1.04-1.45)和HR 1.24(1.05-1.47)。 PERR分析提供了与更广泛的置信区间相似的整体危险比(HR 1.29(0.94-1.63))。曝光组中的AKI风险增加仅存在于接受两种或更多种抗高血压性的那些中。绝对的AKI风险很小。结论:RAAS抑制剂/利尿剂导致AKI的风险增加。然而,AKI风险的绝对增加很小,并且需要在任何潜在利益的背景下考虑。

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