Harold Simmons Center for Kidney Disease Research and Epidemiology, Division of Nephrology, Hypertension and Kidney Transplantation, University of California Irvine, Orange, California, USA.
Tibor Rubin Veterans Affairs Medical Center, Long Beach, California, USA.
Am J Nephrol. 2020;51(9):715-725. doi: 10.1159/000509451. Epub 2020 Aug 10.
Population-based studies show there is a high prevalence of chronic kidney disease (CKD) patients suffering from chronic pain. While opiates are frequently prescribed in non-dialysis-dependent CKD (NDD-CKD) patients, there may be toxic accumulation of metabolites, particularly among those progressing to end-stage renal disease (ESRD). We examined the association of opiate versus other analgesic use during the pre-ESRD period with post-ESRD mortality among NDD-CKD patients transitioning to dialysis.
We examined a national cohort of US Veterans with NDD-CKD who transitioned to dialysis over 2007-14. Among patients who received ≥1 prescription(s) in the Veterans Affairs (VA) Healthcare System within 1 year of transitioning to dialysis, we examined associations of pre-ESRD analgesic status, defined as opiate, gabapentin/pregabalin, other non-opiate analgesic, versus no analgesic use, with post-ESRD mortality using multivariable Cox models.
Among 57,764 patients who met eligibility criteria, pre-ESRD opiate and gabapentin/pregabalin use were each associated with higher post-ESRD mortality (ref: no analgesic use), whereas non-opiate analgesic use was not associated with higher mortality in expanded case-mix analyses: HRs (95% CIs) 1.07 (1.05-1.10), 1.07 (1.01-1.13), and 1.00 (0.94-1.06), respectively. In secondary analyses, increasing frequency of opiate prescriptions exceeding 1 opiate prescription in the 1-year pre-ESRD period was associated with incrementally higher post-ESRD mortality (ref: no analgesic use).
In NDD-CKD patients transitioning to dialysis, pre-ESRD opiate and gabapentin/pregabalin use were associated with higher post-ESRD mortality, whereas non-opiate analgesic use was not associated with death. There was a graded association between increasing frequency of pre-ESRD opiate use and incrementally higher mortality.
基于人群的研究表明,患有慢性疼痛的慢性肾脏病(CKD)患者患病率很高。虽然阿片类药物经常在非透析依赖性 CKD(NDD-CKD)患者中开处方,但代谢物可能会有毒素积累,特别是在那些进展为终末期肾病(ESRD)的患者中。我们研究了 NDD-CKD 患者在进入 ESRD 前使用阿片类药物与进入 ESRD 后死亡率之间的关系,这些患者正在过渡到透析。
我们研究了一个 2007 年至 2014 年期间在美国退伍军人事务部(VA)医疗保健系统中接受 NDD-CKD 过渡到透析的全国性退伍军人队列。在接受≥1 份 VA 医疗保健系统处方的患者中,我们在进入透析前 1 年内,检查了镇痛状态(定义为阿片类药物、加巴喷丁/普瑞巴林、其他非阿片类镇痛药和无镇痛治疗)与进入 ESRD 后死亡率之间的关联,使用多变量 Cox 模型。
在符合入选标准的 57764 名患者中,进入 ESRD 前使用阿片类药物和加巴喷丁/普瑞巴林均与较高的进入 ESRD 后死亡率相关(参考:无镇痛治疗),而非阿片类镇痛药的使用在扩展病例组合分析中与较高的死亡率无关:风险比(95%CI)分别为 1.07(1.05-1.10)、1.07(1.01-1.13)和 1.00(0.94-1.06)。在二次分析中,进入 ESRD 前 1 年中超过 1 次阿片类药物处方的阿片类药物处方的频率增加与进入 ESRD 后死亡率的增加相关(参考:无镇痛治疗)。
在过渡到透析的 NDD-CKD 患者中,进入 ESRD 前使用阿片类药物和加巴喷丁/普瑞巴林与较高的进入 ESRD 后死亡率相关,而非阿片类镇痛药的使用与死亡无关。阿片类药物的使用频率与死亡率呈递增关系。