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活性注射用维生素D与血液透析生存率:一项历史性队列研究。

Activated injectable vitamin D and hemodialysis survival: a historical cohort study.

作者信息

Teng Ming, Wolf Myles, Ofsthun M Norma, Lazarus J Michael, Hernán Miguel A, Camargo Carlos A, Thadhani Ravi

机构信息

Fresenius Medical Care North America, Lexington, Massachusetts, USA.

出版信息

J Am Soc Nephrol. 2005 Apr;16(4):1115-25. doi: 10.1681/ASN.2004070573. Epub 2005 Feb 23.

Abstract

Patients with ESRD commonly experience secondary hyperparathyroidism, a condition primarily managed with activated injectable vitamin D. The biologic effects of vitamin D, however, are widespread, and it is possible that activated injectable vitamin D alters survival in ESRD. This hypothesis was tested in a historical cohort study of incident hemodialysis patients who lived throughout the United States between January 1996 and December 1999. The primary outcome was 2-yr survival among those who survived for at least 90 d after initiation of chronic hemodialysis. During this period, 51,037 chronic hemodialysis patients survived for at least 90 d from the initiation of hemodialysis, and in the ensuing 2 yr, 37,173 received activated injectable vitamin D and 13,864 did not. At 2 yr, mortality rates were 13.8/100 person-years in the group that received injectable vitamin D compared with 28.6/100 person-years in the group that did not (P < 0.001). Cox proportional hazards analyses adjusting for several potential confounders and examining injectable vitamin D therapy as a time-dependent exposure suggested that compared with patients who did not receive injectable vitamin D, the 2-yr survival advantage associated with the group that did receive injectable vitamin D was 20% (hazard ratio, 0.80; 95% confidence interval, 0.76 to 0.83). The incidence of cardiovascular-related mortality was 7.6/100 person-years in the injectable vitamin D group, compared with 14.6/100 person-years in the non-vitamin D group (P < 0.001). The benefit of injectable vitamin D was evident in 48 of 49 strata examined, including those with low serum levels of intact parathyroid hormone and elevated levels of serum calcium and phosphorus, situations in which injectable vitamin D is often withheld. Repeating the entire analysis using marginal structural models to adjust for time-dependent confounding by indication yielded a survival advantage of 26% (hazard ratio, 0.74; 95% confidence interval, 0.71 to 0.79) associated with the injectable vitamin D group. In this historical cohort study, chronic hemodialysis patients in the group that received injectable vitamin D had a significant survival advantage over patients who did not. Randomized clinical trials would permit definitive conclusions.

摘要

终末期肾病(ESRD)患者常出现继发性甲状旁腺功能亢进,这一病症主要通过注射用活性维生素D进行治疗。然而,维生素D具有广泛的生物学效应,注射用活性维生素D有可能改变ESRD患者的生存率。在一项针对1996年1月至1999年12月间美国各地新接受血液透析患者的历史性队列研究中,对这一假设进行了检验。主要结局是慢性血液透析开始后至少存活90天的患者的2年生存率。在此期间,51,037例慢性血液透析患者自透析开始后至少存活了90天,在随后的2年中,37,173例接受了注射用活性维生素D,13,864例未接受。2年后,接受注射用维生素D组的死亡率为13.8/100人年,而未接受组为28.6/100人年(P<0.001)。在对多个潜在混杂因素进行校正并将注射用维生素D治疗作为时间依赖性暴露进行检验的Cox比例风险分析中,结果显示,与未接受注射用维生素D的患者相比,接受注射用维生素D组的2年生存优势为20%(风险比,0.80;95%置信区间,0.76至0.83)。注射用维生素D组心血管相关死亡率为7.6/100人年,非维生素D组为14.6/100人年(P<0.001)。在49个研究分层中的48个分层中,注射用维生素D的益处均很明显,包括那些血清完整甲状旁腺激素水平低以及血清钙和磷水平升高的情况,而在这些情况下通常不使用注射用维生素D。使用边际结构模型重复整个分析以校正因适应证导致的时间依赖性混杂因素后,注射用维生素D组的生存优势为26%(风险比,0.74;95%置信区间,0.71至0.79)。在这项历史性队列研究中,接受注射用维生素D组的慢性血液透析患者比未接受组具有显著的生存优势。随机临床试验将得出明确结论。

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