Friedman Oded, Wald Ron, Goldstein Marc B
Prosserman Centre for Health Research, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.
Nephron Clin Pract. 2008;110(4):c229-34. doi: 10.1159/000167870. Epub 2008 Oct 31.
BACKGROUND/AIMS: Disordered mineral metabolism is independently associated with mortality among chronic dialysis patients. We hypothesized that, upon dialysis start, biochemical markers of mineral metabolism would be better controlled among patients who had received multidisciplinary predialysis care (MDC).
We conducted a retrospective cohort study of incident hemodialysis patients between 2002 and 2005. Corrected calcium (Ca), phosphate (P), calcium-phosphate product (CaxP), and intact parathyroid hormone (iPTH) at the time of dialysis initiation and over the first year thereafter were compared based on prior MDC receipt. Furthermore, we examined the relationship between the duration of MDC and mineral metabolic parameters.
67 patients received MDC and 84 patients received conventional or no nephrologist-based care. Patients who received MDC had a higher iPTH (p = 0.03) both at dialysis initiation and over the subsequent year while Ca, P, and CaxP were not significantly impacted. Among patients who received MDC, mineral metabolic values at dialysis initiation did not differ by duration of predialysis care.
The receipt of MDC had a limited effect on mineral metabolic profiles at the time of and over the first year following chronic hemodialysis initiation. The survival benefits associated with the receipt of MDC may be mediated by mechanisms other than improved mineral metabolic control.
背景/目的:矿物质代谢紊乱与慢性透析患者的死亡率独立相关。我们假设,在开始透析时,接受多学科透析前护理(MDC)的患者矿物质代谢的生化指标能得到更好的控制。
我们对2002年至2005年期间开始进行血液透析的患者进行了一项回顾性队列研究。根据之前是否接受MDC,比较了透析开始时及此后第一年的校正钙(Ca)、磷(P)、钙磷乘积(CaxP)和完整甲状旁腺激素(iPTH)。此外,我们还研究了MDC持续时间与矿物质代谢参数之间的关系。
67例患者接受了MDC,84例患者接受了传统护理或无肾脏科医生参与的护理。接受MDC的患者在透析开始时及随后一年的iPTH均较高(p = 0.03),而Ca、P和CaxP未受到显著影响。在接受MDC的患者中,透析开始时的矿物质代谢值并不因透析前护理的持续时间而有所不同。
接受MDC对慢性血液透析开始时及随后第一年的矿物质代谢状况影响有限。与接受MDC相关的生存益处可能是由改善矿物质代谢控制以外的机制介导的。