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腹膜透析患者血磷水平及其影响因素分析

崔春黎 陈胜芳

同济大学学报(医学版)2011,Vol.32Issue(5):61-64,4.
同济大学学报(医学版)2011,Vol.32Issue(5):61-64,4.DOI:10.3969/j.issn1008-0392.2011.05.013

腹膜透析患者血磷水平及其影响因素分析

Phosphorus levels in peritoneal dialysis patients and related influencing factors

崔春黎 1陈胜芳2

作者信息

  • 1. 同济大学附属同济医院肾内科,上海200065
  • 2. 同济大学附属同济医院营养科,上海200065
  • 折叠

摘要

Abstract

Objective To investigate the phosphorus levels in patients undergoing continuous ambulatory peritoneal dialysis (CAPD) and related influencing factors. Methods Fifty-eight stable CAPD patients were enrolled in the study. Dietary survey was conducted, estimated residual kidney function(KRF) and dialysis adequacy were evaluated. Serum phosphate, calcium, intact parathyroid hormone(IPTH), albumin(ALB) , pre-albumin(PA), lipids, endothelin(ET) and C-reactive protein (CRP) were measured. Results The levels of serum phosphate and IPTH were decreased after dialysis in CAPD patients (P < 0. 01) , 26 of 58 (45% ) patients had hyperphosphatemia. Serum phosphate levels were positively correlated with dietary phosphate, cholesterol, protein and energy intake(r = 0.575,r = 0.449, r = 0. 353 and r = 0.367, respectively;P < 0.01). Serum phosphate levels were not correlated with dialysis adequacy and RRF, but correlated with serum urea nitrogen and creatinine(r = 0.578, r = 0. 560, respectively; P < 0. 01). Serum phosphate levels were positively correlated with serum albumin and pre-albumin ( r = 0. 269, P < 0. 05; r = 0. 404, P < 0. 01 ), and negatively correlated with TC and LDL levels(r= -0.407,r= -0.311 ;P <0.01). Serum phosphate levels were also positively correlated with ET( r = 0.359; P <0.01). Conclusion CAPD contributes to improve calcium-phosphate metabolism disorder. Serum phosphate levels are associated with dietary intake and uremic toxin accumulation. Hyperphosphatemia may stimulate ET release.

关键词

腹膜透析/高磷血症/内皮素

Key words

peritoneal dialysis/ hyperphosphatemia/ endothelin

分类

医药卫生

引用本文复制引用

崔春黎,陈胜芳..腹膜透析患者血磷水平及其影响因素分析[J].同济大学学报(医学版),2011,32(5):61-64,4.

同济大学学报(医学版)

OACSTPCD

1008-0392

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