Hydration Status Does Not Influence Peritoneal Equilibration Test Ultrafiltration Volumes

被引:33
作者
Davenport, Andrew [1 ]
Willicombe, Michelle Kay [1 ]
机构
[1] UCL, Sch Med, UCL Ctr Nephrol, London NW3 2PF, England
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2009年 / 4卷 / 07期
关键词
SOLUTE TRANSPORT RATE; TOTAL-BODY WATER; DIALYSIS PATIENTS; SYSTEMIC INFLAMMATION; MEMBRANE-FUNCTION; FLUID STATUS; HEMODIALYSIS; ICODEXTRIN; WEIGHT;
D O I
10.2215/CJN.01060209
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives: The peritoneal equilibration test (PET) was developed some 25 yr ago and has been used to help prescribe peritoneal dialysis. However, PET is affected by several factors, including diabetes and inflammation. It was speculated that extracellular fluid overload would increase PET ultrafiltration volumes, and therefore the usefulness of the PET in routine clinical practice was audited. Design, setting, participants, & measurements: Data from 211 consecutive patients attending a university teaching hospital for a standard PET who had multifrequency bioimpedance performance were analyzed to determine which factors affected net PET ultrafiltration volumes. Results: Net PET ultrafiltration volume was independent of gender, age, diabetes, residual renal function, peritoneal dialysis prescriptions (modes and dialysates), extracellular fluid volume, or C-reactive protein (CRP). There was an inverse regression with serum albumin and sodium on multiple logistical regression analysis (F = 13.4, P < 0.001 and F = 10.1, P = 0.001, respectively) and a positive regression with 24-h net peritoneal ultrafiltration volumes (F = 15.5, P < 0.001). As expected, there was a strong correlation with net sodium losses (r = 0.99, P < 0001). Conclusions: It was found that PET test ultrafiltration volume in routine clinical practice was not affected by CRP, hyperglycemia, or extracellular fluid volume overload. Ultrafiltration volumes were increased in those patients with reduced serum sodium and albumin, most likely because of inflammation and protein malnutrition. Clin J Am Soc Nephrol 4: 1207-1212, 2009. doi: 10.2215/CJN.01060209
引用
收藏
页码:1207 / 1212
页数:6
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