Impact of dialysis dose and membrane on infection-related hospitalization and death: Results of the HEMO study

被引:164
作者
Allon, M
Depner, TA
Radeva, M
Bailey, J
Beddhu, S
Butterly, D
Coyne, DW
Gassman, JJ
Kaufman, AM
Kaysen, GA
Lewis, JA
Schwab, SJ
机构
[1] Univ Alabama Birmingham, Birmingham, AL USA
[2] Univ Calif Davis, Davis, CA 95616 USA
[3] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[4] Emory Univ, Atlanta, GA 30322 USA
[5] Univ Utah, Salt Lake City, UT 84112 USA
[6] Duke Univ, Durham, NC USA
[7] Washington Univ, St Louis, MO USA
[8] Beth Israel Deaconess Med Ctr, New York, NY 10003 USA
[9] Vanderbilt Univ, Nashville, TN USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2003年 / 14卷 / 07期
关键词
D O I
10.1097/01.ASN.0000074237.78764.D1
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
Infection is the second most common cause of death among hemodialysis patients. A predefined secondary aim of the HEMO study was to determine if dialysis dose or flux reduced infection-related deaths or hospitalizations. The effects of dialysis dose, dialysis membrane, and other clinical parameters on infection-related deaths and first infection-related hospitalizations were analyzed using Cox regression analysis. Among the 1846 randomized patients (mean age, 58 yr; 56% female; 63% black; 45% with diabetes), there were 871 deaths, of which 201 (23%) were due to infection. There were 1698 infection-related hospitalizations, yielding a 35% annual rate. The likelihood of infection-related death did not differ between patients randomized to a high or standard dose (relative risk [RR], 0.99 [0.75 to 1.31]) or between patients randomized to high-flux or low-flux membranes (RR, 0.85 [0.64 to 1.13]). The relative risk of infection-related death was associated (P < 0.001 for each variable) with age (RR, 1.47 [1.29 to 1.68] per 10 yr); co-morbidity score (RR, 1.46 [1.21 to 1.76]), and serum albumin (RR, 0.19 [0.09 to 0.41] per g/dl). The first infection-related hospitalization was related to the vascular access in 21% of the cases, and non-access-related in 79%. Catheters were present in 32% of all study patients admitted with access-related infection, even though catheters represented only 7.6% of vascular accesses in the study. In conclusion, infection accounted for almost one fourth of deaths. Infection-related deaths were not reduced by higher dose or by high flux dialyzers. In this prospective study, most infection-related hospitalizations were not attributed to vascular access. However, the frequency of access-related, infection-related hospitalizations was disproportionately higher among patients with catheters compared with grafts or fistulas.
引用
收藏
页码:1863 / 1870
页数:8
相关论文
共 24 条
[1]  
[Anonymous], 2019, 2019 CHIN DAT PROT C
[2]   Comorbidity assessment in hemodialysis and peritoneal dialysis using the index of coexistent disease [J].
Athienites, NV ;
Miskulin, DC ;
Fernandez, G ;
Bunnapradist, S ;
Simon, G ;
Landa, M ;
Schmid, CH ;
Greenfield, S ;
Levey, AS ;
Meyer, KB .
SEMINARS IN DIALYSIS, 2000, 13 (05) :320-326
[3]   Relationship of dialysis membrane and cause-specific mortality [J].
Bloembergen, WE ;
Hakim, RM ;
Stannard, DC ;
Held, PJ ;
Wolfe, RA ;
Agodoa, LYC ;
Port, FK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1999, 33 (01) :1-10
[4]   Relationship of dose of hemodialysis and cause-specific mortality [J].
Bloembergen, WE ;
Stannard, DC ;
Port, FK ;
Wolfe, RA ;
Pugh, JA ;
Jones, CA ;
Greer, JW ;
Golper, TA ;
Held, PJ .
KIDNEY INTERNATIONAL, 1996, 50 (02) :557-565
[5]  
Cohen G, 1998, J AM SOC NEPHROL, V9, P451
[6]  
COX DR, 1972, J R STAT SOC B, V34, P187
[7]   Effect of dialysis dose and membrane flux in maintenance hemodialysis. [J].
Eknoyan, G ;
Beck, GJ ;
Cheung, AK ;
Daugirdas, JT ;
Greene, T ;
Kusek, JW ;
Allon, M ;
Bailey, J ;
Delmez, JA ;
Depner, TA ;
Dwyer, JT ;
Levey, AS ;
Levin, NW ;
Milford, E ;
Ornt, DB ;
Rocco, MV ;
Schulman, G ;
Schwab, SJ ;
Teehan, BP ;
Toto, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (25) :2010-2019
[8]  
Hoen B, 1998, J AM SOC NEPHROL, V9, P869
[9]   PHYSICOCHEMICAL CHARACTERIZATION OF A POLYPEPTIDE PRESENT IN UREMIC SERUM THAT INHIBITS THE BIOLOGICAL-ACTIVITY OF POLYMORPHONUCLEAR CELLS [J].
HORL, WH ;
HAAGWEBER, M ;
GEORGOPOULOS, A ;
BLOCK, LH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6353-6357
[10]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481