The role of continuous renal replacement therapy in the future treatment of acute renal failure

被引:7
作者
Conger, JD [1 ]
机构
[1] UNIV COLORADO, SCH MED, DEPT MED, BOULDER, CO 80309 USA
关键词
continuous dialysis; oliguria; natriuretic peptides; growth factors; dialysis membranes; vasculature;
D O I
10.1016/S0272-6386(96)90089-X
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
In considering continuous renal replacement therapy (CRRT) in future therapeutic regimens for acute renal failure (ARF), three relevant areas of interest have been examined: changes in the nature and perception of ARF as an illness; the emerging roles of CRRT in ARF management; and the use of dialysis modes in conjunction with newer pharmacologic treatments in ARF, Regarding changing patterns and perceptions of ARF, there are a number of important issues in relation to future therapy, ARF in the 1990s is predominantly a nonoliguric disorder that has a better outcome than oliguric ARF and may have a positive effect on overall mortality compared with previous decades, Rates of increases of serum creatinine (Scr) and blood urea nitrogen (BUN) levels in the current decade are little changed, however, in large part because of catabolism and high protein infusion formulae, Of related interest is recent information that baseline serum creatinine is a poor predictor of subsequent dialysis need and mortality in ARF. Other outcome predictive scoring systems, while improved, still lack the precision for general application in patient treatment decisions, Given that there is increasing evidence of abnormal vascular reactivity predisposing to recurrent ischemia in ARF and new evidence of negative renal effects of bioincompatible dialyzer membranes, the issue of early and intensive dialysis in ARF needs to be re-examined using CRRT with biocompatible membranes, rather than standard intermittent dialysis, Finally, pharmacologic agents currently under study that may have clinical efficacy have variable levels of hypotensive side effects, It is very likely that when combination treatment using dialysis and these newer drugs is considered, it will require CRRT. (C) 1996 by the National Kidney Foundation, Inc.
引用
收藏
页码:S108 / S113
页数:6
相关论文
共 70 条
[1]   NON-OLIGURIC ACUTE RENAL-FAILURE [J].
ANDERSON, RJ ;
LINAS, SL ;
BERNS, AS ;
HENRICH, WL ;
MILLER, TR ;
GABOW, PA ;
SCHRIER, RW .
NEW ENGLAND JOURNAL OF MEDICINE, 1977, 296 (20) :1134-1138
[2]   CALCITONIN-GENE-RELATED PEPTIDE ATTENUATES EXPERIMENTAL ISCHEMIC RENAL-FAILURE IN A RAT MODEL OF REVERSIBLE RENAL ISCHEMIC INSULT [J].
BERGMAN, ASF ;
FALT, K ;
ODARCEDERLOF, I ;
WESTMAN, L ;
TAKOLANDER, R .
RENAL FAILURE, 1994, 16 (03) :351-357
[3]  
BOSWORTH C, 1991, CONTRIB NEPHROL, V93, P13
[4]  
BRAHMAN SAN, 1994, AM J KIDNEY DIS, V23, P788
[5]  
BROWN CB, 1981, CLIN NEPHROL, V15, P90
[6]   THE ASSESSMENT OF RISK-FACTORS IN 462 PATIENTS WITH ACUTE RENAL-FAILURE [J].
BULLOCK, ML ;
UMEN, AJ ;
FINKELSTEIN, M ;
KEANE, WF .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1985, 5 (02) :97-103
[7]  
CANTAROVICH F, 1971, POSTGRAD MED J, V47, P13
[8]   HIGH DOSE FRUSEMIDE IN ESTABLISHED ACUTE RENAL-FAILURE [J].
CANTAROVICH, F ;
GALLI, C ;
BENEDETTI, L ;
CHENA, C ;
CASTRO, L ;
CORREA, C ;
PEREZLOR.J ;
FERNANDEZ, JC ;
LOCATELLI, A ;
TIZADO, J .
BMJ-BRITISH MEDICAL JOURNAL, 1973, 4 (5890) :449-450
[9]  
CANTAROVICH F, 1994, J AM SOC NEPHROL, V5, P389
[10]   ARE ANTIPHOSPHOLIPID ANTIBODIES CLINICALLY RELEVANT IN DIALYSIS PATIENTS [J].
CHEW, SL ;
LINS, RL ;
DAELEMANS, R ;
ZACHEE, P ;
DECLERCK, LS ;
VERMYLEN, J .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1992, 7 (12) :1194-1198