ERYTHROPOIETIN DEFICIENCY AFTER CORONARY-ARTERY BYPASS PROCEDURES

被引:26
作者
LEVINE, EA [1 ]
ROSEN, AL [1 ]
SEHGAL, LR [1 ]
GOULD, SA [1 ]
EGRIE, JC [1 ]
MOSS, GS [1 ]
机构
[1] AMGEN CORP, THOUSAND OAKS, CA USA
关键词
D O I
10.1016/0003-4975(91)90121-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Erythropoietin is the primary regulator of erythropoiesis. Erythropoietin has been shown to increase exponentially in response to linear decreases in hematocrit in normal, unstressed animals. However, the effect of operation, with its attendant stress, on erythropoietin levels is unknown. The purpose of this study is to evaluate the effect of surgical stress on erythropoietin. Twenty otherwise healthy patients scheduled for elective surgical procedures were studied. The cholecystectomy group included 10 patients who underwent cholecystectomy for documented stone disease. Ten patients who underwent coronary artery bypass procedures constituted the coronary artery bypass grafting group. Patients were studied preoperatively as well as on the first and second postoperative days. The hematocrit and erythropoietin levels were similar in both groups preoperatively. The hematocrit in the coronary artery bypass grafting group was lower than that of the cholecystectomy group on postoperative day 1 (0.31 versus 0.36; p < 0.003) and postoperative day 2 (0.30 versus 0.36; p < 0.001). During the first two postoperative days the erythropoietin levels were similar between groups. The data show that postoperative erythropoietin levels are similar after coronary artery bypass grafting, despite more severe anemia, when compared with cholecystectomy. This suggests that after coronary artery bypass grafting there is a relative deficiency of erythropoietin. Administration of recombinant human erythropoietin to patients undergoing surgical procedures could correct the erythropoietin deficiency and accelerate postoperative erythropoiesis.
引用
收藏
页码:764 / 766
页数:3
相关论文
共 27 条
[2]   TRANSFUSION-ASSOCIATED HEPATITIS AND AIDS - WHAT IS THE RISK [J].
BOVE, JR .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (04) :242-245
[3]  
CHRISTENSEN RD, 1989, PEDIATRICS, V83, P793
[4]  
DOUGLAS SW, 1975, BLOOD, V45, P55
[5]   DEVELOPMENT OF RADIOIMMUNOASSAYS FOR HUMAN ERYTHROPOIETIN USING RECOMBINANT ERYTHROPOIETIN AS TRACER AND IMMUNOGEN [J].
EGRIE, JC ;
COTES, PM ;
LANE, J ;
DAS, REG ;
TAM, RC .
JOURNAL OF IMMUNOLOGICAL METHODS, 1987, 99 (02) :235-241
[6]   WHY THE KIDNEY [J].
ERSLEV, AJ ;
CARO, J ;
BESARAB, A .
NEPHRON, 1985, 41 (03) :213-216
[7]  
ERSLEV AJ, 1987, J LAB CLIN MED, V109, P429
[8]   CORRECTION OF THE ANEMIA OF END-STAGE RENAL-DISEASE WITH RECOMBINANT-HUMAN-ERYTHROPOIETIN - RESULTS OF A COMBINED PHASE-I AND PHASE-II CLINICAL-TRIAL [J].
ESCHBACH, JW ;
EGRIE, JC ;
DOWNING, MR ;
BROWNE, JK ;
ADAMSON, JW .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (02) :73-78
[9]   RECOMBINANT-HUMAN-ERYTHROPOIETIN FOR PATIENTS WITH AIDS TREATED WITH ZIDOVUDINE [J].
FISCHL, M ;
GALPIN, JE ;
LEVINE, JD ;
GROOPMAN, JE ;
HENRY, DH ;
KENNEDY, P ;
MILES, S ;
ROBBINS, W ;
STARRETT, B ;
ZALUSKY, R ;
ABELS, RI ;
TSAI, HC ;
RUDNICK, SA .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (21) :1488-1493
[10]  
GOLDWASSER E, 1975, FED PROC, V34, P2285