CARDIAC-FUNCTION AND HEMATOCRIT LEVEL

被引:113
作者
HARNETT, JD
KENT, GM
FOLEY, RN
PARFREY, PS
机构
[1] Division of Nephrology, Health Sciences Centre, Memorial University, St John's
关键词
CARDIOVASCULAR RISK; DIALYSIS; EPOETIN; LEFT VENTRICULAR HYPERTROPHY;
D O I
10.1016/0272-6386(95)90673-8
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
Patients on dialysis have an age-adjusted death rate 3.5 times that of the general population. The most common cause of death in patients on dialysis is cardiovascular disease. We prospectively followed a cohort of 433 patients in three centers for a mean of 41 months. Mean hemoglobin level at the beginning of dialysis was 8.39 (+/-1.7) g/dL, and the mean hemoglobin level during follow-up was 8.84 (+/-1.5) g/dL. Using Cox's regression model, we found that anemia predicted mortality independently of age, diabetes mellitus, cardiac failure, hypoalbuminemia, serum creatinine, mean arterial pressure, or echocardiographic heart disease. The independent relative risk (RR) of mortality was 1.18 per 1.0 g/dL decrease in hemoglobin level. Anemia also independently predicted the de novo occurrence of congestive heart failure when the same covariates were controlled for (RR, 1.49 per 1.0 g/dL decrease). Anemia was also independently predictive of heart failure at the start of dialysis (RR, 1.14 per 1.0 g/dL decrease) and heart failure recurrence (RR, 1.25 per 1.0 g/dL decrease). Left ventricular hypertrophy is present in 75% of patients on dialysis at the start of therapy for end-stage renal disease. It independently predicts mortality. Our prospective cohort study identified increasing age, hypertension, and anemia as risk factors for its development One controlled study and several uncontrolled studies demonstrated improvement (but not complete regression) of elevated left ventricular mass in patients on dialysis treated with recombinant human erythropoietin (epoetin). (C) 1995 by the National Kidney Foundation, Inc.
引用
收藏
页码:S3 / S7
页数:5
相关论文
共 22 条
[1]  
Organ Replacement Register, 1991 Annual Report, (1993)
[2]  
Foley, Parfrey, Harnett, Kent, Martin, Murray, Barre, Clinical and echocardiographic disease in patients starting end-stage renal disease therapy, Kidney Int, 47, pp. 186-192, (1995)
[3]  
Foley, Parfrey, Harnett, Kent, Barre, Uremia-related prognostic factors in dialysis patients: a cohort study from the start of dialysis, JASN, 4, (1993)
[4]  
Harnett, Parfrey, Kent, Foley, Barre, Congestive heart failure in dialysis patients: prevalence, incidence, risk factors and prognosis, JASN, 4, (1993)
[5]  
Silberberg, Racine, Barre, Sniderman, Regression of left ventricular hypertrophy in dialysis patients following correction of anemia with recombinant human erythropoietin, Can J Cardiol, 6, pp. 1-4, (1990)
[6]  
Goldberg, Lundin, Delano, Friedman, Stein, Changes in left ventricular size, wall thickness and function in anemic patients treated with recombinant human erythropoietin, Am Heart J, 124, pp. 424-427, (1992)
[7]  
Low-Friedrich, Grutzmacher, Marz, Bergmann, Schoeppe, Therapy with recombinant human erythropoietin reduces cardiac size and improves heart function in chronic hemodialysis patients, Am J Neprhol, 11, pp. 54-60, (1991)
[8]  
Pascual, Teruel, Moya, Liano, Jimenez-Mena, Ortuno, Regression of left ventricular hypertrophy after partial correction of anemia with erythropoetin in patients on hemodialysis: a prospective study, Clin Nephrol, 35, pp. 280-287, (1991)
[9]  
Martinez-Vea, Bardaji, Garcia, Ridao, Richart, Oliver, Long-term myocardial effects of correction of anemia with recombinant human erythropoietin in aged patients on hemodialysis, Am J Kidney Dis, 19, pp. 353-357, (1992)
[10]  
London, Zins, Pannier, Naret, Berthelot, Jacquot, Safer, Drueke, Vascular changes in hemodialysis patients in response to recombinant human erythropoietin, Kidney Int, 36, pp. 878-882, (1989)