Effect of darbepoetin alfa on exercise tolerance in anemic patients with symptomatic chronic heart failure : A randomized, double-blind, placebo-controlled trial

This study sought to investigate whether darbepoetin alfa, an erythropoiesis-stimulating protein (ESP), improves exercise capacity in patients with symptomatic chronic heart failure (CHF) and anemia. Anemia is common in patients with CHF. In a multicenter, randomized, double-blind, placebo-controlle...

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Published inJournal of the American College of Cardiology Vol. 49; no. 7; pp. 753 - 764
Main Authors PONIKOWSKI, Piotr, ANKER, Stefan D, ROSEN, Stuart D, POOLE-WILSON, Philip A, BANASIAK, Waldemar, COATS, Andrew J. S, MCDONALD, Ken, SZACHNIEWICZ, Joanna, OKONKO, Darlington, LEDWIDGE, Mark, ZYMLINSKI, Robert, RYAN, Enda, WASSERMAN, Scott M, BAKER, Nigel, ROSSER, Dylan
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Science 20.02.2007
Elsevier Limited
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Abstract This study sought to investigate whether darbepoetin alfa, an erythropoiesis-stimulating protein (ESP), improves exercise capacity in patients with symptomatic chronic heart failure (CHF) and anemia. Anemia is common in patients with CHF. In a multicenter, randomized, double-blind, placebo-controlled study, CHF patients with anemia (hemoglobin > or =9.0 to < or =12.0 g/dl) received subcutaneous placebo (n = 22) or darbepoetin alfa (n = 19) at a starting dose of 0.75 microg/kg every 2 weeks for 26 weeks. The primary end point was change in exercise tolerance from baseline to week 27 as measured by peak oxygen uptake (ml/min/kg body weight). Other end points included changes in absolute peak VO2 (ml/min), exercise duration, and health-related quality of life. Differences (95% confidence interval) in mean changes from baseline to week 27 between treatment groups were 1.5 g/dl (0.5 to 2.4) for hemoglobin concentration (p = 0.005), 0.5 ml/kg/min (-0.7 to 1.7) for peak VO2 (p = 0.40), 45 ml/min (-35 to 127) for absolute peak VO2 (p = 0.27), and 108 s (-11 to 228) for exercise duration (p = 0.075). Patients receiving darbepoetin alfa compared with placebo had an improvement in self-reported Patient's Global Assessment of Change (79% vs. 41%, p = 0.01) but no significant differences in the Kansas City Cardiomyopathy and Minnesota Living with Heart Failure Questionnaire scores. Darbepoetin alfa was well tolerated. In patients with symptomatic CHF and anemia, darbepoetin alfa increased and maintained hemoglobin concentrations and improved health-related quality of life. A trend toward increased exercise time but not peak VO2 was observed. (Impact of Darbepoetin Alfa on Exercise Tolerance and Left Ventricular Structure in Subjects With Symptomatic Congestive Heart Failure (CHF) and Anemia; http://clinicaltrials.gov/ct/show/NCT00117234?order = 1; NCT00117234).
AbstractList Effect of Darbepoetin Alfa on Exercise Tolerance in Anemic Patients With Symptomatic Chronic Heart Failure: A Randomized, Double-Blind, Placebo-Controlled Trial Piotr Ponikowski, Stefan D. Anker, Joanna Szachniewicz, Darlington Okonko, Mark Ledwidge, Robert Zymlinski, Enda Ryan, Scott M. Wasserman, Nigel Baker, Dylan Rosser, Stuart D. Rosen, Philip A. Poole-Wilson, Waldemar Banasiak, Andrew J. S. Coats, Ken McDonald In a double-blind, randomized, placebo-controlled trial, 19 anemic heart failure patients (hemoglobin >=9.0 to <=12.0 g/dl) received darbepoetin alfa and 22 patients received placebo every 2 weeks for 26 weeks. Differences (95% confidence interval) in mean changes from baseline to week 27 were: hemoglobin 1.5 g/dl (0.5 to 2.4, p = 0.005), peak Vo20.5 ml/kg/min (-0.7 to 1.7, p = 0.40), absolute peak Vo245 ml/min (-35 to 127; p = 0.27), exercise duration 108 s (-11 to 228, p = 0.075). Patient's Global Assessment of Change improved on drug (79% vs. 41%, p = 0.01). Darbepoetin alfa was well tolerated.
This study sought to investigate whether darbepoetin alfa, an erythropoiesis-stimulating protein (ESP), improves exercise capacity in patients with symptomatic chronic heart failure (CHF) and anemia.OBJECTIVESThis study sought to investigate whether darbepoetin alfa, an erythropoiesis-stimulating protein (ESP), improves exercise capacity in patients with symptomatic chronic heart failure (CHF) and anemia.Anemia is common in patients with CHF.BACKGROUNDAnemia is common in patients with CHF.In a multicenter, randomized, double-blind, placebo-controlled study, CHF patients with anemia (hemoglobin > or =9.0 to < or =12.0 g/dl) received subcutaneous placebo (n = 22) or darbepoetin alfa (n = 19) at a starting dose of 0.75 microg/kg every 2 weeks for 26 weeks. The primary end point was change in exercise tolerance from baseline to week 27 as measured by peak oxygen uptake (ml/min/kg body weight). Other end points included changes in absolute peak VO2 (ml/min), exercise duration, and health-related quality of life.METHODSIn a multicenter, randomized, double-blind, placebo-controlled study, CHF patients with anemia (hemoglobin > or =9.0 to < or =12.0 g/dl) received subcutaneous placebo (n = 22) or darbepoetin alfa (n = 19) at a starting dose of 0.75 microg/kg every 2 weeks for 26 weeks. The primary end point was change in exercise tolerance from baseline to week 27 as measured by peak oxygen uptake (ml/min/kg body weight). Other end points included changes in absolute peak VO2 (ml/min), exercise duration, and health-related quality of life.Differences (95% confidence interval) in mean changes from baseline to week 27 between treatment groups were 1.5 g/dl (0.5 to 2.4) for hemoglobin concentration (p = 0.005), 0.5 ml/kg/min (-0.7 to 1.7) for peak VO2 (p = 0.40), 45 ml/min (-35 to 127) for absolute peak VO2 (p = 0.27), and 108 s (-11 to 228) for exercise duration (p = 0.075). Patients receiving darbepoetin alfa compared with placebo had an improvement in self-reported Patient's Global Assessment of Change (79% vs. 41%, p = 0.01) but no significant differences in the Kansas City Cardiomyopathy and Minnesota Living with Heart Failure Questionnaire scores. Darbepoetin alfa was well tolerated.RESULTSDifferences (95% confidence interval) in mean changes from baseline to week 27 between treatment groups were 1.5 g/dl (0.5 to 2.4) for hemoglobin concentration (p = 0.005), 0.5 ml/kg/min (-0.7 to 1.7) for peak VO2 (p = 0.40), 45 ml/min (-35 to 127) for absolute peak VO2 (p = 0.27), and 108 s (-11 to 228) for exercise duration (p = 0.075). Patients receiving darbepoetin alfa compared with placebo had an improvement in self-reported Patient's Global Assessment of Change (79% vs. 41%, p = 0.01) but no significant differences in the Kansas City Cardiomyopathy and Minnesota Living with Heart Failure Questionnaire scores. Darbepoetin alfa was well tolerated.In patients with symptomatic CHF and anemia, darbepoetin alfa increased and maintained hemoglobin concentrations and improved health-related quality of life. A trend toward increased exercise time but not peak VO2 was observed. (Impact of Darbepoetin Alfa on Exercise Tolerance and Left Ventricular Structure in Subjects With Symptomatic Congestive Heart Failure (CHF) and Anemia; http://clinicaltrials.gov/ct/show/NCT00117234?order = 1; NCT00117234).CONCLUSIONSIn patients with symptomatic CHF and anemia, darbepoetin alfa increased and maintained hemoglobin concentrations and improved health-related quality of life. A trend toward increased exercise time but not peak VO2 was observed. (Impact of Darbepoetin Alfa on Exercise Tolerance and Left Ventricular Structure in Subjects With Symptomatic Congestive Heart Failure (CHF) and Anemia; http://clinicaltrials.gov/ct/show/NCT00117234?order = 1; NCT00117234).
This study sought to investigate whether darbepoetin alfa, an erythropoiesis-stimulating protein (ESP), improves exercise capacity in patients with symptomatic chronic heart failure (CHF) and anemia. Anemia is common in patients with CHF. In a multicenter, randomized, double-blind, placebo-controlled study, CHF patients with anemia (hemoglobin > or =9.0 to < or =12.0 g/dl) received subcutaneous placebo (n = 22) or darbepoetin alfa (n = 19) at a starting dose of 0.75 microg/kg every 2 weeks for 26 weeks. The primary end point was change in exercise tolerance from baseline to week 27 as measured by peak oxygen uptake (ml/min/kg body weight). Other end points included changes in absolute peak VO2 (ml/min), exercise duration, and health-related quality of life. Differences (95% confidence interval) in mean changes from baseline to week 27 between treatment groups were 1.5 g/dl (0.5 to 2.4) for hemoglobin concentration (p = 0.005), 0.5 ml/kg/min (-0.7 to 1.7) for peak VO2 (p = 0.40), 45 ml/min (-35 to 127) for absolute peak VO2 (p = 0.27), and 108 s (-11 to 228) for exercise duration (p = 0.075). Patients receiving darbepoetin alfa compared with placebo had an improvement in self-reported Patient's Global Assessment of Change (79% vs. 41%, p = 0.01) but no significant differences in the Kansas City Cardiomyopathy and Minnesota Living with Heart Failure Questionnaire scores. Darbepoetin alfa was well tolerated. In patients with symptomatic CHF and anemia, darbepoetin alfa increased and maintained hemoglobin concentrations and improved health-related quality of life. A trend toward increased exercise time but not peak VO2 was observed. (Impact of Darbepoetin Alfa on Exercise Tolerance and Left Ventricular Structure in Subjects With Symptomatic Congestive Heart Failure (CHF) and Anemia; http://clinicaltrials.gov/ct/show/NCT00117234?order = 1; NCT00117234).
Author MCDONALD, Ken
ZYMLINSKI, Robert
WASSERMAN, Scott M
ANKER, Stefan D
LEDWIDGE, Mark
OKONKO, Darlington
BANASIAK, Waldemar
ROSSER, Dylan
COATS, Andrew J. S
RYAN, Enda
BAKER, Nigel
SZACHNIEWICZ, Joanna
PONIKOWSKI, Piotr
ROSEN, Stuart D
POOLE-WILSON, Philip A
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Issue 7
Keywords Physical exercise
Human
Heart failure
Anemia
Tolerance
Cardiovascular disease
Patient
Hemopathy
Phlebology
Chronic
Randomization
Heart disease
Double blind study
Exercise tolerance test
Clinical trial
Circulatory system
Cardiology
Darbepoetin alfa
Language English
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PublicationTitle Journal of the American College of Cardiology
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References 17306704 - J Am Coll Cardiol. 2007 Feb 20;49(7):763-4
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Snippet This study sought to investigate whether darbepoetin alfa, an erythropoiesis-stimulating protein (ESP), improves exercise capacity in patients with symptomatic...
Effect of Darbepoetin Alfa on Exercise Tolerance in Anemic Patients With Symptomatic Chronic Heart Failure: A Randomized, Double-Blind, Placebo-Controlled...
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StartPage 753
SubjectTerms Activities of Daily Living
Aged
Anemia
Anemia - etiology
Anemia - physiopathology
Anemia - therapy
Anemias. Hemoglobinopathies
Biological and medical sciences
Body Weight
Cardiology
Cardiology. Vascular system
Cardiomyopathy
Confidence intervals
Darbepoetin alfa
Diseases of red blood cells
Double-Blind Method
Drug dosages
Drug therapy
Erythropoietin - analogs & derivatives
Erythropoietin - therapeutic use
Exercise Test - drug effects
Exercise Tolerance - drug effects
Female
Fitness equipment
Heart
Heart failure
Heart Failure - complications
Heart failure, cardiogenic pulmonary edema, cardiac enlargement
Hematinics - therapeutic use
Hematologic and hematopoietic diseases
Hemoglobins - drug effects
Hospitalization
Humans
Injections, Subcutaneous
Male
Medical sciences
Mortality
Natriuretic Peptide, Brain - blood
Older people
Oxygen Consumption - drug effects
Quality of Life
Questionnaires
Treatment Outcome
Title Effect of darbepoetin alfa on exercise tolerance in anemic patients with symptomatic chronic heart failure : A randomized, double-blind, placebo-controlled trial
URI https://www.ncbi.nlm.nih.gov/pubmed/17306703
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Volume 49
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