Increased mortality after dronedarone therapy for severe heart failure

التفاصيل البيبلوغرافية
العنوان: Increased mortality after dronedarone therapy for severe heart failure
المؤلفون: Lars, Køber, Christian, Torp-Pedersen, John J V, McMurray, Ole, Gøtzsche, Samuel, Lévy, Harry, Crijns, Jan, Amlie, Jan, Carlsen, P, Smedgård
المصدر: Køber, L, Torp-Pedersen, C, McMurray, J J V, Gøtzsche, O, Lévy, S, Crijns, H, Amlie, J, Carlsen, J & Dronedarone Study Group 2008, ' Increased mortality after dronedarone therapy for severe heart failure ', The New England Journal of Medicine, vol. 358, no. 25, pp. 2678-87 . https://doi.org/10.1056/NEJMoa0800456
سنة النشر: 2008
مصطلحات موضوعية: Drug, Adult, Male, medicine.medical_specialty, Heart disease, media_common.quotation_subject, medicine.medical_treatment, Amiodarone, Kaplan-Meier Estimate, Antiarrhythmic agent, Vernakalant, chemistry.chemical_compound, Ventricular Dysfunction, Left, Double-Blind Method, Internal medicine, Cause of Death, medicine, Humans, Treatment Failure, Intensive care medicine, Dronedarone, Kaplan-Meiers Estimate, media_common, Cause of death, Aged, Aged, 80 and over, Heart Failure, business.industry, General Medicine, Middle Aged, medicine.disease, chemistry, Cardiovascular Diseases, Heart failure, Cardiology, Female, business, Anti-Arrhythmia Agents, medicine.drug
الوصف: Udgivelsesdato: 2008-Jun-19 BACKGROUND: Dronedarone is a novel antiarrhythmic drug with electrophysiological properties that are similar to those of amiodarone, but it does not contain iodine and thus does not cause iodine-related adverse reactions. Therefore, it may be of value in the treatment of patients with heart failure. METHODS: In a multicenter study with a double-blind design, we planned to randomly assign 1000 patients who were hospitalized with symptomatic heart failure and severe left ventricular systolic dysfunction to receive 400 mg of dronedarone twice a day or placebo. The primary end point was the composite of death from any cause or hospitalization for heart failure. RESULTS: After inclusion of 627 patients (310 in the dronedarone group and 317 in the placebo group), the trial was prematurely terminated for safety reasons, at the recommendation of the data and safety monitoring board, in accordance with the board's predefined rules for termination of the study. During a median follow-up of 2 months, 25 patients in the dronedarone group (8.1%) and 12 patients in the placebo group (3.8%) died (hazard ratio in the dronedarone group, 2.13; 95% confidence interval [CI], 1.07 to 4.25; P=0.03). The excess mortality was predominantly related to worsening of heart failure--10 deaths in the dronedarone group and 2 in the placebo group. The primary end point did not differ significantly between the two groups; there were 53 events in the dronedarone group (17.1%) and 40 events in the placebo group (12.6%) (hazard ratio, 1.38; 95% CI, 0.92 to 2.09; P=0.12). More increases in the creatinine concentration were reported as serious adverse events in the dronedarone group than in the placebo group. CONCLUSIONS: In patients with severe heart failure and left ventricular systolic dysfunction, treatment with dronedarone was associated with increased early mortality related to the worsening of heart failure. (ClinicalTrials.gov number, NCT00543699.)
تدمد: 1533-4406
DOI: 10.1056/NEJMoa0800456
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7de075875be59fe40ded0138951e329
https://pubmed.ncbi.nlm.nih.gov/18565866
Rights: RESTRICTED
رقم الانضمام: edsair.doi.dedup.....f7de075875be59fe40ded0138951e329
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15334406
DOI:10.1056/NEJMoa0800456