Administration of Nebivolol After Coronary Artery Bypass in Patients with Altered Left Ventricular Function
Autor: | Alain D'Hollander, Jean Louis Leclerc, Luc Barvais, R. J. Kahn, Jean Louis Vincent, Van Nueten L, M Goldstein, Scheijgrond H, De Smet Jm |
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Rok vydání: | 1993 |
Předmět: |
Male
medicine.medical_specialty Cardiac output Adrenergic beta-Antagonists Cardiac index Hemodynamics Nebivolol Postoperative Complications Double-Blind Method Internal medicine Tachycardia Supraventricular Transducers Pressure Humans Medicine Benzopyrans Prospective Studies Coronary Artery Bypass Aged Pharmacology Blood Volume Ejection fraction business.industry Stroke Volume Middle Aged Atenolol Adrenergic beta-1 Receptor Antagonists Echocardiography Doppler medicine.anatomical_structure Ethanolamines Anesthesia Vascular resistance Cardiology Atrial Function Left Female Vascular Resistance Cardiology and Cardiovascular Medicine business Isovolumic relaxation time medicine.drug |
Zdroj: | Europe PubMed Central |
ISSN: | 0160-2446 |
DOI: | 10.1097/00005344-199308000-00013 |
Popis: | This prospective, double-blind study used invasive monitoring and echo-Doppler techniques to compare the hemodynamic effects of nebivolol, a new beta 1-selective beta-blocking agent with those of atenolol in patients recovering from coronary artery bypass grafting surgery. Five milligrams nebivolol and 50 mg atenolol equally decreased heart rate (HR) and blood pressure (BP) but, nebivolol, in contrast to atenolol, caused no decrease in stroke index (SI), cardiac index (CI), and right ventricular ejection fraction (RVEF). These differences appeared to be related in part to different peripheral effects of the two agents because nebivolol administration was associated with a reduction in systemic vascular resistance (SVR). After < or = 10 days of treatment, acceleration of aortic flow velocity increased and isovolumic relaxation time decreased with nebivolol but not with atenolol treatment. Both drugs were equally well tolerated. Therefore, nebivolol shares most of its effects with classical beta 1-blockers but is devoid of the potentially harmful effects on cardiac output (CO) and peripheral resistance. |
Databáze: | OpenAIRE |
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