Interaction of Anesthesia, Beta‐receptor Blockade, and Blood Loss in Dogs with Induced Myocardial Infarction
作者:
Cedric Prys-Roberts,
John Roberts,
Pierre Foëx,
Thomas Clarke,
Meg Bennett,
W. Ryder,
期刊:
Anesthesiology
(OVID Available online 1976)
卷期:
Volume 45,
issue 3
页码: 326-339
ISSN:0003-3022
年代: 1976
出版商: OVID
关键词: Heart,;myocardial infarction; Hemorrhage,;propranolol; Sympathetic nervous system,;beta-adrenergic blockade; Anesthetics;volatile;halo thane
数据来源: OVID
摘要:
The cardiovascular effects of halothane-nitrous oxide anesthesia, and beta-receptor blockade with either propranolol or practolol, were studied in 15 dogs in which severe myocardial infarction had been induced ten days earlier. The hemodynamic responses to blood loss amounting to 25 per cent of estimated blood volume, and its subsequent replacement, were studied before and after induction of beta-receptor blockade. In terms of cardiac output and aortic blood (low acceleration, cardiac performance in the absence of beta-blockade was markedly impaired during steady-state anesthesia, compared with corresponding values in normal dogs. Practolol (2.0 mg/kg) administered during anesthesia induced no significant circulatory change other than a 14 per cent decrease in heart rate and a 25 per cent increase in stroke volume. Propranolol (0.3 mg/kg) caused a comparable reduction of heart rate, but significantly reduced cardiac output (-27 per cent), aortic blood (low acceleration (-26 per cent), and peak L.V power (-19 per cent), and increased systemic vascular resistance (+49 per cent). The two drugs caused comparable shifts of the isoproterenol dose-response curve during anesthesia. Graduated blood loss during anesthesia, to a total of 25 per cent of blood volume, caused consistent circulatory changes (decreased mean arterial pressure, cardiac output, peak LV power, LV minute work) that were essentially similar before and after beta-receptor blockade with either propranolol or practolol. The positive inotropic effect of calcium gluconate during halo thane anesthesia was significantly reduced following either propranolol or practolol, but the hemodynamic responses to changes of systemic vascular resistance induced with acetylcholine or phenylephrine were not modified by beta-receptor blockade.
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