VARIABLE RESPONSE TO ATRIAL-PACING AFTER INTRAVENOUS PROPRANOLOL IN PATIENTS WITH STABLE EXERTIONAL ANGINA

被引:1
作者
DESERVI, S
FERRARIO, M
GHIO, S
CIOFFI, P
ANGOLI, L
BRAMUCCI, E
AIME, E
MONTERICCIO, V
SPECCHIA, G
机构
[1] Divisione di Cardiologia IRCCS, Policlinico S. Matteo, Pavia
关键词
Angina pectoris; Atrial pacing; Coronary haemodynamics; Propranolol;
D O I
10.1093/oxfordjournals.eurheartj.a059640
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effect of propranolol administration on regional coronary haemodynamics were investigated in 14 patients with stable exertional angina and isolated left anterior descending artery disease. Thermodilution was used to measure great cardiac vein flow (GCVF) and anterior regional coronary resistance (ARCR) under control conditions, at peak atrial pacing, after i. v. propranolol administration (0.1 mgkg-1) and at the peak of repeated atrial pacing.Propranolol did not change peak pacing heart rate, systolic blood pressure or double product. Peak pacing GCVF decreased slightly but non-significantly after drug administration from 84±20 to 79±24 ml min-1, while ARCR increased, but again non-significantly, from I.36±0.44 to 1.45±0.45. Analysis of individual patient responses revealed that propranolol prolonged peak pacing time and hence peak pacing heart rate (from 126±24 to 140±23 beats min-1, P<0.05) in five patients. In such patients, peak pacing systolic blood pressure was lower than the pre-propranolol atrial pacing (145±35 vs 165±33, P<0.001) so that double product remained unchanged. Moreover, peak pacing ARCR did not change after propranolol (pre-propranolol 1.47±0.46, after propranolol 1.40±0.56mmHg. ml-1.min, P = ns) while it increased significantly in the nine patients who did not improve after the drug (before propranolol 1.30±0.44, after propranolol 1.48±0.41 mmHg. ml-1.min, P<0.02).These data suggest that the response to atrial pacing after i. v. propranolol administration is variable as some patients tolerate higher heart rates while others do not. Such variability may depend on different effects of the drug on coronary haemodynamics and on factors affecting myocardial oxygen consumption. © 1990 The European Society of Cardiology.
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收藏
页码:997 / 1005
页数:9
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