Harrison M R, Smith M D, Nissen S E, Grayburn P A, DeMaria A N
Division of Cardiology, University of Kentucky, Lexington.
J Am Coll Cardiol. 1988 May;11(5):1002-9. doi: 10.1016/s0735-1097(98)90058-4.
This study evaluated the ability of exercise Doppler echocardiography to identify hemodynamic changes due to cardiac medication. Twenty young healthy volunteers (mean age 30 years) underwent continuous wave Doppler examination from the suprasternal notch at rest, during each stage of a standard exercise protocol and immediately after exercise. On completion of the control test, each subject received either 60 to 80 mg of propranolol or 120 mg of verapamil orally, and the same exercise protocol was repeated after 90 min. During the control test, values for modal velocity, acceleration and flow velocity integral all increased significantly from baseline (p less than 0.0002 for each). When exercise was repeated after propranolol administration, values for all Doppler measurements were significantly altered. Modal velocity at baseline was significantly lower after propranolol when compared with control (0.53 +/- 0.11 versus 0.63 +/- 0.17 m/s; p less than 0.0001). Similarly, modal velocity at maximal exercise was significantly lower after propranolol (1.11 +/- 0.2 versus 1.25 +/- 0.21 m/s; p less than 0.0001). The effect of propranolol on acceleration was even greater, with blunting of baseline (11.4 +/- 2 versus 15.4 +/- 5 m/s per s; p less than 0.0005) and exertional (33.4 +/- 10 versus 56.3 +/- 15 m/s per s; p less than 0.0001) acceleration. The flow velocity integral during exercise was greater after propranolol (14.1 +/- 3.1 versus 10.1 +/- 3.2 cm; p less than 0.0005) than during the control test. Verapamil failed to influence any Doppler-measured index of aortic blood flow.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究评估了运动多普勒超声心动图识别心脏药物引起的血流动力学变化的能力。20名年轻健康志愿者(平均年龄30岁)在静息状态下、标准运动方案的每个阶段以及运动后立即从胸骨上切迹进行连续波多普勒检查。在对照试验完成后,每位受试者口服60至80毫克普萘洛尔或120毫克维拉帕米,90分钟后重复相同的运动方案。在对照试验期间,平均速度、加速度和流速积分值均较基线显著增加(每项p均小于0.0002)。服用普萘洛尔后重复运动时,所有多普勒测量值均发生显著改变。与对照相比,普萘洛尔服用后基线时的平均速度显著降低(0.53±0.11对0.63±0.17米/秒;p小于0.0001)。同样,普萘洛尔服用后最大运动时的平均速度也显著降低(1.11±0.2对1.25±0.21米/秒;p小于0.0001)。普萘洛尔对加速度的影响更大,基线加速度(11.4±2对15.4±5米/秒每秒;p小于0.0005)和运动时加速度(33.4±10对56.3±15米/秒每秒;p小于0.0001)均减弱。运动期间普萘洛尔组的流速积分大于对照试验期间(14.1±3.1对10.1±3.2厘米;p小于0.0005)。维拉帕米未能影响任何多普勒测量的主动脉血流指标。(摘要截断于250字)