Adigun A Q, Ajayi O E, Sofowora G G, Ajayi A A
Department of Medicine, College of Health Sciences, Obafemi Awolowo University, Ile-Ife, Osun State, Nigeria.
Int J Cardiol. 1998 Nov 30;67(1):81-6. doi: 10.1016/s0167-5273(98)00234-4.
A prospective study to evaluate and compare the cardiorespiratory effects and clinical efficacy of the Neurohormonal inhibitors (Captopril 50 mg+prazosin 1 mg only) and direct arteriolar and venular dilators (Intravenous hydralazine 30 mg+oral isosorbide dinitrate 30 mg) used as vasodilator therapy, was undertaken in a randomized, single blind study in 17 Nigerian patients with hypertensive acute left ventricular failure. Both vasodilator regimes separately and significantly reduced the systolic and diastolic blood pressures (P<0.001 ANOVA), heart rate (P<0.001 ANOVA), and the respiratory rate (P<0.05 ANOVA), the double product, but increased the peak expiratory flow rate (P<0.05 ANOVA). However, the neurohormonal antagonists, captopril and prazosin (n=9) caused a statistically significantly greater reduction in heart rate (P<0.05 ANOVA) respiratory rate (P<0.05 ANOVA) and induced a significantly greater increase in the self-paced exercise capacity, 24 h after initiation of treatment, (P<0.02) compared to the hydralazine and isosorbide dinitrate combination (n=8). Five of the nine patients on the neurohormonal antagonist therapy were ambulant at 24 h, compared to none of the eight patients receiving conventional venular and arteriolar dilators hydralazine and isosorbide dinitrate (chi2=5.84 dfi P<0.05). There was a significant inverse correlation between the systolic blood pressure heart rate product, and the distance covered during symptom limited self paced exercise capacity (r=-0.58, P=0.0146 ANOVA). One of eight patients in the hydralazine+isosorbide nitrate combination died, but there was no mortality in the captopril+prazosin group. These findings collectively suggest that captopril+prazosin combination may be a superior vasodilator therapy compared to hydralazine-isosorbide dinitrate, in hypertensive acute pulmonary oedema.
一项前瞻性研究在17例尼日利亚高血压急性左心室衰竭患者中进行,该研究采用随机、单盲设计,旨在评估并比较作为血管扩张剂疗法使用的神经激素抑制剂(仅卡托普利50毫克+哌唑嗪1毫克)与直接小动脉和小静脉扩张剂(静脉注射肼屈嗪30毫克+口服硝酸异山梨酯30毫克)的心肺效应及临床疗效。两种血管扩张剂方案均分别显著降低了收缩压和舒张压(方差分析,P<0.001)、心率(方差分析,P<0.001)以及呼吸频率(方差分析,P<0.05)、双乘积,但增加了呼气峰值流速(方差分析,P<0.05)。然而,与肼屈嗪和硝酸异山梨酯联合用药组(n=8)相比,神经激素拮抗剂卡托普利和哌唑嗪组(n=9)在治疗开始24小时后,心率(方差分析,P<0.05)、呼吸频率(方差分析,P<0.05)的降低在统计学上更为显著,并且自定进度运动能力的增加也更为显著(P<0.02)。接受神经激素拮抗剂治疗的9例患者中有5例在24小时时可下床活动,而接受传统小静脉和小动脉扩张剂肼屈嗪和硝酸异山梨酯治疗的8例患者中无一例可下床活动(卡方检验=5.84,自由度1,P<0.05)。症状受限的自定进度运动能力期间所覆盖的距离与收缩压心率乘积之间存在显著的负相关(r=-0.58,方差分析,P=0.0146)。肼屈嗪+硝酸异山梨酯联合用药组的8例患者中有1例死亡,但卡托普利+哌唑嗪组无死亡病例。这些研究结果共同表明,在高血压急性肺水肿中,与肼屈嗪-硝酸异山梨酯相比,卡托普利+哌唑嗪联合用药可能是一种更优的血管扩张剂疗法。