Flammang D, Waynberger M, Chassing A
Department of Cardiology, Angouleme General Hospital, Saint Michel, France.
Am J Cardiol. 1993 Jun 24;71(17):48E-56E. doi: 10.1016/0002-9149(93)90953-a.
To assess the short- and long-term hemodynamic efficacy of perindopril, 15 patients (12 men and 3 women) diagnosed with congestive heart failure were treated with oral perindopril (4 mg daily) for 3 months in association with digitalis and diuretic maintenance therapy. Patients were in New York Heart Association (NYHA) functional classes III and IV. Underlying cardiopathy was ischemic (6 patients), hypertensive (5 patients), valvular (2 patients), and dilated cardiomyopathy (2 patients). Hemodynamics, angiotensin-converting enzyme (ACE) activity, and perindoprilat (the active metabolite of perindopril) blood titration were measured at 2 periods. Acute assessment was performed over 2 titration days on oral perindopril 2 mg (day 1) and 4 mg (day 2); measurements were performed at rest and at 0, 1, 4, 6, 8, 12, and 24 hours. Chronic assessment was performed after 3 months of treatment with oral perindopril, 4 mg daily. During the study, 1 patient withdrew due to low systolic blood pressure (< 100 mm Hg) and 3 severely impaired patients died due to a worsening of heart failure during the study. Among the 11 remaining patients, 6 were symptomatically improved. On 4 mg perindopril administration, hemodynamic improvement was similar for peak values at both day 2 and at 3 months. At day 2, compared with baseline, cardiac index increased by 21% (p < 0.05) and pulmonary capillary wedge pressure (PCWP) and mean arterial pressure (MAP) decreased by 54% and by 21%, respectively (p < 0.01). Similarly, at 3 months, cardiac index increased by 37% (p < 0.001) and PCWP and MAP decreased by 41% and 19%, respectively (p < 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)
为评估培哚普利的短期和长期血流动力学疗效,对15例诊断为充血性心力衰竭的患者(12例男性和3例女性)进行治疗,给予口服培哚普利(每日4毫克),为期3个月,并联合洋地黄和利尿剂维持治疗。患者均处于纽约心脏协会(NYHA)心功能Ⅲ级和Ⅳ级。基础心脏病包括缺血性(6例)、高血压性(5例)、瓣膜性(2例)和扩张型心肌病(2例)。在两个阶段测量血流动力学、血管紧张素转换酶(ACE)活性和培哚普利拉(培哚普利的活性代谢产物)血药浓度。急性评估在口服培哚普利2毫克(第1天)和4毫克(第2天)的2个滴定日进行;在静息状态以及0、1、4、6、8、12和24小时进行测量。慢性评估在每日口服4毫克培哚普利治疗3个月后进行。研究期间,1例患者因收缩压过低(<100毫米汞柱)退出,3例病情严重的患者在研究期间因心力衰竭恶化死亡。在其余11例患者中,6例症状改善。服用4毫克培哚普利时,第2天和3个月时的峰值血流动力学改善相似。在第2天,与基线相比,心脏指数增加21%(p<0.05),肺毛细血管楔压(PCWP)和平均动脉压(MAP)分别降低54%和21%(p<0.01)。同样,在3个月时,心脏指数增加37%(p<0.001),PCWP和MAP分别降低41%和19%(p<0.01)。(摘要截短于250字)