Catarino C, Serra J, Antunes E, Ferreira R, da Silva N, de Oliveira M, Lousada N, Faria J, Quininha J, Gracias R
Serviço de Cardiologia, Hospital de Santa Marta.
Rev Port Cardiol. 1990 Dec;9(12):969-71.
Evaluate the clinical and hemodynamic efficacy of enalapril in the treatment of severe congestive heart failure, refractory to the classic therapeutics with diuretics and digitalis.
Hospitalized patients (pts) of a cardiac department.
10 pts with a mean age of 57.8 years in whom a Swan-Ganz catheter was placed for 72 hours to monitor the right pressures and cardiac output, with regular control of arterial blood pressure and cardiac frequency. Low doses of enalapril (2.5 mg) were utilized at the start of the treatment and this dose was readjusted depending on the clinic and hemodynamic parameters.
the 10 pts had the following characteristics: Basal-mean pulmonary arterial pressure (PAP) 34.1 mmHg, Pulmonary wedge pressure (PWP) 21.1 mmHg, cardiac output (CO) 4.8 l/min, cardiac index (CI) 2.8 l/min/m2. After 72 hours with enalapril treatment, these measurements were: PAP-23.8 mmHg, PWP-12.6 mmHg, CO-5.2 l/min and Cl-3.0 ll/min/m2. These differences were statistically significant. With a follow-up of 18.4 months, there was also a clinical improvement; of the 4 pts in class III, 2 moved to class II and 2 to class I; the 4 pts in class IV 4 moved to class II; two pts had died.
In severe heart failure, the addition of enalapril to the classic therapy has allowed the immediate improvement of the clinical and hemodynamic indexes and this improvement was maintained in the follow-up period.
评估依那普利治疗重度充血性心力衰竭的临床及血流动力学疗效,这类患者对利尿剂和洋地黄等传统疗法无效。
心内科住院患者。
10例平均年龄57.8岁的患者,置入Swan-Ganz导管72小时以监测右心压力和心输出量,同时定期监测动脉血压和心率。治疗开始时使用低剂量依那普利(2.5毫克),并根据临床和血流动力学参数调整剂量。
10例患者具有以下特征:基础平均肺动脉压(PAP)34.1毫米汞柱,肺楔压(PWP)21.1毫米汞柱,心输出量(CO)4.8升/分钟,心脏指数(CI)2.8升/分钟/平方米。依那普利治疗72小时后,这些测量值分别为:PAP - 23.8毫米汞柱,PWP - 12.6毫米汞柱,CO - 5.2升/分钟,CI - 3.0升/分钟/平方米。这些差异具有统计学意义。随访18.4个月时,临床症状也有所改善;4例III级患者中,2例降至II级,2例降至I级;4例IV级患者均降至II级;2例患者死亡。
在重度心力衰竭中,在传统治疗基础上加用依那普利可使临床和血流动力学指标立即改善,且这种改善在随访期内得以维持。