Privalova E V, Ershov V I, Ermakov A I, Ivanov A S, Baloian G M, Kulagina T I, Aksiuk M A, Dobrovol'skaia T N
Klin Med (Mosk). 2000;78(2):40-2.
A pilot trial of efficiency of enalapril maleate in the treatment of residual pulmonary hypertension was made in 22 patients operated for rheumatic mitral valve defects. Degree I, II and III of pulmonary hypertension was registered in 5, 13 and 4 patients, respectively. Thus, the patients had NYHA functional classes III and IV (22.7 and 77.3%, respectively. Enalapril given for 6 months in a mean daily dose 12.3 +/- 1.57 mg/m2 (5-30 mg a day) normalized pressure in the pulmonary artery in 18.2% of patients. 50% of patients showed hypertension degree I, only one female retained hypertension degree III. To the end of the treatment the functional classes were the following: II--in 68.2%, III--in 27.3% and IV--in 4.5%.
对22例因风湿性二尖瓣病变接受手术的患者进行了马来酸依那普利治疗残余肺动脉高压疗效的初步试验。肺动脉高压I级、II级和III级的患者分别有5例、13例和4例。因此,这些患者的心功能分级为III级和IV级(分别占22.7%和77.3%)。以平均每日剂量12.3±1.57mg/m²(每日5 - 30mg)给予依那普利6个月,18.2%的患者肺动脉压力恢复正常。50%的患者表现为I级高血压,仅1名女性仍为III级高血压。治疗结束时,心功能分级如下:II级占68.2%,III级占27.3%,IV级占4.5%。