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[纽约心脏协会(NYHA)III 级和 IV 级慢性充血性心力衰竭患者卡托普利水平的评估]

[Evaluation of captopril levels in chronic congestive heart failure, stages NYHA III and IV].

作者信息

Mazur-Cichocka M, Michałowicz B, Stasiński T, Wierzchowiecki M

机构信息

II Kliniki Kardiologii Instytutu Kardiologii AM, Poznaniu.

出版信息

Pol Tyg Lek. 1991;46(19-21):375-9.

PMID:1845677
Abstract

Thirty eight patients, aged between 25 and 81 years (mean age 56.9 years) with diagnosed chronic congestive heart failure of NYHA III and IV stages have been examined. The following phases of therapy have been distinguished depending on the used drugs: phase 0--digoxin in a daily dose of 0.25 mg and furosemide in a daily dose of 40-150 mg (mean value 72.4 mg) for 14 days; phase A1A2--nifedipine has been added in a daily dose of 40-80 mg (mean value 64.0 mg), lasting also for 14 days; phase B1B2--captopril (Lopirin--Squibb) has been added to the previous drugs in a daily dose of 25-150 mg (mean value 67.4 mg) in three divided portions for 28 days; phase C1C2--captopril has been withdrawn and drugs as in phase A1A2 have been administered for 14 days. Routine laboratory tests, ECG, a 24-hour ECG-records with Holter's technique, exercise ECG, chest X-ray, and 2D and M echocardiography were performed prior to and after 7 days as well as after each phase of the studies. A significant improvement in the left ventricle functioning assessed with Cubet's echo 2D has been observed in phase B1B2 in comparison with phase A1A2. These parameters have been the following: EF 42.61% vs 31.52%; CO 3.2 vs 2.9 L/min; SV 57.15 vs 44.24 mL (p < .001). Moreover, a decrease in heart volume (X-ray) from 1,145.25 mL to 1,088.25 mL, an increase in exercise tolerance (exercise ECG) in 52.6% of the patients, decrease in Lown's class in 11 out of 24 patients have been noted.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对38例年龄在25至81岁(平均年龄56.9岁)、诊断为纽约心脏病协会(NYHA)III级和IV级慢性充血性心力衰竭的患者进行了检查。根据所使用的药物区分出以下治疗阶段:0期——地高辛每日剂量0.25mg,呋塞米每日剂量40 - 150mg(平均值72.4mg),持续14天;A1A2期——添加硝苯地平,每日剂量40 - 80mg(平均值64.0mg),也持续14天;B1B2期——在前述药物基础上添加卡托普利(洛匹林 - 施贵宝),每日剂量25 - 150mg(平均值67.4mg),分三次服用,持续28天;C1C2期——停用卡托普利,给予与A1A2期相同的药物,持续14天。在研究前、7天后以及每个阶段结束后进行常规实验室检查、心电图、采用动态心电图技术的24小时心电图记录、运动心电图、胸部X线检查以及二维和M型超声心动图检查。与A1A2期相比,B1B2期用二维超声心动图评估的左心室功能有显著改善。这些参数如下:射血分数(EF)42.61%对31.52%;心输出量(CO)3.2对2.9L/分钟;每搏输出量(SV)57.15对44.24mL(p < 0.001)。此外,还注意到心脏体积(X线)从1145.25mL降至1088.25mL,52.6%的患者运动耐量增加(运动心电图),24例患者中有11例洛恩分级降低。(摘要截断于250字)

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