首页 | 本学科首页   官方微博 | 高级检索  
     


A parallel study of enalapril and captopril and 1 year of experience with enalapril treatment in moderate-to-severe essential hypertension
Authors:G S Thind  A Johnson  D Bhatnagar  T W Henkel
Affiliation:2. The Manchester Collaborative Center for Inflammation Research, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK;3. Faculty of Health and Social Care, Edge Hill University, Ormskirk, Lancashire, UK;4. Department of Medical Statistics, University Hospital of South Manchester NHS Foundation Trust, Manchester, UK;5. Centre of Biostatistics, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre; Research and Innovation, Manchester University NHS Foundation Trust, Manchester, UK
Abstract:Angiotensin converting enzyme (ACE) inhibitors, enalapril (5 to 20 mg twice daily) or captopril (25 to 100 mg thrice daily) and matching ACE inhibitor placebos were given to 32 moderate-to-severe essential hypertension patients who were already on 50 mg hydrochlorothiazide daily. Alpha-methyldopa (250 to 500 mg twice daily) was given to 16 patients following 6 weeks of ACE inhibitor therapy. Both enalapril and captopril significantly (p less than 0.05) lowered the supine and upright blood pressures (BPs) (acutely and long-term) without significant reflex heart rate changes. The BPs of enalapril patients were, however, significantly lower (supine diastolic p less than 0.03, supine systolic p less than 0.05, and upright diastolic p less than 0.04) than those of captopril patients when compared by repeated measures of analysis of variance. Eleven enalapril patients have been followed for 1 year with continued BP control. Skin rash occurred in one captopril patient and reversible renal insufficiency developed in two enalapril patients during the first 16 weeks. It is concluded that (although both ACE inhibitors lowered BP, enalapril was more effective than captopril and twice-daily enalapril was well tolerated during 52 weeks of treatment.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号