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Efficacy and tolerability of perindopril in the treatment of essential hypertension in postmenopausal women
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Abstract
Material and methods We studied 667 postmenopausal women (54.9 ± 5.4 years) with mild and moderate hypertension. The treatment period lasted 12 weeks. At the first visit, all the patients started receiving perindopril at the dose of 4 mg per day. After 4 and 8 weeks of treatment, in those subjects where diastolic blood pressure was still ≥ 90 mm Hg and did not decrease by ≥ 10 mm Hg in comparison with the last visit, the dose of perindopril was increased to 8 mg per day. If, after 8 weeks, the patient still had elevated blood pressure values, slow release indapamid at the dose of 1.5 mg per day was added.
Results After 4, 8 and 12 weeks of treatment, the normalization of diastolic blood pressure (< 90 mm Hg) was achieved in 42.4%, 67.6% and 84.3% of cases respectively. 74.2% of treated women responded well to the monotherapy with perindopril. In 8.7% cases indapamid at a dose of 1.5 mg had to be added to 8 mg of perindopril. No serious adverse events were noted during the study. The most frequent adverse event was cough, present in 5.1% of patients. Other adverse events were: headache (1.5%), nausea (1%), fatigue (0.9%) and vertigo (0.7%). Only 2.7% of women discontinued the study due to adverse events. 94.5% of women rated their life comfort during this therapy regimen as good or excellent.
Conclusion Our results show that perindopril - long acting, tissue ACEI, is a very effective and a well tolerated drug in the therapy of hypertension in postmenopausal women.
Abstract
Material and methods We studied 667 postmenopausal women (54.9 ± 5.4 years) with mild and moderate hypertension. The treatment period lasted 12 weeks. At the first visit, all the patients started receiving perindopril at the dose of 4 mg per day. After 4 and 8 weeks of treatment, in those subjects where diastolic blood pressure was still ≥ 90 mm Hg and did not decrease by ≥ 10 mm Hg in comparison with the last visit, the dose of perindopril was increased to 8 mg per day. If, after 8 weeks, the patient still had elevated blood pressure values, slow release indapamid at the dose of 1.5 mg per day was added.
Results After 4, 8 and 12 weeks of treatment, the normalization of diastolic blood pressure (< 90 mm Hg) was achieved in 42.4%, 67.6% and 84.3% of cases respectively. 74.2% of treated women responded well to the monotherapy with perindopril. In 8.7% cases indapamid at a dose of 1.5 mg had to be added to 8 mg of perindopril. No serious adverse events were noted during the study. The most frequent adverse event was cough, present in 5.1% of patients. Other adverse events were: headache (1.5%), nausea (1%), fatigue (0.9%) and vertigo (0.7%). Only 2.7% of women discontinued the study due to adverse events. 94.5% of women rated their life comfort during this therapy regimen as good or excellent.
Conclusion Our results show that perindopril - long acting, tissue ACEI, is a very effective and a well tolerated drug in the therapy of hypertension in postmenopausal women.
Keywords
hypertension in women; menopause; angiotensin converting enzyme inhibitors; perindopril
Title
Efficacy and tolerability of perindopril in the treatment of essential hypertension in postmenopausal women
Journal
Issue
Article type
Original paper
Pages
263-271
Published online
2004-07-22
Page views
779
Article views/downloads
1713
Bibliographic record
Nadciśnienie tętnicze 2004;8(4):263-271.
Keywords
hypertension in women
menopause
angiotensin converting enzyme inhibitors
perindopril
Authors
Jadwiga Kłoś
Krystyna Suchecka-Rachoń
Katarzyna Cybulska
Arleta Wilkins