Comparison of acebutolol with and without hydrochlorothiazide versus carvedilol with and without hydrochlorothiazide in black patients with mild to moderate systemic hypertension

Citation
Iv. Radevski et al., Comparison of acebutolol with and without hydrochlorothiazide versus carvedilol with and without hydrochlorothiazide in black patients with mild to moderate systemic hypertension, AM J CARD, 84(1), 1999, pp. 70-75
Citations number
11
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
AMERICAN JOURNAL OF CARDIOLOGY
ISSN journal
00029149 → ACNP
Volume
84
Issue
1
Year of publication
1999
Pages
70 - 75
Database
ISI
SICI code
0002-9149(19990701)84:1<70:COAWAW>2.0.ZU;2-T
Abstract
In the present study, we assessed the antihypertensive efficacy of acebutol ol 200 mg versus carvedilol 25 mg once daily, given as monotherapy for 3 mo nths to 40 black patients (20 patients in each group, mean age 53 +/- 10 ye ars 24 women) with mean blood pressure (BP) during the day >90 and <110 mm Hg. Patients in whom blood pressure could not be controlled took medication , which was increased at 3-month intervals as follows: step 2, acebutolol 2 00 mg or carvedilol 25 mg plus hydrochlorothiazide 12.5 mg once daily; step 3, acebutolol 400 mg or carvedilol 50 mg plus hydrochlorothiazide 25 mg on ce daily. Overall, significant but modest BP reduction was achieved with bo th beta blockers at 3 months. In the acebutolol group, 24-hour BP decreased from 142 +/- 15/94 +/- 7 mm Hg to 138 +/- 16/89 +/- 8 mm Hg (p <0.005 for diastolic BP at 3 months vs baseline). Mean day BP decreased from 145 +/- 1 5/98 +/- 5 mm Hg to 140 +/- 14/93 +/- 7 mm Hg (p <0.05 for systolic BP and p <0.0005 for diastolic BP at 3 months vs baseline). In the carvedilol grou p, 24-hour BP decreased from 145 +/- 11/93 +/- 6 to 138 +/- 16/87 +/- 9 mm Hg (p <0.05 for systolic BP and p<0.005 for diastolic BP at 3 months vs bas eline). Mean day BP decreased from 149 +/- 10/99 +/- 5 to 141 +/- 16/91 +/- 87 mm Hg (p <0.05 for systolic BP and p<0.0005 for diastolic BP at 3 month s vs baseline). At 12 months, most patients required combination therapy to achieve BP control. The control (mean day diastolic BP <90 mm Hg) and resp onse (mean day diastolic BP decrease greater than or equal to 10 mm Hg) rat es at 12 months were 59% and 82% in the acebutolol and 78% and 78% in the c arvedilol groups, respectively. In conclusion, acebutolol or carvedilol in combination with hydrochlorothiazide, rather than acebutolol or carvedilol alone, should be considered as first-line antihypertensive therapy in black patients with mild to moderate hypertension. (C) 1999 by Excerpta Medica, Inc.