Trough-to-peak ratio and circadian blood pressure profile after treatment with once-daily extended-release diltiazem, 240 mg, in patients with mild-to-moderate essential hypertension

被引:4
作者
Coca, A
Sobrino, J
Soler, J
Modol, J
Palos, MA
Minguez, A
Esque, J
Plana, J
Cases, M
Closas, J
delaSierra, A
机构
[1] HOSP CLIN BARCELONA, BARCELONA, SPAIN
[2] HOSP SANT CAMIL SANT PERE RIBAS, SANT PERE DE RIBES, SPAIN
关键词
diltiazem extended release; hypertension; ambulatory blood pressure monitoring; trough-to-peak ratio;
D O I
10.1097/00005344-199703000-00003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Once-daily diltiazem extended-release 240 mg (Lacerol-HTA Retard) was evaluated for safety, efficacy, and trough-to-peak ratio in a multicenter open study by using 24-h blood pressure (BP) monitoring in mild-to-moderate essential hypertension. After a 4-week washout period, 30 patients (17 men, 13 women) aged 25-76 years, showing a mean daytime diastolic BP (DBP) >90 mm Hg, were treated with diltiazem-ER, 240 mg, given once daily for 8 weeks. Ambulatory BP monitoring was obtained at the end of a 4-week placebo run-in period and during the last week of treatment. A significant reduction of the mean values of clinical BP [161.6 +/- 16.2 to 151.2 +/- 15.6 mm Hg; p < 0.01 for systolic BP (SBP); and 101.1 +/- 4.8 to 93.3 +/- 9.2 mm Hg; p < 0.001 for DBP] was observed at the end of treatment in the group of 30 patients, with no significant changes in heart rate (77.1 +/- 9.9 to 73.1 +/- 11.1 beats/min; p = NS). Likewise, mean values of 24-h SBP, DBP, SBP-load, and DBP-load were significantly reduced. In the group of 21 responders, the average reduction at peak was -18.6 +/- 12.9 mm Hg for SBP and 14.7 +/- 9.5 mm Hg for DBP. The residual effect at trough was -12.2 +/- 14.7 and -8.1 +/- 10 mm Hg, respectively. The trough-to-peak ratio was estimated as 0.66 for SBP and 0.55 for DBP. Long-term variability expressed as the mean standard deviation of BP for the 24-h period was reduced in responders (16.2 +/- 4.3 to 14.6 +/- 2.7 mm Hg for SBP; p = 0.0395; and 12.1 +/- 2.7 to 10.7 +/- 2.5 mm Hg for DBP; p = 0.0019), although no changes were observed in the variation coefficient (10.58-10.57% for SBP and 12.88-12.87% for DBP). We conclude that once-daily diltiazem-ER, 240 mg, was effective and well tolerated. Blood pressure was controlled over the entire period of 24 h, preserving the circadian profile and reducing long-term variability in responders. The significant reduction of both BP values and long-term variability may have implications involving protection from endorgan damage in essential hypertension.
引用
收藏
页码:316 / 322
页数:7
相关论文
共 53 条
[1]  
ANDERSSON KE, 1985, ACTA PHARMACOL TOX, V57, P1
[2]   PHARMACOKINETIC ANALYSIS OF 2 NEW SUSTAINED-RELEASE PRODUCTS OF DILTIAZEM DESIGNED FOR TWICE-DAILY AND ONCE-DAILY TREATMENT [J].
BIALER, M ;
HADAD, S ;
GOLOMB, G ;
BAREL, S ;
SAMARA, E ;
ABUSALACH, O ;
BERKMAN, N ;
DANENBERG, HD ;
BENDAVID, J ;
CARON, D ;
KAPLAN, R ;
TAMIR, A ;
FRIEDMAN, M .
BIOPHARMACEUTICS & DRUG DISPOSITION, 1994, 15 (01) :45-52
[3]   DIURNAL-VARIATIONS OF BLOOD-PRESSURE AND MICROALBUMINURIA IN ESSENTIAL-HYPERTENSION [J].
BIANCHI, S ;
BIGAZZI, X ;
BALDARI, G ;
SGHERRI, G ;
CAMPESE, VM .
AMERICAN JOURNAL OF HYPERTENSION, 1994, 7 (01) :23-29
[4]  
BLACK HR, 1988, CONSULTANT, V28, P145
[5]   DILTIAZEM - A REVIEW OF ITS PHARMACOLOGICAL PROPERTIES AND THERAPEUTIC EFFICACY [J].
CHAFFMAN, M ;
BROGDEN, RN .
DRUGS, 1985, 29 (05) :387-454
[6]  
CLEMENT DL, 1994, J HYPERTENS, V12, pS49
[7]  
COCA A, 1994, J HYPERTENS, V12, pS13
[8]   DOSE-RANGING STUDY OF A NEW, ONCE-DAILY DILTIAZEM FORMULATION FOR PATIENTS WITH STABLE ANGINA [J].
CUTLER, NR ;
EFF, J ;
FROMELL, G ;
BRASS, EP ;
ARCHER, S ;
CHRYSANT, SG ;
FIDDES, R .
JOURNAL OF CLINICAL PHARMACOLOGY, 1995, 35 (02) :189-195
[9]  
DIXON WJ, 1985, BMDP STATISTICAL SOF
[10]   PLACEBO DOES NOT LOWER AMBULATORY BLOOD-PRESSURE [J].
DUPONT, AG ;
VANDERNIEPEN, P ;
SIX, RO .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1987, 24 (01) :106-109