TY - JOUR
T1 - Long-term efficacy of a new, fixed, very-low-dose angiotensin-converting enzyme-inhibitor/diuretic combination as first-line therapy in elderly hypertensive patients
AU - Chalmers, John
AU - Castaigne, Alain
AU - Morgan, Trefor
AU - Chastang, Claude
PY - 2000/3
Y1 - 2000/3
N2 - Objective. To determine the long-term efficacy and safety of a fixed, very-low-dose tablet combining one-half the standard dose of perindopril with one-quarter the standard dose of indapamide as first-line treatment in elderly patients. Design. Double-blind, randomized, placebo-controlled study in an outpatient setting. Patients and interventions. Following a single-blind, placebo run-in period of 4 weeks, patients [65-85 years, with mild-to-moderate essential hypertension or isolated systolic hypertension (ISH)] were randomized to receive one tablet of perindopril 2 mg/indapamide 0.625 mg (Per/Ind) (n = 193) or placebo (n = 190), daily for 12 weeks. After this first 12-week period, all patients on Per/Ind (n = 138) and patients responding to placebo (n = 61) were maintained on their previous regimen for a further 48 weeks. Patients in the placebo group whose blood pressure was not normalized, were switched to Per/Ind (n = 60). Main outcome measure. The primary endpoint was the proportion of patients with blood pressure that normalized between weeks 0 and 60. Results. After 1 year of treatment (intention-to-treat) supine systolic and diastolic blood pressure decreased by 23.0 ± 15.3 mmHg and 13.3 ± 9.4 mmHg with Per/Ind (n = 253: 193 from randomized Per/Ind group and 60 from the placebo group switched at week 12). The mean decreases in systolic blood pressure were similar in essential hypertension and ISH (systolic blood pressure 23.2 versus 22.7 mmHg, respectively). Per/Ind treatment (n = 253) achieved an initial normalization of blood pressure in 96.2% [95% confidence interval (CI) 93.6-98.9%; Kaplan-Meier estimate] of Per/Ind-treated patients; 79.8% (95% CI 74.1-85.5%) of these maintained a normalized blood pressure throughout the 1-year followup. The incidence of adverse events was similarly low in the placebo and active therapy groups. Efficacy and safety results for the over 75 years subgroup were similar to those for the younger elderly subjects. Conclusions. The fixed, very low-dose combination of perindopril 2 mg/indapamide 0.625 mg results in sustained blood pressure control when used as first line treatment of elderly hypertensive patients over 1-year, and is well-tolerated.
AB - Objective. To determine the long-term efficacy and safety of a fixed, very-low-dose tablet combining one-half the standard dose of perindopril with one-quarter the standard dose of indapamide as first-line treatment in elderly patients. Design. Double-blind, randomized, placebo-controlled study in an outpatient setting. Patients and interventions. Following a single-blind, placebo run-in period of 4 weeks, patients [65-85 years, with mild-to-moderate essential hypertension or isolated systolic hypertension (ISH)] were randomized to receive one tablet of perindopril 2 mg/indapamide 0.625 mg (Per/Ind) (n = 193) or placebo (n = 190), daily for 12 weeks. After this first 12-week period, all patients on Per/Ind (n = 138) and patients responding to placebo (n = 61) were maintained on their previous regimen for a further 48 weeks. Patients in the placebo group whose blood pressure was not normalized, were switched to Per/Ind (n = 60). Main outcome measure. The primary endpoint was the proportion of patients with blood pressure that normalized between weeks 0 and 60. Results. After 1 year of treatment (intention-to-treat) supine systolic and diastolic blood pressure decreased by 23.0 ± 15.3 mmHg and 13.3 ± 9.4 mmHg with Per/Ind (n = 253: 193 from randomized Per/Ind group and 60 from the placebo group switched at week 12). The mean decreases in systolic blood pressure were similar in essential hypertension and ISH (systolic blood pressure 23.2 versus 22.7 mmHg, respectively). Per/Ind treatment (n = 253) achieved an initial normalization of blood pressure in 96.2% [95% confidence interval (CI) 93.6-98.9%; Kaplan-Meier estimate] of Per/Ind-treated patients; 79.8% (95% CI 74.1-85.5%) of these maintained a normalized blood pressure throughout the 1-year followup. The incidence of adverse events was similarly low in the placebo and active therapy groups. Efficacy and safety results for the over 75 years subgroup were similar to those for the younger elderly subjects. Conclusions. The fixed, very low-dose combination of perindopril 2 mg/indapamide 0.625 mg results in sustained blood pressure control when used as first line treatment of elderly hypertensive patients over 1-year, and is well-tolerated.
KW - Combination therapy
KW - Elderly
KW - Hypertension
KW - Indapamide
KW - Low-dose
KW - Perindopril
UR - http://www.scopus.com/inward/record.url?scp=0034010827&partnerID=8YFLogxK
U2 - 10.1097/00004872-200018030-00013
DO - 10.1097/00004872-200018030-00013
M3 - Article
C2 - 10726720
AN - SCOPUS:0034010827
VL - 18
SP - 327
EP - 334
JO - Journal of hypertension. Supplement : official journal of the International Society of Hypertension
JF - Journal of hypertension. Supplement : official journal of the International Society of Hypertension
SN - 0952-1178
IS - 3
ER -