Background: Many patients are diagnosed with hypertension each year, making rapid and effective control of blood pressure (BP) crucial. Appropriate first-line treatment is important, and special attention should be paid to the positive effects of lowering BP early. Perindopril 3.5 mg/amlodipine 2.5mg (P3.5/A2.5) is a single-pill combination suitable for first-line use. The doses of each component of the single-pill combination were selected for a first-line setting. Objective: To investigate the effectiveness of the P3.5/ A2.5 combination at lowering BP compared with renin–angiotensin system (RAS)-inhibitor monotherapies, after 1 month of treatment. Methods: Individual patient data from three randomized controlled trials were used to evaluate the efficacy of P3.5/ A2.5 versus RAS-inhibitor monotherapies after 1 month in 5496 patients with hypertension, in a combined analysis. Results: P3.5/A2.5 was well tolerated and significantly more effective at reducing BP after 1 month than RAS-inhibitor monotherapies (perindopril 5mg, irbesartan 150mg or valsartan 80mg). P3.5/A2.5 was associated with a significantly lower SBP (P¼0.002) and DBP (P¼0.005) after 1 month of treatment compared with RAS-inhibitor monotherapies. Conclusion: In a large patient population, early administration of P3.5/A2.5 resulted in a significantly greater BP-lowering effect than perindopril, irbesartan or valsartan monotherapies after 1 month. Reducing BP levels within a month of treatment may reasonably be expected to lead to a reduced risk of cardiovascular events.

Laurent, S., Mancia, G., Poulter, N. (2018). Perindopril 3.5 mg/amlodipine 2.5 mg versus renin^ angiotensin system inhibitor monotherapy as first-line treatment in hypertension: A combined analysis. JOURNAL OF HYPERTENSION, 36(9), 1915-1920 [10.1097/HJH.0000000000001766].

Perindopril 3.5 mg/amlodipine 2.5 mg versus renin^ angiotensin system inhibitor monotherapy as first-line treatment in hypertension: A combined analysis

Mancia G.;
2018

Abstract

Background: Many patients are diagnosed with hypertension each year, making rapid and effective control of blood pressure (BP) crucial. Appropriate first-line treatment is important, and special attention should be paid to the positive effects of lowering BP early. Perindopril 3.5 mg/amlodipine 2.5mg (P3.5/A2.5) is a single-pill combination suitable for first-line use. The doses of each component of the single-pill combination were selected for a first-line setting. Objective: To investigate the effectiveness of the P3.5/ A2.5 combination at lowering BP compared with renin–angiotensin system (RAS)-inhibitor monotherapies, after 1 month of treatment. Methods: Individual patient data from three randomized controlled trials were used to evaluate the efficacy of P3.5/ A2.5 versus RAS-inhibitor monotherapies after 1 month in 5496 patients with hypertension, in a combined analysis. Results: P3.5/A2.5 was well tolerated and significantly more effective at reducing BP after 1 month than RAS-inhibitor monotherapies (perindopril 5mg, irbesartan 150mg or valsartan 80mg). P3.5/A2.5 was associated with a significantly lower SBP (P¼0.002) and DBP (P¼0.005) after 1 month of treatment compared with RAS-inhibitor monotherapies. Conclusion: In a large patient population, early administration of P3.5/A2.5 resulted in a significantly greater BP-lowering effect than perindopril, irbesartan or valsartan monotherapies after 1 month. Reducing BP levels within a month of treatment may reasonably be expected to lead to a reduced risk of cardiovascular events.
Articolo in rivista - Articolo scientifico
Amlodipine; Calcium channel blocker; Combination; First-line indication; Hypertension; Perindopril; Renin–angiotensin system;
English
2018
36
9
1915
1920
none
Laurent, S., Mancia, G., Poulter, N. (2018). Perindopril 3.5 mg/amlodipine 2.5 mg versus renin^ angiotensin system inhibitor monotherapy as first-line treatment in hypertension: A combined analysis. JOURNAL OF HYPERTENSION, 36(9), 1915-1920 [10.1097/HJH.0000000000001766].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/433764
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