Effect of Fixed-dose Combination Amlodipine/Valsartan in Comparison to Two Drug Combination Nebivolol/Valsartan on 24-Hour Ambulatory Blood Pressure

Author:

Hanna Selvia M.1ORCID,Rabea Hoda M.2,Abdelrahim Mohamed E.A.2,Mahmoud Hesham B.3

Affiliation:

1. Cardiovascular Department, Beni-Suef University Hospital, Beni-Suef, Egypt

2. Clinical Pharmacy Department, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt

3. Department of Cardiology, Beni-Suef University Hospital, Beni-Suef, Beni-Suef, Egypt

Abstract

Background: Nebivolol has a dual mechanism of action, exerting a moderate b- block-ade effect and reducing peripheral arterial resistance, as a result, the antihypertensive effect of nebivolol may be higher than that of a potent vasodilator CCB such as amlodipine. Aims: The study evaluated the effect of two nebivolol/valsartan on 24 hour ambulatory blood pres-sure versus amlodipine/valsartan in grade II or III hypertension patients or having uncontrolled BP despite treatment. Ambulatory blood pressure monitoring is a powerful method to monitor the changes in blood pressure over the 24 hour. Materials and Methods: A total of 74 from 90 patients continued the study. Fourty patients re-ceived amlodipine 10 mg/valsartan 160 mg (group I), and thirty-four patients received nebivolol 5 mg/ valsartan 160 mg (group II). Peripheral blood pressure readings were measured at randomiza-tion at 6 and 12 weeks. Ambulatory blood pressure was measured at randomization and 12 weeks. Results: Both drug combinations showed high efficacy in reducing peripheral and 24 hour ambu-latory BP. There was no statistically significant difference between the groups in lowering periph-eral systolic and diastolic blood pressure at 6 and 12 weeks. Furthermore, both groups failed to show any significant difference in reducing 24 hour SBP and DBP. Regarding day SBP, the blood pressure dropped by -5.63 ± 14.87 in group I and -6.25 ± 11.59 in group II (p = 0.844). Also, group I reduced the day DBP average by -2.53 ± 9.83 and group II by -3.61 ± 9.78 (p = 0.640). In addition, both drug combinations had no statistically significant difference in lowering night SBP and DBP average. Conclusion: Both treatment groups reached the target ambulatory blood pressure, and there was no statistically significant difference between both groups as a regard reduction in all ambulatory blood pressure readings.

Publisher

Bentham Science Publishers Ltd.

Subject

Internal Medicine

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