Imperial College London

ProfessorPeterSever

Faculty of MedicineNational Heart & Lung Institute

Professor of Clinical Pharmacology & Therapeutics
 
 
 
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Contact

 

+44 (0)20 7594 1099p.sever

 
 
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Assistant

 

Mrs Yvonne Green +44 (0)20 7594 1100

 
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Location

 

333ICTEM buildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Poulter:2019:10.1007/s40256-018-00314-4,
author = {Poulter, NR and Dolan, E and Gupta, AK and O'Brien, E and Whitehouse, A and Sever, PS},
doi = {10.1007/s40256-018-00314-4},
journal = {American Journal of Cardiovascular Drugs},
pages = {313--323},
title = {Efficacy and safety of incremental dosing of a new single-pill formulation of perindopril and amlodipine in the management of hypertension},
url = {http://dx.doi.org/10.1007/s40256-018-00314-4},
volume = {19},
year = {2019}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - BACKGROUND: Angiotensin-converting enzyme inhibitors and calcium channel blockers in combination are widely recommended in hypertension guidelines. The advantages of single-pill combinations (SPCs) are increasingly recognized, so a dosage-adapted combination of perindopril and amlodipine was developed for the initial management of hypertension. OBJECTIVE: This randomized trial evaluated the blood pressure (BP)-lowering efficacy of four incremental doses of perindopril/amlodipine SPC in adults with mild-to-severe hypertension. METHODS: Eligible patients (N = 1617) were randomized to SPC perindopril 3.5 mg/amlodipine 2.5 mg (i.e., 3.5/2.5 mg) daily, uptitrating as required on a monthly basis up to 14/10 mg until BP < 140/90 mmHg (< 130/80 mmHg in patients with diabetes). The primary endpoint (proportion with controlled BP at each uptitrated dose) was evaluated at 6 months, and safety was evaluated at 9 months; 24-h ambulatory BP measurement and BP variability were also investigated. Control-arm participants (n = 1653) were randomized to irbesartan 150 mg daily, uptitrating over 3 months to irbesartan/hydrochlorothiazide 300/25 mg. RESULTS: Significant increases in BP control were observed with each dosage increment of perindopril/amlodipine, which was well tolerated, rising from 21% (3.5/2.5 mg) to 30% (7/5 mg), 37% (14/5 mg), and 42% (14/10 mg) after 1, 2, 3, and 6 months, respectively. Reductions in mean systolic and diastolic BP occurred with each incremental dose of perindopril/amlodipine. After 6 months, mean BP had fallen by 24.8/10.8 mmHg. Irbesartan-based therapy reduced clinic and 24-h BP similarly to perindopril/amlodipine, but perindopril/amlodipine reduced BP variability more in comparison. CONCLUSIONS: Incremental uptitration with dosage-adapted perindopril/amlodipine SPC is a safe and effective strategy for mana
AU - Poulter,NR
AU - Dolan,E
AU - Gupta,AK
AU - O'Brien,E
AU - Whitehouse,A
AU - Sever,PS
DO - 10.1007/s40256-018-00314-4
EP - 323
PY - 2019///
SN - 1175-3277
SP - 313
TI - Efficacy and safety of incremental dosing of a new single-pill formulation of perindopril and amlodipine in the management of hypertension
T2 - American Journal of Cardiovascular Drugs
UR - http://dx.doi.org/10.1007/s40256-018-00314-4
UR - https://www.ncbi.nlm.nih.gov/pubmed/30919249
UR - http://hdl.handle.net/10044/1/70991
VL - 19
ER -