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      Azilsartan compared to ACE inhibitors in anti-hypertensive therapy: one-year outcomes of the observational EARLY registry

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          Abstract

          Background

          Azilsartan medoxomil (AZL-M), has been demonstrated to be more effective than the other sartans currently in use; however, there is insufficient information available comparing it with ACE-inhibitors. Therefore, we aimed to compare the efficacy, safety, and tolerability of AZL-M with that of ACE-inhibitors in a real life clinical setting.

          Methods

          The EARLY registry is a prospective, observational, national, multicentre registry with a follow-up period of 12 months. There were two principal objectives: 1) documentation of the achievement of target BP values set according to recent national and international guidelines, and 2) description of the safety profile of AZL-M.

          Results

          A total of 3 849 patients with essential arterial hypertension were recruited from primary care offices in Germany. Patients who initiated monotherapy at baseline comprising either AZL-M or an ACE-inhibitor were included at a ratio of seven to three. Results demonstrated that a blood pressure target of <140/90 mmHg was achieved by a significantly greater proportion of patients in the AZL-M group (61.1 %) compared with the ACE-inhibitor group (56.4 %; p < 0.05; OR, 1.21; 95 % CI, 1.03–1.42), with this finding maintained after adjusting for differences in baseline characteristics. AZL-M appeared to have an equivalent safety profile to the ACE-inhibitors, with a similar incidence of adverse events in the two patient groups ( p = 0.73).

          Conclusions

          These data add to the results of previous randomized controlled clinical trials suggesting that, compared with other agents that target the renin–angiotensin system, AZL-M provides statistically significant albeit small improvements in blood pressure control.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12872-016-0222-6) contains supplementary material, which is available to authorized users.

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          Most cited references19

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          Global burden of hypertension: analysis of worldwide data

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            Angiotensin converting enzyme (ACE) inhibitors versus angiotensin receptor blockers for primary hypertension.

            Angiotensin converting enzyme inhibitors (ACE inhibitors) and angiotensin receptor blockers (ARBs) are widely prescribed for primary hypertension (systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg). However, while ACE inhibitors have been shown to reduce mortality and morbidity in placebo-controlled trials, ARBs have not. Therefore, a comparison of the efficacies of these two drug classes in primary hypertension for preventing total mortality and cardiovascular events is important.
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              The comparative effects of azilsartan medoxomil and olmesartan on ambulatory and clinic blood pressure.

              The current study assesses the antihypertensive efficacy and safety of the investigational angiotensin receptor blocker (ARB), azilsartan medoxomil (AZL-M), compared with placebo and the ARB olmesartan medoxomil (OLM-M). This randomized, double-blind, placebo-controlled, multicenter study assessed change from baseline in mean 24-hour ambulatory systolic blood pressure (SBP) following 6 weeks of treatment. Patients with primary hypertension (n=1275) and baseline 24-hour mean ambulatory systolic pressure ≥ 130 mm Hg and ≤ 170 mm Hg were studied; 142 received placebo and the remainder received 20 mg, 40 mg, or 80 mg AZL-M or 40 mg OLM-M. Mean age of participants was 58 ± 11 years, baseline mean 24-hour SBP was 146 mm Hg. Dose-dependent reductions in 24-hour mean SBP at study end occurred in all AZL-M groups. Reduction in 24-hour mean SBP was greater with AZL-M 80 mg than OLM-M 40 mg by 2.1 mm Hg (95% confidence interval, -4.0 to -0.1; P=.038), while AZL-M 40 mg was noninferior to OLM-M 40 mg. The side effect profiles of both ARBs were similar to placebo. AZL-M is well tolerated and more efficacious at its maximal dose than the highest dose of OLM-M. © 2011 Wiley Periodicals, Inc.
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                Author and article information

                Contributors
                +49-621-5032944 , gitta@klilu.de
                peter.bramlage@ippmed.de
                sebastian.potthoff@med.uni-duesseldorf.de
                p.baumgart@clemenshospital.de
                felix.mahfoud@uniklinikum-saarland.de
                dr.buhck@medcommtools.de
                martina.ehmen@takeda.com
                ouarrak@ihf.de
                senges@ihf.de
                roland.schmieder@uk-erlangen.de
                Journal
                BMC Cardiovasc Disord
                BMC Cardiovasc Disord
                BMC Cardiovascular Disorders
                BioMed Central (London )
                1471-2261
                8 March 2016
                8 March 2016
                2016
                : 16
                : 56
                Affiliations
                [ ]Institut für Herzinfarktforschung, Bremser Strasse 79, 67063 Ludwigshafen, Germany
                [ ]Herzzentrum Ludwigshafen, Medizinische Klinik B, Ludwigshafen, Germany
                [ ]Institut für Pharmakologie und präventive Medizin, Mahlow, Germany
                [ ]Universitätsklinikum Düsseldorf, Klinik für Nephrologie, Düsseldorf, Germany
                [ ]Clemens-Hospital Münster, Klinik für Innere Medizin I, Münster, Germany
                [ ]Universitätsklinikum des Saarlandes, Klinik für Innere Medizin III, Homburg/Saar, Germany
                [ ]MedCommTools, Medical-scientific consultancy, Hannover, Germany
                [ ]Takeda Pharma Vertriebs GmbH, Berlin, Germany
                [ ]Universitätsklinikum Erlangen, Medizinische Klinik 4, Schwerpunkt Nephrologie / Hypertensiologie, Erlangen, Germany
                Article
                222
                10.1186/s12872-016-0222-6
                4784379
                26956148
                1f5b6a1d-97e7-499c-9444-723edd3ba51f
                © Gitt et al. 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 21 August 2015
                : 11 February 2016
                Funding
                Funded by: FundRef http://dx.doi.org/http://dx.doi.org/10.13039/100005570, Takeda Pharmaceuticals North America (US);
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2016

                Cardiovascular Medicine
                azilsartan medoxomil (azl-m),hypertension,real world,effectiveness,safety
                Cardiovascular Medicine
                azilsartan medoxomil (azl-m), hypertension, real world, effectiveness, safety

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