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dc.contributor.authorYener, Gul
dc.contributor.authorAran, Sinan
dc.contributor.authorBahceci, Mithat
dc.contributor.authorOzdemir, Kurtulus
dc.contributor.authorGultekin, Fusun
dc.contributor.authorLowe, Wing
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:17:11Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:17:11Z
dc.date.issued2007
dc.identifier.issn1173-2563
dc.identifier.issn1179-1918
dc.identifier.urihttps://dx.doi.org/10.2165/00044011-200727090-00003
dc.identifier.urihttps://hdl.handle.net/20.500.12418/10690
dc.descriptionWOS: 000249359500003en_US
dc.descriptionPubMed ID: 17705570en_US
dc.description.abstractBackground and objective: Recently the PatenT (Prevalence, awareness, treatment and control of hypertension in Turkey) study showed that while the prevalence of hypertension in Turkey is high, effective control of BP is infrequently achieved. This study investigated the efficacy and safety of quinapril (as monotherapy or in combination with hydrochlorothiazide [HCTZ]) for achieving BP control (target < 140/90mm Hg) in Turkish subjects with mild to moderate hypertension. Methods: Two-hundred male and female outpatients aged 19-65 years with mild to moderate hypertension (stage I or II, Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure 7 guidelines) entered this 12-week, open-label study. All subjects received quinapril 20 mg/day for 6 weeks. If BP targets were achieved at week 6, responders were maintained on 20 mg/day-1 if BP targets were not achieved, non-responders were randomised to quinapril 40 mg/day or quinapril 20 mg/day + HCTZ 12.5 mg/day for the remainder of the study. Results: After 6 weeks, 63% of subjects achieved BP targets, and 82% of week-6 responders who continued on quinapril 20 mg/day maintained BP targets at week 12. Of the non-responders, 50% and 52% randomised to quinapril 40 mg/day or quinapril 20 mg/day + HCTZ 12.5 mg/day, respectively, went on to achieve BP targets by week 12. Safety was not compromised with increased dosages or use of combination therapy. Conclusion: Quinapril was an effective and safe treatment for achieving and maintaining recommended BP targets in this sample population. These findings will provide clinicians in Turkey with valuable data on the use of quinapril for effective control and management of hypertension.en_US
dc.language.isoengen_US
dc.publisherADIS INT LTDen_US
dc.relation.isversionof10.2165/00044011-200727090-00003en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleQuinapril for treatment of hypertension in Turkey - Dose titration and diuretic combination treatment strategiesen_US
dc.typearticleen_US
dc.relation.journalCLINICAL DRUG INVESTIGATIONen_US
dc.contributor.departmentAnkara Hosp, Dept Internal Med, Ankara, Turkey -- Istanbul Univ, Cerrahpasa Med Fac, Dept Family Med, Istanbul, Turkey -- Dicle Univ, Fac Med, Dept Endocrinol, Diyarbakir, Turkey -- Selcuk Univ Meram, Fac Med, Dept Cardiol, Konya, Turkey -- Cumhuriyet Univ, Fac Med, Dept Cardiol, Sivas, Turkey -- Pfizer Worldwide Dev Operat, Asia Biometr Ctr, Sydney, NSW, Australiaen_US
dc.identifier.volume27en_US
dc.identifier.issue9en_US
dc.identifier.endpage622en_US
dc.identifier.startpage613en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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