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Effectiveness of Fimasartan and Rosuvastatin Combination Treatment in Hypertensive Patients With Dyslipidemia

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dc.contributor.author엄재선-
dc.contributor.author심지영-
dc.contributor.author박성하-
dc.contributor.author오재원-
dc.contributor.author이상학-
dc.contributor.author이승준-
dc.contributor.author고영국-
dc.contributor.author김병극-
dc.contributor.author홍성진-
dc.contributor.author홍그루-
dc.contributor.author최동훈-
dc.contributor.author장혁재-
dc.contributor.author김중선-
dc.contributor.author안철민-
dc.date.accessioned2020-09-28T11:48:35Z-
dc.date.available2020-09-28T11:48:35Z-
dc.date.issued2020-06-
dc.identifier.issn0149-2918-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/179293-
dc.description.abstractPurpose: The goal of this study was to evaluate the concurrent control rate of hypertension and dyslipidemia by fimasartan and rosuvastatin in patients who were concomitantly prescribed both drugs. Methods: This single-center, cross-sectional study was conducted in 536 patients with hypertension and dyslipidemia who were taking fimasartan and rosuvastatin together for at least 12 weeks. Patients were enrolled from October 2016 to March 2018 at a tertiary hospital in the Republic of Korea. The primary end point was the concurrent control rate of blood pressure (<140/90 mm Hg) and LDL-C. As a secondary end point, the target blood pressure <130/80 mm Hg was adopted in all patients or in high-risk patients with atherosclerotic cardiovascular diseases. Target LDL-C and non-HDL-C levels followed the domestic guidelines. Correlation between blood pressure control and lipid profile was also evaluated. All parameters were assessed in a clinic by board-certified physicians. Findings: Of the total 536 patients, 69% (n = 368) had very high (n = 308) or high (n = 60) cardiovascular risk, with an average age of 65 years; 57% were male. When the target blood pressure was set at 140/90 mm Hg, the proportion of patients meeting the targeting LDL-C level was 40.3% (95% CI, 36.2-44.5; P < 0.001). When applied to the revised blood pressure criteria targeting 130/80 mm Hg, the concurrent control rate dropped by one half to 20.3% (95% CI, 17.2-24.0; P < 0.001). To apply the new blood pressure criteria, more intensive management is mandatory in patients with high or very high cardiovascular risk. There was no positive correlation between the controlled rate of hypertension and dyslipidemia. Implications: Fimasartan and rosuvastatin were shown to have effects on target diseases, but there was no synergistic effect when administered in combination. The higher the cardiovascular risk of the patients, the lower the rate of concurrent control when fimasartan and rosuvastatin were administered simultaneously. More active treatment is therefore required in high-risk patients.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherExcerpta Medica-
dc.relation.isPartOfCLINICAL THERAPEUTICS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleEffectiveness of Fimasartan and Rosuvastatin Combination Treatment in Hypertensive Patients With Dyslipidemia-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorSeung-Jun Lee-
dc.contributor.googleauthorJaewon Oh-
dc.contributor.googleauthorSung-Jin Hong-
dc.contributor.googleauthorIn-Jeong Cho-
dc.contributor.googleauthorSu Rae Kim-
dc.contributor.googleauthorJae-Sun Uhm-
dc.contributor.googleauthorChi Young Shim-
dc.contributor.googleauthorHyuk-Jae Chang-
dc.contributor.googleauthorChul-Min Ahn-
dc.contributor.googleauthorJung-Sun Kim-
dc.contributor.googleauthorByeong-Keuk Kim-
dc.contributor.googleauthorSungha Park-
dc.contributor.googleauthorSang-Hak Lee-
dc.contributor.googleauthorGeu Ru Hong-
dc.contributor.googleauthorYoung-Guk Ko-
dc.contributor.googleauthorDonghoon Choi-
dc.identifier.doi10.1016/j.clinthera.2020.03.019-
dc.contributor.localIdA02337-
dc.contributor.localIdA02213-
dc.contributor.localIdA01512-
dc.contributor.localIdA02395-
dc.contributor.localIdA02833-
dc.contributor.localIdA02927-
dc.contributor.localIdA00127-
dc.contributor.localIdA00493-
dc.contributor.localIdA04403-
dc.contributor.localIdA04386-
dc.contributor.localIdA04053-
dc.contributor.localIdA03490-
dc.contributor.localIdA05648-
dc.relation.journalcodeJ00614-
dc.identifier.eissn1879-114X-
dc.identifier.pmid32376036-
dc.subject.keywordangiotensin receptor blocker-
dc.subject.keywordfimasartan-
dc.subject.keywordhypertension-
dc.subject.keywordrosuvastatin-
dc.contributor.alternativeNameUhm, Jae Sun-
dc.contributor.affiliatedAuthor엄재선-
dc.contributor.affiliatedAuthor심지영-
dc.contributor.affiliatedAuthor박성하-
dc.contributor.affiliatedAuthor오재원-
dc.contributor.affiliatedAuthor이상학-
dc.contributor.affiliatedAuthor이승준-
dc.contributor.affiliatedAuthor고영국-
dc.contributor.affiliatedAuthor김병극-
dc.contributor.affiliatedAuthor홍성진-
dc.contributor.affiliatedAuthor홍그루-
dc.contributor.affiliatedAuthor최동훈-
dc.contributor.affiliatedAuthor장혁재-
dc.citation.volume42-
dc.citation.number6-
dc.citation.startPage1058-
dc.citation.endPage1066.e3-
dc.identifier.bibliographicCitationCLINICAL THERAPEUTICS, Vol.42(6) : 1058-1066.e3, 2020-06-
dc.identifier.rimsid67289-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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