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경증 및 중등도 고혈압 환자에서 Fosinopril 단독 투여에 의한 강압 효과
DC Field | Value | Language |
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dc.contributor.author | 하종원 | - |
dc.date.accessioned | 2023-07-12T00:29:12Z | - |
dc.date.available | 2023-07-12T00:29:12Z | - |
dc.date.issued | 1994-02 | - |
dc.identifier.issn | 1738-5520 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/195132 | - |
dc.description.abstract | Background: The angiotensin-converting enzyme inhibitors have been found to be safe and efficacious in the treatment of essential hypertension. Fosinopril is the first angiotensin-converting enzyme inhibitor from a new class of agents containing phosphorus. This drug is known to be metabolized to almost and equal extent by the hepatic and renal pathways. Methods: This study was performed to investigate the efficacy and safety of oral fosinopril, a new class of phosporus-containing angiotensin converting enzyme inhibitor, on essential hypertension. A single daily dose of 10mg to 20mg fosinopril was administered in 21 hypertensive patients with diastolic blood pressure in the range of 95mmHg-115mmHg while off all other anti-hypertensive agents for 10 weeks. Blood pressure and heart rate were measured every 4 weeks. The complete blood count, blood chemistry by SMA-12, serum electrolytes and urinalysis were performed at 12th week of therapy. Results: 1) Baseline systolic and diastolic blood pressures after 2 weeks of placebo at sitting position were 158.8±15.7 and 99.4±6.3mmHg respectively. There was a statistcally significant reduction of blood pressure after 4 week treatment of fosinopril which was maintained up to 12 weeks of follow-up(158.8±15.7-99.4±6.3mmHg vs 139.3±18.2/86.6±10.3mmHg, p<0.05). 2) The proportion of responders defined by diastolic blood pressures less than 90mmHg or decline more than 10mmHg at 4, 8 and 12 weeks after treatment with fosinopril were 90.5, 95.2, and 95.2% respectively. 3) THere were no significant changes in blood chemistry, serum electrolytes, hematologic findings and heart rate over the treatment period. 4) Three patients experienced severe non-productive cough that required to discontinue the medication. Conclusion: In patients with mild to moderate hypertension, once-daily fosinopril(10mg and 20mg) provided significant anti-hypertensive effects without serious side effects. The 10mg dose was effective in majority of patients and may be considered as a starting dose. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | Korean | - |
dc.publisher | 대한심장학회 | - |
dc.relation.isPartOf | KOREAN CIRCULATION JOURNAL(순환기) | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | 경증 및 중등도 고혈압 환자에서 Fosinopril 단독 투여에 의한 강압 효과 | - |
dc.title.alternative | A Clinical Study on the Anti-Hypertensive Efect of Fosinopril in Mild to Moderate Hypertensive Patients | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | 하종원 | - |
dc.contributor.googleauthor | 임상욱 | - |
dc.contributor.googleauthor | 정남식 | - |
dc.contributor.googleauthor | 심원흠 | - |
dc.contributor.googleauthor | 조승연 | - |
dc.contributor.googleauthor | 김성순 | - |
dc.identifier.doi | 10.4070/kcj.1994.24.1.175 | - |
dc.contributor.localId | A04257 | - |
dc.relation.journalcode | J01953 | - |
dc.identifier.eissn | 1738-5555 | - |
dc.contributor.alternativeName | Ha, Jong Won | - |
dc.contributor.affiliatedAuthor | 하종원 | - |
dc.citation.volume | 24 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 175 | - |
dc.citation.endPage | 181 | - |
dc.identifier.bibliographicCitation | Korean Circulation Journal (순환기), Vol.24(1) : 175-181, 1994-02 | - |
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