Phase IV Study on the Antihypertensive Effect and Safety of Irbesartan in Patients with Mild to Moderate Hypertension and Renal Disease.
- Author:
Soo Young YOON
1
;
Seung Hyeok HAN
;
Jeong Yeob PARK
;
Byoung Keuk KIM
;
Young Su SONG
;
Joo Seong KIM
;
Jung Jung ROH
;
Hyun Jin NOH
;
Sug Kyun SHIN
;
Kyu Hun CHOI
;
Dae Suk HAN
;
Ho Yung LEE
Author Information
1. Department of Internal Medicine, College of Medicine, Yonsei University, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Irbesartan;
Angiotnsin II receptor antagonist;
Hypertension;
Renal disease
- MeSH:
Alkaline Phosphatase;
Angiotensin II;
Bilirubin;
Blood Glucose;
Blood Pressure;
Calcium;
Cholesterol;
Creatinine;
Fasting;
Heart Rate;
Hematocrit;
Humans;
Hypertension*;
Potassium;
Sodium;
Uric Acid
- From:Korean Journal of Nephrology
2000;19(4):731-739
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Irbesartan is a new selective angiotensin II subtype 1 receptor antagonist. We evaluated the efficacy and tolerability of irbesartan in patients with mild to moderate hypertension and renal disease. On 24 hypertensive patients, oral irbesartan 150mg a day was administered. In cases whose seated diastolic blood pressure did not decrease to 85mmHg after treatment for 4 weeks, the dose of irbesartan was increased to 300mg per day. Every 4 weeks, blood pressure, heart rates, and adverse effects were monitored. And we assessed WBC counts, hemoglobin, hematocrits, platelets, creatinine, BUN, total protein, albumin, fasting blood sugar, total cholesterol, AST, ALT, alkaline phosphatase, total bilirubin, sodium, potassium, calcium, uric acid and urine protein/creatinine ratio to evaluate the change of renal and hepatic function and other adverse effects. Seated systolic blood pressure was decreased from 157.1+/-3.1mmHg to 135.5+/-3.7mmHg, and seated diastolic blood pressure was also decreased from 99.2+/-1.7mmHg to 84.3+/-2.5mmHg. Irbesartan was effective in lowering blood pressure in 20 among 24 patients, and the effective rate of this drug was 83.3%. After treatment, a non clinically significant increase of heart rates and statistically significant decrease of total cholesterol level were noted. There was no dose-related adverse effect. We conclude that irbesartan is a safe and effective angiotensin II subtype 1 receptor antagonist for lowering blood pressure in patients with mild to moderate hypertension and renal disease.
