Efficacy and safety of spirapril in mild-to-moderate hypertension
- PMID: 10499560
- DOI: 10.1097/00005344-199908001-00004
Efficacy and safety of spirapril in mild-to-moderate hypertension
Abstract
Spirapril is a new angiotensin-converting enzyme (ACE) inhibitor. It is a prodrug with a resorption of about 50%. The active metabolite spiraprilat reaches maximal plasma concentration within 2-3 h after oral administration. Spirapril can be administered once daily because of its long duration of action caused by an elimination half-life of about 40 h. It undergoes renal and hepatic elimination. In contrast to other ACE inhibitors it has a narrow dose range; therefore, the recommended dose is 6 mg for most patients without the need for dose titration. Spirapril has no relevant drug interactions. In several studies, spirapril was given to patients with mild-to-moderate essential hypertension at doses of 1-24 mg/day. There was an identical blood pressure lowering effect at doses of 6-24 mg/day; doses of 1-3 mg/day were less effective. Twenty-four-hour blood pressure monitoring showed a trough:peak ratio up to 0.84. In studies comparing the effect of spirapril with enalapril, lisinopril, trandolapril or captopril, spirapril was at least as effective as the other substances. Besides treating uncomplicated mild-to-moderate essential hypertension, spirapril can be used in patients with diseases accompanying hypertension such as heart and renal diseases, diabetes mellitus, and lipid disturbances. Possible advantages of spirapril compared to other ACE inhibitors are the dual mechanism of elimination, the lack of need for dose titration and a low incidence of cough.
Similar articles
-
Clinical pharmacokinetics and selective pharmacodynamics of new angiotensin converting enzyme inhibitors: an update.Clin Pharmacokinet. 2002;41(3):207-24. doi: 10.2165/00003088-200241030-00005. Clin Pharmacokinet. 2002. PMID: 11929321 Review.
-
Spirapril. A preliminary review of its pharmacology and therapeutic efficacy in the treatment of hypertension.Drugs. 1995 May;49(5):750-66. doi: 10.2165/00003495-199549050-00008. Drugs. 1995. PMID: 7601014 Review.
-
Partial escape of angiotensin converting enzyme (ACE) inhibition during prolonged ACE inhibitor treatment: does it exist and does it affect the antihypertensive response?J Hypertens. 1992 Aug;10(8):803-12. J Hypertens. 1992. PMID: 1325513 Clinical Trial.
-
Effects of spirapril and captopril on regional blood flow in chronic congestive heart failure: a comparison between a short- and a long-acting angiotensin-converting enzyme inhibitor.J Cardiovasc Pharmacol. 1995 Jan;25(1):105-12. doi: 10.1097/00005344-199501000-00017. J Cardiovasc Pharmacol. 1995. PMID: 7723338 Clinical Trial.
-
[Blood pressure lowering by the ACE-inhibitor spirapril. "24-hour efficacy of real once daily application of spirapril (HERAS Study)"].MMW Fortschr Med. 2003 Oct 2;145(40):46. MMW Fortschr Med. 2003. PMID: 14603605 German. No abstract available.
Cited by
-
Clinical pharmacokinetics and selective pharmacodynamics of new angiotensin converting enzyme inhibitors: an update.Clin Pharmacokinet. 2002;41(3):207-24. doi: 10.2165/00003088-200241030-00005. Clin Pharmacokinet. 2002. PMID: 11929321 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous