Clinical Pharmacokinetics of Vasodilators
- 1 January 1998
- journal article
- review article
- Published by Springer Nature in Clinical Pharmacokinetics
- Vol. 35 (1) , 9-36
- https://doi.org/10.2165/00003088-199835010-00002
Abstract
Stimulating cardiac β1-adrenoceptors with oxyfedrine causes dilatation of coronary vessels and positive inotropic effects on the myocardium. β1-adrenergic agonists increase coronary blood flow in nonstenotic and stenotic vessels. The main indication for the use of the phosphodiesterase inhibitors pamrinone, mirinone, enoximone and piroximone is acute treatment of severe congestive heart failure. Theophylline is indicated for the treatment of asthma, chronic obstructive pulmonary disease, apnea in preterm infants ans sleep apnea syndrome. Severe arterial occlusive disease associated with atherosclerosis can be beneficially affected by elcosanoids. These drugs must be administered parenterally and have a half-life of only a few minutes. Sublingual or buccal preparations of nitrates are the only prompt method (within 1 or 2 min) of terminating anginal pain, except for biting nifedipine capsules. The short half-life (about 2.5 min) of nitroglycerin (glyceryl trinitrate) makes long term therapy impossible. Tolerance is a problem encountered with longer-acting nitric oxide donors. Knowledge of the pharmacokinetic properties of vasodilating drugs can prevent a too sudden and severe blood pressure decrease in patients with chronic hypertension. In considering the administration of a second dose, or another drug, the time necessary for the initially administered drug to reach maximal efficacy should be taken into account. In hypertensive emergencies urapidil, sodium nitroprusside, nitroglycerin, hydralazine and phentolamine are the drugs of choice, with the addition of β-blockers during catecholamine crisis or dissecting aortic aneurysm. Childhood hypertension is most often treated with angiotensin-converting enzyme (ACE) inhibitors or calcium antagonists, primarily nifedipine. Because of the teratogenic risk involved with ACE inhibitors, extreme caution must be exercised when prescribing for adolescent females. The propagation of health benefits to breast-fed infants, combined with more women delaying pregnancy until their fourth decade, has entailed an increase in the need for hypertension management during lactation. Low dose hydrochlorothiazide, propranolol, nifendipine and enalapril or captopril do not pose enough of a risk to preclude breastfeeding in this group. The most frequently used antihypertensive agents during pregnancy are methyldopa, labetalol and calcium channel antagonists. Methyldopa and β-blockers are the drugs of choice for treating mild to moderate hypertension. Prazosin and hydralazine are used to treat moderate to severe hypertension and hydralazine, urapidil or labetalol are used to treat hypertensive emergencies. The use of overly aggressive antihypertensive therapy during pregnancy should be avoided so that adequate uteroplacental blood flow is maintained. Methyldopa is the only drug accepted for use during the first trimester of pregnancy.Keywords
This publication has 95 references indexed in Scilit:
- MoxonidineDrugs, 1992
- Clinical Pharmacokinetics and Kinetic-Dynamic Relationships of Dilevalol and LabetalolClinical Pharmacokinetics, 1991
- Pharmacokinetic Interactions Between Theophylline and Other Medication (Part I)1Clinical Pharmacokinetics, 1991
- Effects of Age on the Elimination of LabetalolClinical Pharmacokinetics, 1989
- Evaluation of theophylline pharmacokinetics in a pediatric population using mixed effects modelsJournal of Pharmacokinetics and Biopharmaceutics, 1989
- The population pharmacokinetics of theophylline in neonates and young infantsJournal of Pharmacokinetics and Biopharmaceutics, 1989
- MilrinoneDrugs, 1988
- Relationship of Pharmacokinetic and Pharmacodynamic Properties of the Organic NitratesClinical Pharmacokinetics, 1988
- Influence of Carvedilol on Blood Glucose and Glycohaemoglobin A1 in Non-Insulin-Dependent DiabeticsDrugs, 1988
- Theophylline Disposition in Patients with Hepatic CirrhosisNew England Journal of Medicine, 1977