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Anesth Analg ; 91(4): 904-9, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11004045

ABSTRACT

We compared the efficacy of the combination of enalaprilat/labetalol with that of enalaprilat/nicardipine to prevent emergence postcraniotomy hypertension. A prospective, randomized open labeled clinical trial was designed to compare the incidence of breakthrough hypertension (systolic blood pressure [SBP] > 140 mm Hg) and adverse effects (hypotension, tachycardia, and bradycardia) between the two drug combinations. Secondarily, the effects of the drugs on SBP, mean blood pressure, and diastolic blood pressure were evaluated over the course of the study. Forty-two patients received enalaprilat 1.25 mg IV at dural closure followed by either multidose nicardipine 2 mg IV or labetalol 5 mg IV to maintain the SBP below 140 mm Hg. SBP was similarly controlled in both groups. There was a marginally smaller incidence of failures and adverse effects with labetalol. Blood pressure profiles were similar for both groups.


Subject(s)
Adrenergic alpha-Antagonists/therapeutic use , Adrenergic beta-Antagonists/therapeutic use , Anesthesia Recovery Period , Antihypertensive Agents/therapeutic use , Brain Neoplasms/surgery , Calcium Channel Blockers/therapeutic use , Craniotomy , Hypertension/prevention & control , Labetalol/therapeutic use , Nicardipine/therapeutic use , Adrenergic alpha-Antagonists/adverse effects , Adrenergic beta-Antagonists/adverse effects , Adult , Aged , Analysis of Variance , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Antihypertensive Agents/adverse effects , Blood Pressure/drug effects , Bradycardia/chemically induced , Calcium Channel Blockers/adverse effects , Chi-Square Distribution , Enalaprilat/therapeutic use , Female , Humans , Hypotension/chemically induced , Incidence , Labetalol/adverse effects , Male , Middle Aged , Nicardipine/adverse effects , Prospective Studies , Tachycardia/chemically induced , Treatment Outcome
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