SAFETY AND EFFICACY OF URAPIDIL AND SODIUM-NITROPRUSSIDE IN THE TREATMENT OF HYPERTENSIVE EMERGENCIES

Citation
Mm. Hirschl et al., SAFETY AND EFFICACY OF URAPIDIL AND SODIUM-NITROPRUSSIDE IN THE TREATMENT OF HYPERTENSIVE EMERGENCIES, Intensive care medicine, 23(8), 1997, pp. 885-888
Citations number
10
Categorie Soggetti
Emergency Medicine & Critical Care
Journal title
ISSN journal
03424642
Volume
23
Issue
8
Year of publication
1997
Pages
885 - 888
Database
ISI
SICI code
0342-4642(1997)23:8<885:SAEOUA>2.0.ZU;2-V
Abstract
Objective: To assess the safety and efficacy of urapidil compared to s odium nitroprusside in the treatment of hypertensive emergencies. Desi gn: randomized, prospective clinical study. Setting: Emergency departm ent in a 2000-bed inner city hospital. Patients: Eighty-one patients w ith hypertensive emergencies defined as elevation of systolic blood pr essure above 200 mmHg and/or diastolic blood pressure above 110 mmHg p lus evidence of end-organ damage were included in the study protocol. The efficacy of therapy was defined as 1) blood pressure reduction bel ow 180/95 mmHg within 90 min and 2) no re-elevation of blood pressure during a 4-h follow-up period in primary responders. The safety of bot h drugs was defined as the number of minor and major side effects duri ng treatment. Interventions: Patients received either sodium nitroprus side (n = 35; continuous intravenous administration with a starting do se of 0.5 mu g/kg per min; increase in increments of 0.5 mu g/kg per m in every 15 min until response to treatment or a maximum of 3 mu g/kg per min) or urapidil (n = 46; intravenous bolus; starting dose: 12.5 m g; repetitive administration of 12.5 mg every 15 min until response or a maximum dose of 75 mg). Measurements and results: Blood pressure wa s measured every 2.5 min by using a non-invasive oscillometric blood p ressure measurement unit. Response to treatment within 90 min was obse rved in 75 (93 %) patients (urapidil: n = 41 [89 %]; nitroprusside: n = 34 [97 %]; p = 0.18). During the follow-up period 8/34 (24 %) patien ts in the nitroprusside group and 1/41 (2 %) patients in the urapidil group exhibited blood pressure re-elevation. Major side effects were o bserved in seven patients receiving nitroprusside and two patients in the urapidil group (p = 0.04). Conclusion: Urapidil is equally effecti ve, compared to sodium nitroprusside, in the treatment of hypertensive emergencies. Due to a smaller number of adverse events, urapidil is a reasonable alternative to nitroprusside in the treatment of hypertens ive emergencies.