Dihydralazine or ketanserin for severe hypertension in pregnancy? Preliminary results
dc.contributor.author | Steyn D.W. | |
dc.contributor.author | Odendaal H.J. | |
dc.date.accessioned | 2011-05-15T16:16:22Z | |
dc.date.available | 2011-05-15T16:16:22Z | |
dc.date.issued | 1997 | |
dc.description.abstract | Objective: To compare the efficacy and safety of intravenous dihydralazine with ketanserin in the management of severe hypertension in the third trimester. Study design: A double blind randomised controlled trial, comparing 5 mg dihydralazine with 10 mg ketanserin after an intravenous infusion of 500 ml of a crystalloid solution. Medication was repeated every 20 min till the therapeutic goal of 90 mm Hg was reached, to a maximum of 4 dosages. Main outcome measures were treatment failures and emergency deliveries for fetal distress. Results: The therapeutic goal was met more often in patients receiving dihydralazine (36/38 compared to 27/42; P<0.01). The need for delivery for fetal distress did not differ (3 after dihydralazine, 1 after ketanserin, P=0.29). No therapy related perinatal loss occurred, but one mother with an undiagnosed phaechromocytoma died 24 h after receiving dihydralazine. Conclusion: Ketanserin in this dosage is less effective to lower diastolic blood pressure. The place of a fluid load prior to dihydralazine needs to be further investigated, as fetal heart rate decelerations were less common-than previously reported. | |
dc.description.version | Article | |
dc.identifier.citation | European Journal of Obstetrics Gynecology and Reproductive Biology | |
dc.identifier.citation | 75 | |
dc.identifier.citation | 2 | |
dc.identifier.issn | 03012115 | |
dc.identifier.other | 10.1016/S0301-2115(97)00123-1 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/13748 | |
dc.subject | dihydralazine | |
dc.subject | ketanserin | |
dc.subject | adult | |
dc.subject | article | |
dc.subject | clinical trial | |
dc.subject | controlled study | |
dc.subject | crystalloid | |
dc.subject | double blind procedure | |
dc.subject | drug efficacy | |
dc.subject | drug safety | |
dc.subject | drug screening | |
dc.subject | female | |
dc.subject | fetus distress | |
dc.subject | human | |
dc.subject | intravenous drug administration | |
dc.subject | major clinical study | |
dc.subject | maternal hypertension | |
dc.subject | priority journal | |
dc.subject | randomized controlled trial | |
dc.subject | third trimester pregnancy | |
dc.subject | treatment outcome | |
dc.subject | Adult | |
dc.subject | Antihypertensive Agents | |
dc.subject | Blood Pressure | |
dc.subject | Dihydralazine | |
dc.subject | Double-Blind Method | |
dc.subject | Female | |
dc.subject | Fetal Death | |
dc.subject | Fetal Distress | |
dc.subject | Heart Rate, Fetal | |
dc.subject | Humans | |
dc.subject | Hypertension | |
dc.subject | Infusions, Intravenous | |
dc.subject | Ketanserin | |
dc.subject | Pregnancy | |
dc.subject | Pregnancy Complications, Cardiovascular | |
dc.title | Dihydralazine or ketanserin for severe hypertension in pregnancy? Preliminary results | |
dc.type | Article |