Insufficient efficacy of intravenous ketanserin in severe early-onset pre-eclampsia
European Journal of Obstetrics & Gynecology and Reproductive Biology , Volume 128 - Issue 1-2 p. 199- 203
Objective: To analyze the efficacy of intravenous ketanserin in controlling blood pressure of severe early-onset pre-eclamptic patients. Study design: Pre-eclamptic patients (n = 47) with a gestational age (GA) between 21 and 32 weeks were treated with intravenous ketanserin in a maximum dosage of 14 mg/h, to obtain a diastolic blood pressure of 90 mmHg or below. The number of patients reaching and maintaining target blood pressure was retrospectively assessed. Patient characteristics associated with an adequate or inadequate response to ketanserin treatment were identified. Results: With a maximum intravenous dosage of ketanserin, target blood pressure was not achieved in 15 (32%) patients. A high systolic blood pressure at the start of treatment was significantly (p = 0.02) associated with failure of ketanserin treatment. The median period of ketanserin treatment in the responding group was 3 days (range 1-10 days). In 26 (55%) of initially successfully treated patients, additional antihypertensive drugs had to be added to maintain adequate blood pressure control. Conclusion: Intravenous ketanserin lacks antihypertensive efficacy in a substantial proportion of severe pre-eclamptic patients, despite high dosages. In patients who initially respond well to ketanserin treatment, additional antihypertensive treatment is often necessary to maintain adequate blood pressure control.
|, , ,|
|European Journal of Obstetrics & Gynecology and Reproductive Biology|
|Organisation||Department of Gynaecology & Obstetrics|
Hanff, L.M, Visser, W, Roofthooft, D.W.E, Vermes, A, Hop, W.C.J, Steegers, E.A.P, & Vulto, A.G. (2006). Insufficient efficacy of intravenous ketanserin in severe early-onset pre-eclampsia. European Journal of Obstetrics & Gynecology and Reproductive Biology, 128(1-2), 199–203. doi:10.1016/j.ejogrb.2005.11.032