Fenoldopam infusion for the treatment of postoperative hypertension

Study Objective: To examine the safety and efficacy of intravenous fenoldopam as compared to placebo for the treatment of postoperative hypertension. Design: Randomized, placebo-controlled, double-blind study. Setting: Community hospital. Patients: 16 ASA I–III hypertensive patients scheduled for no...

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Veröffentlicht in:Journal of clinical anesthesia 1993-09, Vol.5 (5), p.386-391
Hauptverfasser: Goldberg, Michael E., Cantillo, Joaquin, Nemiroff, Mark S., Subramoni, Jaya, Muñoz, Raul, Torjman, Marc, Schieren, Hugh
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container_end_page 391
container_issue 5
container_start_page 386
container_title Journal of clinical anesthesia
container_volume 5
creator Goldberg, Michael E.
Cantillo, Joaquin
Nemiroff, Mark S.
Subramoni, Jaya
Muñoz, Raul
Torjman, Marc
Schieren, Hugh
description Study Objective: To examine the safety and efficacy of intravenous fenoldopam as compared to placebo for the treatment of postoperative hypertension. Design: Randomized, placebo-controlled, double-blind study. Setting: Community hospital. Patients: 16 ASA I–III hypertensive patients scheduled for noncardiac surgical procedures. Interventions: Treatment with fenoldopam or placebo was initiated immediately after other causes of hypertension had been ruled out. Hypertension was defined as a supine systolic blood pressure (SBP) or diastolic blood pressure (DBP) greater than 20% over the patient's preoperative baseline, which was obtained 6 hours prior to the procedure with the patient lying quietly. The baseline consisted of 3 consecutive blood pressure (BP) measurements obtained at 5-minute intervals and not varying by more than 10%. Fenoldopam or placebo infusion was initiated at 0.1 μg/kg/min and increased and decreased as necessary until the therapeutic goal BP was reached or treatment failure had occurred. The therapeutic goal BP was a decrease to at least 10% above the preoperative baseline, and failure of treatment was defined as inability to reach this BP level after 15 minutes at 1.5 μg/kg/min. Measurements and Main Results: BP and heart rate (HR) data were collected consistently throughout the study and 1 hour after termination of infusion. Laboratory studies and 12-lead electrocardiographic results were obtained at the start of the study and repeated 24 hours after termination of infusion. Blood samples were obtained for the measurement of epinephrine, norepinephrine, and dopamine levels and were analyzed using high-performance liquid chromatography with electrochemical detection. Pretreatment BP measurements were significantly elevated from baseline in both groups. Fenoldopam treatment significantly reduced BP to the therapeutic goal in 8 of 8 patients; placebo reduced BP to this goal in only 4 of 8 patients ( p < 0.05). At the end of the titration period, the therapeutic goal BP was not significantly different from baseline in the fenoldopam group. HR was significantly elevated ( p < 0.05) at goal in the fenoldopam group as compared with the placebo group. Fenoldopam administration lowered SBP and DBP to goal in a mean time of 28 minutes versus 42.5 minutes in the placebo group. There were no significant differences in catecholamine levels at any of the measurement periods. Conclusion: Fenoldopam is an effective drug for reducing BP f ollowing hyp
doi_str_mv 10.1016/0952-8180(93)90102-K
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Design: Randomized, placebo-controlled, double-blind study. Setting: Community hospital. Patients: 16 ASA I–III hypertensive patients scheduled for noncardiac surgical procedures. Interventions: Treatment with fenoldopam or placebo was initiated immediately after other causes of hypertension had been ruled out. Hypertension was defined as a supine systolic blood pressure (SBP) or diastolic blood pressure (DBP) greater than 20% over the patient's preoperative baseline, which was obtained 6 hours prior to the procedure with the patient lying quietly. The baseline consisted of 3 consecutive blood pressure (BP) measurements obtained at 5-minute intervals and not varying by more than 10%. Fenoldopam or placebo infusion was initiated at 0.1 μg/kg/min and increased and decreased as necessary until the therapeutic goal BP was reached or treatment failure had occurred. The therapeutic goal BP was a decrease to at least 10% above the preoperative baseline, and failure of treatment was defined as inability to reach this BP level after 15 minutes at 1.5 μg/kg/min. Measurements and Main Results: BP and heart rate (HR) data were collected consistently throughout the study and 1 hour after termination of infusion. Laboratory studies and 12-lead electrocardiographic results were obtained at the start of the study and repeated 24 hours after termination of infusion. Blood samples were obtained for the measurement of epinephrine, norepinephrine, and dopamine levels and were analyzed using high-performance liquid chromatography with electrochemical detection. Pretreatment BP measurements were significantly elevated from baseline in both groups. Fenoldopam treatment significantly reduced BP to the therapeutic goal in 8 of 8 patients; placebo reduced BP to this goal in only 4 of 8 patients ( p &lt; 0.05). At the end of the titration period, the therapeutic goal BP was not significantly different from baseline in the fenoldopam group. HR was significantly elevated ( p &lt; 0.05) at goal in the fenoldopam group as compared with the placebo group. Fenoldopam administration lowered SBP and DBP to goal in a mean time of 28 minutes versus 42.5 minutes in the placebo group. There were no significant differences in catecholamine levels at any of the measurement periods. Conclusion: Fenoldopam is an effective drug for reducing BP f ollowing hypertensive episodes in the postoperative setting. 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Design: Randomized, placebo-controlled, double-blind study. Setting: Community hospital. Patients: 16 ASA I–III hypertensive patients scheduled for noncardiac surgical procedures. Interventions: Treatment with fenoldopam or placebo was initiated immediately after other causes of hypertension had been ruled out. Hypertension was defined as a supine systolic blood pressure (SBP) or diastolic blood pressure (DBP) greater than 20% over the patient's preoperative baseline, which was obtained 6 hours prior to the procedure with the patient lying quietly. The baseline consisted of 3 consecutive blood pressure (BP) measurements obtained at 5-minute intervals and not varying by more than 10%. Fenoldopam or placebo infusion was initiated at 0.1 μg/kg/min and increased and decreased as necessary until the therapeutic goal BP was reached or treatment failure had occurred. The therapeutic goal BP was a decrease to at least 10% above the preoperative baseline, and failure of treatment was defined as inability to reach this BP level after 15 minutes at 1.5 μg/kg/min. Measurements and Main Results: BP and heart rate (HR) data were collected consistently throughout the study and 1 hour after termination of infusion. Laboratory studies and 12-lead electrocardiographic results were obtained at the start of the study and repeated 24 hours after termination of infusion. Blood samples were obtained for the measurement of epinephrine, norepinephrine, and dopamine levels and were analyzed using high-performance liquid chromatography with electrochemical detection. Pretreatment BP measurements were significantly elevated from baseline in both groups. Fenoldopam treatment significantly reduced BP to the therapeutic goal in 8 of 8 patients; placebo reduced BP to this goal in only 4 of 8 patients ( p &lt; 0.05). At the end of the titration period, the therapeutic goal BP was not significantly different from baseline in the fenoldopam group. HR was significantly elevated ( p &lt; 0.05) at goal in the fenoldopam group as compared with the placebo group. Fenoldopam administration lowered SBP and DBP to goal in a mean time of 28 minutes versus 42.5 minutes in the placebo group. There were no significant differences in catecholamine levels at any of the measurement periods. Conclusion: Fenoldopam is an effective drug for reducing BP f ollowing hypertensive episodes in the postoperative setting. 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Design: Randomized, placebo-controlled, double-blind study. Setting: Community hospital. Patients: 16 ASA I–III hypertensive patients scheduled for noncardiac surgical procedures. Interventions: Treatment with fenoldopam or placebo was initiated immediately after other causes of hypertension had been ruled out. Hypertension was defined as a supine systolic blood pressure (SBP) or diastolic blood pressure (DBP) greater than 20% over the patient's preoperative baseline, which was obtained 6 hours prior to the procedure with the patient lying quietly. The baseline consisted of 3 consecutive blood pressure (BP) measurements obtained at 5-minute intervals and not varying by more than 10%. Fenoldopam or placebo infusion was initiated at 0.1 μg/kg/min and increased and decreased as necessary until the therapeutic goal BP was reached or treatment failure had occurred. The therapeutic goal BP was a decrease to at least 10% above the preoperative baseline, and failure of treatment was defined as inability to reach this BP level after 15 minutes at 1.5 μg/kg/min. Measurements and Main Results: BP and heart rate (HR) data were collected consistently throughout the study and 1 hour after termination of infusion. Laboratory studies and 12-lead electrocardiographic results were obtained at the start of the study and repeated 24 hours after termination of infusion. Blood samples were obtained for the measurement of epinephrine, norepinephrine, and dopamine levels and were analyzed using high-performance liquid chromatography with electrochemical detection. Pretreatment BP measurements were significantly elevated from baseline in both groups. Fenoldopam treatment significantly reduced BP to the therapeutic goal in 8 of 8 patients; placebo reduced BP to this goal in only 4 of 8 patients ( p &lt; 0.05). At the end of the titration period, the therapeutic goal BP was not significantly different from baseline in the fenoldopam group. HR was significantly elevated ( p &lt; 0.05) at goal in the fenoldopam group as compared with the placebo group. Fenoldopam administration lowered SBP and DBP to goal in a mean time of 28 minutes versus 42.5 minutes in the placebo group. There were no significant differences in catecholamine levels at any of the measurement periods. Conclusion: Fenoldopam is an effective drug for reducing BP f ollowing hypertensive episodes in the postoperative setting. Fenoldopam use is associated with an increase in HR versus placebo.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>8105829</pmid><doi>10.1016/0952-8180(93)90102-K</doi><tpages>6</tpages></addata></record>
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subjects 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine - administration & dosage
2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine - analogs & derivatives
Adult
Aged
Blood Pressure - physiology
Dopamine
Dopamine Agents - administration & dosage
Double-Blind Method
Epinephrine - blood
Female
Fenoldopam
Heart Rate - physiology
Humans
Hypertension - drug therapy
Hypertension - physiopathology
hypertension, postoperative
Infusions, Intravenous
Male
Middle Aged
Norepinephrine - blood
Postoperative Complications - drug therapy
Postoperative Complications - physiopathology
Surgical Procedures, Operative
title Fenoldopam infusion for the treatment of postoperative hypertension
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