Treatment of acute postoperative hypertension in cardiac surgery patients: An efficacy study of clevidipine assessing its postoperative antihypertensive effect in cardiac surgery-2 (ESCAPE-2), a randomized, double-blind, placebo-controlled trial

被引:60
作者
Singla, Neil [1 ]
Warltier, David C. [2 ]
Gandhi, Sweeta D. [2 ]
Lumb, Philip D. [3 ]
Sladen, Robert N. [4 ]
Aronson, Solomon [5 ]
Newman, Mark F. [5 ]
Corwin, Howard L. [6 ,7 ]
机构
[1] Huntington Mem Hosp, Dept Anesthesia, Pasadena, CA 91105 USA
[2] VA Med Ctr, Dept Anesthesiol, Milwaukee, WI USA
[3] Univ So Calif, Keck Sch Med, Dept Anesthesiol, Los Angeles, CA 90033 USA
[4] Columbia Univ, Coll Phys & Surg, Dept Anesthesiol, New York, NY USA
[5] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
[6] Dartmouth Hitchcock Med Ctr, Dept Med, Lebanon, NH 03766 USA
[7] Dartmouth Hitchcock Med Ctr, Dept Anesthesiol, Lebanon, NH 03766 USA
关键词
D O I
10.1213/ane.0b013e3181732e53
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BACKGROUND: Acute postoperative hypertension is a well-known complication of cardiac surgery and is associated with postoperative morbidity. Clevidipine an ultrashort-acting, third-generation dihydropyridine calcium channel blocker, exerts vascular-selective, arterial-specific vasodilation to decrease arterial blood pressure without negatively impacting cardiac function. In this double-blind, placebo-controlled trial, we examined the efficacy and safety of clevidipine in treating postoperative hypertension in cardiac surgery patients. METHODS: Two hundred six patients undergoing cardiac surgery were randomized preoperatively. Of these, 110 met postrandomization inclusion criteria for the study [systolic blood pressure (SBP) >= 140 mm Hg within 4 h of admission to a postoperative setting clinically assessed as needing SBP reduction by >= 15% from baseline]. Patients received an infusion of either clevidipine (0.4-8.0 mu g kg(-1) min(-1)) or 20% lipid emulsion (placebo) for 30 min to a maximum of 1 h unless treatment failure occurred sooner. The primary end point was the incidence of treatment failure, defined as the inability to decrease SBP by >= 15% from baseline, or the discontinuation of study treatment for any reason within the 30-min period after study drug initiation. RESULTS: Clevidipine-treated patients had a significantly lower incidence of treatment failure than placebo patients [8.2% (5 of 61) vs 79.6% (39 of 49), P < 0.0001]. Treatment success was achieved in 91.8% of clevidipine-treated patients. Median time to target SBP with clevidipine was 5.3 min (95% confidence interval, 4-7 min). No clinically significant increase in heart rate from baseline was observed. Adverse event rates were similar for both treatment groups. CONCLUSIONS: Clevidipine is effective and safe in the rapid treatment of acute postoperative hypertension after cardiac surgery.
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页码:59 / 67
页数:9
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