UF Health Jacksonville, Jacksonville, FL, USA.
Am J Health Syst Pharm. 2024 Oct 23;81(21):e668-e676. doi: 10.1093/ajhp/zxae156.
Evidence has suggested that clevidipine may provide faster blood pressure (BP) reduction with less volume than nicardipine in stroke and cardiothoracic surgery patients, but its use in hypertensive crises has not been well established. The primary objective of this study was to compare the treatment success of clevidipine and nicardipine in hypertensive crisis.
This was a multicenter, retrospective cohort study including patients who received either clevidipine or nicardipine for treatment of hypertensive crisis. The primary outcome was the time from infusion start to attainment of goal BP, defined as the higher value of the guideline-directed 25% reduction in BP or the physician-ordered goal. Secondary outcomes were the time from infusion start to guideline-directed 25% reduction in BP, drug and total volume intake, the time from order entry to BP goal attainment, the number of BP and heart rate excursions, intensive care unit (ICU) length of stay, and study medication cost.
In total, 182 patients were included in the study (103 receiving nicardipine and 79 receiving clevidipine). Time to goal BP was similar between the groups (35 vs 33 minutes for clevidipine vs nicardipine, respectively; P = 0.37). Time to guideline-directed 25% reduction was also similar (P = 0.42). Volume from study drug was significantly less with clevidipine (222 vs 518 mL; P = 0.01); however, the total volume received in the ICU was similar (3,370 vs 3,383 mL; P = 0.43). Percent time in the goal BP range was similar (43.1% vs 42.3%). The cost of clevidipine was $199.37 per vial (based on the average wholesale price as of June 2023). This cost was 682% higher than that for a bag of nicardipine.
Time to goal BP was similar for clevidipine and nicardipine in this population. Any decreases in medication-associated volume with clevidipine were no longer evident when all volume sources were considered. These results show that clevidipine may not provide meaningful benefit in this heterogenous population. The difference in cost does not seem justified given the lack of improvement in clinically relevant outcomes.
有证据表明,在脑卒中患者和心胸外科手术患者中,相比尼卡地平,使用拉贝洛尔可更快地降低血压(BP)且容量更少,但在高血压危象中的应用尚未得到充分证实。本研究的主要目的是比较拉贝洛尔和尼卡地平在高血压危象中的治疗效果。
这是一项多中心、回顾性队列研究,纳入了接受拉贝洛尔或尼卡地平治疗高血压危象的患者。主要结局是从开始输注到达到目标血压的时间,定义为指南指导的血压降低 25%的较高值或医生规定的目标值。次要结局包括从开始输注到达到指南指导的血压降低 25%的时间、药物和总液体摄入量、从医嘱输入到达到血压目标的时间、血压和心率波动的次数、重症监护病房(ICU)的住院时间以及研究药物的费用。
共纳入 182 例患者(尼卡地平组 103 例,拉贝洛尔组 79 例)。两组到达目标血压的时间相似(分别为拉贝洛尔组 35 分钟,尼卡地平组 33 分钟;P = 0.37)。达到指南指导的血压降低 25%的时间也相似(P = 0.42)。拉贝洛尔组的研究药物用量明显较少(222 毫升比 518 毫升;P = 0.01);然而,ICU 内的总液体量相似(3370 毫升比 3383 毫升;P = 0.43)。目标血压范围内的时间百分比相似(43.1%比 42.3%)。拉贝洛尔的成本为每瓶 199.37 美元(基于截至 2023 年 6 月的平均批发价格)。这一成本比尼卡地平一袋高出 682%。
在该人群中,拉贝洛尔和尼卡地平达到目标血压的时间相似。当考虑所有液体来源时,拉贝洛尔与药物相关的容量减少的任何减少都不再明显。这些结果表明,在这种异质人群中,拉贝洛尔可能不会提供有意义的益处。鉴于在临床相关结局方面没有改善,成本差异似乎没有理由。