Department of Hospital Pharmacy, Williamson Medical Center, Franklin, Tennessee.
Department of Hospital Pharmacy, Williamson Medical Center, Franklin, Tennessee; Department of Pharmacy and Pharmaceutical Sciences, Lipscomb University, Nashville, Tennessee.
J Emerg Med. 2024 Oct;67(4):e368-e374. doi: 10.1016/j.jemermed.2024.04.006. Epub 2024 May 3.
Hypertensive crisis is an acute increase in blood pressure >180/120 mm Hg. A titratable antihypertensive agent is preferred to lower blood pressure acutely in a controlled way and prevent an abrupt overcorrection. Nicardipine and clevidipine are both dihydropyridine calcium channel blockers that provide unique benefits for blood pressure control.
The purpose of this study was to compare the efficacy and safety of nicardipine or clevidipine for blood pressure control in the setting of hypertensive crisis.
This was a single-center, retrospective cohort study. Eligible patients received either nicardipine or clevidipine for the treatment of hypertensive crisis. The primary outcome was achievement of 25% reduction in mean arterial pressure at 1 h. The secondary outcome was achievement of a systolic blood pressure (SBP) of <160 mm Hg at 2-6 h from the start of the infusion.
This study included a total of 156 patients, 74 in the nicardipine group and 82 in the clevidipine group. The SBP on admission and at the start of the infusion were similar between groups. There was no difference between groups in achieving a 25% reduction in mean arterial pressure at 1 h. Nicardipine achieved an SBP goal of <160 mm Hg at 2-6 h significantly more often than the clevidipine group (89.2% vs. 73.2%; p = 0.011).
There is no difference between agents for initial blood pressure control in the treatment of hypertensive crisis. Nicardipine showed more sustained SBP control, with a lower risk of rebound hypertension and a significant cost savings compared with clevidipine.
高血压危象是血压突然升高>180/120mmHg。在急性降压时,应首选可滴定的降压药物,以控制血压并防止血压急剧回升。尼卡地平与拉贝洛尔均为二氢吡啶类钙通道阻滞剂,在血压控制方面具有独特的优势。
本研究旨在比较尼卡地平和拉贝洛尔在高血压危象患者中降压的疗效和安全性。
这是一项单中心回顾性队列研究。符合条件的患者接受尼卡地平或拉贝洛尔治疗高血压危象。主要结局是在 1 小时内平均动脉压降低 25%。次要结局是在开始输注后 2-6 小时内收缩压(SBP)<160mmHg。
本研究共纳入 156 例患者,尼卡地平组 74 例,拉贝洛尔组 82 例。两组患者入院时和开始输注时的 SBP 相似。两组患者在 1 小时时平均动脉压降低 25%的差异无统计学意义。尼卡地平组在 2-6 小时达到 SBP<160mmHg 目标的比例明显高于拉贝洛尔组(89.2%比 73.2%;p=0.011)。
在高血压危象的治疗中,初始血压控制药物之间没有差异。与拉贝洛尔相比,尼卡地平的 SBP 控制更持久,且反弹性高血压的风险更低,成本效益比更高。