A 2025 prospective cohort study evaluated the efficacy and safety of clevidipine compared to standard intravenous antihypertensive therapy (labetalol with or without urapidil) for maintaining strict postoperative blood pressure control following carotid endarterectomy (CEA). The study analyzed data from 97 consecutive patients between August 2018 and October 2021, with 44 patients receiving clevidipine and 53 receiving non-clevidipine treatment based on physician preference. The primary outcome measured was the Area Under the Curve for systolic blood pressure outside the institutional target range of 130-145 mmHg (AUC-sBP), normalized per hour during the first six postoperative hours. Despite having higher baseline systolic blood pressure and a greater burden of comorbidities, patients treated with clevidipine demonstrated significantly better adherence to the target blood pressure range, with a median AUC-sBP of 120 mmHg x min/h compared to 240 mmHg x min/h in the non-clevidipine group (p <0.00001). This association remained significant after multivariable adjustment for age, sex, and preoperative systolic blood pressure (adjusted coefficient: -220 mmHg x min/h; 95% CI -293 to -146; p= 0.0001). The mean cumulative clevidipine dose was 58 ± 86 mg administered over 14 ± 10 hours. Importantly, no significant differences were observed between groups in secondary outcomes (including time to achieve initial blood pressure control, need for surgical reintervention, hematoma expansion, ICU length of stay, or in-hospital mortality) or in pre-specified adverse events such as significant hypotension, bradycardia, or new-onset atrial fibrillation. The authors conclude that clevidipine was associated with significantly tighter systolic blood pressure control within the narrow target range during the critical first six hours post-CEA compared to standard therapy with labetalol ± urapidil, without an observed increase in adverse effects, suggesting it may be a valuable option for optimizing postoperative management in this high-risk patient population. However, they acknowledge study limitations including its observational single-center design and recommend prospective randomized trials to confirm these findings. [1]