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Cardiovascular Disease: Heart Failure Diagnosis and Rehabilitation


Tuesday, October 23, 2007

2:30 PM - 4:00 PM

PROLONGED INFUSION OF CLEVIDIPINE RESULTS IN SAFE AND PREDICTABLE BLOOD PRESSURE CONTROL IN PATIENTS WITH ACUTE SEVERE HYPERTENSION

J Varon, MD, FCCP*, W. Peacock, MD, N. Garrison, MD, R. Ebrahimi, MD, L. Dunbar, MD, P. Acosta, MD and C. Pollack, MD

University of Texas Health Science Center, Houston, TX

PURPOSE: Severe hypertension is common and requires rapid, predictable and safe reduction of blood pressure (BP). Clevidipine (CLV) is a novel arterial-selective calcium antagonist with an ultra-short half life (t1/2 ~ 1 min). The purpose of this predefined analysis from the VELOCITY trial was to assess the safety and efficacy of a prolonged infusion of CLV in severe hypertension (HTN).

METHODS: An open-label, single-arm trial was performed at 11 centers across the US. Patients presenting in the emergency department with persistent systolic BP (SBP) >180 or diastolic BP >115 mmHg were eligible. SBP target ranges to be achieved within the first 30 min were selected and patients received CLV infusion via a peripheral line using a non-weight based titration algorithm. Patients were monitored with a BP cuff. The infusion rate was maintained or further titrated after 30 min to the desired long-term (≥18 h) SBP target.

RESULTS: Of the 126 patients in the safety population, 117 (mITT population) were included in the efficacy analysis. The mean age was 53 yrs, 51% were female and 77% were black. Almost all patients (97%) had a history of HTN. Mean baseline SBP was 203 mmHg. After initiating CLV the mean SBP rapidly decreased during the titration period: -12 mmHg (-6%) at 3 min, -34 mmHg (-16.5%) at 15 min and -45 mmHg (-21%) at 30 min. Median time to patients achieving a 15% reduction in SBP was 9.5 min. At 18 h the BP reduction was -55 mmHg (-27%) from baseline. Throughout 18 h, target SBP was maintained at a steady CLV infusion rate. A modest 9 bpm increase in HR was seen at 30 min. After 30 min and up to 18 h HR trended back to baseline. AEs were reported in 10% of patients. No hypotensive events were reported.

CONCLUSION: CLV was safe and effective after prolonged infusion in patients with acute severe HTN.

CLINICAL IMPLICATIONS: CLV offers rapid, predictable and safe BP control in patients with acute severe HTN.

DISCLOSURE: J Varon, Consultant fee, speaker bureau, advisory committee, etc. Consultant and Advisor: The Medicines Company; Other Investigator: The Medicines Company; Product/procedure/technique that is considered research and is NOT yet approved for any purpose. Clevidipine for acute, severe hypertension







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Copyright © 2007 by the American College of Chest Physicians.