Acute Care Hospital Products
NASDAQ: MDCO
Rapid, predictable blood pressure (BP) control is essential for the estimated 30% to 56% of cardiac surgery patients who will require IV antihypertensive therapy during the perioperative period.1 Perioperative BP management is a concern for patients with and without a history of chronic hypertension.2,3 BP control during the postoperative period is also important, as the incidence of postoperative hypertensive crises varies from an estimated 4% to 35% of patients.3
Cleviprex® is the latest-generation IV dihydropyridine calcium channel blocker.4 It has a rapid onset and rapid offset of effect for a predictable pharmacologic response.4 Cleviprex is vascular selective and reduces BP by decreasing systemic vascular resistance.4 Cleviprex is rapidly metabolized in the blood and extravascular tissues, not in the liver or kidney.4 It does not have the potential for blocking or inducing any CYP enzyme, and the potential for Cleviprex to interact with other drugs is low.4
In clinical trials of 215 patients with preoperative or postoperative hypertension (ESCAPE trials), Cleviprex decreased SBP by at least 15% within
30 minutes in more than 90% of patients.5,6 The median time to reach the prespecified target BP reduction of ≥15% was approximately 5 minutes in preoperative patients and approximately 6 minutes in postoperative patients.5,6 Cleviprex demonstrated comparable safety and efficacy to 3 other IV antihypertensive treatments (nitroglycerin, sodium nitroprusside, and nicardipine) in clinical trials comprised of 1,512 cardiac surgery patients who required perioperative or postoperative BP reduction (ECLIPSE trials).7
Cleviprex also rapidly lowered BP to an individualized target BP in ~90% of patients in a clinical study of 126 patients presenting to the emergency department or intensive care unit with severe hypertension (VELOCITY trial).8
Cleviprex is intended for intravenous use. Titrate drug depending on the response of the individual patient to achieve the desired blood pressure reduction. Monitor blood pressure and heart rate continually during infusion, and then until vital signs are stable. Patients who receive prolonged Cleviprex infusions and are not transitioned to other antihypertensive therapies should be monitored for the possibility of rebound hypertension for at least 8 hours after the infusion is stopped.
Cleviprex is contraindicated in patients with allergies to soybeans, soy products, eggs, or egg products; defective lipid metabolism such as pathologic hyperlipemia, lipoid nephrosis, or acute pancreatitis if it is accompanied by hyperlipidemia; and in patients with severe aortic stenosis.
Hypotension and reflex tachycardia are potential consequences of rapid upward titration of Cleviprex. Dihydropyridine calcium channel blockers can produce negative inotropic effects and exacerbate heart failure. Monitor heart failure patients carefully. Cleviprex gives no protection against the effects of abrupt beta-blocker withdrawal.
Most common adverse reactions (> 2%) are headache, nausea, and vomiting.
Cleviprex should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
Maintain aseptic technique while handling Cleviprex. Cleviprex contains phospholipids and can support microbial growth. Do not use if contamination is suspected. Once the stopper is punctured, use and discard within 4 hours.
Please see full Prescribing Information.
References