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del Nido cardioplegia

Development stage
Phase 4
Lead developer
University of Pittsburgh
Modality
Implantable Devices → Device-based Delivery → Drug Delivery Systems, Transdermal Patches → Device-based Delivery → Drug Delivery Systems, Inhalation Devices → Device-based Delivery → Drug Delivery Systems
Administration
Intracoronary, Intracardiac
01

Overview

Del Nido cardioplegia is a specialized myocardial protection solution used to induce cardiac arrest during open-heart surgery. Developed in the early 1990s by Pedro Del Nido and colleagues at the University of Pittsburgh, it was initially designed for pediatric cardiac surgery but has since been widely adopted in adult procedures as well[8][1][9]. The formulation consists of a 4:1 ratio of crystalloid (typically Plasma-Lyte A) to autologous blood. Key components include potassium chloride (to induce depolarized arrest), lidocaine (a sodium channel blocker for membrane stabilization), magnesium sulfate (a calcium channel blocker), mannitol (an osmotic agent and free-radical scavenger), sodium bicarbonate (for pH buffering), and trace calcium from the blood fraction[7][6][8]. The mechanism centers on rapid induction of diastolic arrest, minimizing ischemia-reperfusion injury, stabilizing cell membranes, reducing intracellular calcium overload, and providing osmotic protection against edema. It is typically administered as a single dose at 20 mL/kg with a maximum volume around 1000 mL for adults[1][6][9].

Brand names
del Nido cardioplegia
Other names
del Nido solutionDNCdel Nido cardioplegic solution
02

Targets

NaV (Voltage-gated sodium channels)CACNA1C (Voltage-dependent L-type calcium channel subunit alpha-1C)

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