Cost-reduction strategy for isoproterenol use in radiofrequency catheter ablation procedures
Scott R Parkin1, Jenna M Negrelli1, Charles M Van Gorder1
1Pharmacy Department, Intermountain Medical Center, Murray, UT.
Purpose:
A cost-reduction strategy for isoproterenol use in radiofrequency catheter ablation procedures was evaluated.
Summary:
A medication-use evaluation at a 454-bed tertiary medical center revealed that the cardiac catheterization laboratory was the highest user of isoproterenol. Isoproterenol was removed from all AcuDose-Rx machines Omnicell, Mountain View, CA, and compounding was performed by pharmacy personnel. It was initially provided to the cardiac catheterization laboratory as an 8-µg/mL concentration in 20-mL 0.9% sodium chloride injection syringes with a 24-hour beyond-use date. This resulted in an initial cost savings but with an unacceptably high rate of wastage. Isoproterenol was then compounded as a 4-µg/mL concentration in 30 mL 5% dextrose in water syringes with a 9-day beyond-use date after a thorough literature search supported longer stability with this admixture. After 12 months of our current process, isoproterenol use during radio frequency catheter ablations (RFCAs) in the cardiac catheterization laboratory was reduced by 85%, decreasing the number of ampules used from 11.15 to 1.66 per week.
Conclusion:
A pharmacy-initiated process to mitigate an extraordinary increase in isoproterenol acquisition cost resulted in a reduction in usage in a tertiary care community hospital. Isoproterenol usage was reduced 85% after two different interventions were implemented, which is estimated to save $1,839 per procedure.
More Related Videos
Related Concept Videos
Oxidation-Reduction Reactions
NMR Spectrometers: Radiofrequency Pulses and Pulse Sequences
Block Diagram Reduction
The first step in this process is the identification and relocation of a branch point. A branch point, where a...
Oxymercuration-Reduction of Alkenes
Phase I Reactions: Reductive Reactions
Esters to Alcohols: Hydride Reductions
Lithium aluminum hydride is a source of hydride ions and functions as a nucleophile. The mechanism proceeds in three steps. Firstly, the nucleophilic hydride ion attacks the carbonyl carbon of the ester to form a tetrahedral intermediate. Subsequently, the carbonyl group re-forms,...


