87 System Dose Conversion Protocol Evaluation and Formulary Exclusion of U-500 Insulin

Wednesday, May 18, 2016
Dr. Derek LaBar, Pharm.D., BCPS1 and Dr. Leah Frantzen, Pharm.D., BCPS2
1Department of Pharmacy, HealthEast Care System, Maplewood, MN
2Department of Pharmacy, HealthEast Care System, St. Paul, MN
Service or Program:

To promote safe and cost-effective blood glucose management, HealthEast Hospitals removed U-500 insulin from formulary and implemented a conversion protocol for hospitalized patients.

Justification/Documentation:

The Institute for Safe Medication Practices (ISMP) recognizes an increase in medication errors related to dose conversions of home U-500 insulin to inpatient regimens and has called upon health systems to implement practices that avoid inappropriate dosing.  Inaccurately reported insulin doses is a common error leading to a potential 5-fold overdose when using U-500 insulin.  Standards of practice and protocols are necessary in managing this high risk medication.

Transferability:

Decentralized clinical staff pharmacists are uniquely positioned to provide alternative conversion recommendations to prescribers for all concentrated insulins. In collaboration with the diabetes educators, a protocol was approved by HealthEast’s P&T Committee and Medication Safety Committee. All U-500 orders are converted to a basal/prandial insulin regimen in a 50:50 ratio utilizing insulin glargine and insulin aspart along with a custom resistant correction bolus. Prescriber acceptance of the recommendation is required before initiation of the conversion regimen.

Impact:

An evaluation of this implemented protocol was completed from January 1st, 2015 to December 23rd, 2015.  Ten hospitalized patients with orders to resume home U-500 insulin were reviewed.  Eight of ten (80%) patients were initiated on a pharmacist recommended insulin glargine/insulin aspart regimen per protocol. Of those initiated on the protocol, no hypoglycemic events [blood glucose (BG)<70mg/dl] were documented and four hyperglycemic events (BG>200mg/dl) were documented. No incorrect U-500 insulin dose administrations or safety events have been reported following protocol initiation. Concentrated insulins pose new challenges for pharmacists and implementing U-500 formulary exclusion and conversion protocols further promote safe and cost-effective blood glucose management.