Few validated approaches exist for the transition from intravenous (IV) insulin infusion to subcutaneous (SQ) insulin post-operatively in cardiothoracic surgery patients.
This study aimed to assess whether a pharmacist-driven protocol utilizing basal, prandial, correctional, or correctional-only SQ insulin is safe and efficacious for post-operative glycemic control following 24 h of IV insulin administration.
A retrospective, single-center, observational study investigating outcomes associated with a pharmacist-driven protocol utilizing basal, prandial, correctional, or correctional-only insulin from May 2023 through July 2023 when compared with a historical nursing-driven protocol observed from May 2021 through July 2021. Adult cardiac intensive care unit patients who received an insulin infusion within 24 h of cardiothoracic surgery and subsequently transitioned to SQ insulin were observed. The primary outcome was percentage of blood glucose (BG) readings at goal (140–180 mg/dL). Secondary outcomes included percentage of BG readings in a clinically acceptable range (110–180 mg/dL), hypoglycemia (<70 mg/dL), severe hypoglycemia (<40 mg/dL), administration of rescue dextrose, reinitiation of insulin infusion following transition, and surgical site infection.
Use of a pharmacist-driven protocol improved the percentage of BG readings in goal range when compared with a nursing driven protocol (24.4% vs. 12.4%, p = 0.001). More BG readings were in the clinically acceptable range in the pharmacist-driven group: 69.6% of readings versus 58.5% in the nursing-driven group (p = 0.011). There were fewer hypoglycemic events in the pharmacist-driven group. There were no reports of severe hypoglycemia, further IV insulin requirements, or surgical site infections in either group. Pharmacist compliance to the protocol was high at 92.4%.
A pharmacist-driven protocolized approach to the transition to SQ insulin post-operatively in cardiothoracic patients is both safe and efficacious. The pharmacist-driven protocol resulted in an improved percentage of BG readings in goal range and fewer hypoglycemic events when compared with the historical nursing-driven protocol.