Related Experiment Video
Updated: May 20, 2025

A Pre-Clinical Porcine Model of Orthotopic Heart Transplantation
Published on: April 27, 2019
Effect of sodium glucose cotransporter 2 inhibition immediately prior to heart transplantation
Lisa M Raven1,2,3, Christopher A Muir1,3, Ricardo C Deveza3,4,5
1Department of Diabetes and Endocrinology, St Vincent's Hospital, Sydney, NSW, Australia.
Abstract:
Sodium glucose cotransporter 2 inhibitors (SGLT2i) are an established treatment for heart failure and type 2 diabetes. Guidelines suggest withholding SGLT2i preoperatively due to the risk of ketoacidosis. Orthotopic heart transplantation (OHT) occurs without sufficient notice to cease SGLT2i treatment before surgery. In a retrospective analysis of 163 OHT recipients (40 exposed to SGLT2i, 123 not exposed), we show no increase in rates of mild, moderate, or severe acidosis postoperatively. No cases of ketoacidosis occurred, likely due to the fact that 97% of patients received insulin infusions postoperatively for transient postoperative hyperglycemia. Patients exposed to SGLT2i had shorter length of stay in the intensive care unit and improved adjusted survival overall. These findings support the safety of SGLT2i use up to the time of OHT with routine use of a postoperative insulin infusion.
Insights
Sodium glucose cotransporter 2 inhibitors (SGLT2i) are safe for patients undergoing heart transplantation. SGLT2i use did not increase acidosis risk and was associated with shorter ICU stays and improved survival.
Area of Science:
- Cardiology
- Endocrinology
- Transplantation Medicine
Background:
- Sodium glucose cotransporter 2 inhibitors (SGLT2i) are vital for managing type 2 diabetes and heart failure.
- Current guidelines recommend discontinuing SGLT2i before surgery due to ketoacidosis concerns.
- Orthotopic heart transplantation (OHT) often occurs emergently, precluding preoperative SGLT2i cessation.
Purpose of the Study:
- To evaluate the safety of continuing SGLT2i therapy up to the time of OHT.
- To assess the incidence of postoperative acidosis and ketoacidosis in OHT recipients on SGLT2i.
- To compare outcomes, including ICU length of stay and survival, between SGLT2i-exposed and unexposed OHT patients.
Main Methods:
- Retrospective analysis of 163 OHT recipients.
- Comparison of 40 patients exposed to SGLT2i with 123 patients not exposed.
- Assessment of postoperative acidosis severity and ketoacidosis occurrence.
Main Results:
- No significant increase in mild, moderate, or severe acidosis was observed in the SGLT2i-exposed group.
- Zero cases of ketoacidosis occurred, attributed to routine postoperative insulin infusions for hyperglycemia (97% of patients).
- SGLT2i-exposed patients experienced shorter intensive care unit (ICU) stays and improved overall adjusted survival.
Conclusions:
- Continuing SGLT2i therapy until the time of OHT is safe.
- Routine postoperative insulin infusion effectively mitigates the risk of ketoacidosis in this population.
- SGLT2i use in OHT recipients may be associated with improved clinical outcomes.
Related Concept Videos
Secondary Active Transport
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Glucose Absorption Into the Small Intestine
Heart Failure Drugs: Inotropic Agents

