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.

JHLT Open
|March 27, 2025
PubMed

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 Transport01:55

Secondary Active Transport

One example of how cells use the energy contained in electrochemical gradients is demonstrated by glucose transport into cells. The ion vital to this process is sodium (Na+), which is typically present in higher concentrations extracellularly than in the cytosol. Such a concentration difference is due, in part, to the action of an enzyme “pump” embedded in the cellular membrane that actively expels Na+ from a cell. Importantly, as this pump contributes to the high concentration of...
117.1K
Glucose Transporters01:27

Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
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:
22.3K
Glucose Absorption Into the Small Intestine01:26

Glucose Absorption Into the Small Intestine

Complex carbohydrates consumed cannot be absorbed into the small intestine in their original form. First, they must be hydrolyzed to a monosaccharide form such as glucose or galactose. These monosaccharides are then transported across the intestinal membrane and into the blood via transcellular transport. The intestinal epithelial cells allow the movement of these monosaccharides with a defined 'entry' through membrane transporter proteins present on their apical membrane and...
31.0K
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
476