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Impact of Sodium-glucose Cotransporter 2 Inhibitors on Post-operative Atrial Fibrillation in Cardiothoracic Surgery

Hamad Medical Corporation (HMC) logo

Hamad Medical Corporation (HMC)

Status

Enrolling

Conditions

Atrial Fibrillation

Treatments

Drug: SGLT2 inhibitor

Study type

Observational

Funder types

Industry

Identifiers

NCT06251453
MRC-01-23-470

Details and patient eligibility

About

SGLT2 inhibitors are oral anti-diabetic medications that were found to improve cardiorenal outcomes in patients with type 2 diabetes mellitus (DM), chronic heart failure with reduced and preserved ejection fraction, and chronic kidney disease. Recent evidence suggested that the use of SGLT2 inhibitors resulted in a significant reduction in atrial fibrillation (AF) over a mean follow-up duration of 2.6 years. Given the possible AF protective benefit with SGLT2 inhibitors use.

Full description

we aim to conduct a retrospective cohort study to evaluate the impact of SGLT2 inhibitors use on post-operative AF (POAF) among patients undergoing cardiothoracic surgery, including coronary artery bypass grafting (CABG), valve replacement, and valve repair over a 6-year period (from 1/06/2017 to 1/07/2023). The follow-up period will be the post-operative hospital stay or 30-days, whichever is shorter, and the data will be obtained from the electronic medical records. The study outcomes will include effectiveness outcomes of incidence of POAF regardless of frequency, duration, or intervention used for termination, incidence of paroxysmal POAF, incidence of paroxysmal POAF requiring pharmacological cardioversion, incidence of hemodynamically unstable POAF requiring electrical cardioversion, incidence of persistent POAF (sustained beyond 7 days), incidence of POAF requiring anticoagulation, ischemic stroke, and safety outcomes of euglycemic diabetic ketoacidosis and urinary tract infections (UTI).

Enrollment

3,280 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults > 18 years undergoing cardiothoracic surgery, including CABG, mechanical valve replacement, bioprosthetic valve replacement, or valve repair.
  • Use of SGLT2 inhibitors for a minimum of 1 week prior to surgery regardless of DM status.
  • Resumption of SGLT2 inhibitor after stepping down from the intensive care unit.

Exclusion criteria

  • Known AF on anticoagulation.
  • Chronic kidney disease with CrCl < 25 mL/min.

Trial design

3,280 participants in 2 patient groups

SGLT2 inhibitors users
Description:
Adults undergoing cardiothoracic surgery who had been using SGLT2 inhibitors for a minimum of 1 week before surgery, regardless of diabetes status
Treatment:
Drug: SGLT2 inhibitor
SGLT2 inhibitors non-users
Description:
Adults not receiving SGLT2 inhibitors undergoing cardiothoracic surgery

Trial contacts and locations

2

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Central trial contact

Alaa Rahhal, Msc

Data sourced from clinicaltrials.gov

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