The goal of this clinical trial is to find out whether levothyroxine reduces complications and improves the prognosis of patients with subclinical hypothyroidism (SCH) undergoing coronary artery bypass grafting (CABG). The main questions this study aims to answer are: • Does levothyroxine reduce major adverse cardiovascular events (MACE), including cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and new arrhythmias, in SCH patients undergoing CABG? Researchers will compare patients who take levothyroxine with those who do not. Participants will: * Be randomly assigned to either receive levothyroxine or not * Start the medication one day before surgery if assigned to the treatment group. * Have regular follow-up visits to check thyroid function and cardiovascular events for up to five years after surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
338
Intervention description: Participants assigned to the LT4 group will begin receiving levothyroxine the day before CABG. The initial dose is 25 μg once daily, or 12.5 μg for participants weighing less than 60 kg. The dose will then be adjusted based on thyroid function test results to achieve target TSH levels of 0.4-2.0 μIU/mL.
Department of Internal Medicine, Seoul National University Bundang Hospital
Seongnam-si, South Korea
RECRUITINGA composite of MACE within 4months after surgery
A composite of major adverse cardiovascular events (MACE), including cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and the occurrence of new arrhythmias assessed within 4 months after CABG.
Time frame: within 4months after surgery
Number of participants who experience cardiovascular death within 4 months after surgery
Number of participants who experience cardiovascular death within 4 months after CABG
Time frame: within 4months after surgery
Number of participants who experience nonfatal myocardial infarction within 4 months after surgery
Number of participants who experience nonfatal myocardial infarction within 4 months after CABG
Time frame: within 4months after surgery
Number of participants who experience nonfatal stroke within 4 months after surgery
Number of participants who experience nonfatal stroke within 4 months after CABG
Time frame: within 4months after surgery
Number of participants who experience new arrhythmia within 4 months after surgery
Number of participants who experience new arrhythmia within 4 months after CABG
Time frame: within 4months after surgery
A composite of MACE within 1 year after surgery
A composite of major adverse cardiovascular events (MACE), including cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and the occurrence of new arrhythmias assessed within 1year after CABG
Time frame: within 1 year after surgery
A composite of MACE within 5 year after surgery
A composite of major adverse cardiovascular events (MACE), including cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and the occurrence of new arrhythmias assessed within 5 years after CABG
Time frame: within 5 years after surgery
All-cause mortality within 5 years after surgery
All-cause mortality within 5 years after surgery
Time frame: within 5 years after surgery
Change in LVEF from baseline to 1 year after surgery
Left ventricular ejection fraction (LVEF) will be measured using transthoracic echocardiography at baseline (pre-operative) and at 1 year post-operatively. The outcome will be reported as the mean change in LVEF (%) from baseline to 1 year.
Time frame: From baseline to 1 year after surgery
Change in LV EDD from baseline to 1 year after surgery
Left ventricular end-diastolic diameter (LVEDD) will be measured using transthoracic echocardiography at baseline (pre-operative) and at 1 year post-operatively. The outcome will be reported as the mean change in LVEDD (%) from baseline to 1 year.
Time frame: From baseline to 1 year after surgery
Change in LV ESD from baseline to 1 year after surgery
Left ventricular end-systolic diameter (LV ESD) will be measured using transthoracic echocardiography at baseline (pre-operative) and at 1 year post-operatively. The outcome will be reported as the mean change in LV ESD (%) from baseline to 1 year.
Time frame: From baseline to 1 year after surgery
Change in LVMI from baseline to 1 year after surgery
Left ventricular mass index (LVMI) will be measured using transthoracic echocardiography at baseline (pre-operative) and at 1 year post-operatively. The outcome will be reported as the mean change in LVMI (%) from baseline to 1 year.
Time frame: From baseline to 1 year after surgery
Change in LAMI from baseline to 1 year after surgery
Left atrial volume index (LAMI) will be measured using transthoracic echocardiography at baseline (pre-operative) and at 1 year post-operatively. The outcome will be reported as the mean change in LAMI (%) from baseline to 1 year.
Time frame: From baseline to 1 year after surgery
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