Follow-Up Testing for Patient on Wegovy at 6 Months
At 6 months of Wegovy therapy, you should obtain fasting lipid panel, fasting glucose or hemoglobin A1c, blood pressure measurement, liver function tests, and body weight/BMI to assess treatment efficacy and monitor for improvement in obesity-related comorbidities. 1
Core Metabolic Monitoring
Weight Loss Assessment
- Measure body weight and calculate BMI to determine if patient has achieved ≥5% weight loss, which produces clinically meaningful improvements in cardiometabolic risk factors 1, 2
- Evaluate treatment efficacy at this 6-month timepoint, as guidelines recommend assessment at 12-16 weeks on maximum tolerated dose, and you are now well past that threshold 3
- If weight loss is less than 4-5% at 16 weeks on maximum tolerated dose, consider discontinuing therapy per GLP-1 receptor agonist guidelines 3
Cardiovascular Risk Factor Monitoring
- Fasting lipid panel (total cholesterol, LDL-C, HDL-C, triglycerides) to assess for improvement in dyslipidemia, as GLP-1 receptor agonists demonstrate cardioprotective effects through improved lipid profiles 1, 3
- Blood pressure measurement to evaluate hypertension control, as even modest weight loss of 3-5% produces clinically meaningful reductions in blood pressure 1
- Fasting plasma glucose and/or hemoglobin A1c to screen for prediabetes (fasting glucose 100-125 mg/dL, A1c 5.7-6.4%) and assess for improvement in glucose metabolism 1
Hepatic Assessment
- Liver function tests (ALT, AST) to monitor for improvement in nonalcoholic fatty liver disease, which commonly improves with weight loss 1
- Weight loss has been shown to decrease ALT by 9 U/L and AST by 3 U/L in patients using weight loss interventions 1
Additional Monitoring Considerations
Waist Circumference
- Measure waist circumference as central obesity is an independent risk factor for mortality, and weight loss interventions reduce waist circumference by an average of 4.1 cm 1
- This is particularly important given your patient's metabolic syndrome components (hypertension, hyperlipidemia) 1
Metabolic Syndrome Screening
- Assess for metabolic syndrome criteria: waist circumference ≥88 cm (women) or ≥102 cm (men), triglycerides ≥150 mg/dL, fasting glucose ≥100 mg/dL, blood pressure ≥130/85 mm Hg, HDL-C <40 mg/dL (men) or <50 mg/dL (women) 1
- Your patient already has 2 components (hypertension, hyperlipidemia), making this assessment critical 1
Clinical Decision Points
Treatment Continuation
- Continue Wegovy if patient has achieved ≥5% weight loss, as this threshold produces significant cardiometabolic benefits 2
- Expected weight loss with semaglutide at 6 months is approximately 13-15% in real-world settings 4, 5
- Consider discontinuation if <4-5% weight loss at 16 weeks on maximum tolerated dose, extrapolating from liraglutide guidelines for GLP-1 receptor agonists 3
Long-Term Planning
- Emphasize that long-term use is necessary to maintain weight loss benefits, as discontinuation leads to rapid weight regain 3, 2
- Continue monitoring for gastrointestinal adverse events (nausea, diarrhea, vomiting, constipation), which are the most common side effects 3, 6