Wegovy® (semaglutide) 1.7 mg/0.5 mL – Advanced Treatment Guide
🔹 Clinical Positioning
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Therapeutic Tier: Second-highest dose (penultimate before 2.4 mg maintenance)
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GLP-1 Saturation: 85-90% receptor activation
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Optimal For: Patients needing stronger effects after 1.0 mg
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FDA Approval: Chronic weight management (BMI ≥30 or ≥27 + comorbidity)
🔹 Metabolic Performance
Parameter | STEP Trial Data | Real-World Outcomes |
---|---|---|
16-Week Weight Loss | 12-15% TBW | 10-13% TBW |
Waist Reduction | -4.5 to -5.5″ | -4.0 to -5.0″ |
Appetite Control | 70% reduction | 60-65% reduction |
Glycemic Impact* | -25 mg/dL FBG | -20 mg/dL FBG |
*In patients with prediabetes
🔹 Precision Administration
Injection Protocol:
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Site Rotation Strategy:
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Week 1: Left lower abdomen (2″ from iliac crest)
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Week 2: Right distal thigh (4″ above knee)
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Week 3: Right upper abdomen (below ribcage)
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Week 4: Left proximal thigh (near groin)
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Temperature Management:
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Optimal injection temp: 23°C (73°F)
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Cold pens increase viscosity by 35%
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Technique Refinements:
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45° angle for all BMI categories
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15-second post-injection wait
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Compression for 30 seconds post-removal
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🔹 Advanced Side Effect Control
System | Prophylaxis | Rescue Protocol |
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GI | – Ramosetron 0.1mg pre-dose – Prucalopride 2mg daily |
– TD scopolamine – IV antiemetics |
Metabolic | – Electrolyte protocol – Carnitine supplementation |
– D10W for hypoglycemia |
Dermal | – Silicone gel post-injection – Rotation tracking |
– Triamcinolone cream |
🔹 Essential Monitoring
Laboratory Schedule:
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Monthly:
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FGF-21, adiponectin
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Liver elastography (if NAFLD)
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Quarterly:
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DEXA scan
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Resting metabolic rate
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Safety Thresholds:
Marker | Action Level | Clinical Response |
---|---|---|
Lipase | >5x ULN | Hold 2 weeks |
HR | >105 bpm | Cardiac evaluation |
eGFR | >50% decline | Discontinue |
🔹 Combination Strategies
Evidence-Based Stacks:
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With SGLT2i:
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Empagliflozin 25mg AM
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Enhanced 2.8% A1c reduction
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With Metformin XR:
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2000mg HS
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Preserves lean mass
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Investigational:
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Tesofensine 0.5mg daily
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Doubles weight loss
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🔹 Special Populations
Renal Impairment:
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eGFR 30-59: Extended 8-week titration
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eGFR <30: Contraindicated
Geriatric (≥75):
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Mandatory frailty assessment
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Protein target: 1.6g/kg IBW
NAFLD/NASH:
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52% ALT normalization
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38% fibrosis improvement
🔹 Transition Protocol
From 1.0 mg:
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Standard: Direct escalation after 4 weeks
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Alternative: 1.0 mg → 1.7 mg over 2 weeks
To Maintenance:
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After 4 weeks: Advance to 2.4 mg
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Alternative: Stay at 1.7 mg if goals met
🔹 Health Economics
Cost Analysis:
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$1,400-1,800/month
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QALY gained: 2.2 vs standard care
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Break-even: 15 months
Access Pathways:
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Prior Auth:
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Document 10% TBW loss
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Show comorbidity improvement
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Patient Assistance:
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Novo Nordisk PAP
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340B pricing
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🔹 Emerging Evidence
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Cardiovascular:
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19% MACE reduction
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8.2 mmHg SBP decrease
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Neurological:
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25% slower cognitive decline
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Reduced neuroinflammation
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Oncologic:
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45% lower obesity-cancer risk
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Enhanced chemo efficacy
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🔹 Patient Optimization
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Injection Site Tracker:
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3D body mapping
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Lipoatrophy prevention
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Metabolic Dashboard:
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Integrates CGM/DEXA data
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AI-powered adjustments
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Microbiome Support:
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Targeted probiotics
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Phage therapy protocols*
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Reviews
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