Key Points
            - Use the highest‑yield diagnostic test early; do not let testing delay time‑critical therapy.
- Set objective targets and reassess frequently.
- Plan definitive source control or disease‑specific therapy when indicated; document follow‑up and patient education.
                                        Algorithm
            - Start β-blocker; administer thionamide; after 1–2 h give iodine; add hydrocortisone.
- Treat precipitant; aggressive supportive care (cooling, fluids, nutrition).
- Titrate therapy to clinical response; transition to maintenance and plan for definitive therapy.
                                        Clinical Synopsis & Reasoning
            Severe thyrotoxicosis with multiorgan dysfunction. Start β-blockade; give PTU 500–1000 mg load then 250 mg q4h (or Methimazole 20 mg q4–6h), followed by iodine (SSKI) 1–2 h later to block release. Add hydrocortisone 100 mg IV q8h and supportive care including cooling and fluids.
                                        Treatment Strategy & Disposition
            Stabilize ABCs. Initiate guideline‑concordant first‑line therapy with precise dosing and continuous monitoring. Escalate to advanced/procedural interventions based on explicit failure criteria. Define ICU, step‑down, and ward disposition triggers; involve specialty teams early.
                                        Epidemiology / Risk Factors
            - Risk varies by comorbidity and precipitants; see citations for condition‑specific data.
                                        Investigations
            
              
                | Test | Role / Rationale | Typical Findings | Notes | 
|---|
                
                  | Burch–Wartofsky score (or Japanese Thyroid Association) | Severity | Quantify likelihood | — | 
| TSH/free T4/T3 (do not delay) | Diagnosis | Thyrotoxicosis pattern | — | 
| Infection, MI, PE workup | Triggers | Common precipitants | Treat source | 
                
              
             
                                        High-Risk & Disposition Triggers
            
              
                | Trigger | Why it matters | Action | 
|---|
                
                  | Atrial fibrillation with instability or heart failure | High mortality | ICU; esmolol infusion | 
| Hyperthermia >40°C | Multiorgan failure risk | Active cooling | 
| Sepsis or precipitating surgery | Worsening trigger | Aggressive source control | 
| Pregnancy | Drug selection nuance | Specialist input on thionamide choice | 
| Hepatic failure | PTU risk | Prefer methimazole; monitor LFTs | 
                
              
             
                                        Pharmacology
            
              
                | Medication/Intervention | Mechanism | Onset | Role in Therapy | Limitations | 
|---|
                
                  | Propranolol 20–80 mg PO q6h (or Esmolol infusion) | β-blockade | Minutes | Symptom and rate control | Watch for HF/asthma | 
| PTU 500–1000 mg load then 250 mg q4h (or Methimazole 20 mg q4–6h) | Block synthesis/5'-deiodinase (PTU) | Hours | Core therapy | Hepatotoxicity (PTU) | 
| SSKI 5 drops PO q6h (or Lugol) started 1–2 h after thionamide | Iodine blockade | Hours | Inhibits release | Timing crucial | 
| Hydrocortisone 100 mg IV q8h | Adrenal support/T4→T3 block | Hours | Stress dosing | — | 
| Cholestyramine 4 g PO QID (adjunct) | Peripheral clearance | Days | Severe cases | — | 
                
              
             
                                        Prognosis / Complications
            - Outcome depends on timeliness of diagnosis and definitive therapy; monitor for complications.
                                        Patient Education / Counseling
            - Provide red‑flag education, adherence guidance, and explicit return precautions; arrange timely specialty follow‑up.
                  
        
                  References
                      - ATA hyperthyroidism/thyroid storm guidance — Link