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
            - Assess airway/safety; rule out other causes; identify precipitants.
- Start lactulose and titrate to 2–3 soft stools/day; add rifaximin for secondary prevention.
- Address nutrition (adequate protein), avoid sedatives, and arrange follow‑up with hepatology.
                                        Clinical Synopsis & Reasoning
            Neuropsychiatric dysfunction in cirrhosis. Exclude alternative causes, correct precipitants (GI bleed, infection, dehydration), and treat with lactulose titrated to 2–3 soft stools/day plus rifaximin for prevention of recurrence; counsel on protein intake and avoid sedatives.
                                        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 | 
|---|
                
                  | Ammonia (supportive), infection screen, electrolytes | Etiology | Identify precipitant; ammonia not diagnostic alone | — | 
| Asterixis/mental status staging (West Haven) | Severity | Grade encephalopathy | Serial exams | 
| CT head (atypical focal deficits/trauma) | Rule out alternate | ICH, stroke | — | 
                
              
             
                                        High-Risk & Disposition Triggers
            
              
                | Trigger | Why it matters | Action | 
|---|
                
                  | Airway compromise or severe agitation | Aspiration risk | ICU; airway protection | 
| GI bleeding, infection, or dehydration | Common precipitants | Treat source; volume resuscitation | 
| Renal failure or hyponatremia | Worse outcomes | Optimize fluids; nephrology | 
| Refractory HE despite therapy | Recurrent admissions | Evaluate for TIPS reversal or transplant | 
| Unreliable social support | Safety | Arrange caregiver support; consider admission | 
                
              
             
                                        Pharmacology
            
              
                | Medication/Intervention | Mechanism | Onset | Role in Therapy | Limitations | 
|---|
                
                  | Lactulose 25 mL PO/NG q1–2 h until catharsis then 2–3/day | Ammonia reduction | Hours | First‑line | Rectal route if unable to take PO | 
| Rifaximin 550 mg PO BID (add‑on) | Nonabsorbable antibiotic | Days | Reduce recurrence | Cost considerations | 
| Treat precipitants (e.g., antibiotics for SBP, stop sedatives) | Source control | Hours | Prevent recurrence | — | 
                
              
             
                                        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
                      - AASLD practice guidance on hepatic encephalopathy — Link