Outpatient Management of Chronic Liver Disease
Stable CLD patients require systematic outpatient monitoring every 6-12 months with laboratory testing, imaging surveillance, and aggressive management of underlying etiology and complications to prevent progression to cirrhosis, decompensation, and hepatocellular carcinoma. 1
Initial Assessment and Risk Stratification
Determine Disease Severity Using Non-Invasive Tests
- Obtain FibroScan (transient elastography) or calculate FIB-4 score (age, AST, ALT, platelet count) to assess fibrosis stage, as these non-invasive methods perform well in identifying cirrhosis or minimal fibrosis 1
- Patients with liver stiffness <8 kPa or FIB-4 <1.45 can be followed by general practitioners with annual repeat testing 1
- Patients with liver stiffness ≥10 kPa or FIB-4 >3.25 require hepatology specialist follow-up regardless of other factors 1
- For intermediate values (liver stiffness 8-10 kPa or FIB-4 1.45-3.25), refer to hepatology if metabolic dysfunction-associated steatotic liver disease (MASLD) present or alcohol intake >20 g/day for women or >30 g/day for men 1
Identify and Screen for Underlying Etiology
- Test for HBsAg, anti-HCV antibodies, HIV, ferritin, and transferrin saturation in all patients 1
- If anti-HCV positive, obtain HCV RNA by sensitive molecular method (lower limit <15 IU/ml) 1
- Quantify alcohol consumption at every visit and provide specific counseling to stop all alcohol use, as even moderate amounts (>10 g/day) enhance disease progression 1
- Screen for metabolic syndrome components (obesity, diabetes, hypertension, dyslipidemia) as these accelerate fibrosis progression 1
Laboratory Monitoring Schedule
Every 6-12 Months for All CLD Patients
- Complete blood count with platelet count (surrogate marker for portal hypertension) 1
- Comprehensive metabolic panel including AST, ALT, bilirubin, albumin, and creatinine 1
- Prothrombin time/INR 2
- Note that ALT fluctuates in chronic hepatitis C, so single normal ALT cannot exclude ongoing hepatic injury 1
Every 3-6 Months for Advanced Fibrosis/Cirrhosis
- Liver function tests to track disease progression 3
- Platelet count and albumin as surrogates for hepatic function and portal hypertension 1
Imaging Surveillance
Hepatocellular Carcinoma Screening
- Perform abdominal ultrasound every 6 months in all cirrhotic patients, as HCC develops in 1-4% per year once cirrhosis is established 1, 2
- Continue HCC surveillance indefinitely even after successful viral eradication, as risk persists though reduced 1
Portal Hypertension Assessment
- During routine ultrasound, assess for portosystemic collaterals, splenomegaly, enlarged portal vein diameter, and ascites as signs of clinically significant portal hypertension 1
Management of Underlying Etiology
Chronic Hepatitis C (HCV RNA Positive)
- Refer to hepatologist or infectious disease specialist for direct-acting antiviral therapy, with goal of sustained virologic response (undetectable HCV RNA 12 weeks post-treatment) 1
- After achieving SVR, patients with prior advanced fibrosis/cirrhosis require continued hepatology follow-up despite viral clearance 1
Chronic Hepatitis B (HBsAg Positive)
- Refer to hepatologist for consideration of entecavir 0.5 mg once daily (or 1 mg daily if lamivudine-resistant or decompensated liver disease) 4
- Offer HIV antibody testing before initiating entecavir, as therapy is not recommended for HIV/HBV co-infected patients not receiving HAART 4
- Monitor hepatic function closely for at least several months if anti-HBV therapy is discontinued, as severe acute exacerbations can occur 4
Alcohol-Related Liver Disease
- Prescribe baclofen (up to 80 mg/day) as the only anti-craving medication safe in alcoholic liver disease, as it has been formally tested in cirrhotic patients 3, 5
- Acamprosate 1,998 mg/day represents a safe alternative with no hepatotoxicity risk for 3-6 months 3, 5
- Never use naltrexone in patients with alcoholic liver disease due to significant hepatotoxicity risk 3, 6
- Immediately refer to Alcoholics Anonymous with active encouragement for regular attendance 3, 6
- Implement cognitive behavioral therapy to develop coping skills and address psychological patterns underlying drinking 3, 5
- Complete lifelong abstinence from alcohol is the only acceptable recommendation, as there is no safe amount 3
Metabolic Dysfunction-Associated Steatotic Liver Disease
- Counsel on regular physical activity, maintaining healthy diet, and avoiding weight gain, as weight gain after viral cure increases progression risk 1
- Manage diabetes, hypertension, and dyslipidemia aggressively 1
Vaccination Requirements
Administer hepatitis A and B vaccines to all CLD patients, as acute hepatitis A or B infection can be lethal in patients with chronic liver disease 7
Complication Screening and Management
For Patients with Compensated Advanced Chronic Liver Disease (cACLD)
Varices Screening
- Patients with post-treatment liver stiffness <12 kPa and platelets >150 G/L do not need endoscopy as clinically significant portal hypertension can be ruled out 1
- Patients with liver stiffness >20 kPa and/or platelets <150 G/L should undergo esophagogastroduodenoscopy if not already on non-selective beta-blocker therapy 1
- If varices detected, initiate non-selective beta-blockers for primary prophylaxis 2, 8
Ascites Management
- Mild ascites: restrict sodium and water intake 8, 9
- Moderate ascites: add careful diuresis with spironolactone and furosemide 8, 9
- Severe/refractory ascites: perform large-volume paracentesis with albumin infusion 8, 9
Hepatic Encephalopathy
- Rule out other causes of altered mental status and identify precipitating factors (infection, GI bleeding, constipation, medications) 8, 9
- Initiate lactulose empirically for suspected hepatic encephalopathy 8, 9
- Add rifaximin for maintenance of remission and decreased readmission rates 8
Follow-Up Visit Schedule
Compensated CLD Without Cirrhosis
- Every 6-12 months with laboratory testing and clinical assessment 1, 3
- Repeat non-invasive fibrosis testing annually 1
Compensated Advanced Chronic Liver Disease/Cirrhosis
- Every 3-6 months with comprehensive laboratory testing 3
- Ultrasound every 6 months for HCC surveillance 2
- Annual or biennial endoscopy for variceal screening based on initial findings 2
Decompensated Cirrhosis Post-Hospitalization
- Every 1-3 months to assess medication compliance, monitor liver function, evaluate for complications, and adjust treatment 3, 10
Critical Pitfalls to Avoid
- Never discontinue monitoring patients who achieved viral cure if they had advanced fibrosis/cirrhosis, as HCC and decompensation risk persists 1
- Do not rely on single ALT measurement to exclude active liver disease, as ALT fluctuates and patients can have prolonged normal ALT despite ongoing hepatic injury 1
- Avoid naltrexone entirely in alcoholic liver disease due to hepatotoxicity 3, 6
- Do not assume patients with normal liver tests lack advanced disease, as cirrhosis often remains asymptomatic until decompensation 2
- Never recommend "safe" levels of alcohol consumption to CLD patients, as even moderate intake (>10 g/day) accelerates progression 1, 3
Liver Transplant Evaluation
Refer to transplant center when MELD-Na score ≥15, at first decompensation event, or when HCC is detected within Milan criteria 1, 10
Sample Prescription for Stable CLD Patient
Diagnosis: Chronic Liver Disease [specify etiology: HCV, HBV, alcohol-related, MASLD]
Medications:
- [If HBV+] Entecavir 0.5 mg PO once daily on empty stomach (2 hours after and 2 hours before food) 4
- [If alcohol-related] Baclofen 20 mg PO three times daily (max 80 mg/day) 3, 5
- [If varices present] Propranolol [dose titrated to heart rate 55-60 bpm] 2
- [If ascites] Spironolactone 100 mg + Furosemide 40 mg PO daily 8
- [If hepatic encephalopathy] Lactulose 30 mL PO 2-3 times daily (titrate to 2-3 soft stools/day) 8
Laboratory Orders:
Imaging:
- Abdominal ultrasound every 6 months for HCC screening 2
Referrals:
- Hepatology follow-up every 6 months 1
- Alcoholics Anonymous (if alcohol-related) 3, 6
- Mental health evaluation (if depression or alcohol use disorder) 3
Patient Education: