✉ drhardikahuja@gmail.com 📞 +91 99900 56499
Home Healthcare Services Hepatic Disorders
Hepatology & Liver Care

Hepatic
Disorders &
Liver Disease

Comprehensive Liver Care — From Fatty Liver to Transplant

Dr. Hardik Ahuja, DM Gastroenterologist and LTSI Fellow, provides complete hepatology care — managing fatty liver, viral hepatitis, jaundice, cirrhosis, and liver failure, including liver transplant evaluation and post-transplant follow-up.

🫀 Fatty Liver (NAFLD/NASH)
💛 Jaundice
🦠 Hepatitis A / B / C / E
🔄 Liver Cirrhosis
💧 Ascites
🏥 Transplant Care
Liver Care
35K+
Patients Treated
10+
Years Hepatology
Experience
LTSI
Fellow 2024
Transplant
🫀Fatty Liver
💛Jaundice
🦠Hepatitis B
🔬Hepatitis C
🧪Hepatitis A & E
🔄Cirrhosis
🏥Transplant
220M+
Indians with Fatty Liver
40M+
Hepatitis B Carriers India
10+
Years Hepatology Expertise
100%
Personalised Care Plans
Overview

What Are Hepatic Disorders?

Hepatic (liver) disorders encompass a wide range of acute and chronic conditions affecting the liver — the body's largest internal organ responsible for detoxification, protein synthesis, bile production, fat metabolism, and glucose regulation. India bears one of the highest burdens of liver disease globally, with over 220 million people affected by fatty liver disease and 40 million chronic Hepatitis B carriers.

Dr. Hardik Ahuja is a specialist Hepatologist with dedicated expertise in managing all forms of liver disease — from the earliest stages of fatty liver and viral hepatitis, to complex cirrhosis complications, liver failure, and liver transplant evaluation and post-transplant care.

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Most liver diseases are silent in early stages — they cause no symptoms until significant damage has occurred. Early detection through routine liver function tests, ultrasound, and FibroScan can prevent progression to cirrhosis and liver failure.

Conditions We Treat

Hepatic Disorders — Detailed Guide

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Fatty Liver Disease (NAFLD / NASH / ALD)

Non-alcoholic, alcoholic, and metabolic fatty liver
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Non-Alcoholic Fatty Liver Disease (NAFLD) is the most common liver condition in India, affecting 1 in 3 urban adults. It occurs when excess fat accumulates in liver cells in the absence of significant alcohol use. Risk factors include obesity, Type 2 diabetes, high triglycerides, metabolic syndrome, and PCOD.

NASH (Non-Alcoholic Steatohepatitis) is the aggressive form — fat plus inflammation plus liver cell injury — that can progress to fibrosis, cirrhosis, and liver cancer over 10–20 years. Alcoholic Liver Disease (ALD) ranges from fatty liver to alcoholic hepatitis and cirrhosis in heavy drinkers.

Treatment focuses on weight loss (even 5–10% reduces liver fat significantly), dietary modification, blood sugar and lipid control, and in NASH, medications under Dr. Ahuja's supervision. Regular FibroScan monitoring tracks progression.

FibroScan MonitoringDiet CounsellingMetabolic ManagementReversible if caught early
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Jaundice (Hyperbilirubinaemia)

Yellow discolouration of skin and eyes from elevated bilirubin
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Jaundice is not a disease itself but a symptom of an underlying liver, bile duct, or blood condition. It occurs when bilirubin — a breakdown product of red blood cells — accumulates in the blood due to impaired liver processing or bile duct obstruction.

Common causes: Viral hepatitis (A, B, E), gallstones blocking the bile duct, alcoholic liver disease, drug-induced liver injury, haemolytic anaemia, cirrhosis, and pancreatic or bile duct cancer. Neonatal jaundice in newborns requires immediate evaluation.

Dr. Ahuja identifies the exact cause through blood tests (bilirubin fractions, liver enzymes, viral markers), ultrasound, and MRCP or ERCP if bile duct obstruction is suspected. Treatment is directed at the underlying cause.

Liver jaundiceObstructive jaundiceHaemolytic jaundiceERCP if bile duct block
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Hepatitis B (Chronic & Acute)

India has 40 million chronic HBV carriers — the 2nd largest burden globally
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Hepatitis B Virus (HBV) is transmitted through blood, unprotected sex, or mother-to-child during childbirth. Acute HBV is self-limiting in most adults; however, 5–10% develop chronic infection which, if untreated, leads to cirrhosis (20–30% risk over 20 years) and liver cancer (HCC).

Dr. Ahuja evaluates HBV DNA levels, HBeAg/HBsAg status, liver enzymes, and liver fibrosis stage (FibroScan) to determine who needs antiviral treatment. Tenofovir and Entecavir are highly effective first-line antivirals that suppress HBV DNA and prevent disease progression.

All chronic HBV patients need 6-monthly liver cancer surveillance (AFP + ultrasound). Family members should be screened and vaccinated. Dr. Ahuja provides comprehensive long-term HBV management.

HBV DNA testingAntiviral therapyHCC surveillanceLifelong monitoring
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Hepatitis C (HCV — Now Curable)

Direct-acting antivirals cure Hepatitis C in 8–12 weeks
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Hepatitis C Virus (HCV) is spread through blood contact — shared needles, unscreened blood transfusions (pre-1992), or contaminated medical equipment. Unlike Hepatitis B, HCV is now completely curable with Direct-Acting Antiviral (DAA) therapy in 8–12 weeks with a 95%+ cure rate.

Many HCV patients are asymptomatic for decades while the virus silently causes liver fibrosis and cirrhosis. All adults born between 1945–1965 or with risk factors should be screened with a one-time HCV antibody test. Those with positive antibody need HCV RNA PCR to confirm active infection.

Dr. Ahuja prescribes appropriate DAA regimens (Sofosbuvir-based), monitors treatment response, and confirms cure (Sustained Virological Response at 12 weeks after treatment completion). Even patients with advanced cirrhosis can be cured — though transplant may still be needed for end-stage disease.

DAA therapy (8–12 weeks)95%+ cure rateSVR12 testingCompletely curable
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Hepatitis A & E (Acute Viral Hepatitis)

Waterborne liver infections — common during monsoon in India
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Hepatitis A (HAV) and Hepatitis E (HEV) are transmitted through contaminated food and water — the faeco-oral route. They are especially common during and after monsoon season in India when waterborne contamination increases. Most cases are self-limiting with supportive care.

Symptoms include acute jaundice, fever, nausea, vomiting, dark urine, clay-coloured stools, and right upper abdominal pain. Hepatitis E is particularly dangerous in pregnancy, causing fulminant (rapidly fatal) liver failure in up to 25% of pregnant women — requiring urgent hospital management.

Dr. Ahuja provides supportive management for uncomplicated cases and intensive monitoring for severe or fulminant hepatitis. Hospitalisation is required for inability to eat, coagulopathy, encephalopathy, or fulminant failure. Hepatitis A vaccination is available for prevention.

Self-limiting usuallyHigh-risk in pregnancy (HEV)Supportive careHAV vaccine available
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Liver Cirrhosis & Its Complications

Advanced fibrosis with portal hypertension — requires specialist management
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Cirrhosis is the end-result of prolonged liver inflammation and fibrosis — where normal liver tissue is replaced by scar tissue, impairing liver function and blood flow. Common causes include chronic Hepatitis B, Hepatitis C, alcohol, and NASH. Cirrhosis can be compensated (no symptoms, liver still functioning) or decompensated (complications present).

Complications of Decompensated Cirrhosis:

Ascites (fluid in the abdomen) — managed with diuretics and therapeutic paracentesis. • Variceal bleeding (ruptured oesophageal/gastric varices) — prevented by beta-blockers and endoscopic band ligation (EVL). • Hepatic Encephalopathy (brain dysfunction from ammonia) — treated with lactulose and rifaximin. • Spontaneous Bacterial Peritonitis (SBP) — antibiotic treatment. • Hepatorenal Syndrome — intensive medical management.

Dr. Ahuja manages all complications with regular endoscopic surveillance for varices, FibroScan, LFT monitoring, and timely referral for liver transplant when appropriate.

Variceal surveillanceAscites drainageBand ligation (EVL)Transplant evaluation
Disease Progression

How Liver Disease Progresses — The 5 Stages

Understanding the stages of liver disease is critical. Early intervention at Stages 1–3 can prevent progression to irreversible cirrhosis and liver failure.

🟢 Stage 1

Healthy / Steatosis

Fat accumulation only. No inflammation. Fully reversible with lifestyle changes.

🟡 Stage 2

Hepatitis / NASH

Fat + inflammation + cell injury. Still reversible with treatment and weight loss.

🟠 Stage 3

Fibrosis

Scar tissue forming. Partially reversible. Critical to treat before Stage 4.

🔴 Stage 4

Cirrhosis

Extensive scarring. Irreversible but manageable to prevent decompensation.

Stage 5

Liver Failure / HCC

Liver no longer functions. Transplant evaluation required. Cancer screening essential.

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Dr. Ahuja's goal: Detect liver disease at Stages 1–3 through routine screening and intervene before irreversible cirrhosis develops. A FibroScan takes 10 minutes and can accurately stage liver fibrosis without a biopsy.

When to See a Doctor

Warning Signs of Liver Disease

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Jaundice

Yellow discolouration of skin, eyes (scleral icterus), and dark tea-coloured urine — urgent evaluation needed.

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Abdominal Swelling

Fluid accumulation in the abdomen (ascites) — a sign of advanced liver disease or portal hypertension.

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Vomiting Blood

Haematemesis from ruptured oesophageal varices — a life-threatening emergency requiring immediate endoscopy.

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Confusion / Forgetfulness

Hepatic encephalopathy — brain dysfunction from ammonia build-up in liver failure. Urgent medical attention.

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Persistent Fatigue

Unexplained, severe tiredness with loss of appetite and weight — common early symptom of chronic liver disease.

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Right Upper Pain

Dull ache or heaviness under the right rib cage — may indicate liver inflammation, fatty liver, or hepatitis.

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Emergency signs requiring immediate hospital admission: vomiting blood, severe jaundice with confusion, fever with abdominal pain in cirrhosis patients, or sudden extreme abdomen distension. Call 9990056499 or visit the emergency immediately.

How We Diagnose

Diagnostic Approach at Dr. Ahuja's Clinic

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Clinical History & Examination

Detailed history — alcohol intake, medications, travel, family history, diabetes, obesity. Physical examination for jaundice, liver size, spleen size, ascites, and signs of chronic liver disease (spider naevi, palmar erythema, Dupuytren's contracture).

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Blood Tests — Liver Function Panel

Comprehensive biochemical profile to assess liver damage and function.

LFT (ALT, AST, ALP, GGT)Bilirubin (total & direct)Serum albuminPT / INRCBCViral markers (HBsAg, Anti-HCV, HBV DNA, HCV RNA)AFP (liver cancer screen)
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Ultrasound Abdomen

Non-invasive imaging to assess liver size, echogenicity (fatty liver), bile duct dilation, spleen size, ascites, and focal liver lesions (haemangioma, HCC). Colour Doppler for portal vein flow in suspected portal hypertension.

Fatty liver gradingLiver lesion characterisationPortal vein assessment
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FibroScan (Transient Elastography)

A 10-minute, painless, non-invasive test that measures liver stiffness — accurately staging liver fibrosis from F0 (normal) to F4 (cirrhosis) without the need for a liver biopsy in most patients. Also measures controlled attenuation parameter (CAP) for fat quantification.

Fibrosis staging F0–F4Fat quantification (CAP)No biopsy needed usually
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Advanced Imaging (CT / MRI / MRCP)

For characterisation of liver masses (HCC vs benign), bile duct anatomy (MRCP), staging of liver cancer, or pre-transplant evaluation. Triple-phase CT or MRI with contrast is the gold standard for HCC diagnosis.

HCC diagnosisBile duct anatomy (MRCP)Pre-transplant planning
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Upper GI Endoscopy

In cirrhosis patients — to screen for and grade oesophageal and gastric varices (dilated veins from portal hypertension). Endoscopic band ligation (EVL) is performed to prevent variceal bleeding if high-risk varices are found.

Varices screeningBand ligation (EVL)Portal hypertensive gastropathy
How We Treat

Treatment Approaches

Lifestyle & Metabolic

🥗 Diet, Weight Loss & Metabolic Control

For NAFLD/NASH — even a 5–10% reduction in body weight reduces liver fat by 30–40% and can reverse early fibrosis. Dr. Ahuja provides structured dietary counselling, physical activity plans, and management of diabetes, lipids, and metabolic syndrome in coordination with an endocrinologist.

Antiviral Therapy

💊 Antivirals — HBV & HCV Treatment

Chronic Hepatitis B: Long-term suppression with Tenofovir or Entecavir to prevent cirrhosis and cancer. Hepatitis C: 8–12 week DAA regimen (Sofosbuvir + Velpatasvir or Daclatasvir) — 95%+ cure rate. Dr. Ahuja monitors viral response and manages side effects throughout treatment.

Cirrhosis Management

🔄 Cirrhosis Complication Management

Ascites: diuretics (spironolactone, furosemide) and low-sodium diet; large-volume paracentesis with albumin infusion when needed. Hepatic Encephalopathy: lactulose and rifaximin. Variceal bleeding prevention: propranolol and endoscopic band ligation. SBP: prophylactic norfloxacin.

Endoscopic Interventions

🔬 Endoscopic Procedures for Liver Disease

Endoscopic Variceal Ligation (EVL) to prevent and treat variceal bleeding. ERCP for obstructive jaundice from bile duct stones or strictures. EUS-guided drainage for liver abscesses. These are performed by Dr. Ahuja as part of integrated hepatology care.

Advanced Care

🏥 Liver Transplant Evaluation & Post-Transplant Care

Dr. Hardik Ahuja is an LTSI (Liver Transplant Society of India) Fellow 2024, trained at Indraprastha Apollo Hospital, New Delhi. He provides complete transplant hepatology — evaluating patients for liver transplant candidacy, optimising pre-transplant health, and providing long-term post-transplant immunosuppression management and surveillance.

Transplant candidate evaluation MELD score assessment Pre-transplant optimisation Post-transplant follow-up Immunosuppression management Rejection surveillance
Liver Health Screening

Who Should Get Screened for Liver Disease?

  • Adults with obesity (BMI > 25), Type 2 diabetes, or metabolic syndrome — annual LFT and ultrasound
  • Anyone born between 1945–1980 with unknown hepatitis status — one-time HCV antibody test
  • Healthcare workers, dialysis patients, or those with history of blood transfusions before 1992 — HBsAg and Anti-HCV testing
  • Family members of chronic Hepatitis B patients — HBsAg testing and vaccination if negative
  • Heavy alcohol consumers (more than 14 units/week men, 7 units/week women) — LFT and ultrasound annually
  • Patients on long-term medications (paracetamol, antituberculosis drugs, statins) — periodic LFT monitoring
  • All cirrhosis patients — 6-monthly AFP + ultrasound for liver cancer surveillance
  • Pregnant women — HBsAg and Anti-HCV screening, especially HEV testing if jaundice occurs
Common Questions

Frequently Asked Questions

Can fatty liver be reversed completely?
Yes — in Stages 1–2 (steatosis and early NASH), fatty liver is completely reversible with lifestyle changes. Losing 5–10% of body weight reduces liver fat by 30–40%. Controlling diabetes, triglycerides, and blood pressure also helps. At Stage 3 (fibrosis), partial reversal is possible with treatment. Stage 4 (cirrhosis) is not reversible but can be stabilised to prevent progression and complications.
Is Hepatitis C completely curable?
Yes. Modern Direct-Acting Antiviral (DAA) therapy cures Hepatitis C in 8–12 weeks in over 95% of patients — including those with advanced fibrosis or compensated cirrhosis. The treatment involves oral tablets, has minimal side effects, and requires no injections. A simple blood test (HCV RNA PCR at 12 weeks after completing treatment) confirms cure. Early treatment prevents cirrhosis and liver cancer.
What is FibroScan and why is it important?
FibroScan (transient elastography) is a non-invasive, painless 10-minute test that measures liver stiffness using ultrasound waves, providing an accurate assessment of liver fibrosis stage (F0–F4) and fat content (CAP score). It has largely replaced liver biopsy for routine fibrosis staging in fatty liver and viral hepatitis patients. It is performed in Dr. Ahuja's clinic and the result is available immediately.
How dangerous is cirrhosis? Can I live a normal life?
Compensated cirrhosis (no complications) can be managed effectively with medications, dietary changes, and regular monitoring — many patients live for 15–20+ years with good quality of life. The critical goal is preventing decompensation (ascites, bleeding, encephalopathy). This requires avoiding alcohol, treating the underlying cause, regular endoscopic variceal surveillance, and 6-monthly liver cancer screening. Dr. Ahuja provides structured long-term cirrhosis management plans.
When should a liver transplant be considered?
Liver transplant is considered for decompensated cirrhosis (MELD score ≥15), acute liver failure, certain liver cancers (within Milan criteria), or cirrhosis complications not manageable medically. Dr. Ahuja evaluates transplant candidacy, calculates MELD scores, optimises the patient's condition before listing, and coordinates with transplant surgeons. Post-transplant, he provides long-term immunosuppression management and surveillance for rejection and recurrent disease.
Is alcohol-related liver disease reversible?
Early alcoholic liver disease (fatty liver and early hepatitis) can fully recover with complete alcohol cessation. Alcoholic cirrhosis is not reversible, but stopping alcohol completely halts further progression and can improve liver function significantly. Dr. Ahuja provides supportive counselling and medical management for alcoholic liver disease, and can refer to addiction specialists as needed.

Protect Your Liver. Your Life Depends on It.

Early detection and expert management can prevent fatty liver from becoming cirrhosis, and cirrhosis from becoming liver failure. See Dr. Ahuja today.

📅 Book a Liver Health Check 📞 +91 99900 56499