Specialized Department

Liver Diseases & Hepatology

Specialized hepatology clinic managing cirrhosis, fatty liver disease, viral hepatitis, and biliary conditions.

About the Department

Overview & Specialties

Swasthik Multispeciality Hospital's Liver Diseases and Hepatology Department provides comprehensive diagnostics and advanced treatments for acute and chronic disorders of the liver, gallbladder, and biliary tree. Led by specialized hepatology consultants, our clinic manages conditions like non-alcoholic fatty liver disease (NAFLD/NASH), liver cirrhosis, viral hepatitis, and alcoholic liver injury.

Our department uses non-invasive diagnostics like transient elastography (FibroScan) to assess liver stiffness and fatty deposits without a biopsy. We offer treatments for autoimmune hepatitis, biliary conditions like primary biliary cholangitis, and portal hypertension. We emphasize early diagnosis and prevention to arrest disease progression and protect hepatic function.

At Swasthik, we believe in multidisciplinary care. For advanced liver conditions, we coordinate with gastroenterologists, interventional radiologists, and general surgeons to manage complications like ascites and variceal bleeding. Our patient education programs focus on dietary changes, alcohol rehabilitation, and lifestyle counseling to support recovery and long-term liver health.


Clinical Care

Conditions We Treat

Non-Alcoholic Fatty Liver Disease (NAFLD)

Description: An accumulation of excess fat in liver cells not caused by alcohol consumption.

Symptoms: Often asymptomatic, mild fatigue, dull ache in the upper right abdomen. Causes: Insulin resistance, obesity, high carbohydrate/sugar intake. Risk Factors: Obesity, type 2 diabetes, dyslipidemia, metabolic syndrome. Diagnosis: Abdominal ultrasound, liver function tests, FibroScan. Treatment: Weight loss, healthy low-fat diet, regular exercise, managing blood sugar.

Liver Cirrhosis

Description: Late-stage scarring (fibrosis) of the liver caused by many forms of liver diseases and conditions.

Symptoms: Jaundice, swelling in legs and abdomen (ascites), easy bruising, fatigue, confusion. Causes: Chronic hepatitis B/C, long-term alcohol abuse, advanced NASH. Risk Factors: Excessive alcohol consumption, chronic viral hepatitis, obesity. Diagnosis: Liver function panel, FibroScan, abdominal ultrasound or CT, endoscopy. Treatment: Treating underlying cause, diuretics for ascites, liver transplant evaluation.

Hepatitis B (Chronic)

Description: A serious liver infection caused by the hepatitis B virus (HBV), leading to chronic inflammation.

Symptoms: Fatigue, yellowing of skin/eyes (jaundice), dark urine, joint pain. Causes: Contact with infectious blood, semen, or other body fluids; vertical transmission. Risk Factors: Healthcare workers, unprotected sex, needle sharing, born to infected mothers. Diagnosis: HBsAg blood test, HBV DNA viral load, liver biopsy. Treatment: Antiviral medications (tenofovir, entecavir), regular liver monitoring.

Hepatitis C (Chronic)

Description: An infection caused by the hepatitis C virus (HCV) that attacks the liver and leads to inflammation.

Symptoms: Often silent for decades, fatigue, easily bleeding, poor appetite. Causes: Blood-to-blood contact with an infected person's blood. Risk Factors: History of blood transfusions before screening, sharing needles. Diagnosis: Anti-HCV antibody test, HCV RNA PCR viral load. Treatment: Direct-acting antivirals (DAAs) with a high cure rate.

Alcoholic Liver Disease

Description: Liver damage caused by excess alcohol intake, ranging from fatty liver to alcoholic hepatitis.

Symptoms: Nausea, vomiting, abdominal tenderness, jaundice, fever. Causes: Heavy alcohol consumption over several years. Risk Factors: Heavy drinking, female gender (higher risk for same intake), poor nutrition. Diagnosis: Elevated liver enzymes (AST/ALT ratio > 2), abdominal ultrasound. Treatment: Strict, complete abstinence from alcohol, nutritional support.

Autoimmune Hepatitis

Description: Chronic inflammatory liver disease where the body's immune system attacks liver cells.

Symptoms: Fatigue, joint pain, abdominal discomfort, skin rashes, jaundice. Causes: Autoimmune reaction triggered by genetic factors. Risk Factors: Female gender, history of other autoimmune diseases (lupus, celiac). Diagnosis: Positive antinuclear antibody (ANA) or ASMA, liver biopsy. Treatment: Corticosteroids (prednisolone), immunosuppressants (azathioprine).

Primary Biliary Cholangitis (PBC)

Description: An autoimmune disease causing progressive destruction of the small bile ducts in the liver.

Symptoms: Severe fatigue, intense skin itching (pruritus), dry eyes and mouth. Causes: Autoimmune attack on the intrahepatic bile duct epithelial cells. Risk Factors: Female gender, middle age, family history. Diagnosis: Anti-mitochondrial antibody (AMA) positive, high alkaline phosphatase. Treatment: Ursodeoxycholic acid (UDCA), medications for itching.

Hepatic Encephalopathy

Description: A decline in brain function that occurs as a result of severe liver disease.

Symptoms: Forgetfulness, confusion, personality changes, hand tremors (asterixis), slurred speech. Causes: Accumulation of toxins (like ammonia) in the blood due to liver failure. Risk Factors: Dehydration, gastrointestinal bleeding, infections in cirrhotic patients. Diagnosis: Clinical evaluation, elevated serum ammonia levels. Treatment: Lactulose syrup, rifaximin antibiotic, correcting precipitating factor.

Portal Hypertension

Description: An increase in the blood pressure within the portal vein system, a major complication of cirrhosis.

Symptoms: Ascites, splenomegaly, bleeding from esophageal or gastric varices. Causes: Obstruction of blood flow through the scarred cirrhotic liver. Risk Factors: Advanced liver cirrhosis. Diagnosis: Abdominal ultrasound with Doppler, upper endoscopy. Treatment: Beta-blockers, endoscopic variceal band ligation (EVL), TIPS procedure.

Ascites

Description: An abnormal accumulation of fluid in the peritoneal cavity, commonly complicating liver failure.

Symptoms: Abdominal swelling, rapid weight gain, shortness of breath, feeling full quickly. Causes: High portal vein pressure and low albumin protein levels. Risk Factors: Severe liver cirrhosis, heart failure, abdominal cancer. Diagnosis: Abdominal ultrasound, paracentesis fluid analysis (SAAG ratio). Treatment: Low-sodium diet, diuretic medications (spironolactone), therapeutic paracentesis.

Hepatocellular Carcinoma

Description: The most common primary liver cancer, arising from hepatocytes, often in cirrhotic patients.

Symptoms: Weight loss, upper abdominal pain, worsening ascites, jaundice, palpable liver lump. Causes: Chronic inflammation and cellular mutations from HBV, HCV, or alcohol. Risk Factors: Liver cirrhosis, chronic hepatitis B/C, fatty liver. Diagnosis: Triple-phase CT scan of abdomen, liver MRI, serum Alpha-Fetoprotein (AFP). Treatment: Surgical resection, radiofrequency ablation, chemoembolization (TACE), liver transplantation.

Wilson's Disease

Description: A rare genetic disorder causing copper accumulation in the liver, brain, and other vital organs.

Symptoms: Tremors, difficulty speaking or walking, jaundice, Kaiser-Fleischer rings in eyes. Causes: Inherited mutation in the ATP7B gene. Risk Factors: Family history. Diagnosis: Low serum ceruloplasmin, high 24-hour urine copper excretion, eye exam. Treatment: Chelating agents (penicillamine, trientine), zinc acetate.

Drug-Induced Liver Injury (DILI)

Description: Liver damage caused by medications, herbal remedies, or dietary supplements.

Symptoms: Nausea, fatigue, dark urine, jaundice, itching. Causes: Hepatotoxins or idiosyncratic immune reactions to drugs. Risk Factors: Pre-existing liver disease, taking multiple medications, advanced age. Diagnosis: Diagnosis of exclusion, detailed medication history, liver function tests. Treatment: Discontinuing the offending drug, supportive care, N-acetylcysteine.

Hemochromatosis

Description: A genetic disorder causing the body to absorb too much iron, storing it in organs like the liver.

Symptoms: Joint pain, fatigue, abdominal pain, darkening of skin color ('bronze diabetes'). Causes: Mutations in the HFE gene. Risk Factors: Family history, European ancestry. Diagnosis: High transferrin saturation, high serum ferritin, genetic testing. Treatment: Therapeutic phlebotomy (regular blood removal), iron chelation.

Primary Sclerosing Cholangitis (PSC)

Description: A progressive disease of the bile ducts characterized by inflammation, scarring, and narrowing.

Symptoms: Itching, fatigue, jaundice, upper abdominal pain, fever. Causes: Unknown, highly associated with inflammatory bowel disease. Risk Factors: History of Ulcerative Colitis, male gender, age between 30 and 50. Diagnosis: MRCP (magnetic resonance cholangiopancreatography), ERCP. Treatment: Ursodeoxycholic acid, endoscopic dilation of strictures, liver transplant.