Hepatic Disorders NURS 321

Anatomy of the Hepatic and Biliary System
  • Key Structures:
      - Liver: The central organ of the hepatic system, located below the diaphragm.
      - Gallbladder: Connected via the cystic duct; stores and concentrates bile.
      - Ductal System:
        - Cystic duct: Leads from the gallbladder.
        - Hepatic duct: Leads from the liver.
        - Common bile duct: Formed by the union of the cystic and hepatic ducts.
        - Hepatopancreatic ampulla: The junction where the common bile duct and pancreatic duct enter the duodenum.
        - Pancreas: Consists of the head (near the duodenum), the pancreatic duct, and the tail (near the spleen).
        - Spleen: Located in the left upper quadrant, adjacent to the tail of the pancreas.
        - Duodenum: The first part of the small intestine where bile and pancreatic enzymes are secreted.

Functional Roles of the Liver
  • Primary Functions:
      - Metabolic: Processing of carbohydrates, proteins, and fats.
      - Secretory: Production and secretion of bile for fat digestion.
      - Storage: Storing glucose (as glycogen), vitamins, and minerals.
      - Vascular: Serving as a blood reservoir and filtering blood through the portal system.

  • Core Nursing Concepts:
      - Elimination: The liver's role in detoxifying substances and excreting bilirubin.
      - Nutrition: The liver's role in nutrient metabolism and storage.

Hepatitis: Etiology and Classifications
  • Definition: Inflammation of the liver.

  • Standard Etiology:
      - Viruses: The most common cause of inflammation.
      - Drugs and Alcohol: Especially hepatotoxic substances like Acetaminophen.
      - Chemicals: Exposure to industrial or environmental toxins.
      - Autoimmune Diseases: The body's immune system attacking liver cells.

Viral Hepatitis: Pathophysiology and Staging
  • Viral Agents:
      - Six primary viruses: AA, BB, CC, DD, EE, and GG.
      - Most common types: AA, BB, and CC.
      - Other contributing viruses: Cytomegalovirus (CMVCMV), Epstein-Barr virus (EBVEBV), Herpes virus, Coxsackievirus, and Rubella virus.

  • Pathophysiology Phases:
      - Acute Phase:
        - Duration: 66 months or less.
        - Mechanism: Lysis of hepatocytes caused by cytotoxic cytokines and natural killer cells.
        - Inflammation: Widespread inflammation that may interrupt bile and blood flow.
        - Necrosis: Tissue necrosis occurs during the peak of infection.
        - Regeneration: Liver cells typically regenerate after the infection resolves, restoring normal function.

  - Chronic Phase:
    - Duration: Greater than (>) 66 months; can be lifelong.
    - Mechanism: Persistent inflammation causes progressive fibrosis and ongoing tissue necrosis.
    - Outcomes: Over time, this leads to compromised liver function, Cirrhosis, or Liver Cancer.

Comparative Analysis of Hepatitis A, B, and C
  • Hepatitis A Virus (HAV):
      - Type: Acute only (never chronic).
      - Transmission: Fecal-Oral Route.
      - Sources: Poor personal hygiene, poor sanitation, contaminated food, water, milk, or shellfish.
      - Incubation: 1515 to 5050 days.
      - At-Risk Populations: Daycare workers/attendees, institutionalized individuals, Men who have Sex with Men (MSMMSM).
      - Prevention: Hepatitis A Vaccine and Immune Globulin (IGIG).
      - Diagnostic Test: Anti-HAVHAV IgMIgM (indicated for acute infection).

  • Hepatitis B Virus (HBV):
      - Type: Acute or Chronic.
      - Transmission: Percutaneous, Perinatal, or mucosal exposure to blood/bodily fluids; sexual contact.
      - Sources: Contaminated needles, blood products, tattoos, body piercings, or bites.
      - Incubation: 4545 to 180180 days.
      - At-Risk Populations: Healthcare workers, hemodialysis patients, transplant recipients, unprotected sex (MSMMSM), and injection drug users.
      - Prevention: Hepatitis B Vaccine and Hepatitis B Immune Globulin (HBIGHBIG).
      - Diagnostic Test: HBsAgHBsAg (Hepatitis surface antigen) or Anti-HBcHBc IgMIgM.

  • Hepatitis C Virus (HCV):
      - Type: Acute or Chronic.
      - Transmission: Percutaneous (needles), high-risk sexual activity, blood/blood products (prior to the 1990s1990s).
      - Incubation: 1414 to 180180 days.
      - At-Risk Populations: IV drug users, HIV+HIV+ MSMMSM, individuals receiving blood products before precise screening (1990s1990s).
      - Prevention: No vaccine available; rely on needle safety and safe sex.
      - Diagnostic Test: Anti-HCVHCV (tests for acute or chronic infection).

Clinical Manifestations of Acute Viral Hepatitis
  • Incubation Phase:
      - The period after the virus is acquired; symptoms begin to emerge.

  • Acute Phase (Highly Infectious):
      - Duration: 11 to 66 months.
      - Systemic Symptoms: Fatigue, low-grade fever, myalgias, arthralgias, and headaches.
      - GI Symptoms: Anorexia, weight loss, nausea, vomiting, and abdominal tenderness.
      - Physical Findings: Hepatomegaly, Splenomegaly, and Lymphadenopathy.
      - Icteric Symptoms: Jaundice (yellowing), dark urine (excess bilirubin), clay-colored stools (lack of bile), and pruritus (itching).

  • Convalescent Phase:
      - Duration: Weeks to months (Average: 22 to 44 months).
      - Progression: Fever subsides and jaundice resolves.
      - Organ Recovery: Splenomegaly subsides; hepatomegaly persists but slowly subsides.
      - Persistence: Fatigue and malaise may continue for some time.

Diagnostic Evaluation of Hepatitis
  • Primary Method: Hepatitis antigens and antibodies; viral load (viral level in blood).

  • Liver Function Tests (LFTs):
      - Liver Transaminases: ASTAST, ALTALT, GGTGGT.
      - Enzymes: Alkaline phosphatase, LDHLDH (lactate dehydrogenase).

  • Serums: Serum albumin (decreases in failure), Serum bilirubin (increases).

  • Coagulation: PTTPTT (Prothrombin time) and INRINR.

  • Tissue Analysis: Liver Biopsy (to assess the degree of fibrosis).

Collaborative Care for Viral Hepatitis
  • Acute Management:
      - Rest: Essential for liver cell regeneration.
      - Location: Usually managed at home as an outpatient.
      - Nutrition: Goal is to maintain calorie intake to avoid weight loss. Small, frequent meals; high oral fluid intake; vitamin supplementation.
      - Abstinence: Avoid alcohol and Acetaminophen.

  • Drug Therapy:
      - Supportive: Antiemetics for nausea; Diphenhydramine (Benadryl) for pruritus.
      - Chronic Hepatitis B: Interferon, Nucleoside & nucleotide analogs (antivirals) like lamivudine (Epivir 3TC3TC), adefovir dipivoxil (Hepsera), and Telbivudine (Tyzeka).
      - Chronic Hepatitis C: extαinterferonext{α-interferon}, Direct-acting antivirals (DAAsDAAs), and Ribavirin.

  • Prevention (Healthcare and Personal):
      - Vaccinations (HAVHAV & HBVHBV).
      - Immune globulin (IGIG) for passive immunity post-exposure.
      - Universal (Standard) precautions (PPEs).
      - Disposable, one-time-use needles.

Drug and Chemical Induced Hepatitis
  • Etiology: Hepatotoxic substances, most commonly Acetaminophen and Alcohol.

  • Manifestations: Ranges from a slight elevation in ASTAST and ALTALT to acute alcoholic hepatitis or advanced cirrhosis.

  • Care: Supportive care; immediate removal of the offending substance; potential liver transplantation in severe cases.

Liver Cirrhosis: Pathophysiology and Etiology
  • Definition: Extensive degeneration and destruction of the liver cells where liver lobules are replaced by nodes of scar tissue.

  • Pathophysiology Process:
      - 1.1. Cell necrosis occurs.
      - 2.2. Native liver cells are replaced by scar (fibrotic) tissue.
      - 3.3. Regenerative efforts result in nodules (irregular sizes/shapes) rather than normal lobular structure.
      - 4.4. Abnormal blood flow through the fibrotic tissue leading to portal hypertension and decreased liver function.

  • Etiology:
      - Alcohol abuse.
      - Chronic Hepatitis BB or CC.
      - Biliary issues and NASHNASH (Nonalcoholic steatohepatitis).
      - Genetics and autoimmune diseases.
      - Cardiac problems (secondary to severe right-sided heart failure).

Clinical Manifestations of Cirrhosis
  • Early Phase: Insidious; fatigue and mild GI symptoms; palpable liver.

  • Late Phase Symptoms:
      - Neurologic: Hepatic encephalopathy, peripheral neuropathy, and Asterixis (flapping tremors).
      - Gastrointestinal: Anorexia, dyspepsia, nausea/vomiting, fetor hepaticus (musty breath), esophageal/gastric varices, and hematemesis.
      - Integumentary: Jaundice, spider angioma, palmar erythema, purpura, petechiae, and caput medusae.
      - Hematologic: Anemia, thrombocytopenia, leukopenia, and coagulation disorders.
      - Reproductive: Amenorrhea, testicular atrophy, gynecomastia, and impotence.
      - Metabolic: Potassium deficiency (KK), hyponatremia (NaNa), and hypoalbuminemia.
      - Cardiovascular: Fluid retention, peripheral edema, and ascites.

Complications of Cirrhosis and Management
  • Portal Hypertension: Increased venous pressure in portal circulation leading to splenomegaly, collateral veins, ascites, and varices.

  • Esophageal and Gastric Varices:
      - Risk: Extremely high risk for bleeding/hemorrhage.
      - Prevention: Avoid ASAASA, alcohol, and irritating foods. Treat coughs promptly to prevent rupture.
      - Treatment: Inderal (propranolol); Balloon tamponade (Sengstaken-Blakemore tube); endoscopic procedures.

  • Peripheral Edema and Ascites:
      - Treatment: Limit Na+Na^+ intake; Diuretics; Paracentesis; Peritoneovenous shunt; TIPSTIPS procedure.
      - Concerns: Bacterial peritonitis, dehydration, and hypokalemia.

  • Hepatic Encephalopathy:
      - Cause: Liver cannot convert ammonia to urea; ammonia crosses the blood-brain barrier.
      - Sign: Change in mental status and Asterixis.
      - Care: Lactulose (promote ammonia excretion) and Neomycin; neuro checks; airway protection (ABCsABCs).

Dietary Considerations for Cirrhosis
  • General Diet: High calorie, high carbohydrate, low to moderate fat.

  • Protein Conflict:
      - Low Protein: Needed if encephalopathy is present, but may worsen malnutrition.
      - High Protein: Needed for tissue repair/albumin, but worsens encephalopathy.
      - Standard Recommendation: Small frequent meals with restricted high-protein foods; consult a dietitian.

  • Electrolytes: May need low Sodium (Na+Na^+) and supplementation of KK, MgMg, and Phos.

Fulminant Hepatic Failure (Acute Liver Failure)
  • Definition: Acute liver failure accompanied by hepatic encephalopathy; occurs suddenly.

  • Primary Causes:
      - Combination of Alcohol and Acetaminophen overdose (most common).
      - Hepatotoxic meds: Isoniazid, halothane, sulfa drugs, and NSAIDSNSAIDS.
      - Hepatitis BB Virus (2nd2nd most common cause).

  • Clinical Indicators: First sign is a change in mental status. Jaundice and coagulation abnormalities follow.

  • Complications: Cerebral edema (herniation), renal failure, hypoglycemia, metabolic acidosis, and sepsis.

  • Nursing Care:
      - Early ICU transfer.
      - Decrease ICPICP: Head of Bed (HOBHOB) at 3030 degrees; decrease straining/coughing.
      - Liver transplant is the treatment of choice for stable patients.

Liver Cancer
  • Types: Hepatocellular Carcinoma (HCCHCC), Malignant Hepatoma, Cholangioma.

  • Classification: Primary liver cancer is less common than metastatic disease from other sites (due to the liver's high blood flow filtration).

  • Risk Factors: Hepatitis BB and CC, alcoholic cirrhosis, obesity, diabetes, Hemochromatosis, and NASHNASH.

  • Diagnostics:
      - AFPAFP (alpha fetoprotein levels), Ultrasound, CTCT, MRIMRI, and biopsy.

  • Treatment:
      - Surgery: Excision or liver transplant if localized.
      - Radiofrequency Ablation: Using electrical energy to heat the tumor.
      - Chemoembolization: Direct injection of chemo into arteries feeding the tumor.
      - Chemotherapy: Limited efficacy; Sorafenib (Nexavar) is an option.

Liver Transplantation
  • Candidate Criteria: Based on the MELDMELD (Model for End-Stage Liver Disease) Score.

  • Donors:
      - Cadaveric donors.
      - Living donors (retrieval of the right lobe).

  • Post-Transplant Focus: Focus on rejection prevention, infection control, and psychosocial support for the patient and family.