Viral hepatitis Flashcards

1
Q

What is hepatitis A&E?

A
  1. HAV ⇒ RNA picornavirus. HEV ⇒ calicivirus. Both transmitted via faecal-oral route.
    • HAV → endemic in the developing world. Infection often occurs sub-clinically. Better sanitisation in developed world means it is less common.
    • HEV → endemic in Asia, Africa and Central America.
  2. Hep A = particularly associated with travellers
    - Both have incubation period of 3-6 weeks.
    - Severe Hepatitis in pregnant women = Hep E.
  3. Acute infection only
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2
Q

What are the risk factors for hepA&E?

A
  •  Risk factors: 
  • Living in endemic region 
  • Close personal contact with an infected person 
  • Men who have sex with men 
  • Known foodborne outbreak 
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3
Q

Summarise the epidemiology of viral hepatitis

A
  • HAV is endemic in the developing world
  • Infection often occurs sub-clinically (no clinical findings)
  • Better sanitation in the developed world means that it is less common, age of exposure is higher and, hence, patients are more likely to be symptomatic
  • Annual UK incidence: 5000
  • HEV is endemic in Asia, Africa and Central America
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4
Q

What are the presenting symptoms of hepA&E?

A
  1. Incubation period of HAV and HEV: 3-6 weeks
  2. Prodromal period symptoms (early symptoms)
    - Malaise
    - Anorexia – distaste for cigarettes in smokers
    - Fever
    - Nausea and vomiting
  3. Hepatitis symptoms:
    - Dark urine
    - Pale stools
    - Jaundice lasting around 3 weeks
    - Occasionally, itching and jaundice may last several weeks in HAV infection
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5
Q

What signs of viral hepatitis A&E can be found on physical examination

A
  • Pyrexia
  • Jaundice
  • Tender hepatomegaly
  • Spleen may be palpable
  • ABSENCE of stigmata of chronic liver disease (although some spider naevi may appear transiently)
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6
Q

What investigations are used to diagnose/ monitor hepatitis A&E?

A
  1. LFT’s → raised AST, ALT, ALP, GGT and bilirubin
  2. Raised ESR
  3. Severe → low albumin + high platelets
  4. Serology:
    - HAV ⇒ Anti-HAV IgM present during acute illness, disappears after 3-5 months. Anti-HAV IgG persist indefinitely after infection or vaccination.
    - HEV ⇒ Anti-HEV IgM for active infection, Anti-HEV IgG for past infection.
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7
Q

How is hepatitis A&E managed?

A
  1. Symptomatic Treatment (+ use drugs such as paracetamol with caution due to hepatotoxicity)
  2. Hepatitis A Vaccine (no vaccine for HEV)
  3. Avoid alcohol and excess paracetamol
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8
Q

What complications may arise from hepatitis A&E?

A
  • Fulminant hepatic failure (in a very small proportion of patients but is more common in pregnant women)
  • Cholestatic hepatitis with prolonged jaundice and pruritus can develop after HAV infection
  • Post-hepatitis syndrome: continued malaise for weeks to months
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9
Q

Summarise the prognosis for patients with viral hepatitis

A
  • Recovery is usually within 3-6 weeks
  • Occasionally patients may relapse during recovery
  • There are no chronic sequelae
  • Fulminant hepatic failure has a mortality of 80%
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10
Q

What is hepatitis B&D?

A
  1. HBV ⇒ double-stranded DNA hepadnavirus
    - Transmitted via sexual contact, blood and vertical transmission (from mother to baby)
  2. HDV ⇒ single-stranded RNA virus coated with HbsAg. Defective virus (requires hepatitis B surface antigen to complete its replication and transmission cycle), that may only co-infect with HBV or superinfect people who are already carriers of HBV
    - Chronic Hep B patient with flare up → suspect Hep D superinfection
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11
Q

What are the risk factors for hep B&D?

A

IV drug use, unscreened blood products, infants of HbeAg-positive mothers, sexual contact with HBV carriers, Genetic factors are associated with varying rates of viral clearance

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12
Q

Summarise the epidemiology of viral hepatitis B&D

A
  • Common
  • 1-2 million deaths annually
  • Common in Southeast Asia, Africa and Mediterranean countries
  • HDV is also found worldwide
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13
Q

What are the presenting symptoms of viral hepatitis B&D?

A
  1. Incubation period: 3-6 months
  2. 1-2 week prodrome consisting of:
    - Malaise
    - Headache
    - Anorexia
    - Nausea and vomiting
    - Diarrhoea
    - RUQ pain
    - Serum-sickness type illness may develop (e.g. fever, arthralgia, polyarthritis, urticaria, maculopapular rash)
  3. Jaundice then develops with dark urine and pale stools
  4. Recovery usually within 4-8 weeks
    1% develop fulminant liver failure
  5. Chronic carriage may be diagnosed after routine LFT testing or if cirrhosis or decompensation develops
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14
Q

What signs of viral hepatitis B&D can be found on physical examination

A
  1. Acute
    - Jaundice
    - Pyrexia
    - Tender hepatomegaly
    - Splenomegaly
    - Cervical lymphadneopathy (in 10-20% of patients)
    - Occasionally: urticaria and maculopapular rash
  2. Chronic
    - May be no findings
    - May have signs of chronic liver disease or decompensation
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15
Q

What investigations are used to diagnose/ monitor hep B&D?

A

*Viral Serology
1. Acute HBV → HBsAg positive + IgM anti-HBcAg
- HBsAg is first marker to appear and causes production of anti-HBs.
2. Chronic HBV → HBsAg positive + IgG anti-HBcAg. May be HbeAg positive or negative.
3. HBV Cleared → anti-HbsAg antibody positive + IgG anti-HBcAg
- HbsAg positive indicates acute or chronic infection (ie. still have it). Anti-HbsAg antibody positive indicates immunity through previous immunisation or disease (ie. cleared).
4. Vaccinated against HBV → anti-HbsAg antibody positive (everything else negative, won’t have IgG antibody)
- Can only get antibodies against HbcAg if had infection, not with vaccination
5. HBeAg → marker of infectivity (higher = more infectious)
6. HDV Infection → PCR used for detection

*LFTs → raised AST, ALT, ALP, Bilirubin
*High PT in severe disease
1. PT = sensitive marker of significant liver damage

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16
Q

How is hep B&D managed?

A
  1. Acute HBV → supportive
  2. Chronic HBV → interferon α (antiviral)
  3. Hepatitis B Immunisation
  4. Screen for HIV
  5. Prevention → blood screening, safe sex, instrument sterilisation
  6. Notifiable Disease
17
Q

What complications may arise from hep B&D?

A
  • 1% get fulminant hepatic failure
  • Chronic HBV infection (10% of adults, much higher in neonates)
  • Cirrhosis
  • Hepatocellular carcinoma (HCC)
  • Extrahepatic immune complex disorders (e.g. glomerulonephritis, polyarteritis nodosa)
  • Superinfection with HDV may lead to acute liver failure or more rapidly progressive disease
18
Q

Summarise the prognosis of patients with viral hepatitis B&D

A
  • Adults: 10% of infections become chronic
  • Of the chronic infections, 20-30% will develop cirrhosis
19
Q

What is viral hepatitis C?

A
  • Hepatitis caused by infection with hepatitis C virus (HCV), often following a chronic course (in 80% of cases)
  • HCV ⇒ small, enveloped, single-stranded RNA virus
  • Parenteral Transmission → sexual transmission and vertical transmission
20
Q

What are the 2 types of HepC?

A

Acute <6 months, Chronic >6 months
- Most common type of hepatitis to become chronic

21
Q

What patients are at high risk of HepC?

A

IV drug users, needlestick injury (health care workers), blood transfusion (esp. before 1992)

22
Q

Describe the pathology of hepatitis C

A
  1. The virus is not thought to be directly hepatotoxic
  2. It is the humoral and cell-mediated responses to the viral infection that leads to hepatic inflammation and necrosis
  3. Liver biopsy shows:
    - Chronic hepatitis
    - Lymphoid follicles in portal tracts
    - Fatty change
    - Cirrhosis may be present
23
Q

Summarise the epidemiology of viral hepatitis C

A
  • COMMON
  • Different genotypes of HCV have different geographical prevalence
24
Q

What are the presenting symptoms of hep C?

A
  • 90% of acute infections are ASYMPTOMATIC
  • 10% become jaundiced with mild flu-like illness
  • May be diagnosed after incidental abnormal LFT or in older patients with complications of cirrhosis
25
Q

What are signs of hep C can be found on physical examination?

A
  1. ognise the signs of viral hepatitis on physical examination
    May be NO SIGNS
  2. There may be signs of chronic liver disease (if long-standing HCV infection)
  3. Extra-hepatic manifestations (rare) include:
    - Skin rash
    - Renal dysfunction (due to glomerulonephritis)
26
Q

What investigations are used to diagnose/ monitor viral hepatitis C?

A
  1. HCV Serology → anti-HCV antibodies (IgM = acute, IgG = past exposure or chronic)
  2. RT-PCR → detection of HCV
  3. LFTs
  4. Liver Biopsy → assess degree of inflammation and liver damage. Useful for diagnosing cirrhosis.
27
Q

How is HepC managed?

A
  1. Medical Treatment (Antivirals) → interferon α or ribavirin
    - Needed for acute and chronic Hep C
  2. Screen for HIV
  3. Prevention → screen blood, blood products and organ donors. Instrument sterilisation.
  4. No vaccine available for HCV
28
Q

What complications may arise from viral hepC?

A
  • Fulminant hepatic failure
  • Chronic carriage of HCV
  • Hepatocellular carcinoma
  • Less common: porphyria cutanea tarda, cryoglobulinaemia, glomerulonephritis
29
Q

Summarise the prognosis for patients with viral hepatitis C

A
  • 80% of exposed will progress to chronic carriage
  • Of these, 20-30% will develop cirrhosis over 10-20 years