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Hepatitis C

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Minocycline, Fluoxetine, Levothyroxine, Paracetamol ... BTs, tatoos, medical or dental treatment in developing countries. Contacts of any of these ... – PowerPoint PPT presentation

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Title: Hepatitis C


1
Hepatitis C
2
49 year old woman
  • Hx of depression, acne, Raynauds,
    hypothyroidism.
  • Minocycline, Fluoxetine, Levothyroxine,
    Paracetamol
  • 2 week Hx of general malaise, myalgia, anorexia,
    nausea, fever, cough. No specific symptoms.
  • Pale, normal general, CVS, Resp and GI
    examinations

3
Blood Results
  • Hb 12.1, WCC 2.7 (Ne 1.6), Plt 336
  • Na 138, K3.9, U 3.5, Cr 54
  • ALT 586, Bil 34, AP 364, Alb 42
  • CRP 14

4
Fast-Track Jaundice Clinic
  • No jaundice
  • Normal urine and stools
  • Normal USS
  • Previous blood transfusion in 1985
  • Hx consistent with viral infection or Minocycline
    use

5
Why should we be interested?
  • BMJ 2007 Most cases are undiagnosed
  • Treatable disease
  • Family Planning 2006
  • Primary Care important setting for case finding
  • Cost effective
  • In Tayside 1700 diagnosed. A further 3000 cases
    go undiagnosed
  • New SIGN and NICE guidelines within last year

6
What is it?
  • Blood-borne, infectious, viral disease
  • Can remain viable outside the body
  • Causes liver inflammation (often asymptomatic)
  • Acute infection (first 6 months) 15 20
    symptomatic
  • Fatigue, anorexia, abdo pain, jaundice and
    itching, flu-like symptoms
  • 20-30 clear the virus in first 6 months
  • Remaining 70-80 develop chronic (6 months)
    infection
  • Chronic infection leads to cirrhosis
  • 1-4 p.a develop hepatocelluar Ca.

7
How do you catch it?
  • Blood transfusions/blood products
  • Dirty needles (10 times commoner in IVDUs than
    HIV)
  • Vertical transmission
  • Very little incidence of sexual transmission
  • Former drug users 35yrs at greatest risk (may
    only have injected once)

8
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9
Who should be tested?
  • According to latest SIGN guidelines
  • Past or present IVDU
  • Blood transfusion/products pre 1987
  • BTs, tatoos, medical or dental treatment in
    developing countries
  • Contacts of any of these
  • Unexplained raised ALT
  • Healthcare workers exposure prone treatments
  • Patients on haemodialysis
  • People wit HIV

10
Benefits of testing
  • Availability of treatment
  • Success of treatment
  • Prevention of secondary transmission
  • Disease modifying factors

11
Testing
  • 2 tests available Antibodies (1 yellow top tube)
  • Viral RNA PCR (2 purple top tubes)

12
Referral
  • Should be considered for all patients
  • Specialist treatment important even if supportive
  • Treatment given during acute phase more
    successful
  • Multidisciplinary care should be offered
  • Increases uptake when lifestyles are chaotic
  • Often drug/alcohol abuse

13
Treatment
  • Current treatment is (oral ribavarin) and weekly
    interferon for 6 to 12 months.
  • Trials show cure rates of 50-80
  • Until recently only those with mod-severe
    symptoms being treated
  • Now recommended that mild infection should also
    be treated
  • Treat 3 to 6 months after diagnosing acute Hep C
    (for 24 weeks)
  • 4 genotypes of chronic 12-24 weeks for genotypes
    2 or 3
  • 48 weeks for genotype 1 or 4

14
Improved Treatment Success
  • Genotype 2 or 3
  • Less fibrosis in liver
  • Gender better if female
  • Age better if younger
  • Smaller viral load
  • Lower body weight

15
Adverse Effects
  • Flu-like symptoms (advise paracetamol)
  • Anaemia
  • Depression
  • Skin reactions
  • Thyroid dysfunction
  • Retinopathy
  • Alopecia

16
Progression of Disease
  • Age, gender and ethnicity
  • BMI 25
  • Tobacco smoking
  • Alcohol
  • ALT
  • HIV co-infection

17
Summary The Role of the GP
  • Prevention primary and secondary traansmission
  • Detection awareness of at-risk groups
  • Knowledge of presenting symptoms
  • Testing
  • Treatment and its adverse effects
  • Monitoring
  • Disease modifying factors
  • Support

18
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