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 Occupational exposure to blood-borne pathogens is a
well recognised hazard to health care workers (HCW).
 Adherence to standard infection control practices is
the best way to prevent blood-borne infections in the
health care setting.
 However, accidental exposure still happens.
First aid
 Immediately following any exposure, the wound should be
washed immediately and thoroughly with soap and water.
 Antiseptics are not necessary as there is no evidence of
their efficacy.
 Wounds should not be sucked.
 The exposed HCW should then seek medical advice for
proper wound care and post-exposure management.
Reporting
 The institution should ensure that a mechanism is in
place and made known to all HCW to facilitate
reporting and management of sharps injury and
mucosal exposure in the occupational setting.
 Clear documentation and investigation of the
circumstances of exposure are necessary.
 A surveillance system of exposure events should be set
up with a view to avoidance of similar incidents.
Counselling
 Until infection is ruled out, health care staff
potentially exposed to HBV, HCV, or HIV infected
blood should refrain from donating blood, plasma,
organs, tissue or semen.
 Safer sex with condom is advisable.
Hepatitis B
 The risk of contracting HBV infection through
occupational exposure ranges from 18% to 30%,
depending on the type of exposure, the body fluid
involved and the infectivity of the source.
 Percutaneous injuries with hollow-bored, blood-filled
needles from a patient positive with HBeAg carry the
highest risk of infection at 37-62%.
Management of accidental
exposure to HBV
 All health care staff with potential risk of exposure to
blood and body fluids are advised to receive hepatitis
B vaccination as soon as possible for their own safety.
 Subjects with anti-HBs titre ≥ 10 mIU/mL 1-4 months
after vaccine completion are considered as
responders.
 Non-responders are those with no detectable
antiHBs and hypo-responders refer to those whose
anti-HBs titre are between 0-10 mIU/mL.
 Both non- and hypo-responders should complete a
second 3-dose vaccine series and retested at the
completion of the second vaccine series.
 Nonresponders to the initial 3-dose vaccine series
have a 41% chance of responding to a second 3-dose
series.
 Though antibody levels fall gradually over time, those
who have mounted an initial response following the 3-
dose regimen could achieve effective protection upon a
subsequent challenge, regardless of the titre of
antiHBs at the time of exposure.
 This is referred to as the anamnestic response.
 The efficacy of hepatitis B immunoglobulin (HBIG)
and HBV vaccine for postexposure protection in
occupational exposure can be referenced from
perinatal transmission.
 A single dose of HBIG lowers the infection rate of
infants born to HBsAg positive mothers from 92% to
54% at 1 year.
 With multiple doses, HBIG becomes 70-75% effective.
 The efficacy of protection is further increased to 85-
95% by adding a standard HBV vaccination regimen to
HBIG.
 The need for HBIG administration and HBV
vaccination depends on the exposure, and HBV status
of the source and the exposed.
 Individuals who lack HBsAg and have not previously
developed satisfactory immune response to the virus
may be susceptible.
 They could be offered HBIG for immediate protection
upon significant exposure to HBV.
 Individualised approach on risk assessment is
recommended for the management of a health care
worker with unknown response to hepatitis B
vaccination, one who has been exposed to an unknown
source or a source with unknown hepatitis status.
 In such circumstances, the HBV status of the source
and/or the exposed should be determined.
 The exposed person may be managed as in the case of
an injury involving an HBsAg positive source person if
the HBV status of the source cannot be ascertained.
Hepatitis C
 HCV is not transmitted as efficiently as HBV.
 The estimated risk of contracting hepatitis C through
needlestick injury involving HCV-infected blood is
1.8% (range 0-7%).
 In a meta-analysis, the risk of transmission was shown
to be greater if the source was HCV RNA positive.
Management of accidental
exposure to HCV
 One principle of HCV post-exposure management is to
identify those with acute HCV infection and refer them to
specialists for further evaluation.
 At baseline, HCV antibody should be tested for both the
source (with informed consent) and the exposed.
 Sera should also be stored for at least one year.
 For the exposed, testing should be repeated at 6 months,
and 12 months if the source is HIV-HCV co-infected.
 If the source person is known to be HCV infected or is
an injecting drug user with unknown HCV status,
baseline ALT should be considered in addition to HCV
Ab.
 Furthermore, HCV Ab, ALT and HCV-RNA should be
determined between 6 to 8 weeks in order to capture
those who develop acute hepatitis.
 Those who do should be promptly referred to
specialists for further evaluation.
 Currently, there is no effective vaccine or
chemoprophylactic agent for preventing HCV
infection after accidental occupational exposure.
 Therapy (interferon or pegylated interferon, with or
without ribavirin) may prevent chronic HCV infection
when administered to patients with acute hepatitis.
 The sustained virological response may be up to 94-
100% when treatment is started within 24 weeks of
symptom onset.
 26% of patients with acute HCV infection would have
spontaneous resolution without treatment.
 Patients who have acute hepatitis C should be
promptly evaluated by experts in this field.
Thank you

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management of hbv & hcv needle stick injury

  • 1.
  • 2.  Occupational exposure to blood-borne pathogens is a well recognised hazard to health care workers (HCW).  Adherence to standard infection control practices is the best way to prevent blood-borne infections in the health care setting.  However, accidental exposure still happens.
  • 3.
  • 4.
  • 5. First aid  Immediately following any exposure, the wound should be washed immediately and thoroughly with soap and water.  Antiseptics are not necessary as there is no evidence of their efficacy.  Wounds should not be sucked.  The exposed HCW should then seek medical advice for proper wound care and post-exposure management.
  • 6. Reporting  The institution should ensure that a mechanism is in place and made known to all HCW to facilitate reporting and management of sharps injury and mucosal exposure in the occupational setting.  Clear documentation and investigation of the circumstances of exposure are necessary.  A surveillance system of exposure events should be set up with a view to avoidance of similar incidents.
  • 7. Counselling  Until infection is ruled out, health care staff potentially exposed to HBV, HCV, or HIV infected blood should refrain from donating blood, plasma, organs, tissue or semen.  Safer sex with condom is advisable.
  • 8. Hepatitis B  The risk of contracting HBV infection through occupational exposure ranges from 18% to 30%, depending on the type of exposure, the body fluid involved and the infectivity of the source.  Percutaneous injuries with hollow-bored, blood-filled needles from a patient positive with HBeAg carry the highest risk of infection at 37-62%.
  • 9. Management of accidental exposure to HBV  All health care staff with potential risk of exposure to blood and body fluids are advised to receive hepatitis B vaccination as soon as possible for their own safety.  Subjects with anti-HBs titre ≥ 10 mIU/mL 1-4 months after vaccine completion are considered as responders.
  • 10.  Non-responders are those with no detectable antiHBs and hypo-responders refer to those whose anti-HBs titre are between 0-10 mIU/mL.  Both non- and hypo-responders should complete a second 3-dose vaccine series and retested at the completion of the second vaccine series.
  • 11.  Nonresponders to the initial 3-dose vaccine series have a 41% chance of responding to a second 3-dose series.  Though antibody levels fall gradually over time, those who have mounted an initial response following the 3- dose regimen could achieve effective protection upon a subsequent challenge, regardless of the titre of antiHBs at the time of exposure.  This is referred to as the anamnestic response.
  • 12.  The efficacy of hepatitis B immunoglobulin (HBIG) and HBV vaccine for postexposure protection in occupational exposure can be referenced from perinatal transmission.  A single dose of HBIG lowers the infection rate of infants born to HBsAg positive mothers from 92% to 54% at 1 year.  With multiple doses, HBIG becomes 70-75% effective.  The efficacy of protection is further increased to 85- 95% by adding a standard HBV vaccination regimen to HBIG.
  • 13.  The need for HBIG administration and HBV vaccination depends on the exposure, and HBV status of the source and the exposed.  Individuals who lack HBsAg and have not previously developed satisfactory immune response to the virus may be susceptible.  They could be offered HBIG for immediate protection upon significant exposure to HBV.
  • 14.  Individualised approach on risk assessment is recommended for the management of a health care worker with unknown response to hepatitis B vaccination, one who has been exposed to an unknown source or a source with unknown hepatitis status.  In such circumstances, the HBV status of the source and/or the exposed should be determined.  The exposed person may be managed as in the case of an injury involving an HBsAg positive source person if the HBV status of the source cannot be ascertained.
  • 15.
  • 16. Hepatitis C  HCV is not transmitted as efficiently as HBV.  The estimated risk of contracting hepatitis C through needlestick injury involving HCV-infected blood is 1.8% (range 0-7%).  In a meta-analysis, the risk of transmission was shown to be greater if the source was HCV RNA positive.
  • 17. Management of accidental exposure to HCV  One principle of HCV post-exposure management is to identify those with acute HCV infection and refer them to specialists for further evaluation.  At baseline, HCV antibody should be tested for both the source (with informed consent) and the exposed.  Sera should also be stored for at least one year.  For the exposed, testing should be repeated at 6 months, and 12 months if the source is HIV-HCV co-infected.
  • 18.  If the source person is known to be HCV infected or is an injecting drug user with unknown HCV status, baseline ALT should be considered in addition to HCV Ab.  Furthermore, HCV Ab, ALT and HCV-RNA should be determined between 6 to 8 weeks in order to capture those who develop acute hepatitis.  Those who do should be promptly referred to specialists for further evaluation.
  • 19.  Currently, there is no effective vaccine or chemoprophylactic agent for preventing HCV infection after accidental occupational exposure.  Therapy (interferon or pegylated interferon, with or without ribavirin) may prevent chronic HCV infection when administered to patients with acute hepatitis.
  • 20.  The sustained virological response may be up to 94- 100% when treatment is started within 24 weeks of symptom onset.  26% of patients with acute HCV infection would have spontaneous resolution without treatment.  Patients who have acute hepatitis C should be promptly evaluated by experts in this field.
  • 21.