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18.10   Post-exposure prophylaxis

18.10.1            Specific hepatitis B immunoglobulin (HBIG) is available for passive protection and is normally used in combination with hepatitis B vaccine to confer passive/active immunity after exposure.  Guidance is given in ‘Exposure to hepatitis B virus; guidance on post exposure prophylaxis’.  PHLS Hepatitis Subcommittee.  CDR Review 1992:2;R97-R101.  A summary of this guidance is given in the following table.

18.10.2            Whenever immediate protection is required, immunisation with the vaccine should be combined with simultaneous administration of hepatitis B immunoglobulin (HBIG) at a different site.  It has been shown that passive immunisation with HBIG does not suppress an active immune response.  A single dose of HBIG (usually 500iu for adults; 200iu for the newborn) is sufficient for healthy individuals.  If infection has already occurred at the time of immunisation, virus multiplication may not be inhibited completely, but severe illness and, most importantly, the development of the carrier state may be prevented.

18.10.3   Immunoglobulin should be administered as soon as possible after exposure.  In babies born to hepatitis B carrier mothers it should be given not later than 48 hours after birth (but see 18.11.1) and in other types of exposure it should preferably be given with 48 hours and certainly no later than a week after exposure.

18.10.4   There is no evidence associating the administration of HBIG with acquisition of HIV infection.  Not only does the processing of the plasma from which it is prepared render it safe, but the screening of blood donations is now routine practice.

18.11     Groups requiring post-exposure prophylaxis

18.11.1   Babies born to mothers who are HBeAg positive carriers, who are HBsAg positive without e markers (or where e marker status has not been determined), or who have had acute hepatitis during pregnancy.

Active/passive immunisation is recommended (see 18.4.4).  All babies of HBsAg positive mothers are e-antigen positive, HBsAg positive without e markers (or where e-marker status has not been determined) or had acute hepatitis during pregnancy will require HBIG.  The first dose of vaccine should be given at birth or as soon as possible thereafter.  HBIG should be given at a contralateral site at the same time; arrangements for the supply of HBIG should be made well in advance.  If administration of HBIG is delayed for more than 48 hours, advice should be sought from a local Consultant in Communicable Disease Control, CPHM (CD & EH), a Consultant in Medical Microbiology/Consultant Virologist or from the PHLS Communicable Disease Surveillance Centre or SCIEH.

18.11.2   Persons who are accidentally inoculated, or who contaminate the eye or mouth or fresh cuts or abrasions of the skin, with blood from a known HBsAg positive person.  Individuals who sustain such accidents should wash the affected area well with soap and warm water and seek medical advice.  Advice about prophylaxis after such accidents should be obtained by telephone from the nearest Public Health Laboratory or from the CPHM on call for the local Health Board in Scotland.  Advice following accidental exposure may also be obtained from the Hospital Control of Infection Officer or the Occupational Health Services.

Health care workers who have already been successfully immunised should be given a booster dose of vaccine unless they are known to have adequate protective levels of antibody.

18.11.3  Sexual partners (and in some circumstances a family contact judged to be at high risk) of individuals suffering from acute hepatitis B, and who are seen within one week of onset of jaundice in the contact.

HBV Prophylaxis for reported exposure incidents

 

HIV status of person exposed

Significant Exposure

Non–Significant Exposure

HbsAg postive source

Unknown source

HbsAg negative source

Continued risk

No further risk

£ 1 dose HB vaccine
pre-exposure

Accelerated course
of HB vaccine*
HBIG x 1

Accelerated course of HB vaccine*

Initiate course of HB vaccine

Initiate course
of HB vaccine

No HBV
prophylaxis Reassure

³   2 doses HB vaccine pre-exposure(anti-HBs not known)

One dose of HB vaccine followed by second dose one month later

One dose of HB vaccine

Finish course of HB vaccine

Finish course
of HB vaccine

No HBV prophylaxis. Reassure

Known responder to HB vaccine (anti-HB’s > 10miU/ml )

Consider booster dose of HB vaccine

Consider booster dose of HB vaccine

Consider booster dose of HB vaccine

Consider booster dose of HB vaccine

No HBV prophylaxis. Reassure

Known non-responder to HB vaccine (anti-HB’s < 10miU/ml 2-4 months post immunisation)

HBIG x 1
Consider booster dose of HB vaccine

HBIG x 1
Consider booster dose of HB vaccine

No HBIG
Consider booster dose of HB vaccine

No HBIG Consider booster dose of HB vaccine

No prophylaxis. Reassure

 

* An accelerated course of vaccines consists of doses spaced at 0, 1 and 2 months.

A booster dose may be given at 12 months to those at continuing risk of exposure to HBV.

Source: PHLS Hepatitis Subcommittee. CDR Review 1992:2;R97-R101. (Further Details and explanation of definitions are contained in this article.)

 

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Authored by A G M Campbell. Chairman, Joint Committee on Vaccination and Immunisation.
© Crown copyright 1996