PAINFUL GUIDELINES (BBV healthcare worker, BBV in dialysis, HAV) Flashcards
A healthcare worker with hep B is on antiviral therapy. How often should they have viral load checked?
Every 6 months
If they stop antivirals:
2 tests 6 months apart
( the first being no less than 6 months after ceasing
treatment)
Therefore if someone stops antivirals
or after a minimum of 12 months after stopping a course is when they could resume EPP (Is that correct?)
With regards to a BBV exposure what is a patient notification exercise?
When should it be performed?
A look back exercise discussed in UKAP guidance.
If a HCW is diagnosed with a BBV, need to do a risk assessment of risk of transmission (based on incubation periods, level of viraemia, EPP). Patients potentially exposed may then be contacted and offered testing
Done on a case by case assessment by UKAP, but you can voluntarily do one locally
(this is a change from earlier guidance when it used to be that large scale PNE were performed)
What is the name of the assessment tool for herpes B risk exposure and its key features?
5 key points
McGill protocol
-was there adequate first aid
-what sort of exposure (ie mucosal splash/break in skin integrety)
-how deep was the bite
-where was the bite (head and face higher risk than limbs)
-monkey has to be a macaque (a healthy one low estrisk)
Surgeon with HbSAg positive v/l 100
What do you do
Case by case which may result in no action
Recheck 10 days later
If it goes above 200 then would stop
Ensure UKAP-OHR registrered
All bloods under IVS
Monitor 6 monthly if DNA
If HBsAg postive how often to check viral loads
4 weeks apart for initital clearance, <200
Then 6 monthly
HCV exposed healthcare worker
6, 12, 24 weeks
PCR at each- Abs at 12 and 24
BBV assessment required pre dialysis
HBsAg anti-HBc anti-HBs
HCV IgG (if high risk recent consider HCV RNA)
HIV Ab / Ag combined
Frequency of monitoring of hep B immunity for dialysis patients
Ant- Hbs anually
Hep B surface antibody >100 mIU/ml, Hep surface Ag 6 monthly
If Hep B surface < 100mIU/ml: 3 monthly
If under 100 in last 6 months then give booster
Methods for reduction of BBV transmission in renal units
Vaccination
Regular testing
Segration of HBV positive-with HBV
Dialyisis away from base
Stratify high, intermed and low risk countried for dialysis away from base
Low risk countries:
UK, Europe, US, Canada, Australia, New Zealand and Japan
High risk countries:
Indian subcontinent, parts of Africa
Intermediate risk countries:
Rest of the world including South East Asia, South America, Middle East
Protocol for enhanced surveillance
Protocol for enhanced surveillance following a new case of BBV infection
HBV The exposed cohort should be tested for HBsAg and those who have not
demonstrated anti-HBs levels ≥ 100 mIU/ml in the preceding 12 months should
be re-tested every 2 weeks for at least 3 months after the last exposure to the index case.
For patients who have previously been immunised and shown to have responded,
a booster dose of vaccine should be considered.
In non-responders, or where status is unknown, HBIG and an accelerated course
of vaccine should be considered.
HCV The exposed cohort should be tested for HCV RNA by PCR at 2-weekly intervals
until 3 months after the last exposure to the index case, particularly if the index case
seroconverted whilst receiving dialysis on the unit (i.e. when (s)he would have had a
high viral load during the acute phase of infection).
HIV Undertake a risk analysis. If the index case seroconverted whilst receiving dialysis on
the unit (i.e. when (s)he would have had a high viral load during the acute phase of
infection) consider HIV RNA testing of the exposed cohort by PCR at 2-weekly
intervals until 3 months after the last exposure.
Procedure for individual returning after dialysis away from base in risk countries: 4 marks
Assess
Segregated dialysis
Test for BBV
Should have been vaccinated prior
Depending on the risk of BBV exposure we recommend the following level of surveillance:
Low risk
Continue with HCV Ab and HBsAg screening as per routine practice.
Segregation not required
Intermediate Risk
HCV Ab (or HCV RNA) every 2 weeks for 3 months
HBsAg every 2 weeks for 3 months
HIV Ag/Ab if indicated by risk assessment
High risk
HCV Ab (or HCV RNA) every 2 weeks for 3 months
HBsAg every 2 weeks for 3 months
HIV Ag/Ab if indicated by risk assessment
Our previous guidelines have suggested that enhanced surveillance for HBV is not required if immune with
HBsAb level >100 mIU/mL in the last 12 months. However, antibody titres can fall over time, leading some
patients to become unprotected. In view of this and in an attempt to reduce the level of complexity in the
guidelines, which can lead to errors if misinterpreted, we have recommended same level of surveillance
irrespective of HBsAb levels.
Regarding segregation:
Medium risk: If initial screening is negative,
machine and patient
segregation not required
High risk: segregate for 3 months
For dialysis: Defintion of a non-responder to vaccine- <100 (?units), 8 weeks following primary vaccinations
And strategy to overcome this
If between 10-100: give booster
If <10 repeat whole course
Exposed to HBV on dialysis unit, HB surface antibody level of 70. What do you do?
Give dose of vaccine only
(if Hbs antibody within 6 months of exposure is between 10-100 vaccinate, if less than 10 and exposure is within last 7 days give HBig)
Dose if HBIG for adults (people over 10 years of age)