CDC recommends baseline assessment of antibodies within
48 hours of exposure, reflexed when positive to nucleic acid testing for HCV RNA
with up to 6 months’ interval testing depending on results and source patient’s
status.
The Centers for Disease Control and Prevention (CDC) in an
update to its algorithm for testing healthcare workers potentially exposed to
hepatitis C virus (HCV) is now recommending an antibodies test 4 to 6 months
following exposure. This is based on the agency’s current understanding of early
HCV infection viral dynamics. CDC is also calling for preferential HCV RNA tests
in source patients to respond to the increasing incidence of acute HCV infection
among injectable drug users.
The new report reflects updated guidance from
the American Association for the Study of Liver Diseases and the Infectious
Diseases Society of America that recommends treatment of acute HCV
infection.
Workers treating patients can get exposed through blood, bodily
fluids, or sharps injuries. “Although sharps injury prevention measures have led
to overall exposure decreases in recent decades, blood and body fluid exposures,
including sharps injuries, continue to occur,” wrote the authors of the
guidance, who published their recommendations in CDC’s Morbidity and Mortality
Weekly Report.
CDC developed this guidance in conjunction with occupational
health and viral hepatitis epidemiology experts.
Guideline authors recommend
two pathways for testing source patients: a nucleic acid test or NAT, or an
antibody test (anti-HCV), following up with an HCV RNA if positive. NAT is the
preferred route, especially when the source patient has engaged in high-risk
behaviors such as injecting drugs.
The guideline recommends the following
protocol for testing workers:
Baseline testing for anti-HCV followed by
reflex to a NAT for HCV RNA within 48 hours after the exposure. Testing may take
place simultaneously with source-patient testing.
If the source patient’s
status calls for follow-up testing (an HCV RNA positive or anti-HCV positive
result with unavailable HCV RNA or if the infection status is unknown), workers
should receive a NAT for HCV RNA at 3–6 weeks post-exposure.
If HCV RNA is
negative at 3–6 weeks post-exposure, a final test for anti-HCV at 4–6 months
post-exposure should take place.
In the event a worker is exposed to blood or
body fluids from a source patient who tests HCV RNA negative but positive for
HCV antibody, follow up testing isn’t necessary, except in cases where specimen
mishandling compromises test results or if the worker starts showing signs of
infection.
Patients or workers with positive HCV RNA results should be
referred to further care and evaluation for treatment. Workers who remain
anti-HCV negative after 4–6 months don’t require further follow-up, although an
additional test for HCV RNA might be considered for individuals with
immunocompromised systems or liver disease.
The guideline authors also
recommended against HCV post-exposure prophylaxis (PEP) with direct-acting
antiviral (DAA) therapy. Their rationale: HCV transmission risk from
percutaneous and mucocutaneous exposures is very low. In most cases, it makes no
sense to give DAA to exposed healthcare workers due to potential side effects.
“Furthermore, efficient duration of PEP has not been established,” the authors
added.