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Transcript
Back to REPORTABLE DISEASES
REPORTABLE
DISEASES
TOOLKIT
Acute Flaccid Paralysis
(AFP)
Reporting Obligations
Confirmed and suspected cases shall be reported to
local Health Unit.
REPORTING FORM
Epidemiology
Aetiologic Agent:
AFP is a clinical syndrome, typically characterized by rapid
onset weakness, which may include respiratory and bulbar
weakness. AFP is a broad clinical syndrome with an array of
diagnostic possibilities, and may be the result of infectious
or non-infectious agents. Surveillance is conducted in
an attempt to identify cases of AFP and to investigate all
reported cases for evidence to rule out poliomyelitis (polio),
which is essential for maintaining Canada’s polio-free status.
AFP may be caused by a number of agents. The immunemediated condition Guillain-Barré Syndrome (GBS) is the
most common cause of AFP in Canada. The causes of AFP,
some of which lead to GBS, include, but are not limited to,
enteroviruses (including poliovirus), adenoviruses, acute
West Nile virus infection, Campylobacter spp., transverse
myelitis, peripheral neuropathy, acute non-bacterial
meningitis, brain abscess, China syndrome, post-polio
sequelae, tick paralysis, myasthenia gravis, porphyria and
botulism. Poliomyelitis must be distinguished from other
paralytic conditions by isolation of poliovirus from stool.
Clinical Presentation:
Acute onset of focal weakness or paralysis, characterized as
flaccid without other obvious cases (e.g., trauma).
The most characteristic feature of AFP associated with
paralytic polio is its asymmetric distribution (not affecting
both sides equally), which affects some muscle groups while
sparing others, with fever present at onset. The most typical
pattern is involvement of one leg only, or on arm, although
this occurs less often. It is less common for both legs or
both arms to be affected.
AFP due to Guillain-Barré Syndrome (GBS) may present as
symmetrical paralysis and may progress for up to 10 days.
Modes of transmission:
Depends on causative agent.
Incubation Period:
Depends on the causative agent.
Period of Communicability:
Varies, depending on causative agent.
References
1. Ministry of Health and Long Term Care, Infectious Diseases Protocol, 2015.
Information for
Health Care
Professionals
Risk Factors/Susceptibility
Depends on causative agent.
Diagnosis & Laboratory Testing
Clinically confirmed case: Acute onset of focal weakness or
paralysis characterized as flaccid (reduced tone) without other
obvious cause (e.g. trauma) in children <15 years old. Cases of
Guillain-Barré Syndrome (GBS) should be included as cases of
Acute Flaccid Paralysis (AFP). Transient weakness (e.g. post-ictal
weakness) should not be reported.
AFP is a syndrome which can be caused by a number of
pathogens. The following laboratory testing (of stool,
respiratory secretions, cerebrospinal fluid (CSF) and other
appropriate clinical specimens) is used to rule out poliomyelitis
and/or determine pathogens causing AFP:
• Stool samples - collection of two stool samples within
two weeks (up to six weeks) after the onset of paralysis
for viral studies and campylobacter
• Viral throat swab
yy Serology testing is not recommended for diagnosis of polio
or non-polio enterovirus infection
yy Depending on the clinical presentation, a nasopharyngeal
swab, and/or cerebrospinal fluid (CSF) may be collected to
assist with the investigation
yy Neurologic investigations, as appropriate, should take place
(electromyography, nerve conduction studies, MRI, CT)
Please see additional information (Quick Links) from Public
Health Ontario –“Summary of AFP and EV-D68 testing
surveillance & reporting and AFP/EV-D68 Case Report Forms”.
TESTING INFORMATION & REQUISITION
Treatment & Case Management
Treatment is under the direction of the attending health
care provider.
Routine Practices are recommended for hospitalized cases
and additional precautions would depend on the causative
organism.
Immediate case investigation and specimen collection is
essential by Public Health staff to rule out polio as a source
of infection, maintain Canada’s polio-free certification status,
and determine the source of infection.
Additional Resources
1. PHAC. “Poliomyelitis (Polio) Vaccine- Preventable Diseases,
December 4, 2013.”
2. Public Health Ontario. “Enterovirus D68 (includes AFP Testing and
Reporting).”
3. Heymann, D.L. Control of Communicable Disease Manual (19th Ed.).
Washington, American Public Health Association, 2008.
Leeds, Grenville & Lanark District Health Unit © 2013