Poliomyelitis Disease Investigation Guideline
Poliomyelitis Disease Investigation Guideline
Poliomyelitis Disease Investigation Guideline
Investigation Guideline
CONTENT:
VERSION DATE:
Investigation Protocol:
Investigation Guideline
02/2012
03/2009
03/2009
Revision History:
Date
Replaced
Comments
02/2012
03/2009
Released 03/2009
Version 02/2012
Poliovirus Infection
Disease Management and Investigative Guidelines
CASE DEFINITION Poliomyelitis, Paralytic (CDC 2010)
Case Classification:
Confirmed: Acute onset of a flaccid paralysis of one or more limbs with
decreased or absent tendon reflexes in the affected limbs, without other
apparent cause, and without sensory or cognitive loss; AND in which the
patient:
has a neurologic deficit 60 days after onset of initial symptoms; or
has died; or
has unknown follow-up status.
Probable: Acute onset of a flaccid paralysis of one or more limbs with
decreased or absent tendon reflexes in the affected limbs, without other
apparent cause, and without sensory or cognitive loss
Comment: All suspected cases of paralytic poliomyelitis are reviewed by a panel of
expert consultants before final classification occurs. Confirmed cases are then further
classified based on epidemiologic and laboratory criteria. 1
LABORATORY ANALYSIS
Isolation of wild poliovirus constitutes a public health EMERGENCY.
To determine whether virus is wild type- or vaccine-associated polio may
require that isolates or specimens be sent to the KDHEL
Specimens for culture that may yield poliovirus:
Stool: likelihood is highest, contributes to diagnostic evaluation but does
not constitute proof of causal association
Pharyngeal swabs: intermediate probability of isolation
Blood or spinal fluid: very low probability of isolation but is diagnostic
Serological testing (Complement Fixation (CF) or Neutralization (N)):
Helpful in supporting or ruling out the diagnosis of paralytic polio
May be falsely negative in immunocompromised persons
Neutralizing antibodies appear early and may be at high levels by the time
the patient is hospitalized so a fourfold titer cannot be demonstrated
Vaccinated persons would also have measurable titers
Serology cannot differentiate between wild and vaccine-related polio virus.
Sutter RW, Brink EW, Cochi SL, et al. A new epidemiologic and laboratory classification system for
paralytic poliomyelitis cases. Am J Public Health 1989;79:495-8.
Kansas Disease Investigation Guidelines
Version 02/2012
Poliovirus Infection, Page 2
EPIDEMIOLOGY
Since the introduction of the of polio vaccine, most of the worlds population is
considered polio-free. In the United States, cases of paralytic poliomyelitis are
extremely rare. In1980-94, an average of 8 cases of paralytic polio were
reported annually; all of which were related to vaccine-associated paralytic
poliomyelitis (VAPP). To reduce the risk of VAPP, a new polio vaccination
schedule (i.e., inactivated polio vaccine (IPV) for doses 1 and 2, oral polio
vaccine (OPV) for doses 3 and 4) was recommended in 1997 and then an allIPV immunization schedule was initiated in 2000. Risk factors for paralytic
poliomyelitis include larger inocula of poliovirus, increasing age, pregnancy,
strenuous exercise, tonsillectomy, and intramuscular injections administered
while the patient is infected with poliovirus. Today in the U.S., polio can occur
when under-immunized travelers and immigrants import the virus from areas of
the world where it is still prevalent (i.e., Sub-Saharan Africa and southern Asia).
Worldwide, the number of polio cases has fallen from an estimated 350,000 in
1988 to fewer than 1300 in 2010a decline of more than 99% in reported
cases. Three regions of the world are certified polio freethe Americas,
Europe, and the Western Pacific. Only four polio-endemic countries (countries
that have never interrupted the transmission of wild poliovirus) remain
Afghanistan, India, Nigeria, and Pakistan.
DISEASE OVERVIEW
A. Agent:
Polio is caused by poliovirus, with antigenic types 1, 2, and 3. Type 1 is most
often the agent in paralytic illnesses. Type 2 is most often associated with
vaccine-associated cases.
B. Clinical Description:
Poliomyelitis is an acute illness ranging in severity from inapparent infection to
paralytic disease. The fatality rate ranges between 2-10%. Symptoms include
fever, headache, nausea and vomiting, stiffness in neck and back, with or
without paralysis. Paralysis is typically flaccid, asymmetric and most commonly
affects the lower extremities. Any recovery from paralysis usually begins within
1 month. Between 25 - 40% of persons who contracted paralytic poliomyelitis
in childhood may develop post-polio syndrome 30 - 40 years later. This
syndrome is characterized by muscle pain, exacerbation of existing weakness,
and/or development of new paralysis or weakness. In children, 90% of all
infections are asymptomatic.
Vaccine-associated poliomyelitis can occur in a recipient 7 to 21 days after oral
polio vaccine administration or in susceptible contacts of the vaccine recipient
20 to 29 days after vaccine administration. Adults have a slightly increased risk
of vaccine-associated paralytic poliomyelitis.
C. Reservoirs:
Humans.
D. Mode(s) of Transmission:
Transmission is primarily through the fecal-oral route. However, the virus can
be transmitted by indirect contact with infectious saliva or feces, or by
contaminated sewage or water.
E. Incubation Period:
Range 3-35 days; usually 7-14 days for paralytic poliomyelitis.
F. Period of Communicability:
Infectivity is greatest 7-10 days before and after onset of symptoms. In
symptomatic and asymptomatic cases, poliovirus is found in pharyngeal
secretions 36 hours and in the feces 72 hours after exposure. Poliovirus can
remain present in the stool from 3 to 6 weeks.
G. Susceptibility and Resistance:
Persons who are immunodeficient are at increased risk for acquiring polio.
Lifelong, type specific immunity follows natural infection.
H. Treatment: Supportive only.
I. Vaccines:
IPV, a killed polio vaccine, is administered via injection and is used as part
of the routine all-IPV immunization schedule in the U.S.
OPV, a live polio vaccine, is used in many parts of the world. When the risk
of wild-type polio transmission is greater than the risk of possible VAPP, it is
the vaccine of choice for polio outbreak control.
Kansas Disease Investigation Guidelines
Version 02/2012
INVESTIGATOR RESPONSIBILITIES
1)
2)
3)
4)
Use current case definition, to confirm diagnosis with the medical provider.
Conduct a case investigation to identify potential source of infection.
Conduct contact investigation to identify additional cases.
Identify whether the source of infection is major public health concern.
Possibility of wild poliovirus or vaccine-related cause
Under-immunized population within the community.
Distinguish between failure to vaccinate and vaccine failure.
5) Initiate control and prevention measures to prevent spread of disease.
6) Complete and report information requested in the Kansas electronic
surveillance system.
7) As appropriate, use the disease fact sheet to educate individuals or groups
and the notification letter to alert physicians and emergency rooms.
Environmental
None.
Education
1) Persons in communities with low vaccination coverage should be warned of the
potential risk for poliomyelitis and informed of vaccine availability.
2) If a situation calls for the use of OPV, those exposed to the vaccine or to the
recipient should be made aware of the risks of VAPP.
Supporting Materials