This document provides an overview of poliomyelitis (polio), including its introduction, epidemiology, clinical manifestations, diagnosis, treatment and prevention. Some key points: - Polio is a viral infection that can cause paralysis. It was first described in 1799 and primarily infects the gastrointestinal tract. - Through vaccination efforts starting in the 1950s, polio has been eliminated in most developed countries. Global eradication efforts have reduced endemic countries from 125 to 3 between 1988-2012. - Polio spreads through the fecal-oral route or oral secretions. There is no animal reservoir - humans are the only known carrier. Vaccines including both inactivated (Salk) and

1. Poliomyelitis

2. Introduction
 Greek poliós= "grey", myelós= marrow, and the suffix -
itis= inflammation
 First described by British physician Micheal Underwood in 1799
referring to it as "debility of the lower extremities.“
 A viral infection most often recognized by acute onset of flaccid
paralysis.
 Primarily an infection of human alimentary tract, but may infect
CNS in very small no. (i.e <1%)
 Infection results in a spectrum of clinical manifestations……

3. Problem statement
World
 A worldwide problem in pre vaccination era
 With the wide use of polio vaccine from 1954 disease
being eliminated from most of the developed countries
 In 1988 WHA resolved to eradicate the disease globally
 Since than no. of endemic countries reduced from 125 in
1988 to 3 in 2012.
 Reported cases worldwide decreased by 51% (1352 in
2010 to 650 in 2011)

4. Cont…
India
No reported cases since January 2011 (last
case reported in 13th Jan 2011, Howrah,
West Bengal)
Considered polio-free since February 2012
Attained the status of eradication in 13th
January 2014

5. Epidemiology

6. Agent factors
Agent
Poliovirus: belongs to “Picorna” viruses which are
small RNA-containing viruses.
Three serotypes- 1, 2 & 3 giving no cross
immunity
Long survival in environment….lives upto 4hours
in water and 6 hours in faeces in cold
enviornment.
Readily destroyed by heat (e.g. pasteurization of
milk, and chlorination of water).

7. Reservoir of infection
 Man is the only reservoir of infection of poliomyelitis.
 Man: cases and carriers
 Cases: all clinical forms of disease
 Most of the infections are subclinical- dominant role in spread of
infection
 Estimated subclinical infection ranges from 75 to 1000 per clinical case
 No chronic cases or animal sources documented
Foci of infection
 Pharynx: the virus is found in the oropharyngeal secretions.
 Small intestine: the virus finds exit in stools.

8. Modes of transmission
Since foci of infection are the throat and small intestines,
poliomyelitis spreads by two routes:
Oral-oral infection: direct droplet infection
Faeco-oral infection:
– Through contaminated foods. Vehicles include milk, water, or any
others that may be contaminated by handling, flies, dust….
– Hand to mouth infection.
Polio virus has the ability to survive in cold environments.
Overcrowding and poor sanitation provide opportunities for
exposure to infection

9. Period of communicability
 Estimated to about 2 weeks
 Cases: 7 to 10 days before and after the onset of symptoms.
 Virus is excreted commonly for 2 to 3 weeks, sometimes as
long as 3 to 4 months in faeces.
 In polio cases, infectivity in the pharyngeal foci is around one
week, and in the intestinal foci 6-8 weeks.
Incubation Period: 7-14 days

10. Host factors
Age:
 All age groups; children(6 MONTHS TO 3 YEARS most susceptible)
 more than 95% reported in infancy and childhood with over 50% of them
in infancy.
Sex:
 no sex ratio differences, but in some countries, males are infected more
frequently than females in a ratio 3:1.
Risk factors:
 Fatigue, trauma,im injections, tonsillectomy, immunizing agents like alum
containing DPT vaccine and excessive muscular exercise…
Immunity:
 Immunity by maternal antibodies till the age of 6months
 Immunity conferred by natural infection fairly solid but doesn’t protects
against the reinfection by other strains

11. Environmental factors
Rainy season (june to september)
Environmental sources- food, flies and water
Overcrowding and poor sanitation-
oppourtinities

12. Clinical spectrum

13. Inapparent infection
 Occurs approximately in 91-96% of poliovirus infection.
 Incidence is more than 75 to 1000 times the clinical
cases.
 No clinical manifestations, but infection is associated
with acquired immunity.
 Recognition only by virus isolation or rising antibody titre.

14. Clinical poliomyelitis
Abortive polio (minor illness):
 Occurs approximately in 4-8% of the infection.
 Causes only a mild or self limiting illness due to
viraemia.
 Mild systemic manifestations for 1-2 days
 Some abortive cases so mild to pass unnoticed.
 Patient recovers quickly.
 Manifestations:
 Moderate fever
 Upper respiratory manifestations: pharyngitis and sore throat
 Gastrointestinal manifestations: vomiting, abdominal pain,
and diarrhea.

15. Cont…..
Involvement of the CNS (major illness):
 Affects a small proportion of the clinical cases
 Takes two forms: Non-paralytic and Paralytic polio.
Non paralytic polio:
 Occurs approximately in one per cent of all infections.
 Presenting features are stiffness and pain in neck and back.
 Disease lasts for 2-10 days.
 Recovery is rapid.

16. Cont…
Paralytic polio:
 Occurs in less then one per cent of infections.
 The virus enters the CNS and causes varying degree of disability
with destruction of the motor nerve cells, but not the sensory
nerve cells.
 Forms: spinal, bulbar, and bulbospinal.
 Paralysis usually appears within 4 days (around 7-10 days from
onset of disease).
 History of fever at the time of paralysis- suggestive of polio.
 Progression of paralysis reaches maximum by 4th day (4-7 days)

17. Cont….
 Other symptoms- malaise, anorexia, vommiting, headache, sore
throat, constipation and headache.
 Signs of meningeal irritation
 Tripod sign may be present
 Assymetrical, patchy flaccid paralysis, of descending type
affecting the proximal group of muscle the most
 Deep tendon reflexes (DTR) deminished before the the onset of
paralysis.
 Cranial nerve involvement seen in bulbar and bulbospinal
paralytic poliomyelitis
 Facial assymetry, difficulty in swallowing weakness of voice;
respiratory insuffiency may lead to death

19. Spinal polio
Different spinal nerves are involved
Injury of the anterior horn cells of the spinal cord
causing tenderness, weakness, and flaccid
paralysis of the corresponding striated muscles.
The lower limbs are the most commonly affected.

20. Bulbar polio
Nuclei of the cranial nerves are involved, causing
weakness of the supplied muscles, and maybe
encephalitis.
Bulbar manifestations include dysphagia, nasal voice,
fluid regurgitation from the nose, difficult chewing, facial
weakness and diplopia
Paralysis of the muscles of respiration is the most
serious life-threatening manifestation.
Bulbospinal polio
 Combination of both spinal and bulbar forms

21. Polio infection
Polio infection
Inapparent infection Clinical poliomyelitis
Abortive polio
(minor illness)
Involvement of CNS
(major illness)
Paralytic
polio
Non-paralytic
polio
Spinal polio
Bulbar polio
Bulbospinal polio

22. Complications and case fatality
 Respiratory complications: pneumonia, pulmonary edema
 Cardiovascular complications: myocarditis, cor pulmonale.
 Late complications: soft tissue and bone deformities,
osteoporosis, and chronic distension of the colon.
 Case fatality: varies from 1% to 10% according to the form
of disease (higher in bulbar), complications and age (
fatality increases with age).

23. Diagnosis and laboratory testing
Laboratory studies critical to rule out or confirm the
diagnosis of paralytic poliomyelitis.
 Virus isolation
 The likelihood of poliovirus isolation is highest from stool
specimens,
 Intermediate from pharyngeal swabs, and very low from blood
or spinal fluid.
 Serologic testing
A four-fold titer rise between the acute and convalescent
specimens suggests poliovirus infection.

24. Prevention
General prevention:
Health promotion through environmental
sanitation.
Health education (modes of spread,
protective value of vaccination).

25. Cont….
Seroprophylaxis by immunoglobulins:
Not a practical way of giving protection
because it must be given either or before or
very shortly after exposure to infection.
Dose-(0.25-0.3 ml/kg of body weight).
Immunized status after a few weeks

26. Active immunization
Inactivated (Salk) vaccine
 Contains 3 serotypes of vaccine virus
 Route of administration-intramuscular/ Subcutaneous.
 Schedule
 First dose given at the age of 6 weeks
 Next 2 doses 1-2 months apart
 4th dose after 6-12 month of 3rd dose
 Additional doses prior to school entry
 Repeated doses every 5 year after that till age of 18
 Highly effective in producing immunity to poliovirus
 >90% immune after 2 doses
 >99% immune after 3 doses
 Duration of immunity not known with certainty

27. Cont…
Oral (Sabin) Polio Vaccine
 Contains 3 serotypes of vaccine virus
 Route of administration-intramuscular/ Subcutaneous.
 Schedule
 Zero dose vaccination recommended in hospital delivery
 First dose given at the age of 6 weeks
 Next 2 doses 1-2 months apart
 One booster dose 12-18 months later recommended
 Highly effective in producing immunity to poliovirus
 50% immune after 1 dose
 >95% immune after 3 doses
 Immunity probably lifelong
 Shed in stool for up to 6 weeks following vaccination

28. Salk versus Sabin vaccine
IPV (Salk) OPV (Sabin)
killed formolised virus
Given SC or IM
Induces circulating antibodies, but
not local (intestinal immunity)
Prevents paralysis but does not
prevent reinfection
Not useful in controlling epidemics
More difficult to manufacture and is
relatively costly
Does not require stringent conditions
during storage and transportation. Has
a longer shelf life.
live attenuated virus
given orally
immunity is both humoral and
intestinal. induces antibody quickly
Prevents paralysis and prevents
reinfection
Can be effectively used in controlling
epidemics.
Easy to manufacture and is cheaper
Requires to be stored and
transported at subzero temperatures,
and is damaged easily.

29. Epidemiological Investigations
Epidemic
 Occurrence of 2 or more local cases caused by the same virus in any
4-weeks period
 Sample of faeces to be collected from all the cases and suspected
cases and subjected to lab testing
 If possible, paired sera to be tested
– First specimen at the clinical suspicion
– Second at the period of convalescence
 An increase in antibody titre provides confirmatory evidence
 OPV should be provided to all persons over 6 weeks age who are not
completely immunize de or immune status unknown in the epidemic
area

30. Thank you