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Japanese
Encephalitis
 Devlop Shrestha
Prepared By:
• Japanese encephalitis is a mosquito borne encephalitis
caused by group B arbovirus
• Zoonotic disease
• Transmitted by the bite of infected Culex mosquitoes
• No man to man transmission of disease
• No man to mosquito spread of disease
Introduction
Host
Environment
Agent
Time
Epidemiological Determinants
• Group B Arbo virus (Japanese Encephalitis virus) is
causative agent
• Comes under genus: Flavi virus
• ssRNA & enveloped virus
• Based on the envelope gene, 5 genotype have been
discovered (I-V)
• Transmitted by Culex mosquitoes.
Agent
Agent
Host
EnvironmentAgent
Time
Epidemiological Determinants
Natural host
 Pig
Wading birds
 Accidental host
Human (dead end host)
Age : Children less than 15 years
Host
Host
EnvironmentAgent
Time
Epidemiological Determinants
• Viral transmission is high in
i. Rural agricultural area (flooding irrigation is
practised)
ii. Rainy season
Environment
Because the vector mosquito
 Breeds in irrigated rice fields, shallow ditches
and pools.
 Are common in rainy season
• Vector = culex
mosquitoes (Culex
tritaeniorhyncus ,
Culex vishnui)
Natural cycle & transmission of the
disease
• The vector is responsible
for
 Pig – Mosquito- Pig
cycle
 Birds- Mosquito – Bird
cycle.
• After 9-12 days of viral
entry in mosquito , they
can transmit virus to
other hosts.
Natural cycle & transmission of the
disease
Virus enters the body through the bite of mosquitoes
After multiplication in local and regional lymph nodes,
viremia of varying duration occurs
Virus is transported to target organ (brain) via blood
Virus proliferate and damages the neuronal tissues , thereby
elicits nervous manifestation
Pathogenesis
• Incubation period : 5 - 15 days
• Course of disease in man is divided into 3 stages
i. Prodromal stage
ii. Acute encephalitic stage
iii. Late stage and sequelae
Clinical features
i. Prodromal stage
• Lasts for 1-6 days
• Fever
• Headache
• Gastrointestinal disturbances
• Lethargy
• Malaise
i. Prodromal stage
• Fever (38 to 40.7 degree Celsius)
• Nuchal rigidity
• Convulsion
• Difficulty in speech
• Dystonia
• Ocular palsies
• Paralysis
• Tremor
• Altered sensorium progressing to Coma
ii. Acute Encephalitic Stage
• Begins when active inflammation is at an end
• Neurological sign become stationary or tend to
improve
• Convalescence may be prolonged
• Commonly patients have residual neurological
deficit.
iii. Late stage and sequelae
Common symptoms
of
Japanese Encephalitis
Common symptoms
of
Japanese Encephalitis
Other symptoms include disorientation, coma,
seizures, spastic paralysis and ultimately death.
Of those who survive, 20%–30% suffer from
permanent intellectual, behavioural or
neurological problems such as paralysis,
recurrent seizures or the inability to speak.
• Most important viral encephalitis in Asia, especially in rural and
suburban areas where rice culture and pig farming coexist.
• Has also occurred rarely and sporadically in northern Australia
and parts of the Western Pacific.
• In the late 1980s, Burke and Leake estimated that 50 000 new
cases of JE occurred annually among the 2.4 billion people
living in the 16 Asian countries considered endemic at that time
(approximate overall annual incidence: 2 per 100 000).
• Incidence group:
Total population (endemic + non-endemic areas)
Aged 0–14 years is 1000.9 million
Aged ≥ 15 years, 2692.7 million
Global scenario
Global scenario
Reported AES and laboratory confirmed JE
cases by districts FY 2073/2074
National immunization coverage FY 2073/2074
Above table shows antigens wise coverage at national level during FY 2073/74.
Figure shows the three years (2015, 2016 and 2017) trends of immunization
coverage.
Clinical Diagnosis
o Clinical Suspect
– Febrile illness of variable severity associated with
neurological symptoms
o Probable Case
– Suspected case in close geographical and temporal
relationship to a laboratory confirmed case of AES / JE in
an outbreak
o Confirmed Case
– Suspect case with confirmed laboratory result.
– Virus isolation from brain tissues , increased titre of IgM
antibody in serum and CSF etc.
• No specific antiviral medicine available for JE
• Clinical management is supportive
• Fluid and electrolyte balance is must during
the acute phase of the disease
• Seizures management is necessary
• Airway management is crucial
Treatment of Japanese Encephalitis
• 3 types of vaccines are available against JE
Mouse brain derived killed vaccines
Cell culture derived killed vaccine
Cell cultured derived live attenuated vaccine
Prevention of JE
 Nakayama or Beijing strains are used
 Widely used vaccine in the past
 0.5 ml < 3yr and 1 ml>3 yrs subcutaneously
 2 primary dose 4 weeks apart, booster dose after 1
year and subsequently 3 yearly interval until 10-15
years
 Has severe adverse effect
 Banned from 2007 in India
Mouse Brain derived killed Vaccine
 Also called as SA 14-14-2 vaccine
 Widely used nowadays
 equally good childhood protection is obtained by a
single primary dose followed by a single booster dose
after 1 year
 Safer upto 15 years of age
 0.5 ml subcutaneously
 Not recommended for adult
 Highly effective for use during mass campaign.
Live attenuated Vaccines
• Control measures involves 2 strategies
Control of Reservoir
Control of Vector
Control measures for JE
• Pigs acts as amplifying host so pig rearing
should be discouraged in areas where rice
cultivation is wide spread.
• Inactivated vaccines or modified live vaccines
can be used for vaccinating Swine.
Control of Reservoir
Insecticide spraying should be done in breeding
places such as paddy fields.
Eco-management of paddy fields can be done.
Ultra low volume insecticide spraying by fogging has
been found helpful to some extent
Sterile male technique is a novel approach.
Control of Vector
• Park's Textbook of Preventive & Social Medicine, K. Park
24th edition
Chapter IV
Page no. 302, 303 & 304
• WHO website : https://who.int
• Annual health report 2073/2074
Chapter 2
Page no. 10, 11, 21 & 22
References
Japanese encephalitis_6th batch_NAIHS_Devlop Shrestha

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Japanese encephalitis_6th batch_NAIHS_Devlop Shrestha

  • 2. • Japanese encephalitis is a mosquito borne encephalitis caused by group B arbovirus • Zoonotic disease • Transmitted by the bite of infected Culex mosquitoes • No man to man transmission of disease • No man to mosquito spread of disease Introduction
  • 3.
  • 5. • Group B Arbo virus (Japanese Encephalitis virus) is causative agent • Comes under genus: Flavi virus • ssRNA & enveloped virus • Based on the envelope gene, 5 genotype have been discovered (I-V) • Transmitted by Culex mosquitoes. Agent
  • 8. Natural host  Pig Wading birds  Accidental host Human (dead end host) Age : Children less than 15 years Host
  • 10. • Viral transmission is high in i. Rural agricultural area (flooding irrigation is practised) ii. Rainy season Environment Because the vector mosquito  Breeds in irrigated rice fields, shallow ditches and pools.  Are common in rainy season
  • 11. • Vector = culex mosquitoes (Culex tritaeniorhyncus , Culex vishnui) Natural cycle & transmission of the disease
  • 12. • The vector is responsible for  Pig – Mosquito- Pig cycle  Birds- Mosquito – Bird cycle. • After 9-12 days of viral entry in mosquito , they can transmit virus to other hosts. Natural cycle & transmission of the disease
  • 13. Virus enters the body through the bite of mosquitoes After multiplication in local and regional lymph nodes, viremia of varying duration occurs Virus is transported to target organ (brain) via blood Virus proliferate and damages the neuronal tissues , thereby elicits nervous manifestation Pathogenesis
  • 14. • Incubation period : 5 - 15 days • Course of disease in man is divided into 3 stages i. Prodromal stage ii. Acute encephalitic stage iii. Late stage and sequelae Clinical features
  • 15. i. Prodromal stage • Lasts for 1-6 days • Fever • Headache • Gastrointestinal disturbances • Lethargy • Malaise i. Prodromal stage
  • 16. • Fever (38 to 40.7 degree Celsius) • Nuchal rigidity • Convulsion • Difficulty in speech • Dystonia • Ocular palsies • Paralysis • Tremor • Altered sensorium progressing to Coma ii. Acute Encephalitic Stage
  • 17. • Begins when active inflammation is at an end • Neurological sign become stationary or tend to improve • Convalescence may be prolonged • Commonly patients have residual neurological deficit. iii. Late stage and sequelae
  • 19. Common symptoms of Japanese Encephalitis Other symptoms include disorientation, coma, seizures, spastic paralysis and ultimately death. Of those who survive, 20%–30% suffer from permanent intellectual, behavioural or neurological problems such as paralysis, recurrent seizures or the inability to speak.
  • 20. • Most important viral encephalitis in Asia, especially in rural and suburban areas where rice culture and pig farming coexist. • Has also occurred rarely and sporadically in northern Australia and parts of the Western Pacific. • In the late 1980s, Burke and Leake estimated that 50 000 new cases of JE occurred annually among the 2.4 billion people living in the 16 Asian countries considered endemic at that time (approximate overall annual incidence: 2 per 100 000). • Incidence group: Total population (endemic + non-endemic areas) Aged 0–14 years is 1000.9 million Aged ≥ 15 years, 2692.7 million Global scenario
  • 22. Reported AES and laboratory confirmed JE cases by districts FY 2073/2074
  • 23. National immunization coverage FY 2073/2074 Above table shows antigens wise coverage at national level during FY 2073/74.
  • 24. Figure shows the three years (2015, 2016 and 2017) trends of immunization coverage.
  • 25. Clinical Diagnosis o Clinical Suspect – Febrile illness of variable severity associated with neurological symptoms o Probable Case – Suspected case in close geographical and temporal relationship to a laboratory confirmed case of AES / JE in an outbreak o Confirmed Case – Suspect case with confirmed laboratory result. – Virus isolation from brain tissues , increased titre of IgM antibody in serum and CSF etc.
  • 26. • No specific antiviral medicine available for JE • Clinical management is supportive • Fluid and electrolyte balance is must during the acute phase of the disease • Seizures management is necessary • Airway management is crucial Treatment of Japanese Encephalitis
  • 27. • 3 types of vaccines are available against JE Mouse brain derived killed vaccines Cell culture derived killed vaccine Cell cultured derived live attenuated vaccine Prevention of JE
  • 28.  Nakayama or Beijing strains are used  Widely used vaccine in the past  0.5 ml < 3yr and 1 ml>3 yrs subcutaneously  2 primary dose 4 weeks apart, booster dose after 1 year and subsequently 3 yearly interval until 10-15 years  Has severe adverse effect  Banned from 2007 in India Mouse Brain derived killed Vaccine
  • 29.  Also called as SA 14-14-2 vaccine  Widely used nowadays  equally good childhood protection is obtained by a single primary dose followed by a single booster dose after 1 year  Safer upto 15 years of age  0.5 ml subcutaneously  Not recommended for adult  Highly effective for use during mass campaign. Live attenuated Vaccines
  • 30.
  • 31.
  • 32. • Control measures involves 2 strategies Control of Reservoir Control of Vector Control measures for JE
  • 33.
  • 34. • Pigs acts as amplifying host so pig rearing should be discouraged in areas where rice cultivation is wide spread. • Inactivated vaccines or modified live vaccines can be used for vaccinating Swine. Control of Reservoir
  • 35. Insecticide spraying should be done in breeding places such as paddy fields. Eco-management of paddy fields can be done. Ultra low volume insecticide spraying by fogging has been found helpful to some extent Sterile male technique is a novel approach. Control of Vector
  • 36. • Park's Textbook of Preventive & Social Medicine, K. Park 24th edition Chapter IV Page no. 302, 303 & 304 • WHO website : https://who.int • Annual health report 2073/2074 Chapter 2 Page no. 10, 11, 21 & 22 References