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NIPAH VIRUS
By:
Dr Harivansh Chopra
Dr Abhishek Agarwal
Introduction
• Nipah virus (NiV) infection is a newly
emerging zoonosis that causes severe
disease in both animals and humans
• It is named after the Malaysian Village
from where it was first discovered.
Introduction
• Nipah virus causes a range of
illnesses from asymptomatic
(subclinical) infection to acute
respiratory illness and fatal
encephalitis.
Introduction
• Nipah virus is closely related to Hendra
virus.
• Both are members of the
genus Henipavirus, a new class of virus
in the Paramyxoviridae family.
NIPAH Virus : A public Health Problem
• Though Nipah virus has caused
only a few outbreaks, it infects a
wide range of animals and causes
severe disease and death in
people, making it a public health
concern.
Distribution
nipahvirus-180525062654 (1).pdf
Problem
• 1st Case reported from Malaysia in 1998
• 1st Outbreak in south east asia was in Bangladesh in 2001
• 1st Outbreak in India was in Siliguri killing over 33 Health workers
• Recent Outbreak was in Kerela, killed upto 11 health workers
• Till now over 457 cases of Nipah Virus has been reported killing
more then 252 persons
Agent: Nipah Virus
Paramyxovirus
Highly pathogenic
Closely related to Hendra virus
Epidemiology
Incubation Period
4 – 18 days
Host
• Reservoir Host: Fruit Bats
• Amplifier Hosts: Pig and Horses
• Dead End Host: Humans
Epidemiology
nipahvirus-180525062654 (1).pdf
Epidemiology
ENVIRONMENT
• Cases are more in Winter and Spring (December–May).
– Breeding Season of bats
– Date palm sap harvesting season
Transmission cycle of Nipah Virus
Direct Transmission: Pig to Human
• Direct human contact with infected
pigs was identified as the
predominant mode of transmission
in humans when it was first
recognized in Malaysia. (outbreak
of Nipah virus, 1998-99)
Direct Transmission: Human to Human
• The evidence of human to human
transmission of Nipah Virus was first
reported from India.
• During the outbreak in Siliguri, 33 health
workers and hospital visitors became ill after
exposure to patients hospitalized with Nipah
Virus, suggesting nosocomial infection.
Body fluids responsible for human to human
transmission of Nipah Virus
Cerebrospinal Fluid
Respiratory Secretions
Saliva
Urine
Direct Transmission: Bat to
Human
• Direct transmission of Nipah
Virus from fruit bats to
humans has been reported
during Bangladesh
Outbreak.
Indirect Transmission: Fruit Bat
• The natural host of the virus are
fruit bats of the Pteropodidae
Family, Pteropus genus
• In India the sub species Pteropus
giganteus is the causative agent
Fluids from bats transmitting the disease
• Virus present in its excretions and secretions
– Urine
– Semen
– Saliva
– Excreta
Indirect Transmission: Date palm sap
• Drinking of date palm sap,
possibly contaminated by fruit
bats may have been responsible
for the transmission of Nipah
Virus to Humans.
Indirect Transmission: Date palm sap
• Fruit bats also consume date
palm sap and can contaminate it
with saliva, urine feces.
• This is the means by which
Nipah Virus is thought to have
been transmitted from infected
fruit bats to humans.
Case Definition : Suspected Nipah Case
High Grade Fever with :-
• acute onset of altered mental status, or
• Seizure, or
• Headache, or
• acute onset of cough with shortness of breath
Case Definition : Probable Nipah Case
• Suspect cases, and/or who
died before complete
diagnostic specimens could
be collected, including a
serum antibody test 14 days
after onset of illness
Death: 14
days of onset
of illness
Case Definition : Confirmed Nipah Case
i) IgM antibody
ii) RNA identified by RT-PCR
iii) isolation of Nipah Virus
Confirmed Nipah case: Suspected/probable case
having:
Clinical Features
• The classical form is an acute and
rapidly progressive encephalitis with or
without respiratory involvement in all
age groups.
Clinical Features
• The Nipah encephalitis presents with 3–14 days of
fever and headache, followed by drowsiness,
disorientation and mental confusion.
• The acute encephalitis progresses then to coma
within 24–48 hours, with high mortality rate.
Clinical Features
• The respiratory involvement consists of non-productive
cough during the early part of the disease, which can
evolve later to severe acute lower respiratory disease,
i.e., from breathing difficulties to acute respiratory
distress syndrome (ARDS)
Clinical Features
• Post-encephalitis sequelae have been commonly
observed in NiV infection.
• One third of Nipah survivors in Bangladesh have
moderate to severe objective neurological dysfunction
7–30 months after infection
Lab Diagnosis
Serology
PCR
ELISA
Virus Isolation
Neutralization test
Treatment : Supportive
• Fluid maintenance and electrolyte balance.
• Nutrition
• Anticonvulsant
• Oropharyngeal suction in closed circuit.
Treatment : Supportive
• Oxygen inhalation using disposable cannula.
• Bronchodilators through large spacer
devices.
• Severely ill individuals may require Intensive
Care Unit (ICU) support
Treatment: Drug
• Ribavirin:
• Monoclonal Antibodies (Post exposure therapy)
Prevention
• hand hygiene
• injection safety
• facial protection
• glove and gown wearing
• waste disposal,
Prevention
• Linen cleaning
• Environmental cleaning
• Patient care equipment and
• Respiratory Hygiene
Prevention
# Avoid intake of
fruits bitten by
animals
Prevention
# Proper handling of
specimen
Prevention
# Strong Disease
Surveillance
Prevention
Alvac Canary Pox Vaccine
(Presently for cat)
Human trials are underway
Reach us at:
Dr Harivansh Chopra: harichop@gmail.com
Dr Abhishek Agarwal: abhishek3april@gmail.com

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nipahvirus-180525062654 (1).pdf

  • 1. NIPAH VIRUS By: Dr Harivansh Chopra Dr Abhishek Agarwal
  • 2. Introduction • Nipah virus (NiV) infection is a newly emerging zoonosis that causes severe disease in both animals and humans • It is named after the Malaysian Village from where it was first discovered.
  • 3. Introduction • Nipah virus causes a range of illnesses from asymptomatic (subclinical) infection to acute respiratory illness and fatal encephalitis.
  • 4. Introduction • Nipah virus is closely related to Hendra virus. • Both are members of the genus Henipavirus, a new class of virus in the Paramyxoviridae family.
  • 5. NIPAH Virus : A public Health Problem • Though Nipah virus has caused only a few outbreaks, it infects a wide range of animals and causes severe disease and death in people, making it a public health concern.
  • 8. Problem • 1st Case reported from Malaysia in 1998 • 1st Outbreak in south east asia was in Bangladesh in 2001 • 1st Outbreak in India was in Siliguri killing over 33 Health workers • Recent Outbreak was in Kerela, killed upto 11 health workers • Till now over 457 cases of Nipah Virus has been reported killing more then 252 persons
  • 9. Agent: Nipah Virus Paramyxovirus Highly pathogenic Closely related to Hendra virus Epidemiology
  • 11. Host • Reservoir Host: Fruit Bats • Amplifier Hosts: Pig and Horses • Dead End Host: Humans Epidemiology
  • 13. Epidemiology ENVIRONMENT • Cases are more in Winter and Spring (December–May). – Breeding Season of bats – Date palm sap harvesting season
  • 14. Transmission cycle of Nipah Virus
  • 15. Direct Transmission: Pig to Human • Direct human contact with infected pigs was identified as the predominant mode of transmission in humans when it was first recognized in Malaysia. (outbreak of Nipah virus, 1998-99)
  • 16. Direct Transmission: Human to Human • The evidence of human to human transmission of Nipah Virus was first reported from India. • During the outbreak in Siliguri, 33 health workers and hospital visitors became ill after exposure to patients hospitalized with Nipah Virus, suggesting nosocomial infection.
  • 17. Body fluids responsible for human to human transmission of Nipah Virus Cerebrospinal Fluid Respiratory Secretions Saliva Urine
  • 18. Direct Transmission: Bat to Human • Direct transmission of Nipah Virus from fruit bats to humans has been reported during Bangladesh Outbreak.
  • 19. Indirect Transmission: Fruit Bat • The natural host of the virus are fruit bats of the Pteropodidae Family, Pteropus genus • In India the sub species Pteropus giganteus is the causative agent
  • 20. Fluids from bats transmitting the disease • Virus present in its excretions and secretions – Urine – Semen – Saliva – Excreta
  • 21. Indirect Transmission: Date palm sap • Drinking of date palm sap, possibly contaminated by fruit bats may have been responsible for the transmission of Nipah Virus to Humans.
  • 22. Indirect Transmission: Date palm sap • Fruit bats also consume date palm sap and can contaminate it with saliva, urine feces. • This is the means by which Nipah Virus is thought to have been transmitted from infected fruit bats to humans.
  • 23. Case Definition : Suspected Nipah Case High Grade Fever with :- • acute onset of altered mental status, or • Seizure, or • Headache, or • acute onset of cough with shortness of breath
  • 24. Case Definition : Probable Nipah Case • Suspect cases, and/or who died before complete diagnostic specimens could be collected, including a serum antibody test 14 days after onset of illness Death: 14 days of onset of illness
  • 25. Case Definition : Confirmed Nipah Case i) IgM antibody ii) RNA identified by RT-PCR iii) isolation of Nipah Virus Confirmed Nipah case: Suspected/probable case having:
  • 26. Clinical Features • The classical form is an acute and rapidly progressive encephalitis with or without respiratory involvement in all age groups.
  • 27. Clinical Features • The Nipah encephalitis presents with 3–14 days of fever and headache, followed by drowsiness, disorientation and mental confusion. • The acute encephalitis progresses then to coma within 24–48 hours, with high mortality rate.
  • 28. Clinical Features • The respiratory involvement consists of non-productive cough during the early part of the disease, which can evolve later to severe acute lower respiratory disease, i.e., from breathing difficulties to acute respiratory distress syndrome (ARDS)
  • 29. Clinical Features • Post-encephalitis sequelae have been commonly observed in NiV infection. • One third of Nipah survivors in Bangladesh have moderate to severe objective neurological dysfunction 7–30 months after infection
  • 31. Treatment : Supportive • Fluid maintenance and electrolyte balance. • Nutrition • Anticonvulsant • Oropharyngeal suction in closed circuit.
  • 32. Treatment : Supportive • Oxygen inhalation using disposable cannula. • Bronchodilators through large spacer devices. • Severely ill individuals may require Intensive Care Unit (ICU) support
  • 33. Treatment: Drug • Ribavirin: • Monoclonal Antibodies (Post exposure therapy)
  • 34. Prevention • hand hygiene • injection safety • facial protection • glove and gown wearing • waste disposal,
  • 35. Prevention • Linen cleaning • Environmental cleaning • Patient care equipment and • Respiratory Hygiene
  • 36. Prevention # Avoid intake of fruits bitten by animals
  • 39. Prevention Alvac Canary Pox Vaccine (Presently for cat) Human trials are underway
  • 40. Reach us at: Dr Harivansh Chopra: harichop@gmail.com Dr Abhishek Agarwal: abhishek3april@gmail.com