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Identify the Disease
Measles
(Rubeola)
Dr . Anuradha Davey
Associate Professor
Community Medicine
Introduction
• Measles means- Red Spots
• It is Acute Viral exanthematous fever and
leading cause of VPD
• Most contagious disease known
– And if ds is introduced in a virgin community- 90%
of population will be affected
– Immunity level needed to interrupt transmission is
94% or higher
• Prior to vaccination- epidemic after every 2-3
yrs
• After vaccination- Interval increased to 5 years
and peak of intensity decreased
• Epidemic occur when susceptible population
reached around 40%
Clinical features
3 stages
• Prodromal
• Eruptive phase
• Post Eruptive phase
Prodromal phase
Prodromal:
begins at 10 days after exposure and last for 4 days
– Fever
– Coryza
– Sneezing
– Nasal discharge
– Cough
– Redness of eyes
– Lacrimation
– Photophobia
– May be vomiting or diarrhoea
• KOPLIK SPOT: 1-2 day before or after
appearance of rash: small bluish-white spot on
red base, smaller than head of a pin, against
first and second lower molar tooth.
“Pathognomic”
Koplik Spot
Eruptive phase:
Rash appearance: after 4days of fever or 14 days
of exposure
– Dusky red, Maculo-papular rash ( pathognomic)
– Discrete, confluent, blotchy
– Begin behind the ear, in few hrs face and neck, down body
in 2-3 days
– Disappear in another 3-4 days in same order
– Patient normally improves by 3rd day of rash and
uncomplicated case recover within 7-10 days of onset of
disease
– Brownish discoloration lasting for 2 months or so
During this phase, virus excrete from tear, nasal & throat
secretion, urine, blood
Measles Rash-3rd day
Brownish discoloration of rash
 Rash are because of circulating antibodies ,
result from interaction of T cells with virus
infected cells in small blood vessels
 Patient with defective CMI- no rash
Post eruptive phase
• Decreased immunity: chances of secondary
infection
• Loss of weight
• Growth retardation
• Diarrhoea
• Cancrum oris
• Pyogenic infection
• Candidiasis
• Reactivation of pulmonary TB
Complications
• Measles associated diarrhoea
• Pneumonia (most common cause of death)
• Respiratory tract infection
• Otitis media
Complications…Measles
• Encephalitis (4-7 d after onset of rash) : 1: 1000 → 15%
die
• Sub acute sclerosing pan encephalitis: rare(1: 3,00,000)
• develop many yrs after measles infection.
• Diagnosis by CF AB in CSF. Fatal →
severe personality changes, myoclonic seizures, motor
impairment,coma and death over course of several
months to years
EPIDEMIOLOGY
Agent
Transmission
Host
Environment
Agent
Category: Viral Disease-RNA paramyxovirus
 Only one serotype- so life long immunity
• Easily destroyed by sunlight, acids and drying
• BUT At sub zero temp: virus retain infectivity,
Agent…..
• Source of Infection: Case or subclinical case
No carrier stage
Infective material: secretion from nose, throat,
respiratory tract
• Direct- Person to person: droplet infection (the virus
can survive for atlest two hours in fine droplets)
• Indirect: droplet nuclei, articles freshly soiled with
discharges
Entry point : respiratory tract
• Conjunctiva
Transmission
Communicability: prodromal phase and eruption of
rashes.
4 days before and 4 days after the appearance of rash.
Host factor
• Age: 6 mths to 3 year in developing countries
and around 5 years in developed
• Sex: equal in both sex but mortality following acute
measles in greater in females at all age
Immunity: If no previous immunity: all ages are
susceptible
•One attack gives life long immunity
•Second attack is 90%
•Immunity after vaccination is life lasting
•Maternal ab persists from 6-9 mths after birth
Host continued…….
• Increased risk of developing severe or fatal measles
in the following cases:
– Malnutrition (measles can precipitate kwashiorkor
in borderline cases)
– Vit A Deficiency
– Severe immunological disorder such as advanced
HIV Infection-
Environment
• Tropical zone: dry season
• Temperate zone: winter
Overcrowding favours transmission
Incubation period:
From exposure to onset of fever: 10 days and
From exposure to appearence of rash: 14 days
•Overcrowding favours transmission
Mini measles by passing the RT (through vaccination) : 7
days
• Measles infection during pregnancy→
spontaneous abortion, LBW, premature
delivery
• Atypical Measles Syndrome: high fever,
pneumonia, pleural effusion, edema of hands
& feet, hepatic abn, unusual rash
↓
seen in persons who received killed measles
vaccine in the past & who were subsequently
exposed to measles virus
Prevention and Control
• Active Immunization- Primary method of
prevention
• Passive immunization- Administration of
Immunoglobins
• General measures
Diagnosis
• History of contact with a case
• C/F: maculopapular rash & koplik spots are
pathognomic
• Lab:
A four fold rise in in measles antibody titre in
acute or convalescent serum
IgG antibodies appear shortly after rash,peak
in 2 to 4 weeks and last for lifetime
Viral particles can be demonstrated using RT-
PCR
Active Immunization
• Type of vaccine: Live attenuated vaccine- as freeze
dried product (Chick embro or Human Diploid Cell line(
Edmonston Zagreb strain vaccine)
• Reconstitution: by cooled sterile diluents, must not
be frozen
• Sensitive to light : so kept in covered glass vials and
reconstituted vaccine must be used in 6 hours
Continued….
• Dose: 0.5 ml,
• Route: S/c or IM
• Age: 9 months
– THREE situation where vaccine can be given at 6
months if measles outbreak in India
Malnourished child
HIV (Asymptomatic ) infection
and repeat dose at 6-9 mth with 4 weeks interval
Contraindications: Pregnancy
immunocompromised
anaphylactic reaction to neomycin, gelatin
or other components of vaccine
 Immune response: humoral and cellular response with
lower Ab titer
 Reaction: Mini measles illness 5-10 days after
immunisation (15-20% of the vaccinees)
Fever lasts for 1-2 days and rashes last for 3-4 days
Immunity: develops after 11-12 days
99% protection when given at 12 month and 90%
protection when given at 9 month because of slow
sero conversion
Passive immunization
• Normal human Immunoglobins
• Dose: 0.25ml/kgbw
• Within 6 days
• Indication: vulnerable susceptible households
contacts like immunocompromised children
General measures
• Isolation : for one week from appearance of
rash
• Articles soiled with secretions or fluids from
vesicles s/b incinerated or treated with
disinfectants
• Reporting of outbreaks to local health
authorities
Treatment
• No specific treatment
• Supportive therapy-
– Fever(antipyretics)
– Dehydration (ORS)
– Gen. Nutritional support
– Antibiotic-for secondary bacterial infection
– Vit A supplementation
Dose: 2 doses 24 hours apart
supplementaty doses: 6mth- 1 year: one lakh IU
above 1 year: 2 lakh IU every 6 mthly
Definition of Elimination of Measles
by WHO
Absence of endemic measles for more than 12
months in the presence of adequate
surveillance
Indicator of measles Elimination:
• Sustained measles incidence <1/100,000
population
Why Measles can be eliminated…
• One sero type
• Life long immunity
• No chronic carrier state
• No animal reservoir
• Virus is easily destroyed
WHO Strategy for elimination
Catch up
Keep up
Follow up
• 1. Catch up: one time nation wide
vaccination campaign targeting usually all
children from 9mths to 14 yrs regardless
of previous h/o vaccination or ds
.
Continued….
2. Keep up: Routine services aimed at vaccinating
more than 95% of each successive birth cohort
3. Follow up: Subsequent nation wide vaccination
campaign after every 2-4 years targeting all children
born after catch up campaign
First two are the supplementary vaccination
campaign
Measles vaccination with HIV infection
• Asymptomatic HIV infection: Measles is not a
contraindication.
– It is given at 6 months and additional dose at 9
months
• Severely immuno-compromised: Measles
contraindicated
•Thank you

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Measles

  • 2.
  • 3.
  • 4. Measles (Rubeola) Dr . Anuradha Davey Associate Professor Community Medicine
  • 5. Introduction • Measles means- Red Spots • It is Acute Viral exanthematous fever and leading cause of VPD • Most contagious disease known – And if ds is introduced in a virgin community- 90% of population will be affected – Immunity level needed to interrupt transmission is 94% or higher
  • 6. • Prior to vaccination- epidemic after every 2-3 yrs • After vaccination- Interval increased to 5 years and peak of intensity decreased • Epidemic occur when susceptible population reached around 40%
  • 7. Clinical features 3 stages • Prodromal • Eruptive phase • Post Eruptive phase
  • 9. Prodromal: begins at 10 days after exposure and last for 4 days – Fever – Coryza – Sneezing – Nasal discharge – Cough – Redness of eyes – Lacrimation – Photophobia – May be vomiting or diarrhoea
  • 10. • KOPLIK SPOT: 1-2 day before or after appearance of rash: small bluish-white spot on red base, smaller than head of a pin, against first and second lower molar tooth. “Pathognomic”
  • 12. Eruptive phase: Rash appearance: after 4days of fever or 14 days of exposure – Dusky red, Maculo-papular rash ( pathognomic) – Discrete, confluent, blotchy – Begin behind the ear, in few hrs face and neck, down body in 2-3 days – Disappear in another 3-4 days in same order – Patient normally improves by 3rd day of rash and uncomplicated case recover within 7-10 days of onset of disease – Brownish discoloration lasting for 2 months or so During this phase, virus excrete from tear, nasal & throat secretion, urine, blood
  • 15.  Rash are because of circulating antibodies , result from interaction of T cells with virus infected cells in small blood vessels  Patient with defective CMI- no rash
  • 16. Post eruptive phase • Decreased immunity: chances of secondary infection • Loss of weight • Growth retardation • Diarrhoea • Cancrum oris • Pyogenic infection • Candidiasis • Reactivation of pulmonary TB
  • 17. Complications • Measles associated diarrhoea • Pneumonia (most common cause of death) • Respiratory tract infection • Otitis media
  • 18. Complications…Measles • Encephalitis (4-7 d after onset of rash) : 1: 1000 → 15% die • Sub acute sclerosing pan encephalitis: rare(1: 3,00,000) • develop many yrs after measles infection. • Diagnosis by CF AB in CSF. Fatal → severe personality changes, myoclonic seizures, motor impairment,coma and death over course of several months to years
  • 20. Agent Category: Viral Disease-RNA paramyxovirus  Only one serotype- so life long immunity • Easily destroyed by sunlight, acids and drying • BUT At sub zero temp: virus retain infectivity,
  • 21. Agent….. • Source of Infection: Case or subclinical case No carrier stage Infective material: secretion from nose, throat, respiratory tract
  • 22. • Direct- Person to person: droplet infection (the virus can survive for atlest two hours in fine droplets) • Indirect: droplet nuclei, articles freshly soiled with discharges Entry point : respiratory tract • Conjunctiva Transmission Communicability: prodromal phase and eruption of rashes. 4 days before and 4 days after the appearance of rash.
  • 23. Host factor • Age: 6 mths to 3 year in developing countries and around 5 years in developed • Sex: equal in both sex but mortality following acute measles in greater in females at all age Immunity: If no previous immunity: all ages are susceptible •One attack gives life long immunity •Second attack is 90% •Immunity after vaccination is life lasting •Maternal ab persists from 6-9 mths after birth
  • 24. Host continued……. • Increased risk of developing severe or fatal measles in the following cases: – Malnutrition (measles can precipitate kwashiorkor in borderline cases) – Vit A Deficiency – Severe immunological disorder such as advanced HIV Infection-
  • 25. Environment • Tropical zone: dry season • Temperate zone: winter Overcrowding favours transmission Incubation period: From exposure to onset of fever: 10 days and From exposure to appearence of rash: 14 days •Overcrowding favours transmission Mini measles by passing the RT (through vaccination) : 7 days
  • 26. • Measles infection during pregnancy→ spontaneous abortion, LBW, premature delivery • Atypical Measles Syndrome: high fever, pneumonia, pleural effusion, edema of hands & feet, hepatic abn, unusual rash ↓ seen in persons who received killed measles vaccine in the past & who were subsequently exposed to measles virus
  • 27. Prevention and Control • Active Immunization- Primary method of prevention • Passive immunization- Administration of Immunoglobins • General measures
  • 28. Diagnosis • History of contact with a case • C/F: maculopapular rash & koplik spots are pathognomic • Lab: A four fold rise in in measles antibody titre in acute or convalescent serum IgG antibodies appear shortly after rash,peak in 2 to 4 weeks and last for lifetime Viral particles can be demonstrated using RT- PCR
  • 29. Active Immunization • Type of vaccine: Live attenuated vaccine- as freeze dried product (Chick embro or Human Diploid Cell line( Edmonston Zagreb strain vaccine) • Reconstitution: by cooled sterile diluents, must not be frozen • Sensitive to light : so kept in covered glass vials and reconstituted vaccine must be used in 6 hours
  • 30. Continued…. • Dose: 0.5 ml, • Route: S/c or IM • Age: 9 months – THREE situation where vaccine can be given at 6 months if measles outbreak in India Malnourished child HIV (Asymptomatic ) infection and repeat dose at 6-9 mth with 4 weeks interval Contraindications: Pregnancy immunocompromised anaphylactic reaction to neomycin, gelatin or other components of vaccine
  • 31.  Immune response: humoral and cellular response with lower Ab titer  Reaction: Mini measles illness 5-10 days after immunisation (15-20% of the vaccinees) Fever lasts for 1-2 days and rashes last for 3-4 days Immunity: develops after 11-12 days 99% protection when given at 12 month and 90% protection when given at 9 month because of slow sero conversion
  • 32. Passive immunization • Normal human Immunoglobins • Dose: 0.25ml/kgbw • Within 6 days • Indication: vulnerable susceptible households contacts like immunocompromised children
  • 33. General measures • Isolation : for one week from appearance of rash • Articles soiled with secretions or fluids from vesicles s/b incinerated or treated with disinfectants • Reporting of outbreaks to local health authorities
  • 34. Treatment • No specific treatment • Supportive therapy- – Fever(antipyretics) – Dehydration (ORS) – Gen. Nutritional support – Antibiotic-for secondary bacterial infection – Vit A supplementation Dose: 2 doses 24 hours apart supplementaty doses: 6mth- 1 year: one lakh IU above 1 year: 2 lakh IU every 6 mthly
  • 35. Definition of Elimination of Measles by WHO Absence of endemic measles for more than 12 months in the presence of adequate surveillance Indicator of measles Elimination: • Sustained measles incidence <1/100,000 population
  • 36. Why Measles can be eliminated… • One sero type • Life long immunity • No chronic carrier state • No animal reservoir • Virus is easily destroyed
  • 37. WHO Strategy for elimination Catch up Keep up Follow up • 1. Catch up: one time nation wide vaccination campaign targeting usually all children from 9mths to 14 yrs regardless of previous h/o vaccination or ds .
  • 38. Continued…. 2. Keep up: Routine services aimed at vaccinating more than 95% of each successive birth cohort 3. Follow up: Subsequent nation wide vaccination campaign after every 2-4 years targeting all children born after catch up campaign First two are the supplementary vaccination campaign
  • 39. Measles vaccination with HIV infection • Asymptomatic HIV infection: Measles is not a contraindication. – It is given at 6 months and additional dose at 9 months • Severely immuno-compromised: Measles contraindicated