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PRESENTED BY
SAMITA KHATIWADA
III YR BSC. NURSING
The Teratogenic property of
the infection was documented
by an Australian
ophthalmologist Norman
McAlister Gregg, in 1941
 Rubella, commonly known as German
measles, is a disease caused by Rubella virus.
The name is derived from the Latin, meaning
little red.
 Rubella is also known as German measles
because the disease was first described by
German physicians, Friedrich Hoffmann, in the
mid-eighteenth century.
 Rubella is a disease caused by the rubella virus.
 Also known as German Measles or 3 day
measles
 Rubella is usually a mild illness.
 Most people who have had rubella or the
vaccine are protected against the virus for the
rest of their lives.
 Because of routine vaccination against rubella
since 1970 , rubella is now rarely reported
 Rubella virus is single
stranded RNA virus
 Diameter 50 – 70 nm
 Enveloped Spherical
 Virus multiply in the
cytoplasm of infected cell
AGENT
ENVIRONMENTHOST
• Caused by an RNA virus of the togavirus
family.
• It can be propagated in cell culture
Agent
• Large no of rubella infections are Sub- clinical.
Source of
Infection
• It is much less communicable than measles.
• It probably extends from a week before
symptoms to about a week after rash appears.
Period of
communicability
AGE
•Disease of childhood (3-10 years)
IMMUNITY
•One attacks results in life long immunity;
second attacks are rare.
• 40 % of women of child bearing age are
susceptible to rubella in India,
 Disease usually occurs in a seasonal
pattern i.e. in temperate zones during
the later winter and spring, with
epidemics of every 4-9 years
 The virus is transmitted directly from person to
person by droplet nuclei from nose and throat.
 The portal of entry is via the respiratory route.
 The virus can cross the placenta and infect the
foetus in uterus, leading to congenital rubella
in new born
2-3 weeks Average 18
days
 Malaise
 Low grade fever
 Morbilliform rash
 Rash starts on Face
Extremities
 Rarely lasts more than 5
days
 No features of the rash
give clues to definitive
diagnosis of Rubella.
 "Rubella infection in
pregnant women during
the first three months of
pregnancy may result in
the baby being born with
birth defects or
congenital rubella
syndrome.
Occurs in Neonates and Childhood
 Lasts for 13 – 15 days
 Leads to development of antibodies
 The appearance of antibodies
coincides the appearance of
suggestive immulogic basis for the
rash
 In 20 – 50 % cases of primary
infections are subclinical
 Congenital rubella syndrome (CRS) refers to
infants born with defects secondary to
intrauterine infection.
 It occurs if the infant has IgM rubella
antibodies shortly after birth or IgG antibodies
persist for more than 6 months, by the time
maternally derived antibodies would have
disappeared.
 the most common and major defects are
deafness, cardiac malformations and cataracts.
deafness cataracts PDA
 Other defects includes
 Glaucoma
 Retinopathy
 Microcephalus
 Cerebral palsy
 Intrauterine growth retardation
 Hepato-splenomegaly
 Mental and motor retardation
 Throat swab culture for virus isolation and
serology.
 Haemagglutination inhibition test (HAI)
 Others includes ELISA test and radio-immune
assay.
 There is no specific treatment for Rubella;
management is a matter of responding to
symptoms to diminish discomfort.
 Rubella vaccine is given to children at 15
months of age as a part of the MMR (measles-
mumps-rubella) immunization.
 Isolation of the patient.
 Strict avoidance of close contact with patient.
 Vaccination to girls(11-14 years), duration of
immunity pffered being 10 years.
 Other precautionary measures are needed as
applied to air borne infection.
 The MMR vaccine is a mixture of three live
attenuated viruses, administered via injection
for immunization against measles, mumps
and rubella.
 It is generally administered to children around
the age of one year, with a second dose before
starting school (i.e. age 4/5).
 The second dose is not a booster; it is a dose to
produce immunity in the small number of
persons (2-5%) who fail to develop measles
immunity after the first dose.
Rubella
Rubella

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Rubella

  • 1.
  • 3. The Teratogenic property of the infection was documented by an Australian ophthalmologist Norman McAlister Gregg, in 1941
  • 4.  Rubella, commonly known as German measles, is a disease caused by Rubella virus. The name is derived from the Latin, meaning little red.  Rubella is also known as German measles because the disease was first described by German physicians, Friedrich Hoffmann, in the mid-eighteenth century.
  • 5.  Rubella is a disease caused by the rubella virus.  Also known as German Measles or 3 day measles  Rubella is usually a mild illness.  Most people who have had rubella or the vaccine are protected against the virus for the rest of their lives.  Because of routine vaccination against rubella since 1970 , rubella is now rarely reported
  • 6.  Rubella virus is single stranded RNA virus  Diameter 50 – 70 nm  Enveloped Spherical  Virus multiply in the cytoplasm of infected cell
  • 8. • Caused by an RNA virus of the togavirus family. • It can be propagated in cell culture Agent • Large no of rubella infections are Sub- clinical. Source of Infection • It is much less communicable than measles. • It probably extends from a week before symptoms to about a week after rash appears. Period of communicability
  • 9. AGE •Disease of childhood (3-10 years) IMMUNITY •One attacks results in life long immunity; second attacks are rare. • 40 % of women of child bearing age are susceptible to rubella in India,
  • 10.  Disease usually occurs in a seasonal pattern i.e. in temperate zones during the later winter and spring, with epidemics of every 4-9 years
  • 11.  The virus is transmitted directly from person to person by droplet nuclei from nose and throat.  The portal of entry is via the respiratory route.  The virus can cross the placenta and infect the foetus in uterus, leading to congenital rubella in new born
  • 12. 2-3 weeks Average 18 days
  • 13.  Malaise  Low grade fever  Morbilliform rash  Rash starts on Face Extremities  Rarely lasts more than 5 days  No features of the rash give clues to definitive diagnosis of Rubella.
  • 14.
  • 15.  "Rubella infection in pregnant women during the first three months of pregnancy may result in the baby being born with birth defects or congenital rubella syndrome.
  • 16.
  • 17. Occurs in Neonates and Childhood  Lasts for 13 – 15 days  Leads to development of antibodies  The appearance of antibodies coincides the appearance of suggestive immulogic basis for the rash  In 20 – 50 % cases of primary infections are subclinical
  • 18.  Congenital rubella syndrome (CRS) refers to infants born with defects secondary to intrauterine infection.  It occurs if the infant has IgM rubella antibodies shortly after birth or IgG antibodies persist for more than 6 months, by the time maternally derived antibodies would have disappeared.
  • 19.  the most common and major defects are deafness, cardiac malformations and cataracts. deafness cataracts PDA
  • 20.  Other defects includes  Glaucoma  Retinopathy  Microcephalus  Cerebral palsy  Intrauterine growth retardation  Hepato-splenomegaly  Mental and motor retardation
  • 21.  Throat swab culture for virus isolation and serology.  Haemagglutination inhibition test (HAI)  Others includes ELISA test and radio-immune assay.
  • 22.  There is no specific treatment for Rubella; management is a matter of responding to symptoms to diminish discomfort.
  • 23.  Rubella vaccine is given to children at 15 months of age as a part of the MMR (measles- mumps-rubella) immunization.  Isolation of the patient.  Strict avoidance of close contact with patient.  Vaccination to girls(11-14 years), duration of immunity pffered being 10 years.  Other precautionary measures are needed as applied to air borne infection.
  • 24.  The MMR vaccine is a mixture of three live attenuated viruses, administered via injection for immunization against measles, mumps and rubella.  It is generally administered to children around the age of one year, with a second dose before starting school (i.e. age 4/5).  The second dose is not a booster; it is a dose to produce immunity in the small number of persons (2-5%) who fail to develop measles immunity after the first dose.