Rubella slide

3,590 views 25 slides May 23, 2020
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About This Presentation

Rubella slide


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PRESENTED BY :- MR. ROMAN BAJRANG BASIC BS.C NURSING 2 ND YEAR RELIANCE INSTITUTE OF 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 ENVI R ONME N T H O S T

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 com m u n ic a bility

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 catara c ts 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.
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