Chicken Pox & Rubella

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CHICKEN POX &

RUBELLA
Introduction
 Chickenpox or varicella is a highly
contagious disease caused by the
varicella-zoster virus (VZV). It can cause
an itchy, blister-like rash (vesicular rash),
fever and malaise. The rash first appears
on the chest, back, and face, and then
spreads over the entire body.
Epidemiological
determinants
 AGENT :
Varicella-zoster virus/ Human (alpha)
herpes virus 3
 SOURCE OF INFECTION:
Oropharyngeal secretions and lesions of
skin and mucosa.
HOST FACTORS
 Children under 10 years of age.
ENVIORNMENTAL FACTORS
 Poor personal hygiene
 Over crowding
MODE OF TRANSMISSION
 Droplet infection
 Droplet nuclei
 Face to face contact
 Cross the placental barrier (CONGENITAL
VARICELLA)
Incubation period
The average incubation period for
varicella is 14 to 16 days after
exposure to a varicella or a herpes
zoster rash, with a range of 10 to 21
days.
Clinical features
 Divided into two stages :
 PRE-ERUPTIVE STAGE
 ERUPTIVE STAGE
PRE-ERUPTIVE STAGE

 Onset is sudden
 Mild or moderate fever
 Pain in back, shivering and malaise
 Lasts for 24 hours in children and 2-3
days in adults
ERUPTIVE STAGE

(a) DISTRIBUTION:
 Rash (first sign when fever starts), it first appears on the

trunk where it is abundant and then comes on face, arms


and legs.
 Density of eruption diminishes centrifugally

 Mucosal surfaces are also involved

(b) RAPID EVOLUTION:


 Once the chickenpox rash appears, it goes through three

phases: Raised pink or red bumps (papules), which break


out over several days. Small fluid-filled blisters (vesicles),
which form in about one day and then break and leak.
Crusts and scabs, which cover the broken blisters and take
several more days to heal. Vesicles are dewdrop like.
(c) PLEOMORPHISM:
 All stages of rash may be seen

simultaneously at one time, in same


area.
(d) FEVER:
 Fever does not run high

 Exacerbations with each fresh crop of

eruption
complications
 Sepsis
 Hemorrhages
 Dehydration
 Pneumonia
 Inflammation of the brain (encephalitis)
 Toxic shock syndrome
 Acute retinal necrosis
 Reye's syndrome ( acute encephalopathy
associated with fatty degeneration of the viscera)
 Foetal deaths and birth defetcs
Laboratory diagnosis
 Rarely required as clinical signs are
usually clear-cut.
 VZV DNA using PCR
 Cell culture from vesicular fluid, crusts,
saliva
Control
 No specific treatment
 Tetracycline to prevent secondary
infection
 Notification to health authorities
 Isolation from school for only on week
 Contact with susceptible is avoided
 Concurrent disinfection of the articles
soiled by discharges
Preventive measures
 VZIG:
I/M within 72 hours
12.5 units/kg body weight up to a
maximum of 625 units, with a repeated
dose in 3 weeks.
 VACCINE:
A live attenuated vaccine (12-18
months)
MMRV
RUBELLA
 Also called as GERMAN MEASLES
 Acute, childhood infection
 Mild and have short duration (3 days)
 Low grade fever, maculopapular rash
 Infection in early pregnancy may lead to
serious congenital defects including
foetal death.
EPIDEMOLOGICAL DETERMINANTS

AGENT:
 RNA virus of Toga virus family

 Recovered from the nasopharynx, throat,

blood, CSF and urine


HOST FCTORS:
 Age: 3-10 years

 Immunity: one attack results in life-long

immunity
ENVIORNMENTAL FACTORS:
 Temperate zones during the late winter

and spring
TRANSMISSION
 Person to person by droplets from nose
and throat and droplet nuclei
 Portal of entry is respiratory route
 Can cross the placenta (vertical)
Incubation period
 2-3 weeks, average 18 days
Clinical features
 5o-65% are asymptomatic
 The signs and symptoms of rubella are often
difficult to notice, especially in children.
 PRODROMAL:
 Mild fever of 102 F
 Headache
 Stuffy or runny nose
 Red, itchy eyes
 LYMPHADENOPATHY:
Enlarged, tender lymph nodes at the base of the
skull, the back of the neck and behind the ears
 RASH:
A fine, pink,macular rash that begins on
the face (24 hours) and quickly spreads
to the trunk and then the arms and legs,
before disappearing in the same order
 Aching joints, especially in young women
Complications
 Arthralgia
 Encephalitis
 Thrombocytopenia purpura
 Congenital malformations
CONGENITAL RUBELLA
Congenital rubella syndrome (CRS) is an
illness in infants that results from
maternal infection with rubella virus
during pregnancy. When rubella
infection occurs during early pregnancy,
serious consequences occurs such as:
 miscarriages,
 stillbirths, and a constellation of severe
birth defects in infants–can result.
 CLASSIC TRIAD:
1. cataracts
2. congenital heart disease (most commonly patent
ductus arteriosus or peripheral pulmonary artery
stenosis)
3. hearing impairment
 congenital glaucoma
 retinopathy
 hepatosplenomegaly,
 microcephaly
 developmental delay
 meningoencephalitis

Laboratory diagnosis
 It can go unrecognized unless it is an
epidemic
 Virus isolation and serology
 Haemagglutination inhibition test
 Detection of IgG ntibody
Preventive measures

 Active immunization with live attenuated


vaccine
 RUBELLA VACCINE:
 RA 27/3 vaccine (produced in human diploid
fibro-blast)
 Single dos, 0.5ml, S/C
 Infants under 1 year should not be
vaccinated
 Contraindicated in pregnancy
 MMR Vaccine
 Rubella can be prevented with MMR
vaccine. This protects against three
diseases: measles, mumps, and rubella.
 CDC recommends children get two
doses of MMR vaccine, starting with the:
 first dose at 12-15 months
 second dose at 4-6 years

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