VARICELLA (CHICKEN POX)
VARICELLA (CHICKEN POX)
Virology:
Varicella
zoster virus (VZV), included in the family Herpesviridae
Epidemiology:
Varicella zoster virus infection occurs worldwide.
Seroprevalence
at
age 20 is typically 95%. Primary infection with VZV causes
chickenpox,
which is primarily a disease of childhood, although
it
may occur at any age and is more severe in adults, with a
higher
incidence of serious complications such as pneumonitis.
Reactivation
of latent VZV in sensory ganglia causes herpes
zoster
(shingles). The absolute incidence of zoster is higher in
adults, but not if
corrected for prior exposure to VZV.
Reservoir: Man
Mode of Transmission:
Person-to-person, by
direct contact or droplet spread from
cases of chicken pox or
herpes zoster.
Incubation Period:
13–21 days.
Infectious Period:
From 2 days before the
onset of rash until the lesions are
crusted. Scabs are
noninfectious.
1-Fetal Infection
If infection occurs at
less than 26-weeks gestation, there is a
small risk of fetal malformation
(microcephaly, hydrocephalus,
limb hypoplasia,
cutaneous scarring and ophthalmic defects).
The risk is highest
during the first trimester (3%). Infection just
before or shortly after
delivery may be followed by neonatal
infection, which can be
severe.
2-Infection in Neonates
Neonates of mothers who
develop varicella <5 days before or
shortly after delivery
will not be protected by maternal IgG
and may develop severe
disseminated infection. They should
receive VZIG (see below)
and be monitored for 14–16 days
for signs of infection,
which should be treated promptly with
aciclovir. Some
recommend prophylactic acyclovir for these
neonates. Herpes zoster
during pregnancy poses no threat to
mother or child, since
by definition, the mother will have anti-
VZV IgG and this will
protect the neonate.
Clinical Features:-
• There is a mild
prodrome of malaise, fever, headache and
rhinitis.
• The rash
develops as crops of vesicles each
appearing on an
erythematous base (“dewdrop on a rose
petal”).Vesicles rapidly
progress to umbilicated papules,
pustules and scabs.
Distribution is typically central
on head, trunk and arms,
and also the palate or gums. New
crops continue to appear
for up to 7 days. Fever remains
elevated for 4–5 days
after onset of rash.
Pulmonary disease during varicella is often due to
secondary bacterial
pneumonia, usually with Streptococcus
pneumoniae, Haemophilus influenzae or Staphylococcus
aureus. Staphylococcal septicemia may occur.
Investigations:
Light Microscopy of Vesicle Contents
Reveals multinucleate
giant cells (Tzanck preparation);
electron microscopy
shows large numbers of herpes virus
particles. Methods are
available for the rapid detection of
VZV antigens in vesicle
fluid. Retrospectively diagnosis can be
confirmed by serology.
CXR
CXR shows widespread
patchy shadowing; may show military
mottling. Residual pulmonary
fibrosis and CXR calcifications
may occur in survivors.
Differential Diagnosis:
• Infectious
vesicular rashes include:
– Herpes simplex
infection
– Hand, foot and mouth
disease
– Disseminated
gonococcal infection
• Noninfectious causes include:
– Stevens-Johnson
syndrome
– Pemphigus
– Pemphigoid
In atypical cases,
vesicular impetigo due to Staphylococcus
aureus
or GAS can be confused.
Treatment:
Supportive
Care
• Antipyretic
paracetamol and non-aspirin drug
• Plenty of fluid
intakes
• Soothing agents like
lotion calamine over the affected skin
• Antipruritic: In
troublesome itching condition.
Antiviral
Treatment (Not Usually Required)
Aciclovir shortens and
reduces the severity of illness but
must be given early
(ideally <24 hours) to have a significant
effect. Aciclovir is not
recommended for routine use in
immune-competent
children. Intravenous acyclovir is indicated
in the following circumstances:
• Immuno-compromised
patients (including those with AIDS)
• Neonates and if there
is evidence of severe or disseminated
disease (30 mg/kg in
three divided dose IV for 10 days)
• In particular,
ophthalmic disease, pneumonitis or
encephalitis.
Complications:
• Bacterial super-infection
of the rash is common Streptococcus
followed by Staphylococcus,
sepsis, scarlet fever. In severe
cases, varicella
gangrenosum (Streptococcus)
• Hemorrhagic chickenpox
• Many patients have
mild hepatitis
• Mucositis may cause
dysuria
• Varicella pneumonitis
is more common in immune-compromised
patients
• It may progress
rapidly, with hypoxia and tachypnea
• Encephalitis
(cerebellitis): Chickenpox cerebellitis is an
important cause of acute
ataxia in children with good
prognosis
Other
CNS complications:
– GBS
– Transverse myelitis
• Thrombocytopenia and
disseminated intravascular
coagulopathy: Occur very
rarely and may cause hemorrhagic
varicella, with bleeding
into vesicles. All complications are
commoner in the immune-compromised.
Prevention:
Chicken
pox is very contagious.
•
Isolation
•
Rest at home to keep away from close human contact until
the
lesions are crusted.
Vaccination:
Live attenuated varicella-zoster
virus (Oka strain), obtained
from human diploid cell culture.
Indications
• A single dose of
vaccine is recommended in children ≥12
months of age. For
children ≥12 years, 2 doses at 4-week
interval. Currently,
however, 2 doses are recommended
irrespective of age
after 12-month age
• For active
immunization, from age 12 months onwards at
a dose of 0.5 mL, to be
given subcutaneously
•
Varicella and MMR vaccine
can be given in same date at
different sites, if not
given they should be given at 4-weeks
interval. They can be
given combined by single injection
MMRV vaccine at 12
months of age through 12 years of age.
This MMRV vaccine may be
used both first and second dose
of MMR and varicella
vaccine. Breakthrough infection may
occur after first dose
of varicella vaccine and manifests as
modified chickenpox
(milder form).
Contraindications
• Acute severe febrile
illness
• Lymphocyte count
<1200/cumm.)
Adverse
Effects
• Local reaction (pain,
erythema)
• Generalized rash (maculopapular).
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