| Varicella-Zoster
Varicella-zoster virus belongs to the
herpes group
of viruses and is the etiologic agent of varicella (chickenpox), the
most
common childhood disease associated with a rash.
Epidemiology
- Chickenpox occurs most frequently
during
childhood with
about 90% of adults having evidence of seropositivity.
- Very contagious with about 80% of
household contacts
becoming infected.
- Approximately 200 deaths per year in
the
United States
and 6000-9000 hospital admissions.
- Incubation period is 10-21 days and
the
contagious period
is 1-2 days prior to the rash and about 5 days after the rash begins
when
all lesions are crusted.
- Transmission is primarily from direct
contact with patients
who have varicella infection and occasionally by air-borne spread of
droplets.
- Immunity is lifelong with rare second
cases reported.
Most "second" cases are a result of a wrong primary diagnosis
- After primary infection, the virus may
be
dormant in
the dorsal root ganglion and become activated clinically as "shingles".
Clinical Manifestations
- After a 1-2 day of mild prodromal
symptoms, the child
will break out with rash usually on the trunk. The rash will start as
macular
red lesions and proceed to papules, vesicles, pustules, and then
crusted
lesion. They come out in crops and there are lesions present of
different
stages. May have involvement of the mucous membranes and this may help
distinguish chickenpox from insect bites
- The rash is very pruritic but systemic
symptoms are
mild.
- Teenagers and adults may become very
ill
with high fevers
and the development of pneumonia.
- Congenital varicella infections are
rare
because of
the high incidence of maternal immunity. Pregnant woman who develop
chickenpox
during the first or second trimester may deliver a neonate with the
congenital
varicella syndrome. Findings may consist of limb anomalies, SGA, eye
changes
including chorioretinitis,cataracts, and scarring.
- Neonates born to mothers who acquire
varicella 5 days
prior to delivery or 2` days after delivery have a high incidence of
serious
infections and death. Treatment with VZIG has improved the outcome in
these
neonates. Neonates who develop varicella after this period are generaly
not sicker than infants and older chldren.
- Infections in immunocompromised
children
are associated
with life-threatening illness.
Complications
- Secondary bacterial infections of skin
lesions. Usually
S.aureus or S.pyogenes.
- Necrotizing fasciitis may follow
secondary
infection
with S.pyogenes
- Secondary infections of the lung with
S.pyogenes causing
a severe pneumonia
- Cerebellar ataxia- common after
varicella
infection
- Encephalitis, aseptic meningitis,
transverse myelitis
- Primary varicella pneumonia
- Reye syndrome- incidence decreased
over
past 15 years.
Severe vomiting and mental status changes. Has beeen associated with
the
use of aspirin.
- Hemorrhagic chickenpox.
- Shingles
- results from reactivation of dormant
virus in the dorsal
ganglia.
- adults, there is usually no
underlying
condition that
leads to reactivation. Lesions are mostly confined to the trunk.
- Follows dermatome distribution and
rarely painful. Usually
pruritic.
- Isolation unnecessary as long as
lesions
are covered.
- Highest incidence in children who
had
primary infection
when they were less than one year of age.
Treatment
- Antipruritic measures- Calamine
lotion typically,
soothing baths with the addition of oatmeal, and Benadryl PO. Keep the
child's fingernails short.
- May return to school after all the
lesions
are crusted,
which is about 5-7 days after appearance.
- Acyclovir- routine use in varicella
not
recommended.
In immunocompromised hosts, teenagers, and adults, acyclovir may be
given
orally to help decrease the symptoms. It can be administered orally and
should be started within 12 hours of the appearance of the first
lesions.
- Some new literature has demonstrated
the
effectiveness
of post-exposure immunization in preventing the development of disease.
Active Immunization
- The immunization, a live attenuated
vaccine, is recommended
for all children by ACIP and the AAP between 12-18 months
- Children <13 years need one dose
and> 13, two doses
4-8 weeks apart.
- May be given concomitantly with the
MMR,
but if given
separately, one month apart
- Excellent antibody response (95%) and
immunity has not
been shown to wane in follow-up studies of 10 years duration.
- Rare breakthrough cases of chickenpox
in
prior immunized
individuals have been mild
- Post vaccination rashes are uncommon
and
virus has rarely
been isolated from these lesions
- Vaccine should not be given to
immunocompromised hosts
including patients receiving chemotherapy, or taking 2 mg./kg./day
prednisone
for greater than a month.
- HIV patients with mild or no symptoms
and
CD$=T-lymphocyte
percentage > 25% may receive the vaccine.
- Children in households with
immunocompromised hosts
or pregnant women, may receive the vaccine. If they break out with a
rash,
contact should be avoided with the immunocompromised individual.
- Patients receiving steroids should be
off
them for 1
month prior to giving the vaccine and the use of nasal or inhaled
steroids
is not a contraindication to the vaccine.
Passive Immunization-Varicella-Zoster
Immune Globulin
(VZIG)
- Indications- should be given as
soon as exposure
occurs but may be effective if given 96 hours later.
- Immunocompromised individuals
- newborns of mothers who acquire
varicella 5 days prior
to or 2 days after delivery
- Exposed premis < 28 weeks or <
1000 grams
- Exposed premis > 28 weeks whose
mother has not had chickenpox
- Susceptible adults
- Susceptible pregnant mothers. VZIG
may
decrease symptoms
in the pregnant mother but the virus may still be transimitted
to
the fetus.
References
- Committee
on Infectious Disease. Varicella Vaccine Update. Pediatrics. 2000;
105(1):136-141.
- Fisher, RG and Edwards KM. Varicella
Zoster. Pediatrics
in Review. 1998; 19:62-67.
- McCrary ML, Severson J and Tyring SK.
Varicella Zoster
Virus. Journal of the American Academy of Dermatology. 1999; 41(1):1-14.
- Resnick SD. New Aspects of
Exanthematous
Diseases of
Childhood. Dermatologic Clinics. 1997; 15(2):257-266.
- Walther RR. What is New in Clinical
Research of Viral
Diseases of the Skin. Dermatologic Clinics. 1997; 15(1):189-196.
- Watson B et. al. Postexposure
Effectiveness of Varicella Vaccine. Pediatrics. 2000;
105(1):84-88.
- M. Vasquez et. al. The
Effectiveness of Varicella Vaccine in Clinical Practice. NEJM
Vol 344 Numbeer 13 pages 955-961. March 29, 2001
- Ziebold C. et al. Severe
complications of Varicella in a Previously Healthy Children in Germany:
A 1-Year Survey. Pediatrics November 2001 e79
- Galil Karin et al. Outbreak
of Varicella at a Day-care Center Desptie Vaccination NEJM Vol
347(24)
pp. 1909-1915 December 12, 2002
- Tugwell BD et al. Chicknpox
Outbreak in a Highly Vaccinated Population. Pediatrics
2004;113:455
- Feder H, HossD. Herpes
Zoster in Otherwise Helathy Children. Pediatric Infectious
Disease.
May 2004
- Nguyen H.Q. Decline in
Mortality Due
to
Varicella after
Implementation of Varicella Vaccination in the United States.
NEJM
Feb 3, 2005
- Hudspeth M. Varicella-Zoster
Immune
Globulin Pediatrics in Review September 2005
- Chaves S. et al. Loss of
Vaccine Induced Immunity to Varicella over Time
<>NEJM March 15, 2007
15. MMWR Prevention
of Varicella June 2007
16. Gershonn A. Varicella
Zoster Virus Infections. Pediatrics in Review January 2008
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