Chickenpox is a highly contagious illness caused by primary infection with
varicella zoster virus (VZV). It generally begins with
conjunctival and
catarrhal symptoms and then characteristic spots appearing in two or three waves, mainly on the body and head rather than the hands and becoming itchy raw
pockmarks, small open sores which heal mostly without scarring.
Chickenpox has a 10-21 day incubation period and is spread easily through aerosolized droplets from the
nasopharynx of ill individuals or through direct contact with secretions from the rash. Following primary infection there is usually lifelong protective immunity from further episodes of chickenpox.
Chickenpox is rarely fatal, although it is generally more severe in adults than in children. Pregnant women and those with a suppressed immune system are at highest risk of serious complications. The most common late complication of chicken pox is
shingles, caused by reactivation of the varicella zoster virus decades after the initial episode of chickenpox.
Signs and symptomsChickenpox is a highly contagious disease that spreads from person to person by direct contact or through the air from an infected person's coughing or sneezing. Touching the fluid from a chickenpox
blister can also spread the disease. A person with chickenpox is contagious from one to two days before the rash appears until all blisters have formed scabs. This may take 5-10 days.
[1] It takes from 10-21 days after contact with an infected person for someone to develop chickenpox.
[2]The chickenpox lesions (blisters) start as a two to four millimeter red
papule which develops an irregular outline (a rose petal). A thin-walled, clear vesicle (dew drop) develops on top of the area of redness. This "dew drop on a rose petal" lesion is very characteristic for chickenpox. After about eight to 12 hours the fluid in the vesicle gets cloudy and the vesicle breaks leaving a crust. The fluid is highly contagious, but once the lesion crusts over, it is not considered contagious. The crust usually falls off after seven days sometimes leaving a crater-like scar. Although one lesion goes through this complete cycle in about seven days, another hallmark of chickenpox is the fact that new lesions crop up every day for several days. Therefore it may be a week before new lesions stop appearing and existing lesions crust over. Children are not to be sent back to school until all lesions have crusted over.
[3]Chickenpox is highly contagious and is spread through the air when infected people cough or sneeze, or through physical contact with fluid from lesions on the skin.
Zoster, also known as shingles, is a reactivation of chickenpox and may also be a source of the virus for susceptible children and adults. It is not necessary to have physical contact with the infected person for the disease to spread. Those infected can spread chickenpox before they know they have the disease - even before any rash develops. People with chickenpox, in fact, can infect others from about two days before the rash develops until all the sores have crusted over, usually four or five days after the rash starts.
Infection in Pregnancy and Neonates
Varicella infection in pregnant women can lead to viral transmission via the placenta and infection of the foetus. If infection occurs during the first 28 weeks of gestation, this can lead to foetal varicella syndrome (also known as congenital varicella syndrome). Effects on the foetus can range in severity from underdeveloped toes and fingers to severe anal and bladder malformation. Possible problems include:
Damage to brain:
encephalitis,
microcephaly,
hydrocephaly,
aplasia of brain
Damage to the eye (optic stalk, optic cap, and lens vesicles),
microphthalmia,
cataracts,
chorioretinitis,
optic atrophyOther neurological disorder: damage to cervical and lumbosacral
spinal cord, motor/sensory deficits, absent deep
tendon reflexes, anisocoria/
Horner's syndromeDamage to body:
hypoplasia of upper/lower extremities, anal and bladder
sphincter dysfunction
Skin disorders: (
cicatricial) skin lesions,
hypopigmentationInfection late in gestation or immediately post-partum is referred to as neonatal varicella. Maternal infection is associated with premature delivery. The risk of the baby developing the disease is greatest following exposure to infection in the period 7 days prior to delivery and up to 7 days post-partum. The nenoate may also be exposed to the virus via infectious siblings or other contacts, but this is of less concern if the mother is immune. Newborns who develop symptoms are at a high risk of pneumonia and other serious complications of the disease.
[4]Causes
Chickenpox is a highly contagious illness caused by acute primary (initial) infection with
varicella zoster virus (VZV).
Pathophysiology
Chickenpox is usually acquired by the inhalation of airborne respiratory droplets from an infected host. The highly contagious nature of VZV explains the epidemics of chickenpox that spread through schools as one child who is infected quickly spreads the virus to many classmates. High viral titers are found in the characteristic vesicles of chickenpox; thus, viral transmission may also occur through direct contact with these vesicles, although the risk is lower.
After initial inhalation of contaminated respiratory droplets, the virus infects the
conjunctivae or the
mucosae of the
upper respiratory tract. Viral proliferation occurs in regional
lymph nodes of the upper respiratory tract 2-4 days after initial infection and is followed by primary viremia on postinfection days 4-6. A second round of viral replication occurs in the body's internal organs, most notably the
liver and the
spleen, followed by a secondary
viremia 14-16 days postinfection. This secondary viremia is characterized by diffuse viral invasion of
capillary endothelial cells and the
epidermis. VZV infection of cells of the
malpighian layer produces both intercellular and intracellular
edema, resulting in the characteristic vesicle.
Exposure to VZV in a healthy child initiates the production of host
immunoglobulin G (IgG),
immunoglobulin M (IgM), and
immunoglobulin A (IgA)
antibodies; IgG antibodies persist for life and confer immunity.
Cell-mediated immune responses are also important in limiting the scope and the duration of primary varicella infection. After primary infection, VZV is hypothesized to spread from
mucosal and
epidermal lesions to local
sensory nerves. VZV then remains latent in the
dorsal ganglion cells of the sensory nerves. Reactivation of VZV results in the clinically distinct syndrome of herpes zoster (shingles).
DiagnosisThe diagnosis of varicella is primarily clinical. In a non-immunized individual with typical
prodromal symptoms associated with the appropriate appearing rash occurring in "crops", no further investigation would normally be undertaken.
If further investigation is undertaken, confirmation of the diagnosis can be sought through either examination of the fluid within the vesicles, or by testing blood for evidence of an acute immunologic reposnse. Vesicle fluid can be examined with a
Tsanck smear, or better with examination for
direct fluorescent antibody. The fluid can also be "cultured", whereby attempts are made to grow the virus from a fluid sample. Blood tests can be used to identify a response to acute infection (IgM) or previous infection and subsequent immunity (IgE).
[5]Prenatal diagnosis of foetal varicella infection can be performed using
ultrasound, though a delay of 5 weeks following primary maternal infection is advised. A
PCR (DNA) test of the mother's
amniotic fluid can also be performed, though the risk of
spontaneous abortion due to the
amniocentesis procedure is higher than the risk of the baby developing foetal varicella syndrome.
[4]Prevention
Main article: Varicella vaccineA
varicella vaccine has been available since 1995 to inoculate against the disease. Some countries require the varicella vaccination or an exemption before entering elementary school. Protection is not lifelong and further vaccination is necessary five years after the initial immunization.
[6]In the
United Kingdom, varicella antibodies are measured in women with no history of the disease as part of routine of prenatal care. By 2005 all
National Health Service personnel had determined their immunity and been immunized if they were non-immune and have direct patient contact. Population-based immunization against varicella is not otherwise practiced in the UK. It is feared that there would be a greater number of cases of shingles in adults, until the vaccination was given to the entire population—because adults who have had chickenpox as a child are less likely to have shingles in later life if they have been exposed occasionally to the chickenpox virus (for example by their children). This is because the exposure acts as a booster vaccine.
[7][8]TreatmentThere is no evidence to support the effectiveness of topical application of
calamine lotion, a topical barrier preparation containing zinc oxide in spite of its wide usage and excellent safety profile.
[9] It is important to maintain good hygiene and daily cleaning of skin with warm water to avoid secondary bacterial infection.
If exposure to varicella in certain 'at risk' populations is confirmed (immunosuppressed individuals, pregnant seronegative women, neonates), anti-varicella zoster immunoglobulin may be given prior to onset of disease symptoms.
Infection in otherwise healthy adults tends to be more severe and active; treatment with antiviral drugs (e.g.
acyclovir) is generally advised. Patients of any age with depressed immune systems or extensive eczema are at risk of more severe disease and should also be treated with antiviral medication. In the U.S., 55 percent of chickenpox deaths are in the over-20 age group, even though they are a tiny fraction of the cases.
PrognosisChickenpox infection tends to be milder the younger a child is and symptomatic treatment, with a little
sodium bicarbonate in baths or
antihistamine medication to ease itching,
[10] and
paracetamol (acetaminophen) to reduce fever, are widely used. Ibuprofen can also be used on advice of a doctor. However,
aspirin or products containing aspirin must not be given to children with chickenpox (or any fever-causing illness), as this risks causing the serious and potentially fatal
Reye's Syndrome.
[11]Symptoms in adults tend to be more severe, though incidence is much less common. Infection in adults is associated with greater morbidity and mortality due to
pneumonia,
hepatitis and
encephalitis. In particular, up to 10% of pregnant women with chickenpox develop pneumonia, the severity of which increases with onset later in gestation. In England and Wales, 75% of deaths due to chickenpox are in adults.
[4]Inflammation of the brain, or
encephalitis, can occur in immunocompromised individuals. This is more dangerous with
shingles.
[12]Necrotizing fasciitis[13] is also a rare complication.
Patients with
Crohn's disease or any IBD, because of the use of immunosuppressive drugs, are at serious risk of complications from varicella zoster virus.
Later in life, any chickenpox viruses that remain dormant in the nerves can reactivate, causing shingles.
Secondary bacterial infection of skin lesions, manifesting as impetigo, cellulitis, and erysipelas, is the most common complication in healthy children.
o Staphylococci and streptococci are the most commonly implicated bacterial pathogens. o Bacterial superinfection may predispose to scarring. Localized bacterial superinfection rarely may manifest in septicemia, culminating in secondary bacterial pneumonia, otitis media, or necrotizing fasciitis.
Disseminated primary varicella infection, usually seen in the immunocompromised or adult populations, may have high morbidity. Ninety percent of cases of varicella pneumonia occur in the adult population. Rarer complications of disseminated chickenpox also include myocarditis, hepatitis, and glomerulonephritis.
Central nervous system complications of primary VZV infection may occur, albeit very rarely. Reye syndrome, Guillain-Barré syndrome, acute cerebellar ataxia, and encephalitis have all been documented to occur after VZV infection.
Thrombocytopenia and purpura secondary to VZV infection have been described in more than 100 patients.
o Hemorrhagic complications are more common in the immunocompromised or immunosuppressed populations, although healthy children and adults have been affected. Five major clinical syndromes have been described: febrile purpura, malignant chickenpox with purpura, postinfectious purpura, purpura fulminans, and anaphylactoid purpura.
o These syndromes have variable courses, with febrile purpura being the most benign of the syndromes and having an uncomplicated outcome. In contrast, malignant chickenpox with purpura is a grave clinical condition that has a mortality rate of greater than 70%. The etiology of these hemorrhagic chickenpox syndromes is not known.
EpidemiologyPrimary varicella is an endemic disease. Cases of varicella are seen throughout the year but, like other viruses spread by the respiratory route eg. measles and rubella, they are seen more commonly in the winter and early spring. This is unlike that for enteroviruses and lends some support to the view that varicella is spread mainly by the respiratory route. Herpes zoster, in contrast, occurs sporadically and evenly throughout the year. Varicella is one of the classic diseases of childhood, with the highest prevalence occurring in the 4 - 10 years old age group. Like rubella, infection is uncommon in preschool children. Varicella is highly communicable, with an attack rate of 90% in close contacts. Most people become infected before adulthood but 10% of young adults remain susceptible. However, this pattern of infection is not universal, eg. in rural India, varicella is predominantly a disease of adults, the mean age of infection being 23.4 years. It was suggested that this could be due to interference by other respiratory viruses that the children are exposed to at an early age.
Historically, varicella has been a disease predominantly affecting preschool and school-aged children. Although mostly noted in preschool and primary levels, the said disease has also been noticed among adults, with the pocks being more darker andthe scars more prominent than their younger counterparts.
HistoryOne history of medicine book credits
Giovanni Filippo (
1510–
1580) of
Palermo with the first description of varicella (chickenpox). Subsequently in the
1600s, an
English physician named
Richard Morton described what he thought a mild form of
smallpox as "chicken pox." Later, in
1767, a physician named
William Heberden, also from England, was the first physician to clearly demonstrate that chickenpox was different from smallpox. However, it is believed the name chickenpox was commonly used in earlier centuries before doctors identified the disease.
There are many explanations offered for the origin of the name chickenpox:
Samuel Johnson suggested that the disease was "less dangerous", thus a "chicken" version of the pox;
the specks that appear looked as though the skin was pecked by chickens;
the disease was named after
chick peas, from a supposed similarity in size of the seed to the lesions;
the term reflects a corruption of the Old English word giccin, which meant itching.
As "pox" also means curse, in medieval times some believed it was a plague brought on to curse children by the use of black magic.
From ancient times,
neem has been used by
Indians to alleviate the external symptoms of itching and to minimise scarring. Neem baths (neem leaves and a dash of
turmeric powder in water) are commonly given for the duration. Neem branches are hung at the entrance of households to announce that illness to visitors. Neem branches are kept handy by the affected person to gently brush the skin, to soothe the itching sensation.
During the medieval era,
oatmeal was discovered to soothe the sores, and oatmeal baths are today still commonly given to relieve itching.
