Varicella Zoster Infection

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    ID conference

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    A 46 year old woman

    Admission date : 21/2/54

    Case SLE Dx 2550

    DLE

    ANA speckle pattern titer 1:1280

    Anti nRNP/Sm +ve, Anti SS-A +ve Current medication HCQ 1x1, Prednisolone 7.5

    mg/day

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    Hospital course Overlap syndrome (SLE with scleroderma)

    Develop RPGN >> Kidney biopsy : LN class II

    with severe vascular occlusion Double pulse methylprednisolone and IVCY 2

    courses 19/1/54

    Prednisolone 15 mg/day

    ESRD>> regular HD 31/1/54

    This admission due to volume overload

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    Hospital course VAP with ARDS 13/3/54

    Transfer to MICU 17/3/54

    Sputum culture : P. aeruginosa Rx with Ceftazidime for 14 days

    Weaning ventilator 27/3/54

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    Hospital course Chicken pox

    30/3/54 developed papulovesicular rash at Ltarm and Lt thigh

    History of exposure to chicken pox at RCU 10-14/3/54

    CBC : WBC 15,200 PMN 73% Band 5%Eo 2% L 11% Hct 22% Plt 225,000

    LFT : D. bili 0.12 T. bili 0.27SGOT 58 SGPT 24

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    Hospital course Isolation

    Acyclovir 250 mg IV q 8 hr

    No development of new lesions and turn to crustin 3 days

    Continue acyclovir for 7 days

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    Varicella-zoster

    infection

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    Varicella-zoster virus (VZV) :

    herpesviruses

    Distinct forms of disease: Varicella (chickenpox): Primary VZV infection

    results in the diffuse vesicular rash.

    Herpes zoster(shingles): Endogenous

    reactivation of latent VZV typically results in alocalized skin infection

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    Transmission routesAirborne transmission

    Contact with aerosolized droplets from

    nasopharyngeal secretions

    Direct cutaneous contact with vesicle fluid

    from skin lesions

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    Viremia Double-stranded, linear DNA virus

    Lipid-containing envelope with glycoproteinspikes.

    Localized replication with concurrent replication inregional lymph nodes by 4-6 days

    Primary viremic phase with seeding of thereticuloendothelial system

    Secondary phase : after 9 days and persiststhrough the development of skin lesions

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    Incubation period Incubation period : 8 -21 days

    Average : 14-16 days

    Infectivity : last from 48 hours prior to the onset ofrash until skin lesions have fully crusted.

    Administration of varicella zoster immune

    globulin (VZIG) following exposure can prolong

    the incubation period from 21 days to 28 days.

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    Reinfection

    Second episodes of varicella infection in

    immunocompetent individuals rarely occur

    Subclinical reinfection with VZV is common

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    CLINI

    CALMANIFES

    TATIONS

    Occurs during childhood

    Benign self-limited illness

    Severe disease : adolescents, adults, andimmunosuppressed or

    immunocompromised

    Secondary cases : more severe thanprimary cases

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    Uncomplicated varicella

    Develop within fifteen days after the exposure

    Prodrome of fever, malaise, or pharyngitis, loss of

    appetite Development of a generalized vesicular rash within

    24 hours.

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    Macule, papule, pustule, vesicular rash : formation

    generally stops within 4 days

    Pruritic

    Crusted papules : 6 days in normal host

    Different stages

    Face, trunk and extremities

    Crusts tend to fall off within about one to two weeks

    Temporary area of hypopigmentation

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    IMMUNOS

    UPPRESSED

    HOS

    TS

    Underlying malignancy

    Steroid use or immunosuppressive therapy

    HIV infection

    Solid organ transplantation

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    Clinical manifestation

    Vesicles > 1 week

    Large and hemorrhagic skin lesions

    Susceptible for disseminated varicella

    Disseminated intravascular coagulation

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    Diagnosis Clinical signs and symptoms

    Tzanck smear Multinucleated giant cell

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    Laboratory testing

    PCR : rapid and sensitive

    Specimen from skin lesion, CSF, BAL, blood

    Direct fluorescent antibody (DFA) active vesicular skin lesions

    Serologic testing :

    protection against subsequent infection.

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    Complication

    Skin/soft tissue infections

    Bacterial skin infections are one of the most

    common complications. Streptococcal or staphylococcal pathogens.

    Invasive group A streptococcal infections :

    cellulitis, myositis/necrotizing fasciitis,

    bacteremia, streptococcal toxic shock syndrome.

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    Complication

    Neurologic complications

    Encephalitis

    Reye syndrome Transient focal deficits

    Aseptic meningitis

    Transverse myelitis

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    Complication: Encephalitis

    Acute cerebellar ataxia : children Complete recovery

    Diffuse encephalitis : adult delirium, seizures, and focal neurologic signs

    20% of varicella-related hospitalizations

    Develop toward the end of the first week

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    Complication

    Pneumonia

    Risk factors : cigarette smoking, pregnancy,

    immunosuppression, and male sex Insidious onset within one to six days :

    progressive tachypnea, dyspnea, and dry cough,hemoptysis

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    Complication

    Hepatitis Asymptomatic or subclinical transaminase

    elevation

    Immunosuppressed hosts including transplantrecipients and AIDS patients

    Acute abdominal or back pain

    Fulminant liver failure with disseminatedintravascular coagulation (DIC) andgastrointestinal hemorrhage

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    THERAPY

    Symptomatictreatment

    Antihistamines : symptomatic treatment of

    pruritis Acetaminophen : treat fever

    Avoid significant excoriation and secondarybacterial infection.

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    THERAPY

    Antiviral therapy Acyclovir: effective for varicella if given during

    the first 24 hours of rash Dose :

    Children : 20 mg/kg PO qid for 5 days

    Adult : 800 mg IV qid for 5 days

    Immunocompromised host: 10 mg/kg IV q 8 hr

    (up to 500 mg IV q 8 hr) for 7 days

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    Children

    Significantly : fewer lesions, reduced the

    number of days of fever

    Developed equivalent antibody responsesto those given placebo.

    No clinically important differences to

    complications

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    Acyclovir should be given

    Older children (greater than 12 years of age)

    Secondary household cases

    History of chronic cutaneous or cardiopulmonarydisorders, since secondary bacterial infectionsmay have severe consequences

    Children taking intermittent oral or inhaled steroidtherapy

    Children taking chronic salicylates. (higher risk ofdeveloping Reye syndrome)

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    Adult

    Most adults have uncomplicated varicella.

    Varicella pneumonia has mortality 10-30%.

    Acyclovir should be initiated within 24 hr ofsymptom onset.

    Acyclovir had no effect on the course of the

    illnessafter 25 - 72 hr

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    Immunocompromised host Mortality rate of 7-14%

    Acyclovir reduced the risk of visceral

    dissemination and severe complications Intravenous acyclovir should be given even

    if > 24 hours

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    Prevention

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    Varicella Vaccine Immunogenicity

    and Efficacy Detectable antibody

    97% of children 12 months-12 years following 1

    dose 99% of persons 13 years and older after 2 doses

    70%-90% effective against any varicella

    disease

    95%-100% effective against severe

    varicella disease

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    Varicella Breakthrough Infection

    Immunity appears to be long-lasting for

    most recipients

    Breakthrough disease much milder than inunvaccinated persons

    No consistent evidence that risk of

    breakthrough infection increases with timesince vaccination

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    Minimum Intervals Between Doses ofV

    aricellaV

    accine 12 months

    through 12 years

    of age 13 years of age or

    older

    3 months

    4 weeks

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    Varicella

    Vaccine

    Adverse

    Reactions

    Local reactions (pain, erythema) 19% (children) 24% (adolescents and adults)

    Rash 3%-4% may be maculopapular rather

    than vesicular average 5 lesions

    Systemic reactions not common

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    Post-exposure prophylaxis

    ASSESSMENTOF EXPOSURE RISK

    Transmission rate 90%

    Negative history of varicella No prior vaccination

    Close indoor contact lasting one hour or more

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    Post-exposure prophylaxis

    Active immunization

    Live attenuated varicella virus vaccines

    Contraindicated for immunocompromised hosts prevention of infection and lessening of disease

    severity

    Ideally administered within 3 days of exposure

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    Post-exposure prophylaxis

    PASSIVE IMMUNIZATION

    Effective in prevention 60%

    Immunosuppressed patients

    Pregnant women

    administered within 96 hours of exposure

    Monitored for varicella for 28 days

    If develop varicella : promp treatment with acyclovir

    vaccine should be given after 5 months have passed

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    Post-exposure prophylaxis

    Varicella zoster immune globulin (VZIG)

    Dose : 125 units/10 kg (max 625 units)

    Intravenous immune globulin (IVIG)

    If VariZIG cannot be administered

    Dose : 400 mg/kg IV once

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    Prevention andcontrol of varicella

    in hospitals

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    IMPORTANCE OF VARICELLAASA

    NOSOC

    OMIAL

    INFECT

    ION Highly contagious

    Associated with serious complications

    Infection in pregnant women may lead tocongenital varicella syndrome

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    Nosocomial exposure to varicella Removal of susceptible staff from patient

    contact following VZV exposures

    Administration of prophylaxis to patientsand employees

    Time and effort of hospital staff inevaluating potential VZV exposures.

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    Prevention

    Employees without a definitive history of

    VZV infection should undergo serologic

    testing. Routine varicella immunization for

    susceptible health care workers.

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    Management of patients exposed toVZV

    Confirm source case has VZV infection.

    Define exposed patient.

    Susceptible patients are placed on airborneprecautions or private negative pressureroom.

    Considered for post-exposure prophylaxis.