Management of Smallpox Vaccine Adverse Events Department of Health and Human Services Centers for Disease Control and Prevention February 2003.

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Presentation transcript:

Management of Smallpox Vaccine Adverse Events Department of Health and Human Services Centers for Disease Control and Prevention February 2003

Management of Smallpox Vaccine Adverse Events Learning Objectives: – Describe the treatment and management of vaccinia adverse events (AEs) – Describe the use of Vaccinia Immune Globulin (VIG) and Cidofovir

Adverse Events Associated with Smallpox Vaccine Inadvertent inoculation Ocular vaccinia Generalized vaccinia Eczema vaccinatum Progressive vaccinia Post-vaccinial Encephalopathy Encephalomyelitis Fetal Vaccinia

Local Skin Reactions Irritation from Adhesive Dressing

Non-Specific Rashes Erythematous Patches

Dermatologic Manifestations of Hypersensitivity Reactions Erythema Multiforme

Dermatologic Manifestations of Hypersensitivity Reactions Stevens-Johnson Syndrome

Vaccinia Specific Adverse Events Inadvertent Inoculation

Vaccinia Specific Adverse Events Keratitis

Manage in consult with ophthalmologist Consider off-label use of topical ophthalmic trifluridine or vidarabine Balance with risk of drug toxicity Continue until periocular and/or lid lesions heal and scabs fall off Treatment of Ocular Infections Guidance for Clinicians

Consider VIG when keratitis NOT present Useful with severe blepharitis or blepharoconjunctivitis Weigh risks and benefits if keratitis present Use VIG for other severe vaccinia disease, even if keratitis present Consider prophylaxis against bacterial infection Enroll in studies Treatment of Ocular Infections Guidance for Clinicians

Prevention of Contact Transmission Proper hand-hygiene Healthcare Setting – Cover with gauze – Cover gauze with semi-permeable dressing – Until scab separates Non-Healthcare Setting – Cover with gauze – Wear sleeve over site

Generalized Vaccinia

Eczema Vaccinatum

Progressive Vaccinia

Post-Vaccinial Encephalitis Diagnostic and Management None for specific diagnosis of PVE Diagnosis of exclusion – Consider other infectious or toxic etiologies 15-25% mortality rate 25% varying neurological deficits VIG not recommended

Fetal Vaccinia

Prophlyaxis of High-Risk Groups Accidentally Exposed VIG NOT recommended Vigilant clinical follow-up Do NOT administer VIG with smallpox vaccine Exclude those with contraindications

Vaccinia Immune Globulin Immunoglobulin fraction of plasma Antibodies to vaccinia from vaccinated donors Previously-licensed IM product (Baxter) – Contains 0.01% thimerosal New IV products in production Obtain as IND product through CDC and DoD

Vaccinia Immune Globulin Indications RecommendedInadvertent Inoculation - severe Eczema vaccinatum Generalized vaccinia – severe or underlying illness Progressive vaccinia Not Recommended Inadvertent Inoculation – Not severe Generalized vaccinia – mild or limited Non-specific rashes, EM, SJS Post-vaccinial encephalitis ConsiderOcular complications

Vaccinia Immune Globulin Side Effects - Mild Local Pain Tenderness Swelling Erythema From few hours to 1 or 2 days

Vaccinia Immune Globulin Side Effects - Moderate Joint Pain Diarrhea Dizziness Hyperkinesis Drowsiness Pruritis Rash Perspiration Vasodilation

Vaccinia Immune Globulin Contraindications Allergic reaction to thimerosal History of severe reaction with IG preparations IgA Deficiency Vaccinia keratitis, except in some cases Pregnancy Theoretical risks as with all human plasma

VIG Administration VIG-IM 0.6ml/kg IM, preferably in buttock or anterolateral aspect of thigh Divide doses > 5ml Refer to package insert

Cidofovir Nucleotide analogue of cytosine Some antiviral activity against orthopoxviruses Administer under IND protocol, only Released by CDC and DoD if: – No response to VIG – Patient near death – All inventories of VIG exhausted

Cidofovir Side Effects Renal toxicity Neutropenia Proteinuria Decreased intraocular pressure Anterior uveitis/iritis Metabolic acidosis

Cidofovir Admin 5 mg/kg IV over 60 minute period Consider 2nd dose one week later if no response Adjust dose for renal function Assess baseline and post-admin renal function IV hydration (1L of 0.9% saline IV) 3 doses oral probenicid (25 mg/kg per dose)

For More Information CDC Smallpox website National Immunization Program website