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Complete Summary

GUIDELINE TITLE

Updated interim CDC guidance for use of smallpox vaccine, cidofovir, and vaccinia immune globulin (VIG) for prevention and treatment in the setting of an outbreak of monkeypox infections.

BIBLIOGRAPHIC SOURCE(S)

  • Centers for Disease Control and Prevention. Updated interim CDC guidance for use of smallpox vaccine, cidofovir, and vaccinia immune globulin (VIG) for prevention and treatment in the setting of an outbreak of monkeypox infections. Atlanta (GA): Centers for Disease Control and Prevention; 2003 Jun 25. 7 p. [14 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Centers for Disease Control and Prevention. Interim guidance for use of smallpox vaccine, cidofovir, and vaccinia immune globulin (VIG) for prevention and treatment in the setting of an outbreak monkeypox infections. Atlanta (GA): Centers for Disease Control and Prevention; 2003 Jun 12. 6 p.

COMPLETE SUMMARY CONTENT

 
SCOPE
 METHODOLOGY - including Rating Scheme and Cost Analysis
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 BENEFITS/HARMS OF IMPLEMENTING THE GUIDELINE RECOMMENDATIONS
 CONTRAINDICATIONS
 IMPLEMENTATION OF THE GUIDELINE
 INSTITUTE OF MEDICINE (IOM) NATIONAL HEALTHCARE QUALITY REPORT CATEGORIES
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

SCOPE

DISEASE/CONDITION(S)

Monkeypox infection

GUIDELINE CATEGORY

Management
Prevention
Treatment

CLINICAL SPECIALTY

Family Practice
Infectious Diseases
Internal Medicine
Pediatrics
Preventive Medicine

INTENDED USERS

Advanced Practice Nurses
Allied Health Personnel
Health Care Providers
Nurses
Physician Assistants
Physicians
Public Health Departments

GUIDELINE OBJECTIVE(S)

To provide guidance on the use of smallpox vaccine, cidofovir and vaccinia immune globulin (VIG) for purposes of monkeypox outbreak control

TARGET POPULATION

Adults and children diagnosed with or exposed to monkeypox including:

  • Investigators of suspected human and animal monkeypox
  • Health care workers
    • caring for confirmed monkeypox cases or recently involved in such care
    • selected to care for suspected monkeypox patients
  • Clinical laboratory workers
  • Close contacts, household contacts and others who have had close or intimate contact with confirmed human cases, and who are within 4 days of initial direct exposure to a monkeypox case
  • Persons who have been exposed to a recently acquired prairie dog or other small mammals from implicated distributors

INTERVENTIONS AND PRACTICES CONSIDERED

  1. Smallpox vaccine (available under an investigational new drug [IND] protocol sponsored by CDC)
  2. Vaccinia immune globulin (considered but not recommended)
  3. Cidofovir (considered only for life-threatening monkeypox infections)

MAJOR OUTCOMES CONSIDERED

  • Efficacy of smallpox vaccination for prevention of monkeypox
  • Risk of death from smallpox vaccine

METHODOLOGY

METHODS USED TO COLLECT/SELECT EVIDENCE

Searches of Electronic Databases

DESCRIPTION OF METHODS USED TO COLLECT/SELECT THE EVIDENCE

Not stated

NUMBER OF SOURCE DOCUMENTS

Not stated

METHODS USED TO ASSESS THE QUALITY AND STRENGTH OF THE EVIDENCE

Not stated

RATING SCHEME FOR THE STRENGTH OF THE EVIDENCE

Not applicable

METHODS USED TO ANALYZE THE EVIDENCE

Review

DESCRIPTION OF THE METHODS USED TO ANALYZE THE EVIDENCE

Not stated

METHODS USED TO FORMULATE THE RECOMMENDATIONS

Not stated

RATING SCHEME FOR THE STRENGTH OF THE RECOMMENDATIONS

Not applicable

COST ANALYSIS

A formal cost analysis was not performed and published cost analyses were not reviewed.

METHOD OF GUIDELINE VALIDATION

Peer Review

DESCRIPTION OF METHOD OF GUIDELINE VALIDATION

Not stated

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Note: Because of the potential seriousness of this disease, the Centers for Disease Control and Prevention (CDC) has developed interim guidance to balance the risks of smallpox vaccination against the risks posed by exposure to monkeypox infection. This interim guidance will be re-evaluated as more information becomes available.

Smallpox vaccine for controlling outbreaks of monkeypox would be available under an investigational new drug (IND) protocol sponsored by CDC.

General Recommendations

It is important that vaccinators, as currently occurs in the pre-event smallpox vaccination program, screen potential vaccinees for precautions and contraindications to smallpox vaccination and evaluate vaccination sites for a successful vaccination (i.e., a major reaction at the site 6-8 days after vaccination). Persons without a successful vaccine take should be revaccinated within 2 weeks of the most recent exposure to monkeypox. State and local health departments should provide information on how vaccinees should seek consultation on evaluation of vaccination sites for major reactions or for potential complications of vaccination.

Rash illnesses suspected to be monkeypox should be confirmed by laboratory evaluation, which, in addition to determining the presence of monkeypox, should have the capability to detect varicella, vaccinia and other relevant viruses. Laboratory confirmation of monkeypox cases is particularly important before recommending vaccination to persons with close or intimate contact with a monkeypox case and considered to have contraindications to smallpox vaccination in the pre-event smallpox vaccination (e.g., pregnant women, persons with eczema, and children aged <1 year). Intimate contact refers to contact resulting in exposure to body fluids or lesions of ill persons or ill animals. The period of communicability (i.e., exposure period for contacts) for humans may be from 1 day before onset of rash up to 21 days after rash or illness onset or when all rash lesions have scabbed over. The period of communicability (i.e., exposure period for contacts) for animals may be from 1 day before onset of illness up to 21 days after rash or illness onset or when the ill animal is removed from possible exposure with the contact, or when the animal’s clinical illness ends and all rash lesions have scabbed over. As general guidance, for purposes of smallpox exposure (for human-to-human transmission), close contact has been defined as >3 hours of direct (face-to-face) exposure within 6 feet; this is reasonable guidance for exposure to monkeypox from humans as well. In animal care settings, close contact has been defined as direct exposure within 6 feet of an animal suspected to have monkeypox with respiratory symptoms such as nasal discharge, cough, or conjunctivitis in a setting where the animal has been manipulated (e.g., an exam room). However, judgment must be applied to determine the significance of contact in individual exposure situations.

Who Should be Vaccinated?

Vaccination sites should be managed as recommended for HCWs in the pre-event smallpox vaccination program. Persons who care for recently vaccinated children should be particularly vigilant to observe recommended standard and contact infection control precautions with the vaccination site. Persons without a vaccine take by day 7 should only be revaccinated if within 2 weeks of most recent exposure.

  • Persons who have been exposed to a recently acquired prairie dog or other small mammals from implicated distributors

    Smallpox vaccination should be recommended for persons who have, within the past 4 days, had direct physical (intimate) contact with ill prairie dogs or other ill small mammals meeting the probable or confirmed case definitions for monkeypox from implicated distributors acquired since April 15 within the affected areas. The interim case definition for animal cases of monkeypox. Vaccination should be considered for persons who are within 2 weeks of most recent exposure. In addition, vaccination can be considered for persons who have close contact with an ill animal that meets the probable or confirmed animal case definition. Close contact is defined as direct exposure within 6 feet of a probable or confirmed monkeypox case in an animal with respiratory symptoms such as nasal discharge, cough, or conjunctivitis in a setting where the animal has been manipulated (e.g., an exam room). Smallpox vaccination is not recommended for persons exposed to a healthy animal.

These recommendations may change should evidence show that other symptomatically ill small mammals pose significant risk for human monkeypox.

Vaccination sites should be managed as recommended for HCWs in the pre-event smallpox vaccination program. Persons who care for recently vaccinated children should be particularly vigilant to observe recommended standard and contact infection control precautions with the vaccination site. Persons without a vaccine take by day 7 should only be revaccinated if within 2 weeks of most recent exposure.

Veterinary health care workers should observe recommended infection control practices including use of personal protective equipment when appropriate, even if vaccinated. It is anticipated that fit-tested N95 respirators will not be available in most veterinary facilities; when currently N95 or comparable respirators are unavailable, surgical masks should be worn to protect against transmission through contact or large droplets. Exposed veterinarians and staff without N95 (or comparable) respirator protection who have direct or close contact to animals with monkeypox should be vaccinated according to the guidelines. Interim guidance for infection control and exposure management in the health-care and community setting for patients with possible monkeypox virus infection.

Interim guidance on appropriate handling of routine clinical laboratory specimens from animals suspected or confirmed to be infected with monkeypox.

Contraindications to Smallpox Vaccination (Refer to the "Contraindications" field)

Vaccinia Immune Globulin (VIG)

No data are available on the effectiveness of VIG in treatment of monkeypox complications. VIG has no proven benefit in the treatment of smallpox complications. It is unknown whether a person with severe monkeypox infection will benefit from treatment with VIG, however, its use may be considered in such instances. VIG can be considered for prophylactic use in an exposed person with severe immunodeficiency in T-cell function for whom smallpox vaccination following exposure to monkeypox is contraindicated.

Cidofovir

No data are available on the effectiveness of cidofovir in treatment of human monkeypox cases. However, cidofovir has proven anti-monkeypox viral activity in in vitro and in animal studies. It is unknown whether a person with severe monkeypox infection will benefit from treatment with cidofovir, however, its use may be considered in such instances. Cidofovir has significant toxicity and should only be considered for treatment of severe monkeypox infections, not for prophylactic use.

Clinical consultation on the use of VIG and cidofovir is available from staff at each state health department in the affected states. In addition, clinical consultation is available from staff at the CDC.

Vaccination of Veterinarians, Veterinary and Animal Control Staff

Similar to health care workers, at this time pre-exposure smallpox vaccination is not recommended for unexposed veterinarians, veterinary staff, and animal control officers in the affected areas, but routine use of appropriate standard, contact and air-borne infection control measures should be stressed.

Persons who may be involved in field investigations involving potentially infected animals should be vaccinated in advance. This recommendation will be re-evaluated as more information becomes available.

Laboratory workers (e.g., veterinary pathologists) at designated reference laboratories who handle specimens from ill prairie dogs or other ill small mammals meeting the probable or confirmed case definitions for monkeypox from implicated distributors acquired since April 15 within the affected states should be vaccinated as recommended for field investigators or health care workers anticipated to have future contact with suspected monkeypox cases.

Reporting of Adverse Events Associated with Smallpox Vaccination

Serious adverse events after smallpox vaccination should be reported to the Vaccine Adverse Event Reporting System (VAERS). Refer to the original guideline document for details.

CLINICAL ALGORITHM(S)

Not applicable

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is not specifically stated. In most instances, only limited data are available on which to directly base recommendations and thus the guidance is primarily based on expert opinion. This interim Centers for Disease Control and Prevention (CDC) guidance was developed using the best available information about the benefits and risks of smallpox vaccination, vaccinia immune globulin and cidofovir for prevention and/or management of smallpox, monkeypox and complications of vaccinia infection.

BENEFITS/HARMS OF IMPLEMENTING THE GUIDELINE RECOMMENDATIONS

POTENTIAL BENEFITS

Limited information is available on efficacy of smallpox vaccination for prevention of monkeypox. The data suggest that pre-exposure smallpox vaccination is highly effective (>85%) in protecting persons exposed to monkeypox from disease. No information is available on the efficacy of post-exposure vaccination. Data which suggest smallpox vaccination following exposure to smallpox is effective in preventing or ameliorating disease, suggest that post-exposure smallpox vaccination should have similar impact against monkeypox. Data from investigations in Africa in the 1980s suggested that in household settings, secondary transmission occurred to about 8% to 15% of contacts. Among infected human cases, reported mortality rates have ranged from 1% to 10%, the risk of death from smallpox vaccine is estimated to be 1-2 per million vaccinees.

POTENTIAL HARMS

  • Complications of smallpox vaccination
  • Cidofovir has significant toxicity and should only be considered for treatment of severe monkeypox infections, not for prophylactic use.

CONTRAINDICATIONS

CONTRAINDICATIONS

The nature of exposure should be assessed carefully for health care workers (HCWs), household, close or intimate contacts who have been exposed within the past 2 weeks to a probable or confirmed animal case or confirmed human case of monkeypox, but who have contraindications to smallpox vaccine receipt in the pre-event smallpox setting. If there are difficulties in obtaining rapid laboratory confirmation, the state health department should be urgently consulted. The risk of monkeypox disease for persons with a close or intimate exposure to confirmed monkeypox cases is believed to be greater than the risk of adverse events resulting from vaccinia exposure for most persons for whom smallpox vaccination would be otherwise contraindicated in the pre-event smallpox vaccination setting. In the post-exposure setting, the benefit of vaccination outweighs the risk of vaccination. In this setting, most contraindications are considered precautions to vaccination. In persons with close or intimate exposure within the past 2 weeks to a confirmed human case or probable or confirmed animal case of monkeypox, neither age, pregnancy, nor a history of eczema are contraindications to receipt of smallpox vaccination. These conditions are precautions and not contraindications. Active eczematous disease is more concerning, but in instances when the potential vaccinee has had true close or intimate exposure, the risk of contracting monkeypox would likely still be greater than the risk of complications of smallpox vaccination. Appropriate site care should be used to prevent transmission of smallpox vaccine (vaccinia virus) from vaccinated persons to other non-vaccinated household members.

Smallpox vaccination is still contraindicated for:

  1. Persons who have severe immunodeficiency in T-cell function, defined as:
    • Human immunodeficiency virus (HIV)-infected adults with CD4 lymphocyte count less than 200 (or age appropriate equivalent counts for HIV infected children);
    • Solid organ, bone marrow transplant recipients or others currently receiving high dose immunosuppressive therapy (i.e., 2 mg/kg body weight or a total of 20 mg/day of prednisone or equivalent for persons whose weight is > 10 kg, when administered for > 2 weeks); and
    • Persons with lymphosarcoma, hematological malignancies, or primary T-cell congenital immunodeficiencies.
  2. Persons with life-threatening allergies to latex or to smallpox vaccine or any of its components (polymyxin B, streptomycin, chlortetracycline, neomycin).

These persons have a risk of severe complications from smallpox vaccination that may approach or exceed the risk of disease from monkeypox exposure. Consultation with state and local health departments and the Centers for Disease Control and Prevention (CDC) should be sought regarding judgments about vaccination of such persons in the post-exposure setting.

IMPLEMENTATION OF THE GUIDELINE

DESCRIPTION OF IMPLEMENTATION STRATEGY

An implementation strategy was not provided.

IMPLEMENTATION TOOLS

Patient Resources

For information about availability, see the "Availability of Companion Documents" and "Patient Resources" fields below.

INSTITUTE OF MEDICINE (IOM) NATIONAL HEALTHCARE QUALITY REPORT CATEGORIES

IOM CARE NEED

Getting Better
Staying Healthy

IOM DOMAIN

Effectiveness

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Centers for Disease Control and Prevention. Updated interim CDC guidance for use of smallpox vaccine, cidofovir, and vaccinia immune globulin (VIG) for prevention and treatment in the setting of an outbreak of monkeypox infections. Atlanta (GA): Centers for Disease Control and Prevention; 2003 Jun 25. 7 p. [14 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2003 Jun 12 (revised 2003 Jun 25)

GUIDELINE DEVELOPER(S)

Centers for Disease Control and Prevention - Federal Government Agency [U.S.]

SOURCE(S) OF FUNDING

United States Government

GUIDELINE COMMITTEE

Not stated

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Not stated

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Centers for Disease Control and Prevention. Interim guidance for use of smallpox vaccine, cidofovir, and vaccinia immune globulin (VIG) for prevention and treatment in the setting of an outbreak monkeypox infections. Atlanta (GA): Centers for Disease Control and Prevention; 2003 Jun 12. 6 p.

GUIDELINE AVAILABILITY

Electronic copies: Available from the Centers for Disease Control and Prevention (CDC) Web site.

Print copies: Available from the Centers for Disease Control and Prevention, MMWR, Atlanta, GA 30333. Additional copies can be purchased from the Superintendent of Documents, U.S. Government Printing Office, Washington, DC 20402-9325; (202) 783-3238.

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

The following are available:

  • Fact sheets: basic information about monkeypox. Atlanta (GA): Centers for Disease Control and Prevention (CDC); 2003 Jun 12. 2 p.
  • Questions and answers about monkeypox. Atlanta (GA): Centers for Disease Control and Prevention (CDC); 2003 Jul 7. 4 p.
  • What pet owners should know about monkeypox. Atlanta (GA): Centers for Disease Control and Prevention (CDC); 2003 Jun 27. 4 p.
  • What pet shop owners should know about monkeypox. Atlanta (GA): Centers for Disease Control and Prevention (CDC); 2003 Jun 27. 4 p.
  • What you should know about monkeypox. Atlanta (GA): Centers for Disease Control and Prevention (CDC); 2003 Jun 12. 2 p.
  • Smallpox vaccine and monkeypox. Atlanta (GA): Centers for Disease Control and Prevention (CDC); 2003 Jul 7. 2 p.

Electronic copies of these and other related materials are available from the CDC Web site.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This summary was completed by ECRI on June 23, 2003. It was updated by ECRI on July 8, 2003. The information was not verified by the guideline developer.

COPYRIGHT STATEMENT

No copyright restrictions apply.

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