09/26/2024 ÐÇ¿ÕÓéÀÖ¹ÙÍø Issues Alert for Prevention Strategies for U.S. Travelers Visiting Countries with Clade I Mpox Outbreaks

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  • Level: Laboratory Advisory
  • Audience: Clinical Laboratory Professionals
LOCS: Laboratory Outreach Communication System

Prevention strategies for U.S. travelers

On September 23, 2024, the U.S. Centers for Disease Control and Prevention (ÐÇ¿ÕÓéÀÖ¹ÙÍø) issued a about the ongoing outbreak of clade I monkeypox virus (MPXV). Initial HAN messages about clade I mpox outbreaks were issued via HAN in December 2023 and HAN in August 2024.

Although there is an ongoing that began in 2022, no domestic cases of clade I mpox have been identified in the U.S. at this time. Active monitoring for mpox continues to occur in the United States. Follow ÐÇ¿ÕÓéÀÖ¹ÙÍø's to protect against clade II MPXV infection and to also protect against clade I MPXV.

For all laboratories performing mpox testing using an orthopoxvirus or monkeypox virus (MPXV) generic test without any additional clade-specific testing occurring, ÐÇ¿ÕÓéÀÖ¹ÙÍø recommends that laboratories send clinical specimens collected from patients who traveled from the Democratic Republic of the Congo, its neighboring countries, or any country with clade I mpox cases, or had close or intimate contact with symptomatic people from these countries, to a laboratory that can perform clade-specific testing as quickly as possible. If clade-specific testing is warranted but is not available in a jurisdiction, to a capable public health laboratory or to ÐÇ¿ÕÓéÀÖ¹ÙÍø is encouraged. Specimen submission to ÐÇ¿ÕÓéÀÖ¹ÙÍø can be coordinated through your . Due to mutations that may impact clade-specific PCR tests, laboratories should use a test that targets a viral essential gene (e.g., the ÐÇ¿ÕÓéÀÖ¹ÙÍø NVO test) as part of a testing strategy to ensure mpox cases are not missed.

Laboratories using ÐÇ¿ÕÓéÀÖ¹ÙÍø's non-variola orthopoxvirus (NVO) test should continue submitting the duplicate specimen to ÐÇ¿ÕÓéÀÖ¹ÙÍø from all patients with positive NVO test results for routine MPXV clade-specific testing if they are not performing clade-specific testing in their laboratory. Specimens that cannot be accepted at ÐÇ¿ÕÓéÀÖ¹ÙÍø for clinical testing under Clinical Laboratory Improvement Amendments (CLIA) will be redirected for surveillance purposes and tested, providing critical data on MPXV clade(s) circulating in the United States. Some non-ÐÇ¿ÕÓéÀÖ¹ÙÍø laboratories may have other options available for clade-specific testing (e.g., molecular testing or genetic sequencing). These laboratories should alert their and ÐÇ¿ÕÓéÀÖ¹ÙÍø ([email protected]) if results from such tests indicate detection of clade I MPXV.

Please review the HAN for more information, including recommendations for clinicians and public health practitioners, travelers, and the public.

We encourage you to share this message widely with your network(s).

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The Laboratory Outreach Communication System

Laboratory Outreach Communication System (LOCS) | Division of Laboratory Systems (DLS)

Center for Laboratory Systems and Response (CLSR)

Centers for Disease Control and Prevention (ÐÇ¿ÕÓéÀÖ¹ÙÍø)

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