Title
Measles Case Laboratory Confirmation Guidelines
Law
Doh Administrative Order No. No. 2012-0003
Decision Date
Feb 8, 2012
The Department of Health establishes guidelines to enhance laboratory confirmation of suspected measles cases, aiming to strengthen surveillance, improve immunization efforts, and achieve the goal of measles elimination in the country.
A

Objectives

  • General: Strengthen laboratory capacity toward measles elimination.
  • Specific:
    • Enhance measles case-based surveillance.
    • Improve detection of rubella through measles surveillance.
    • Evaluate immunization activities on measles and rubella control.
    • Establish dried blood spot (DBS) and nasopharyngeal swab (NPS) as laboratory confirmation methods.
    • Implement standards in collection, handling, storage, and transport of DBS and NPS samples.

Scope and Coverage

  • Applies to entire health sector: public and private health facilities at national and local government levels involved in disease surveillance and response.

Definitions and Abbreviations

  • Case Investigation Form (CIF): Standard epidemiological reporting form.
  • Cluster: Two or more suspected measles cases within 7-21 days and geographically or epidemiologically linked.
  • Contacts: Persons living or in close contact with case during infectious period (5 days before to 5 days after rash onset).
  • Disease Reporting Unit (DRU): Health facilities like hospitals, labs, ports, rural health units.
  • Epidemiologically-linked case: Suspected measles case linked to lab-confirmed case.
  • Immunoglobulin M (IgM): Antibody confirming measles infection.
  • Measles and rubella surveillance units defined (PESU, RESU).
  • Suspected measles case defined by fever, rash, and symptoms like cough or conjunctivitis.

Policies

  • Targets 90% measles mortality reduction and 95% immunization coverage of infants.
  • Follow-up Supplemental Immunization Activities (SIAs) every 3-4 years recommended.
  • Case-based surveillance with laboratory testing essential.
  • Regional action plans and resolutions endorse measles elimination by 2012.
  • Control of congenital rubella syndrome prioritized through MR/MMR vaccines.
  • WHO-UNICEF strategy includes high immunization coverage, a second immunization opportunity, enhanced surveillance, and proper clinical management.

Implementing Mechanism: Laboratory Procedures

  • Laboratory confirms suspected measles by serology (anti-measles IgM), molecular detection, or virus isolation.
  • Serum IgM testing remains the gold standard; one serum specimen to be collected from all suspected cases within 28 days of rash onset.
  • Alternative specimen: Dried Blood Spot (DBS) used where serum collection or specimen storage is difficult.
  • Oropharyngeal/Nasopharyngeal swabs collected within 5 days of rash onset for virus isolation, especially in clusters.
  • Sample collection protocols vary by cluster size to optimize viral isolation.
  • Viral isolation differentiates indigenous vs imported measles transmission.

Roles and Responsibilities

  • Research Institute for Tropical Medicine (RITM): receives and tests specimens, builds lab capacity, collaborates with WHO.
  • National Epidemiology Center (NEC): oversees surveillance implementation, technical support, specimen logistics, data management.
  • Centers for Health Development (CHD): regional coordination, investigation, specimen management, lab result dissemination.
  • Provincial Epidemiology and Surveillance Units (PESU), Provincial Health Office (PHO), and Rural Health Units (RHU): case coordination, data handling, specimen shipping, logistics support.
  • Hospitals: investigate all suspected cases thoroughly, collect and transport specimens properly, maintain documentation.

Funding

  • Laboratory and logistic expenses primarily borne by RITM with DOH and WHO support.
  • Freight and handling costs borne by CHDs in accordance with government accounting rules.

Repealing Clause

  • Previous orders inconsistent with this administrative order are revised, modified, repealed, or rescinded.
  • Other provisions not affected remain valid.

Effectivity

  • The order took effect immediately upon issuance on February 8, 2012, by Secretary of Health Enrique T. Ona, MD.

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