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Supplement F: Laboratory Guidance

Public Health Guidance for Community-Level Preparedness and Response to Severe Acute Respiratory Syndrome (SARS) Version 2/3*

NOTICE

Since 2004, there have not been any known cases of SARS reported anywhere in the world. The content in this Web site was developed for the 2003 SARS epidemic. But, some guidelines are still being used. Any new SARS updates will be posted on this Web site.

Contents of this Section

Title

Section PDF

Summary
I. Rationale and Goals
II. Lessons Learned
III. Diagnostic Assays
IV. CDC’s Laboratory Diagnostics Plan
Appendix F1: Proficiency Testing for Public Health Laboratories Performing SARS-CoV EIA and RT-PCR Diagnostics
Appendix F2: SARS-CoV Specimen Testing Guidelines: RT-PCR and Serology
Appendix F3: Guidelines for Clinicians: The Consent Process for SARS-CoV RT-PCR and EIA Testing at CDC and Public Health Laboratories
Appendix F4: Guidelines for Collecting Specimens from Potential SARS Patients
Appendix F5: Laboratory Biosafety Guidelines for Handling and Processing Specimens Associated with SARS-CoV
Appendix F6: Guidelines for Medical Surveillance of Laboratory Personnel Working with SARS-CoV
Appendix F7: Fact Sheet for Clinicians: Interpreting SARS-CoV Test Results from CDC and Other Public Health Laboratories
Appendix F8: Guidelines for Laboratory Diagnosis of SARS-CoV Infection

Footnote *


This version of Supplement F includes additional guidance on the types of specimens to collect for SARS-CoV testing and the optimal timing for collection. Three new appendices have been included:

  • Appendix F3: Guidelines for Clinicians: The Consent Process for SARS-CoV RT-PCR and EIA Testing at CDC and Public Health Laboratories
  • Appendix F6: Guidelines for Medical Surveillance of Laboratory Personnel Working with SARS-CoV
  • Appendix F8: Guidelines for Laboratory Diagnosis of SARS-CoV Infection

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