We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us

Download Mobile App




Update on Diagnostic Testing for SARS

By HospiMedica staff writers
Posted on 11 Jun 2003
Guidelines on diagnostic testing for severe acute respiratory syndrome (SARS) have been issued by the US Centers for Disease Control and Prevention (Atlanta, GA, USA).

According to these guidelines, initial diagnostic testing should include chest radiograph, pulse oximetry, blood cultures, sputum Gram's stain and culture, and testing for viral respiratory pathogens, notably influenza A and B and respiratory syncytial virus. More...
A specimen for Legionella and pneumococcal urinary antigen testing should also be considered. Clinicians should save any available clinical specimens (respiratory, blood, serum) for additional testing until a specific diagnosis is made. Acute and convalescent (more than 21 days after onset of symptoms) serum samples should be collected from each patient diagnosed with SARS.

The CDC recommends that clinicians evaluating suspected cases use standard precautions (including hand hygiene) together with airborne (e.g., N-95 respirator) and contact (gowns and gloves) precautions. Until the mode of transmission has been defined more precisely, eye protection should also be worn for all patient contact.

Assays for laboratory diagnosis of SARS-CoV (coronavirus) infection include enzyme-linked immunosorbent assay (ELISA), indirect fluorescent-antibody assay, and reverse transcription polymerase chain reaction (RT-PCR) assays of appropriately collected specimens. However, warns the CDC, the absence of SARS-CoV antibody from serum obtained less than 21 days after illness onset, a negative PCR test, or a negative viral culture does not exclude coronavirus infection and is not considered a definitive laboratory result. In these cases, a convalescent serum specimen obtained more than 21 days after illness is needed to determine infection.

All SARS diagnostic assays are still under evaluation and none has been approved for a number of reasons. In the first days of illness, SARS patients produce only a small amount of the virus, unlike other viruses. This means a test has to be very sensitive. Also, before any test can be reliable, it has to be tested on many specimens known to contain the virus in order to be certain it is accurate. In the meantime, the CDC is offering an experimental PCR-based diagnostic test for SARS to about 100 specialized US laboratories around the country to gauge the effectiveness of the test. Patients will be asked to provide written consent before testing.

"The quick reaction to SARS by the CDC, at the global level, has been exceptional,” said Jared Schwartz, M.D., Ph.D., secretary-treasurer of the College of American Pathologists. "This most recent announcement of an experimental polymerase chain reaction (PCR) diagnostic test for SARS illustrates the CDC's aggressive reaction to this emerging disease.”




Related Links:
Centers for Disease Control

Gold Member
Handheld Blood Glucose Analyzer
STAT-Site
Radiology Monitor
MDNC-6121 Barco Nio Color 5.8MP
Hypodermic Syringe
SurTract™ Safety Syringe
Medical-Grade Display
HL2316SHTB
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to HospiMedica.com and get access to news and events that shape the world of Hospital Medicine.
  • Free digital version edition of HospiMedica International sent by email on regular basis
  • Free print version of HospiMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of HospiMedica International in digital format
  • Free HospiMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Critical Care

view channel
Image: The new, inexpensive stick-on sweat sensor measures lipid levels, offering a noninvasive way to continuously monitor cholesterol and triglycerides. (Image Credit: California Institute of Technology)

Wearable Patch Enables Continuous Noninvasive Cholesterol and Triglyceride Monitoring

Cholesterol and triglyceride testing typically relies on phlebotomy and intermittent lipid panels, limiting real-time assessment of cardiovascular and metabolic risk. Noninvasive monitoring could reduce... Read more

Surgical Techniques

view channel
Image: Phasix Mesh is a fully resorbable monofilament scaffold designed for rapid tissue incorporation, combining synthetic mesh repair strength with biologic graft-like remodeling. (Photo courtesy of BD)

Resorbable Mesh Evaluated to Prevent Incisional Hernias After Abdominal Surgery

Incisional hernia is a common complication after abdominal surgery and can necessitate additional interventions and prolonged recovery. Preventive strategies remain limited, and there are currently no... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.