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.

LabMedica

Download Mobile App
Recent News Expo Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Blood Culture Assay Generates Rare False Positives

By LabMedica International staff writers
Posted on 15 Jul 2010
A test kit for detecting methicillin-resistant Staphylococcus aureus (MRSA) can very occasionally give false-negative results.

The assay detects the presence of MRSA and S. aureus (SA) in a Gram-positive culture bottle (GPCB) in less than an hour. Other current culture-based testing methods for GPCB require an additional 18 to 48 hours for determination of MRSA or SA.

The kit is the Xpert MRSA/SA Blood Culture Assay, manufactured by Cepheid (Sunnyvale, CA, USA). The company has issued a voluntary recall due the increased reports of false negatives for MRSA. Cepheid stated that the test does not need to be returned to the company. The Class 1 recall covers all kits made and distributed from October 21, 2008, through June 21, 2010.

The company stresses that the product can still be used and report results of MRSA positive/SA positive as such. However, when customers obtain a result of MRSA negative/SA positive, the company recommends conducting further antimicrobial susceptibility testing using the U.S. Food and Drug Administration (FDA; Rockville, MD, USA) approved methods for an accurate MRSA finding.

Because the test has the rare potential to generate false-negative MRSA results, patients with MRSA infections may receive incorrect treatment or delayed care, according to an alert sent by MedWatch, the FDA's safety information and adverse event reporting program. So far, only one adverse event was reported to the agency through its medical device reporting process.

MRSA and SA are the causative pathogen in up to 35% of severe sepsis cases, which strikes 750,000 people annually in the U.S. Cepheid has identified the emergence of novel MRSA strain types as one cause of the false negatives in an ongoing "failure investigation." The investigation has yet to determine fully the remaining causes of the erroneous results.

Related Links:

Cepheid
FDA



Gold Member
Quality Control Material
iPLEX Pro Exome QC Panel
Collection and Transport System
PurSafe Plus®
New
Gram-Negative Blood Culture Assay
LIAISON PLEX Gram-Negative Blood Culture Assay
Specimen Radiography System
TrueView 200 Pro

Latest Microbiology News

Microfluidic Platform Assesses Neutrophil Function in Sepsis Patients
15 Jul 2010  |   Microbiology

New Diagnostic Method Confirms Sepsis Infections Earlier
15 Jul 2010  |   Microbiology

New Markers Could Predict Risk of Severe Chlamydia Infection
15 Jul 2010  |   Microbiology