Immunoassay for Clostridium difficile toxins A and B. Requests with only a written order and no test number indicated will be processed according to Default Testing for Routine Microbiology.
A separate specimen is required for culture or for the toxin B cytotoxin assay.
1 - 2 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
For more information, please view the literature below.
0.5 g or 0.5 mL liquid stool
Sterile screw-cap container or stool transport (Para-Pak® white clean vial), no preservative. “Cool Whip” containers, denture cups, or other similar containers often leak or even explode during transport and may be rejected by the laboratory.
Specimen should be kept refrigerated and transported to the laboratory within 24 hours of collection. If a longer period is required, the specimen should be frozen at -20°C or lower.
Up to 72 hours from collection (stability provided by manufacturer or literature reference)
After 72 hours (stability provided by manufacturer or literature reference)
Specimens from patients less than two years of age; inappropriate specimen transport conditions (eg, room temperature) or transport device; unlabeled specimen or name discrepancy between specimen and request label; specimen received after prolonged delay (usually more than 72 hours); specimens other than stool; leaking specimen; specimen received in denture cup, "Cool Whip" container, margarine container, or similar container
Aid in the diagnosis of antibiotic-associated diarrheal disease and pseudomembranous colitis
Detection of toxins A and B by enzyme immunoassay has a sensitivity approaching 90%, so multiple specimens may need to be tested. Performance characteristics have not been established in a pediatric population.
Enzyme immunoassay (EIA) for Clostridium difficile toxins A and B
C difficile can produce two toxins, designated A and B, that have pathogenic effects in humans. Antibiotic-associated pseudomembranous colitis has been shown to result from the action of these two toxins. This disease has been associated with clindamycin use but it is now recognized that pseudomembranous colitis can follow administration of virtually any antibiotic. More than 70% of the cases in a large series were associated with cephalosporin therapy.1 The clinical spectrum of antibiotic-induced syndromes caused by C difficile includes patients with symptoms of acute abdomen with little or no diarrhea, as well as cases with fulminant life-threatening diarrhea. Nosocomial transmission and reinfection with different strains occurs as do spontaneous cases without prior antimicrobial therapy. In cases where cessation of antibiotic therapy does not produce a response, specific therapy with oral vancomycin, metronidazole, or oral bacitracin may be effective. Detection of the toxins produced by C difficile (rather than culture of the organism) is important in the determining therapy of this potentially fatal disease. The routine use of culture does not seem appropriate because of the costs and the high rate of recovery of strains which do not produce toxin.
|Order Code||Order Code Name||Order Loinc||Result Code||Result Code Name||UofM||Result LOINC|
|086207||C difficile Toxins A+B, EIA||34468-9||182238||C difficile Toxins A+B, EIA||34468-9|
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