Techniques | Criteria | Advantages | Limitations | References | |||||
---|---|---|---|---|---|---|---|---|---|
Simple to perform | Simple to interpret | Specimen type | Turnaround time | Sensitivity (%) | Specificity (%) | ||||
TC | Good | Good | Stool | 2-7 days | High | Low | Due to its high sensitivity, it is recommended as a reference method; it allows performing strain typing and antimicrobial suitability test | Long turnaround time; need to be combined with another method | 8,18,85 |
CTA | Fair | Good | Stool filtrate | 48-72 hours | High | High | Has acceptable sensitivity and specificity, and it is inexpensive | Labor-intensive, long turnaround time, and lack of harmonization | 18,85,86 |
EIA for detecting GDH | Good | Good | Stool | Rapid 2-6 hours | Low | Low | Quick to produce results, and simple to use | Lacks specificity, high false-positive rate, and should be used in combination with another method | 8,18,85,87 |
EIA for detecting toxins A or B | Good | Good | Stool | Rapid 2-6 hours | Low | Moderate | Quick to produce results, and simple to use | Insensitive enough in the detection of toxin-producing isolates of C. difficile in comparison to other techniques such as TC or CTA. High false-negative rate | 8,18,85,87 |
NAAT | Good | Good | Stool | Rapid 2 hours | High | Low/moderate | Rapid and highly sensitive | Identify carriers of toxigenic C. difficile who have no symptoms. Genetic variation in tcdB or tcdA genes might lead to false-negative results. Expensive | 8,85,87,90 |
TC: toxigenic culture, CTA: cell cytotoxicity assay, GDH: glutamate dehydrogenase, NAAT: nucleic acid amplification test, EIA: enzyme immunoassay