Common Stool Studies for Diarrhea
Fresh diarrheal stool samples should be tested for Salmonella, Shigella, Campylobacter, Yersinia, C. difficile, and Shiga toxin-producing E. coli (STEC) in symptomatic patients, with additional testing based on specific risk factors and clinical presentation. 1
Standard Testing Panel
The optimal specimen for laboratory diagnosis is a diarrheal stool sample (one that takes the shape of the container), which provides greater detection rates compared to rectal swabs.
Core Tests:
- Bacterial culture for:
- Salmonella
- Shigella
- Campylobacter
- Yersinia (especially in school-aged children with right lower quadrant pain)
- E. coli O157:H7 (using chromogenic agar)
- Shiga toxin testing (to detect non-O157 STEC serotypes)
- C. difficile toxin testing (for patients >2 years with history of antimicrobial use in the previous 8-12 weeks) 1, 2
Additional Testing Based on Clinical Presentation:
For Bloody Diarrhea:
- Priority testing for STEC (both O157:H7 culture and Shiga toxin)
- Blood cultures (if systemic symptoms present) 1, 2
For Travelers:
- Consider parasitic testing for diarrhea lasting ≥14 days
- Test for C. difficile if antimicrobials were used in the preceding 8-12 weeks 1
For Immunocompromised Patients:
- Broader testing including:
- Cryptosporidium
- Cyclospora
- Cystoisospora
- Microsporidia
- Mycobacterium avium complex
- Cytomegalovirus 1
Special Considerations for Testing
When to Test for Specific Pathogens:
- Vibrio species: For patients with large-volume rice-water stools, exposure to brackish/salt water, consumption of raw shellfish, or travel to cholera-endemic regions 1
- Parasites: For travelers with diarrhea lasting >14 days, standard approach includes microscopic examination of 3 stool samples collected on different days 1
- Blood cultures: For infants <3 months, patients with signs of septicemia, suspected enteric fever, systemic manifestations, immunocompromised patients, or travelers from enteric fever-endemic areas 1
Modern Diagnostic Approaches:
- Multiplex molecular panels: These can detect multiple pathogens (bacterial, viral, and parasitic) simultaneously with higher sensitivity than traditional methods 1, 2
- Molecular testing for parasites: Enzyme immunoassay tests (e.g., Giardia antigen) or nucleic acid amplification tests have largely replaced traditional microscopy in many settings 1
Caveats and Pitfalls
Interpretation challenges: Molecular tests detect DNA, not necessarily viable organisms, which may lead to false positives 1
Unnecessary testing: Routine stool cultures have traditionally been costly and ineffective when used indiscriminately. For hospitalized patients (>3 days), testing for common community pathogens is rarely useful unless there are specific clinical or epidemiological reasons 3
C. difficile testing considerations:
- High rates of asymptomatic colonization in children <2 years make testing results difficult to interpret
- Only test unformed/diarrheal stools (reject formed stool) 1
Specimen quality matters: Fresh stool provides significantly higher detection rates (49%) compared to rectal swabs (9%) for most pathogens 1, 2
Consider non-infectious causes: If initial testing is negative or symptoms persist >14 days, consider conditions like inflammatory bowel disease, irritable bowel syndrome, or bile acid malabsorption 1
By following a targeted approach to stool testing based on clinical presentation and risk factors, clinicians can improve diagnostic yield while reducing unnecessary testing and costs.