Table 3.
Comparison of Laboratory Diagnostic Tests for Amebiasis
| Method | Sensitivity, % [Reference] | Specificity, % [Reference] |
Advantages | Disadvantages |
|---|---|---|---|---|
| Microscopy | <60% [4] | - | Widely available | Poor sensitivity and specificity; cannot differentiate from other Entamoeba spp. |
| Screens for other parasites | Multiple stools need to be submitted | |||
| Minimal equipment and reagents required | Skilled observer required; time-consuming | |||
| Serology | 65%–92% [16] | >90% [16] | High sensitivity and specificity, useful adjunct to stool studies | Serology remains positive for years after resolution of infection, so less helpful in endemic areas; more useful in travelers |
| Rapid turnaround | Antibody response is often detectable by the time of presentation but may need to be repeated in 7–10 days if initially negative | |||
| Stool antigen detection | 0%–88% [42] | >80% [42] | May have high sensitivity in endemic areas but reduced sensitivity in nonendemic areas | Poor sensitivity for amebic liver abscess |
| Simple to perform, rapid turnaround time, and commercially available combined tests exist to detect several enteroparasites | Requires fresh, not fixative preserved stool for analysis | |||
| PCR | 92%–100% [42] | 89%–100% [42] | Gold standard; high sensitivity and specificity for colitis and liver abscess with increasing availability | More expensive; cost may limit use in resource-limited settings |
| Rapid turnaround; automated systems reduce technician time and risk of contamination | Requires analysis instruments, kits, and skilled technician | |||
| Can be combined with multiplex panels to detect multiple enteric pathogens at a time |
Abbreviation: PCR, polymerase chain reaction.