Advantages |
Excellent sensitivity (0.01–1/μL depending on method and expertise) |
Earlier detection of new infections (up to four days before blood smears) |
Quantification across a wide range of parasite densities |
Species identification |
Potential for strain identification to distinguish new and recrudescent infections |
Samples can be batched for high throughput |
Disadvantages |
Can be time consuming |
Expensive |
Extensive training required |
Mixed infections require more elaborate assay designs and can undermine some assays |
Standardization is complicated (across multiple sites, various assay platforms) |
Requires provisions to avoid cross-contamination of samples |