Ova and Parasite (O&P) Examinations
Introduction |
Macroscopic |
Microscopic |
Microscopic Examination - Ova and Parasite Examination
Introduction |
Direct Wet Smear |
Concentration |
Permanent Stained Smear
Permanent Stained Smear
Introduction |
Trichrome Stain |
Iron Hematoxylin Stain |
Modified Iron Hematoxylin Stain |
Procedure Review
Iron Hematoxylin Stain
Introduction |
Formulas |
Procedures |
Results and Reporting |
Procedure Notes |
Procedure Limitations |
Results and Reporting
Protozoan trophozoites and cysts will be readily seen, although helminth eggs and larvae may not be easily identified because of excess stain retention (wet smears from the concentration procedure[s] are recommended for detection of these organisms). Yeasts (single and budding cells and pseudohyphae) and humans cells (macrophages, PMNs, and RBCs) can be identified. The following quantitation chart can be used for examination of permanent stained smears with the oil immersion lens (100 x objective; total magnification of x 1,000).
Quantitation of parasites, cells, yeasts, and artifacts
Quantity |
No. 10 oil immersion fields ( x 1,000) |
Few |
2 |
Moderate |
3-9 |
Many |
10 |
- Report the organism and stage (do not use abbreviations).
Examples: Entamoeba coli trophozoites and Dientamoeba fragilis trophozoites
- Quantitate the number of B. hominis seen (rare, few, moderate, many). Do not quantitate other protozoa.
Example: Many Blastocystis hominis
- Note and quantitate the presence of human cells.
Example: Moderate WBCs, few RBCs, few macrophages, rare Charcot-Leyden crystals
- Report and quantitate yeast cells.
Example: Many budding yeast cells and few pseudohyphae
- Save positive slides for future reference. Label prior to storage (name, patient number, organisms present).