Thick film interpretation: Difference between revisions
From MalariaETC
No edit summary |
No edit summary |
||
| Line 12: | Line 12: | ||
<span style="font-size:90%">The features described make this approach highly sensitive for parasite detection, but also introduces staining inconsistencies and possible disruption of parasites, analysis therefore requires experienced microscopists who are aware of protential artefacts and have experience in thick blood film interpretation. Typial appearnces of a case of ''P.falciparum'' with easily detected trophozoites is shown below.</br></br> | <span style="font-size:90%">The features described make this approach highly sensitive for parasite detection, but also introduces staining inconsistencies and possible disruption of parasites, analysis therefore requires experienced microscopists who are aware of protential artefacts and have experience in thick blood film interpretation. Typial appearnces of a case of ''P.falciparum'' with easily detected trophozoites is shown below.</br></br> | ||
<gallery mode="nolines" heights=200px widths=200px> | <gallery mode="nolines" heights=200px widths=200px> | ||
File:TF1b.jpg|<span style="font-size:80%">Low magnification view for scale</span>|link={{filepath:TF1b.jpg}} | File:TF1b.jpg|<span style="font-size:80%">Low magnification view for scale, 3 regions marked</span>|link={{filepath:TF1b.jpg}} | ||
File:TF1c.jpg|<span style="font-size:80%">Region A: a single disrupted trophozoite</span>|link={{filepath:TF1c.jpg}} | File:TF1c.jpg|<span style="font-size:80%">Region A: a single disrupted trophozoite</span>|link={{filepath:TF1c.jpg}} | ||
File:TF1d.jpg|<span style="font-size:80%">Region B: 2 trophozoites in one group</span>|link={{filepath:TF1d.jpg}} | File:TF1d.jpg|<span style="font-size:80%">Region B: 2 trophozoites in one group</span>|link={{filepath:TF1d.jpg}} | ||
Revision as of 12:52, 10 February 2025
| OVERVIEW OF THICK FILMS |
A thick film is prepared by placing a small drop of blood on a slide then spreading it in a circular motion. The thick layer acheived is then air-dried without fixation.
The principles are:
- The blood will therefore be many layers thick (around 6-20) compared with the single layer of a thin film
- The erythrocytes are unfixed so will be lysed during staining appearning only as debris.
- The Giemsa stain will therefore stain and distinguish the remaining white cells, parasites.
- This allows parasites to be detected with high sensitivity using fewer microscopic fields
The features described make this approach highly sensitive for parasite detection, but also introduces staining inconsistencies and possible disruption of parasites, analysis therefore requires experienced microscopists who are aware of protential artefacts and have experience in thick blood film interpretation. Typial appearnces of a case of P.falciparum with easily detected trophozoites is shown below.
-
Low magnification view for scale, 3 regions marked
-
Region A: a single disrupted trophozoite
-
Region B: 2 trophozoites in one group
-
Region C:
"
Comparison of Thick and Thin Films for Malaria Diagnosis
| Feature | Thick Film | Thin Film |
|---|---|---|
| Sensitivity | Higher (detects low parasitaemia ~5–10 parasites/µL) | Lower (~50 parasites/µL required for reliable detection) |
| Parasite Concentration | Blood elements are lysed, concentrating parasites | RBCs remain intact, parasites are more spread out |
| Species Identification | Poor—RBC morphology lost, difficult to differentiate Plasmodium species | Excellent—Parasite morphology and RBC characteristics aid species identification |
| Quantification | Difficult—parasite density estimation is less precise | Easier—parasites can be counted per number of RBCs |
| Preparation Time | Longer—requires air drying before staining (≥30 min) | Faster—fixed immediately and stained |
| Staining Challenges | Requires careful staining to avoid artefacts and over-staining | More consistent staining, clearer morphology |
| Expertise Required | High—difficult to distinguish artefacts from parasites | Moderate—clearer structures, easier interpretation |
| Use Case | Best for initial parasite detection, particularly in low parasitaemia cases | Best for confirming species and quantifying parasitaemia |