Thick film interpretation

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.
IMAGE
The principles are:

• The blood layer will be many layers thick (varying from 6-20 accross the specimen)
• The erythrocytes are unfixed, so will be lysed during staining appearing only as debris.
• The Giemsa stain will stain and distinguish the remaining white cells and parasites.
• This concentration effect allows parasites to be detected with high sensitivity

Typical appearances of a case of P.falciparum with easily detected trophozoites are shown below.

• 

  Low magnification view for scale, 3 regions marked

• 

  Region A: a single disrupted trophozoite

• 

  Region B: 5 trophozoites in three group

• 

  Region C: 2 trophozoites in one group

"

Note the differences in recognition - the typical ring form and vacuole of the parasite are not as easy to distinguish and chromatin dots may appear to separate from parasite cytoplasm while the absence of intact red cells takes away important clues to parasite size and distribution. This is illustrated in the image below

• 

  Low magnification view for scale, 3 regions marked

Some strengths and weaknesses of each approach are summarised in the table below:

COMPARISON OF THICK AND THIN FILMS
Feature	Thick Film	Thin Film
Sensitivity for detection	Higher: detects low parasitaemia ~5–10 parasites/µL	Lower: generally needs ~50 parasites/µL for reliable detection)
Species Identification	Poor: RBC morphology lost and species-specific features may be difficult	Excellent: Parasite morphology and RBC characteristics are readily observed
Quantification of parasitaemia	Difficult: requires estimation so is imprecise	Easier: parasites can be counted per number of RBCs
Preparation and staining	Longer: requires air drying before careful staining to avoid artefact	Faster: films are fixed and stained immediately with clearer morphology

---