Blood Film

Download as pptx, pdf, or txt
Download as pptx, pdf, or txt
You are on page 1of 20

A blood smear (blood film):

is a glass microscope slide coated on one side with a thin layer of venous blood. The slide is stained with a dye, usually Wrights stain or leishman stain and examined under a microscope .

Aim of blood smear


Examination of thin blood films is important in the following states: investigation of anaemia, assessment of RBC and platelets morphology Identification of parasites ,infections and other conditions which produce changes in the appearance of blood cells differential count of leukocytes.

A blood film report can provide rapidly , low cost and useful information about a patients condition.

Making blood films


Three basic steps to make blood film:
1.

Preparation of blood smear.

2.
3.

Fixation of blood smear.


Staining of blood smear.

BLOOD SMEAR
Specimen:
Peripheral

blood smear made from EDTA-anticoagulated blood.

Smears should be made within 1 hour of blood collection from EDTA specimens stored at room temperature to avoid alteration of cell morphology
Blood

smears can also be made from finger stick blood directly onto slide.

Equipment Clean slides Blood capillary tube or micropipette 10 L EDTA tubes Lancets and syringes . Cotton and alcohol (disinfectant) Leishman stain Normal saline

Procedure:
Fill a capillary tube three-quarter full with the anticoagulated specimen. 2. Place a drop of blood, about 2 mm in diameter approximately an inch from the frosted area of the slide. 3. Place the slide on a flat surface, and hold the narrow side of the non frosted edge between your left thumb and forefinger. 4. With your right hand, place the smooth clean edge of a second (spreader) slide on the specimen slide, just in front of the blood drop. 5. Hold the spreader slide at a 30 angle, and draw it back against the drop of blood.
1.

Procedure:
6. Allow the blood to spread almost to the edges of the

slide. 7. Push the spread forward with one light, smooth, and fluid motion. A thin film of blood in the shape of a bullet with a feathered edge will remain on the slide. 8. Label the frosted edge with patient name, ID# and date. 9. Allow the blood film to air-dry completely before staining. (Do not blow to dry. The moisture from your breath will cause RBC artifact.)

Steps for Blood Film

The shape of blood film

Collection of Blood
1.
The second or third finger is usually selected and cleaned.

4.
Slide must always be grasped by its edges.

2.
Puncture at the side of the ball of the finger.

5.
Touch the drop of blood to the slide from below.

3.
Gently squeeze toward the puncture site.

Preparing thin films


1.
Touch one drop of blood to a clean slide. . 2-hold the spreader at 30degree angle.

3
Pull the drop of blood across the first slide in one motion.

4
Wait to dry before fixing and staining.

The thickness of the spread when pulling

Is determined by:
1.

2. 3.

The angle of the spreader slide. (the greater the angle, the thicker and shorter the smear). Size of the blood drop. Speed of spreading

Leishman's stain
1- Air dry slides . 2- Flood with Leishman's stain for three minutes. 3- Dilute the stain on the slide with an equal amount of buffered water, pH 6.8, adding the water slowly with a plastic Pasteur pipette and mixing by sucking the stain up and down with the pipette. 4- Leave the slide for approximately 7-10 minutes. 5- Wash off excess stain with slowly-running tap water. 6- flood slide for one minute with buffered water, pH ( 6.8). 7- Dry the slide .

Characteristics of A Good Smear:


1. Surface : even and uniform , free from ridges
2. 3. 4. 5.

,waves and holes. Length : About 2.5 cm long , the blood smear should occupy the central portion of the slide. Margin: The blood smear should not touch the edges Film consist of three parts: head , body and tail . Tail end :will be gradually thin ,without any serrated ends .

The shape of blood film

Sources of error
Irregular spread with ridges and long tail: Edge of

spreader dirty or chipped; dusty slide

Holes in film: Slide contaminated with fat or grease. Irregular leucocyte and platelet distribution, especially

in tail: poor film-making technique Film too short and too thick: spreader held at incorrect angle
Film extending to end of slide: blood drop too large Short thin film: blood drop too small Film extends to edge of slide: spreader too wide or not

positioned correctly

Cellular degenerative changes: delay in fixing, inadequate

fixing time or methanol contaminated with water

Examples of unacceptable smears

You might also like