Skip to document
This is a Premium Document. Some documents on Studocu are Premium. Upgrade to Premium to unlock it.

Platelet estimation lab1

The notes are lifted from the discussion of the professors.
Course

Medical Laboratory Science (BS MLS 1)

360 Documents
Students shared 360 documents in this course
Academic year: 2020/2021
Uploaded by:
0followers
11Uploads
36upvotes

Comments

Please sign in or register to post comments.

Preview text

H E M A T O L O G Y P a g e | 1

PLATELET ESTIMATION  Every laboratory derived their own platelet estimation

PBS Preparation:

  1. EDTA blood EDTA– anticoagulant of choice in platelet counting; preserve morphology of platelets; distinguishable platelets; no significant change in shape/appearance of platelets
  2. Glass slide
  3. Wright stain

Platelet count:

  1. Microscope
  2. Immersion oil Under OIO, choose zone of

morphology →

Count platelets in

10 fields →

Average of 10 OIFs x PEF

zone of morphology – area where you evaluate morphology of red cells; where we start differential count; where we start counting platelets  PEF- platelet estimation factor

 Average of platetels in 10 OIFs: must be whole number

 Platelets: not perfectly circular bodies; may change in shape when outside

blood vessels; may show projections (may be normal/ abnormal – like in

microclots formation )

 Describe plateltes:

 Deep-blue to purple colored bodies  Circular or with changed shape (but still counted)  1/9 the size of normal RBCs

PLATELET ESTIMATION FACTOR

 Derived by correlating a machine count and a smear count30 specimens from health subjects  Machine count  Prepare PBS for each Automation : cells are counted in the principle of their size  Mean cell volume: RBC  Mean platelet volume: platelet  Make use of Coulter principle: body passes through a direct current  direct current disturbed: disturbance is counted as an impulse  1 impulse: 1 cell  Any increase in size of platelets: decrease the count of RBCs  Any clot formation/aggregation of platelets (confused as bigger size): increase the count of RBCs

Count and record number of platelets in 10 consecutive fields

Divide the total number of platelets found by 10 to obtain average number per single OIF

= total number of platelets 10

For each specimen, divide the corresponding machine count by average number of platelets per OIF to obtain individual PEFs

= machine count average number of platelets per OIF

Add all individual PEF from 30 specimens and divide by 30 to obtain average PEF

=PEF1 + PEF2 + ⋯ PEF30 30

H E M A T O L O G Y P a g e | 2

Machine count – expressed in SI unit (150 = 150x10 9 /L); just copy Smear count – average from 10 OIFs

iPEF =

MC

SC

PEF =

total iPEF 30

PEF =

528

30

= 𝟏𝟖

Sample problem: patient X  need to obtain estimated platelet count

DO NOT SAY ABNORMAL/NORMAL: instead write ADEQUATE/DECREASED/INCREASED We do not report (release results) of quantitative estimated platelet count – only report adequate/decreased/increased

Was this document helpful?
This is a Premium Document. Some documents on Studocu are Premium. Upgrade to Premium to unlock it.

Platelet estimation lab1

Course: Medical Laboratory Science (BS MLS 1)

360 Documents
Students shared 360 documents in this course
Was this document helpful?

This is a preview

Do you want full access? Go Premium and unlock all 2 pages
  • Access to all documents

  • Get Unlimited Downloads

  • Improve your grades

Upload

Share your documents to unlock

Already Premium?
HEMATOLOGY P a g e | 1
PLATELET ESTIMATION
Every laboratory derived their own platelet estimation
PBS Preparation:
1. EDTA blood
EDTA anticoagulant of choice in platelet counting; preserve morphology of platelets; distinguishable platelets; no significant change in
shape/appearance of platelets
2. Glass slide
3. Wright stain
Platelet count:
1. Microscope
2. Immersion oil
Under OIO,
choose zone of
morphology
Count platelets in
10 fields
Average of 10
OIFs x PEF
zone of morphology area where you evaluate morphology of red cells; where we
start differential count; where we start counting platelets
PEF- platelet estimation factor
Average of platetels in 10 OIFs: must be whole number
Platelets: not perfectly circular bodies; may change in shape when outside
blood vessels; may show projections (may be normal/ abnormal like in
microclots formation)
Describe plateltes:
Deep-blue to purple colored bodies
Circular or with changed shape (but still counted)
1/9 the size of normal RBCs
PLATELET ESTIMATION FACTOR
Derived by correlating a machine count and a smear count
30 specimens from health subjects
Machine count
Prepare PBS for each
Automation: cells are counted in the principle of their size
Mean cell volume: RBC
Mean platelet volume: platelet
Make use of Coulter principle: body passes through a direct current direct current disturbed: disturbance is counted as an
impulse 1 impulse: 1 cell
Any increase in size of platelets: decrease the count of RBCs
Any clot formation/aggregation of platelets (confused as bigger size): increase the count of RBCs
Count and record
number of
platelets in 10
consecutive fields
Divide the total
number of platelets
found by 10 to obtain
average number per
single OIF
=total number of platelets
10
For each specimen, divide the
corresponding machine count
by average number of platelets
per OIF to obtain individual
PEFs
=machine count
average number of platelets per OIF
Add all individual PEF
from 30 specimens
and divide by 30 to
obtain average PEF
=PEF1 + PEF2 + PEF30
30

Why is this page out of focus?

This is a Premium document. Become Premium to read the whole document.