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BLEEDING TIME  Standard procedure for collecting

blood
– Time required for a standardized skin
 Use non-dominant hand because it
wound to stop bleeding
was less callous
– In-vivo measurement of a platelet
 When blood start to appear start to
function (adhesiveness)
count
– Provides an estimate of the integrity of
 Do not wipe the first blood drop
the platelet plug and thereby measures
 Every 30 seconds-blot the blood
the interaction between the capillaries
using filter paper
and platelets
 Note: as u blot blood do not apply
– First original test for platelet function
pressure on patient finger
before aggregation test
 After blot apply pressure
– Single platelet function test although
 Every blot is equivalent to 30
there are certain factors affecting the
seconds
test
 Blot becomes smaller and smaller
– If platelet count of patient is normal or
coz nagkakaroon na ng plug
quantitatively count which is normal
 Possible mistakes: too much apply
but there is still bleeding so assess
pressure
function of platelets
 Make sure there is ample space on
– Can detect congenital and acquired
blood in blotting paper to avoid
– TIME IT TAKES FOR BLEEDING TO STOP
mixing
– Measure how long bleeding stop
 2-6 mins
– Depend on the size and site of injury
– platelet plug not always relying on METHOD:
platelet adhesion but somehow
1. Sterile Blood Lancet
bleeding time can give rough estimate
2. Stopwatch
how capable platelet to form plug
3. Sterile Filter Paper or clean tissue paper
– 2-9 mins 4. Gauze pads or cotton balls
5. 70% Alcohol or Povidone Iodine Solution
Nowadays more on aggregation test for
assessing platelet function PROCEDURE
In-vitro measurement of platelet 1. Obtain a piece of filter paper and stopwatch.
adhesiveness- PLATELET RETENTION TEST 2. Moisten a piece of cotton with 70% alcohol or
Bleeding on vital parts the more severe Povidone iodine and thoroughly cleanse the ball
bleeding of the patient’s middle or ring finger.
Bleeding time involve skin puncture with 3. Allow the skin to air dry
standard depth 2-4mm to hit capillary bead 4. Make a puncture wound 2-4mm deep in the
earlobe or finger with a disposable blood lancet.
METHODS FOR BLEEDING TIME 5. Start the stopwatch immediately.
6. Being careful not touch the puncture site.
A. Duke’s Method Blot the filter paper every 30 seconds, until the
 1912 first described by dukes and bleeding stops (no more blood adhere on
modified by Ivy’s paper)
 Puncture site: finger  Make sure to make spaces between blots
 Simple and quite easy to do 7. Record the bleeding time.
 Recording: 2 mins and 30 secs
o Add 30 seconds – 5 th blot (no more blood 3. Place the sphygmomanometer on the upper
attaches to filter paper) arm.
Increments of 30 seconds
NOTE: Should be the blood flow more than 15 4. Moisten a piece of cotton with 70% alcohol
minutes. Discontinue the test and report and or Povidone iodine solution and thoroughly
test as “greater than 15 minutes” cleanse the puncture site.

5. Apply the cuff and inflate to 40 mmHg, and


B. Modified Ivy’s Method – best method to
hold at this exact pressure for the duration of
assess platelet adhesiveness
the test NOTE: The time between inflation and
 Puncture site: forearm
incision should be 30 to 60 seconds
 Apply constant amount of pressure
on arm (40mmHg) 6. After applying the pressure cuff and
 Better than DUKE’s METHOD preparing the tessiet. Make 3 same punctures
because of constant pressure with a disposable lancet (1mm wide and 3 mm
 More accurate deep) NOTE: Avoid subcutaneous veins
 Single puncture will do
 As blood appear start timing 7. Start the stopwatch immediately.
 No need to apply pressure 8. After 30 seconds, wipe the flow of blood with
 Viscous, core muscle so blood not the filter paper. (Bring the paper close to the
total comes out easily incision, but do not touch the paper directly to
 Make sure not to puncture any the incision, so as not to disturb the formation
portion with veins because of veins of the platelet plug.)
were puncture more blood come-
falsely elevated 9. Blot each site with filter paper every 30
 If u hit veins sign is purge of blood seconds thereafter, until no blood stains the
and dark blood paper.
 9 mins 10. Stop the timer when only clear fluid is
 Best procedure: constant pressure is applied absorbed onto the filter paper. The bleeding
on the arm with use of blood pressure cuff – 40 time is determine to the nearest 30 seconds.
mmHg 11. Release the pressure of the
sphygmomamoter.
Ballar surface of the forearm – forearm
12. Record the bleeding time for each of the
o Careful to not hit the vein to not cause puncture.
falsely elevated result
o Constant pressure is applied 13. Get the average of the bleeding time in
o 2 – 3 punctures: Average is computed minutes and seconds

PROCEDURE

1. Obtain a piece of filter paper, stopwatch and SOURCES OF ERROR


sphygmomanometer. 1. If body hair will interfere, lightly shave the
2. Position the patient’s arm with the volar area.
surface exposed.
2. Patients should be advised of a potential to FACTORS AFFECTING BLEEDING TIME
produce a scar. This can usually be avoided by
1. Elasticity of the cut tissue –surrounding blood
the use of a butterfly bandage for 24 hours
vessels
3. Aspirin and aspirin containing products may
2. Ability of the blood vessel to constrict and
cause a prolonged bleeding time for up to 2
retract: bleeding time is indirect test to assess
weeks
Integrity of vessels
4. A standardized cut is necessary for valid
If there Injury then blood vessels
results. Too little pressure on the device and the
constrict so if vessel is intact, have
wound will be shallow or non-existent. Too
enough collagen and healthy expect
much pressure and the wound will be too deep.
that your bleeding will be controlled
This is the one area where standardization has
not been completely controlled. 3. Mechanical and chemical action of platelets
in the formation of hemostatic plug
5. Low skin temperature produces constriction
of the capillary vessels, resulting decreased  Skin thickness: callous, scars, hairs
blood flow.  Size and depth of wound- 2-4mm
required
!!Precaution: Be sure to maintain a cuff
 < 100 x 109 /L – bleeding time will be
pressure of 40 mmHg throughout the test. If prolonged
bleeding does not diminish after 15 minutes,
discontinue the test. Report the test as “greater Quantitatively and qualitatively
than 15 minutes” problem on platelets affect the bleeding
time
C. Coply-Lalitch Method - Both involve
Time not to take aspirin- 24 hours
immersion of the wounded finger in a because it has anti-platelet activity;
sterile NSS warmed at 37oC until bleeding cyclooxygenase-inhibit the formation of
stops txa2 which essential in forming clot
Immerse puncture site at 37’C Aspirin makes bleeding time falsely
water bath and check if there still elevated
had bleeding
ABNORMAL BLEEDING TIME:
D. Adelson-Crosby Method  Thrombocytopenia
E. Mac-farlanes method – same principle with  Hypofibrinogenemia
Adelson Crosby method by it only uses earlobe  vWF disorder – VWF essential for adhesion
and problem affecting fibrinogen
as the site of puncture.
 Connective tissue disorder – such as Marfan’s
F. Aspirin tolerance test – assess the effect of a  If bleeding stop immediately – puncture is not
standard dose of aspirin on the Duke’s Bleeding deep enough
Time Blood vessel problem

 Aspirin inhibits cyclooxygenase BLEEDING


 If platelet count is normal, and bleeding time
 Do not take aspirin for 24 hours prior to test is prolonged. Possible problem on:
o Vessel disorder
o Qualitative platelet disorder o Drugs: platelets
and NSAIDS REFERENCE VALUE
 2 – 9 minutes

Earlobe- mas maraming nerve ending and


cannot facilitate flow of blood

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