Approach to a bleeding disorder: These presentation has the approach for a patient of bleeding disorder. it has History, physical finding, Investigations.
3. Introduction
Bleeding, technically known as
hemorrhaging, is the loss of blood escaping
from the circulatory system.
Bleeding can occur internally, where blood
leaks from blood vessels inside the body, or
externally, either through a natural opening
such as the mouth, nose,
ear, urethra, vagina or anus, or through a
break in the skin.
3
4. 4
Bleeding arises due to either traumatic
injury, underlying medical condition, or a
combination.
'Medical bleeding' denotes hemorrhage as a
result of an underlying medical condition
Blood can escape from blood vessels as a
result of 3 basic patterns of injury:
Intravascular changes - changes of the blood
within vessels (e.g. ↓ clotting factors)
5. 5
Intramural changes - changes arising within
the walls of blood vessels (e.g. aneurysms)
Extravascular changes - changes arising
outside blood vessels (e.g. infection)
Certain medical conditions can also make
patients susceptible to bleeding.
These are conditions that affect the normal
"hemostatic" functions of the body.
Hemostasis involves several components.
The main components of the hemostatic
system include platelets and
the coagulation system.
8. History taking
8
For most hemorrhagic conditions,
history plays an important role in
diagnosing the cause.
For a hemorrhagic condition the history
should determine the site or sites of
bleeding, the severity and duration of
hemorrhage, and the age at symptom
onset.
9. 9
Was the bleeding spontaneous or after
trauma? Does bruising occur
spontaneously?
One should determine if symptoms
correlate with the degree of injury or
trauma. Are there lumps with bruises for
which there is minimal trauma?
Was there a previous personal or family
history of similar problems?
recent transfusion?
10. Cont’d…
10
If there has been joint pain, swelling or
limitation of movement
If there has been bleeding from umbilical
stump
If there has been previous surgery or
significant dental procedures, was there any
increased bleeding?
Delayed or slow healing of superficial injuries
may suggest a hereditary bleeding disorder.
In postpubertal females, it is important to take
a careful menstrual history.
Medications such as aspirin, other non-
11. 11
Note:
Once the child is beyond the neonatal period,
thrombotic symptoms are relatively rare until
adulthood.
In the neonate, physiologic deficiencies of
procoagulants and anticoagulants cause the
hemostatic mechanism to be dysregulated
Even in the absence of a family history, the
presence of thrombosis in the child or teenager
should trigger an evaluation of the individual for
a hereditary or acquired predisposition to
12. 12
Non-steroidal anti-inflammatory drugs
such as ibuprofen, mefenamic acid, etc.
and aspirin inhibit platelet function
whereas anticonvulsants,
antihistaminics, antituberculous drugs
especially rifampicin are known to cause
thrombocytopenia.
The overall health of the patient also is a
clue to the cause of bleeding. Congenital
bleeding disorders and ITP usually
occur in children who are otherwise well.
13. Physical Examination
13
Physical examination offers further clues to
the diagnosis
Is it bleeding? e.g. fixed drug eruption,
erythema nodosum, viral exanthem and
mosquito bites The examination should
determine the presence of petechiae,
ecchymoses, hematomas, hemarthroses, or
mucous membrane bleeding.
14. 7/19/2014
approach to pediatrics bleeding
disorders 14
Patients with defects in platelet/blood
vessel wall interaction usually have
mucous membrane bleeding; petechiae
on the skin and mucous membranes;
and small, ecchymotic lesions of the
skin sometimes associated with
hematomas.
Individuals with a clotting factor
deficiency such as factor VIII or factor IX
deficiency have symptoms of deep
bleeding into muscles and joints with
18. 18
Petechiae are pathognomonic of
platelet-related bleeding
Bruises in any area that appear
excessively large for the degree of
trauma or those with underlying
palpable hematomas may be seen in
patients with significant bleeding
disorders
Swelling of any joint without a history of
significant trauma is definitely abnormal.
Similarly, deep tissue and intramuscular
bleeds should prompt the diagnosis of a
20. 20
If it is bleeding, then is it localized or
generalized? A single site involved, it is
more likely to be a localized bleeding
rather than a generalized bleeding
disorder
If generalized, is it platelet type or
coagulation type of bleeding? Is it
congenital/hereditary or acquired
disorder? Symptoms of a longer
duration are indicative of a congenital
disorder such as von Willebrand Disease
(vWD) or coagulation-factor deficiencies
21. 7/19/2014
approach to pediatrics bleeding
disorders 21
Look for hepatosplenomegaly
Do a rectal exam for evidence of GI bleeding
Look for physical signs and symptoms of
diseases related to capillary fragility: Petechiae
secondary to coughing, sneezing, Valsalva
maneuver, blood pressure measurement.
Note: The possibility of physical abuse must be
considered in the evaluation of any child with
unusual patterns of bruising or bleeding.
23. Laboratory Investigation
Tests for Platelet
I. Platelet count
II. Bleeding
Time(BT)
Tests for
coagulation
factors
I.ProthrombinTi
me(PT)
II. Activated Partial
Thromboplastin
Time(aPTT)
III.Thrombin
24. Platelet count must be done in a suspected
bleeding disorder.
Bleeding Time (BT)
Significance
Assess Primary Hemostatic defect(vessel
wall or platelet).
Dependent on adequate functioning of plt.
& Bl.Vs.
Range
4-8 min
Platelet count & Bleeding
Time
25. Causes of prolonged BT
I. Thrombocytopenia.
II. VWD.
III. Platelet function disorder
IV. Disorder of blood vesseles.
Interpretation
26. Significance
Reflects overall activity of the Extrinsic
Pathway.
Most sensitive to changes in Factor V,VII,X.
Lesser to Factor I & II.
Principle
Platelet poor plasma+Tissue
Thromboplastin+Calcium
In Presence of F VII Extrinsic pathway is
activated & clot
formed
Prothrombin Time(PT)
27. Causes of prolonged PT
1. Deficiency of Factor VII,X,V,II,I
2. Vit K deficiency
3. Liver disease
4. Oral anticoagulants
Interpretatio
n
28. Significance
Reflects efficiency of Intrinsic Pathway.
Sensitive to changes in Factor VIII,IX,XI,XII.
Also sensitive to heparin & circulating
anticoagulants.
The test measures the clotting time of plasma
after the activation of contact
So it indicates the overall efficiency of the
Intrinsic pathway
Normal range
26 to 40 seconds.
Activated Partial Thromboplastin
Time
(aPTT)
29. Causes of prolonged aPTT
1. Deficiency of Factor VIII(Hemophilia A).
2. Deficiency of Factor IX(Hemophilia B).
3. Heparin therapy.
4. Circulating anticoagulants.
5. Liver disease.
Interpretation
30. Significance
Asses the final step of coagulation i.e.
conversion of fibrinogen to fibrin in presence
of thrombin.
Bypasses Extrinsic & Intrinsic pathway.
Principle
Thrombin is added to plasma and the clotting
time is
measured.
TT is affected by the concentration and reaction
of fibrinogen and by the presence of inhibitory
substances.
Normal range
A patient’s TT should be within 2 s of the control
Thrombin
Time(TT)
31. Causes of prolonged TT
1. Disorders of fibrinogen-
Afibrinogenaemia.
Hypofibrinogenaemia.
Dysfibrinogenaemia.
2. Liver disease.
3. heparin therapy.
.
Interpretati
on
32. Relevant 2nd line investigations are carried
out with each of the patterns of abnormalities
in first line tests.
2nd Line Investigation
36. Mixing study
Correction test using PT or aPTT
PRINCIPLE
Unexplained prolongation of PT
or aPTT can be investigated
with simple correction test by
mixing the pt`s plasma with
normal plasma.
Correction (should be within
few seconds) indicates a
possible factor deficiency,
whereas failure to correct
suggests the presence of an
inhibitor.
METHOD
Perform a PT and/or aPTT on
control, patient`s,and a 50:50
mixture of the control and pt`s
plasma.
40. Reptilase & Ancord are purified enzymes
from snake.
May be used to replace Thrombin in TT
test.
Snake venom is not inhibited by heparin
Normal time for clotting in presence of
Heparin.
Clotting time will be prolonged in
presence of decreased Fibrinogen.
Reptilase or Ancord
Time
43. References
43
1. American Academy of pediatrics
(http://pedsinreview.aappublications.org/cgi/
content/full/29/4/121)
2. Nelson Textbook of Pediatrics, 18th ed.
3. Current Pediatric Diagnosis & Treatment ,
18th edition
4. Pediatrics on call journal, may 2005 vol.2
issue 5
5. Up to date