Acquired bleeding disorders Flashcards

1
Q

Most prevalent between acquired and inherited coagulation disorders

A

Acquired more common than inherited

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2
Q

How many coagulation factors are affected in acquired coagulation disorders

A

More than 1

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3
Q

Classification of acquired coagulation disorders

A
Deficiency of vitamin k
liver function related
Antibody induced
Drug/transfusion induced
Interference from abnormal proteins
Consumptive coagulopathy
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4
Q

Why will a deficiency of vitamin k cause coagulation disorders

A

This is because some coagulation factors are vitamin k dependant

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5
Q

How does poor liver function cause coagulation disorders

A

This is because a lot of coagulation factors are produced in the liver.

Hepatitis, cirrhosis, hepatocellular ca etc

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6
Q

How do antibodies cause coagulation disorders

A

Antibodies can be produced against certain factors necessary for coagulation

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7
Q

Vitamin K is important in the synthesis of these coagulation factors

A

factor 2, 7,9, 10

which are important factors in all the pathways, hence without it none of the pathways can function

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8
Q

Sources of vitamin k

A

green vegetables, bacterial synthesis in the gut

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9
Q

In what circumstances does vitamin k deficiency occur

A

Newborn
Biliary obstruction
Malabsorption
Inhibition of vitamin k

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10
Q

Why does vitamin K deficiency occur in the newborn

A

Newborn does not eat green vegetables, and their gut is not well developed to synthesize vitamin k

Breast milk contains low amount of vitamin k

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11
Q

Causes of malabsorption syndrome

A

surgery, tropical sprue, gluten sensitive enteropathy

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12
Q

warfarin and vitamin k

A

warfarin is a vitamin k antagonist

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13
Q

The abscence of vitamin k leads to the production of

A

PIVKA. Protein induced in vitamin k absence which in themselves lead to a bleeding tendency

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14
Q

Antibodies being produced against certain factors may be

A

Induced or spontaneous

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15
Q

Von willebrands disease is

A

Autoimmune with antibodies being produced against von willebrands factor

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16
Q

How does massive transfusion cause coagulation disorders

A

They dilute coagulation factors of receiver. Donors blood does not carry all the factors due to duration of preservation etc .

Anticoagulants are present in blood during preservation to keep it from clotting. massive transfusion will cause anticoagulant effect to be pronounced.

17
Q

How does interference from abnormal proteins cause coagulation factor disorder

A

Abnormal proteins like plasma cell myelomas and paraproteins coat the surface of platelets leading to poor function

They also interfere with fibrin formation

18
Q

Initiators of consumptive coagulopathy

A

vessel wall damage
tissue factor release
platelet aggregation

19
Q

Initiators of consumptive coagulopathy

A
infections
malignancies
obstetric complications
Hypersensitivity reaction
widespread tissue damage
vascular abnormalities
hypothermia
heat stroke
acute hypoxia
20
Q

Haemorrhagic disease of the newborn

A

Acquired bleeding disorder in the newborn

21
Q

What causes HDN

A

Vitamin k deficiency

Liver cell immaturity

22
Q

Presentation of HDN

A

Bleeding from second to fourth day of life

23
Q

Diagnosis of HDN

A

Normal platelet count
Prolonged PT
Prolonged APTT

24
Q

Prophylaxis for HDN

A

Vitamin K

25
Q

Treatment for HDN

A

1mg of vitamin K every 6 hours

In case of severe bleeding use prothrombin complex concentrate

26
Q

What causes bleeding in patient with liver dx

A

Biliary obstruction leads to impaired absorption of vitamin k which is fat dependent

Vitamin k dependent factors are affected

Dysfibrogenemia

Reduction of other coagulation factors

DIC

Oesophageal varices

27
Q

Diagnosis of liver dx

A

Underlying dx features
Deranged liver enzymes
Reduced albumin
Raised PT and APTT

28
Q

Prophylaxis for liver dx

A

5mg/day Vitamin K

29
Q

If person is bleeding in liver dx

A

10mg iv vitamin k slowly
Prothrombin complex
Fresh frozen plasma

30
Q

DIC

A

Coagulation system triggered into overdrive with coagulation factors used up and reduced in number and the formation of microthrombi in the vascular system

31
Q

DIC characterised by

A
End organ damage
Bleeding
Consumption of platelets
Thrombotic syndrome
gangrene
32
Q

Investigation of DIC

A

Check for underlying disease

Full blood count i.e low platelets, fibrinogen, increased PT,APTT, fibrin degradation products, D-dimers

Hemolytic anemia due to microangiopathy

33
Q

Treatment of DIC

A
Treat underlying cause
Treat bleeding with ;
FFP
Platelets
Cryoprecipitate
Red cells
Treat thrombus with heparin