Acquired bleeding disorders Flashcards

(33 cards)

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

25
Treatment for HDN
1mg of vitamin K every 6 hours | In case of severe bleeding use prothrombin complex concentrate
26
What causes bleeding in patient with liver dx
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
Diagnosis of liver dx
Underlying dx features Deranged liver enzymes Reduced albumin Raised PT and APTT
28
Prophylaxis for liver dx
5mg/day Vitamin K
29
If person is bleeding in liver dx
10mg iv vitamin k slowly Prothrombin complex Fresh frozen plasma
30
DIC
Coagulation system triggered into overdrive with coagulation factors used up and reduced in number and the formation of microthrombi in the vascular system
31
DIC characterised by
``` End organ damage Bleeding Consumption of platelets Thrombotic syndrome gangrene ```
32
Investigation of DIC
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
Treatment of DIC
``` Treat underlying cause Treat bleeding with ; FFP Platelets Cryoprecipitate Red cells Treat thrombus with heparin ```