JB-Haematology Flashcards

1
Q

treatment for a DVT in patients with anti-phospholipid syndrome

A

Lifelong warfarin

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2
Q

Diagnostic test for hereditary spherocytosis

A

EMA bind test

(None if clear dx)

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3
Q

Who gets G6PD

A

Men (x linked recessive)
African and Mediterranean

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4
Q

Treatment for hereditary spherocytosis

A

Acute haemolytic crisis -> transfuse/ supportive

Folate replacement
Splenectomy

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5
Q

Most common inherited bleeding disorder

A

Von Willibrans disease

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6
Q

How is VWF disease inherited

A

AD (most common in UK)

Rarely AR

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7
Q

VWF disease on clotting screen

A

Prolonged clotting time
APPT maybe prolonged (affects factor 8)

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8
Q

What disease can CLL transform to

A

High-grade lymphoma
NON HODGKINS
Richters transformation

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9
Q

What must be started when warfarin is commenced

A

Cover with LMWH
Prothrombotic first 2 -7 days as less protein C and S as much shorter half life (natural anti-coagulant)

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10
Q

How many days of LMWH cover on wafarin

A

At least 5
More if INR is less than 2

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11
Q

Why may skin necrosis occur on a patient starting warfarin

A

Hereditary protein C/S deficiency
Warfarin drops C and S levels further
Micro clots in skin -> necrosis

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12
Q

Treatment of Venus sinus thrombosis

A

LMWH (warfarin longer term)

Cannot used DOACs!

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13
Q

Difference between using prothrombin concentrate (octeplex) in warfarin vs DOAC

A

Warfarin reverses as provides clotting factors which warfarin stopped body making

Does not reverse DOAC. Used provides extra so hopefully some Xa is made.

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14
Q

Can a patient on a DOAC have surgery if PT and APTT is normal

A

No - not a reliable measure

Need anti X-a level (same as LMWH)

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