Hemophilia Flashcards

1
Q

Clinical manifestations of bleeding disorders

A

bleeding, petechia, purpura, melena, ecchymosis, spontaneous bleeding (epistaxis), hematuria

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2
Q

How are bleeding disorders accquired

A

inherited through x-linked genes

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3
Q

What deficiency is hemophilia A

A

factor VIII

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4
Q

What deficiency is hemophilia B

A

factor IX

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5
Q

Where does hemophilia affect the most

A

GI tract and joints

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6
Q

What population does hemophilia affect the most

A

men

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7
Q

When are signs of hemophilia present

A

after injury

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8
Q

When does joint bleeding usually occur for the first time

A

when a child starts walking

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9
Q

What can recurrent injury and bleeding cause

A

inflammation leading to joint fibrosis, contractures, and arthritis

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10
Q

How are hemophilia A/B classified

A

mild, moderate, or severe based on amount of clotting factors present

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11
Q

What does PT (prothrombin time) measure

A

clotting time for extrinsic pathway

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12
Q

What does aPTT (partial thromboplastin time) measure

A

clotting time for the intrinsic pathway

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13
Q

What test is used for VIII and IX

A

aPTT

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14
Q

What is the main treatment

A

replacement/demand treatment

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15
Q

Risk of not receiving prophylactic therapy

A

risk that bleeding will cause damage before replacement demand therapy is received

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16
Q

Con of prophylactic therapy

A

intensive and expensive

17
Q

Desmopressin

A

lab made hormone used to prevent bleeding for factor VIII

18
Q

Antifibrinolytic use

A

used to stop bleeding especially before dental work

19
Q

Types of antifibrinolytic meds

A

tranexamic acid, epsilon aminocaproic acid

20
Q

When are monoclonal antibodies used

A

in patients with factor VIII or IX antibodies in the bloodstream

21
Q

What does bleeding in joints cause

A

tightness in joints, movement temporarily lost, and damage is caused

22
Q

s/s of brain bleed

A

long painful headaches, neck pain and stiffness, vomiting, sleepiness, sudden change in behavior, sudden weakness, double vision, seizures, convulsions