121214 cases Flashcards

1
Q

giant platelets are characteristic of

A

ITP

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2
Q

mucocutaneous bleeding

A

generally able to see

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3
Q

course of ITP in child vs adult?

A

in children-resolves more frequently. caused commonly by viruses

in aduldts-can get chronic form (from viruses, autoimmune conditions, drugs)

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4
Q

tx for ITP?

A

initially: corticosteroids
IVIG
if refractory: splenectomy (spleen is site of platelet destruction and the primary source of Ig)

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5
Q

D dimer

A

clot production and breakdown

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6
Q

when doing a question on bleeding, what to consider FIRST?

A

mucocutaneous or deep bleeding?

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7
Q

ITP vs DIC in terms of how pt looks

A

ITP-relatively ok

DIC-not well

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8
Q

how to separate out hemophilia from von willebrand dis

A

von willebrand–mucosal bleeding

hemophilia–deep tissue bleeding

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9
Q

if have history of mucosal bleeding and normal PT&PTT, what tests should you do?

A

consider PFA-100

then tests of von Willebrand factor

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10
Q

inheritance pattern of hemophilia

A

X linked recessive

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11
Q

hemophilia–which factors?

A

8 and 9

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12
Q

desmopressin (DDAVP) is used for

A

von Willebrand’s disease
it promotes vWF release from endothelial cells

in severe dis, may use viral-inactivated VWF-FVIII concentrate

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13
Q

types of bleeding in secondary hemostasis defect

A
joint bleeding-hemarthrosis
muscle hemorrhage
soft tissue
life threatening bleeding
surgery
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14
Q

if pt has very heavy periods, what can result?

A

iron deficiency anemia

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15
Q

clinical symptoms of von willdbrand dis

A

mucosal bleeding, esp epistaxis and menorrhagia
post-op bleeding
bleeding from oral cavity
gastrointestinal bleeding

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16
Q

von willebrand’s disease causes what kind of hemostasis-impairment?

A

primary (mucocutaneous bleeding)