Bleeding Disorders Flashcards

1
Q

what is hemorrhagic disorder ?

A

it is a group of disorders of widely difeering etiology which have in common an abnormal tendency to bleed due to a defect in the mechanism of heamostasis

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2
Q

BD due to vascular defect ?

A

hereditary haemorrhagic telangiectasis
ehlers danlos disease
purpura simplex
senile purpura
polyarteritis nodosa

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3
Q

bleeding disorder of platelet abnormalities >

A

thrombocytopenia
thrombathenia
thrombpcytosis
thrombocythaemia

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4
Q

BD of coagulation defect ?

A

H A & B
Von willebrand disease

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5
Q

screening test for BD ?

A

BT
CT
PT
APTT
TT
PC

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6
Q

Normal BT ?

A

<6min

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7
Q

Normal CT ?

A

6-12 MIN

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8
Q

PT ???

A

9-12 sec

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9
Q

APTT ??

A

32-40 sec

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10
Q

TT ??

A

10-14 sec

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11
Q

PC ?

A

1.5-4 laks/mm3

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12
Q

BT prolonged in which D ?

A

ITP

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13
Q

CT + APTT prolonged= ??

A

Haemophilia A + B

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14
Q

BT CT APTT TT all prolonged = ??

A

DIC

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15
Q

Confirmatory test of ITP?

A

Bone marrow
—- inc megakaryopoiesis
Anti-platelet AB

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16
Q

CBC of ITP ?

A

all = Normal
Platelet count = dec

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17
Q

screening test result of ITP ?

A

BT = prolonged
CT APTT PC TT = dec

18
Q

cause of prolong TT ?

19
Q

APTT what ??

A

time required for clotting to take place in intrinsic pathway

20
Q

Other name of DIC ?

A

consumption coagulopathy
defibrination syndrome 448

21
Q

PT what ?

A

time required for clot in extrinsic pathway

22
Q

causes of thrombocytopenia?

23
Q

VWF disease which one prolonged ?

A

BT CT APTT

24
Q

VWd confirmatory test ?

A

factor VIII ASSAY = normal/dec
VWF assat = dec/nai

25
Q

PC normal
but BT prolonged why ?

A

platelet adhesion defect resulting from VWF deficiency

26
Q

WHich parhway defect in H >

A

intricnsic

26
Q

why factor-VIII is dec in VWF ?

A

VWF prevents the lysis of factor-VIII

27
Q

WHY APTT is prolonged in Haemophilia >

A

APTT is prolobged due to inc in 1 2 5 8 9 10 factor
factor 8 specific for APTT

28
Q

cardinal sign of haemophilia >

A

haemoarthrosis

29
Q

Hx presentation of Haempohilia <

A

circumcision
tooth extraction

29
Q

carrier of hemophilia?

30
Q

when female are affected in hemophilia?

A

affected father + carrier mother
turners syndrome
lionization of normal X chromosome

31
Q

common site of muscle hematoma in hemophilia <

A

psoas
calf muscle

32
Q

confirmatory Dx of haemophilia <

A

H-A= factor VIII assya = dec
H-B= factor IX assay = dech

33
Q

which type of anemia in DIC >

A

MICROCYTIC hemolytic anemia

34
Q

confirmatory test of DIC >

A

FDP
fibrin degradation protein

35
Q

in which case BT & CT both prolonged >

36
Q

immune mechanism cause of thrombocytopenia <

A

ITP
post traumatic purpura
drug - vancomycin + quinine

=== Platelet survival; dec

37
Q

dec consumption of P in thrombocytopenia?

A

DIC
microangiopathic hemolytic anemia

viral - dengue
HIV

38
Q

Dec P production in thrombocytopenia ???

A

leukaemia
lymphoma
aplastic anemia
fanconi anemia
liver disease
myeloma
myelofibrosis
437