7 Flashcards

1
Q

neutrophil speed of response

A

few hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

potential complications myelodysplastic syndrome

A

AML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

myelodysplastic syndromes

A

group of cancers in which immature blood cells in the bone marrow do not mature and therefore do not become healthy blood cells.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

presentation type 2 vWD

A

bleeding more frequently and heavier than type 1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

decreased production causes of thrombocytopenia

A

bone marrow failure
aplasia
infiltration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

presentation leukostasis

A
  • fundal haemorrhages
  • dyspnoea
  • hypoxia
  • venous congestion
  • altered conciousness
  • resp failure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

mortality rate severe acute GVHD

A

70%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

management acute myeloid leukaemia

A

chemo

  • allogenic stem cell transplantation
  • ATRA
  • arsenic trioxide
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

essential investigations AML

A
  • blood count + film
  • bone marrow aspirate
  • cytogenetics
  • immunophenoytyping
  • CSF examination
  • targeted molecular genetics for children
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

management sickle cell chest crisis

A

O2
analgesia
close observation as can deteriorate quickly
transfusion top up or exchange

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

management immune thrombocytopenia purpura/ immune thrombocytopenia

A
  • steroids
  • IV IgG
  • splenectomy
  • thrombopoeitin anologues
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

define type 2 vWD

A

qualitative vWD deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

if only 1 parent has vWD problem, what are the chances of child developing each type vWD

A

type 1+2 50%

type 3 - 0%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

management haemoarthrosis

A
resting and icing the joint.
elevating the affected limb.
taking pain medications.
draining the blood from the joint.
having surgery to clean out or replace the joint (if resulting arthritis is severe enough)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is haemophilia B

A

genetic deficiency of factor IX

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

coagulation causes of haemostasis

A
  • thrombocythaemia

- insoluble fibrin formation

17
Q

causes of primary haemostasis

A

vessel wall damage

vasoconstriction -> platelet adhesion -> platelet aggregation

18
Q

when does DIC occur

A

septicaemia
malignancy
eclampsia

19
Q

what happens in DIC

A

consumption of platelets and clotting factors as a result of clot formation being greater than fibrinolysis leading to bleeding

20
Q

describe microvascular disorder

A

when the small arteries (not the main ones) of the heart are damaged
results in diffuse ischaemia
principally found in DIC

21
Q

secondary prevention DVT/ PE

A

depends on cause
anticoagulate 3 months if brought on by a trigger
lifelong if persistent risk factors

22
Q

what is D dimer

A

product of fibrin breakdown