2 Flashcards

1
Q

define graft vs. host disease

A

an immune condition occurring after transplant when donor immune cells attack recipient patient hosts tissues

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2
Q

explain autologous stem cell transplant

A

bone marrow is removed, frozen and reinfused after potent chemotherapy has been given

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3
Q

what drugs are used to prevent immunosuppression

A
  • immunosuppressants
  • rapamycin
  • cyclosporin
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4
Q

life long prophylaxis for stem cell crisis (HbS)

A
  • vaccinations
  • penicillin
  • malarial prophylaxis
  • folic acid
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5
Q

define thrombocytopenic purpura

A

isolated low platelet count with normal bone marrow in the absence of other causes of low platelets

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6
Q

chronic myeloid leukaemia

A

white blood cancer that grows slowly
bone marrow produces too many myeloid cells – immature white blood cells that are not fully developed and do not work properly.

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7
Q

causes leukostasis

A
  • too many platelets
  • AML
  • CML
  • ALL
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8
Q

examples of acquired bleeding disorders

A
  • liver and renal failure
  • thrombocytopenia
    drugs:
  • warfarin
  • heparin
  • aspirin
  • rivaroxaban
  • apixaban
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9
Q

define hyper acute organ rejection

A

type II hypersensitivity reaction
within hours
preformed antibodies bind to ABO? HLA on graft
graft destroyed by vascular thrombosis

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10
Q

define type IIII hypersensitivity reaction

A
  • slowest
  • T cell mediated
  • 2->3 days to develop
  • delayed hypersensitivity
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11
Q

management von willebrand disease

A
  • vWF concentrate of DDAVP
  • transexamic acid
  • COCP
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12
Q

presentation type 3 vWD

A
  • most severe and rarest
  • bleeding from mouth nose and gut common
  • joint and muscle bleeds can occur after injury
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13
Q

cause of type 2 hypersensitivity reaction

A

ANTIBODY DEPENDANT

  • blood transfusion
  • haemolytic disease of newborn
  • drug induced haemolysis
  • graves disease
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14
Q

management options type 1 hypersensitivity reaction

A
  • antihistamines
  • epinephrine
  • prevention
  • desensitisation
  • corticosteroids
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15
Q

management severe primary immunodeficiency

A
  • antibodies against a wide range of pathogens
  • Ig IV/ subcutaneous
  • plasma screened for HIV and hep B/C
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16
Q

types HbS related painful vaso-occlusion

A
  • bone
  • chest
  • stroke
17
Q

what is adult haemoglobin composed of

A
  • haem molecule
  • 2 alpha chains
  • 2 beta chains
18
Q

presentation G6PD deficiency

A
  • fatigue
  • neonatal jaundice
  • anaemia
  • splenomegaly
  • pigmented gallstones
  • intravascular haemorrhage
  • haemoglobinuria
19
Q

what different areas of immune system could primary immunodeficiency be in

A

components of innate

stages of lymphocyte development

responses of mature lymphocytes to antigen stimulation

20
Q

describe Von Willebrand disease

A

genetic disroder

missing/ defective vWF

21
Q

management haemophilia A/ B

A

factor VIII/ IX

desmopressin

tranexamic acid

22
Q

describe articular bleeding (bleeding into joint)

A
  • hot
  • pain
  • not moving
  • positioned in most comfortable position