Haematology Flashcards

1
Q

where is the cellular component of blood produced?

A

marrow

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2
Q

what does a full blood count measure?

A

number and size of cells

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3
Q

what is the condition associated with lack of haemoglobin?

A

anaemia

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4
Q

cells that are too big are?

too small?

A

macrocytic

microcytic

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5
Q

what is WCC?

A

quantity of white blood cells

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6
Q

too many white blood cells?

too few?

A

leucocytosis

leukopenia

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7
Q

too few platelets?

too many?

A

thrombocytopenia

thrombocythaemia

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8
Q

what is a blood film test?

A

smear of red blood cells examined under a microscope

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9
Q

what is neutrophilia?

A

increase in neutrophil production caused by an acute infection

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10
Q

what is malaria?

A

red blood cells deteriorate because of parasites

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11
Q

how are bone marrow samples done?

A

taken from iliac crest/sternum

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12
Q

what are tests to measure coagulation?

A

activated prothrombin time APTT

INR

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13
Q

what pathway causes APTT?

what is a normal prothrombin time?

A

intrinsic pathway

12-13 secs

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14
Q

reasons for lack of haemoglobin in anaemia?

A

lack of raw materials
production problems
longevity problems

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15
Q

what raw materials are needed for haemoglobin to form?

A

iron, vit B12, folate

erythropoietin

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16
Q

why might there be a lack of iron and folic acid?

A

usually dietary, rarely malabsorption

increase in lack of when pregnant

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17
Q

lack of vit b12 caused by?

what kind of anaemia does it cause?

A

autoimmune diseases affect absorption of B12

pernicious anaemia

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18
Q

what do you see on a blood film of someone with anaemia?

A

very pale cells = hypochromic

micocytic smaller cells

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19
Q

why might there be production problems to do with erythropoiten?

A

renal failure

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20
Q

reasons for production problems do to with bone marrow ?

A

aplastic anaemia - no cells
chemotherapy/immunosuppressants
haematological malignancy
anaemia of chronic disease - any chronic inflam process

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21
Q

what are reasons for blood loss causing lack of haemoglobin?

A

bowel - majority
menstruation
trauma/post op
other organs - unusual

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22
Q

wjhat is haemolysis?

A

destruction of cells in circulation

e.g autoimmunity, sickle cell anaemia, thalassemia

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23
Q

lack of what raw materials cause macorcytic cells?

A

B12, folate deficiency

24
Q

what are some symptoms of anaemia?

A

tired, weak, breathless, dizzy, palpitations

25
signs of anaemia?
pale, rapid pulse, oral feautres
26
management of anaemia?
history and exam | establish type - fbc, blood film, levels of iron, folate, b12
27
treatment of anaemia?
iron sulphate folic acid, B12 erythropoietin severe/symptomatic - blood transfusion
28
dental - oral abnormalities caused by? why be careful with GA? what should you verify in an anaemic pt?
iron, b12, folate o2 capacity reduced, sickle cell status
29
what is a neutropenia? caused by?
an inadequate number of neutrophils | bone marrow failure, auntoimmune disease
30
what infections can occur in the mouth?
candida, viral herpes simplex, commensal bacteria
31
dentally be aware of what? do to with white blood cell disorders
chemo pts - bone marrow affected be aware of who is at risk avoid invasive tx
32
what is leukemia?
proliferation of immature cells in blood/bone marrow
33
what is lymphoma?
proliferation of lymphocytes | confined to nodes, liver, spleen, bone marrow
34
acute leukaemia, acute - common in who? what is seen on a blood film?
kids | full of lymphocytes
35
chronic leukaemia, common in who?
adults | can transform to acute
36
increased risk of what with leukaemia?
risk of infection, anaemia, bleeding
37
types of lymphoma?
hodgkins, non hodgkins
38
hodgkins lymphoma systemic factors?
lymphadenopathy | fever, weight loss, night sweats
39
non hodgkins common in? | prognosis?
older pt's | poorer
40
tx of lymphoma?
``` transfusions, infection management chemo radio bone marrow transplant - autologous, allogenic novel therapies ```
41
dental relevance of lymphomas?
atypical infections, bleeding, lymphadenopathy, gum infiltration
42
what does rate of coagulation depend on?
number and functioning ability of platelets
43
3 stages of a clot formation?
vasoconstriction, platelet aggregation, coagulation cascade
44
problems with platelets forming?
deficiencys of raw materials production - bone marrow failure destruction - immune mediated
45
immune mediated conditions causing platelet destruction?
portal hypertension - spleen sequestrian | auntoimmune thrombocytopenic purpura
46
aggregation problems - reason? tx?
platelet function impaired/ medical therapy - aspririn or copidogrel tx of underlying cause platelet transfusion maybe necessary
47
coagulation cascade problems? gen deficiency ? specific deficiency?
gen - protein - liver disease/malnutrition spec. - coagulation - haemophilia, von wilebrands disease drugs - warfarin/heparin
48
what is haemophilia A? B?
A - x lined genetic disorder - absence of VIII clotting factor B - " , IX clotting factor
49
what is von wilebrands disease?
autosomal dominant - platelet factor VIII function problem
50
tx of lack of clotting factors?
factor replacement, prophylactic
51
what does DDAVP do?
increases factor VIII levels
52
what does tranexamic acid do?
inhibits clot breakdown
53
dentally, what to be aware of with pt's with coagulation problems?
risk management, trauma avoidance, prep for suspected bleeding associated conditions - HIV, hepatitis
54
what is warfarin used for?
atrial fib, heart valves, PE, DVT interferes with clotting factor activity INR checked
55
what is heparin used for?
DVT, PE | injectable
56
what is - petechiae, purpura, ecchymoses?
cutaneous bleeding larger bleeds brusing bc bleeding
57
what is menhagva? haemoturina?
excess menstrual bleeding | urinary tract bleeding