Haemotology Flashcards

1
Q

Name the different types of blood types and what they are ? how common are they? (%s)

A
0= A+B antibodies 43%
A= A antigens B antibodies 45%
B= B antigens A antibodies 9% 
AB= A + B antigens 3%
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2
Q

Which blood type is the universal donor and which is the universal recipient

A
o = donor
ab = recipient
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3
Q

Describe rhesus D pregnancy problem

A

Mum Rh -ve baby rh+-e. When born babies rbcs get into maternal blood and mum makes Anti D IgG against the Rh +ve. If the mum then has another baby that is Rh +ve. IgG crosses placenta and attacks babies RBCs

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4
Q

How do we prevent rh D pregnancy problem

A

give mum Anti D Anti bodies against the RBCs after pregnancy so she doesnt make them herself (antinatal prophylaxis)

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5
Q

What do you do when testing between patient serum and donor cells prior to blood issue

A

select blood type to match on basis of ABO/ Rh group

mix serum and cells first to test if reaction

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6
Q

Name some risks of a blood transfusion

A
reactions - febrile and allergic
infection -bac virus protazon prion
iron overload -cant excrete
anaphylaxis
viral transmission- HIV, HEP  B
RBC antibodies - alloimmunisation 
fluid overload
TRALI

hypocalaemia + dilution of clotting factors on a massive transfusion

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7
Q

How much blood in the body?

Composition of blood?

A

5L.

45% RBC, 55% PLASMA, 1% WBC+ PLATELET

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8
Q

Name the stuff in the blood that helps with immunity

A

WBC, antibodies, acute phase proteins

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9
Q

difference between serum and plasma and blood

A

plasma is centrifuged blood

serum is without clotting factors

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10
Q

functions of a RBC

A

acts as a buffer, gas exchange

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11
Q

normal Hb levels

A

male 13.5-18

female 11.5-13.5 - less because of menstruation and decreased circulating vol

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12
Q

what is the haematocrit

A

% of blood that is red cells (often proportional to haemoglobin)

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13
Q

How many platelets in the blood and how long do they last

A

7-14 days .

150

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14
Q

Descrive the 3 granulocytes

A

eosinophils
neutrophils
basophils

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15
Q

eosinophils

A

vital or antiparasite immunity and important in allergic responce
linked to 1gE
biloben nucleus

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16
Q

basophils

A
function not clear, may be important against parasites and anaphalaxis 
dark blue granules
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17
Q

neutrophils

A

phagocytose bacteria and kill (H2o2 and free radicals)
multi lobed nucleus
lifespan 8 hours
2-7%

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18
Q

what are monocytes

A

macrophages
phagocytose dead or dying cells or foreign material
may contain phagocytic vacuoles

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19
Q

whats the difference between MCV and MCH

and name some disease in each

A

MCV = mean corpuscular volume - cell size
small in microcytic anaemia
large in macrocytic anaemia

MCH is how red they are
pale in hypochromic anaemia

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20
Q

what is polycythaemia

A

RBC overproduction in the marrow

or decrease plasma (pseudopolycythameia) - caused by alcohol

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21
Q

name 3 general causes of anaemia

A

decreased RBC production
increased RBC destruction
increased RBC loss

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22
Q

Name 4 causes of microcytic anaemia

A

Thalassaemia (a+b globin chains )
Iron deficience
Chronic disease - body tries to decrease amount in inflammation
Sideroblastic anaemia (congenital)

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23
Q

what is a reticulocyte

A

an immature RBC

around for one day before becomes a RBC

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24
Q

whats the most common cause of microcytic anaemia

A

blood loss via parasites

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25
descrive 3 causes of macrocytic anaemia
- bone marrow trying to compensate for blood loss (haemorrhage and haemolysis) - marrow dysfunction 2y to renal liver and thyroid dysfunction or chemo or leukaemia - megaloblastic anaemia
26
what is megaloblastic anaemia
caused by b12 or folate deficiency , abnormal maturation of RBC
27
what is a marker for macrocytic anaemia
reticulocyte counts
28
what is thrombocytosis
platelet overproduction - normally a reaction ro inflammatory/infection
29
what is thrombocytopenia
decreased platelets. consumption by clots, infection, liver disease
30
philia penia cytosis | mean what?
philia - increased penia - decreased cytosis - increased
31
common causes of ? 1) neutrophilia 2) neutropenia 3) monocytosis 4) eosinophilia
1) reaction to infection 2) under production and over consumption 3) chronic inflammation 4) parasites, fungi, allergies
32
What is virchows triad
clots occur due to : - stasis of blood - changes in blood composition - disturbed vessel - vascular wall injury
33
type of bloot clot in aa and vv and what you give to treat them
aa - platelet ASPRIN | vv - fibrin WARFRIN
34
1 What does prothrombin time measure 2 how long is normal 3 what do we use it for
1 activity of extrinsic pathway 2 usually 9-12 s 3 use this to monitor the effect of warfarin
35
name 2 diseases the prothrombin time will be longer
liver disease and DIC
36
1 what does the APPT measure 2 how long is normal 3 what do we use it for
1 activity of intrinsic pathway 2 22-32s 3 unfractioned heparin ad hirudin
37
name some diseases the APPT is prolonged in
haemophilia A&B, liver disease, lupus anticoagulant, von willebrands disease, DIC
38
1 what does the thromin time measure | 2 how long is normal
1 final common pathway | 2 13-20
39
name 1 treatment and 3 pathological diseases that can increased thrombin time
heparin liver disease DIC dysfibrinogenaemia
40
1 what is the template bleeding time | 2 how long is normal
1 measures in vivo. razor cute 5mm cuts in skin excess blood removed gently time from cut to bleeding stopped is measured 2 normally 2-8 minute
41
Name a limitations of the clotting cascade model
1 explains how it clots in a test tube not in mammal
42
which model is more accurate representation of blood clotting
cell based model
43
describe the final common clotting pathway
prothrombin(2) to thrombin triggers fibrinogen(1) to fibrin . FXIII cross links fibrin to form strong clot
44
1 What are D dimers 2 what are they used for 3 Normal amounts
1) fragment of fibrinogen created when its chopped into pieces. 2) thery're increased if a clot is present so can be used to rule out clots in the worried well 3) normally 250 if
45
What causes haemophilia A and haemophilia B
A- reduced CF 8 | B - reduced CF 9
46
who gets haemophilia and why
both genes on the X chromosome so sex linked so only present in males
47
how does haemophilia present
arthritis - bleeding into joins as baby boy starts to walk | causes prolonges APTT (180 seconds)
48
how do you treat haemophilia
factor replacement intravenously either to treat current bleeding or prophylactically to prevent bleeding
49
What is Disseminated Intravascular Coagulation
microscopic clots form in the circulation, when platelets and clotting factors run out bleed horrendously
50
what can trigger DIC
infection, malignancy, pregnancy complications, massive bleeding
51
how do you treat DIC
identify the cause and remove it, can use plasma and platelet transfusions to buy time whilst treating the cause
52
what is transfusion coagulopathy
occurs when a massive transfusion platelets and clotting factors depleted. circulation becomes acidotic and hypothermic the temp and ph changes further from norm therefor CFs and platelets dont work
53
2 things that can case dysfunctional platelets
drugs . asprin clopidogrel abcizimab | 2y to liver disease
54
1 what can dysfunctional platelets lead to? | 2 how do you treat it
1 bleeding from mucosal surfaces e.g nosebleeds gum bleeds GI bleeds 2 remove cause
55
causes of low platelets
liver disease or marrow failure or ITP
56
1 what can low platelets lead to? | 2 how do you treat it
1 mucosal bleeding problems | 2 platelet transfusion + procoagulant drugs to prevent bleed
57
name 2 causes of aa clot and 3 of vv clot
stroke and MI | DVT PE and AF/cardio-embolism
58
thrombolysis of aa clots?
tPA - activated plasmin | heparin
59
prevention of aa clots?
platelet inhibition - eg asprin, clopidogrel, abciximab | reduce atheroma - statins to lower cholesterol, treat diabetes, bp, smoking
60
thrombolysis of vv clots?
immediately using HEPARIN high dose | medium term use warfarin
61
prevention of vv clots?
keep patients mobile - elastic stockings to maintain venous return. prophylactic heparin
62
what is warfarin
vit K antag for vit k dependent clotting factors, 2, 7,9,10
63
how long does warfarin take to work
49-72 hours
64
how does heparin work
inactivates factor 10 and 2(prothrombin)
65
difference between LMWH and UFH and one positive of both
LMWH fomed by cleavage of unfractioned heparines LMWH - consistent UFH - easily reversible
66
how do you administer heparin and warfarin
heparin iv | wafarin oral
67
what is INR used for
warfarin use and acute liver damage