anaemia Flashcards

1
Q

why gaviscon -> anarmia

A

iron best absorbed in acidic env

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2
Q

what transports Fe into enterocyte

A

DMT1

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3
Q

what transports Fe from enterocyts into blood

A

ferroportin

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4
Q

what gets the iron off haem

A

haem oxygenase

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5
Q

what carries fe in blood

A

transferrin

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6
Q

which type of Fe can be absorbed ino enterocye

A

Fe2+

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7
Q

who reduces Fe3+ to Fe2+

A

reductase or anti ox like vit C

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8
Q

which enzyme blocks ferroportin

A

hepcidin

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9
Q

where is hepcidin made

A

liver

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10
Q

what Fe ox state is it carried in by transferrin

A

3+

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11
Q

how is iron used in normal cells

A

mitochondria use it in cytochrome enzyems

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12
Q

liver releases ferritin in acute inflammation. what does this mean?

A

in eg RA, serum ferritin can be high even in anaemia

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13
Q

doctor name for bone marrow

A

myeloid tissue

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14
Q

where does erythropoiesis happen

A

red bone marrow

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15
Q

what happens in yellow bone marrow

A

lymphopoiesis

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16
Q

what controls rate of erythropoiesis

A

EPO

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17
Q

where EPO made

A

kidneys interstitial cells near proximal tubules

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18
Q

what causes ++EPO

A

low oxygen

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19
Q

what does EPO do

A

increase erythroblast maturation and pro erythroblast formation

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20
Q

where foetal erythropoiesis

A

You - yolk sac 3-8 wks
Like - Liver 6wk - birth
Split - spleen 8-28 wk
Bonanas - bone marrow18wk to adult

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21
Q

how does reticulocyte get out of BM

A

diapedesis

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22
Q

what molecule causes colour of faeces

A

stercobilin

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23
Q

what molecule causes colour of wee

A

urobilin

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24
Q

what is Haem - Fe2+

A

unconjugated bilirubin

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25
where does unconjugated bilirubin go?
liver bound to albumin in the blood
26
what heppens to bilirubin in the liver
gets conjugated with glucoronic acid -> bilirubin diglucoronide
27
how is bilirubin gotten rid of
secreted in bile
28
where is erythrocyte destruction
spleen by macrophages
29
what is glossitis
inlfammation and depapillation of the tongue
30
what is koilonychia
spoon shaped nails
31
what is angular cheilitis
swelling at corners of mouth
32
weird symptom of IDA
pica - eating non-food such as dirt or ice
33
name 5 tests for IDA
34
IDA in older adult or younger with no obvious apparent cause
CHECK FOR GI MALIGNANCY
35
what does haptoglobin do
mop up free haemoglobin in the blood
36
haemolytic anaemia divided into
DAT + DAT- DAT + indicates the presence of immunoglobulin (Ig)G, IgM, IgA or complement (usually C3d) bound to the red cell membrane so basically very likely to be autoimmune condition DAT - haemoglobinopathies membranopathies infections
37
DAT - haemoglobinopathy example
sickle cell
38
is sickle cell DAT+
no
39
infection that can cause haemolytic anaemia
malaria clostridium
40
how does acute haemolytic anaemia present?
pt is bright yellow
41
why is patient bright yellow
too much conjugated bilirubin
42
what testresults in acute haemolytic anaemia
haemoglobinuria haemoglobinaemia
43
risk factor for caridac arrest in acute haemolytic anaemia
acute hyperkalemia
44
jaundice, splenomegally and pigment gallstones are signs of
acute haemolytic anaemia
45
what is alloimmune haemolytic anaemia
you develop antibodies to transfused blood Or neonatal - mum's antibodies start to haemolyse baby blood
46
3 problem areas in RBC that can lead to haemolytic anaemia
enzymes membrane haemoglobin misspelling
47
what is intravascular haemolytic anaemia
48
what is extravascular haemolytic anaemia
49
why splenomegaly in what is intravascular haemolytic anaemia
extramedullary haematopeosis - making rbc in red pulp of spleen
50
which membrane proteins can go wrong to cause hereditary spherocytosis
Heterogeneous – deficiencies of spectrin (41.5%), ankyrin (1.5%), band 3 (17%), band 4.2 (21.5%)
51
hereditary spherocytosis mode of inheritance
AD
52
what is this common inherited maemolytic anaemia
spherocytosis
53
why pt urine normal in day and black at night
Paroxysmal nocturnal haemoglobinuria
54
what is cause of Paroxysmal nocturnal haemoglobinuria
problem with RHAG complement mediated
55
what is tx for Paroxysmal nocturnal haemoglobinuria? Moa?
eculizumab - binds C5 protein so can't be activated
56
sickle cell mutation
point - glu is now val
57
reticulocyte count in sickle
3-4-500
58
sickle hallmarks
ischaemia shortened rbc lifespan ++inflammation could be pyrexia vasoocclusion infection stroke in children
59
most common enzymopathy
G6PD
60
meds to avoid in G6PD
Dapsone. Methylene blue. Nitrofurantoin. Pegloticase. Phenazopyridine. Primaquine. Rasburicase. Tafenoquine. Chemicals to avoid. Naphthalene (an ingredient found in moth balls)
61
G6PD mode of inheritance
X linked but female pts are seen
62
G6PD
63