red cells + acquired anaemias Flashcards

1
Q

factors influencing ‘normal range’ of haemoglobin levels

A
age
sex
ethnic origin 
time of day sample taken 
time to analysis
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2
Q

male haemoglobin reference ranges

A

12-70: 140-180

>70: 116-156

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3
Q

female haemoglobin reference ranges

A

12-70: 120-160

> 70: 108-143

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4
Q

general features of anaemia

A
tiredness
pallor 
breathlessness
swelling of ankles (heart failure) 
dizziness (adjustment of BP)
chest pain - myocardial ischaemia
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5
Q

anaemia causes: problem with production in bone marrow

A

cellularity
stroma
nutrients - not enough iron, folate etc

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6
Q

anaemia causes: problem with red cell

A

membrane
haemoglobin
enzymes

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7
Q

anaemia causes: problems with destruction and loss

A

blood loss
haemolysis
hypersplenism - pooling of blood in spleen

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8
Q

red cell indices

A

automated measurement of red cell size and haemoglobin content

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9
Q

MCH

A

mean cell haemoglobin

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10
Q

MCV

A

mean cell volume (cell size)

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11
Q

hypochromic microcytic anaemia

A

small pale cells

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12
Q

normochromic normocytic anaemia

A

huge number of anaemias

normal amount of Hb and avg normal cell size

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13
Q

macrocytic anaemia

A

big red cells

bigger cells but usually with less Hb - usually pale

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14
Q

hypochromic microcytic anaemia first investigation to do

A

serum ferritin - measure of body iron store

if low = iron deficiency

if normal/inc = thalassaemia, 2ry anaemia (sideroblastic anaemia)

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15
Q

normochromic normocytic anaemic first investigation to do

A

reticulocyte count

if bleeding or haemolysis this count will increase

low if bone marrow nor working

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16
Q

first investigation to do if macrocytic anaemia

A

B12/folate + bone marrow

commonest cause = B12 or folate deficiency

if B12 + folate normal then bone marrow problem e.g. malignancy

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17
Q

hypochromic microcytic anaemia: secondary anaemia

A

normal ferritin with abnormal iron utilisation if background inflammation

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18
Q

intake and loss of dietary iron

A

absorbed by duodenum

lost by intestinal cells (+ menstruation in women)

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19
Q

dietary iron absorption

A
  • iron from diet can be haem or non-haem
  • enter through villi of duodenum, ferroportin transports it across into circulatin
  • bind to transferrin which carries it to liver (if needed for making blood) or to liver where it is stored as ferritin
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20
Q

hepcidin

A

synthesised by hepatocytes in response to increased iron levels, binds to ferroportin and inactivates it

stops you absorbing more iron than you need

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21
Q

iron and inflammation

A

iron can be redirected into inflammatory processes

hepcidin switches on to allow this to happen

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22
Q

signs of iron deficiency

A

kooilonychia
angular chelitis
atrophic tongue

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23
Q

causes of iron deficiency

A

GI blood loss
menorrhagia
malabsorption - gasterectomy, coeliac

24
Q

management of iron deficiency

A

correct deficiency - oral iron usually sufficient (IV if intolerant), blood transfusion rarely indicated

correct cause - diet, ulcer therapy, gynae intervention, surgery e.g. tumour

25
normochromic normocytic anaemia: reticulocyte count increased
- acute blood loss | - haemolysis: inc breakdown of cells
26
normochromic normocytic anaemia: reticulocyte count normal/low
secondary anaemia e.g. due to renal impairment, chronic disease hypoplasia marrow infiltration
27
secondary anaemia
anaemia of chronic disease mostly hypochromic microcytic
28
secondary anaemia: defective iron utilisation
- increased hepcidin in inflammatin | - ferritin often elevated (acute phase reactant)
29
secondary anaemia: underlying diseases
infection inflammation malignancy
30
haemolytic anaemi
accelerated red cell destruction (low Hb) | compensation by bone marrow (inc reticulocytes)
31
extravascular haemolysis
extravascular haemolysis in macrophages of reticuloendothelial cells normal process increased in haemolysi s e.g. red cell abnormal shape and removed faster can get exageration of normal process as cells recognised as foreign by reticuloendothelial system
32
intravascular haemolysi s
pathological red cells bust in circulation free Hb in circulation toxic to kidneys, free radicals cause inflammation sick people or haemoglobinopathies e.g. sickle cell
33
congenital haemolytic anaemias
hereditary spherocytosis G6PD deficiency haemoglobinopathy HbSS
34
acquired haemolytic anemias
autoimmune haemolytic anaemia (extravascular) - exaggerated removal of red cells from circulation mechanical e.g. artificial valve leaking (intravasc) severe infection/DIC (intravasc) PET/HUS/TTP (intravasc)
35
immune haemolytic anaemias
mostly extravascular
36
non-immune haemolytic anaemias
mostly intravascular
37
direct antiglobulin test
if suspicion someone has immune haemolysis detects antibody or complement on red cell membrane
38
direct antiglobulin test: reagent
anti-human IgG antibody or anti-complement antiboy reagent will bind if there is antibody on red cell surface and cause agglutinatin in vitro (cells stick together)
39
direct antiglobulin test resultd
positive - immune mediated | negative - non-immune mediated
40
immune haemolysis: warm autoantibody
bind to cells at body temp only autoimmune drugs CLL
41
immune haemolysis: cold autoantibody
only bind when cold CHAD infections lymphoma
42
immune haemolysis: alloantibody
antibody against transfused cells transfusion reaction
43
extravascular haemolysis - blood film
spherocytes on film - due to damaged membrane agglutination in cold AIHA
44
intravascualr haemolysis - blood film
red cell fragments - schistocytes
45
haemolytic anaemia investigations
``` FBC reticulocyte count blood film serum bilirubin, LDH serum haptoglobin ```
46
haemolytic anaemia management
support marrow function - folic acid correct cause - immunosuppression if autoimmune (steroids, treat trigger e.g. lymphoma) remove site of red cell destruction - splenectomy consider transfusion
47
macrocytic anaemia investigations
B12/folate assay and blood film megaloblastic = b12/folate deficiency non-megaloblastic = myelodysplasia, marrow infiltration, drugs e.g.methotrexate
48
vitamin B12 absorption
dietary B12 binds to intrinsic factor (made by parietal cells) B12-IF complex attaches to specific IF receptors in distal ileum B12 bounded by transcobalamin II in portal circulation for transport to marrow/other tissues
49
B12 deficiency causes
pernicious anaemia | gastric/ileal disease
50
folate deficiency causes
dietary inc requirements (haemolysis) GI pathology e.g. coeliac
51
why do get lemon yellow tinge in B12/folate def anaemia
bilirubin, LDH | red cells friable
52
pernicious anaemia
commonest cause of B12 def in western pop autoimmune disease antibodies against intrinsic factor, parietal cells malabsorption of dietary B12
53
why to symptoms/signs of pernicious anaemia take 1-2yrs to show
takes time to run through b12 stores | bit of passive absorption in small intestine
54
megalobastic anaemia treatment
replace vitamin
55
B12 replacement
B12 IM injection loading dose then 3mo maintenance
56
folate replacement
oral folate replacement ensure B12 normal if neuropathic symptoms
57
other causes of macrocytosis
``` alcohol drugs - methotrexate, antiretrovirals, hydroxycarbamine disordered liver function hyperthyroidism myelodysplasia ```