Red cells 2 - acquired anaemias Flashcards

1
Q

What does normal haemoglobin depend on?

A

sex, age, ethnicity, time sample taken etc..

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2
Q

Normal male Hb values

A

12-70 (140-180)

>70 (116-156)

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3
Q

Normal female Hb values

A

12-70 (120-160)

>70 (108-143)

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4
Q

clinical features of anaemia

A
SOB 
pallor
tiredness 
dizziness 
ankle swelling
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5
Q

Underlying causes clinical features of anaemia

A

bleeding eg menorrhagia, GI bleed
malabsorption eg diarrhoea
splenomegaly and jaundice

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6
Q

bone marrow pathophysiology anaemia

A

cellularity, stroma, nutrients

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7
Q

RBC pathophysiology anaemia

A

membrane, enzymes, haemoglobin

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8
Q

destruction/loss anaemia pathophysiology

A

bleeding
haemolysis
hypersplenism

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9
Q

MCV

A

mean cell volume = cell size

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10
Q

MCH

A

mean cell haemoglobin

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11
Q

3 morphological types of anaemia

A

hypochromic microcytic
normochromic normocytic
macrocytic

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12
Q

What you would measure in each of the 3 morphological types of anaemia

A
Hm = Serum ferritin 
Nn = Reticulocyte count
M = Vit B12/folate or bone marrow
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13
Q

serum ferritin results and what they mean

A
low = iron deficiency anaemia 
normal/high = secondary anaemia, thalassaemia
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14
Q

Is there a pathway for excess iron excretion?

A

no

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15
Q

What happens to absorbed iron?

A

bound to mucosal ferritin and shedded OR

transported across basement membrane by ferroportin

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16
Q

What is iron bound to in plasma?

A

transferrin

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17
Q

What is iron stored in cells as?

18
Q

hepcidin

A

produced by hepatocytes
bind to ferroportin and stop iron absorption
chronic anaemia of inflammatory diseased

19
Q

History - iron deficiency anaemia

A

dyspepsia/Gi bleed, menorrhagia, diet, increased requirement eg pregnancy, malabsorption eg coeliac

20
Q

Examination - iron deficiency anaemia

A

koilonychia
tongue atrophy and angular cheilitis
abdominal and rectal

21
Q

managing iron deficiency anaemia

A

oral iron (IV if intolerant)
rarely blood transfusion
diet, ulcer therapy, gynae etc..

22
Q

Reticulocyte findings and what it means

A

increased - acute blood loss/haemolysis

decreased - marrow infiltration , secondary anaemia

23
Q

haemolytic anaemia - 2 main things

A

increased red cell destruction = decrease Hb

compensation by bone marrow = increase Reticulocyte count

24
Q

extravascular and intravascular haemolysis

A
extravascular = reticuloendothelial system and immune mediated 
intravascular = in vessels, non immune mediated
25
congenital haemolysis
hereditary spherocytosis enzyme deficiency haemoglobinopathy
26
acquired haemolysis
``` autoimmune mechanical (heart valve), PET, DIC, infection ```
27
Direct antiglobulin test
detects antibody or complement on RBC | reagent is anti human IgG or anti complement
28
DAGT results and what they mean
``` +ve = immune mediated -ve = non-immune mediated ```
29
How to find out if patient is haemolysing
``` FBC reticulocyte count blood film serum bilirubin heptaglobin ```
30
How to find out the mechanism of haemolysis
AGT, urine, blood film
31
managing haemolysis
support marrow function - folic acid autoimmune - steroids splenectomy, transfusion? remove valve, infection, sepsis etc
32
secondary anaemia type
normochromic normocytic
33
megaloblastic anaemia
B12/folate deficiency
34
non-megaloblastic anaemia
marrow infiltrate | drugs
35
appearance of megaloblastic anaemia
yellow tinge - bilirubin
36
Vitamin B12 absorption
binds to intrinsic factor made by parietal cells | absorbed in distal ileum
37
commonest cause of B12 deficiency
pernicious anaemia
38
pernicious anaemia
auto antibodies directed against INTRINSIC FACTOR
39
How long does it take for pernicious anaemia symptoms to appear?
1-2 years
40
megaloblastic anaemia treatment
B12 - im injection | oral folate --> ensure B12 levels normal if neuropathic symptoms
41
other causes of macrocytosis
drugs eg ART, methotrexate hypothyroidism alcohol disordered liver function