Anaemia Flashcards

(27 cards)

1
Q

How is anaemia broadly defined

A

Hb level less than 13 in men and less than 12 in women

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2
Q

What are the 3 microcytic anaemias

A

iron deficiency anaemia
anaemia of chronic disease
thalassaemia

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3
Q

What are some causes of iron deficiency anaemia

A

reduced uptake - IBD,malnutrition,coeliac

increased loss- GI malignancy , IBD, menstruation

increased demand - pregnancy

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4
Q

What are symptoms of IDA

A

fatigue
SOB
pallor
palpitations
atrophic glossitis
post-cricoid webs
angular stomatitis
koilonychia

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5
Q

What investigations are required

A

FBC- hypochromic microcytic anaemia

blood film-
pencil cells, anisopoikilocytosis
hypochromic
microcytic
target cells

Serum ferritin - LOW

TIBC/transferrin- high– due to less iron being bound

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6
Q

What is stepwise management for those with IDA

A

treat underlying cause

oral iron replacement
-Oral ferrous sulphate/fumarate

Iron-rich diet

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7
Q

What are some side effects of iron supplements

A

black stools, constipation and nausea

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8
Q

What is Anaemia of chronic disease

A

chronic disease state - infection, malignancy, diabetes, autoimmune disorders

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9
Q

What are some symptoms that someone with ACD may have

A

fatigue
pallor
SOB with physical activity

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10
Q

What investigations are required and what will the investigations show

A

FBC- low Hb
serum iron < 15

TIBC- low

ferritin - normal / high

blood film - starts normocytic then leads to microcytic

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11
Q

How do you manage ACD

A

treat underlying cause

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12
Q

What is thalassaemia

A

two types
alpha and beta
beta thalassemia major is most severe type

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13
Q

What is the epidemiology od beta thalassaemia

A

more likely to affect those of mediterranean origin

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14
Q

What is the epidemiology of alpha thalassemia

A

more common in asians

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15
Q

What is beta thalassemia major

A

absence of beta globin chains
chromosome 11

autosomal recessive trait

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16
Q

What are features of beta thalassemia major

A

presents in first year of life with failure to thrive and
hepatosplenomegaly

microcytic anaemia

HbA2 and HbF raised

HbA absent

17
Q

What is management for beta thalassemia major

A

repeated transfusions
- however can lead to iron overload and result in organ failure

iron chelation therapy hence more important

DESFERRIOXAMINE

18
Q

What is alpha thalassemia

A

2 separate alpha globin genes are located on each chromosome 16

19
Q

What does the clinical severity of alpha thalassemia depend on

A

number of alpha globulin alleles affected

-1/2 affected - blood film is hypochromic and microcytic
Hb level is normal

3 affected -
hypochromic microcytic anaemia with splenomegaly . Hb H disease

4 - death in utero

20
Q

What are the 2 types of macrocytic anaemia

A

megaloblastic
normoblastic

21
Q

What are causes of megaloblastic anaemia

A

vit B12 deficiency
folate deficiency

nutrietnst which are essential to DNA synthesis

22
Q

What are causes of vit B12 deficiency

A

insufficient dietary intake
gastric pathology - pernicious anemia
small bowel pathology - ileal resection, IBD , malbsorption disorders

23
Q

What are causes of folate deficiency

A

reduced dietray intake
increased metabolic demand- pregnancy , malignancy
malabsorption disorders
antifolate drugs

24
Q

What are some antifolate drugs

A

phenytoin

methotrexate

trimethoprim

25
what can B12 deficiency cause
sub-acute combined cord degeneration loss of proprioception and vibration absent jerk reflexes and peripheral neuropathy
26
How do you treat megaloblastic anaemia
replace vit B12 FIRST !! then folate
27
What are some causes of normoblastic anaemia
alcohol liver disease hypothyroidism pregnancy reticulocytosis myelodysplasia drugs- AZATHIOPRINE