35.3 Anaemia Flashcards

1
Q

at birth what is the Hb/MCV/MCH relative to adult?

A

all higher than normal the begins to drop off

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2
Q

when is the nadir for Hb/MCV/MCH

A

2 months

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3
Q

2 things to looks at when you see a low haemoglobin

A

MCV

Reticulocyte count: are they producing?

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4
Q

iron deficiency anaemia, if ferritin is what level = diagnostic?

A

<10ug/L

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5
Q

ferritin goes up in?

A

infection
malignancy
liver disease

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6
Q

how much iron to treat anaemia?

A

6mg/kg/day of elemental iron
1ml/kg/day of ferro-liquid
treatment for 3 months

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7
Q

when to check for response with iron therapy?

A

1-2 weeks

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8
Q

restrict milk in anaemia?

A

500ml

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9
Q

how to tell if child has cow’s milk protein intolerance?

A

hopyalbuminaemic
bleeds from gut
managed by boiling cow’s milk

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10
Q

when do alpha chain disorder manifest?

A

birth, persists throughout life

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11
Q

when do beta chain disorder manifest?

A

3-6months persists

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12
Q

when do gamma chain disorder manifest?

A

birth, declines after

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13
Q

what is thalassaemia intermedia?

A

can be homozygous or variety, not requiring transfusions

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14
Q

problem with transfusion dependent thalassaemia?

A

iron overload,

need chelator, daily

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15
Q

what to investigate if think thalassaemia?

A

FBC
Film
HB electrophoresis/Hb studies
Ferritin

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16
Q

2 main causes of megaloblastic anaemia?

A
B12 - deficiency in mother
-vegans
-missing ileum
-selective malabsorption
Folate - not as much
17
Q

why do ppl with hereditary spherocytosis get more gallstones?

A

increased breakdown of RBCs, more bilirubin, more load on liver

18
Q

hereditary spherocytosis bad complication?

A

aplastic crises secondary to parvovirus

19
Q

what happens in a G6PD attack?

A
  • oxidative hemolysis
  • get brown urine
  • jaundice
20
Q

if G6PD is x-linked, how do girls get it?

A
  • homozygous
  • turner’s
  • girls’ inactivate one of their Xs early on
  • balance translocation
21
Q

G6PD, 2 things life-threatening?

A
  • fava beans

- naphthalene

22
Q

what is diagnostic on blood film for G6PD?

A

bite and blister cells and irregularly contracted cells

23
Q

who to look for if suspect sickle cell?

A
  • african
  • middle eastern descent
  • abdo pain and leg pain
24
Q

when to refer to paed haematologist?

A
  • macrocytic anaemia
  • haemoglobinopathies
  • haemolytic anaemias
  • anaemia+splenomegaly
  • anaemia with neutropenia/thrombocytopenia
25
Q

iron supplementation in thalassemia?

A

NOPE

contraindicated, iron overload