Anaemia Flashcards

1
Q

what the symptoms of anaemia?

A
fatigue 
dyspnoea 
faintness 
palpitations 
headache
tinnitus 
angina
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2
Q

whats are the signs of anaemia?

A
conjunctival and skin pallor 
glossitis 
koilonychia 
stomatitis 
tachycardia 
ES murmur
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3
Q

A microcytic anaemia is when there is low MCV. What causes it?

A

IDA
thalassaemia
sideroblastic anaemia
chronic disease (some)

TICS

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4
Q

A normocytic anaemia is when there is a normal MCV. What causes it?

A
Acute blood loss 
Anaemia of chronic disease 
Bone marrow failure 
renal failure 
hypothyroidism 
haemolysis
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5
Q

A macrocytic anaemia is when there is a high MCV. What causes it?

A

B12 or folate deficiency
Alcohol xs
Reticulocytosis
myelodysplastic syndrome

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6
Q

What causes IDA?

A

GI blood loss (Golden rule IDA in males and postmenopausal women is GI blood loss until proven otherwise)

Menstruation

Malabsorption i.e coeliacs

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7
Q

what investigations are done in IDA and what are their results?

A

Hb, MCV and MCH
- all are low

Blood film

  • microcytic, hypochromic RBCS
  • Anisocytosis (RBCs of varying size)
  • Poikilocytosis (RBCs of varying shape)

Serum ferritin and serum iron
- both low

Total iron binding capacity
- increased

Coeliac serology

OGD and colonoscopy

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8
Q

what is the treatment of IDA?

A

Oral iron replacement

  • Ferrous sulphate
  • Ferrous Gluconate
  • Ferrous fumarate

Ascorbic acid
- increases iron absorption

IV iron replacement

  • iron dextron
  • sodium ferric gluconate complex
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9
Q

what are the side effects of iron replacement?

A

Nausea, GI upset, diarrhoea/constipation, black stools

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10
Q

what is thalassaemia?

A

a relative lack of globin genes leading to decreased globin production and subsequent low Hb

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11
Q

how many alpha globin genes are there and where are they located?

A

4 located on Ch16

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12
Q

how many beta globin genes are there and where are they located?

A

2 on Ch11

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13
Q

how does missing alpha globin genes manifest?

A

missing 1 gene - mild microcytosis

missing 2 genes = microcytosis, increased red cell count and sometimes very mild anaemia

missing 3 genes = significant anaemia and bizzare small red cells known as HbH disease as the B-chains join together

Missing 4 = not compatible with life

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14
Q

how is HbH disease managed?

A

blood transfusions during periods of stress

Hepatosplenomegaly
lef ulcers
jaundice

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15
Q

how does B-thalassaemia major manifest physically and on blood analysis?

A

skull deformities
hepatosplenomegaly
osteopenia

FBC shows microcytic anaemia and leucocyte and platelet derrangement

blood smear shows microcytic RBCs with irregular teardrop shape

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16
Q

how is B-thalassaemia managed? what are the side effects of this management?

A

life long blood transfusions

can lead to;

  • endorcrine failure
  • liver disease
  • cardiac toxicity
17
Q

what are the S&S of sickle cell disease?

A

Fhx

persistent pain in skeleton, chest and/or abdomen

Dactylitis i.e swollen hands/feet

18
Q

how is sickle cells disease investigated?

A

Hb electrophoresis

Blood smear - nucleated RBCs, sickle shaped cells

FBC - anaemia

19
Q

how is sickle cell disease managed?

A

hydroxycarbamide

L-glutamine

Abx and immunisation for hyposplenism

Bone marrow transplant

20
Q

how can sickle cell crisis manifest and how is treated?

A

Stroke, Acute chest syndrome, dactiliyits, hyposplenism, kidney infarct, priapism

managed with IV opiates, crossmatch, septic screen, IV fluids, keep warm, 02

21
Q

what are the signs of B12 deficiency and how is treated?

A

pallor
Glossitis
Cheliosis
Neuropsychriatric i.e irritiability, depression, paraesthesiae
Neurological = peipheral neuropathy, paraesthesiae and absent reflexes

treat with hydroxocobalamin

22
Q

what lab tests indicates haemolytic anaemia?

A

Increased RBC breakdown

  • anaemia with normal/increased MCV
  • increased bilirubin
  • increased urinary urobilinogen
  • increased serum LDH (released from RBCs)

RBC production
- increased reticulocytes causing increased MCV

23
Q

what are the signs and symptoms of haemolytic anaemia?

A
jaundice 
dark urine 
hepatosplenomegaly 
gallstones (increased bilirubin) 
Anaemia symptoms 
Leg ulcers (poor bloodflow)
24
Q

what are the causes of immune mediated/coombs +ve haemolytic anaemia?

A

Drug induced
Autoimmune haemolytic anaemia
Isoimmune e.g transfusion reaction

25
Q

what are the causes of Coombs negative haemolytic anaemia?

A

Autoimmune hepatitis

Hep B and C

26
Q

what are the causes of microangiopathic haemolytic anaemia?

A

haemolytic uraemic syndrome
thrombotic thrombocytopenic purpure
DIC
Pre-eclampsia

27
Q

Outline Warm AIHA

A

IgG mediated

Casued by CLL, lymphoma, drugs, autoimmune disease

RBCs spherocytic and polychromic

Treat with steroids/immunosupression and/or splenectomy

28
Q

Outline cold AIHA

A

IgM mediated

causes a chronic anaemia worsened by cold

may follow infection e.g Mycoplasma or EBV

treatment = keep warm and usually self limiting