Microcytic Anaemia Flashcards
What causes microcytic anaemia
- iron deficiency
- thalassaemia
- sideroblastic anaemia
- anaemia of chronic disease
- GI cancer (increases with age)
- hookworm infestation in developing countries
What is the main cause of iron deficiency anaemia
- iron deficiency anaemia usually occurs as a result of blood loss through the GI tract or through menesturation
What drugs can cause iron deficiency anaemia
- NSAIDs and aspirin account for 10-15% of iron deficiency anaemia
What does thalassaemia cause anaemia
- thalassaemias cause anaemia in the carrier state (trait) but people are usually only symptomatic when both parents are affected (thalassaemia major)
What investigations do you carry out
- do a FBC and then repeat it to confirm the initial blood count and establish if abnormal results are stable or progressive
- if results are abnormal request an examination of a peripheral blood film
- test for coeliac disease (anti-tissue transglutaminase antibodies)
- upper and lower GI investigations
- autoimmune gastritis (gastrin and parietal cell antibodies)
- helicobacter pylori (urea breath test)
What investigations distinguish between iron deficiency anaemia and thalassaemia trait
- Serum ferritin - decreases in iron deficiency anaemia but remains normal in thalassaemia trait
- haemoglobin A2 quantitation - increase in beta thalassaemia trait but normal in alpha thalassaemia trait
what use can a reticulocyte count do
- differentiates anaemia due to underproduction (low if untreated iron deficiency anaemia) from that due to red blood cell loss or destruction (raised in haemolytic, bleeding and during treatment for iron deficiency)
what should you do if someone has microcytic anaemia and is either a man or postmenopausal women
- need investigation of upper and lower GI tract unless there is bleeding from a non gastrointestinal source
when should premenopausal women be investigated with microcytic anaemia
- premenopausal women with GI symptoms and iron deficiency anaemia
- all premenopausal women should be screened for coeliac disease
- aged over 50 have a family history of colon cancer need investigation of the lower GI tract
when do you refer patients
- Refer patients to the gastrointestinal department whether or not they have gastrointestinal symptoms
- Refer women to a gynaecologist if there is a structural abnormality on pelvic ultrasonography, menorrhagia unresponsive to medical management, or postmenopausal bleeding
- Refer patients to a haematology service when the type of anaemia is in doubt, laboratory findings suggest iron deficiency anaemia but there has been a poor response to oral iron supplements, or when further haematological investigations, such as bone marrow examination or an investigation of bleeding state, cannot be carried out in primary care.
what is the treatment for iron deficiency anaemia
Ferrous
sulphate 200 mg three times daily is effective
What might thalassaemia trait coexist with
Thalassaemia trait may coexist with iron deficiency anaemia and should be considered (by repeating haemoglobin A2 quantitation) when a microcytic anaemia fails to respond to iron supplementation
to avoid iron overload in patients what should you monitor
- monitor serum ferritin levels only when there is a dual cause for anaemia (as in iron deficiency anaemia with thalassaemia trait or with anaemia of chronic disease)
what happens to - serum ferritin level - serum iron level - total iron binding capacity - transferrin saturation - haemoglobin electrophoresis and quantitation of haemoglobin A2 in iron deficiency anaemia
- serum ferritin level = decreased
- serum iron level = decreased
- total iron binding capacity = increased
- transferrin saturation = decreased
- haemoglobin electrophoresis and quantitation of haemoglobin A2 = normal
what happens to - serum ferritin level - serum iron level - total iron binding capacity - transferrin saturation - haemoglobin electrophoresis and quantitation of haemoglobin A2 in thalassaemia trait
- serum ferritin level = normal
- serum iron level = normal
- total iron binding capacity = increased
- transferrin saturation = normal
- haemoglobin electrophoresis and quantitation of haemoglobin A2 = increased haemoglobin A2 in beta thalassaemia trait, normal in alpha thalassaemia trait