Haematology - Autoimmune haemolytic anaemia
Diagnosing and managing autoimmune haemolytic anaemia. By Professor David Roberts
HAEMATOLOGY RESOURCE CENTREOur series of articles on haematology covers a wide range of topics to broaden your knowledge of this vast area. Our articles are written by expert haematologists from across the UK but are focussed on what is useful and practical in primary care.
Topics covered include the anaemias, haemato-oncology, and myeloproliferative disease.
Diagnosing and managing autoimmune haemolytic anaemia. By Professor David Roberts
One cause for a high Hb level in adults is polycythaemia vera, writes Dr Jecko Thachil
This myeloproliferative disorder is mainly seen in men aged over 50, writes Dr Jecko Thachil
This group of rare metabolic disorders can be diagnosed using appropriate biochemical tests, says Dr David Rees
The most important cause of this alloimmune disease is formation of antibodies to the rhesus D antigen. By Dr Denise Bonney
Pre-eclampsia is relatively common but can become life-threatening, says Professor David Roberts.
The early recognition and referral of patients with TTP is essential, says Professor David Roberts.
Management depends on the clinical circumstances, say Dr Shruthi Patel and Dr John Hanley.
GPs need to be aware of the risks and benefits of receiving blood, explains Dr Megan Rowley.
Read the article on disseminated intravascular coagulation then answer these three questions to check your understanding. You may want to document your answers and any learning points to save in your CPD folder along with the article.
This life-threatening condition has many triggers.
Deficiency can be caused by blood loss, malabsorption or increased requirement.
In the first of our new series on haematology, Dr Amit Patel discusses sickle cell anaemia.
This condition predominantly affects the elderly. By Dr Anicee Danaee and Dr Deepti Radia.
Contributed by Dr Ana Filipa Barroso, a research fellow in obstetric haematology at Barts and the London NHS Trust

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