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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Managing the problem of pain in adolescents with sickle cell disease
Neill Westerdale1, Tina Jegede
1Department of Haematology, Guy's and St Thomas' Hospital Trust, London.
Abstract:
Sickle cell disease can be particularly painful during adolescence for several biomedical and psychosocial reasons that lead to an increase in the number of vaso-occlusive episodes. These can cause pain and tissue damage. Nurses must be aware of the range of pharmacological and psychological approaches available to help these patients.
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Assessment: