Paediatric Protocols/Guidance
Acute Guidance
- Acute abdominal pain in children with Sickle Cell disease
- Acute Anaemia
- Acute Chest Syndrome
- Chronic Transfusion in Thalassaemia
- Monitoring and management of endocrine complications in children with transfusion dependent thalassemia (TDT)
- Endocrine complications in children with Thalassaemia
- Exchange Transfusion
- Hydroxycarbamide in Sickle Cell disease
- Inpatient Specialist Management of acutely unwell children with haemoglobinopathies
- Iron overload and chelation therapy
- Management of Hyperhaemolysis in patients with Sickle Cell disease
- Management of Priapism in Sickle Cell disease
- Painful Sickle Cell crisis (management)
- Physiotherapy guideline for the acute management of paediatric & adult patients with Sickle Cell disease
- Stem Cell Transplant
- Stroke and other CNS manifestations
- Surgery and Anaesthesia
- Transcranial Doppler (TCD) screening for Sickle Cell disease
- Diagnosis and Management of Non-Transfusion-Dependent Thalassaemia (NTDT) phenotypes
- Vaccination
Guidance due for review is being considered by the SPAH Guidance subgroups. Information contained within the guidance has been approved to remain in the website.
