Author: Roy, Noémi B. A.; Telfer, Paul; Eleftheriou, Perla; de la Fuente, Josu; Drasar, Emma; Shah, Farrukh; Roberts, David; Atoyebi, Wale; Trompeter, Sara; Layton, D. Mark; Lugthart, Sanne; Stuartâ€Smith, Sara; Chakravorty, Subarna; Wright, Josh; Porter, John; Inusa, Baba; Howard, Jo
Title: Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVIDâ€19 pandemic Cord-id: gluzoods Document date: 2020_5_10
ID: gluzoods
Snippet: With the developing COVIDâ€19 pandemic, patients with inherited anaemias require specific advice regarding isolation and changes to usual treatment schedules. The National Haemoglobinopathy Panel (NHP) has issued guidance on the care of patients with sickle cell disease, thalassaemia, Diamond Blackfan anaemia (DBA), congenital dyserythropoietic anaemia (CDA), sideroblastic anaemia, pyruvate kinase deficiency and other red cell enzyme and membrane disorders. Cascading of accurate information for
Document: With the developing COVIDâ€19 pandemic, patients with inherited anaemias require specific advice regarding isolation and changes to usual treatment schedules. The National Haemoglobinopathy Panel (NHP) has issued guidance on the care of patients with sickle cell disease, thalassaemia, Diamond Blackfan anaemia (DBA), congenital dyserythropoietic anaemia (CDA), sideroblastic anaemia, pyruvate kinase deficiency and other red cell enzyme and membrane disorders. Cascading of accurate information for clinicians and patients is paramount to preventing adverse outcomes, such as patients who are at increased risk of fulminant bacterial infection due to their condition or its treatment erroneously selfâ€isolating if their fever is mistakenly attributed to a viral cause, delaying potentially lifeâ€saving antibiotic therapy. Outpatient visits should be minimised for most patients, however some, such as first transcranial dopplers for children with sickle cell anaemia should not be delayed as known risk of stroke will outweigh the unknown risk from COVIDâ€19 infection. Blood transfusion programmes should be continued, but specific changes to usual clinical pathways can be instituted to reduce risk of patient exposure to COVIDâ€19, as well as contingency planning for possible reductions in blood available for transfusions. Bone marrow transplants for these disorders should be postponed until further notice. With the current lack of evidence on the risk and complications of COVIDâ€19 infection in these patients, national data collection is ongoing to record outcomes and eventually to identify predictors of disease severity, particularly important if further waves of infection travel through the population.
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