Sickle-Cell Disease and Stroke: Quality of Life of Patients in a Chronic Transfusion Regimen from the Caregivers’ Perspective

Author:

Cerqueira Maria Aline Ferreira de1ORCID,Couto Luciana Maria Fortes Magalhães Castelo Branco2ORCID,Parente Mírian Perpétua Palha Dias2ORCID,Llerena Juan Clinton3ORCID

Affiliation:

1. Hematology and Hemotherapy Center of Piauí, Teresina, PI, Brazil

2. State University of Piauí, Teresina, PI, Brazil

3. Fernandes Figueira National Institute of Women’s, Children’s and Adolescents’ Health (IFF-FIOCRUZ), Rio de Janeiro, RJ, Brazil

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference25 articles.

1. Epidemiology and disease burden of sickle cell disease in France: A descriptive study based on a French nationwide claim database

2. Brasil. Ministério da Saúde. Secretaria de Atenção à Saúde. Secretaria de Ciência, Tecnologia e Insumos Estratégicos. Portaria Conjunta no 05, de 19 de fevereiro de 2018. Aprova o Protocolo Clínico e Diretrizes Terapêuticas da Doença Falciforme. Disponível em https://www.gov.br/saude/pt-br/assuntos/protocolos-clinicos-e-diretrizes-terapeuticas-pcdt/arquivos/2018/doenca-falciforme-pcdt.pdf/view. Acessado em 17 de janeiro de 2022]

3. Sickle cell disease: A primary care update

4. Neurologic Complications of Sickle Cell Disease

5. Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography

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