Advances in Sickle Cell Disease

Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's parents. The most common type is known as sickle cell anaemia (SCA). It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. This leads to a rigid, sickle-like shape under certain circumstances.


In the present book, fifteen typical literatures about sickle cell disease published on international authoritative journals were selected to introduce the worldwide newest progress, which contains reviews or original researches on sickle cell crisis, acute chest syndrome, malaria prevention, vaso-occlusive crisis, avascular necrosis, etc. We hope this book can demonstrate advances in sickle cell disease as well as give references to the researchers, students and other related people.

Components of the Book:
  • Chapter 1
    Sickle cell disease, sickle trait and the risk for venous thromboembolism: a systematic review and meta-analysis
  • Chapter 2
    Use of autologous bone marrow stem cell implantation for osteonecrosis of the knee in sickle cell disease: a preliminary report
  • Chapter 3
    Efficacy of autologous stem cell-based therapy for osteonecrosis of the femoral head in sickle cell disease: a five-year follow-up study
  • Chapter 4
    Safety and effectiveness of antimalarial therapy in sickle cell disease: a systematic review and network meta-analysis
  • Chapter 5
    Prevalence of Plasmodium falciparum and non-P. falciparum infections in a highland district in Ghana, and the influence of HIV and sickle cell disease
  • Chapter 6
    Low-dose methotrexate in sickle-cell disease: a pilot study with rationale borrowed from rheumatoid arthritis
  • Chapter 7
    Prevention of Morbidity in sickle cell disease - qualitative outcomes, pain and quality of life in a randomised cross-over pilot trial of overnight supplementary oxygen and auto-adjusting continuous positive airways pressure (POMS2a): study protocol for a randomised controlled trial
  • Chapter 8
    Adapting medical guidelines to be patient-centered using a patient-driven process for individuals with sickle cell disease and their caregivers
  • Chapter 9
    Development and feasibility of a home-based education model for families of children with sickle cell disease
  • Chapter 10
    Verbal autopsy as a tool for identifying children dying of sickle cell disease: a validation study conducted in Kilifi district, Kenya
  • Chapter 11
    Hepatic Overexpression of Hemopexin Inhibits Inflammation and Vascular Stasis in Murine Models of Sickle Cell Disease
  • Chapter 12
    Advances in Sickle Cell Therapies in the Hydroxyurea Era
Readership: Students, academics, teachers and other people attending or interested in sickle cell disease.
Gildasio Daltro, Prof. Edgar Santos Hospital Complex, Federal University of Bahia, Salvador, Brazil

Paula Braga Daltro, Health Science Institute, Federal University of Bahia, Salvador, Brazil

Gildasio Cerqueira Daltro, Prof. Edgar Santos Hospital Complex, Salvador, Brazil

Vitor Fortuna, Health Science Institute, Federal University of Bahia, Salvador, Brazil

Silvia R. Brandalise, Boldrini Children’s CenterCampinasBrazil

Rosemary Assis, Department of Psychology, Paulista University, Campinas, Brazil

and more...
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