Sickle cell disease is the most common inherited blood disorder, affecting millions of people worldwide. Although sickle cell disease can be found in various areas of the world, it predominantly affects individuals of African or Hispanic heritage. The hallmark clinical symptoms are due to vaso-occlusion, which occurs when the blood vessels are obstructed by sickled red cells. The most common symptom of vaso-occlusion is moderate-to-severe pain. Severe complications include acute chest syndrome, stroke, and pneumonia. Clinicians and patients with sickle cell disease may have difficulty treating the painful episodes owing to the subjective nature of pain and lack of knowledge of the disease.
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Univ Birmingham, Med Sch, Birmingham B15 2TT, W Midlands, EnglandUniv Birmingham, Med Sch, Birmingham B15 2TT, W Midlands, England
Booker, Matthew J.
Blethyn, Kate L.
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Univ Birmingham, Med Sch, Birmingham B15 2TT, W Midlands, EnglandUniv Birmingham, Med Sch, Birmingham B15 2TT, W Midlands, England
Blethyn, Kate L.
Wright, Christine J.
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City Hosp, Sickle Cell & Thalassaemia Ctr, Birmingham B18 7QH, W Midlands, EnglandUniv Birmingham, Med Sch, Birmingham B15 2TT, W Midlands, England
Wright, Christine J.
Greenfield, Sheila M.
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Univ Birmingham, Dept Primary Care & Gen Practice, Birmingham B15 2TT, W Midlands, EnglandUniv Birmingham, Med Sch, Birmingham B15 2TT, W Midlands, England
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Yale New Haven Med Ctr, Dept Pharm Serv, 20 York St, New Haven, CT 06504 USAYale New Haven Med Ctr, Dept Pharm Serv, 20 York St, New Haven, CT 06504 USA
Zassman, Stefanie M.
Zamora, Francis J.
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Yale New Haven Med Ctr, Dept Pharm Serv, 20 York St, New Haven, CT 06504 USAYale New Haven Med Ctr, Dept Pharm Serv, 20 York St, New Haven, CT 06504 USA
Zamora, Francis J.
Roberts, John D.
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Yale Univ, Yale Canc Ctr, New Haven, CT USAYale New Haven Med Ctr, Dept Pharm Serv, 20 York St, New Haven, CT 06504 USA