Manual red cell exchange transfusion to avert sickle cell related complications

Sickle cell-beta thalassemia is a double heterozygous state. Red cell exchange (RCE) transfusion reduces the concentration of sickle cells without increasing the hematocrit or whole-blood viscosity. It can be performed manually or by erythrocytapheresis. RCE transfusion is an effective tool for both...

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Detalles Bibliográficos
Autores principales: Mehra, Ruhi A., Gupta, Seema A., Borkar, D. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327770/
https://www.ncbi.nlm.nih.gov/pubmed/30692802
http://dx.doi.org/10.4103/ajts.AJTS_128_16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327770/
https://www.ncbi.nlm.nih.gov/pubmed/30692802
http://dx.doi.org/10.4103/ajts.AJTS_128_16

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