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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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Bibliografski detalji
Izdano u:Asian J Transfus Sci
Glavni autori: Mehra, Ruhi A., Gupta, Seema A., Borkar, D. B.
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications & Media Pvt Ltd 2018
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6327770/
https://ncbi.nlm.nih.gov/pubmed/30692802
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ajts.AJTS_128_16
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