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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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| Udgivet i: | Asian J Transfus Sci |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Medknow Publications & Media Pvt Ltd
2018
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| Fag: | |
| Online adgang: | 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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