Optimal blood transfusion therapy in haemoglobinopathies
For reasons of time, this short talk will be confined to the optimal frequency, timing, indications and dosing of blood transfusion. Blood transfusion protocols in thalassaemia syndromes are more widely agreed (1) than for sickle disorders but questions still remain about optimal Hb levels, timing a...
Main Author: | John Porter |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2018-04-01
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Series: | Thalassemia Reports |
Subjects: | |
Online Access: | https://www.pagepressjournals.org/index.php/thal/article/view/7477 |
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