Autor: |
Ganesh Kasinathan, Jameela Sathar |
Jazyk: |
angličtina |
Rok vydání: |
2021 |
Předmět: |
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Zdroj: |
Clinical Case Reports, Vol 9, Iss 6, Pp n/a-n/a (2021) |
Druh dokumentu: |
article |
ISSN: |
2050-0904 |
DOI: |
10.1002/ccr3.4226 |
Popis: |
Abstract Hyperhemolysis syndrome (HS) is characterized by the occurrence of severe anemia with post‐transfusion hemoglobin and hematocrit levels being markedly lower than those present prior to transfusion. A high index of suspicion of HS in a multi‐transfused thalassemia patient allows prompt institution of therapy resulting in improved survival outcome. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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