Sickle cell disease is a genetic disorder characterized by the presence of hemoglobin S. This hemoglobin has a low affinity for oxygen, allowing a good oxygenation of tissues with low levels of hemoglobin. Therefore, blood transfusions are not necessary to correct basal anemia, but are indispensable in the treatment and prevention of some complications. Detailed indications for blood transfusions are presented, as well as the different types of transfusion usually performed: simple, exchange and hypertransfusion. Finally, reference is made to the preferable blood components to be used, complications related with transfusion, the preventive measures to be taken and the need for a patient's transfusion record.Sickle cell disease is a genetic ...
A collection of genetic red blood cell disorders refers a disease called sickle cell disease (SCD). ...
Background Sickle cell disease is one of the commonest severe monogenic disorders in the world, due ...
La drépanocytose est une hémoglobinopathie aux formes et aux sévérités cliniques très hétérogènes qu...
This is a review of the literature as regards the indications for blood transfusion in SCD, complica...
A Drepanocitose é uma doença genética caracterizada pela presença de uma hemoglobina anormal (Hb S)....
Blood transfusions are sometimes required, most usually to treat severe anaemia, in patients with si...
Graham R Serjeant Sickle Cell Trust (Jamaica), Kingston, Jamaica Abstract: Homozygous sickle cell (S...
Sickle cell disease was first described by Herrick in 1910. This disease involves an abnormality of ...
Sickle cell disease was first described by Herrick in 1910. This disease involves an abnormality of ...
Introduction. Hypertransfusion refers to chronic blood transfusion therapy aimed at ameliorating dis...
Chronic red blood cell transfusions remain an essential part of supportive treatment in patients wit...
Copyright © 2010 Radha Raghupathy et al. This is an open access article distributed under the Creati...
Sickle cell-beta thalassemia is a double heterozygous state. Red cell exchange (RCE) transfusion red...
Chronic red blood cell transfusions remain an essential part of supportive treatment in patients wit...
Sickle cell disease is a group of disorders that affects hemoglobin, and causes distorted sickle- or...
A collection of genetic red blood cell disorders refers a disease called sickle cell disease (SCD). ...
Background Sickle cell disease is one of the commonest severe monogenic disorders in the world, due ...
La drépanocytose est une hémoglobinopathie aux formes et aux sévérités cliniques très hétérogènes qu...
This is a review of the literature as regards the indications for blood transfusion in SCD, complica...
A Drepanocitose é uma doença genética caracterizada pela presença de uma hemoglobina anormal (Hb S)....
Blood transfusions are sometimes required, most usually to treat severe anaemia, in patients with si...
Graham R Serjeant Sickle Cell Trust (Jamaica), Kingston, Jamaica Abstract: Homozygous sickle cell (S...
Sickle cell disease was first described by Herrick in 1910. This disease involves an abnormality of ...
Sickle cell disease was first described by Herrick in 1910. This disease involves an abnormality of ...
Introduction. Hypertransfusion refers to chronic blood transfusion therapy aimed at ameliorating dis...
Chronic red blood cell transfusions remain an essential part of supportive treatment in patients wit...
Copyright © 2010 Radha Raghupathy et al. This is an open access article distributed under the Creati...
Sickle cell-beta thalassemia is a double heterozygous state. Red cell exchange (RCE) transfusion red...
Chronic red blood cell transfusions remain an essential part of supportive treatment in patients wit...
Sickle cell disease is a group of disorders that affects hemoglobin, and causes distorted sickle- or...
A collection of genetic red blood cell disorders refers a disease called sickle cell disease (SCD). ...
Background Sickle cell disease is one of the commonest severe monogenic disorders in the world, due ...
La drépanocytose est une hémoglobinopathie aux formes et aux sévérités cliniques très hétérogènes qu...