Red cell exchange transfusions remain an effective but possibly underutilized therapy in the acute and chronic treatment of sickle cell disease. In sickle cell disease, increased blood viscosity can cause compli-cations when the hemoglobin exceeds 10 g/dL even if this is due to simple transfusion. Red cell exchange can provide needed oxygen carrying capacity while reducing the overall viscosity of blood. Acute red cell exchange is useful in acute infarctive stroke, in acute chest and the multi-organ failure syndromes, the right upper quadrant syndrome, and possibly priapism. Neither simple or exchange transfusions are likely to hasten resolution of an acute pain episode. Red cell exchange transfusion is an effective but perhaps underutilize...
Red cell transfusion has an important role in the management of sickle cell disease (SCD) in both em...
Red blood cell exchange is the process of removing red blood cells from a patient and replacing them...
Background: Thirteen cases of priapism seen in adult patients with sickle cell disease (SCD) were tr...
Acute chest syndrome (ACS) is a life-threatening complication of sickle cell disease (SCD) with bloo...
Sickle cell-beta thalassemia is a double heterozygous state. Red cell exchange (RCE) transfusion red...
Graham R Serjeant Sickle Cell Trust (Jamaica), Kingston, Jamaica Abstract: Homozygous sickle cell (S...
Chronic blood transfusions are very important in the care of sickle-cell patients in danger for morb...
Chronic transfusion in sickle cell disease (SCD) remains the gold standard therapy for stroke preven...
This is a review of the literature as regards the indications for blood transfusion in SCD, complica...
INTRODUCTION: Despite several documented challenges, Hematopoietic Stem cell Transplantation (HSCT) ...
Sickle cell disease is a genetic disorder characterized by the presence of hemoglobin S. This hemogl...
BACKGROUND: Red blood cell (RBC) transfusions remain essential in the treatment of patients with sic...
Blood transfusions are sometimes required, most usually to treat severe anaemia, in patients with si...
Sickle cell disease was first described by Herrick in 1910. This disease involves an abnormality of ...
Delayed hemolytic transfusion reactions (DHTR) are potentially life-threatening complications observ...
Red cell transfusion has an important role in the management of sickle cell disease (SCD) in both em...
Red blood cell exchange is the process of removing red blood cells from a patient and replacing them...
Background: Thirteen cases of priapism seen in adult patients with sickle cell disease (SCD) were tr...
Acute chest syndrome (ACS) is a life-threatening complication of sickle cell disease (SCD) with bloo...
Sickle cell-beta thalassemia is a double heterozygous state. Red cell exchange (RCE) transfusion red...
Graham R Serjeant Sickle Cell Trust (Jamaica), Kingston, Jamaica Abstract: Homozygous sickle cell (S...
Chronic blood transfusions are very important in the care of sickle-cell patients in danger for morb...
Chronic transfusion in sickle cell disease (SCD) remains the gold standard therapy for stroke preven...
This is a review of the literature as regards the indications for blood transfusion in SCD, complica...
INTRODUCTION: Despite several documented challenges, Hematopoietic Stem cell Transplantation (HSCT) ...
Sickle cell disease is a genetic disorder characterized by the presence of hemoglobin S. This hemogl...
BACKGROUND: Red blood cell (RBC) transfusions remain essential in the treatment of patients with sic...
Blood transfusions are sometimes required, most usually to treat severe anaemia, in patients with si...
Sickle cell disease was first described by Herrick in 1910. This disease involves an abnormality of ...
Delayed hemolytic transfusion reactions (DHTR) are potentially life-threatening complications observ...
Red cell transfusion has an important role in the management of sickle cell disease (SCD) in both em...
Red blood cell exchange is the process of removing red blood cells from a patient and replacing them...
Background: Thirteen cases of priapism seen in adult patients with sickle cell disease (SCD) were tr...