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Protocols - Hemorio

Protocols - Hemorio

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ADVERSE EFFECTS RELATED TO THE TRANSFUSIONS IN FALCIFORM DISEASE:<br />

In addition to the inherent adverse effects to any and all blood transfusion, there is one, in particular, that it<br />

may attack the person who has Falciform Disease, which is:<br />

BYSTANDER HEMOLYSIS: that, by definition, is a complication of the late hemolytic reaction, in which the<br />

red blood cells of the receptor are destroyed during an immune hemolytic reaction.<br />

2 – TRANSFUSIONAL CONDUCT AT THE MAJOR THALASSEMIA AND INTERMEDIATE<br />

HYPERTRANSFUSION: the subjects will be transfused every 2 to 3 weeks, with the purpose to keep the<br />

Hb at least 10 g/dl and less than 15g/dL.<br />

INDICATIONS:<br />

- Major thalassemia – all cases<br />

- Intermediate thalassemia – with facial changes, retardation in the growth, pathologic fractures and/or<br />

extramedullary hematopoiesis.<br />

CHARACTERISTICS OF THE TRANSFUSIONAL COMPONENTS<br />

Transfuse de-leukocytated blood prophylactically.<br />

Transfuse phenotyped blood for the antigens Rh and Kell (Rh1, Rh2, Rh3, Rh4, K1).<br />

Whenever possible, also respect the antigens Fy a and Fy b , Jk a and Jk b , S and s.<br />

In allo-immunizing subjects, transfuse red blood cells destituted of the antigen(s) against which the subject<br />

has developed the antibody, in addition to mandatory respect the antigens Rh1, Rh2, Rh3, Rh4, K1, Fy a and<br />

Fy b , Jk a and Jk b , S and s.<br />

The interval between each transfusion will be determined case by case, due to the usage of transfusion<br />

and the levels of pre-transfusion hemoglobin. As a general rule, this interval must be of two to three<br />

weeks.<br />

The volume to be transfused must also be determined case by case, due to the weight of the subject and<br />

the response to the transfusions.<br />

The serum dosage of ferritin of the subject must be verified every three months. Levels of ferritin above<br />

1,000 µg% indicate that the case must be evaluated and discussed jointly by the Hemotherapy and<br />

Hematology Services.<br />

3 – TRANSFUSIONAL CONDUCT AT THE HERITABLE SPHEROCYTOSIS AND G6PD DEFICIENCY<br />

- Transfusions when symptomatic and hemoglobin

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