The treatment of various complications of sickle cell disease has included red cell exchange in the past, and the development of automated pheresis equipment has greatly simplified such exchanges. Traditionally, the patient's red cells have been exchanged while their plasma was returned to them. Rec
Improved method for automated red cell exchange in sickle cell disease
β Scribed by Oswaldo Castro; Helga Finke-castro; Debra Coats
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 661 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0733-2459
No coin nor oath required. For personal study only.
β¦ Synopsis
An improvcd method for intermittent-flow erythrocytapheresis in patients with sickle cell disease is reported. The method. a modification of the standard red cell exchange procedure for the Haemonetics 30s unit, dilutes with physiologic saline the patient's blood as i ! flows from the draw line and before it reachcs the centrifugation bowl. The blood dilution (approximately 1.6 parts saline to I part blood) is used only during the first two passes. when the proportion of sickle erythrocytes in the patient's blood is still high. Only that amount of bowl supernatant (saline-diluted plasma) necessary to maintain extracorporeal volume below 500 ml is returned to the patient. The method described largely prevents the clumping of sickle erythrocytes in the centrifugation bowl, a complication frcquently encountered with the Haemonetics 30s unit. Thus, changing the bowl between passes is avoided.
Furthermore. the sickle red cells can be collected with the first pass and cryoprescrvcd for possible future uscs including the option of autotransfusion.
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Sickle cell disease (SCD) patients are prone to develop complications that include stroke, acute chest syndrome, and other crises. Some of these complications require chronic transfusion therapy or red cell exchange (RCE), either for therapeutic or prophylactic reasons. Due to a discrepancy of red c
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