Positive effects of ultrasound‐guided peripheral IV insertion on pediatric sickle cell anemia/thalassemia patients receiving automated red cell exchange procedures or chronic transfusion therapy
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DOI: 10.1002/jca.21856
Abstract: Peripheral vascular access and venipuncture are major causes of distress and anxiety for children and their parents. This is especially difficult for patients with hemoglobinopathies (thalassemia major and sickle cell disease) who require chronic blood… read more here.
Keywords: red cell; cell exchange; automated red; cell ... See more keywords
Algorithm‐based selection of automated red blood cell exchange procedure goals reduces blood utilization in chronically transfused adults with sickle cell disease
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DOI: 10.1002/jca.22004
Abstract: Automated red cell exchange (RCE) is a common treatment for patients with sickle cell disease (SCD). Two key parameters are used to determine the volume of blood for RCE to reduce sickle hemoglobin (eg, HbS):… read more here.
Keywords: cell; cell disease; cell exchange; blood ... See more keywords
Comprehensive guide to managing a chronic automated red cell exchange program in sickle cell disease
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DOI: 10.1002/jca.22014
Abstract: Sickle cell disease (SCD) is associated with significant morbidity and mortality, and limits both the quality and quantity of life. Transfusion therapy, specifically automated red cell exchange (aRCE), plays a key role in management of… read more here.
Keywords: red cell; cell; program; cell disease ... See more keywords
Procedural adverse events in pediatric patients with sickle cell disease undergoing chronic automated red cell exchange
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DOI: 10.1111/trf.16807
Abstract: Chronic automated red cell exchange (RCE) is increasingly employed for sickle cell disease (SCD). There is a paucity of data on the incidence of RCE adverse events (AEs) and potential patient and procedural risk factors… read more here.
Keywords: red cell; cell; chronic automated; cell exchange ... See more keywords