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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
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Management of cesarean delivery in a parturient with sickle cell disease

D Romano1, H Craig1, D Katz1

  • 1Department of Anesthesiology, Perioperative and Pain Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.

International Journal of Obstetric Anesthesia
|October 16, 2019
PubMed

Chronic hemolysis and intermittent vaso-occlusion in sickle cell disease can lead to recurrent blood transfusions with related complications such as antibody formation and rarely, life-threatening reactions. We report a case of a parturient who presented with complications of sickle cell disease and who later had fetal compromise that required an emergent cesarean delivery. Complex management decisions were made, aided by technologies such as rotational thromboelastometry, quantitative blood loss analysis and cell salvage.

Keywords:
Cell salvageCesarean deliveryHyperhemolysis syndromePregnancySickle cell anemia

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