Abstract:Individuals with sickle cell disease (SCD) who undergo surgery with general anesthesia have higher rates of postoperative complications. Randomized clinical trials have shown a benefit for transfusing SCD patients to a goal hemoglobin concentration of 10 g/dL. Preoperative management for patients with Hb SC or Hb Sβ+ -thalassemia is unclear because hemoglobin concentrations are frequently ≥ 10 g/dL. Pre-surgical risk assessment tools utilized in non-SCD patients may have a role in predicting adverse outcomes i… Show more
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