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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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[Sickle cell crisis: inpatient management]

Léonore Genet1, Francesco Grandoni2,3, Lorenzo Alberio2,3

  • 1Service de médecine interne, Département de médecine, Centre hospitalier universitaire vaudois et Université de Lausanne, 1011 Lausanne.

Revue Medicale Suisse
|November 21, 2024
PubMed
Summary

Sickle cell anemia, a common monogenic disease, is increasing globally, including in Switzerland. Prompt management of acute events like vaso-occlusive crises is key to improving patient outcomes and life expectancy.

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