Crises drépanocytaires: prise en charge hospitalière [Sickle cell crisis: inpatient management]

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UNIL restricted access
State: Public
Version: Final published version
License: CC BY-NC-ND 4.0
Serval ID
serval:BIB_9BD13AB5C815
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Crises drépanocytaires: prise en charge hospitalière [Sickle cell crisis: inpatient management]
Journal
Revue medicale suisse
Author(s)
Genet L., Grandoni F., Alberio L., Gavillet M., Benmachiche M.
ISSN
1660-9379 (Print)
ISSN-L
1660-9379
Publication state
Published
Issued date
20/11/2024
Peer-reviewed
Oui
Volume
20
Number
896
Pages
2154-2159
Language
french
Notes
Publication types: English Abstract ; Journal Article
Publication Status: ppublish
Abstract
Sickle cell anemia is the world's most common monogenic disease, with a steady rise in the number of cases also in Switzerland. It presents as regenerative anemia and recurrent vaso-occlusive episodes, which can impact all organs. Acute and chronic complications increase morbidity and mortality, significantly reducing life expectancy compared to the general population. Optimal and multidisciplinary management of acute events is essential to improve patients' quality of life and overall prognosis. Vaso-occlusive crises and acute chest syndrome are the two most frequent acute complications. Their treatment, described here, is threefold: analgesia, treatment of causative factors and prevention of further complications.
Keywords
Humans, Anemia, Sickle Cell/therapy, Anemia, Sickle Cell/complications, Anemia, Sickle Cell/epidemiology, Inpatients, Switzerland/epidemiology
Pubmed
Create date
25/11/2024 16:07
Last modification date
26/11/2024 7:15
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