Early risk factors for acute chest syndrome in sickle cell anemia: A pediatric study
Mohamed Condé, Florie Bouvier, Roselyne Brat, Salim Ferrani, Régis Hankard, Philippe Connes, Georges Dimitrov

TL;DR
This study identifies early risk factors for acute chest syndrome in children with sickle cell anemia during emergency department visits.
Contribution
The study introduces three early risk factors for acute chest syndrome progression in pediatric sickle cell anemia patients.
Findings
Diffuse pain, night-time pain occurrence, and increased C-Reactive protein are significant risk factors for acute chest syndrome.
ACS was not significantly associated with opiate use, elevated leucocyte count, or decreased red blood cell count.
Early identification of risk factors in the Emergency Department can improve hospital management for sickle cell anemia patients.
Abstract
Acute chest syndrome (ACS) is a life-threatening complication of sickle cell anemia (SCA). Most often, ACS occurs during the progression of a painful vaso-occlusive crisis (VOC) in vulnerable patients. The present study aimed to identify early risk factors for ACS progression, focusing on patient assessments in a pediatric Emergency Department. In this study (2016–2022) concerning exclusively the SS and Sβ0 sickle cell disease genotypes, severe VOC encounters progressing to ACS were compared to uncomplicated severe VOCs. Medical history, clinical and laboratory data were collected for both groups. Out of 280 severe VOC encounters without initial respiratory symptoms, 40 progressed to life-threatening acute chest syndrome. The forty ACS (age 8.5 ± 4.3 years, 37% females) were compared with 240 severe VOCs (9.3 ± 4.4 years, 46% females). ACS was positively correlated with the occurrence…
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Taxonomy
TopicsHemoglobinopathies and Related Disorders · Blood groups and transfusion · Iron Metabolism and Disorders
