# Early risk factors for acute chest syndrome in sickle cell anemia: A pediatric study

**Authors:** Mohamed Condé, Florie Bouvier, Roselyne Brat, Salim Ferrani, Régis Hankard, Philippe Connes, Georges Dimitrov

PMC · DOI: 10.1371/journal.pone.0336567 · 2025-11-14

## 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.

## Key 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 of VOC at night, diffuse (multifocal) pain and increased C-Reactive protein (p < 0.05). The multivariable modelling, using generalized linear mixed-effects models, defined three risk factors for ACS occurrence: diffuse pain, night-time pain occurrence, and increased C-Reactive protein (p < 0.01). Increased use of opiates in the Emergency Department, elevated total leucocyte count, breath rate, and decreased red blood cell count were not significantly associated with ACS occurrence (p > 0.05). The initial evaluation of SCA patients’ acute pain in the Emergency Department is crucial for subsequent management during hospitalization.

## Linked entities

- **Genes:** FDFT1 (farnesyl-diphosphate farnesyltransferase 1) [NCBI Gene 2222], Sb_0 (serine proteinase stubble) [NCBI Gene 105214948]
- **Diseases:** sickle cell anemia (MONDO:0011382), acute chest syndrome (MONDO:0005632)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** SCA (MESH:D000755), pain (MESH:D010146), VOC (MESH:D001157), ACS (MESH:D056586)
- **Chemicals:** opiates (MESH:D053610), VOCs (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12617906/full.md

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Source: https://tomesphere.com/paper/PMC12617906