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Published on: December 6, 2016
Prevalence of and risk factors for obstructive sleep apnea in children with sickle cell: a multicentric cross
Albraa Abulhamail1, Ahmad AlShebli2, Leeena Merdad3
1College of Medicine, King Abdulaziz University Hospital, King Abdulaziz University, Jeddah, Saudi Arabia. caandor@icloud.com.
Insights
Obstructive sleep apnea syndrome (OSAS) affects 22% of children with sickle cell disease (SCD). Adenotonsillar hypertrophy and periodic limb movements are significant risk factors for OSAS in this vulnerable pediatric population.
Area of Science:
- Pediatric Sleep Medicine
- Hematology
- Public Health
Background:
- Obstructive sleep apnea syndrome (OSAS) is a common comorbidity in children with sickle cell disease (SCD).
- Understanding the prevalence and risk factors of OSAS in pediatric SCD patients is crucial for early diagnosis and management.
Purpose of the Study:
- To determine the prevalence of OSAS among children with SCD in Jeddah, Saudi Arabia.
- To identify risk factors associated with OSAS in this population.
Main Methods:
- A multicenter cross-sectional study involving 150 children with SCD aged 2-18 years.
- The Pediatric Sleep Questionnaire (PSQ) was used for OSAS screening.
- Data collected included patient demographics, SCD type, and history of related conditions.
Main Results:
- The prevalence of OSAS was 22% (33 out of 150 children) based on PSQ scores.
- Adenotonsillar hypertrophy (adjusted odds ratio [aOR] 5.5) and periodic limb movements (aOR 9.0) were significant risk factors for OSAS.
- Other associated factors in bivariate analysis included nationality and education level.
Conclusions:
- OSAS is highly prevalent in children with SCD.
- Targeted screening for OSAS is recommended in pediatric SCD patients, particularly those with adenotonsillar hypertrophy or periodic limb movements.
Abstract:
The prevalence of obstructive sleep apnea syndrome (OSAS) is elevated in some high-risk populations. Children with sickle cell disease (SCD) are known to have many comorbidities, including OSAS. The objectives of this study were to assess the prevalence of and risk factors for OSAS among children with SCD in two major tertiary health care facilities in Jeddah, Saudi Arabia. This multicenter cross-sectional study took place in two major tertiary health care facilities-King Abdulaziz University Hospital and King Khalid National Guard Hospital, Jeddah, Saudi Arabia. Children with SCD who were admitted between January 2010 and December 2017 were enrolled. The Pediatric Sleep Questionnaire (PSQ) was used to screen for OSAS. Data were collected from 150 children with SCD aged between 2 and 18 years. Eighty-five percent of the children had sickle cell anemia (SCA) with HbSS, and the rest had sickle beta-thalassemia (HbS/ß-thalassemia). Based on the PSQ, 33 of the 150 (22%) children had OSAS (score ≥ 7). The average score on the PSQ was 3.8/22 (± 3.8). A history of adenotonsillar hypertrophy was found to be a significant risk factor in bivariate and multivariate analyses [aOR 5.5; 95% CI 1.84-16.35 (P < 0.001)]. The odds of having OSAS were ninefold higher in children who had periodic limb movements than in those who did not after adjustment [95% CI 1.75-48.03 (P < 0.001)]. OSAS is a highly prevalent disease among children with SCD. Many factors were associated with OSAS in the bivariate analysis, including nationality, education level, a history of adenotonsillar hypertrophy, and a history of periodic limb movements.
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