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Airway Abnormalities in Children Operated for Congenital Heart Disease: Clinical characteristics and risk factors
Fatma Al Kindi1,2,3, Rand Al Harthy1,2,3, Saif Awlad Thani2,4
1Child Health Department, Al Nahda Hospital, Ministry of Health, Muscat, Oman.
Insights
Airway abnormalities (AAs) are common in children with congenital heart disease (CHD). Prematurity is a risk factor for AAs, leading to longer ventilation times in these complex pediatric cases.
Area of Science:
- Pediatric Cardiology
- Thoracic Surgery
- Congenital Abnormalities
Background:
- Congenital heart disease (CHD) is the most frequent congenital defect.
- Airway abnormalities (AAs) are significant comorbidities in CHD patients, increasing complexity and morbidity.
Purpose of the Study:
- To identify common AAs in children with CHD.
- To determine risk factors associated with AAs in this population.
- To analyze clinical outcomes in children with CHD and concurrent AAs.
Main Methods:
- A case-control study was conducted on children under 13 with CHD who had cardiothoracic surgery.
- Cases had concurrent AAs; controls had CHD without AAs, matched for age and gender.
- Data were collected between January 2016 and December 2018 at the National Genetic Centre in Oman.
Main Results:
- The prevalence of AAs in children with CHD was 5.5%.
- Vascular compressions (47.4%) and airway malacia (23.1%) were the most frequent AAs.
- Prematurity was a significant risk factor (OR 3.2), and AAs were associated with longer invasive ventilation durations.
Conclusions:
- AAs are critical comorbidities in pediatric CHD.
- Increased clinical vigilance and early AA investigation are recommended for children with CHD.
- Further prospective studies are needed to understand long-term implications.
Objectives:
Congenital heart disease (CHD) is the most common congenital defect, with airway abnormalities (AAs) representing significant comorbidities that contribute to increased morbidity and clinical complexity. This study aimed to identify the most common AAs, associated risk factors, and clinical outcomes in children with CHD.
Methods:
This case-control study included children aged under 13 years with CHD who underwent cardiothoracic surgery between 1 January 2016 and 31 December 2018 at the National Genetic Centre in Oman. Cases were children with concurrent AAs, while controls were age- and gender-matched children with CHD but without AAs.
Results:
The prevalence of concomitant AAs in children with CHD in the cohort was 5.5%. The most common AAs were vascular compressions (47.4%), followed by airway malacia (23.1%). Chest computed tomography was the most frequently utilised diagnostic modality. Prematurity was significantly more common among children with AAs (odds ratio: 3.2, 95% confidence interval: 1.1-11.1; P = 0.016), and the duration of invasive ventilation was significantly longer (P = 0.013).
Conclusion:
AAs are important comorbidities in children with CHD. This study highlights the need for increased clinical vigilance and early investigation of AAs in this population. Prospective studies are warranted to further assess the long-term implications of these findings.
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