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Early lung function testing in infants with aortic arch anomalies identifies patients at risk for airway obstruction
Charles Christoph Roehr1, Silke Wilitzki, Bernd Opgen-Rhein
1Department of Neonatology, Charité Universitätsmedizin Berlin, Berlin, Germany. christoph.roehr@charite.de
Insights
Infants with aortic arch anomalies (AAA) face airway obstruction risks. Neonatal lung function testing (LFT) effectively identifies and monitors these risks in infants with right-sided (RAAA) and double-sided (DAAA) aortic arch anomalies.
Area of Science:
- Pediatric Cardiology
- Respiratory Medicine
- Medical Imaging
Background:
- Aortic arch anomalies (AAA) are rare cardiovascular conditions.
- Right-sided (RAAA) and double-sided (DAAA) aortic arch anomalies can lead to airway obstruction in infants.
- Neonatal lung function testing (LFT) is utilized to assess airway obstruction in infants with AAA.
Purpose of the Study:
- To investigate the degree of airway obstruction in infants diagnosed with aortic arch anomalies (AAA).
- To evaluate the utility of neonatal lung function testing (LFT) in identifying and monitoring airway obstruction in infants with RAAA and DAAA.
Main Methods:
- Seventeen infants (10 RAAA, 7 DAAA) with prenatal AAA diagnosis underwent LFT.
- Measurements included tidal breathing flow-volume loops (TBFVL), airway resistance (R(aw)) via bodyplethysmography, and maximal expiratory flow (V'(max)FRC) using rapid thoracic-abdominal compression.
- V'(max)FRC was analyzed using Z-scores relative to normative data.
Main Results:
- Abnormal LFT findings were present in both RAAA and DAAA infants.
- DAAA infants showed significantly more expiratory flow limitations and increased R(aw) compared to RAAA infants.
- While R(aw) correlated with V'(max)FRC Z-scores, no significant difference in V'(max)FRC Z-scores was found between RAAA and DAAA groups. Four infants (24%) were at high risk for airway obstruction.
Conclusions:
- Infants with both RAAA and DAAA are susceptible to airway obstruction.
- Early LFT is crucial for identifying and monitoring these infants.
- This monitoring can guide therapeutic interventions before the onset of clinical symptoms.
Background:
Aortic arch anomalies (AAA) are rare cardio-vascular anomalies. Right-sided and double-sided aortic arch anomalies (RAAA, DAAA) are distinguished, both may cause airway obstructions. We studied the degree of airway obstruction in infants with AAA by neonatal lung function testing (LFT).
Patients And Methods:
17 patients (10 RAAA and 7 DAAA) with prenatal diagnosis of AAA were investigated. The median (range) post conception age at LFT was 40.3 (36.6-44.1) weeks, median body weight 3400 (2320-4665) g. Measurements included tidal breathing flow-volume loops (TBFVL), airway resistance (R(aw)) by bodyplethysmography and the maximal expiratory flow at functional residual capacity (V'(max)FRC) by rapid thoracic-abdominal compression (RTC) technique. V'(max)FRC was also expressed in Z-scores, based on published gender-, age and height-specific reference values.
Results:
Abnormal lung function tests were seen in both RAAA and DAAA infants. Compared to RAAA infants, infants with DAAA had significantly more expiratory flow limitations in the TBFVL, (86% vs. 30%, p<0.05) and a significantly increased R(aw) (p = 0.015). Despite a significant correlation between R(aw) and the Z-score of V'(max)FRC (r = 0.740, p<0.001), there were no statistically significant differences in V'(max)FRC and it's Z-scores between RAAA and DAAA infants. 4 (24%) infants (2 RAAA, 2 DAAA) were near or below the 10(th) percentile of V'(max)FRC, indicating a high risk for airway obstruction.
Conclusion:
Both, infants with RAAA and DAAA, are at risk for airway obstruction and early LFT helps to identify and to monitor these infants. This may support the decision for therapeutic interventions before clinical symptoms arise.
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