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Updated: Feb 20, 2026

Point-of-Care Ultrasound: A Review of Ultrasound Parameters for Predicting Difficult Airways
Published on: April 7, 2023
Interrater Reliability of Point-of-Care Ultrasound for Predicting Post-Extubation Stridor in Pediatrics
April Slamowitz1, Shannon Moriarty1, Matthew Taylor2
1Division of Pediatric Critical Care Medicine, Cohen Children's Medical Center, Northwell Health, New Hyde Park, New York, USA.
Insights
Laryngeal air column width difference (LACWD) measured by point-of-care ultrasound (POCUS) did not reliably predict post-extubation stridor (PES) in pediatric patients. The technique showed poor consistency between different providers, limiting its clinical use.
Area of Science:
- Pediatric Critical Care Medicine
- Point-of-Care Ultrasound (POCUS)
- Respiratory Physiology
Background:
- Post-extubation stridor (PES) is a significant complication in pediatric patients after endotracheal intubation, often associated with laryngeal edema.
- Laryngeal air column width difference (LACWD), measured via POCUS, has been proposed as a potential predictor of PES.
Purpose of the Study:
- To evaluate the predictive value of LACWD for PES in pediatric patients.
- To examine the correlation between LACWD and endotracheal tube (ETT) cuff pressure.
- To assess the interrater reliability of LACWD measurements by POCUS-trained providers.
Main Methods:
- A prospective observational study involving 51 mechanically ventilated pediatric patients (0-18 years).
- LACWD was measured using bedside POCUS; duplicate scans were performed by different providers to assess interrater reliability.
- PES was identified by inspiratory stridor; reliability was quantified using intraclass correlation coefficients (ICCs).
Main Results:
- PES occurred in 14% of the study population.
- No significant difference in LACWD was observed between patients with and without PES.
- LACWD measurements demonstrated excellent intrarater reliability (ICC >0.95) but poor interrater reliability (ICC = 0.27).
Conclusions:
- LACWD measurements did not reliably predict PES in pediatric patients and exhibited poor interrater reliability.
- The current POCUS technique for LACWD measurement lacks the necessary reproducibility for widespread clinical application among different providers.
- Further advancements in POCUS techniques may be needed to enhance feasibility and reliability for routine bedside use in pediatric critical care.
Objectives:
Post-extubation stridor (PES) is a serious complication in pediatric patients following endotracheal intubation and is linked to laryngeal edema. Prior studies suggest that the laryngeal air column width difference (LACWD), measured by point-of-care ultrasound (POCUS), may predict PES. There is a critical need to evaluate whether such techniques can be reliably reproduced among typical providers in the pediatric critical care setting. We aimed to assess the predictive value of LACWD for PES, examine its correlation with endotracheal tube (ETT) cuff pressure, and determine whether LACWD can be measured consistently by multiple POCUS-trained providers.
Methods:
We conducted a prospective observational study of 51 mechanically ventilated pediatric patients aged 0-18 years. LACWD was measured using bedside POCUS. A subset underwent duplicate scans by different providers to assess interrater reliability. PES was defined by the presence of inspiratory stridor. Intra- and interrater reliability were evaluated using intraclass correlation coefficients (ICCs).
Results:
PES occurred in 14% of patients. There was no significant difference in LACWD between PES and non-PES groups. LACWD showed no correlation with ETT cuff pressure. Intrarater reliability for LACWD measurements was excellent (ICC >0.95), but interrater reliability was poor (ICC = 0.27 for LACWD).
Conclusions:
LACWD did not reliably predict PES and showed poor interrater reliability, raising concerns about its practical utility in pediatrics. While POCUS remains an appealing non-invasive tool, our study demonstrates that the current technique lacks the reproducibility required for clinical application across providers. Future advancements may improve feasibility, but current methods are not yet suitable for routine bedside use.
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