High-flow nasal cannula versus nasal cannula for advanced bronchoscopy
Regina Pikman Gavriely, Ophir Freund, Amir Bar-Shai, Evgeni Gershman

TL;DR
This paper responds to questions about a study comparing high-flow nasal cannula and nasal cannula during bronchoscopy procedures.
Contribution
The authors clarify aspects of their bronchoscopy study, including preoxygenation and intervention protocols.
Findings
The response addresses concerns raised about preoxygenation methods used in the study.
The authors explain how intervention protocols may have influenced their results.
Clarifications are provided to improve understanding of the study's methodology.
Abstract
We read with interest the correspondence of our colleagues to our article titled “Laryngeal mask airway or high-flow nasal cannula versus nasal cannula for advanced bronchoscopy: a randomised controlled trial” [1], and would like to respond to their remarks. Providing some answers that explain aspects questioned by colleagues, such as preoxygenation and intervention protocols, and their influence on our results https://bit.ly/4qBr4X1
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Taxonomy
TopicsAirway Management and Intubation Techniques · Tracheal and airway disorders · Lung Cancer Diagnosis and Treatment
Reply to Y. Cao:
We read with interest the correspondence of our colleagues to our article titled “Laryngeal mask airway or high-flow nasal cannula versus nasal cannula for advanced bronchoscopy: a randomised controlled trial” [1], and would like to respond to their remarks.
Firstly, the authors are right that pre-oxygenation was different than normally used in real-world practice with high-flow nasal cannula (HFNC). This was done to enable blind allocation, as patients were unaware of the method of oxygenation. We agree that the implementation of HFNC may indeed lengthen the apnoeic time and further delay or prevent hypoxia during the procedure due to the de-nitrogenation effect and oxygen reservoir expansion of HFNC. Compared to the studies cited in our paper and by the authors [2, 3], which included only endo-bronchial ultrasound, almost half of our cases had additional bronchoscopic procedures, which could possibly explain the higher rates of desaturation. We also used an approximate flow of 45 L·min^−1^, while in the other two trials higher oxygen flows were utilised. It is important to point out that considering the sample size in our study and those mentioned, the 26% rate of desaturation in our trial is not statistically different from the 10–13% in others. Of note, despite the lack of HFNC pre-oxygenation in our study, the HFNC group had the lowest rate of desaturation, an advantage that indeed can be magnified by extending its use to the pre-oxygenation period.
Secondly, the authors mention the higher levels of CO_2_ found in the HFNC group compared to the nasal cannula or laryngeal mask groups. In our cohort, respiratory interventions in the nasal cannula group mainly included oxygen enrichment via the bronchoscope port, chin lift and jaw thrust (leading to reopening of airway and return to spontaneous ventilation). In six cases where these methods did not provide a solution for the desaturation, temporary mask ventilation was provided, and three of these patients were ultimately switched to laryngeal mask airway support. When used, masked ventilation was applied for less than one minute, hence any effect on overall CO_2_ levels might not be significant. Still, we agree with the authors that these actions might have affected our results, given that we performed an intention-to-treat analysis. Other than the already-mentioned possible mechanisms for this trend in our discussion, the difference between procedural and post-procedural CO_2_ levels in the HFNC groups might be explained by the mouth position. Per protocol in both HFNC and NC groups bronchoscopy was done via a bite block mouth piece, thus keeping the mouth open. The open mouth position during bronchoscopy could lower the pressure generated by the HFNC by over 50% [4, 5], which is not the case after procedure cessation when the bite block it taken out and the mouth is closed. While the peak levels of CO_2_ were statistically higher in the HFNC during the procedure, this might not be clinically significant (mean 65.6 versus 60.1 mmHg), moreover there was no difference in the change of CO_2_ level from baseline in between groups.
We hope that these explanations provide more insight into our work and urge other studies in this field in order to improve the respiratory support methods for bronchoscopic examinations.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Pikman Gavriely R, Freund O, Tiran B, et al. Laryngeal mask airway or high flow nasal cannula versus nasal cannula for advanced bronchoscopy: a randomised controlled trial. ERJ Open Res 2025; 11: 00421-2024. doi:10.1183/23120541.00421-2024 PMC 1180893239931666 · doi ↗ · pubmed ↗
- 2Douglas N, Ng I, Nazeem F, et al. A randomised controlled trial comparing high-flow nasal oxygen with standard management for conscious sedation during bronchoscopy. Anaesthesia 2018; 73: 169–176. doi:10.1111/anae.1415629171661 · doi ↗ · pubmed ↗
- 3Irfan M, Ahmed M, Breen D. Assessment of high flow nasal cannula oxygenation in endobronchial ultrasound bronchoscopy: a randomized controlled trial. J Bronchol Interv Pulmonol 2021; 28: 130. doi:10.1097/LBR.000000000000071933105418 · doi ↗ · pubmed ↗
- 4Gray AJ, Nielsen KR, Ellington LE, et al. Tracheal pressure generated by high-flow nasal cannula in 3D-Printed pediatric airway models. Int J Pediatr Otorhinolaryngol 2021; 145: 110719. doi:10.1016/j.ijporl.2021.11071933894521 PMC 10549990 · doi ↗ · pubmed ↗
- 5Zhang J, Lin L, Pan K, et al. High-flow nasal cannula therapy for adult patients. J Int Med Res 2016; 44: 1200–1211. doi:10.1177/030006051666462127698207 PMC 5536739 · doi ↗ · pubmed ↗
