A comment on oral vs. nasal intubation and post-extubation laryngeal injury


Türe N.

EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, vol.1, no.1, pp.2-3, 2025 (SCI-Expanded)

Abstract

A comment on oral vs. nasal intubation and post-extubation laryngeal injury

Nurullah TÜRE1

To the editor,

I read with great interest the report by Meena & Gill [1], which prospectively and commendably under clinician blinding assessed early laryngoscopic findings after extubation. The pragmatic design and timely endoscopic verification make a useful contribution to the perioperative airway literature. However, two clarifications would strengthen reproducibility and align the conclusions with the study’s design.

The analysis records “intubation duration,” which appears to reflect time to achieve intubation rather than the total time patients remained intubated during surgery the latter being the physiologically relevant dose for pressure and friction- mediated injury. Crucially, cuff pressure (and its time course) was not measured. Because both total intubation time and cuff pressure-time exposure are primary determinants of mucosal ischemia and contact trauma, their omission likely induces nondifferential exposure misclassification, biasing route comparisons toward no difference. Even if the two routes truly differ under longer anesthesia or higher cuff pressures, the current specification would dilute that signal. Minimal remediation is possible by reporting anesthesia/airway time from records, stratifying by case length, and conducting sensitivity analyses that model plausible cuff-pressure ranges.

Airway route was chosen by surgical indication and anesthesiologist preference a classic confounding by indication setting. With a modest sample and few moderate-to-severe events, a standard multivariable model cannot reliably control imbalances in case mix (operative field, positioning, instrumentation such as Magill forceps, operator effects In this context, a non-significant p-value is not evidence of equivalence; it only indicates insufficient power to detect a difference. An appropriate inference framework would prespecify a clinically meaningful non-inferiority margin (e.g., absolute risk difference ≤ 10%), estimate effect sizes with 95% CIs, and use balancing methods (propensity scores/ IPTW) to address allocation bias. Absent these elements, concluding that routes “demonstrated comparable rates and severity” overstates what the design can support.

Re-analyzing the cohort with total intubation time and a cuff-pressure proxy, balanced route comparison, and effect-size/CIs within a non-inferiority framework would align statistical claims with physiologic plausibility and strengthen the paper’s clinical takeaway without altering its prospective spirit.