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Preoperative Airway Images for Difficult Airway Prediction (AI-AIRWAY)

7 juli 2026 uppdaterad av: Murat Ferhat Ferhatoğlu, Memorial Atasehir Hospital

Multimodal Artificial Intelligence for Image-Based Prediction of Difficult Airway: A Prospective Observational Study

This prospective observational study will evaluate whether commonly available multimodal artificial intelligence models can predict difficult laryngoscopy and difficult intubation using standardized preoperative airway photographs. Adult patients scheduled for elective surgery requiring endotracheal intubation will undergo an eight-view preoperative airway photography protocol. The anonymized image sets will be assessed by ChatGPT, Gemini, and Grok using the same structured prompt. Their predictions will be compared with expert anesthesiologist image-based assessments, conventional airway evaluation findings, and prospectively recorded intraoperative airway outcomes. The primary aim is to determine the diagnostic performance of AI models for predicting difficult intubation. A key secondary aim is to evaluate their performance for predicting difficult laryngoscopy. The study is intended to explore whether image-based AI assessment may support preoperative airway risk stratification as a clinician-supervised screening tool.

Studieöversikt

Status

Aktiv, inte rekryterande

Detaljerad beskrivning

Preoperative airway assessment is important for identifying patients at risk for difficult laryngoscopy or difficult intubation. However, conventional bedside airway predictors have limited accuracy when used alone. Multimodal artificial intelligence models may provide additional image-based information by evaluating visible anatomical features from standardized preoperative airway photographs.

In this prospective observational study, adult patients undergoing elective surgery requiring endotracheal intubation will be enrolled between June and September 2026. Each participant will undergo standardized eight-view airway photography during the pre-anesthetic evaluation. The image set will include frontal facial, lateral profile, maximal mouth opening, modified Mallampati, neck extension, and anterior neck views. Images will be anonymized before assessment.

The same image sets will be independently evaluated by multimodal AI models, including ChatGPT, Gemini, and Grok, using an identical structured prompt. The AI models will provide categorical and binary predictions for difficult laryngoscopy and difficult intubation based only on visible image-based anatomical features. No intraoperative outcome data, expert predictions, or conventional airway assessment results will be provided to the AI models.

AI-generated predictions will be compared with expert anesthesiologist image-based assessments, conventional airway evaluation parameters, and prospectively recorded intraoperative reference outcomes. Difficult laryngoscopy will be defined as Cormack-Lehane grade III or IV. Difficult intubation will be defined using objective intraoperative criteria, including more than one intubation attempt, need for bougie or stylet assistance, rescue use of video laryngoscopy or supraglottic airway device, intubation time exceeding 60 seconds, or Intubation Difficulty Scale score greater than 5.

The study will assess the sensitivity, specificity, positive predictive value, negative predictive value, accuracy, receiver operating characteristic performance, and agreement between AI models and expert anesthesiologist assessments. The findings may help clarify whether multimodal AI can serve as a clinician-supervised adjunct for preoperative difficult airway risk stratification.

Studietyp

Observationell

Inskrivning (Beräknad)

319

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Kadıköy
      • Istanbul, Kadıköy, Turkiet (Türkiye), 34734
        • Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Adult patients scheduled for elective surgical procedures requiring endotracheal intubation at Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital.

Beskrivning

Inclusion Criteria:

  • Age 18 years or older
  • Scheduled for elective surgery requiring endotracheal intubation
  • Able to cooperate with the standardized preoperative airway photography protocol
  • Able to provide written informed consent

Exclusion Criteria:

  • Age younger than 18 years
  • Emergency surgery
  • Refusal or inability to provide informed consent
  • Inability to cooperate with the standardized photographic protocol
  • Known craniofacial or cervical deformity
  • History of major head and neck surgery or radiotherapy
  • Obstruction of key anatomical landmarks by facial hair, dressings, cervical collars, or other external devices
  • Incomplete or poor-quality image sets despite repeated acquisition
  • Missing clinical airway assessment data
  • No endotracheal intubation performed
  • Airway difficulty could not be reliably evaluated
  • Planned awake fiberoptic intubation or other preplanned advanced airway technique because of known difficult airway

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Elective Surgery Patients Requiring Endotracheal Intubation
Adult patients scheduled for elective surgery requiring endotracheal intubation who will undergo standardized preoperative airway photography and prospective intraoperative airway outcome recording.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Diagnostic Performance of Multimodal AI Models for Predicting Difficult Intubation
Tidsram: From preoperative airway photography to completion of intraoperative endotracheal intubation, up to 1 day
The primary outcome is the diagnostic performance of multimodal artificial intelligence models for predicting true difficult intubation based on standardized preoperative airway photographs. Difficult intubation will be determined using prospectively recorded intraoperative reference criteria, including more than one intubation attempt, need for bougie or stylet assistance, rescue use of video laryngoscopy or supraglottic airway device, intubation time exceeding 60 seconds, or Intubation Difficulty Scale score greater than 5. Diagnostic performance will be assessed using sensitivity, specificity, positive predictive value, negative predictive value, accuracy, and receiver operating characteristic analysis.
From preoperative airway photography to completion of intraoperative endotracheal intubation, up to 1 day

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Diagnostic Performance of Multimodal AI Models for Predicting Difficult Laryngoscopy
Tidsram: From preoperative airway photography to completion of intraoperative laryngoscopy, up to 1 day
The key secondary outcome is the diagnostic performance of multimodal artificial intelligence models for predicting true difficult laryngoscopy based on standardized preoperative airway photographs. Difficult laryngoscopy will be defined as Cormack-Lehane grade III or IV recorded during intraoperative airway management. Diagnostic performance will be assessed using sensitivity, specificity, positive predictive value, negative predictive value, accuracy, and receiver operating characteristic analysis.
From preoperative airway photography to completion of intraoperative laryngoscopy, up to 1 day

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

25 juni 2026

Primärt slutförande (Beräknad)

1 september 2026

Avslutad studie (Beräknad)

1 september 2026

Studieregistreringsdatum

Först inskickad

7 juli 2026

Först inskickad som uppfyllde QC-kriterierna

7 juli 2026

Första postat (Faktisk)

14 juli 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

14 juli 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

7 juli 2026

Senast verifierad

1 juli 2026

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

IPD-planbeskrivning

Individual participant data will not be shared due to privacy and confidentiality considerations, particularly because the study involves preoperative airway images. De-identified aggregate data will be presented in the final analysis and publication.

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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