Comparative Effectiveness of an Artificial Air Pocket Device to Delay Asphyxiation in Supine Individuals Critically Buried in Avalanche Debris

Author:

Strapazzon Giacomo12,Rauch Simon13,Malacrida Sandro1,Dal Cappello Tomas1,Governo Enrica4,Catuzzo Bruna4,Mrakic-Sposta Simona5,Urgesi Margherita4,Falla Marika16,Cavoretto Gianluca4,Visetti Enrico47,Giardini Guido4,Brugger Hermann1,Prato Federico248

Affiliation:

1. Institute of Mountain Emergency Medicine, Eurac Research, Bolzano, Italy

2. Corpo Nazionale Soccorso Alpino e Speleologico, Milano, Italy

3. Department of Anesthesia and Intensive Care Medicine, F. Tappeiner Hospital, Merano, Italy

4. Mountain Medicine Center, Azienda Sanitaria Valle d’Aosta, Aosta, Italy

5. Institute of Clinical Physiology, National Research Council, Milano, Italy

6. Center for Mind/Brain Sciences, University of Trento, Rovereto, Italy

7. Department of Anesthesia and Intensive Care, Gruppo Policlinico di Monza, Monza, Italy

8. Department of Emergency Medicine, Azienda Ospedaliero-Universitaria Maggiore della Carità, Novara, Italy

Abstract

ImportanceApproximately 70% of individuals critically buried in avalanche debris die within 35 minutes as a result of asphyxial cardiac arrest. An artificial air-pocket device (AAPD) that separates inhaled air from exhaled air may delay the onset of severe hypoxemia and eventual asphyxia during snow burial.ObjectiveTo investigate the efficacy of a new AAPD during snow burial in a supine position.Design, Setting, and ParticipantsThis comparative effectiveness trial was performed in winter 2016 with data analysis in November 2016 and November 2022. Each trial used a simulated critical avalanche burial scenario, in which a trough was dug in a snow pile and an additional air pocket of 0.5 L volume was punched into the lateral wall for each control trial. All participants were buried in a supine position. Trials could be voluntarily terminated at any time, with a maximum length of 60 minutes; trials were automatically terminated if the participant’s peripheral oxygen saturation (Spo2) dropped to less than 84%.ExposuresEach participant conducted 2 trials, one in which they breathed into the AAPD (intervention trial) and the other in which they breathed into the prepared air pocket (control trial).Main Outcomes and MeasuresMeasurements included Spo2, cerebral oxygenation, ventilatory parameters, respiratory gas concentrations, and visual-analogue scales. Kaplan-Meier survival curves and rank test for matched survival data were used to analyze the total burial time in each trial.ResultsA total of 13 volunteers (9 men; mean [SD] age, 33 [8] years) were exposed to the intervention and control trials. Intervention trials were terminated less often (2 of 13 trials) as a result of hypoxemia than control trials (11 of 12 trials). Similarly, survival curves showed a longer duration of burial in the intervention compared with the control trials for the time to reach an Spo2 less than 84% (rank test for matched survival data: P = .003). The intervention trials, compared with the control trials, also had slower rates of decrease in fraction of inspired oxygen (mean [SD] rate, −0.8 [0.4] %/min vs −2.2 [1.2] %/min) and of increase in fraction of inspired carbon dioxide (mean [SD] rate, 0.5 [0.3] %/min vs 1.4 [0.6] %/min) and expired ventilation per minute (mean [SD] rate, 0.5 [1.0] L/min2 vs 3.9 [2.6] L/min2).Conclusions and RelevanceThis comparative effectiveness trial found that the new AAPD was associated with delaying the development of hypoxemia and hypercapnia in supine participants in a critical burial scenario. Use of the AAPD may allow a longer burial time before asphyxial cardiac arrest, which might allow longer times for successful rescue by companions or by prehospital emergency medical services.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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