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Intra-breath arterial oxygen oscillations detected by a fast oxygen sensor in an animal model of acute respiratory distress syndrome

BACKGROUND: There is considerable interest in oxygen partial pressure (Po(2)) monitoring in physiology, and in tracking Po(2) changes dynamically when it varies rapidly. For example, arterial Po(2) ([Formula: see text]) can vary within the respiratory cycle in cyclical atelectasis (CA), where [Formu...

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Detalles Bibliográficos
Autores principales: Formenti, F., Chen, R., McPeak, H., Murison, P. J., Matejovic, M., Hahn, C. E. W., Farmery, A. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364062/
https://www.ncbi.nlm.nih.gov/pubmed/25631471
http://dx.doi.org/10.1093/bja/aeu407
Descripción
Sumario:BACKGROUND: There is considerable interest in oxygen partial pressure (Po(2)) monitoring in physiology, and in tracking Po(2) changes dynamically when it varies rapidly. For example, arterial Po(2) ([Formula: see text]) can vary within the respiratory cycle in cyclical atelectasis (CA), where [Formula: see text] is thought to increase and decrease during inspiration and expiration, respectively. A sensor that detects these [Formula: see text] oscillations could become a useful diagnostic tool of CA during acute respiratory distress syndrome (ARDS). METHODS: We developed a fibreoptic Po(2) sensor (<200 µm diameter), suitable for human use, that has a fast response time, and can measure Po(2) continuously in blood. By altering the inspired fraction of oxygen ([Formula: see text]) from 21 to 100% in four healthy animal models, we determined the linearity of the sensor's signal over a wide range of [Formula: see text] values in vivo. We also hypothesized that the sensor could measure rapid intra-breath [Formula: see text] oscillations in a large animal model of ARDS. RESULTS: In the healthy animal models, [Formula: see text] responses to changes in [Formula: see text] were in agreement with conventional intermittent blood-gas analysis (n=39) for a wide range of [Formula: see text] values, from 10 to 73 kPa. In the animal lavage model of CA, the sensor detected [Formula: see text] oscillations, also at clinically relevant [Formula: see text] levels close to 9 kPa. CONCLUSIONS: We conclude that these fibreoptic [Formula: see text] sensors have the potential to become a diagnostic tool for CA in ARDS.