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Article Abstract

The present study describes the magnitude and spatial distribution of lung strain in healthy anesthetized, mechanically ventilated dogs with and without positive end-expiratory pressure (PEEP). Total lung strain (LS) has a dynamic (LS) and a static (LS) component. Due to lung heterogeneity, global lung strain may not accurately represent regional total tissue lung strain (TS), which may also be described by a regional dynamic (TS) and static (TS) component. Six healthy anesthetized beagles (12.4 ± 1.4 kg body weight) were placed in dorsal recumbency and ventilated with a tidal volume of 15 ml/kg, respiratory rate of 15 bpm, and zero end-expiratory pressure (ZEEP). Respiratory system mechanics and full thoracic end-expiratory and end-inspiratory CT scan images were obtained at ZEEP. Thereafter, a PEEP of 5 cmHO was set and respiratory system mechanics measurements and end-expiratory and end-inspiratory images were repeated. Computed lung volumes from CT scans were used to evaluate the global LS, LS, and LS during PEEP. During ZEEP, LS was assumed zero; therefore, LS was the same as LS. Image segmentation was applied to CT images to obtain maps of regional TS, TS, and TS during PEEP, and TS during ZEEP. Compliance increased ( = 0.013) and driving pressure decreased ( = 0.043) during PEEP. PEEP increased the end-expiratory lung volume ( < 0.001) and significantly reduced global LS (33.4 ± 6.4% during ZEEP, 24.0 ± 4.6% during PEEP, = 0.032). LS by PEEP was larger than the reduction in LS; therefore, LS at PEEP was larger than LS at ZEEP ( = 0.005). There was marked topographic heterogeneity of regional strains. PEEP induced a significant reduction in TS in all lung regions ( < 0.05). Similar to global findings, PEEP-induced TS was larger than the reduction in TS; therefore, PEEP-induced TS was larger than TS at ZEEP. In conclusion, PEEP reduced both global and regional estimates of dynamic strain, but induced a large static strain. Given that lung injury has been mostly associated with tidal deformation, limiting dynamic strain may be an important clinical target in healthy and diseased lungs, but this requires further study.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964072PMC
http://dx.doi.org/10.3389/fvets.2022.839406DOI Listing

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