Abstract

BackgroundVentilator-induced diaphragmatic dysfunction is a serious complication associated with higher ICU mortality, prolonged mechanical ventilation, and unsuccessful withdrawal from mechanical ventilation. Although neurally adjusted ventilatory assist (NAVA) could be associated with lower patient-ventilator asynchrony compared with conventional ventilation, its effects on diaphragmatic dysfunction have not yet been well elucidated.MethodsTwenty Japanese white rabbits were randomly divided into four groups, (1) no ventilation, (2) controlled mechanical ventilation (CMV) with continuous neuromuscular blockade, (3) NAVA, and (4) pressure support ventilation (PSV). Ventilated rabbits had lung injury induced, and mechanical ventilation was continued for 12 h. Respiratory waveforms were continuously recorded, and the asynchronous events measured. Subsequently, the animals were euthanized, and diaphragm and lung tissue were removed, and stained with Hematoxylin-Eosin to evaluate the extent of lung injury. The myofiber cross-sectional area of the diaphragm was evaluated under the adenosine triphosphatase staining, sarcomere disruptions by electron microscopy, apoptotic cell numbers by the TUNEL method, and quantitative analysis of Caspase-3 mRNA expression by real-time polymerase chain reaction.ResultsPhysiological index, respiratory parameters, and histologic lung injury were not significantly different among the CMV, NAVA, and PSV. NAVA had lower asynchronous events than PSV (median [interquartile range], NAVA, 1.1 [0–2.2], PSV, 6.8 [3.8–10.0], p = 0.023). No differences were seen in the cross-sectional areas of myofibers between NAVA and PSV, but those of Type 1, 2A, and 2B fibers were lower in CMV compared with NAVA. The area fraction of sarcomere disruptions was lower in NAVA than PSV (NAVA vs PSV; 1.6 [1.5–2.8] vs 3.6 [2.7–4.3], p < 0.001). The proportion of apoptotic cells was lower in NAVA group than in PSV (NAVA vs PSV; 3.5 [2.5–6.4] vs 12.1 [8.9–18.1], p < 0.001). There was a tendency in the decreased expression levels of Caspase-3 mRNA in NAVA groups. Asynchrony Index was a mediator in the relationship between NAVA and sarcomere disruptions.ConclusionsPreservation of spontaneous breathing using either PSV or NAVA can preserve the cross sectional area of the diaphragm to prevent atrophy. However, NAVA may be superior to PSV in preventing sarcomere injury and apoptosis of myofibrotic cells of the diaphragm, and this effect may be mediated by patient-ventilator asynchrony.

Highlights

  • Ventilator-induced diaphragmatic dysfunction is a serious complication associated with higher intensive care unit (ICU) mortality, prolonged mechanical ventilation, and unsuccessful withdrawal from mechanical ventilation

  • controlled mechanical ventilation (CMV) control mechanical ventilation, NAVA neurally adjusted ventilatory assist, PSV pressure support ventilation; bpm, beats per minutes, NA not available, Partial pressure of arterial oxygen (PaO2) partial pressure of arterial oxygen, Fraction of inspired oxygen (FIO2) fraction of inspired oxygen, Partial pressure of arterial carbon dioxide (PaCO2) partial pressure of arterial carbon dioxide; electrical activity of the diaphragm (Edi), electrical activity of diaphragm with no significant difference in the subsequent values

  • Muscle protein degradation There was a tendency in the decreased expression levels of Caspase-3 messenger ribonucleic acid (mRNA) in NAVA groups (CMV vs NAVA vs PSV, compared with the baseline control group: 15.0 [5.7–22.6] vs 11.1 [7.96–17.3] vs 27.6 [18.2– 52.6], p = 0.065)

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Summary

Introduction

Ventilator-induced diaphragmatic dysfunction is a serious complication associated with higher ICU mortality, prolonged mechanical ventilation, and unsuccessful withdrawal from mechanical ventilation. Ventilator-induced diaphragm dysfunction (VIDD) [1,2,3,4,5] occurs in 30–80% of critically ill patients undergoing mechanical ventilation [6], and may be associated with prolonged mechanical ventilation and increased intensive care unit (ICU) and hospital mortality [5,6,7]. Most cases of ineffective inspiratory effort occur during the expiratory phase on the ventilator. This failure to trigger mechanical breaths might result in activation of the diaphragm even while it is lengthening -i.e. eccentric contraction [21,22,23,24]. No studies have demonstrated a relationship between ventilator asynchrony and diaphragmatic injury

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