key: cord-0728685-jnond059
authors: Dres, Martin; Bassi, Gianluigi Li
title: Reducing Ventilator-associated Brain Injury by Diaphragm Neurostimulation: Racking the Diaphragm to Protect the Brain?
date: 2021-03-30
journal: Am. j. respir. crit. care med
DOI: 10.1164/rccm.202110-2312ed
sha: 1812905b014980e18de78686844a3edda5bd3677
doc_id: 728685
cord_uid: jnond059

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Racking the Diaphragm to Protect the Brain?

Mechanical ventilation is of paramount importance in improving the survival of patients suffering from respiratory failure, as most recently confirmed by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. Notwithstanding, it is well established that mechanical ventilation has unfavorable effects, some of them being likely to worsen the prognosis of the primary disease, for which mechanical ventilation was indicated. Among the harmful effects associated with the use of mechanical ventilation, it has become evident that ventilation in critically ill patients can augment or cause lung injury, leading to ventilator-induced lung injury (1) . Therefore, providing a lung-protective ventilation-limiting stress and strain-is currently the basis of good clinical practice in critical care settings. However, this approach requires putting the respiratory muscles at rest, which may lead to ventilator-induced diaphragmatic dysfunction (2) . Besides ventilator-induced lung injury and ventilator-induced diaphragmatic dysfunction, studies have also reported a strong association between the use of mechanical ventilation and delirium in the ICU (3) and long-term cognitive impairment in acute respiratory distress syndrome survivors who are ventilated for prolonged periods (4, 5) . The causal association between mechanical ventilation and neurocognitive dysfunction is extremely difficult to investigate and multifactorial, encompassing nonmodifiable factors such as pre-ICU cognitive impairment, sepsis, and acute illness severity and modifiable factors such as use of opiates, benzodiazepines, and anticholinergic drugs. In addition, mechanical ventilation generates cyclic alveolar collapse and overstretching, causing local and systemic inflammation (6) , potentially leading to neurological injury and ventilatorassociated brain injury. The concept of ventilator-associated brain injury is supported by several findings confirming hippocampal neuronal cell apoptosis (7) , but the long-term impact is still not fully elucidated, considering the plasticity and regenerative capacity of specific hippocampal regions, such as the dentate gyrus (8) . Whether ventilator-associated brain injury is mediated though a systemic (hyper)inflammatory or a neural pathway is unclear, and further investigations will have to address this point.

In this issue of the Journal, Bassi and colleagues (pp. 1391-1402) provided thought-provoking insights on ventilator-associated brain injury and a novel preventive intervention (9) . They used a porcine model to investigate a hybrid strategy of 50-hour mechanical ventilation, including synchronized diaphragmatic neurostimulation. Neurostimulation of the diaphragm was provided through a catheter advanced up to the superior vena cava through the left subclavian, which stimulated the phrenic nerve to reduce ventilator pressure-time product by 15-20%. The intriguing hypothesis was that a "physiological" mechanical ventilation, generated by the contraction of the diaphragm and a preserved ventilation homogeneity, would reduce inflammation and modulate the pulmonary afferent signal, leading to mitigation of cellular apoptosis in the hippocampus. Four interventions were investigated: lungprotective mechanical ventilation, diaphragm neurostimulation either every other breath or every breath in synchrony with lung-protective mechanical ventilation, or no ventilation. During the experimental protocol, the investigators applied consistent sedation protocols among all ventilated groups and therapeutic regimens to control hemodynamics, temperature, and gas exchanges. Interestingly, the heart rate variability was used as a surrogate of autonomic nervous system activity. Significantly greater apoptotic indices, microglia percentages, and reactive astrocyte percentages were found in the mechanical ventilation group in comparison with the other groups, suggesting a protective effect of diaphragm neurostimulation on hippocampal injury. In addition, blood biomarkers of brain injury were significantly lower in the group that had every breath in synchrony with lung-protective mechanical ventilation. Yet, systemic markers of inflammation and lung injury scores were similar between the groups, which may imply that hippocampal apoptosis, rather than being triggered by the inflammatory pathway, was possibly caused by a neuropathway of injury.

This study brings to light important new knowledge about pathophysiology of ventilator-associated brain injury and a promising therapeutic advance. This study will certainly have further concrete dividends and the authors should be commended for such a complex investigation in animals mechanically ventilated up to 50 hours. Indeed, a main strength of the study was the accurate modeling of settings and interventions routinely applied in critically ill patients and the extensive panel of assessments to corroborate the authors' hypothesis. The rather long use of diaphragmatic neurostimulation is also reassuring, specifically considering that no major adverse events were recorded.

However, a few important factors should be considered to appropriately infer from these novel findings and extrapolate the evidence to clinical practice. First, the findings highlighted by Bassi and colleagues suggested association and not causality between mechanical ventilation and brain injury; thus, the mechanistic process of the brain-lung interaction remains to be elucidated. Second, the authors reported evidence of hippocampal apoptosis associated with mechanical ventilation, which does not necessarily indicate that in clinical settings this would translate in relevant clinical symptoms, such as delirium or cognitive impairment after 50 hours of mechanical ventilation. Indeed, to distinguish between a permanent loss of cells and a reversible atrophy is pivotal, and it is still uncertain the association between ventilator-associated brain injury and longterm neurological disabilities. Further investigations will have to feed the gap between histological data and clinical outcomes in critically ill patients and in particular should address whether diaphragmatic neurostimulation could exert any benefit in patients on mechanical ventilation with neurological injury (i.e., traumatic brain injury). Although in the study by Bassi and colleagues, insertion through the left subclavian vein ensured optimal bilateral phrenic nerves stimulation, theoretically access through the left jugular vein (a privileged vascular access for clinicians) might provide comparable results. Irrespective, in patients with brain injury, potential risk of catheter-related venous thrombosis and intracranial hypertension should be also considered and explored in future investigations. Along the same line, the preliminary nature of these findings should be emphasized. Because findings were obtained from a model of mechanical ventilation without lung injury, reservations remain on the benefits in the context of overwhelming lung inflammation. In addition, animals were kept supine whereas mechanically ventilated patients are most commonly in the semirecumbent position, possibly modifying risks of brain injury (10) . Third, the hemodynamic effect of diaphragm neurostimulation on cerebral perfusion warrants further investigation, specifically in light of some potential interspecies differences in cerebral blood flow autoregulation that could have overexpressed deleterious effects of mechanical ventilation. Finally, the safety of the novel intervention was marginally appraised by the current investigation, and although no major adverse events were found, long-term stimulation of the phrenic nerve, beyond 50 hours, will be essential to ensure potential translatability into clinical settings.

In conclusion, the study by Bassi and colleagues undoubtedly provides a significant contribution to the field, introducing new applications of mechanical ventilation-synchronized phrenic nerve stimulation to hinder neurological dysfunction. Although acknowledging possible limitations of preclinical tests in animal models of mechanical ventilation, these pioneering results-if confirmed in models of critical illnesses-could provide robust new evidence to be translated into clinical trials. 

Ventilator-induced lung injury

Ventilator-induced diaphragmatic dysfunction

Delirium as a predictor of mortality in mechanically ventilated patients in the intensive care unit

Neuropsychological sequelae and impaired health status in survivors of severe acute respiratory distress syndrome

Canadian Critical Care Trials Group. Functional disability 5 years after acute respiratory distress syndrome

Effects of cyclic opening and closing at low-and high-volume ventilation on bronchoalveolar lavage cytokines

Mechanical ventilation triggers hippocampal apoptosis by vagal and dopaminergic pathways

Functional neurogenesis in the adult hippocampus

Transvenous diaphragm neurostimulation mitigates ventilationassociated brain injury

Hippocampal damage during mechanical ventilation in trendelenburg position: a secondary analysis of an experimental study on the prevention of ventilator-associated pneumonia