Transvenous Diaphragm Neurostimulation Mitigates Ventilation-associated Brain Injury

• Published in: American journal of respiratory and critical care medicine Vol. 204; no. 12; pp. 1391 - 1402
• Main Authors: Bassi, Thiago G., Rohrs, Elizabeth C., Fernandez, Karl C., Ornowska, Marlena, Nicholas, Michelle, Gani, Matt, Evans, Doug, Reynolds, Steven C.
• Format: Journal Article
• Language: English
• Published: United States American Thoracic Society 15.12.2021
• Subjects: Animals; Apoptosis; Brain Injuries - diagnosis; Brain Injuries - etiology; Brain Injuries - pathology; Brain Injuries - prevention & control; Clinical trials; Diaphragm (Anatomy); Diaphragm - innervation; Electric Stimulation Therapy - methods; Encephalitis - diagnosis; Encephalitis - etiology; Encephalitis - pathology; Encephalitis - prevention & control; Female; Hippocampus - pathology; Inflammation; Lung cancer; Original; Phrenic Nerve; Respiration, Artificial - adverse effects; Respiration, Artificial - methods; Swine; Treatment Outcome; Ventilation; apoptosis; ICU; post-ICU syndrome; mechanical ventilators; brain injuries
• ISSN: 1073-449X; 1535-4970; 1535-4970
• DOI: 10.1164/rccm.202101-0076OC

Mechanical ventilation (MV) is associated with hippocampal apoptosis and inflammation, and it is important to study strategies to mitigate them. To explore whether temporary transvenous diaphragm neurostimulation (TTDN) in association with MV mitigates hippocampal apoptosis and inflammation after 50 hours of MV. Normal-lung porcine study comparing apoptotic index, inflammatory markers, and neurological-damage serum markers between never-ventilated subjects, subjects undergoing 50 hours of MV plus either TTDN every other breath or every breath, and subjects undergoing 50 hours of MV (MV group). MV settings in volume control were Vt of 8 ml/kg, and positive end-expiratory pressure of 5 cm H O. Apoptotic indices, microglia percentages, and reactive astrocyte percentages were greater in the MV group in comparison with the other groups (  < 0.05). Transpulmonary pressure at baseline and at study end were both lower in the group receiving TTDN every breath, but lung injury scores and systemic inflammatory markers were not different between the groups. Serum concentrations of four neurological-damage markers were lower in the group receiving TTDN every breath than in the MV group (  < 0.05). Heart rate variability declined significantly in the MV group and increased significantly in both TTDN groups over the course of the experiments. Our study found that mechanical ventilation is associated with hippocampal apoptosis and inflammation, independent of lung injury and systemic inflammation. Also, in a porcine model, TTDN results in neuroprotection after 50 hours, and the degree of neuroprotection increases with greater exposure to TTDN.