Respiratory Failure Clinical Trial
Official title:
Feasibility of Phrenic Nerve Block to Mitigate Self-inflicted Lung Injury in ARF Patients Under Mechanical Ventilation on Spontaneous Breathing
The purpose of this single-centered, proof of concept study is to determine whether it is feasible to perform a phrenic nerve block to reduce diaphragm electrical activity and, therefore, inspiratory effort and if such block reduces self-inflicted lung injury on patients under mechanical ventilation on spontaneous breathing. Ten patients will be monitored with electrical impedance tomography, NAVA catheter, and esophageal balloon. Using a nerve stimulator and an ultrasound, we will identify the phrenic nerve on its cervical portion bilaterally and administer perineural low-dose lidocaine. Diaphragm electrical activity, transpulmonary pressure and data on ventilation distribution will be continuously collected. The study will be over once the patient presents the same diaphragm electrical activity and transpulmonary pressure as before the phrenic nerve block.
The use of protective mechanical ventilation has improved prognosis on patients with Acute
Respiratory Failure. The association of neuromuscular blockade in the first 48-72h has
additionally contributed to a higher survival rate. Such improvement may be due to the
reduction of transpulmonary pressures caused by the patient's inspiratory effort. To achieve
appropriate neuromuscular blockade, highes doses of both neuromuscular blocking agents and
sedatives are required. Therefore, such a strategy usually causes muscular atrophy, including
the diaphragm.
Because of the augmented neural drive of such patients, exacerbated by inflammation and
pulmonary edema, the consequent high tidal volume and transpulmonary pressure cannot be
reduced by the newest sedatives. In fact, some of these sedatives may even deteriorate
ventilatory dyssynchrony. Our intention is to verify a novel approach: whether is possible to
reduce the inspiratory effort of patients without the use of systemic neuromuscular blocking
agents.
Our objective in this proof of concept study is to determine the feasibility the use of
phrenic nerve blockade to decrease transpulmonary pressure and tidal volume, as well as
quantify its effects on esophageal pressure, diaphragmatic electrical activity,
transpulmonary pressure and ventilation distribution in patients on spontaneous breathing. It
is expected that such intervention will reduce diaphragm electrical activity, leading to
lower transpulmonary pressure, tidal volume and driving pressures.
All patients will be submitted to the same intervention. Respiratory mechanics, ventilation
distribution, diaphragm electrical activity, heart rate, mean arterial pressure and
peripheral saturation will be collected throughout the study. Once the patient presents the
same diaphragmatic electrical activity and transpulmonary pressure as before the phrenic
nerve block, the study will be over.
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