Acute Lung Injury Clinical Trial
Official title:
Effects of Recruitment Maneuvers in Patients With Acute Brain Injury and Acute Lung Injury
Development of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) in patients with severe brain injury has been associated with poor outcome. The application of lung recruitment maneuvers (RM) for a short period of time to open collapsed alveoli and reverse hypoxemia in early ARDS has been recommended. However, little is known about the cerebral and vascular effects of RM in brain injury patients with ALI/ARDS. The aim of this study is to assess the effects of a single standardized RM on oxygenation and on systemic and cerebral hemodynamics in severe brain injury patients with ALI/ARDS.
Patients with severe brain injury comprise a significant portion of admissions to critical
care units. These patients are unable to adequately protect their airways and are usually
intubated and mechanically ventilated. The goal of mechanical ventilation in patients with
brain injury is to optimize blood gas exchange while minimizing intrathoracic pressure to
avoid interference with cerebral venous drainage.Over the last 20 years, a plethora of
experimental and clinical data have shown that mechanical ventilation can cause or aggravate
lung damage in patients with acute lung injury (ALI) and the acute respiratory distress
syndrome (ARDS). The aim of this pilot study was to assess the effects of a single
standardized recruitment maneuver (RM) on oxygenation and on systemic and cerebral
hemodynamics in severe brain injury patients with ALI/ARDS.
Only patients with brain injury, as defined by a Glasgow Coma Score <13, admitted into the
Trauma and Surgical intensive care unit (ICU) will be studied.
After obtaining informed consent, a RM will be performed by switching the ventilator from
assist/control ventilation to continuous positive airway pressure (CPAP) and applying a
pressure of 40 cmH2O for 40 sec (11). After the RM, patients have been ventilated in
pressure control ventilation and PEEP will be gradually reduced in decremental steps every 3
respiratory cycles starting with PEEP at 30 cm H2O, maintaining a maximum peak pressure of
40 cmH2O during this procedure until pre-RM PEEP levels are achieved. The RM will be
discontinued if any of the following changes developed during the procedure: (i) ≥20%
changes in baseline systemic blood pressure, (ii) ICP ≥20 mmHg, or (iii) SaO2 ≤90%. After
the RM is performed, respiratory mechanics, arterial and SjO2 blood samples and systemic and
cerebral hemodynamics will be obtained at 30 min and 8 hours.
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Observational Model: Case-Only, Time Perspective: Prospective
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