Understanding and Improving Dysphagia After Mechanical Ventilation
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Deglutition Disorders
- Sponsor
- Johns Hopkins University
- Enrollment
- 58
- Locations
- 1
- Primary Endpoint
- Number of participants aspirating during fiberoptic endoscopic swallow study
- Status
- Terminated
- Last Updated
- 3 years ago
Overview
Brief Summary
An early intervention for swallowing disorders (i.e., dysphagia) during endotracheal intubation may improve patient outcomes. The investigators propose treatment sessions targeting sensorimotor integration, strength, and range of motion during oral endotracheal intubation with mechanical ventilation to reduce or prevent dysphagia and aspiration (food or liquids entering the airway), establish a solid foundation in understanding reasons for swallowing impairment after extubation from mechanical ventilation and learn new methods to reduce or prevent these problems.
Detailed Description
The overall goals of this study are to evaluate patients with acute respiratory failure from the time they are orally intubated in the ICU to: 1) investigate tongue weakness and other pathophysiological aspects of dysphagia, and 2) evaluate, in a Phase II clinical trial, a novel, multimodal, sensorimotor intervention conducted during intubation to reduce or prevent dysphagia after extubation. Patients who are expected to be intubated with mechanical ventilation for \>96 hours will be consecutively enrolled shortly after intubation. Laryngeal function, tongue strength, swallowing pathophysiology, and breathing-swallowing coordination will be evaluated with valid and reliable standardized measures. While orally intubated, patients in the treatment group will receive a novel, early, sensorimotor intervention for 60-minutes daily, 5 times per week, targeting improved swallowing physiology and kinematics to reduce aspiration and dysphagia. These daily sessions will continue until the completion of a modified barium swallow study conducted within approximately 2 days after extubation, and thereafter standard clinical care will resume. Patients in the control group will receive standard clinical care during intubation and throughout their hospital stay. All patients will be followed to hospital discharge to determine the pathophysiological and clinical impact of the proposed intervention. Knowledge from this study will provide important data for this novel intervention and provide a critical foundation for understanding the physiological mechanisms of dysphagia and aspiration after intubation in patients with acute respiratory failure. With success, this investigation will help shift clinical practice patterns to consider early intervention with the goal of reducing the frequency and severity of swallowing impairment leading to aspiration and additional medical complications.
Investigators
Eligibility Criteria
Inclusion Criteria
- •≥18 years old
- •Required mechanical ventilation via an oral endotracheal tube
Exclusion Criteria
- •Unable to understand or speak English due to a language barrier
- •Unable to understand or speak English due to a cognitive impairment
- •Barium sulfate allergy
- •Pregnancy
- •Presence of any cardiac pacing device (including temporary epicardial pacing) without an underlying cardiac rhythm as confirmed by treating physician or diaphragmatic pacer
- •Nasal endotracheal intubation during the present admission
- •Patient is not expected to require ≥48 hours of intubation
- •Pre-existing dysphagia/aspiration, voice or cognitive disorder
- •Reflux with history of known or suspected aspiration
- •Presence of a central nervous system, neuromuscular or connective tissue disease (e.g., stroke, Guillain-Barre, scleroderma)
Outcomes
Primary Outcomes
Number of participants aspirating during fiberoptic endoscopic swallow study
Time Frame: participants will be evaluated an expected average of 48 hours after extubation