Ultrasound Evaluation of Respiratory Muscles During Mechanical Ventilation Weaning in ICU Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBursa Sevket Yilmaz Training and Research Hospital

About this trial

Patients with pneumonia who require invasive mechanical ventilation in the intensive care unit (ICU) often experience difficulties during the process of being separated from the breathing machine (weaning). Failure of weaning is associated with longer ventilation duration, prolonged ICU stay, and increased risk of complications and death. Therefore, simple and reliable bedside tools are needed to better understand respiratory muscle function and to help predict weaning outcomes.

This prospective, observational, single-center study aims to evaluate respiratory muscle function using bedside ultrasound in adult ICU patients with pneumonia receiving invasive mechanical ventilation. The diaphragm, parasternal intercostal muscles, and anterior scalene muscles will be assessed using ultrasound during the weaning process. Measurements will be performed serially, starting from the first day when patients demonstrate meaningful spontaneous breathing effort and continuing until successful extubation, tracheostomy, or ICU mortality.

Ultrasound measurements of muscle thickness and thickening fraction will be analyzed in relation to weaning outcomes. In addition, ventilator parameters and commonly used weaning indices will be recorded at the time of each ultrasound assessment. The findings of this study are expected to improve understanding of respiratory muscle involvement during weaning and may contribute to earlier identification of patients at risk of weaning failure.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Admission to the intensive care unit with a diagnosis of pneumonia

Receiving invasive mechanical ventilation via endotracheal intubation

Expected to undergo a weaning process from mechanical ventilation

Disqualifiers

Known neuromuscular disease affecting respiratory muscles

High cervical spinal cord injury

History of major neck, thoracic, or diaphragmatic surgery

Acute thoracic trauma or pneumothorax

Trial design

Treatments tested in this trial

  • No intervention (observational study)

Treatment groups

150 Participants
are divided into 1 treatment group