None listed
Conditions
Brief summary
The TARGET Study is a prospective, randomised controlled trial, evaluating two standard techniques of tracheal puncture during insertion of percutaneous tracheostomies: the traditional landmark method versus the ultrasound guided method. Percutaneous Dilatational Tracheostomy (PTD) is a frequently performed invasive procedure in the Intensive Care setting, where complications both immediate and short term can contribute to significant morbidity and mortality. It is increasingly recognised that lateral (off midline) and craniocaudal (too high up or too low down) malposition of PDTs may result in greater incidence of both short and long term complications. The use of ultrasonography in placing tracheostomies is well described in the literature. We aim to evaluate the use of realtime ultrasound guidance for the tracheal puncture, which is the most important determining element in positioning the tracheostomy, to determine which method results in better midline and craniocaudal placement. Better midline and cranio-caudal placement in turn may decrease complications and improve clinically significant surrogate markers of outcome.
Interventions
Real time ultrasound guidance will be used to determine tracheal midline and cranio-caudal distance (i.e number of tracheal rings) from the cricoid catilage to determine the the site of the tracheal puncture which is the initial step in a percutaneous dilatational tracheostomy. A bronchoscopic image will be taken after the puncture which will be used to evaluate the puncture position during data analysis. After the puncture, insertion of the tracheostomy will proceed as per the routine used for insertion of a percutanous dilatational tracheostomy. The entire procedure is expected to last between 15-30 minutes.
Sponsors
Study design
Eligibility
Inclusion criteria
All adult intensive care patients where a decision has been made to insert a percutaneous dilatational tracheostomy
Exclusion criteria
Under 18 years old Pregnant women