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Evaluation of a Specialised Tracheostomy Team for the Management of Patients With a Tracheostomy Cannula in a Belgium General Hospital: A Retrospective Study.

Management of Patients With a Tracheostomy Cannula by a Specialised Team in a Belgium General Hospital: A Retrospective Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07755969
Enrollment
200
Registered
2026-08-10
Start date
2026-08-01
Completion date
2027-03-31
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hospital, Multidisciplinary Care Team, Outcomes, Tracheostomy Patients

Keywords

Multidisciplinary tracheostomy team, Tracheostomy care, Hospitalised patients with a tracheostomy, Retrospective study, Clinical outcomes, Trachea cannula, tracheostomy related care

Brief summary

Patients admitted to intensive care units (ICUs) frequently require prolonged mechanical ventilation. Difficulties in weaning from mechanical ventilation represent an important indication for performing a tracheotomy, which involves creating a temporary opening in the trachea into which a cannula is inserted. This procedure is often confused with a tracheostomy, in which a permanent stoma is created. Tracheotomy offers several clinical benefits, including increased patient comfort, reduced sedation requirements, decreased work of breathing, improved oral hygiene, a lower risk of ventilator-associated pneumonia, and lower mortality. With the increasing use of the percutaneous technique, the procedure is increasingly performed by intensivists. Consequently, the number of patients with a tracheostomy cannula in the ICU is increasing. Following clinical stabilisation, these patients are transferred to inpatient wards throughout the hospital according to their underlying pathology. However, nurses working on these wards encounter tracheostomy-related care less frequently, which may include suctioning, wound care, cannula care, and decannulation. Despite the availability of clinical procedures and protocols, a lack of knowledge, skills, and confidence in providing safe tracheostomy-related care persists. This increases the risk of complications such as cannula obstruction, infection, hypoxaemia, dislodgement, and bleeding. To address this issue, specialised multidisciplinary tracheostomy teams are increasingly being implemented. The aim of this retrospective study is to answer the following research question: What is the impact of a specialised multidisciplinary tracheostomy team on clinical outcomes in hospitalised patients with a tracheostomy cannula?

Interventions

OTHERThe implementation of the specialised multidisciplinary tracheostomy team.

The intervention of interest is the implementation of the specialised multidisciplinary tracheostomy team, which provides structured, team-based care for patients with a tracheostomy cannula.

Sponsors

Vitaz
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Hospitalisation between 2010 and 2026 in VITAZ (general hospital, Belgium) * Age ≥18 years. * Presence of a tracheostomy cannula (tracheotomy, permanent tracheostomy, or laryngectomy). * Curative and palliative patients will be included.

Exclusion criteria

* Ambulatory care * Day hospitalisation

Design outcomes

Primary

MeasureTime frameDescription
Tracheo(s)tomy-related ICU readmissionthrough study completion, an average of 1 yearOccurrence of readmission to the intensive care unit due to tracheo(s)tomy cannula-related problems.
Successful decannulationthrough study completion, an average of 1 yearSuccessful decannulation of the tracheo(s)tomy cannula according to predefined criteria derived from the literature. The proportion of patients achieving successful decannulation will be compared between the pre-intervention and post-intervention cohorts.
Tracheo(s)tomy-related complicationsthrough study completion, an average of 1 yearOccurrence of predefined canulla-related complications, including airway obstruction, wound infection, bleeding, ... .
Performance of FEESthrough study completion, an average of 1 yearPerformance of a fibreoptic endoscopic evaluation of swallowing (FEES) during hospitalisation.

Secondary

MeasureTime frameDescription
Total hospital length of staythrough study completion, an average of 1 yearFrom hospital admission until hospital discharge
Use of high-flow oxygen therapy or active humidificationthrough study completion, an average of 1 yearUse of high-flow oxygen therapy and/or active humidification during hospitalisation.
Time to tracheo(s)tomythrough study completion, an average of 1 yearNumber of days from hospital admission to the performance of the tracheo(s)tomy.
Time from ICU admission to transfer to an inpatient wardthrough study completion, an average of 1 yearDuration of intensive care unit stay before transfer to an inpatient ward.
Length of ICU stay following canulla-related readmissionthrough study completion, an average of 1 yearDuration of intensive care unit stay following readmission due to cannula-related problems.
Mortality due to cannulla-related complicationsthrough study completion, an average of 1 yearOccurrence of death attributable to tracheo(s)tomy- or cannula-related complications.
Use of a speaking valvethrough study completion, an average of 1 yearOccurrence and use of a speaking valve during hospitalisation.
Responsible medical disciplinethrough study completion, an average of 1 yearLocation and discipline responsible for tracheostomy placement.

Countries

Belgium

Contacts

CONTACTLisa Christiaens, MSc
brecht.serraes@vitaz.be+3237606060

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026