Post Oesophagectomy Outcomes in a Single Regional Centre in Australia
Condition(s) studied
Investigational drug(s) / intervention(s)
No Intervention: Observational Cohort: No intervention - retrospective observational study
Study summary
Literature review/rationale for project
* Oesophageal cancer is associated with a grim prognosis despite many advances in treatment. Oesophagectomy is a key component of the care of patients who are candidates for curative treatment, however it is associated with substantial morbidity.
* Several studies have suggested that oesophagectomies performed at higher volume tertiary centres are associated with lower morbidity and mortality than lower volume centres, and this has prompted changes to policy in countries such as Great Britain, Canada and the Netherlands with regards to the centralisation of these cases. A higher volume centre within Australia is likely to perform 6 or more procedures per year.
* Currently within Australia, centralisation on a large scale has not occurred. This has been limited in part by resource provision and geographical barriers. Therefore, oesophagectomies in Australia are still routinely performed in regional centres. However, there is a paucity of recent outcomes data from these centres.
Aims/objectives
* Retrospective review of oesophagectomies undertaken in a single regional centre in Tasmania, Australia over 10 years (January 2014 to December 2023)
* Assess outcomes (long and short-term complications and mortality) and compare to morbidity and mortality rates from larger international centres
Eligibility
Primary outcome measure(s)
- mortality — from date of surgery to end of study (November 2024) for a timeframe up to 10 years
date of death from any cause or date of palliation whichever came first - Anastomotic leak — from date of surgery to end of study period (Nov 2024), assessed up to 10 years
Grade 1-3, diagnosed radiologicaly, requiring intervention (surgical or non-surgical) - Length of stay — from date of surgery to discharge date of hospital admission, approximately 2-4 weeks in most cases but assessed up to 12 weeks
total inpatient hospital stay and total ICU length stay
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Launceston General Hospital | Launceston | Tasmania |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06662513 on ClinicalTrials.gov ↗ ← All trials in Australia