About this trial
A postoperative high-acuity model of care (ARRC) has been shown, in a prospective cohort study of approximately 850 patients, to produce a marked improvement in patient and hospital outcomes, and hospital costs, in medium risk patients (Ludbrook G et al., JAMA Surgery 2023).
The goal of this observational study is to examine the outcomes after non-cardiac surgery of a larger group of medium risk patients receiving different forms of care -ARRC and usual ward care. The main questions it aims to answer are:
what are the outcomes for patients and hospital after the different forms of care, who receives benefit from high acuity care, what underlies the improved outcomes seen with high acuity care.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Scheduled for elective or unplanned surgery
Scheduled to stay in hospital at least one night after surgery
30-day mortality of 0.5% to 8% by the US National Safety and Quality Improvement Program risk score (NSQIP)
Disqualifiers
Undergoing cardiac surgery
Scheduled for postoperative Intensive Care Unit management
Trial population
Patients undergoing surgery at Royal Adelaide Hospital
Trial design
Cohort
Prospective
Treatments tested in this trial
ARRC
Other interventionEligible for ARRC and managed in ARRC unit
Usual Care
Other interventionEligible for ARRC but managed elsewhere as no ARRC bed available
Treatment groups
Trial outcomes
Primary outcomes
Days at Home after surgery
number of days spent at usual place of residence within 90 days after surgery
Secondary outcomes
in-hospital complications
medical emergency response level complications
mortality
mortality out to 1 year after surgery
cost-effectiveness
cost per Day at Home improvement compared to usual care - Incremental cost-effectiveness ratio
Sponsors and contacts
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University of Adelaide
Lead sponsor
Royal Adelaide Hospital
Collaborator