The difference between intervention and control period will be calculated. Treatment at the GPC means having a record at the GPC.
| Group | Value | 95% CI |
|---|---|---|
| Triage With Referral to Primary Care | 599 | |
| Triage Without Referral to Primary Care | 0 |
Last reviewed · How we verify
Triaging and Referring in Adjacent General and Emergency Departments
NA trial testing Triage with referral to primary care in Triage in 8,158 participants. Completed in 31 December 2019.
| Lead sponsor | Universiteit Antwerpen |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | health services research |
| Enrollment | 8,158 |
| Start date | 4 January 2019 |
| Primary completion | 31 December 2019 |
| Estimated completion | 31 December 2019 |
| Sites | 2 locations across Belgium |
Universiteit Antwerpen — full company profile →
Eligibility, any sex, with Triage. Patients with the condition only — healthy volunteers not accepted.
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
The difference between intervention and control period will be calculated. Treatment at the GPC means having a record at the GPC.
| Group | Value | 95% CI |
|---|---|---|
| Triage With Referral to Primary Care | 599 | |
| Triage Without Referral to Primary Care | 0 |
Time frame: For the individual patient: only during their stay at the emergency department or general practice cooperative.. Reporting threshold: 5%. Adverse-event reports describe events observed during the trial — not all are caused by the drug.
| Reaction | System | Triage With Referral to Pr… | Triage Without Referral to… |
|---|---|---|---|
| Ruptured Abdominal Aortic Artery | Blood and lymphatic system disorders | — | — |
Most-reported serious reactions: Ruptured Abdominal Aortic Artery.
Data from ClinicalTrials.gov NCT03793972 adverse events section.
Introduction: Patients who might also go to the general practitioner (GP) frequently consult emergency departments (ED). This leads to additional costs for both government and patient and a high workload for emergency physicians in Flanders. The Belgian government wants to address this problem by improved collaboration between EDs and general practice cooperatives (GPCs). Intervention: Patients presenting at the ED during out-of-hours (OOH) will be triaged and allocated to the most appropriate service. For this purpose the Manchester Triage System (MTS) which is commonly used in Flemish hospitals, will be extended (eMTS). By doing so a trained nurse will be able to diverge suitable patients towards the GPC. Methodology: The investigators will conduct a cluster randomised controlled trial in which eligible ED patients will be diverged to the GPC using the eMTS. The investigators will collect data using the iCAREdata database. The investigators will study the use of the eMTS, the effectiveness and effects of triage, work load changes, epidemiology at both departments, patient safety, health insurance (HIS) and patient expenditures. Furthermore, facilitators and barriers will be studied and an incident analysis of problem cases will be performed. Outcome: The primary outcome is the proportion of patients who enter the ED and are handled by the GP after triage. Secondary outcome measurements are related to safety: referral rate to the ED by the GP, proportion of patients not following the triage advice and file review for selected patients.
5 peer-reviewed publications reference this trial (live from Europe PMC):
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