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Surgical Emergency Flows and Delays in Admission to the Operating Room

Flows of Emergency Surgery and Delay in Admission to the Operating Room: a Multicenter Prospective Observational Study in France

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04585529
Acronym
ACUTE-FLOW
Enrollment
1149
Registered
2020-10-14
Start date
2020-10-05
Completion date
2021-03-15
Last updated
2021-05-26

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

Conditions

Emergencies, Postoperative Complications, Surgery

Keywords

delay, organization

Brief summary

French hospitals treat non-elective surgery according to three organizational models: in a dedicated multi-specialty emergency operative room (OR), in a dedicated OR within a specialized surgical platform or in any available OR from a list of non-dedicated OR. Some triage algorithms for the classification of non-elective surgery have been described but are not routinely applied. The rate of delay in the management of non-elective surgery in France is not known. Reducing this delay decreased mortality and morbidity in urgent surgery (McIsaac D, et al., CMAJ 2017). Optimizing the flow of non-elective surgery represents a major challenge. The main objective of this study is to determine the rate of delay in admission to the OR in emergency surgery through a multicenter prospective observational study in France. All patients requiring urgent surgical management (\<72 hours) will be included. The ideal time for surgery was previously defined by surgeons according to the NEST classification (NEST 1: within minutes; NEST 2: \< 1 hour; NEST 3: \< 4 hours; NEST 4: \< 12 hours; NEST 5: \< 48 hours; NEST 6: \< 72 hours). For each patient, the ratio between the observed time (actual Time To Surgery \[aTTS\] ) and the ideal time (ideal Time To Surgery \[iTTS\]) will be determined. The delay is identified by aTTS/iTTS ratio \>1.

Interventions

None listed

Sponsors

Société Française d'Anesthésie et de Réanimation
CollaboratorOTHER
University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

any patient meeting the Following two criteria * at least 18 ys old * decision for unplanned surgery (which should be performed within 72 hours according to the protocol) * in one of the following hospitals: Lille University hospital, Grenoble University hospital, Strasbourg University hospital, Paris University hospitals (Européen Georges Pompidou, Beaujon, H. Mondor), Lyon University hospital (Hôpital E. Herriot, Lyon Sud), Angers University hospital, Anthony Private hospital).

Exclusion criteria

* obstetrics * interventional radiology * endoscopies

Design outcomes

Primary

MeasureTime frameDescription
Incidence of OR admission delay (delay = aTTS / iTTS > 1)30 dayshours

Secondary

MeasureTime frameDescription
OR Admission delay according to the period of work (day, night, and week-end)30 dayshours
OR Admission delay according to the NEST classification30 dayshours
delays related to organisational causes30 dayshours
delays related to material causes30 dayshours
OR Admission delay according to the three organizational model30 dayshours
Impact of the delay on ICU length of stay30 daysdays
Impact of the delay on hospital length of stay30 daysdays
Impact of the delay on mortality30 days
Impact of the delay on morbidity30 days
delays related to human causes30 dayshours

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026