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Morbidity and Mortality: Surgery and Standardized Transmission in Operating Room

Morbidity and Mortality in Operating Room: Surgery and Standardized Communication

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05440331
Acronym
HIATUS
Enrollment
1120
Registered
2022-06-30
Start date
2023-09-08
Completion date
2026-10-31
Last updated
2025-11-19

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

Conditions

Major Surgery

Keywords

Major surgery, Morbility, Mortality, Training in peroperative, Handover, Anaesthetist, Nurse anaesthetist

Brief summary

The primary objective of the study is to evaluate the efficacy of standard handover with AnesList© between physician anesthesists in operating room, for a complete transmission for a patient, on the occurence of event as death, serious complications or rehospitalization in month of postoperative after major surgery.

Detailed description

The secondary objectives are: * to analysis the impact of the transmission on: 1. the occurence of different events: re-hospitalization, serious complications, death at one month; 2. the duration of initial ICU stay and of hospitalization; 3. the duration of the transmission; 4. the quality of the transmission by the physician leaving operating room. * to evaluate the condition of the transmission * to study the persistence of the use of the AnesList© at 6 months after the end of inclusions in the center * to evaluate the satisfaction on AnesList© and on the training with the tool and the obstacles of its utilization * to evaluate the morbility-mortality in the centers of the centers before, during and 6 months after the beginning of the study.

Interventions

OTHERTraining with AnesList©

Training with AnesList© as tool

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patient aged \> 18 years; * Patients with score ASA I-IV; * Requiring urgent or planned surgery; * Major surgery (duration of surgery \> 2 hours, requiring a hospital stay of at least 1 night): orthopedics, cardiac, vascular, thoracic, visceral, ENT, plastic surgery; * Handover between two anesthesists defined as a definitive relay between one physician anaesthesist and another in operating room; * Intensive care anesthesists and nurse anaesthetist working in investigator center during the study; * Affiliated to a social security system; * No-opposition to participating to the study.

Exclusion criteria

* Transmission between physician anaesthesist and nurse anaesthetist; * Medical transmission occurs out of anesthesia care out of operating room; * Medical transmission occurs in transitory manner (for example: coffee time, lunch time); * Patients enrolled in an another ongoing study of surgical intervention.

Design outcomes

Primary

MeasureTime frameDescription
The occurence of adverse eventsat 1 monthDeath, serious complications and re-hospitalization will be noted in order to evaluate the efficacy of standardized transmission with AnesList©.

Secondary

MeasureTime frameDescription
The duration of hospitalizationthrough study completion, an average of 18 monthsThe length of initial hospitalization will be noted.
Evaluate of the condition of transmissionthrough study completion, an average of 18 monthsBy the presence or intervention of anaesthetics-nurse, recorded or not the transmission in medical files.
Utilization of the AnesList© by anaesthesists at 6 monthsat 6 monthsOnly for intervention group: use on cell phone or with printed form: the use will be noted.
The duration of ICU staythrough study completion, an average of 18 monthsThe length of initial ICU stay will be noted.
Interaction with study nursethrough study completion, an average of 18 monthsThe study nurse will evaluate the existence and composite of the interaction between the anesthesist who receiving the transmission and the nurse.
Morbi-mortalitythrough study completion, an average of 18 monthsThe method of chronological series will be used to analysis the morbi-mortality in investigator center.
Quality of medical transmissionthrough study completion, an average of 18 monthsScale will be noted by anaesthesists between 0 and 22: 20% of recorded transmission will be noted.

Countries

France

Contacts

Primary ContactDominique FLETCHER, MD, PhD
dominique.fletcher@aphp.fr+33 (0)661177035
Backup ContactAicha KASSOUL, MD
aicha.kassoul@aphp.fr+ 33 (0)633855997

Outcome results

None listed

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