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CompletedNCT06411496Updated May 13, 2024

Creation, Implementation and Validation of Intra- and Postoperative Risk Prediction Models

An observational study in Postoperative Complications and Risk Factors, sponsored by Hospital Galdakao-Usansolo. Completed at 1 site in Spain. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-05-13.

Sponsored by Hospital Galdakao-Usansolo · Observational

Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
112,745
Ages
18 Years and older
Sex
All
01

Study summary

This project aims to create and validate surgical risk prediction models for the prediction of complications in patients pending surgery during the operation, in the immediate postoperative period and up to one month after discharge.

At present there is no risk assessment system in place, except for the ASA scale which is mainly based on the subjective impression of the facultative, who assesses it in the universal preoperative consultations that we have planned in the system. In this project we intend to provide robust models, based on the analysis of data from patients in 4/5 Basque hospitals, i.e. generated in our population.

Read the detailed description

A three-phase study has been designed:

  1. st phase: Derivation and internal validation of the predictive model by means of a reprospective cohort study in which patients operated on at the Galdakao-Usansolo Hospital (HGU), Urduliz Hospital (HU), Basurto University Hospital (HUB), Donostia University Hospital (HUD) and Araba University Hospital (HUA) will be recruited. Hospital universitario de Donostia (HUD) and Hospital universitario de Araba (HUA) over XXX years and data will be obtained from the preoperative period until the month of discharge from the operation. For the identification and creation of these models, machine learning techniques will be used with the main purpose of identifying variables not described in the literature. Machine learning is the most important branch of Artificial Intelligence. Within Machine Learning, supervised learning is the most widely used area. Supervised learning allows computers to learn to perform tasks by discovering and exploiting complex patterns in large amounts of data. In the specific case of data from electronic medical records, Machine Learning algorithms allow us to use the historical data of each patient so that the computer learns to anticipate future events in a personalised way.
  2. nd phase: External validation of the models created in the first phase in a cohort of patients operated on in 2020 in the same centres. The methodology proposed by Debray et al. will be applied.
  3. rd phase: Evaluation of results after the implementation of the models in the EHR of the Galdakao-Usansolo Hospital in the form of an 'Action Guide'. Based on the risk stratification carried out in the previous phases, the anaesthesia department will create recommendations for action according to the level of risk. The percentages of mortality and intra- and postoperative complications will be compared by means of a quasi-experimental intervention study, comparing the results of the HGU hospital where the risk scale and the consequent recommendations will be implemented, before and after its implementation, and also comparing them with the percentages of patients who become complicated and/or die in HU, HUB, HUD and HUA, where the usual clinical practice will be followed, based on the ASA scale. This prospective cohort, once the risk scale has been implemented, will also be used for external validation (2020-2021).

Socio-demographic and clinical variables (main diagnosis, comorbidities, treatments, previous interventions, intraoperative data, post-operative data, procedures performed during hospitalisation, and complications up to one month after hospital discharge) and laboratory parameters will be collected.

This information will be extracted from osabide\'s global data exploitation system, Oracle Business Intelligence, and the laboratory data will be extracted from the information systems of the clinical laboratories of the centres involved.

02

Conditions studied

  • Postoperative Complications
  • Risk Factors
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Surgical patients at Galdakao-Usansolo Hospital between 2019 and 2022. We used anonymized patient level data from patients in waiting list to be intervened in four public hospitals in Basque Country. Participating hospitals serve a population of approximately 1.2 million and provide tertiary referral services to the surrounding region.

Inclusion criteria

  • Patients over 18 years of age pending scheduled or urgent surgery in non-cardiac surgery.

Exclusion criteria

Exclusion Criteria:

  • Surgery performed under local anaesthesia
  • Paediatric Surgery
  • Obstetric Patient
  • Cardiac Surgery
04

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
112,745 participants (actual)
Patient registry
No

Groups and cohorts

  • Scheduled or urgent surgery

    This is a retrospective cohort study recruiting surgical patients at Galdakao-Usansolo Hospital between 2019 and 2022. We used anonymized patient level data from patients in waiting list to be intervened in four public hospitals in Basque Country.

05

What researchers measure

Primary outcomes

  1. Death intraoperatively and up to one month after surgery

    yes/not

    Time frame: One-month

Secondary outcomes

  1. Intensive care unit admission

    yes/not

    Time frame: One month

  2. intra-operative complications

    Categorical variable

    Time frame: Complications during the intervention

  3. readmission

    yes /not

    Time frame: One month

06

Study locations

1 site
  • Hospital Galdakao Usansolo
    Galdakao, Bizkaia 48960, Spain
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06411496
Lead sponsor
Hospital Galdakao-Usansolo
Responsible party
Susana García Gutiérrez (Colaborator, Hospital Galdakao-Usansolo) — Principal investigator
First posted
May 13, 2024
Start date
Jun 1, 2018
Primary completion
Jan 1, 2019
Completion
Jun 1, 2023
Last update
May 13, 2024

Study contacts

Francisco Mendoza, MD
principal investigator · Galdakao-Usansolo Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2024. You cannot join it, but the record below documents what was studied.

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