Design and Validation of a Preoperative Calculator for "Textbook Outcome" After Bariatric Surgery (BARCINO)

Sponsor
Hospital Universitari de Bellvitge (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT06044116
Collaborator
(none)
6,000
1
36
166.6

Study Details

Study Description

Brief Summary

The present study aims to design, develop and validate a preoperative calculator for "Textbook Outcome" after bariatric surgery, in orther to calculate the possibility of not achieving "Textbook outcome" based on the characteristics of the patient and the proposed surgical technique.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Morbid obesity is considered the great epidemic of our century. It is regarded as the first non-traumatic cause of death in the western population and it is also progressively beginning to affect developing countries. The latest epidemiological studies estimate that in Spain more than 15% of the population has overweight and about 5% has morbid obesity.

    Obesity treatment is multidisciplinary, from lifestyle and dietary changes to surgery. Amongst the different available treatments, bariatric surgery is the only cost-effective in patients with morbid obesity. Bariatric surgery provides better results compared to both pharmacological treatments (which are less available and less effective) and lifestyle changes. Furthermore, as well as weight loss, it guarantees a better control of comorbidities, reducing the risk of cardiovascular disease, morbidity and mortality, improving quality of life. There are several currently standardized bariatric surgical techniques. These techniques can be restrictive (such as sleeve gastrectomy or SG), hypoabsorptive (such as duodenal switch or DS and single anastomosis duodeno-ileal bypass with sleeve gastrectomy or SADI-S) or mixed (such as gastric bypass or GBP). The indication will depend on factors such as the patient's BMI, their metabolic comorbidities or the experience of the surgical team, among others. All of them have been shown to be safe in experienced teams, with rates of mortality equal to or less than 0.5% and morbidity less than 10%.

    However, although postoperative risks are low, they have to be taken into account in each case individually, along with the potential benefits of surgery as accurately as possible, so the decision whether or not to perform surgical procedure in a consensual manner with the patient can be based on objective data.

    Recently, a new concept of measuring postoperative results called "Textbook outcome" (TO) has been introduced. It is a multidimensional measure that is obtained from the sum of several traditional surgical measures: the absence of postoperative complications, no prolongation of hospital stay, no mortality, and no readmissions. The TO reflects what is considered the "ideal" postoperative evolution. In bariatric surgery, TO has been defined as hospital stay equal to or less than 2 days, absence of complications in the first 30 days after surgery, no readmission once discharged in the first 30 days after surgery, and no mortality during the stay hospitalization or during the first 30 days after surgery. Additionally, an ordered TO has been created, ordering these quality indicators from worst to best: mortality, severe complications, readmission, mild complications and prolonged hospitalization stay. The fact of ordering the results with this ordered TO allows to find different combinations of these five indicators in the same patient. It does not happen if, as previously, the combination of all the results of the different parameters generate a binomial result. The ordered TO also has the advantage that allows to identify in the results some individual differences for each hospital, thus making it possible to detect variations between hospitals that can help to improve the quality of surgery and of the hospital in particular, and therefore, improve the clinical result of bariatric surgery, which is not possible with the binomial result since it does not provide information to individual hospitals on which aspect is significantly worse than in the other hospitals. The order of parameters mentioned above was based on expert advice and evidence from the literature regarding what patients considered to be a quality improvement assistant care.

    Currently, there is not any tool that calculates preoperatively the risk of not presenting a TO in some of its degrees.

    The optimal values of the preoperative variables that allow patients to achieve TO have not been studied either. The aim of this study is to create a calculator that allows calculating the risk that each patient has of not achieving TO based on the patient's variables and the selected surgical technique. This tool could provide relevant information for the patient in the process of informed consent for the surgery, as well as assist in the choice of surgical technique in clinical practice in each specific case. The development of the calculator is intended to be done with the help of machine learning. The Machine learning statistics techniques are a branch of artificial intelligence that allow great flexibility to capture complex non-linear relationships especially when using large amounts of data. The situation where we find ourselves due to the rapid expansion of the COVID-19 pandemic has found doctors and the rest of health professionals unprottected to face with the difficulty of giving an adequate and rapid response to the patients.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    6000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Design and Validation of a Preoperative Calculator for "Textbook Outcome" After Bariatric Surgery: Project BARCINO (BARiatric Surgery Calculator Nomogram for Textbook Outcome)
    Actual Study Start Date :
    Jan 1, 2022
    Anticipated Primary Completion Date :
    Oct 1, 2023
    Anticipated Study Completion Date :
    Jan 1, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    Calculator design

    5.000 patients of the entire cohort of 6.000 patients will be used for the design of the risk calculator

    Internal validation

    1.000 patients of the entire cohort of 6.000 patients will be used for the design of the risk calculator

    External validation

    Another surgical group from outside Spain will be contacted for external validation

    Outcome Measures

    Primary Outcome Measures

    1. Textbook outcome [From surgery to 30 days after surgery or hospital discharge (if hospital discharge is longer than 30 days after surgery)]

      Perfect postoperative couse, defined as: Hospital stay nor more than 2 days, no complications during the first 30 days after surgery, no hospital readmision during the first 30 days after surgery AND no mortality during hospital stay and/or the first 30 days after surgery.

    Secondary Outcome Measures

    1. Severity of postoperative complications [From surgery to 30 days after surgery]

      Postoperative complications staged with the Clavien-Dindo score

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients who underwent bariatric surgery using laparoscopic SG, laparoscopic BPG, laparoscopic DS, laparoscopic SADI-S or revisional surgery, from 2015 to 2021 both included.
    Exclusion Criteria:
    • Patients who underwent bariatric surgery using another primary surgical technique that does not be laparoscopic SG, laparoscopic BPG, laparoscopic DS or laparoscopic SADI-S or patients who underwent bariatric surgery outside the established period (2015-2021).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital Universitari de Bellvitge L'Hospitalet De Llobregat Barcelona Spain 08907

    Sponsors and Collaborators

    • Hospital Universitari de Bellvitge

    Investigators

    • Principal Investigator: Javier Osorio, MD, PhD, Hospital Universitari de Bellvitge

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Javier Osorio, Javier Osorio, Chief of Bariatric and Metabolic surgical Unit, Hospital Universitari de Bellvitge, Hospital Universitari de Bellvitge
    ClinicalTrials.gov Identifier:
    NCT06044116
    Other Study ID Numbers:
    • HUB-INF-BARCINO
    First Posted:
    Sep 21, 2023
    Last Update Posted:
    Sep 21, 2023
    Last Verified:
    Sep 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Javier Osorio, Javier Osorio, Chief of Bariatric and Metabolic surgical Unit, Hospital Universitari de Bellvitge, Hospital Universitari de Bellvitge
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 21, 2023