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XGBoost for Predict Incisional Hernia

Development and Internal Validation of a Machine Learning Model to Predict the Occurrence of Incisional Hernia After a Midline Laparotomy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05718999
Acronym
XGB&IncHern
Enrollment
1000
Registered
2023-02-08
Start date
2023-01-30
Completion date
2023-11-30
Last updated
2023-02-27

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

Conditions

Incisional Hernia

Brief summary

The objective of this study is to develop a predictive model of IH based on machine learning with the use of the XGBoost technique, this will help surgeons in charge of abdominal wall closure to have objective support to determine high-risk patients and in them modify the closure technique or use a mesh according to their choice or the degree of contamination of the abdominal cavity.

Detailed description

Retrospective and observational study. The predictions will make using machine learning models. The programs use the scikit-learn, xgboost and catboost Python packages for modeling. The evaluation of models will be using fourfold cross-validation, the receiver operating characteristic (ROC) curve, the area under the ROC curve (AUC), and accuracy metrics calculated on the union of the test sets of the cross-validation. The most critical factors and their contribution to the prediction will identify using a modern tool of explainable artificial intelligence called SHapley Additive exPlanations (SHAP).

Interventions

DIAGNOSTIC_TESTNot intervention

Not having intervention is an observational study

Sponsors

Hospital Regional de Alta Especialidad del Bajio
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* Patients older than 18 years of age * Postoperative midline exploratory laparotomy, who underwent urgent or scheduled surgery, regardless of their underlying diagnosis, * included between January 2010 and December 2016 and who completed 24 months of follow-up after surgery initial surgery.

Exclusion criteria

* Reoperated for any cuestion diferent to present of hernia * Management of open abdomen

Design outcomes

Primary

MeasureTime frameDescription
Incisional Hernia24 monthsincidence of Incisional hernia (the incisional hernia was defined according to the EHS guidelines as: a mass in the abdominal wall with or without visceral outlet or palpable in the surgical site determined by clinical examination or tomography).

Secondary

MeasureTime frameDescription
Facial dehiscence30 daysIncidence of fascial dehiscence (the fascial dehiscence is the presentation of separation of fascie with leakage of contents from the abdominal cavity

Countries

Mexico

Contacts

Primary ContactEdgard Efren Lozada Hernández, Dr
edgardlozada@hotmail.com+524772745801

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026