Assessing Intensive Care Unit (ICU) Indications: Human vs. ChatGPT-4o Predictions (ICU)

April 13, 2026 updated by: Aycan KURTARANGİL DOĞAN, Bursa Yuksek Ihtisas Training and Research Hospital

Evaluation of the Accuracy of Intensive Care Unit (ICU) Admission Indications in Emergency Department Patients: A Comparison Between Clinical Decisions and ChatGPT-4o Prediction

This retrospective study evaluates the accuracy of ICU admission indications by comparing clinical decisions with predictions from ChatGPT-4. Patient data, including demographics, vital signs, laboratory results, imaging findings, and clinical decisions, will be retrospectively collected and documented systematically using Case Report Forms. The model will be trained using ICU admission guidelines and tasked to predict ICU needs based on collected patient data. This study aims to systematically assess the alignment between AI-based predictions and clinical decisions for ICU admissions.

Study Overview

Detailed Description

This study has a retrospective design. The medical data of patients admitted to the emergency department and consulted to the anesthesiology and reanimation clinic for ICU indications will be collected retrospectively. Demographic information, vital signs, laboratory results, imaging findings, and clinical decisions of the patients will be recorded. These data will be systematically collected for each patient using an individual Case Report Form.

Inclusion Criteria for the Study:

Patients aged 18 years and older who were consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department will be included in the study.

Exclusion Criteria for the Study:

Patients consulted to the anesthesiology and reanimation clinic for ICU indications from inpatient services.

Patients consulted to the anesthesiology and reanimation clinic from the emergency department for reasons other than ICU indications.

Patients consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department but with insufficient recorded data (patients with data loss).

Model Training and Prediction Analysis:

ChatGPT-4 will be trained according to the guidelines in "Yoğun Bakım Hasta Kabul Kriterleri (Rehberleri)" by Çiftçi B, Erdoğan C, and Demiraran Y (5). The collected patient data will be presented to the ChatGPT-4 model to obtain predictions regarding whether the patients require ICU admission. The predictions made by ChatGPT will be compared with clinical decisions, and accuracy rate, false positive rate, and false negative rate will be analyzed.

Statistical Analysis Methods to Be Used in the Study:

Accuracy Rate: The rate at which ChatGPT correctly predicts ICU indications will be calculated.

False Positive Rate: The rate at which ChatGPT predicts ICU need for patients who do not require ICU admission will be evaluated.

False Negative Rate: The rate at which ChatGPT predicts no ICU need for patients who require ICU admission will be analyzed.

Kappa Statistics: The agreement between ChatGPT predictions and clinical decisions will be measured.

ROC Curve and AUC: The performance of ChatGPT will be evaluated using the ROC curve and AUC.

The Case Report Form used for each patient ensures detailed and systematic data collection of clinical information, aiming to meaningfully compare the alignment of ChatGPT's predictions with clinical decisions.

Study Type

Observational

Enrollment (Actual)

624

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bursa, Turkey (Türkiye)
        • Bursa Yuksek Ihtisas Training and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

500

Description

Inclusion Criteria:

  • Patients aged 18 years and older who are consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department will be included in the study.

Exclusion Criteria:

  • Patients consulted to the anesthesiology and reanimation clinic for ICU indications from inpatient services.
  • Patients consulted to the anesthesiology and reanimation clinic from the emergency department for reasons other than ICU indications.
  • Patients consulted to the anesthesiology and reanimation clinic for ICU indications from the emergency department but with insufficient recorded data (patients with data loss)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Accuracy rate of ChatGPT-4 in predicting ICU indications
Time Frame: 3 month
3 month
False positive rate
Time Frame: 3 month
3 month
False negative rate
Time Frame: 3 month
3 month

Secondary Outcome Measures

Outcome Measure
Time Frame
Kappa statistic
Time Frame: 3 month
3 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: İlkay Ceylan, ceylanilkay@yahoo.com

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2024

Primary Completion (Actual)

November 30, 2024

Study Completion (Actual)

February 28, 2025

Study Registration Dates

First Submitted

December 6, 2024

First Submitted That Met QC Criteria

December 6, 2024

First Posted (Actual)

December 10, 2024

Study Record Updates

Last Update Posted (Actual)

April 14, 2026

Last Update Submitted That Met QC Criteria

April 13, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • BYIEAH-INKA

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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