2.1. Study design and population
This cross-sectional study was carried out in the Emergency Department of Tertiary Research Hospital, which has a high capacity, accepts both personal admission and ground and air ambulance patient transfers, and has many facilities for examinations and consultation to all surgical departments.
All patients aged 18 years and over who applied between July 20, 2023, at 8.00 am and July 21, 2023, at 8.00 am were consecutively included in the study. Patients under the age of 18 and those who did not accept the study were excluded. Accordingly, 745 patients were included in the study.
2.2. Establishment of Expert Committee:
An Expert Committee (EC) consisting of five volunteers from our fourth-year resident physicians was formed. This committee had a four-hour theoretical training with case examples on the ESI triage system on December 20, 2023. A single instructor completed the training program to ensure the standardization of the training content. Firstly, theoretical information about the introduction of ESI and the contents of the categories were explained and then the cases were discussed.
2.3. Ethical statements
This study was approved by the local ethics committee on July 12, 2023 (Decision No: E2-23-4509). Patients were recruited by the Declaration of Helsinki. Patients participating in the study were asked to read and approve the informed consent form of their own free will.
2.4. Data collection
Vital signs (blood pressure, oxygen saturation, pulse, and body temperature) of the patients who were admitted to the ED and accepted the study were recorded on the case form together with their age, gender, method of admission, chief complaint, state of consciousness, comorbidities (diabetes mellitus, hypertension, coronary artery disease, congestive heart failure, chronic kidney disease, cerebrovascular accident, liver failure).
Two monitors (GE Medical Systems, B40 Patient Monitor®, GE Medical Systems Information Technologies, Inc.) were used during the triage process. Blood pressure, pulse rate, and saturation values were measured and recorded automatically with this monitor. The Temporal thermometer (Mesilife, DT-8806 Non-Contact Forehead Infrared Thermometer) was used for body temperature measurement.
2.5. Scoring system
2.5.1. Emergency Severity Index
With ESI triage, patients who ‘have risk of wait’ and who 'require urgent intervention' are identified primarily. The triage category of other patients is then determined according to the estimated number of available resources. The ESI application uses four basic decision stages for this purpose. Four key questions exist when determining a patient's triage category [4].
1. Is the patient in a life-threatening case, or is the patient dying?
2. Is the patient unable to wait?
3. How many resources will the patient need to use during the diagnosis and treatment process?
4. What are the patient's vital signs?
Accordingly, patients are triaged by classifying them from the highest urgency category (one) to the lowest urgency category (five).
2.6. Triage category determination and patient grouping
The information recorded in the case form was organized as follows: "A 70-year-old male patient was admitted to the ED by Emergency Medical Service (EMS) ambulance with complaints of abdominal pain and constipation. It was learned that the patient's complaint of constipation had been going on for nine months, abdominal pain had been present for two days and there was no stool discharge for one day. The patient had a known history of malignancy and coronary angiography. The general condition of the patient was good, he was conscious, orientated, and co-operative. His blood pressure was 110/70 mmHg, pulse rate was 97 beats/min, oxygen saturation was 94% and body temperature was 36.3 °C. What is the patient's triage score according to ESI?". All 745 real-time cases were converted into text during November 2023.
The triage scores of all cases were evaluated independently and simultaneously by ChatGPT ver.4 (November 2023) in Turkish language, and the results were recorded.
The results obtained were analyzed both for the whole patient group and for individual ESI categories. Finally, ESI-1 and 2 categories were evaluated as high acuity groups; dichotomous data was created as "severe" and "mild," and subgroup analysis was performed.
2.7. Statistical analyses
The study's statistical analyses were performed with IBM SPSS Statistics for Windows, Version 20.0 (Armonk, NY: IBM Corp). Distribution analyses of continuous variables were performed by the Shapiro-Wilk Test, comparisons between two groups for normally distributed continuous variables were performed by the Independent Samples-t Test, and comparisons between two groups for non-normally distributed variables were performed by the Mann Whitney-U test. For comparisons of categorical data, Pearson Chi-Square and Fisher's Exact test were used according to the case.
The median value of the results of ESI, which is an ordinal parameter obtained by the evaluations of five members of the EC, was accepted as the gold standard. The agreement analysis of the EC and ChatGPT was evaluated with the Kappa statistic. For Kappa coefficients, <0.20 was considered poor, 0.21 to 0.40 reasonable, 0.41 to 0.60 moderate, 0.61 to 0.80 good, and 0.81 to 1.00 high concordance. As a result of this analysis, diagnostic accuracy statistics such as specificity and sensitivity were also given. This analysis was repeated for individual ESI categories. In addition, dichotomous data was created as "severe" and "mild" according to the high urgency group; like the general analysis, the power of ChatGPT to distinguish this group was also analyzed. The P < 0.05 level was used as the statistical significance criterion. All statistical analyses were completed in January 2024.