- Study Design and Setting
This retrospective cross-sectional study analyzed the medical records of patients presenting to the emergency department (ED) with vertigo who underwent non-contrast brain computed tomography (CT) scans. The study was conducted at the emergency department of King Abdulaziz Medical City in Riyadh from January 1, 2021, to October 27, 2024. All eligible patients who met the inclusion criteria during this period were identified systematically through a review of electronic health records.
- Study Population
Patients were included if they were aged 18 years or older, presented to the ED with a chief complaint of vertigo or spinning motion sensation, had a Glasgow Coma Scale score of 15, showed no neurological deficits on neurological examination, and underwent non-contrast brain CT scanning as part of their clinical evaluation. Patients were excluded if they had positive neurological deficits on examination, alcohol intoxication at presentation, patients who were involved in head or neck trauma prior to their vertigo complaint, pregnancy, known peripheral causes of vertigo such as vestibular disorders, or incomplete medical records with missing essential data.
- Data Collection
Medical records were systematically reviewed to extract demographic, clinical, and radiological data from electronic health records, emergency department documentation, radiology reports, and nursing documentation. Demographic variables included age, recorded as both continuous and categorical data, with groups defined as follows: 18-30, 31-40, 41-50, 51-60, and greater than 60 years. Additionally, gender was classified as male or female. Clinical variables encompassed a medical history review for the presence of hypertension, diabetes mellitus, dyslipidemia, ischemic heart disease, cerebrovascular accident, malignancy, hypothyroidism, sickle cell disease, and other significant medical conditions. A composite variable termed "any comorbid condition" was created and defined as the presence of one or more of the conditions.
- Outcome Definition
Non-contrast brain CT scan results were classified into two primary categories based on radiological interpretation. Unremarkable scans were defined as those showing no acute pathological findings, while positive findings included the presence of acute pathology such as acute infarction, intracranial hemorrhage, space-occupying lesions, or features suggestive of increased intracranial pressure. Board-certified radiologists performed all CT interpretations as part of routine clinical care, and classifications were verified through a systematic review of the official radiology reports.
- Statistical Analysis
Continuous variables were assessed for normality using appropriate statistical tests and visual inspection of data distributions. Normally distributed continuous variables are presented as the mean plus or minus the standard deviation, while non-normally distributed variables are reported as the median with the interquartile range. Categorical variables are presented as frequencies and percentages. Demographic and clinical characteristics were summarized using standardized descriptive statistics appropriate for medical research publications.
Bivariate associations between categorical variables and CT scan results were assessed using chi-square tests for independence when all expected cell counts were five or greater and Fisher's exact tests when any expected cell count was less than five. Statistical significance was defined as a p-value less than 0.05 for all analyses. Variables demonstrating statistical significance or clinical relevance in bivariate analysis were considered for inclusion in multivariable modeling.
A multivariable logistic regression model was constructed to identify independent predictors of positive CT scan findings. Variables included in the final model were selected based on clinical relevance, statistical significance in bivariate analysis with a threshold of p < 0.20, and the absence of multicollinearity, as assessed by variance inflation factors of less than 10. The final model included age group (with 18-30 years as the reference category), gender (with female as the reference category), and any comorbid condition (with no comorbidities as the reference category). Results are presented as odds ratios with 95% confidence intervals.
- Model Performance and Validation
Model performance was evaluated using multiple metrics, including the Akaike Information Criterion for model comparison, pseudo-R-squared values to assess explained variance, and receiver operating characteristic curve analysis with calculation of the area under the curve. Model assumptions were verified through examination of residual plots and assessment of influential observations. The goodness of fit was evaluated using appropriate statistical tests.
- Data Management and Quality Assurance
Comprehensive data cleaning procedures were implemented to ensure the quality and accuracy of the data. This included identification and removal of duplicate records, validation of age entries through extraction of numeric values from mixed text and numeric fields, standardization of gender categories, and verification of CT result classifications through double-checking of radiology reports. Missing data were handled using complete case analysis, with patients having missing essential variables, including age, gender, or CT results, excluded from the final analysis dataset.
- Ethical Considerations
This study was conducted in accordance with the principles outlined in the Declaration of Helsinki and all applicable regulatory requirements. Institutional Review Board approval was obtained from King Abdullah International Medical Research Center (KAIMRC) under Protocol Number [NRR24/058/8]. All patient data were de-identified prior to analysis to ensure privacy protection and confidentiality. Given the retrospective nature of the study, the requirement for informed consent was waived by the IRB.
- Sample Size and Statistical Power
No formal sample size calculation was performed as this represented a comprehensive retrospective analysis of all eligible patients during the specified study period. Post-hoc power analysis indicated adequate statistical power exceeding 80% to detect clinically meaningful associations given the observed effect sizes and final sample size.