This study aimed to determine clinical obesity diagnosis(1) and Edmonton Obesity Staging System for Paediatrics (EOSS_P)(2) severity in treatment-seeking adolescents with obesity.
A cross-sectional secondary analysis was conducted using baseline data from the ‘Fast Track to Health’ study (2018-2023), which recruited 141 adolescents (13-17years) with obesity and ≥1 cardiometabolic complication from two paediatric hospitals in Sydney and Melbourne. Comprehensive clinical assessments including anthropometry, blood tests, psychosocial questionnaires and paediatrician reviews were used to classify participants according to diagnostic (Lancet) and staging criteria (EOSS_P Stage 0 to 3). Descriptive statistics determined obesity severity and Chi-square tests examined subgroup differences by sex, study site and completion status.
Most participants met the Lancet Commission diagnostic criteria for clinical obesity (n=97, 68.8%) followed by pre-clinical obesity (n=42, 29.8%), and no obesity (n=2, 1.4%). Significant differences were observed by sex, with males more likely to present with clinical obesity (p=0.021). There were no differences by site or completion status. EOSS-P showed most participants were classified as Stage 2 (n=67, 47.5%) or 3 (n=43, 30.5%), indicating the presence of clinically significant health complications. Mental health (Stage 2, n=71, 50.4%) and social domains (Stage 3, n=33, 23.4%) mostly contributed to higher staging. Subgroup differences by sex demonstrated females more likely to be Stage 1 (p=0.011) in metabolic domain. In the mental domain, Pearson’s Chi-square was not statistically significant (p=0.52), suggesting no association, however the Likelihood Ratio was significant (p=0.05), indicating a potential association with females more likely to be Stage 2.
The Lancet Commission and EOSS-P frameworks provide clinical insight beyond BMI alone. All participants had cardiometabolic complications associated with weight, yet some did not meet the diagnostic criteria for clinical obesity. There may be unintended bias with females less likely to meet Lancet diagnostic criteria despite no differences in overall severity according to EOSS-P.