PT - JOURNAL ARTICLE AU - Albert M Li AU - Hung K So AU - Chun T Au AU - Crover Ho AU - Joseph Lau AU - Siu K Ng AU - Victor J Abdullah AU - Tai F Fok AU - Yun K Wing TI - Epidemiology of obstructive sleep apnoea syndrome in Chinese children: a two-phase community study AID - 10.1136/thx.2010.134858 DP - 2010 Nov 01 TA - Thorax PG - 991--997 VI - 65 IP - 11 4099 - http://thorax.bmj.com/content/65/11/991.short 4100 - http://thorax.bmj.com/content/65/11/991.full SO - Thorax2010 Nov 01; 65 AB - Objective To determine the prevalence and risk factors of obstructive sleep apnoea syndrome (OSAS) in Chinese children using a two-phase community-based study design.Methods Children from 13 primary schools were randomly recruited. A validated OSAS screening questionnaire was completed by their parents. Children at high risk of OSAS and a randomly chosen low-risk group were invited to undergo overnight polysomnographic study and clinical examination. The the sex-specific prevalence rate was measured using different cutoffs (obstructive apnoea hypopnoea index ≥1, ≥1.5, ≥3 and ≥5 and obstructive apnoea index ≥5) and risk factors associated with OSAS were evaluated with logistic regression.Results 6447 completed questionnaires were returned (out of 9172 questionnaires; 70.3%). 586 children (9.1%; 405 boys and 181 girls) children belonged to the high-risk group. A total of 619 (410 and 209 from the high and low-risk group, respectively) subjects underwent overnight polysomnagraphy. Depending on the cutoffs, the prevalence rate of childhood OSAS varied from 4.8% to 40.3%. Using the International Criteria of Sleep Disorders version II, the OSAS prevalence for boys and girls was 5.8% and 3.8%, respectively. Male gender, body mass index z-score and increased adenoid and tonsil size were independently associated with OSAS.Conclusions The prevalence rate of OSAS in children was contingent on the cutoff used. The inclusion of symptoms as a part of the diagnostic criteria greatly reduced the prevalence. A further prospective and outcome study is needed to define a clinically significant diagnostic cutoff for childhood OSAS.