TY - JOUR
T1 - Diagnostic meta-analysis of the Pediatric Sleep Questionnaire, OSA-18, and pulse oximetry in detecting pediatric obstructive sleep apnea syndrome
AU - Wu, Chia-Rung
AU - Tu, Yu-Kang
AU - Chuang, Li-Pang
AU - Gordon, Christopher
AU - Chen, Ning-Hung
AU - Chen, Pin-Yuan
AU - Hasan, Faizul
AU - Kurniasari, Maria D.
AU - Susanty, Sri
AU - Chiu, Hsiao-Yean
PY - 2020/12
Y1 - 2020/12
N2 - The aim of this meta-analysis was to compare the pooled sensitivity and specificity of the Pediatric Sleep Questionnaire (PSQ), Obstructive Sleep Apnea Questionnaire (OSA-18), and pulse oximetry (PO) according to OSAS severity. Three electronic databases were searched for studies evaluating sensitivity and specificity of the three tools against the apnea–hypopnea index measured using overnight in-laboratory or in–home polysomnography in children and adolescents from inception until January 11, 2020. A random-effects bivariate model was used to estimate the summary sensitivity and specificity of the tools. We identified 39 studies involving 6131 clinical and community children (aged 2.9–16.7 y). The PSQ exhibited the highest sensitivity (74%) for detecting symptoms of mild pediatric OSAS. The PSQ and PO had comparable sensitivity in screening moderate and severe pediatric OSAS (0.82 and 0.89 vs 0.83 and 0.83, respectively). PO yielded superior specificity in detecting mild, moderate, and severe pediatric OSAS (86%, 75%, and 83%, respectively) than did the PSQ and OSA-18 (all p < 0.05). Age, percentage of girls, index test criteria, methodology quality, and sample size significantly moderated sensitivity and specificity. For early detection of pediatric OSAS, the combined use of PSQ and PO is recommended when polysomnography is not available. PROSPERO Registration number: CRD42018090571.
AB - The aim of this meta-analysis was to compare the pooled sensitivity and specificity of the Pediatric Sleep Questionnaire (PSQ), Obstructive Sleep Apnea Questionnaire (OSA-18), and pulse oximetry (PO) according to OSAS severity. Three electronic databases were searched for studies evaluating sensitivity and specificity of the three tools against the apnea–hypopnea index measured using overnight in-laboratory or in–home polysomnography in children and adolescents from inception until January 11, 2020. A random-effects bivariate model was used to estimate the summary sensitivity and specificity of the tools. We identified 39 studies involving 6131 clinical and community children (aged 2.9–16.7 y). The PSQ exhibited the highest sensitivity (74%) for detecting symptoms of mild pediatric OSAS. The PSQ and PO had comparable sensitivity in screening moderate and severe pediatric OSAS (0.82 and 0.89 vs 0.83 and 0.83, respectively). PO yielded superior specificity in detecting mild, moderate, and severe pediatric OSAS (86%, 75%, and 83%, respectively) than did the PSQ and OSA-18 (all p < 0.05). Age, percentage of girls, index test criteria, methodology quality, and sample size significantly moderated sensitivity and specificity. For early detection of pediatric OSAS, the combined use of PSQ and PO is recommended when polysomnography is not available. PROSPERO Registration number: CRD42018090571.
KW - Diagnostic meta-analysis
KW - Obstructive sleep apnea syndrome
KW - Pediatric
UR - http://www.scopus.com/inward/record.url?scp=85088930898&partnerID=8YFLogxK
U2 - 10.1016/j.smrv.2020.101355
DO - 10.1016/j.smrv.2020.101355
M3 - Review article
C2 - 32750654
SN - 1087-0792
VL - 54
SP - 1
EP - 9
JO - Sleep Medicine Reviews
JF - Sleep Medicine Reviews
M1 - 101355
ER -