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DC Field | Value | Language |
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dc.contributor.author | Horne R.S.C. | en |
dc.contributor.author | Nixon G.M. | en |
dc.contributor.author | Ranasinha S. | en |
dc.contributor.author | Weichard A. | en |
dc.contributor.author | Davey M.J. | en |
dc.date.accessioned | 2021-05-14T14:28:07Z | en |
dc.date.available | 2021-05-14T14:28:07Z | en |
dc.date.copyright | 2014 | en |
dc.date.created | 20150112 | en |
dc.date.issued | 2015-02-02 | en |
dc.identifier.citation | Sleep and Biological Rhythms. Conference: 26th ASM of Australasian Sleep Association and Australasian Sleep Technologists Association: Sleep Frontiers, Sleep DownUnder 2014. Perth, WA Australia. Conference Publication: (var.pagings). 12 (SUPPL. 1) (pp 53), 2014. Date of Publication: October 2014. | en |
dc.identifier.issn | 1446-9235 | en |
dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/42180 | en |
dc.description.abstract | Introduction: Formally defining the presence of obstructive sleep apnoea (OSA) in a snoring child requires polysomnography (PSG), a test with limited availability. In this study we aimed to examine which combination of clinical factors, oximetry and actigraphy measures provide the most effective model for prediction of moderate-severe OSA (MS OSA) for possible use as a tool outside specialist centres. Method(s): Children referred for PSG for possible OSA were recruited prospectively and underwent clinical investigations including: OSA-18 questionnaire, physical examination, and home overnight oximetry (Masimo Radical 2-sec averaging time) with concurrent actigraphy. Variables assessed for inclusion in the predictive model were: age, gender, OSA-18 (total, sub-scale and individual question scores), BMI z-score, tonsil size, Mallampati score, Friedman pharyngeal score, Angle's dental malocclusion score, oximetry parameters (SpO2 nadir, dips below 90%/h, dips of 4%/h, pulse rate (PR) standard deviation and PR increases of 15 bpm/h), and movement fragmentation index from actigraphy. The primary outcome variable dichotomised the obstructive respiratory disturbance index from PSG into <5/h (primary snoring/ mild OSA) and >=5/h (MS OSA). Stepwise forward elimination logistic regression was used to define significant variables (p > 0.1) and a model was then developed to predict MS OSA. Result(s): 89 children (38F; mean +/- SD age 5.5 +/- 2.5 y) with full PSG results were included. 37 (42%) had MS OSA. OSA-18 Q16 (parent concerned child not getting enough air), dental malocclusion score, SpO2 nadir and PR increases of 15 bpm/h were identified as significant predictor variables and the model was developed on these parameters, dividing SpO2 nadir and PRI15 into tertiles and OSA-18 Q16 scores into two categories. ROC analysis gave an area under the curve of 0.88 using this model, indicating very good discrimination. 81% of children were correctly classified, with sensitivity 82%, specificity 81%, positive predictive value 77% and negative predictive value 85%. Conclusion(s): We have developed a clinical risk score for having moderate-severe OSA that has very good discrimination properties and correctly classifies 81% of children referred for PSG. | en |
dc.language | English | en |
dc.language | en | en |
dc.publisher | Blackwell Publishing | en |
dc.title | A prediction model for the presence of moderate/severe obstructive sleep apnoea in childhood based on clinical findings and oximetry. | en |
dc.type | Conference Abstract | en |
dc.identifier.affiliation | Paediatric - Respiratory and Sleep (Melbourne Children's Sleep Centre) | - |
dc.identifier.doi | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/sbr.12082 | en |
local.date.conferencestart | 2014-10-09 | en |
dc.identifier.source | 71748072 | en |
dc.identifier.institution | (Nixon, Weichard, Horne) Ritchie Centre, MIMR-PHI Institute of Medical Research, Melbourne, Australia (Ranasinha) School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia (Nixon, Davey) Melbourne Children's Sleep Centre, Monash Children's Hospital, Melbourne, Australia | en |
dc.description.address | G.M. Nixon, Ritchie Centre, MIMR-PHI Institute of Medical Research, Melbourne, Australia | en |
dc.description.publicationstatus | CONFERENCE ABSTRACT | en |
local.date.conferenceend | 2014-10-11 | en |
dc.rights.statement | Copyright 2015 Elsevier B.V., All rights reserved. | en |
dc.identifier.affiliationext | (Nixon, Weichard, Horne) Ritchie Centre, MIMR-PHI Institute of Medical Research, Melbourne, Australia | - |
dc.identifier.affiliationext | (Ranasinha) School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia | - |
dc.identifier.affiliationmh | (Nixon, Davey) Melbourne Children's Sleep Centre, Monash Children's Hospital, Melbourne, Australia | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
item.openairetype | Conference Abstract | - |
crisitem.author.dept | Paediatric - Respiratory and Sleep (Melbourne Children's Sleep Centre) | - |
Appears in Collections: | Conferences |
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