2013
DOI: 10.1002/ppul.22867
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Obstructive sleep apnea in infancy: A 7‐year experience at a pediatric sleep center

Abstract: The etiologies of OSA in infants are different when compared to older children. PSG is feasible and a valuable tool in the diagnosis of OSA in infants and may help determine timely and appropriate evaluation and interventions. Clinical improvement in symptoms and resolution of PSG parameters were noted following medical and/or surgical interventions. Prospective studies need to be done to ascertain the long-term outcome of infants diagnosed with OSA to assess the benefits of early intervention on their neuroco… Show more

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Cited by 40 publications
(38 citation statements)
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“…In a 2014 report, Ramgopal et al 5 found that craniofacial abnormalities were a risk factor for OSA during infancy. They also found that craniofacial abnormalities was indication for PSG in 16% of their cohort, which is within range of our 2012 findings.…”
Section: Discussionmentioning
confidence: 99%
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“…In a 2014 report, Ramgopal et al 5 found that craniofacial abnormalities were a risk factor for OSA during infancy. They also found that craniofacial abnormalities was indication for PSG in 16% of their cohort, which is within range of our 2012 findings.…”
Section: Discussionmentioning
confidence: 99%
“…4 For otherwise healthy children with suspected OSA, performing outpatient PSG is considered a reasonable option for work-up; however, many children with significant medical comorbidities may undergo inpatient PSG within the first year of life. Over the past 10 years, multiple authors have reported an association between OSA and conditions such as laryngomalacia [5][6][7] and craniofacial anomalies. 5,8,9 Given that these conditions are commonly diagnosed in early infancy, one would expect that children with laryngomalacia or craniofacial anomalies and signs of sleep disordered breathing (SDB) would be more likely to undergo inpatient PSG than older, otherwise healthy children.…”
Section: Introductionmentioning
confidence: 99%
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“…Çocuklarda da oranı bilinmemekle birlikte yine erkek çocuklarda daha sık olmak üzere genel görülme sıklığı yaklaşık %1 olarak tahmin edilmektedir (6,7). Genel görülme sıklığı yüksek olmamakla birlikte, eşlik eden diğer bazı hastalıklardan, örneğin genetik bozukluklar, reflü, laringomalazi ve kraniyofasiyal anomali varlığında görülme sıklığı %35 gibi oldukça yüksek olabilmektedir (8).…”
Section: Epidemiyolojiunclassified
“…5 Bazı genetik bozuklukların varlığı, obezite ve kısa ve kalın boyun, retrognati, mikrognati, makroglossi, hipertrofik tonsil ve adenoidler, büyük uzun yumuşak damak gibi kraniyofasiyal anomaliler hastalıkla ilişkili predispozan faktörler olarak gös-terilmektedir. 6 Klinik semptomlar arasında ise tanıklı apne, huzursuz uyku, uyku sırasında çok hareket etme belirtilmektedir. Ancak çocukların uyku sırasında boğuluyormuş gibi hissetmeleri ve nefes alamadıklarını tarif etmeleri daha nadir karşılaşılan bir durumdur.…”
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