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DOI 10.1186/s13023-021-01792-7

Медицинская библиотека · Orphanet journal of rare diseases · 2021

Obstructive sleep apnea in Norwegian adults with achondroplasia: a population-based study.

Fredwall Svein O, Øverland Britt, Berdal Hanne, Berg Søren, Weedon-Fekjær Harald, Lidal Ingeborg B, Savarirayan Ravi, Månum Grethe

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Previous studies have found a high prevalence of obstructive sleep apnea (OSA) in children with achondroplasia, but clinical studies on this complication in adults with achondroplasia are lacking.

OBJECTIVES

This population-based, cross-sectional study investigated the prevalence, severity, and predictive factors of OSA in Norwegian adults with achondroplasia.

METHODS

We collected clinical data on 49 participants. Participants without a preexisting diagnosis of OSA had an overnight sleep registration. OSA was defined as an apnea-hypopnea index (AHI) ≥ 5 plus characteristic clinical symptoms, or AHI ≥ 15. We used the Berlin Questionnaire to assess clinical symptoms of OSA.

RESULTS

OSA was found in 59% (29/49) of the participants (95% confidence interval 44 to 73%), of whom 59% (17/29) had moderate to severe OSA (AHI ≥ 15), and 48% (14/29) were previously undiagnosed. Variables predictive of OSA were: excessive daytime sleepiness; unrested sleep; loud snoring; observed nocturnal breathing stops; hypertension; age > 40 years; and BMI > 30 kg/m2.

CONCLUSION

OSA was highly prevalent in Norwegian adults with achondroplasia, which we believe is representative of this population worldwide. Follow-up of adults with achondroplasia should include assessment of symptoms and signs of OSA, with a low threshold for conducting an overnight sleep registration if findings suggestive of OSA are present.

Для цитирования: Fredwall Svein O, Øverland Britt, Berdal Hanne, Berg Søren, Weedon-Fekjær Harald, Lidal Ingeborg B, Savarirayan Ravi, Månum Grethe. Obstructive sleep apnea in Norwegian adults with achondroplasia: a population-based study.. Orphanet journal of rare diseases. 2021. DOI: 10.1186/s13023-021-01792-7.

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