Publication:
Obstructive Sleep Apnea in patients with Cystic Fibrosis and non-Cystic Fibrosis Bronchiectasis and its relation with clinical parameters

Simple item page
dc.contributor.authorVEZİR, DUYGU
dc.contributor.authorKOCAKAYA, DERYA
dc.contributor.authorCEYHAN, BERRİN
dc.contributor.authorsVezir D., Balcan B., KOCAKAYA D., Cinar C., Olgun S., CEYHAN B.
dc.date.accessioned2023-06-21T08:25:09Z
dc.date.available2023-06-21T08:25:09Z
dc.date.issued2022-09-01
dc.description.abstractObjective: This study was designed to assess obstructive sleep apnea (OSA) in adult patients with cystic fibrosis (CF) and non-CF bronchiectasis (BE) and to relate it with clinical characters. Methods: 35 CF (27yrs) and 35 non-CF (24yrs) BE patients were included. Demographic characteristics, medications, comorbidities, BMI, dyspnea scales, pulmonary functions, sputum cultures, exacerbations, and hospitalizations were recorded. Epworth Sleepiness Scale (ESS) questionnaire was filled and polysomnography was performed for each patient. Results: ESS scores did not show any significant difference between CF and non-CF BE patients. 37 (53%) of all patients had OSA. There was no significant difference for OSA risk between CF and non-CF BE patients (54% vs 51%, respectively). Male gender was found to be a risk factor for OSA (68% of males vs 41% of females, respectively, p:0.026). Total sleep time, sleep efficiency, sleep latency, time spent awake after falling asleep, ODI, AHI, AHI in supine position and REM phase did not show any significant difference between CF and non-CF patients. CF patients had significantly lower mean oxygen saturation (p:0.001) and lowest oxygen saturation (p:0.0024) levels and higher heart rate (p:0.02) compared to non-CF BE patients. Multiple logistic regression analysis of all patients revealed male gender and disease duration as risk factors for OSA (p:0.023 and p:0.041 respectively).
dc.identifier.citationVezir D., Balcan B., KOCAKAYA D., Cinar C., Olgun S., CEYHAN B., "Obstructive Sleep Apnea in patients with Cystic Fibrosis and non-Cystic Fibrosis Bronchiectasis and its relation with clinical parameters", EUROPEAN RESPIRATORY JOURNAL, cilt.60, 2022
dc.identifier.doi10.1183/13993003.congress-2022.1486
dc.identifier.issn0903-1936
dc.identifier.urihttps://hdl.handle.net/11424/290467
dc.identifier.volume60
dc.language.isoeng
dc.relation.ispartofEUROPEAN RESPIRATORY JOURNAL
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectGöğüs Hastalıkları ve Allerji
dc.subjectSağlık Bilimleri
dc.subjectMedicine
dc.subjectInternal Medicine Sciences
dc.subjectChest Diseases and Allergy
dc.subjectHealth Sciences
dc.subjectSOLUNUM SİSTEMİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectRESPIRATORY SYSTEM
dc.subjectCLINICAL MEDICINE
dc.subjectClinical Medicine (MED)
dc.subjectSolunum Bakımı
dc.subjectAkciğer ve Solunum Tıbbı
dc.subjectRespiratory Care
dc.subjectPulmonary and Respiratory Medicine
dc.subjectApnoea / Hypopnea
dc.subjectAdults
dc.subjectOrphan diseases
dc.titleObstructive Sleep Apnea in patients with Cystic Fibrosis and non-Cystic Fibrosis Bronchiectasis and its relation with clinical parameters
dc.typearticle
dspace.entity.typePublication
local.avesis.idbdf68fa3-f777-4e9f-8a94-6431c7048694
local.indexed.atWOS
relation.isAuthorOfPublicationfedbd09a-b3b0-4906-82b5-e0f2c2bbd28a
relation.isAuthorOfPublication2771cdd6-7c3b-45a8-89fe-a429a2950516
relation.isAuthorOfPublication14f2d015-b03a-45e7-bb38-e82572308bca
relation.isAuthorOfPublication.latestForDiscoveryfedbd09a-b3b0-4906-82b5-e0f2c2bbd28a

Files

Collections

Research Outputs