Polisomographic Investigation of Sleep Disorders in Patients with Sickle Cell Anemia and Evaluation of the Effect on the Prognosis

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dc.authoridBabayigit, Cenk/0000-0001-9760-6081
dc.contributor.authorDikmen, Nursel
dc.contributor.authorOkuyucu, Emine Esra
dc.contributor.authorGuntel, Murat
dc.contributor.authorUcar, Edip
dc.contributor.authorIlhan, Gul
dc.contributor.authorBabayigit, Cenk
dc.contributor.authorKaradag, Mehmet
dc.date.accessioned2024-09-18T20:57:05Z
dc.date.available2024-09-18T20:57:05Z
dc.date.issued2022
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractOBJECTIVE: The aim of this study is to identify sleep disorders in adults with sickle cell disease and to examine the effects of accompanying sleep disorders on the prognosis of sickle cell disease. MATERIAL AND METHODS: Twenty-eight patients followed up with a diagnosis of sickle cell disease and 22 healthy volunteers were included in our study. RESULTS: Both groups had similar characteristics in terms of age, gender, and body mass index. More obstructive sleep apnea syndrome was detected in the sickle cell group than in healthy volunteers. Statistically, the sickle cell patient group had higher apnea-hypopnea index and lower nighttime oxygen desaturation. As the degree of obstructive sleep apnea syndrome increased in the sickle cell group, it was found that there were more emergency admissions and hospitalization due to painful crises and/or acute chest syndrome in the last 1 year. Also, lower sleep efficiency was found in the sickle cell disease patient group. In the sickle cell group, it was found that the restless leg syndrome severity was statistically significantly more. CONCLUSION: As hypoxia deepens in sickle cell patients, mortality and morbidity due to the disease increase significantly. Comorbid sleep disturbances in sickle cell patients exacerbate nocturnal hypoxia and negatively affect the prognosis of the disease. Therefore, patients with sickle cell disease should be questioned in detail in terms of obstructive sleep apnea syndrome and, if necessary, polysomnographic evaluation should be performed to provide treatment for sleep disorders in the early period.en_US
dc.description.sponsorshipHatay Mustafa Kemal University Scientific Research Projects Coordinator [18.A.007]en_US
dc.description.sponsorshipOur study was supported by Hatay Mustafa Kemal University Scientific Research Projects Coordinator (Project Number: 18.A.007).en_US
dc.identifier.doi10.5152/TurkThoracJ.2022.21199
dc.identifier.endpage224en_US
dc.identifier.issn2149-2530
dc.identifier.issue3en_US
dc.identifier.pmid35579228en_US
dc.identifier.scopus2-s2.0-85131004450en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage218en_US
dc.identifier.trdizinid1175486en_US
dc.identifier.urihttps://doi.org/10.5152/TurkThoracJ.2022.21199
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1175486
dc.identifier.urihttps://hdl.handle.net/20.500.12483/12279
dc.identifier.volume23en_US
dc.identifier.wosWOS:000841463900004en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherAvesen_US
dc.relation.ispartofTurkish Thoracic Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectSleep apnea syndromeen_US
dc.subjectsickle cell anemiaen_US
dc.subjecthypoxiaen_US
dc.subjectthe restless leg syndromeen_US
dc.titlePolisomographic Investigation of Sleep Disorders in Patients with Sickle Cell Anemia and Evaluation of the Effect on the Prognosisen_US
dc.typeArticleen_US

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