Relationship between depression, anxiety, quality of life and vaso-occlusive crisis in adolescents with sickle cell disease

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dc.authorscopusid23095569900
dc.authorscopusid35489765100
dc.authorscopusid35502849500
dc.authorscopusid21743370800
dc.contributor.authorOzer, Cahit
dc.contributor.authorYengil, Erhan
dc.contributor.authorAcipayam, Can
dc.contributor.authorKokacya, Mehmet Hanifi
dc.date.accessioned2024-09-19T15:41:26Z
dc.date.available2024-09-19T15:41:26Z
dc.date.issued2014
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractAims: To explore the relationship between frequency of pain episodes and depression, anxiety, and health related quality of life (HRQOL) in adolescents with sickle cell disease (SCD). Materials and methods: Ten males and twelve females, between the ages of 12 and 19, selected during admittance to pediatric hematology outpatients of city hospital with a vaso-occlusive crisis in the period between September 2012 and February 2013, were included in the study. Beck Depression (BDI) and Anxiety Inventories (BAI), and Short Form Health Survey (SF-36) were used to evaluate depression, anxiety and HRQOL. Results: Nine (40.9%) of the adolescents with SCD had BDI scores higher or equal to 17. In the whole group, 3 (13.6%) patients did not have anxiety, while 14 (63.6%) of them had mild and 4 (18.2%) had moderate anxiety. Physical and mental components of HRQOL were not correlated to BDI and BAI scores. Patients with frequent pain episodes (>10 annually) were found to have tendency to depression and anxiety while their mental and physical components of HRQOL were lower than patients with infrequent pain episodes (<5 annually). Conclusion: Depression and anxiety in adolescents with SCD was found relatively high, while Physical and Mental components of HRQOL were relatively low. However, Physical and Mental Health of the patients was not affected from depression and anxiety presence. Pain episode frequency might be the main determinant of higher depression and anxiety and lower HRQOL component scores.en_US
dc.identifier.endpage339en_US
dc.identifier.issn0393-6384
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-84898471979en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage335en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12483/14260
dc.identifier.volume30en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherActa Medica Mediterraneaen_US
dc.relation.ispartofActa Medica Mediterraneaen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAdolescenten_US
dc.subjectAnxietyen_US
dc.subjectDepressionen_US
dc.subjectQuality of lifeen_US
dc.subjectSickle cell diseaseen_US
dc.titleRelationship between depression, anxiety, quality of life and vaso-occlusive crisis in adolescents with sickle cell diseaseen_US
dc.typeArticleen_US

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