Living with pain in ankylosing spondylitis: a qualitative study

dc.authorid Cinar, Fatma Ilknur/0000-0001-6394-8331
dc.authorid Cinar, Muhammet/0000-0002-6150-3539
dc.authorscopusid 35387400800
dc.authorscopusid 54400060600
dc.authorscopusid 24463296200
dc.authorscopusid 16040539000
dc.authorscopusid 12773262600
dc.authorscopusid 6701629907
dc.contributor.author Bagcivan, Gulcan
dc.contributor.author Cinar, Fatma Ilknur
dc.contributor.author Cinar, Muhammet
dc.contributor.author Oflaz, Fahriye
dc.contributor.author Uzun, Senay
dc.contributor.author Pay, Salih
dc.date.accessioned 2024-05-25T11:18:08Z
dc.date.available 2024-05-25T11:18:08Z
dc.date.issued 2015
dc.department Okan University en_US
dc.department-temp [Bagcivan, Gulcan; Cinar, Fatma Ilknur; Pay, Salih] Gulhane Mil Med Acad, Sch Nursing, Ankara, Turkey; [Cinar, Muhammet] Gulhane Mil Med Acad, Sch Med, Div Rheumatol, Ankara, Turkey; [Oflaz, Fahriye] Okan Univ, Sch Hlth Sci, Dept Nursing, Istanbul, Turkey; [Uzun, Senay] Yeditepe Univ, Dept Nursing & Hlth Serv, Fac Hlth Sci, Istanbul, Turkey en_US
dc.description Cinar, Fatma Ilknur/0000-0001-6394-8331; Cinar, Muhammet/0000-0002-6150-3539 en_US
dc.description.abstract Background: Despite various quantitative studies reporting that pain is among the most serious problem in ankylosing spondylitis (AS), no detailed qualitative studies address how pain affects the life of patients with AS. Aim: To explore AS patients' experiences with pain and its effect on their lives. Design: Descriptive qualitative study. Methods: Data were collected by individual in-depth interviews. Colaizzi's phenomenological data analysis was performed. Results: During periods of pain, participants indicated that they experienced difficulty with performing their daily routine activities and meeting their personal needs. Pain also prevented them from fulfilling their responsibilities in their families, inhibited their social relations, and posed problems at their workplace. Due to the negative effects of pain in their lives, the participants felt helplessness, fear, stress, sadness, and unhappiness. Conclusions: Added to being asked about the quantity of pain, patients with AS should be questioned about how pain affects their lives. en_US
dc.identifier.citationcount 19
dc.identifier.doi 10.1080/10376178.2016.1157028
dc.identifier.endpage 147 en_US
dc.identifier.issn 1037-6178
dc.identifier.issn 1839-3535
dc.identifier.issue 2-3 en_US
dc.identifier.pmid 26902427
dc.identifier.scopus 2-s2.0-84973440897
dc.identifier.scopusquality Q2
dc.identifier.startpage 135 en_US
dc.identifier.uri https://doi.org/10.1080/10376178.2016.1157028
dc.identifier.uri https://hdl.handle.net/20.500.14517/300
dc.identifier.volume 51 en_US
dc.identifier.wos WOS:000375908400003
dc.identifier.wosquality Q3
dc.language.iso en
dc.publisher Routledge Journals, Taylor & Francis Ltd en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.scopus.citedbyCount 20
dc.subject ankylosing spondylitis en_US
dc.subject pain en_US
dc.subject qualitative research en_US
dc.subject life experiences en_US
dc.subject pain experiences en_US
dc.title Living with pain in ankylosing spondylitis: a qualitative study en_US
dc.type Article en_US
dc.wos.citedbyCount 17

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