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Clinicians' views about the experience of disability due to low back pain. Results from a focus group study

dc.rights.licenseopenen_US
dc.contributor.authorCEDRASCHI, Christine
dc.contributor.authorCAMPELLO, Marco
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSALMI, Louis Rachid
dc.contributor.authorCOTE, Pierre
dc.date.accessioned2021-01-19T09:24:13Z
dc.date.available2021-01-19T09:24:13Z
dc.date.issued2020
dc.identifier.issn1432-0932 (Electronic) 0940-6719 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/25860
dc.description.abstractEnPurpose For clinicians, treating the cause of non-pathological low back pain (LBP) is central. For patients, it is how LBP limits their activities of daily living. Little is known about clinicians’ understanding of disability and the patient’s perspective. We conducted a qualitative study to examine how clinicians involved in the care of patients with BP describe and define disability, its associated changes, and rehabilitation. Methods Two focus groups (FGs) were conducted with spine specialists including eleven confirmed orthopedic surgeons and neurosurgeons, ten advanced residents, and five other clinicians. Participants were questioned about their views on disability, what it means to them and to the patients. Responses were collected by two independent observers using Metaplan techniques. Large stickers were used to collect participants’ responses/ideas; the stickers were posted on billboards so the FGs could check them during the discussion. Metaplan was used to aggregate responses. Results Disability was viewed as a major source of physical limitations, difficulties in performing daily activities, associated with emotional distress, and raising legitimacy issues. Changes in roles engaged the social component. Considered from the patients’ perspective, negative emotions and social issues were emphasized, along with the patients’ resources. For rehabilitation, the participants emphasized patient-centered care, teamwork, and objectives for care. Conclusion The participants pointed to disability as an umbrella term for impairments, activity limitations, and participation restrictions. They underlined the necessity for clinicians to help patients define their level of optimal functioning when faced with BP, utilizing adaptation and teamwork within the therapeutic relationship.
dc.language.isoENen_US
dc.subjectIETO
dc.title.enClinicians' views about the experience of disability due to low back pain. Results from a focus group study
dc.title.alternativeEur Spine Jen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s00586-020-06463-yen_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed32436076en_US
bordeaux.journalEuropean Spine Journalen_US
bordeaux.page1953-1958en_US
bordeaux.volume29en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue8en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamIETOen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03166165
hal.version1
hal.date.transferred2021-03-11T09:25:41Z
hal.exporttrue
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