2022
DOI: 10.1080/09638288.2022.2130447
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Clinical conversations in the management of chronic musculoskeletal pain in vulnerable patient populations: a meta-ethnography

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Cited by 4 publications
(8 citation statements)
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“…In terms of methods, 26 studies were qualitative (38.8%), 30 were quantitative (44.7%; which included randomized controlled/clinical trials), four were mixed-methods (5.9%), and seven were reviews (10.4%; including literature, narrative, meta-ethnography, and systematic). 16 , 27–32 The most frequently cited method of data collection was interviews ( n = 21, 31.3%), followed by questionnaires/surveys ( n = 15, 22.3%). Most studies focused generally on chronic pain ( n = 49, 73.1%), with the remaining focusing on specific chronic pain conditions, including migraine, fibromyalgia, sickle cell disease, diabetic neuropathy, HIV-related pain, irritable bowel syndrome, hip or knee osteoarthritis, and back, neck, or knee pain.…”
Section: Resultsmentioning
confidence: 99%
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“…In terms of methods, 26 studies were qualitative (38.8%), 30 were quantitative (44.7%; which included randomized controlled/clinical trials), four were mixed-methods (5.9%), and seven were reviews (10.4%; including literature, narrative, meta-ethnography, and systematic). 16 , 27–32 The most frequently cited method of data collection was interviews ( n = 21, 31.3%), followed by questionnaires/surveys ( n = 15, 22.3%). Most studies focused generally on chronic pain ( n = 49, 73.1%), with the remaining focusing on specific chronic pain conditions, including migraine, fibromyalgia, sickle cell disease, diabetic neuropathy, HIV-related pain, irritable bowel syndrome, hip or knee osteoarthritis, and back, neck, or knee pain.…”
Section: Resultsmentioning
confidence: 99%
“…A large portion of the studies did not specify a theory or guiding conceptual framework ( n = 28, 41.7%). Of those studies that used a framework ( n = 39, 58.2%), examples include Black feminist thought and critical arts-based inquiry, 35 participatory action research, 55 Gadamerian philosophical hermeneutics, 36 two nested hierarchical models (Bronfenbrenner’s bioecological model and social ecological model), 16 the National Institute on Aging Health Disparities Research Framework, 31 Newman’s theory, 48 the sociology of illness experience, 60 Rhodes’ risk environment framework, 61 Bronfenbrenner’s process–person–context–time model, 46 Neuman’s systems model, 62 the life course perspective, 45 and the biopsychosocial model. 28 , 30 , 32 , 43 , 63 , 64 We noted that studies that drew on theory offered more fulsome understandings of and approaches to marginalization, which sheds light on the structures underpinning aspects of chronic pain experiences among marginalized groups.…”
Section: Resultsmentioning
confidence: 99%
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“…Ethnographic research also reveals how cultural beliefs, rituals, and social norms influence the experience and management of pain. These studies underscore the importance of considering cultural context in understanding and addressing pain (Dupuis, 2022, Emerson, et. al., 2023, Silverman, Baroiller & Hemer, 2021.…”
Section: Anthropological Perspectives On Painmentioning
confidence: 87%
“…Additionally, healthcare providers’ own implicit biases, differences in patient/provider expectations, and cultural and linguistic disparities further feed into the negative stigmatization of patients with chronic pain, limit access to pain treatments, impact diagnostic decision-making, and iatrogenically create a negative feedback loop [ 11 ]. To combat disjointed care, providers must work together with their patients, listen to their patients’ lived experiences, and explore their perspectives that may better reduce bias and inequities and increase empathy and health outcomes [ 12 , 13 ].…”
Section: Discussionmentioning
confidence: 99%