Abstract:Objective
The concept of coping with disease appears frequently in the literature; however, there is no precise definition of coping. The aim of this study is to clarify coping concept, and to identify its attributes, antecedents, and consequences in patients with multiple sclerosis.
Methods
Rodgers' evolutionary method of concept analysis was used to clarify the concept of coping. A literature review was conducted with key terms ‘multiple sclerosis’, ‘coping’, ‘adjustm… Show more
“…The selfcare agency and quality of life of the patients with MS decreased, and their adaptation levels were affected because of some factors, such as experiencing balance problems (27%), the use of a wheelchair (12%) and a walking stick (21%), wearing glasses (28%), the presence of family members who provided care (10%), being unemployed (54%), comorbidities (32%), being a primary school graduate (38%), having children (70%), being a dominant female participant (76%), and being younger than 45 years (62%). Besides, these findings have been supported by some studies reporting that the quality of life of patients with MS is lower than others 21,22 and by the study of Hyarat et al 15 conducted with patients with MS, which reported that patients with a low quality of life also showed a low level of adaptation to MS.…”
Section: Discussionmentioning
confidence: 55%
“…The statement in the literature that the quality of life of patients with MS is lower than others supports these findings. 15,20,21 In addition, Dehghani et al 22 stated that the adaptation levels of individuals who conceded the disease were strong and consistent. Multiple sclerosis causes depression, pain, and balance problems that disrupt the physical, social, and psychological independence of patients, 23 and these problems vary from person to person.…”
BACKGROUND: Multiple sclerosis (MS) is an inflammatory and demyelinating disorder of the central nervous system. The patients with MS have some difficulties in physical, social, and psychological functions. This study was carried out to determine the relationship between the adaptation levels of patients with MS to the disease and their self-care agency levels. METHODS: This study used a descriptive design and was carried out in a university hospital's neurology clinic and outpatient clinic between July 2019 and March 2020. The sample size was determined as 258 using the known universe sampling method. Data were collected using the "Adaptation to Chronic Illness Scale," the "Self-Care Agency Scale," and a "Patient Identification Form." Spearmen correlation analysis was used to evaluate the data. RESULTS: The mean age of the patients participating in the study was 41.36 (0.74) years, 74% of them had MS for more than 3 years, 58% had their last attack more than a year ago, and 27% had balance problems. The adaptation levels of patients to the disease (76.79 [0.57]) and their self-care agency (88.42 [1.34]) were slightly higher than the moderate level. A moderate-level, significant, and positive correlation was found between the adaptation level of the patients to the chronic illness and their self-care agency levels (r = 0.310, P = .000). CONCLUSION: It was concluded that there was a moderate-level, significant, and positive correlation between the patients' level of adaptation to MS disease and the level of their self-care agency. We recommend the provision of supportive professional training to patients with MS on their disease.
“…The selfcare agency and quality of life of the patients with MS decreased, and their adaptation levels were affected because of some factors, such as experiencing balance problems (27%), the use of a wheelchair (12%) and a walking stick (21%), wearing glasses (28%), the presence of family members who provided care (10%), being unemployed (54%), comorbidities (32%), being a primary school graduate (38%), having children (70%), being a dominant female participant (76%), and being younger than 45 years (62%). Besides, these findings have been supported by some studies reporting that the quality of life of patients with MS is lower than others 21,22 and by the study of Hyarat et al 15 conducted with patients with MS, which reported that patients with a low quality of life also showed a low level of adaptation to MS.…”
Section: Discussionmentioning
confidence: 55%
“…The statement in the literature that the quality of life of patients with MS is lower than others supports these findings. 15,20,21 In addition, Dehghani et al 22 stated that the adaptation levels of individuals who conceded the disease were strong and consistent. Multiple sclerosis causes depression, pain, and balance problems that disrupt the physical, social, and psychological independence of patients, 23 and these problems vary from person to person.…”
BACKGROUND: Multiple sclerosis (MS) is an inflammatory and demyelinating disorder of the central nervous system. The patients with MS have some difficulties in physical, social, and psychological functions. This study was carried out to determine the relationship between the adaptation levels of patients with MS to the disease and their self-care agency levels. METHODS: This study used a descriptive design and was carried out in a university hospital's neurology clinic and outpatient clinic between July 2019 and March 2020. The sample size was determined as 258 using the known universe sampling method. Data were collected using the "Adaptation to Chronic Illness Scale," the "Self-Care Agency Scale," and a "Patient Identification Form." Spearmen correlation analysis was used to evaluate the data. RESULTS: The mean age of the patients participating in the study was 41.36 (0.74) years, 74% of them had MS for more than 3 years, 58% had their last attack more than a year ago, and 27% had balance problems. The adaptation levels of patients to the disease (76.79 [0.57]) and their self-care agency (88.42 [1.34]) were slightly higher than the moderate level. A moderate-level, significant, and positive correlation was found between the adaptation level of the patients to the chronic illness and their self-care agency levels (r = 0.310, P = .000). CONCLUSION: It was concluded that there was a moderate-level, significant, and positive correlation between the patients' level of adaptation to MS disease and the level of their self-care agency. We recommend the provision of supportive professional training to patients with MS on their disease.
“…Our results showed that emotional reactions and anxiety were expressed due to a sudden physical change during for example experiences of MS symptoms. As was shown by Dehghani et al 29 , the maintenance of emotional balance, acceptance of the disease and self-regulation are favorable factors for coping with MS. Our results as well show that emotional reactions related to general stress were expressed frequently. A new result we could add to literature is that emotional reactions to general stress seem to be a way to cope in persons with MS.…”
Multiple sclerosis (MS) is an auto-immune disease in which the body’s immune system attacks the central nervous system. The demyelination of the nerve fibers can lead to physical, emotional, and cognitive impairments. We wanted to learn about challenges of living with the illness and how people deal with stress. 128 individuals with MS from Austria and the US participated in the qualitative interviews. We interviewed participants and coded their answers using inductive grounded theory. We asked three open-ended questions to inquire about life since being diagnosed with MS as well as about dealing with stress. Life shifts since diagnosis involved ‘experiencing limitations’ and could be categorized in ‘emotional changes’, ‘changes with work’, ‘changes in social interaction’, ‘physical changes’, ‘changes in the medical context’. For dealing with stress active (strategies and activities) and passive coping strategies (avoid/ignore) were employed. General stress reactions were expressed in areas of emotional, physical and /or lifestyle. We recommend developing interventions in three core areas for the MS population: (1) dealing with life changes and significant experiences with MS, (2) focusing on the areas where life shifts took place, (3) focusing on active coping with stress and discussing consequences of passive coping strategies.
“…Quality assessing final articles selected for a principle-based concept analysis using recognised tools such as the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) checklist (von Elm et al, 2007) for quantitative studies and the consolidated for reporting qualitative research (COREQ) checklist (Tong et al, 2007) for qualitative studies (e.g. Dehghani et al, 2018) were reviewed. Yet, existing tools are not suitable or developed for principle-based concept analysis.…”
Section: Quality Assessmentmentioning
confidence: 99%
“…Principle-based concept analysis can include qualitative, quantitative and mixed-methods research and grey literature. Guidelines such as the Centre for Reviews and Dissemination guidelines for the University of York, UK (CRD, 2009) can be followed which have been used in a previous principle-based concept analysis (Dehghani et al, 2018). Other suitable guidelines include Cochrane (e.g.…”
The study aimed to provide a detailed description of a process to conduct a phased principle-based concept analysis and to introduce quality criteria assessment for a phased principle-based concept analysis. Concept analysis explores how a concept is described, used and measured in the literature. This conceptual understanding is important to guide translational research to direct the development of evidence-based practice. The principle-based concept analysis is one approach of concept analysis used in published work, but the literature is lacking in articles clearly describing how to conduct it in practice. This article provides a methodology utilising a phased approach and by advancing on previous work; this approach includes a combination of a systematic search, quality criteria and qualitative analysis with principle-based concept analysis. Quality criteria for a phased principle-based concept analysis is introduced to critically assess articles against the four principles: epistemology, pragmatic, linguistic and logical. These improvements to the methodology promote transparency, rigour and replicability. This comprehensive systematic approach will aid future phased principle-based concept analyses and enable future comparisons of concept development, advancement and related concepts to improve the evidence base.
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