scispace - formally typeset
Open AccessJournal ArticleDOI

Promoting chronic disease management in persons with complex social needs: A qualitative descriptive study:

Reads0
Chats0
TLDR
The aims of this project were to describe the challenges related to availability, accessibility, and acceptability faced by socially complex patients with Chronic Obstructive Pulmonary Disease who were eligible, but declined enrollment in a traditional Chronic Disease Management Program (CDMP).
Abstract
While there are both ethical and practical imperatives to address health inequity issues related to chronic disease management for persons with social complexity, existing programs often do not appropriately address the needs of these individuals. This leads to low levels of participation in programs, suboptimal chronic disease management, and higher health-care utilization. The aims of this project were to describe the challenges related to availability, accessibility, and acceptability faced by socially complex patients with Chronic Obstructive Pulmonary Disease (COPD) who were eligible, but declined enrollment in a traditional Chronic Disease Management Program (CDMP). Using a qualitative descriptive study approach informed by a health equity lens, interviews with participants, managers, and a focus group with providers were used to gather data addressing the above aims. Qualitative data were analyzed using Braun and Clarke's theoretical thematic analysis approach. The ability of participants to manage chronic disease was profoundly influenced by contextual and personal factors, such as poverty, disability, personal attitudes and beliefs (including shame, mistrust, and hopelessness), and barriers inherent in the organization of the health-care system. The existing chronic disease management program did not adequately address the most critical needs of socially complex patients. Challenges with accessibility and acceptability of chronic disease management and health services played important roles in the ways these socially complex participants managed their chronic illness. The individualistic approach to self-management of chronic illness inherent in conventional CDMP can be poorly aligned with the needs, capacity, and circumstances of many socially complex patients. Innovative models of care that promote incremental and guided approaches to enhancing health and improving self-efficacy need further development and evaluation.

read more

Citations
More filters
Journal ArticleDOI

Life Expectancy and Mortality Rates in the United States, 1959-2017

TL;DR: US life expectancy increased for most of the past 60 years, but the rate of increase slowed over time and life expectancy decreased after 2014, with the largest relative increases occurring in the Ohio Valley and New England.

Effectiveness of interventions targeting frequent users of emergency departments: a systematic review

TL;DR: It appears to be beneficial to patients and justifiable for hospitals to implement case management for frequent users in the framework of a clear and consensual definition of frequent users and standardized outcome measures.
Journal ArticleDOI

Qualitative Research Methods in Chronic Disease: Introduction and Opportunities to Promote Health Equity

TL;DR: The authors provide an overview of data collection, sampling, and analysis for qualitative research, and describe research questions that can be addressed by applying qualitative methods across the continuum of chronic disease research, with an emphasis on priority areas to enhance health equity across the evidence generation continuum.
Journal ArticleDOI

Associations Between Patients' Unmet Social Needs and Self-Reported Health Confidence at One Primary Care Clinic.

TL;DR: Results of this quality improvement project suggest that patients with unmet social needs may have decreased perceived ability to manage health problems, and if interventions addressing un met social needs can increase health confidence.
Journal ArticleDOI

Tailored or adapted interventions for adults with chronic obstructive pulmonary disease and at least one other long‐term condition: a mixed methods review

TL;DR: In this paper, the authors evaluated the effectiveness of telemonitoring, pulmonary rehabilitation, treatment optimisation, water-based exercise training, and case management for COPD in terms of the following outcomes: quality of life, exacerbations, functional status, all cause and respiratory-related hospital admissions, mortality, pain, and depression and anxiety.
References
More filters
Journal ArticleDOI

Using thematic analysis in psychology

TL;DR: Thematic analysis is a poorly demarcated, rarely acknowledged, yet widely used qualitative analytic method within psychology as mentioned in this paper, and it offers an accessible and theoretically flexible approach to analysing qualitative data.
Journal ArticleDOI

Evidence suggesting that a chronic disease self-management program can improve health status while reducing hospitalization: a randomized trial.

TL;DR: An intervention designed specifically to meet the needs of a heterogeneous group of chronic disease patients, including those with comorbid conditions, was feasible and beneficial beyond usual care in terms of improved health behaviors and health status.
Journal ArticleDOI

Patient empowerment in theory and practice: Polysemy or cacophony?

TL;DR: The analysis of how the term "empowerment" has been used in relation to the care and education of patients with chronic conditions over the past decade revealed a number of guiding principles and values.
Journal ArticleDOI

Patient self-management: a key to effectiveness and efficiency in care of chronic disease.

TL;DR: There is no cure for chronic disease; instead, management over time is essential.
Journal ArticleDOI

Reconsidering patient empowerment in chronic illness: a critique of models of self-efficacy and bodily control.

TL;DR: The process of relinquishing control is as central to empowerment as is the process of gaining control, as a "successful" process of empowerment occurs when patients come to terms with their threatened security and identity with their treatment, and may be facilitated by health-care providers through the use of narratives.
Related Papers (5)