How chronic conditions are understood, experienced and managed within African communities in Europe, North America and Australia: A synthesis of qualitative studies.

Journal: PloS one

Volume: 18

Issue: 2

Year of Publication: 2023

Affiliated Institutions:  Institute of Advanced Studies, University College London, London, United Kingdom. Department of Population Health Sciences, Spencer Fox Eccles School of Medicine, University of Utah, Salt Lake City, Utah, United States of America. Department of Health Policy, Planning and Management, School of Public Health, University of Ghana, Legon, Accra, Ghana. Faculty of Education, Health and Human Sciences, University of Greenwich, London, United Kingdom. Department of Non-communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom. Department of Public Health, Amsterdam Public Health Research Institute, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Abstract summary 

This review focuses on the lived experiences of chronic conditions among African communities in the Global North, focusing on established immigrant communities as well as recent immigrant, refugee, and asylum-seeking communities. We conducted a systematic and narrative synthesis of qualitative studies published from inception to 2022, following a search from nine databases-MEDLINE, EMBASE, PsycINFO, Web of Science, Social Science Citation Index, Academic Search Complete, CINAHL, SCOPUS and AMED. 39 articles reporting 32 qualitative studies were included in the synthesis. The studies were conducted in 10 countries (Australia, Canada, Denmark, France, Netherlands, Norway, Sweden, Switzerland, United Kingdom, and the United States) and focused on 748 participants from 27 African countries living with eight conditions: type 2 diabetes, hypertension, prostate cancer, sickle cell disease, chronic hepatitis, chronic pain, musculoskeletal orders and mental health conditions. The majority of participants believed chronic conditions to be lifelong, requiring complex interventions. Chronic illness impacted several domains of everyday life-physical, sexual, psycho-emotional, social, and economic. Participants managed their illness using biomedical management, traditional medical treatment and faith-based coping, in isolation or combination. In a number of studies, participants took 'therapeutic journeys'-which involved navigating illness action at home and abroad, with the support of transnational therapy networks. Multi-level barriers to healthcare were reported across the majority of studies: these included individual (changing food habits), social (stigma) and structural (healthcare disparities). We outline methodological and interpretive limitations, such as limited engagement with multi-ethnic and intergenerational differences. However, the studies provide an important insights on a much-ignored area that intersects healthcare for African communities in the Global North and medical pluralism on the continent; they also raise important conceptual, methodological and policy challenges for national health programmes on healthcare disparities.

Authors & Co-authors:  de-Graft Aikins Ama A Sanuade Olutobi O Baatiema Leonard L Adjaye-Gbewonyo Kafui K Addo Juliet J Agyemang Charles C

Study Outcome 

Source Link: Visit source

Statistics
Citations :  World Health Organzation. Noncommunicable diseases 2021.
Authors :  6
Identifiers
Doi : e0277325
SSN : 1932-6203
Study Population
Male
Mesh Terms
Male
Other Terms
Study Design
Narrative Study,Cross Sectional Study
Study Approach
Qualitative,Systemic Review
Country of Study
Publication Country
United States