Triggers and factors associated with moral distress and moral injury in health and social care workers: A systematic review of qualitative studies
View/ Open
Author
Beadle, Emily S.
Walecka, Agnieszka
Sangam, Amy V.
Moorhouse, Jessica
Winter, Matthew
Munro Wild, Helen
Trivedi, Daksha
Casarin, Annalisa
Attention
2299/27999
Abstract
Objective: At some point in their career, many healthcare workers will experience psychological distress associated with being unable to take morally or ethically correct action, as it aligns with their own values; a phenomenon known as moral distress. Similarly, there are increasing reports of healthcare workers experiencing long-term mental and psychological pain, alongside internal dissonance, known as moral injury. This review examined the triggers and factors associated with moral distress and injury in Health and Social Care Workers (HSCW) employed across a range of clinical settings with the aim of understanding how to mitigate the effects of moral distress and identify potential preventative interventions. Methods: A systematic review was conducted and reported according to recommendations from Cochrane and Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Searches were conducted and updated regularly until January 2024 on 2 main databases (CENTRAL, PubMed) and three specialist databases (Scopus, CINAHL, PsycArticles), alongside hand searches of study registration databases and other systematic reviews reference lists. Eligible studies included a HSCW sample, explored moral distress/injury as a main aim, and were written in English or Italian. Verbatim quotes were extracted, and article quality was assessed via the CASP toolkit. Thematic analysis was conducted to identify patterns and arrange codes into themes. Specific factors like culture and diversity were explored, and the effects of exceptional circumstances like the pandemic. Results: Fifty-one reports of 49 studies were included in the review. Causes and triggers were categorised under three domains: individual, social, and organisational. At the individual level, patients’ care options, professionals’ beliefs, locus of control, task planning, and the ability to make decisions based on experience, were indicated as elements that can cause or trigger moral distress. In addition, and relevant to the CoVID-19 pandemic, was use/access to personal protection resources. The social or relational factors were linked to the responsibility for advocating for and communication with patients and families, and professionals own support network. At organisational levels, hierarchy, regulations, support, workload, culture, and resources (staff and equipment) were identified as elements that can affect professionals’ moral comfort. Patients’ care, morals/beliefs/standards, advocacy role and culture of context were the most referenced elements. Data on cultural differences and diversity were not sufficient to make assumptions. Lack of resources and rapid policy changes have emerged as key triggers related to the pandemic. This suggests that those responsible for policy decisions should be mindful of the potential impact on staff of sudden and top-down change. Conclusion: This review indicates that causes and triggers of moral injury are multifactorial and largely influenced by the context and constraints within which professionals work. Moral distress is linked to the duty and responsibility of care, and professionals’ disposition to prioritise the wellbeing of patients. If the organisational values and regulations are in contrast with individuals’ beliefs, repercussions on professionals’ wellbeing and retention are to be expected. Organisational strategies to mitigate against moral distress, or the longer-term sequalae of moral injury, should address the individual, social, and organisational elements identified in this review.
Publication date
2024-06-30Published in
PLoS ONEPublished version
https://doi.org/10.1371/journal.pone.0303013Other links
http://hdl.handle.net/2299/27999Metadata
Show full item recordRelated items
Showing items related by title, author, creator and subject.
-
The Experience of Being a Trainee Clinical Psychologist From a Black and Minority Ethnic Group: A Qualitative Study
Shah, Snehal (2010-12-22)Aim: The existing evidence-base indicates that the experience of being a Black and Minority Ethnic (BME) trainee clinical psychologist is under-researched. The aim of the current study was to capture the broader training ... -
Challenges and coping strategies when caring for terminally ill persons with cancer: perspectives of family caregivers
Biney, Antoinette; Sarfo, Jacob Owusu; Poku, Collins Atta; Deegbe, David Atsu; Atibila, Fidelis; Ti-enkawol Nachinab, Gilbert; Anaba, Emmanuel; Dzansi, Gladys; Attafuah, Priscilla Yeye Adumoah (2024-12-30)Introduction: Terminal illness is an irreversible illness that, without life-sustaining procedures, usually results in death or permanent disability from which recovery is unlikely. When involved, family caregivers are ... -
Quality science from quality measurement: The role of measurement type with respect to replication and effect size magnitude in psychological research
Kornbrot, Diana; Wiseman, Richard; Georgiou, George (2018-02-12)The quality of psychological studies is currently a major concern. The Many Labs Project (MLP) and the Open-Science-Collaboration (OSC) have collected key data on replicability and statistical effect sizes. We build on ...