Article Text
Viewpoint
Why shared decision making is not good enough: lessons from patients
Abstract
A closer look at the lived illness experiences of medical professionals themselves shows that shared decision making is in need of a logic of care. This paper underlines that medical decision making inevitably takes place in a messy and uncertain context in which sharing responsibilities may impose a considerable burden on patients. A better understanding of patients’ lived experiences enables healthcare professionals to attune to what individual patients deem important in their lives. This will contribute to making medical decisions in a good and caring manner, taking into account the lived experience of being ill.
- Education for Health Care Professionals
- Health Personnel
- Quality of Health Care
Statistics from Altmetric.com
Linked Articles
- The concise argument
Read the full text or download the PDF:
Other content recommended for you
- What makes a ‘good doctor’? A critical discourse analysis of perspectives from medical students with lived experience as patients
- Narrative-based learning for person-centred healthcare: the Caring Stories learning framework
- Bringing narratives from physicians, patients and caregivers together: a scoping review of published research
- Evaluation of tumour response after gamma knife radiosurgery for residual vestibular schwannomas based on MRI morphological features
- What do we know about patients’ perspectives and expectations relating to palliative and end-of-life care in advanced liver disease? A systematic review of qualitative literature using ENTREQ guidelines
- Listening, learning, caring: exploring assemblages of, ethics of and pathways to care for avoidant restrictive food intake disorder (ARFID)
- What can art history offer medical humanities?
- Narrative Medicine Theory and Practice: the Double Helix Model
- Constitution of Long COVID illness, patienthood and recovery: a critical synthesis of qualitative studies
- Narrative medicine to investigate the quality of life and emotional impact of inherited retinal disorders through the perspectives of patients, caregivers and clinicians: an Italian multicentre project