UNLABELLED: Temporomandibular disorders (TMDs) are a common group of chronic disorders (illnesses) that health care providers can find difficult to diagnose and explain. Similar difficulties in the diagnosis of other chronic conditions have been shown to have a negative impact on health. An understanding of TMD patients' experiences and journey through care could indicate time points and strategies to help patients. OBJECTIVE: To develop a robust empirically derived map of TMD sufferers' journey through care. METHODS: A qualitative study using semi-structured interviews was undertaken using a purposive sample of patients with TMDs. Analysis followed the principles of the constant comparative method where data collection and thematic analysis occurred concurrently and continued until data saturation (n = 29). RESULTS: The experiences of patients could be grouped into three key stages: genesis of problem, seeking help in primary care and secondary care intervention. A wide variety of negative effects were described throughout these stages. An empirically derived map of the patients' reported journey through care emerged. CONCLUSIONS: The experiences of patients with TMDs mirror experiences of other types of chronic illness. Mapping the journey through care for TMDs highlights the potential for interaction between the stages of the journey and the individual's illness. It may be possible to target interventions at specific stages on the map to help minimize the psychosocial effects of TMDs.
UNLABELLED: Temporomandibular disorders (TMDs) are a common group of chronic disorders (illnesses) that health care providers can find difficult to diagnose and explain. Similar difficulties in the diagnosis of other chronic conditions have been shown to have a negative impact on health. An understanding of TMDpatients' experiences and journey through care could indicate time points and strategies to help patients. OBJECTIVE: To develop a robust empirically derived map of TMD sufferers' journey through care. METHODS: A qualitative study using semi-structured interviews was undertaken using a purposive sample of patients with TMDs. Analysis followed the principles of the constant comparative method where data collection and thematic analysis occurred concurrently and continued until data saturation (n = 29). RESULTS: The experiences of patients could be grouped into three key stages: genesis of problem, seeking help in primary care and secondary care intervention. A wide variety of negative effects were described throughout these stages. An empirically derived map of the patients' reported journey through care emerged. CONCLUSIONS: The experiences of patients with TMDs mirror experiences of other types of chronic illness. Mapping the journey through care for TMDs highlights the potential for interaction between the stages of the journey and the individual's illness. It may be possible to target interventions at specific stages on the map to help minimize the psychosocial effects of TMDs.
Authors: Brenda C Lovette; Sarah M Bannon; Daphne Catherine Spyropoulos; Ana-Maria Vranceanu; Jonathan Greenberg Journal: J Pain Res Date: 2022-07-29 Impact factor: 2.832
Authors: Justin Durham; Matthew Breckons; Vera Araujo-Soares; Catherine Exley; Jimmy Steele; Luke Vale Journal: BMC Oral Health Date: 2014-01-21 Impact factor: 2.757