Fragmented care and missed opportunities: the experiences of adults with myasthenia gravis in accessing and receiving allied health care in Australia.
Autor: | Devlin, Isobel, Williams, Katrina L., Shrubsole, Kirstine |
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Předmět: |
ALLIED health education
MYASTHENIA gravis HEALTH services accessibility RESEARCH methodology MEDICAL care PATIENT-centered care INTERVIEWING COMMUNITY health services QUALITATIVE research PATIENTS' attitudes HEALTH care teams COMMUNICATION MEDICAL referrals DESCRIPTIVE statistics THEMATIC analysis DATA analysis software MEDICAL needs assessment ADULTS |
Zdroj: | Disability & Rehabilitation; Jul2023, Vol. 45 Issue 15, p2488-2496, 9p |
Abstrakt: | Although allied health services are important adjuncts to medical care for people with myasthenia gravis (MG), the underutilisation of these services is not well understood within the Australian context. It is critical to explore patients' perceptions to develop services that meet consumer needs. This study, therefore, sought to obtain insight into MG patients' perspectives and experiences, in addition to the outcomes, of accessing allied health services. Thirteen Australian adults with MG participated in semi-structured interviews. Qualitative analysis was conducted inductively using thematic content analysis. Four themes were identified: (1) missed opportunities and unmet care needs were common, due to frequent patient–provider communication breakdowns and a lack of referral protocols, (2) personal factors – patient self-advocacy influenced their perceived need, with some lacking confidence to seek help, (3) perceived benefit and health provider capacities – most valued allied health despite differing perceptions of health professionals' attitudes, skills, and willingness to learn, and (4) a resultant fragmentation of care between services was universal. Findings highlighted a need for clear referral pathways, coordinated multidisciplinary care, improved access to community-based services and education for allied health professionals about MG. Adults with myasthenia gravis (MG) report a lack of referral pathways to allied health services, leading to unmet needs and fragmented care. Although there is a perceived benefit to allied health care, experiences are impacted by health provider capacity and attitudes. There needs to be an overall shift towards multidisciplinary care for people with MG, and the development of clear referral pathways. Specific education about MG should be available for allied health professionals to improve their knowledge and skills in treating this population. [ABSTRACT FROM AUTHOR] |
Databáze: | Complementary Index |
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