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- W4387302102 abstract "In 2022, two clinical practice guidelines were published, one for allied health and nursing assessment and management of individuals with Duchenne muscular dystrophy (DMD) and the other, for the management of paediatric Charcot-Marie-Tooth disease (CMT). Over the last 10 years, there has been a proliferation of practice guidelines and standards of care for neuromuscular disorders. However, very little is known about adherence to and implementation of these guidelines by health professionals delivering neuromuscular care. To develop strategies for guideline implementation, we must first understand what evidence-to-practice gaps exist as well as the enablers and barriers to the uptake of guideline recommendations. This project will explore health professionals’ awareness of and adherence to the recently published DMD and CMT guidelines via an online survey administered on the REDCap platform (hosted by Murdoch Children's Research Institute). Health professionals (medical, nursing and allied health) who manage the clinical care and treatment of individuals with DMD and/or children and young people with CMT across Australia and New Zealand will be invited to participate in this once-only survey. The survey will be distributed to all Australian and New Zealand neuromuscular clinics and centres and through community health networks and professional associations. The overall aim is to determine current practice and implementation of clinical practice guidelines for neuromuscular disorders, specifically DMD and CMT and in particular relating to assessment and outcome measures (DMD) and exercise, physical activity and nutritional status (CMT). The findings from this project will provide preliminary evidence around awareness of guidelines, as well as enablers and barriers to compliance with guidelines. This information will be used to design tailored guideline implementation strategies and inform further research in the uptake of clinical practice guidelines. In 2022, two clinical practice guidelines were published, one for allied health and nursing assessment and management of individuals with Duchenne muscular dystrophy (DMD) and the other, for the management of paediatric Charcot-Marie-Tooth disease (CMT). Over the last 10 years, there has been a proliferation of practice guidelines and standards of care for neuromuscular disorders. However, very little is known about adherence to and implementation of these guidelines by health professionals delivering neuromuscular care. To develop strategies for guideline implementation, we must first understand what evidence-to-practice gaps exist as well as the enablers and barriers to the uptake of guideline recommendations. This project will explore health professionals’ awareness of and adherence to the recently published DMD and CMT guidelines via an online survey administered on the REDCap platform (hosted by Murdoch Children's Research Institute). Health professionals (medical, nursing and allied health) who manage the clinical care and treatment of individuals with DMD and/or children and young people with CMT across Australia and New Zealand will be invited to participate in this once-only survey. The survey will be distributed to all Australian and New Zealand neuromuscular clinics and centres and through community health networks and professional associations. The overall aim is to determine current practice and implementation of clinical practice guidelines for neuromuscular disorders, specifically DMD and CMT and in particular relating to assessment and outcome measures (DMD) and exercise, physical activity and nutritional status (CMT). The findings from this project will provide preliminary evidence around awareness of guidelines, as well as enablers and barriers to compliance with guidelines. This information will be used to design tailored guideline implementation strategies and inform further research in the uptake of clinical practice guidelines." @default.
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- W4387302102 date "2023-10-01" @default.
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- W4387302102 title "P95 Implementing clinical guidelines for neuromuscular disorders" @default.
- W4387302102 doi "https://doi.org/10.1016/j.nmd.2023.07.402" @default.
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