Lang Tali, McLean Iain, Shin Jenna, Jackson Victoria, Lawrenson Isobel, Zipper Belinda, Yeung Alex, Evans Andrew, Dewson Grant
Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Department of Medical Biology, University of Melbourne, Parkville, Melbourne, VIC, Australia.
NPJ Parkinsons Dis. 2025 Apr 30;11(1):104. doi: 10.1038/s41531-025-00968-3.
There is limited data about experiences of people with Parkinson's (PwP) in Australia. This study, initiated and co-designed by PwP, surveyed 385 participants nationally (335 fully completed the questionnaire). Participants living in capital and regional city centers reported satisfaction with clinical care during diagnostic consultation at approximately 40%, with satisfaction less in rural areas (26%). 68% of participants reported inadequate involvement in discussions about treatment and care planning and 77% were dissatisfied with the support following diagnosis. Respondents reported low referral rates to allied health services such as physiotherapy (22%) and mental health services (17%). Feedback indicated support could improved by increased access to Parkinson's disease Clinical Nurse Specialists and to educational resources and support. Findings highlight the need to establish Australian guidelines for Parkinson's clinical management, greater resourcing for clinicians including development of educational programs, and creation of Australian-centric educational resources to improve quality of care for PwP.
关于澳大利亚帕金森病患者(PwP)经历的数据有限。这项由帕金森病患者发起并共同设计的研究,在全国范围内调查了385名参与者(335人完整填写了问卷)。居住在首府和地区城市中心的参与者对诊断咨询期间的临床护理满意度约为40%,农村地区的满意度较低(26%)。68%的参与者表示在治疗和护理计划讨论中参与不足,77%的人对诊断后的支持不满意。受访者报告称,转介到物理治疗(22%)和心理健康服务(17%)等联合健康服务的比例较低。反馈表明,增加帕金森病临床护理专家的可及性、教育资源和支持,有助于改善支持情况。研究结果强调,需要制定澳大利亚帕金森病临床管理指南,为临床医生提供更多资源,包括开展教育项目,并创建以澳大利亚为中心的教育资源,以提高对帕金森病患者的护理质量。