Receiving the news of a diagnosis of motor neuron disease: What does it take to make it better?
MetadataShow full item record
Our objectives were to identify the experiences of people with MND in receiving the diagnosis and to determine which aspects of breaking this bad news were associated with greater satisfaction with the way the diagnosis was delivered to them. An anonymous postal survey was facilitated by all MND associations in Australia, in 2014, and centred on the SPIKES protocol for communicating bad news. Of the patients (n?=?248, response rate 29%), 36% were dissatisfied with the delivery of the diagnosis and gave low ratings on the ability/skills of their neurologists to deliver the diagnosis. It was evident that the longer the patients spent with their neurologists during breaking such bad news, the more they were satisfied and the higher they rated the neurologists’ abilities/skills. The largest significant differences between neurologists rated as having high or low skills in delivering the diagnosis were in four domains: 1) responding empathically to the feelings of patient/family; 2) sharing the information and suggesting realistic goals; 3) exploring what patient/family are expecting or hoping for; and 4) making a plan and following through. In conclusion, with over one-third of patients dissatisfied with their experience, there is room for improvement in the practice of neurologists in specified areas that could form the basis for changing practice, and the development of standards and protocols likely to have implications at the international level.
Showing items related by title, author, creator and subject.
Breaking the news of a diagnosis of motor neurone disease: A national survey of neurologists’ perspectivesAoun, Samar; Breen, Lauren; Edis, R.; Henderson, R.; Oliver, D.; Howting, D.; O'Connor, M.; Birks, C. (2016)Communication of the diagnosis of MND is daunting for patients and neurologists. This study aimed to establish a knowledge base of current Australian practice of breaking the news of an MND diagnosis, to assess the ...
Australian family carer responses when a loved one receives a diagnosis of Motor Neurone Disease—“Our life has changed forever”O'Connor, M.; Aoun, Samar; Breen, Lauren (2018)While the experiences of family members supporting a person with a terminal illness are well documented, less is known about the needs of carers of people with neurological diseases, in particular, Motor Neurone Disease ...
Family carers' experiences of receiving the news of a diagnosis of Motor Neurone Disease: A national surveyAoun, Samar; Breen, Lauren; Oliver, D.; Henderson, R.; Edis, R.; O'Connor, M.; Howting, D.; Harris, R.; Birks, C. (2017)Family carers have a central role in the care and support of people with MND and face the challenges of the disease from diagnosis to progression and the multiple losses of MND, but their support needs are often neglected. ...