Literature DB >> 16963405

How does current care practice influence the experience of a new diagnosis of motor neuron disease? A qualitative study of current guidelines-based practice.

Heino Hugel1, Nicky Grundy, Sally Rigby, Carolyn A Young.   

Abstract

Management during the diagnostic phase of MND is considered an important influence on the patient's further disease course. Guidelines for the management of MND have been developed, but little is known on how recommended practices influence patients' experience of a new diagnosis of MND. We undertook an interview-based study exploring issues surrounding the diagnosis of MND in a sample of consecutive patients recently diagnosed at a neurosciences centre. Data were analysed with Interpretative Phenomenological Analysis (IPA). Thirteen patients were recruited to the study. The major themes identified in descending order were 'Family/carers', 'Communication of the diagnosis', 'Reaction to the diagnosis', 'Physical difficulties', 'Time before diagnosis', 'Information', 'Future', 'Coping with the diagnosis' and 'Formal support'. Communication was perceived satisfactory if handled according to existing guidelines. Physical difficulties impacted considerably on patients' lives. Delays in the diagnostic process appeared in various interviews. Five patients were avoiding information following the diagnosis. Some patients commented on an increasing number of uncoordinated services becoming involved after their diagnosis. This study supports the current international guidelines for MND care around diagnosis from the patients' perspective and underlines the importance of a multi-disciplinary, coordinated approach for patients with MND from diagnosis onwards.

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Year:  2006        PMID: 16963405     DOI: 10.1080/14660820600601051

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  7 in total

1.  Emotional distress and well-being among people with motor neurone disease (MND) and their family caregivers: a qualitative interview study.

Authors:  Cathryn Pinto; Adam W A Geraghty; Lucy Yardley; Laura Dennison
Journal:  BMJ Open       Date:  2021-08-17       Impact factor: 3.006

2.  Engaging in patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis: the views of health professionals.

Authors:  Anne Hogden; David Greenfield; Peter Nugus; Matthew C Kiernan
Journal:  Patient Prefer Adherence       Date:  2012-09-27       Impact factor: 2.711

Review 3.  Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis.

Authors:  Andrew Soundy; Nicola Condon
Journal:  Front Psychol       Date:  2015-05-12

4.  Gastrostomy uptake in motor neurone disease: a mixed-methods study of patients' decision making.

Authors:  Julie Labra; Anne Hogden; Emma Power; Natalie James; Victoria M Flood
Journal:  BMJ Open       Date:  2020-02-25       Impact factor: 2.692

5.  What influences patient decision-making in amyotrophic lateral sclerosis multidisciplinary care? A study of patient perspectives.

Authors:  Anne Hogden; David Greenfield; Peter Nugus; Matthew C Kiernan
Journal:  Patient Prefer Adherence       Date:  2012-11-27       Impact factor: 2.711

6.  The experiences of, and need for, palliative care for people with motor neurone disease and their informal caregivers: A qualitative systematic review.

Authors:  Kate Flemming; Victoria Turner; Samantha Bolsher; Bill Hulme; Elizabeth McHugh; Ian Watt
Journal:  Palliat Med       Date:  2020-04-14       Impact factor: 4.762

7.  Healthcare Utilisation and Satisfaction with Care in Patients with Amyotrophic Lateral Sclerosis - An Observational Study.

Authors:  Marie Kierkegaard; Kristina Gottberg; Sverker Johansson; Susanne Littorin; Petter Sandstedt; Charlotte Ytterberg; Lotta Widén Holmqvist
Journal:  J Neuromuscul Dis       Date:  2021
  7 in total

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