دورية أكاديمية

Familial amyloid polyneuropathy: elaboration of a therapeutic patient education programme, 'EdAmyl'.

التفاصيل البيبلوغرافية
العنوان: Familial amyloid polyneuropathy: elaboration of a therapeutic patient education programme, 'EdAmyl'.
المؤلفون: Théaudin, Marie, Cauquil, Cécile, Antonini, Teresa, Algalarrondo, Vincent, Labeyrie, Céline, Aycaguer, Sophie, Clément, Mireille, Kubezyk, Marie, Nonnez, Géraldine, Morier, Agnès, Bourges, Catherine, Darras, Amandine, Mouzat, Laurence, Adams, David
المصدر: Amyloid; Dec2014, Vol. 21 Issue 4, p225-230, 6p
مصطلحات موضوعية: TRANSTHYRETIN, AMYLOIDOSIS treatment, AUTONOMIC nervous system, PATIENT education, EDUCATION & training services industry, MEDICAL needs assessment, QUALITATIVE research, TEACHING & society, SOCIETIES
مستخلص: Background: Transthyretin-related amyloidosis (ATTR) is an autosomal dominant disease affecting the peripheral and autonomic nervous system, heart, eyes and kidneys. It is the most disabling hereditary polyneuropathy in adults. The French National Reference centre for this disease was accredited in 2005 with 10 lines of action. One of them is to inform and educate patients about their disease to improve their care and reduce morbidities. We thus decided to elaborate a therapeutic patient education (TPE) programme, starting with patients' needs assessment. Methods: A qualitative research study was conducted with one-to-one semi-structured interviews of selected individuals. Recorded interviews were analysed to identify the skills that patients need to acquire. A TPE programme was elaborated on the basis of these findings. Results: Seven patients, one asymptomatic carrier and two healthy spouses were interviewed. Analysis of the interviews showed that interviewees had a good knowledge of the disease and its symptoms but they had difficulties explaining the disease mechanism and did not have an adequate knowledge of the available treatment options, although they knew that liver transplant might halt progression of the disease. ATTR amyloidosis appeared to have a major negative impact on the patient's physical and mental well-being. Patients feared loss of autonomy and having to require assistance from their relatives and spouses. All interviewees were keen to participate in a TPE programme. Based on this needs assessment, we identified seven skills that patients need to acquire and several pedagogical goals to be achieved during the education programme. An interdisciplinary team then elaborated a complete TPE programme. Conclusion: Elaboration of a TPE programme for ATTR amyloidosis required to obtain useful information from the patients themselves, and their relatives, concerning their perception of their disease. This needs' assessment constituted the basis for designing the first TPE programme, to our knowledge, for ATTR amyloidosis. After translation, this programme could be applied in other EU countries and worldwide for this rare disease. [ABSTRACT FROM AUTHOR]
Copyright of Amyloid is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:13506129
DOI:10.3109/13506129.2014.941463