2026-04-29T07:25:39Zhttps://repisalud.isciii.es/rest/oai/request
oai:repisalud.isciii.es:20.500.12105/182702024-11-28T15:29:16Zcom_20.500.12105_15322com_20.500.12105_2051col_20.500.12105_16927
Repisalud author Hurtado, María M. author Quemada, Casta author García-Herrera, José María author Morales-Asencio, José Miguel authoraffiliation [Hurtado,MM; Quemada,C; García-Herrera,JM] Mental Health Unit, Regional University Hospital, Málaga, Spain. [Hurtado,MM; Quemada,C; Morales-Asencio,JM] Institute of Biomedical Research of Málaga (IBIMA), Málaga, Spain. [Morales-Asencio,JM] Faculty of Health Sciences, University of Málaga, Málaga, Spain. 2024-02-19T15:25:17Z 2024-02-19T15:25:17Z 2021-02-23 1369-6513 http://hdl.handle.net/10668/4251 http://hdl.handle.net/20.500.12105/18270 33621426 10.1111/hex.13193 1369-7625 Health Expectations : An International Journal of Public Participation in Health Care and Health Policy ntroduction: The aim of this study is to analyse different ways of participation dur ing the development of a clinical guideline to improve the early detection of psycho sis and to deploy a comprehensive treatment plan to improve prognosis and social integration. Materials and method: The clinical guideline was developed using the ADAPTE method with the participation of 40 authors and 80 external reviewers. The process was divided into three major phases: set up, adaptation and finalization. During adap tation and completion, a total of 44 patients and 18 family caregivers were involved.Results and conclusions: The different roles assumed by the patients and their family caregivers were described, depending on the panel in which they participated, with diverse grades of complexity: a user as author, integration of the results of qualitative research with the participation of local users and family caregivers, 13 users as indi vidual external reviewers and the participation of users and caregiver organizations in the external review. In the guideline, contributions from patients during the quali tative research were included in an innovative way, placing them just behind the rec ommendations. On the other hand, the results of the family caregivers’ study were included in a specific area of uncertainty. Further, the expressed point of view was considered as the collective demands of users and family caregivers’ organizations in the cost-benefit analysis made by the organizing committee. There were diverse ways to conduct direct patient participation during the guideline development, en suring that their individual experiences contributed significantly to the final version. eng ADAPTE methodology Clinical guidelines Patients involvement Psychoses Schizophrenia Guía de práctica clínica Participación del paciente Trastornos neurocognitivos Esquizofrenia Cuidadores Use of the ADAPTE method to develop a clinical guideline for the improvement of psychoses and schizophrenia care: Example of involvement and participation of patients and family caregivers research article