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Parkinson's disease progressively limits patients at different levels and as a result family members play a key role in their care. However, studies show lack of an integrative approach in Primary Care to respond to the difficulties and psychosocial changes experienced by them. The aim of this study is to evaluate the effects of a multidisciplinary psychoeducational intervention focusing on improving coping skills, the psychosocial adjustment to Parkinson's disease and the quality of life in patients and family carers in a Primary Care setting. Methods: This quasi-experimental study with control group and mixed methods was designed to evaluate a multidisciplinary psychoeducational intervention. Based on the study power calculations, 100 people with Parkinson's disease and 100 family carers will be recruited and assigned to two groups. The intervention group will receive the ReNACE psychoeducational intervention. The control group will be given a general educational programme. The study will be carried out in six community-based health centres. The results obtained from the two groups will be collected for evaluation at three time points: at baseline, immediately after the intervention and at 6 months post-intervention. The results will be measured with these instruments: the Quality of Life Scale PDQ-39 for patients and the Scale of Quality of Life of Care-givers SQLC for family carers, and for all participants the Psychosocial Adjustment to Illness scale and the Brief COPE Inventory. Focus groups will be organised with some patients and family carers who will have received the ReNACE psychoeducational intervention and also with the healthcare professionals involved in its development. Discussion: An important gap exists in the knowledge and application of interventions with a psychosocial approach for people with PD and family carers as a whole. This study will promote this comprehensive approach in Primary Care, which will clearly contribute in the existing knowledge and could reduce the burden of PD for patients and family carers, and also in other long-term conditions.

Findings generated from this concept analysis can raise awareness of Living with chronic illness so that this process could be assessed in a correct and uniform way in the clinical community and improved when needed.

Fundamento. La incidencia de errores de administración de medicación (EAM) es alta y costosa para pacientes e instituciones sanitarias. En su ocurrencia intervienen factores humanos y del entorno de trabajo. El objetivo de este trabajo es identificar los factores del entorno de trabajo que se relacionan con la ocurrencia de EAMs en el ámbito hospitalario. Metodología. Se llevó a cabo una revisión narrativa de la literatura. Se incluyeron 8 artículos tras revisar las bases de datos MEDLINE, CINAHL y COCHRANE LIBRARY, durante el periodo 2002-2012. Resultados. Las distracciones e interrupciones, la sobrecarga de trabajo, el diseño de las unidades y las características del material han sido destacados entre los factores del entorno de trabajo que intervienen en la ocurrencia de errores de administración de medicación. Conclusiones. La creación de artefactos organizacionales para reducir las interrupciones; la implicación del paciente en la administración de medicación; la introducción de nuevas tecnologías y la mejora del etiquetado de los medicamentos puede ayudar a reducir la incidencia de errores de administración de medicación. Para avanzar en la identificación y gestión de factores precursores de errores de administración de medicación se recomienda la realización de estudios de cohortes prospectivas o revisiones.