The patient experience of having a stoma and its relation to nursing practice: implementation of qualitative evidence through clinical pathways

The aim of this article is to explore patients' experiences of having a stoma, in particular those relating to: emotion and social issues; changes in quality of life; feelings of fear, shame or frustration because of the altered lifestyle; and changes in roles and relationships and in their soc...

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Published in:Gastrointestinal nursing Vol. 14; no. 3; pp. 39 - 46
Main Authors: Capilla-Díaz, Concepción, Black, Pat, Bonill-de las Nieves, Candela, Gómez-Urquiza, Jose Luis, Zambrano, Sandra Hernández, Montoya-Juárez, Rafael, Gálvez-González, María, Martín-Muñoz, Begoña, Sánchez-Crisol, Inmaculada, Rivas-Marín, Concepción, Reina-Leal, Liliana Marcela, Pérez-Marfil, María Nieves, Hueso-Montoro, César
Format: Journal Article
Language:English
Published: London MA Healthcare 01-04-2016
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Abstract The aim of this article is to explore patients' experiences of having a stoma, in particular those relating to: emotion and social issues; changes in quality of life; feelings of fear, shame or frustration because of the altered lifestyle; and changes in roles and relationships and in their social environment. This article is part of a research project that employs a three-step method, including a metasynthesis method for international qualitative research, the development of clinical pathways for nursing diagnoses, interventions and outcomes, and the implementation and evaluation of these clinical pathways. This article describes the first phase of the research. The results show that, internationally, there are many similarities in the ways in which individuals with a stoma cope with having a stoma.
AbstractList The aim of this article is to explore patients' experiences of having a stoma, in particular those relating to: emotion and social issues ; changes in quality of life; feelings of fear, shame or frustration because of the altered lifestyle; and changes in roles and relationships and in their social environment. This article is part of a research project that employs a three-step method, including a metasynthesis method for international qualitative research, the development of clinical pathways for nursing diagnoses, interventions and outcomes, and the implementation and evaluation of these clinical pathways. This article describes the first phase of the research. The results show that, internationally, there are many similarities in the ways in which individuals with a stoma cope with having a stoma. References
The aim of this article is to explore patients' experiences of having a stoma, in particular those relating to: emotion and social issues; changes in quality of life; feelings of fear, shame or frustration because of the altered lifestyle; and changes in roles and relationships and in their social environment. This article is part of a research project that employs a three-step method, including a metasynthesis method for international qualitative research, the development of clinical pathways for nursing diagnoses, interventions and outcomes, and the implementation and evaluation of these clinical pathways. This article describes the first phase of the research. The results show that, internationally, there are many similarities in the ways in which individuals with a stoma cope with having a stoma.
Author Martín-Muñoz, Begoña
Sánchez-Crisol, Inmaculada
Black, Pat
Gálvez-González, María
Capilla-Díaz, Concepción
Pérez-Marfil, María Nieves
Rivas-Marín, Concepción
Hueso-Montoro, César
Reina-Leal, Liliana Marcela
Gómez-Urquiza, Jose Luis
Montoya-Juárez, Rafael
Bonill-de las Nieves, Candela
Zambrano, Sandra Hernández
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Cano Arana A (B12) 2010
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Title The patient experience of having a stoma and its relation to nursing practice: implementation of qualitative evidence through clinical pathways
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