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Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain
OBJECTIVES: The aim of this study was to explore the views and experiences of a group of Spanish women suffering from chronic migraine (CM). SETTING: Headache clinic at a university hospital in Madrid (Spain). PARTICIPANTS: Purposeful sampling of patients that attended a specialised headache clinic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724120/ https://www.ncbi.nlm.nih.gov/pubmed/28827275 http://dx.doi.org/10.1136/bmjopen-2017-017851 |
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author | Palacios-Ceña, Domingo Neira-Martín, Beatriz Silva-Hernández, Lorenzo Mayo-Canalejo, Diego Florencio, Lidiane Lima Fernández-de-las-Peñas, César García-Moreno, Héctor García-Azorín, David Cuadrado, María Luz |
author_facet | Palacios-Ceña, Domingo Neira-Martín, Beatriz Silva-Hernández, Lorenzo Mayo-Canalejo, Diego Florencio, Lidiane Lima Fernández-de-las-Peñas, César García-Moreno, Héctor García-Azorín, David Cuadrado, María Luz |
author_sort | Palacios-Ceña, Domingo |
collection | PubMed |
description | OBJECTIVES: The aim of this study was to explore the views and experiences of a group of Spanish women suffering from chronic migraine (CM). SETTING: Headache clinic at a university hospital in Madrid (Spain). PARTICIPANTS: Purposeful sampling of patients that attended a specialised headache clinic for the first time between June 2016 and February 2017 was performed. The patients included were females aged 18–65 and with positive diagnoses of CM according to the International Classification of Headache disorders (third edition, beta version), with or without medication overuse. Accordingly, 20 patients participated in the study with a mean age of 38.65 years (SD 13.85). DESIGN: Qualitative phenomenological study. METHODS: Data were collected through in-depth interviews, researchers’ field notes and patients’ drawings. A thematic analysis was performed following appropriate guidelines for qualitative research. RESULTS: Five main themes describing the significance of suffering emerged: (a) the shame of suffering from an invisible condition; (b) treatment: between need, scepticism and fear; (c) looking for physicians’ support and sincerity and fighting misconceptions; (d) limiting the impact on daily life through self-control; and (e) family and work: between understanding and disbelief. The disease is experienced as an invisible process, and the journey to diagnosis can be a long and tortuous one. Drug prescription by the physician is greeted with distrust and scepticism. Patients expect sincerity, support and the involvement of their doctors in relation to their disease. Pain becomes the main focus of the patient’s life, and it requires considerable self-control. The disease has a strong impact in the work and family environment, where the patient may feel misunderstood. CONCLUSIONS: Qualitative research offers insight into the way patients with CM experience their disease and it may be helpful in establishing a more fruitful relationship with these patients. |
format | Online Article Text |
id | pubmed-5724120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57241202017-12-19 Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain Palacios-Ceña, Domingo Neira-Martín, Beatriz Silva-Hernández, Lorenzo Mayo-Canalejo, Diego Florencio, Lidiane Lima Fernández-de-las-Peñas, César García-Moreno, Héctor García-Azorín, David Cuadrado, María Luz BMJ Open Qualitative Research OBJECTIVES: The aim of this study was to explore the views and experiences of a group of Spanish women suffering from chronic migraine (CM). SETTING: Headache clinic at a university hospital in Madrid (Spain). PARTICIPANTS: Purposeful sampling of patients that attended a specialised headache clinic for the first time between June 2016 and February 2017 was performed. The patients included were females aged 18–65 and with positive diagnoses of CM according to the International Classification of Headache disorders (third edition, beta version), with or without medication overuse. Accordingly, 20 patients participated in the study with a mean age of 38.65 years (SD 13.85). DESIGN: Qualitative phenomenological study. METHODS: Data were collected through in-depth interviews, researchers’ field notes and patients’ drawings. A thematic analysis was performed following appropriate guidelines for qualitative research. RESULTS: Five main themes describing the significance of suffering emerged: (a) the shame of suffering from an invisible condition; (b) treatment: between need, scepticism and fear; (c) looking for physicians’ support and sincerity and fighting misconceptions; (d) limiting the impact on daily life through self-control; and (e) family and work: between understanding and disbelief. The disease is experienced as an invisible process, and the journey to diagnosis can be a long and tortuous one. Drug prescription by the physician is greeted with distrust and scepticism. Patients expect sincerity, support and the involvement of their doctors in relation to their disease. Pain becomes the main focus of the patient’s life, and it requires considerable self-control. The disease has a strong impact in the work and family environment, where the patient may feel misunderstood. CONCLUSIONS: Qualitative research offers insight into the way patients with CM experience their disease and it may be helpful in establishing a more fruitful relationship with these patients. BMJ Publishing Group 2017-08-21 /pmc/articles/PMC5724120/ /pubmed/28827275 http://dx.doi.org/10.1136/bmjopen-2017-017851 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Qualitative Research Palacios-Ceña, Domingo Neira-Martín, Beatriz Silva-Hernández, Lorenzo Mayo-Canalejo, Diego Florencio, Lidiane Lima Fernández-de-las-Peñas, César García-Moreno, Héctor García-Azorín, David Cuadrado, María Luz Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain |
title | Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain |
title_full | Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain |
title_fullStr | Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain |
title_full_unstemmed | Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain |
title_short | Living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in Spain |
title_sort | living with chronic migraine: a qualitative study on female patients’ perspectives from a specialised headache clinic in spain |
topic | Qualitative Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724120/ https://www.ncbi.nlm.nih.gov/pubmed/28827275 http://dx.doi.org/10.1136/bmjopen-2017-017851 |
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