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Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment
BACKGROUND: Pulmonary fibrosis (PF) is a rare, progressive disease that affects patients and their loved ones on many levels. We sought to better understand the needs and interests of PF patients and their loved ones (collectively “reader-participants”) by systematically analyzing their engagement w...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709949/ https://www.ncbi.nlm.nih.gov/pubmed/26754048 http://dx.doi.org/10.1186/s12890-016-0167-7 |
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author | Albright, Karen Walker, Tarik Baird, Susan Eres, Linda Farnsworth, Tara Fier, Kaitlin Kervitsky, Dolly Korn, Marjorie Lederer, David J. McCormick, Mark Steiner, John F. Vierzba, Thomas Wamboldt, Frederick S. Swigris, Jeffrey J. |
author_facet | Albright, Karen Walker, Tarik Baird, Susan Eres, Linda Farnsworth, Tara Fier, Kaitlin Kervitsky, Dolly Korn, Marjorie Lederer, David J. McCormick, Mark Steiner, John F. Vierzba, Thomas Wamboldt, Frederick S. Swigris, Jeffrey J. |
author_sort | Albright, Karen |
collection | PubMed |
description | BACKGROUND: Pulmonary fibrosis (PF) is a rare, progressive disease that affects patients and their loved ones on many levels. We sought to better understand the needs and interests of PF patients and their loved ones (collectively “reader-participants”) by systematically analyzing their engagement with the World Wide Web (the current version referred to as Web 2.0). METHODS: Data were collected from three PF-focused, interactive websites hosted by physician-investigators with expertise in PF. All data generated by reader-participants for approximately 10 months were downloaded and then analyzed using qualitative content analysis methods. RESULTS: PF experts posted 38 blog entries and reader-participants posted 40 forum entries. Blogs received 363 responses, and forum entries received 108 responses from reader-participants. Reader-participants primarily used the three websites to seek information from or offer a contribution to the PF community. Information was sought about PF symptoms, diagnosis, prognosis, treatments, research, pathophysiology, and disease origin; reader-participants also made requests for new posts and pleas for research and sought clarification on existing content. Contributions included personal narratives about experiences with PF, descriptions of activities or behaviors found to be helpful with PF symptoms, resources or information about PF, and supportive comments to other PF sufferers. CONCLUSIONS: PF patients and their loved ones engage the Web 2.0 environment at these PF-focused sites to satisfy their needs to better understand PF and its impacts and to support others facing similar challenges. Clinicians may find it beneficial to encourage PF patients’ involvement in internet forums that foster dynamic, bi-directional information sharing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0167-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4709949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47099492016-01-13 Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment Albright, Karen Walker, Tarik Baird, Susan Eres, Linda Farnsworth, Tara Fier, Kaitlin Kervitsky, Dolly Korn, Marjorie Lederer, David J. McCormick, Mark Steiner, John F. Vierzba, Thomas Wamboldt, Frederick S. Swigris, Jeffrey J. BMC Pulm Med Research Article BACKGROUND: Pulmonary fibrosis (PF) is a rare, progressive disease that affects patients and their loved ones on many levels. We sought to better understand the needs and interests of PF patients and their loved ones (collectively “reader-participants”) by systematically analyzing their engagement with the World Wide Web (the current version referred to as Web 2.0). METHODS: Data were collected from three PF-focused, interactive websites hosted by physician-investigators with expertise in PF. All data generated by reader-participants for approximately 10 months were downloaded and then analyzed using qualitative content analysis methods. RESULTS: PF experts posted 38 blog entries and reader-participants posted 40 forum entries. Blogs received 363 responses, and forum entries received 108 responses from reader-participants. Reader-participants primarily used the three websites to seek information from or offer a contribution to the PF community. Information was sought about PF symptoms, diagnosis, prognosis, treatments, research, pathophysiology, and disease origin; reader-participants also made requests for new posts and pleas for research and sought clarification on existing content. Contributions included personal narratives about experiences with PF, descriptions of activities or behaviors found to be helpful with PF symptoms, resources or information about PF, and supportive comments to other PF sufferers. CONCLUSIONS: PF patients and their loved ones engage the Web 2.0 environment at these PF-focused sites to satisfy their needs to better understand PF and its impacts and to support others facing similar challenges. Clinicians may find it beneficial to encourage PF patients’ involvement in internet forums that foster dynamic, bi-directional information sharing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0167-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-12 /pmc/articles/PMC4709949/ /pubmed/26754048 http://dx.doi.org/10.1186/s12890-016-0167-7 Text en © Albright et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Albright, Karen Walker, Tarik Baird, Susan Eres, Linda Farnsworth, Tara Fier, Kaitlin Kervitsky, Dolly Korn, Marjorie Lederer, David J. McCormick, Mark Steiner, John F. Vierzba, Thomas Wamboldt, Frederick S. Swigris, Jeffrey J. Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment |
title | Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment |
title_full | Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment |
title_fullStr | Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment |
title_full_unstemmed | Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment |
title_short | Seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment |
title_sort | seeking and sharing: why the pulmonary fibrosis community engages the web 2.0 environment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709949/ https://www.ncbi.nlm.nih.gov/pubmed/26754048 http://dx.doi.org/10.1186/s12890-016-0167-7 |
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