Development of rapid guidelines : 2. A qualitative study with who guideline developers

ABSTRACT: Background: Situations such as public health emergencies and outbreaks necessitate the development and publication of high-quality recommendations within a condensed timeframe. For example, WHO has produced examples of and guidance for the development of rapid guidelines (RGs). However, mo...

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Autores:
Flórez Gómez, Iván Darío
Morgan, Rebecca L.
Falavigna, Maicon
Kowalski, Sérgio C.
Zhang, Yuan
Etxeandia Ikobaltzeta, Itziar
Santesso, Nancy
Wiercioch, Wojtek
Schünemann, Holger J.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2018
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/33967
Acceso en línea:
https://hdl.handle.net/10495/33967
https://health-policy-systems.biomedcentral.com/articles/10.1186/s12961-018-0329-6
Palabra clave:
Guideline
Guía
Emergencies
Urgencias Médicas
Methodology
Metodología
Practice Guideline
Guía de Práctica Clínica
Guideline development
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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repository_id_str
dc.title.spa.fl_str_mv Development of rapid guidelines : 2. A qualitative study with who guideline developers
title Development of rapid guidelines : 2. A qualitative study with who guideline developers
spellingShingle Development of rapid guidelines : 2. A qualitative study with who guideline developers
Guideline
Guía
Emergencies
Urgencias Médicas
Methodology
Metodología
Practice Guideline
Guía de Práctica Clínica
Guideline development
title_short Development of rapid guidelines : 2. A qualitative study with who guideline developers
title_full Development of rapid guidelines : 2. A qualitative study with who guideline developers
title_fullStr Development of rapid guidelines : 2. A qualitative study with who guideline developers
title_full_unstemmed Development of rapid guidelines : 2. A qualitative study with who guideline developers
title_sort Development of rapid guidelines : 2. A qualitative study with who guideline developers
dc.creator.fl_str_mv Flórez Gómez, Iván Darío
Morgan, Rebecca L.
Falavigna, Maicon
Kowalski, Sérgio C.
Zhang, Yuan
Etxeandia Ikobaltzeta, Itziar
Santesso, Nancy
Wiercioch, Wojtek
Schünemann, Holger J.
dc.contributor.author.none.fl_str_mv Flórez Gómez, Iván Darío
Morgan, Rebecca L.
Falavigna, Maicon
Kowalski, Sérgio C.
Zhang, Yuan
Etxeandia Ikobaltzeta, Itziar
Santesso, Nancy
Wiercioch, Wojtek
Schünemann, Holger J.
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Investigación Clínica en Enfermedades del Niño y del Adolescente - Pediaciencias
dc.subject.decs.none.fl_str_mv Guideline
Guía
Emergencies
Urgencias Médicas
Methodology
Metodología
Practice Guideline
Guía de Práctica Clínica
topic Guideline
Guía
Emergencies
Urgencias Médicas
Methodology
Metodología
Practice Guideline
Guía de Práctica Clínica
Guideline development
dc.subject.proposal.spa.fl_str_mv Guideline development
description ABSTRACT: Background: Situations such as public health emergencies and outbreaks necessitate the development and publication of high-quality recommendations within a condensed timeframe. For example, WHO has produced examples of and guidance for the development of rapid guidelines (RGs). However, more information is needed to understand the experiences and perceptions of guideline developers. This is the second of a series of three articles addressing methodological issues around RGs. This study describes the perceptions and experiences of guideline developers at WHO about RGs. Methods: We conducted interviews consisting of open- and closed-ended questions with guideline developers at WHO. Our analysis described the definition and rationale of RGs, the differences from regular guidelines with regard to timelines from topic definition until publication, barriers to identifying the evidence and the lack of a standard methodology to develop RGs. Results: We interviewed 10 participants, the majority of whom were comfortable with the current WHO definition of RGs. Most stated that the rationale for developing RGs should be in response to new evidence about efficacy, cost-effectiveness or safety. Respondents differed with regards to the amount of time RGs should take. While the majority of participants agreed that guidelines should be based on a systematic review, this step in the process was considered the most time and resource intensive. Challenges for developing RGs included limited personnel and financial resources as well as the lack of evidence. Facilitators, in turn, that may improve RG development include additional financial and personnel resources as well as the use of virtual meetings. Conclusions: While our study suggests a strong need and rationale for the development of RGs, standardisation of timelines and guidance on panel composition, peer-review process, conduct of meetings and sources of permissible evidence require further research.
publishDate 2018
dc.date.issued.none.fl_str_mv 2018
dc.date.accessioned.none.fl_str_mv 2023-03-13T20:30:27Z
dc.date.available.none.fl_str_mv 2023-03-13T20:30:27Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.issn.none.fl_str_mv 1478-4505
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/33967
dc.identifier.doi.none.fl_str_mv 10.1186/s12961-018-0329-6
dc.identifier.url.spa.fl_str_mv https://health-policy-systems.biomedcentral.com/articles/10.1186/s12961-018-0329-6
identifier_str_mv 1478-4505
10.1186/s12961-018-0329-6
url https://hdl.handle.net/10495/33967
https://health-policy-systems.biomedcentral.com/articles/10.1186/s12961-018-0329-6
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Health Res. Policy Syst.
dc.relation.citationendpage.spa.fl_str_mv 9
dc.relation.citationissue.spa.fl_str_mv 62
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 16
dc.relation.ispartofjournal.spa.fl_str_mv Health Research Policy and Systems
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dc.publisher.place.spa.fl_str_mv Londres, Inglaterra
dc.publisher.faculty.spa.fl_str_mv sin facultad - programa
institution Universidad de Antioquia
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spelling Flórez Gómez, Iván DaríoMorgan, Rebecca L.Falavigna, MaiconKowalski, Sérgio C.Zhang, YuanEtxeandia Ikobaltzeta, ItziarSantesso, NancyWiercioch, WojtekSchünemann, Holger J.Grupo de Investigación Clínica en Enfermedades del Niño y del Adolescente - Pediaciencias2023-03-13T20:30:27Z2023-03-13T20:30:27Z20181478-4505https://hdl.handle.net/10495/3396710.1186/s12961-018-0329-6https://health-policy-systems.biomedcentral.com/articles/10.1186/s12961-018-0329-6ABSTRACT: Background: Situations such as public health emergencies and outbreaks necessitate the development and publication of high-quality recommendations within a condensed timeframe. For example, WHO has produced examples of and guidance for the development of rapid guidelines (RGs). However, more information is needed to understand the experiences and perceptions of guideline developers. This is the second of a series of three articles addressing methodological issues around RGs. This study describes the perceptions and experiences of guideline developers at WHO about RGs. Methods: We conducted interviews consisting of open- and closed-ended questions with guideline developers at WHO. Our analysis described the definition and rationale of RGs, the differences from regular guidelines with regard to timelines from topic definition until publication, barriers to identifying the evidence and the lack of a standard methodology to develop RGs. Results: We interviewed 10 participants, the majority of whom were comfortable with the current WHO definition of RGs. Most stated that the rationale for developing RGs should be in response to new evidence about efficacy, cost-effectiveness or safety. Respondents differed with regards to the amount of time RGs should take. While the majority of participants agreed that guidelines should be based on a systematic review, this step in the process was considered the most time and resource intensive. Challenges for developing RGs included limited personnel and financial resources as well as the lack of evidence. Facilitators, in turn, that may improve RG development include additional financial and personnel resources as well as the use of virtual meetings. Conclusions: While our study suggests a strong need and rationale for the development of RGs, standardisation of timelines and guidance on panel composition, peer-review process, conduct of meetings and sources of permissible evidence require further research.COL00587849application/pdfengBMC (BioMed Central)Londres, Inglaterrasin facultad - programahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Development of rapid guidelines : 2. 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