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...
- 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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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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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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1478-4505 |
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https://hdl.handle.net/10495/33967 |
| dc.identifier.doi.none.fl_str_mv |
10.1186/s12961-018-0329-6 |
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https://health-policy-systems.biomedcentral.com/articles/10.1186/s12961-018-0329-6 |
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1478-4505 10.1186/s12961-018-0329-6 |
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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. |
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9 |
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62 |
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1 |
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16 |
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Health Research Policy and Systems |
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http://creativecommons.org/licenses/by/2.5/co/ |
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https://creativecommons.org/licenses/by/4.0/ |
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application/pdf |
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BMC (BioMed Central) |
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Londres, Inglaterra |
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sin facultad - programa |
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Universidad de Antioquia |
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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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