Transparent development of the WHO rapid advice guidelines.

Emerging health problems require rapid advice. We describe the development and pilot testing of a systematic, transparent approach used by the World Health Organization (WHO) to develop rapid advice guidelines in response to requests from member states confronted with uncertainty about the pharmacol...

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Main Authors: Holger J Schünemann, Suzanne R Hill, Meetali Kakad, Gunn E Vist, Richard Bellamy, Lauren Stockman, Torbjørn Fosen Wisløff, Chris Del Mar, Frederick Hayden, Timothy M Uyeki, Jeremy Farrar, Yazdan Yazdanpanah, Howard Zucker, John Beigel, Tawee Chotpitayasunondh, Tran Tinh Hien, Bülent Ozbay, Norio Sugaya, Andrew D Oxman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-05-01
Series:PLoS Medicine
Online Access:https://doi.org/10.1371/journal.pmed.0040119
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author Holger J Schünemann
Suzanne R Hill
Meetali Kakad
Gunn E Vist
Richard Bellamy
Lauren Stockman
Torbjørn Fosen Wisløff
Chris Del Mar
Frederick Hayden
Timothy M Uyeki
Jeremy Farrar
Yazdan Yazdanpanah
Howard Zucker
John Beigel
Tawee Chotpitayasunondh
Tran Tinh Hien
Bülent Ozbay
Norio Sugaya
Andrew D Oxman
author_facet Holger J Schünemann
Suzanne R Hill
Meetali Kakad
Gunn E Vist
Richard Bellamy
Lauren Stockman
Torbjørn Fosen Wisløff
Chris Del Mar
Frederick Hayden
Timothy M Uyeki
Jeremy Farrar
Yazdan Yazdanpanah
Howard Zucker
John Beigel
Tawee Chotpitayasunondh
Tran Tinh Hien
Bülent Ozbay
Norio Sugaya
Andrew D Oxman
author_sort Holger J Schünemann
collection DOAJ
description Emerging health problems require rapid advice. We describe the development and pilot testing of a systematic, transparent approach used by the World Health Organization (WHO) to develop rapid advice guidelines in response to requests from member states confronted with uncertainty about the pharmacological management of avian influenza A (H5N1) virus infection. We first searched for systematic reviews of randomized trials of treatment and prevention of seasonal influenza and for non-trial evidence on H5N1 infection, including case reports and animal and in vitro studies. A panel of clinical experts, clinicians with experience in treating patients with H5N1, influenza researchers, and methodologists was convened for a two-day meeting. Panel members reviewed the evidence prior to the meeting and agreed on the process. It took one month to put together a team to prepare the evidence profiles (i.e., summaries of the evidence on important clinical and policy questions), and it took the team only five weeks to prepare and revise the evidence profiles and to prepare draft guidelines prior to the panel meeting. A draft manuscript for publication was prepared within 10 days following the panel meeting. Strengths of the process include its transparency and the short amount of time used to prepare these WHO guidelines. The process could be improved by shortening the time required to commission evidence profiles. Further development is needed to facilitate stakeholder involvement, and evaluate and ensure the guideline's usefulness.
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spelling doaj.art-5a51f17ead154367847cbb1dacf36a6d2022-12-21T20:35:05ZengPublic Library of Science (PLoS)PLoS Medicine1549-12771549-16762007-05-0145e11910.1371/journal.pmed.0040119Transparent development of the WHO rapid advice guidelines.Holger J SchünemannSuzanne R HillMeetali KakadGunn E VistRichard BellamyLauren StockmanTorbjørn Fosen WisløffChris Del MarFrederick HaydenTimothy M UyekiJeremy FarrarYazdan YazdanpanahHoward ZuckerJohn BeigelTawee ChotpitayasunondhTran Tinh HienBülent OzbayNorio SugayaAndrew D OxmanEmerging health problems require rapid advice. We describe the development and pilot testing of a systematic, transparent approach used by the World Health Organization (WHO) to develop rapid advice guidelines in response to requests from member states confronted with uncertainty about the pharmacological management of avian influenza A (H5N1) virus infection. We first searched for systematic reviews of randomized trials of treatment and prevention of seasonal influenza and for non-trial evidence on H5N1 infection, including case reports and animal and in vitro studies. A panel of clinical experts, clinicians with experience in treating patients with H5N1, influenza researchers, and methodologists was convened for a two-day meeting. Panel members reviewed the evidence prior to the meeting and agreed on the process. It took one month to put together a team to prepare the evidence profiles (i.e., summaries of the evidence on important clinical and policy questions), and it took the team only five weeks to prepare and revise the evidence profiles and to prepare draft guidelines prior to the panel meeting. A draft manuscript for publication was prepared within 10 days following the panel meeting. Strengths of the process include its transparency and the short amount of time used to prepare these WHO guidelines. The process could be improved by shortening the time required to commission evidence profiles. Further development is needed to facilitate stakeholder involvement, and evaluate and ensure the guideline's usefulness.https://doi.org/10.1371/journal.pmed.0040119
spellingShingle Holger J Schünemann
Suzanne R Hill
Meetali Kakad
Gunn E Vist
Richard Bellamy
Lauren Stockman
Torbjørn Fosen Wisløff
Chris Del Mar
Frederick Hayden
Timothy M Uyeki
Jeremy Farrar
Yazdan Yazdanpanah
Howard Zucker
John Beigel
Tawee Chotpitayasunondh
Tran Tinh Hien
Bülent Ozbay
Norio Sugaya
Andrew D Oxman
Transparent development of the WHO rapid advice guidelines.
PLoS Medicine
title Transparent development of the WHO rapid advice guidelines.
title_full Transparent development of the WHO rapid advice guidelines.
title_fullStr Transparent development of the WHO rapid advice guidelines.
title_full_unstemmed Transparent development of the WHO rapid advice guidelines.
title_short Transparent development of the WHO rapid advice guidelines.
title_sort transparent development of the who rapid advice guidelines
url https://doi.org/10.1371/journal.pmed.0040119
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