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2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema

BACKGROUND: We published the Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema (HAE; C1 inhibitor [C1-INH] deficiency) and updated this as Hereditary angioedema: a current state-of-the-art review: Canadian Hungarian 2007 International...

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Autores principales: Bowen, Tom, Cicardi, Marco, Farkas, Henriette, Bork, Konrad, Longhurst, Hilary J, Zuraw, Bruce, Aygoeren-Pürsün, Emel, Craig, Timothy, Binkley, Karen, Hebert, Jacques, Ritchie, Bruce, Bouillet, Laurence, Betschel, Stephen, Cogar, Della, Dean, John, Devaraj, Ramachand, Hamed, Azza, Kamra, Palinder, Keith, Paul K, Lacuesta, Gina, Leith, Eric, Lyons, Harriet, Mace, Sean, Mako, Barbara, Neurath, Doris, Poon, Man-Chiu, Rivard, Georges-Etienne, Schellenberg, Robert, Rowan, Dereth, Rowe, Anne, Stark, Donald, Sur, Smeeksha, Tsai, Ellie, Warrington, Richard, Waserman, Susan, Ameratunga, Rohan, Bernstein, Jonathan, Björkander, Janne, Brosz, Kristylea, Brosz, John, Bygum, Anette, Caballero, Teresa, Frank, Mike, Fust, George, Harmat, George, Kanani, Amin, Kreuz, Wolfhart, Levi, Marcel, Li, Henry, Martinez-Saguer, Inmaculada, Moldovan, Dumitru, Nagy, Istvan, Nielsen, Erik W, Nordenfelt, Patrik, Reshef, Avner, Rusicke, Eva, Smith-Foltz, Sarah, Späth, Peter, Varga, Lilian, Xiang, Zhi Yu
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921362/
https://www.ncbi.nlm.nih.gov/pubmed/20667127
http://dx.doi.org/10.1186/1710-1492-6-24
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author Bowen, Tom
Cicardi, Marco
Farkas, Henriette
Bork, Konrad
Longhurst, Hilary J
Zuraw, Bruce
Aygoeren-Pürsün, Emel
Craig, Timothy
Binkley, Karen
Hebert, Jacques
Ritchie, Bruce
Bouillet, Laurence
Betschel, Stephen
Cogar, Della
Dean, John
Devaraj, Ramachand
Hamed, Azza
Kamra, Palinder
Keith, Paul K
Lacuesta, Gina
Leith, Eric
Lyons, Harriet
Mace, Sean
Mako, Barbara
Neurath, Doris
Poon, Man-Chiu
Rivard, Georges-Etienne
Schellenberg, Robert
Rowan, Dereth
Rowe, Anne
Stark, Donald
Sur, Smeeksha
Tsai, Ellie
Warrington, Richard
Waserman, Susan
Ameratunga, Rohan
Bernstein, Jonathan
Björkander, Janne
Brosz, Kristylea
Brosz, John
Bygum, Anette
Caballero, Teresa
Frank, Mike
Fust, George
Harmat, George
Kanani, Amin
Kreuz, Wolfhart
Levi, Marcel
Li, Henry
Martinez-Saguer, Inmaculada
Moldovan, Dumitru
Nagy, Istvan
Nielsen, Erik W
Nordenfelt, Patrik
Reshef, Avner
Rusicke, Eva
Smith-Foltz, Sarah
Späth, Peter
Varga, Lilian
Xiang, Zhi Yu
author_facet Bowen, Tom
Cicardi, Marco
Farkas, Henriette
Bork, Konrad
Longhurst, Hilary J
Zuraw, Bruce
Aygoeren-Pürsün, Emel
Craig, Timothy
Binkley, Karen
Hebert, Jacques
Ritchie, Bruce
Bouillet, Laurence
Betschel, Stephen
Cogar, Della
Dean, John
Devaraj, Ramachand
Hamed, Azza
Kamra, Palinder
Keith, Paul K
Lacuesta, Gina
Leith, Eric
Lyons, Harriet
Mace, Sean
Mako, Barbara
Neurath, Doris
Poon, Man-Chiu
Rivard, Georges-Etienne
Schellenberg, Robert
Rowan, Dereth
Rowe, Anne
Stark, Donald
Sur, Smeeksha
Tsai, Ellie
Warrington, Richard
Waserman, Susan
Ameratunga, Rohan
Bernstein, Jonathan
Björkander, Janne
Brosz, Kristylea
Brosz, John
Bygum, Anette
Caballero, Teresa
Frank, Mike
Fust, George
Harmat, George
Kanani, Amin
Kreuz, Wolfhart
Levi, Marcel
Li, Henry
Martinez-Saguer, Inmaculada
Moldovan, Dumitru
Nagy, Istvan
Nielsen, Erik W
Nordenfelt, Patrik
Reshef, Avner
Rusicke, Eva
Smith-Foltz, Sarah
Späth, Peter
Varga, Lilian
Xiang, Zhi Yu
author_sort Bowen, Tom
collection PubMed
description BACKGROUND: We published the Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema (HAE; C1 inhibitor [C1-INH] deficiency) and updated this as Hereditary angioedema: a current state-of-the-art review: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema. OBJECTIVE: To update the International Consensus Algorithm for the Diagnosis, Therapy and Management of Hereditary Angioedema (circa 2010). METHODS: The Canadian Hereditary Angioedema Network (CHAEN)/Réseau Canadien d'angioédème héréditaire (RCAH) http://www.haecanada.com and cosponsors University of Calgary and the Canadian Society of Allergy and Clinical Immunology (with an unrestricted educational grant from CSL Behring) held our third Conference May 15th to 16th, 2010 in Toronto Canada to update our consensus approach. The Consensus document was reviewed at the meeting and then circulated for review. RESULTS: This manuscript is the 2010 International Consensus Algorithm for the Diagnosis, Therapy and Management of Hereditary Angioedema that resulted from that conference. CONCLUSIONS: Consensus approach is only an interim guide to a complex disorder such as HAE and should be replaced as soon as possible with large phase III and IV clinical trials, meta analyses, and using data base registry validation of approaches including quality of life and cost benefit analyses, followed by large head-to-head clinical trials and then evidence-based guidelines and standards for HAE disease management.
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spelling pubmed-29213622010-08-14 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema Bowen, Tom Cicardi, Marco Farkas, Henriette Bork, Konrad Longhurst, Hilary J Zuraw, Bruce Aygoeren-Pürsün, Emel Craig, Timothy Binkley, Karen Hebert, Jacques Ritchie, Bruce Bouillet, Laurence Betschel, Stephen Cogar, Della Dean, John Devaraj, Ramachand Hamed, Azza Kamra, Palinder Keith, Paul K Lacuesta, Gina Leith, Eric Lyons, Harriet Mace, Sean Mako, Barbara Neurath, Doris Poon, Man-Chiu Rivard, Georges-Etienne Schellenberg, Robert Rowan, Dereth Rowe, Anne Stark, Donald Sur, Smeeksha Tsai, Ellie Warrington, Richard Waserman, Susan Ameratunga, Rohan Bernstein, Jonathan Björkander, Janne Brosz, Kristylea Brosz, John Bygum, Anette Caballero, Teresa Frank, Mike Fust, George Harmat, George Kanani, Amin Kreuz, Wolfhart Levi, Marcel Li, Henry Martinez-Saguer, Inmaculada Moldovan, Dumitru Nagy, Istvan Nielsen, Erik W Nordenfelt, Patrik Reshef, Avner Rusicke, Eva Smith-Foltz, Sarah Späth, Peter Varga, Lilian Xiang, Zhi Yu Allergy Asthma Clin Immunol Review BACKGROUND: We published the Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema (HAE; C1 inhibitor [C1-INH] deficiency) and updated this as Hereditary angioedema: a current state-of-the-art review: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema. OBJECTIVE: To update the International Consensus Algorithm for the Diagnosis, Therapy and Management of Hereditary Angioedema (circa 2010). METHODS: The Canadian Hereditary Angioedema Network (CHAEN)/Réseau Canadien d'angioédème héréditaire (RCAH) http://www.haecanada.com and cosponsors University of Calgary and the Canadian Society of Allergy and Clinical Immunology (with an unrestricted educational grant from CSL Behring) held our third Conference May 15th to 16th, 2010 in Toronto Canada to update our consensus approach. The Consensus document was reviewed at the meeting and then circulated for review. RESULTS: This manuscript is the 2010 International Consensus Algorithm for the Diagnosis, Therapy and Management of Hereditary Angioedema that resulted from that conference. CONCLUSIONS: Consensus approach is only an interim guide to a complex disorder such as HAE and should be replaced as soon as possible with large phase III and IV clinical trials, meta analyses, and using data base registry validation of approaches including quality of life and cost benefit analyses, followed by large head-to-head clinical trials and then evidence-based guidelines and standards for HAE disease management. BioMed Central 2010-07-28 /pmc/articles/PMC2921362/ /pubmed/20667127 http://dx.doi.org/10.1186/1710-1492-6-24 Text en Copyright ©2010 Bowen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Bowen, Tom
Cicardi, Marco
Farkas, Henriette
Bork, Konrad
Longhurst, Hilary J
Zuraw, Bruce
Aygoeren-Pürsün, Emel
Craig, Timothy
Binkley, Karen
Hebert, Jacques
Ritchie, Bruce
Bouillet, Laurence
Betschel, Stephen
Cogar, Della
Dean, John
Devaraj, Ramachand
Hamed, Azza
Kamra, Palinder
Keith, Paul K
Lacuesta, Gina
Leith, Eric
Lyons, Harriet
Mace, Sean
Mako, Barbara
Neurath, Doris
Poon, Man-Chiu
Rivard, Georges-Etienne
Schellenberg, Robert
Rowan, Dereth
Rowe, Anne
Stark, Donald
Sur, Smeeksha
Tsai, Ellie
Warrington, Richard
Waserman, Susan
Ameratunga, Rohan
Bernstein, Jonathan
Björkander, Janne
Brosz, Kristylea
Brosz, John
Bygum, Anette
Caballero, Teresa
Frank, Mike
Fust, George
Harmat, George
Kanani, Amin
Kreuz, Wolfhart
Levi, Marcel
Li, Henry
Martinez-Saguer, Inmaculada
Moldovan, Dumitru
Nagy, Istvan
Nielsen, Erik W
Nordenfelt, Patrik
Reshef, Avner
Rusicke, Eva
Smith-Foltz, Sarah
Späth, Peter
Varga, Lilian
Xiang, Zhi Yu
2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
title 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
title_full 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
title_fullStr 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
title_full_unstemmed 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
title_short 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
title_sort 2010 international consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921362/
https://www.ncbi.nlm.nih.gov/pubmed/20667127
http://dx.doi.org/10.1186/1710-1492-6-24
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