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Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease

BACKGROUND: Aspirin – exacerbated respiratory disease can prove difficult to control. Oral aspirin desensitization is effective, but has adverse effects and may not be cardio-protective at the high doses needed. OBJECTIVE: To examine the effectiveness of aspirin administered in lower doses via the n...

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Autores principales: Howe, Rachel, Mirakian, Rita M, Pillai, Prathap, Gane, Simon, Darby, Yvonne C, Scadding, Glenis K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114086/
https://www.ncbi.nlm.nih.gov/pubmed/25097720
http://dx.doi.org/10.1186/1939-4551-7-18
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author Howe, Rachel
Mirakian, Rita M
Pillai, Prathap
Gane, Simon
Darby, Yvonne C
Scadding, Glenis K
author_facet Howe, Rachel
Mirakian, Rita M
Pillai, Prathap
Gane, Simon
Darby, Yvonne C
Scadding, Glenis K
author_sort Howe, Rachel
collection PubMed
description BACKGROUND: Aspirin – exacerbated respiratory disease can prove difficult to control. Oral aspirin desensitization is effective, but has adverse effects and may not be cardio-protective at the high doses needed. OBJECTIVE: To examine the effectiveness of aspirin administered in lower doses via the nose. METHODS: An audit of 121 patients with aspirin exacerbated respiratory disease (AERD), 105 of whom were treated with intranasal lysine aspirin in gradually increasing doses following positive lysine aspirin challenge. RESULTS: Treatment was associated with subjective symptomatic improvement or stabilization in 60 of 78 patients at 3 months and 19 of 27 at 12 months. Nasal inspiratory peak flow, olfaction, exhaled and nasal nitric oxide levels were significantly improved (p < 0.05 for all). Patients with positive skin prick tests and those with later onset (>40 years) AERD improved more than non-atopics and those with early onset AERD. Asthma outcomes over 1 year were assessed by questionnaire in 22 patients on lysine aspirin and in 20 who were positive on challenge but who either refused treatment or took it only briefly (less than or equal to 3 months). There was a significant decrease in emergency visits (p = 0.0182), hospitalization (p = 0.0074) and oral steroid use (p = 0.004) in those on nasal lysine aspirin for a year. Gastrointestinal side effects occurred in 3.8%, lower than those reported for oral aspirin therapy. Conclusions and Clinical Relevance This form of therapy might reduce the need for expensive monoclonal antibodies in AERD patients.
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spelling pubmed-41140862014-08-05 Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease Howe, Rachel Mirakian, Rita M Pillai, Prathap Gane, Simon Darby, Yvonne C Scadding, Glenis K World Allergy Organ J Original Research BACKGROUND: Aspirin – exacerbated respiratory disease can prove difficult to control. Oral aspirin desensitization is effective, but has adverse effects and may not be cardio-protective at the high doses needed. OBJECTIVE: To examine the effectiveness of aspirin administered in lower doses via the nose. METHODS: An audit of 121 patients with aspirin exacerbated respiratory disease (AERD), 105 of whom were treated with intranasal lysine aspirin in gradually increasing doses following positive lysine aspirin challenge. RESULTS: Treatment was associated with subjective symptomatic improvement or stabilization in 60 of 78 patients at 3 months and 19 of 27 at 12 months. Nasal inspiratory peak flow, olfaction, exhaled and nasal nitric oxide levels were significantly improved (p < 0.05 for all). Patients with positive skin prick tests and those with later onset (>40 years) AERD improved more than non-atopics and those with early onset AERD. Asthma outcomes over 1 year were assessed by questionnaire in 22 patients on lysine aspirin and in 20 who were positive on challenge but who either refused treatment or took it only briefly (less than or equal to 3 months). There was a significant decrease in emergency visits (p = 0.0182), hospitalization (p = 0.0074) and oral steroid use (p = 0.004) in those on nasal lysine aspirin for a year. Gastrointestinal side effects occurred in 3.8%, lower than those reported for oral aspirin therapy. Conclusions and Clinical Relevance This form of therapy might reduce the need for expensive monoclonal antibodies in AERD patients. World Allergy Organization 2014-07-29 /pmc/articles/PMC4114086/ /pubmed/25097720 http://dx.doi.org/10.1186/1939-4551-7-18 Text en Copyright © 2014 Howe 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 credited. 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 Original Research
Howe, Rachel
Mirakian, Rita M
Pillai, Prathap
Gane, Simon
Darby, Yvonne C
Scadding, Glenis K
Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease
title Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease
title_full Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease
title_fullStr Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease
title_full_unstemmed Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease
title_short Audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease
title_sort audit of nasal lysine aspirin therapy in recalcitrant aspirin exacerbated respiratory disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114086/
https://www.ncbi.nlm.nih.gov/pubmed/25097720
http://dx.doi.org/10.1186/1939-4551-7-18
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