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Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days

BACKGROUND: One fourth of the adult population in Europe suffer from respiratory allergy. Subcutaneous-allergen-specific-immunotherapy (SCIT) has long-term disease modifying effect on disease specific Health-Related Quality of Life (HRQoL). The purpose of this study was to assess the effect of SCIT...

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Autores principales: Petersen, Karin D, Kronborg, Christian, Larsen, Jørgen N, Dahl, Ronald, Gyrd-Hansen, Dorte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846409/
https://www.ncbi.nlm.nih.gov/pubmed/24229439
http://dx.doi.org/10.1186/1939-4551-6-15
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author Petersen, Karin D
Kronborg, Christian
Larsen, Jørgen N
Dahl, Ronald
Gyrd-Hansen, Dorte
author_facet Petersen, Karin D
Kronborg, Christian
Larsen, Jørgen N
Dahl, Ronald
Gyrd-Hansen, Dorte
author_sort Petersen, Karin D
collection PubMed
description BACKGROUND: One fourth of the adult population in Europe suffer from respiratory allergy. Subcutaneous-allergen-specific-immunotherapy (SCIT) has long-term disease modifying effect on disease specific Health-Related Quality of Life (HRQoL). The purpose of this study was to assess the effect of SCIT on alternative disease outcomes in patients with grass-pollen and/or house dust mite induced allergic rhino-conjunctivitis and/or an asthma diagnosis. Focus was on expressing outcomes in terms of generic quality of life (Quality-Adjusted-Life-Years (QALY)) and reductions in sick days. METHODS: The study was a multi-centre study with prospective follow-up. 248 patients were initiated on SCIT. The disease specific Rhino-conjunctivitis Quality of Life Questionnaire (RQLQ) and two generic (HRQoL) instruments 15D and EQ-5D were used at baseline and at follow-up. The outcome measures included change in; disease severity, RQLQ-scores, number of days with symptoms- and number of sick days per year and finally changes in generic HRQoL and thus, QALY. Disease severity was assessed by specialist doctors; severity of rhino-conjunctivitis was classified according to the Allergic Rhinitis and its Impact on Asthma (ARIA) and asthma severity according to the Global Initiative for Asthma (GINA guideline). The remaining outcome measures were assessed by the patients in questionnaires at baseline and at follow-up. An intension to treat approach was applied. For missing items imputation of sample mean base-line values or follow-up values were used after specified criteria. The effect of SCIT on rhino-conjunctivitis and/or asthma diagnoses was analysed at follow-up using three logistic regression models. RESULTS: The disease severity showed significantly improved disease control. Mean RQLQ-score was reduced from 3.02 at baseline to 2.00 at follow-up. Average annual days with symptoms were reduced from 189 to 145 days whilst annual sick days were reduced from 3.7 to 1.2 days. The 15D-score increased from 0.83 to 0.86 and the EQ-5D-score from 0.70 to 0.77, which indicated an annual gain per patient of 0.03-0.06 QALY. CONCLUSIONS: Allergic patients suffering from rhino-conjunctivitis alone or rhino-conjunctivitis and asthma experience significantly increased HRQoL and they gain 0.03-0.06 QALY, when treated with SCIT for one year. TRIAL REGISTRATION: The study was registered at ClinicalTrials.gov with the identifier: NCT01486498.
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spelling pubmed-38464092013-12-03 Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days Petersen, Karin D Kronborg, Christian Larsen, Jørgen N Dahl, Ronald Gyrd-Hansen, Dorte World Allergy Organ J Original Research BACKGROUND: One fourth of the adult population in Europe suffer from respiratory allergy. Subcutaneous-allergen-specific-immunotherapy (SCIT) has long-term disease modifying effect on disease specific Health-Related Quality of Life (HRQoL). The purpose of this study was to assess the effect of SCIT on alternative disease outcomes in patients with grass-pollen and/or house dust mite induced allergic rhino-conjunctivitis and/or an asthma diagnosis. Focus was on expressing outcomes in terms of generic quality of life (Quality-Adjusted-Life-Years (QALY)) and reductions in sick days. METHODS: The study was a multi-centre study with prospective follow-up. 248 patients were initiated on SCIT. The disease specific Rhino-conjunctivitis Quality of Life Questionnaire (RQLQ) and two generic (HRQoL) instruments 15D and EQ-5D were used at baseline and at follow-up. The outcome measures included change in; disease severity, RQLQ-scores, number of days with symptoms- and number of sick days per year and finally changes in generic HRQoL and thus, QALY. Disease severity was assessed by specialist doctors; severity of rhino-conjunctivitis was classified according to the Allergic Rhinitis and its Impact on Asthma (ARIA) and asthma severity according to the Global Initiative for Asthma (GINA guideline). The remaining outcome measures were assessed by the patients in questionnaires at baseline and at follow-up. An intension to treat approach was applied. For missing items imputation of sample mean base-line values or follow-up values were used after specified criteria. The effect of SCIT on rhino-conjunctivitis and/or asthma diagnoses was analysed at follow-up using three logistic regression models. RESULTS: The disease severity showed significantly improved disease control. Mean RQLQ-score was reduced from 3.02 at baseline to 2.00 at follow-up. Average annual days with symptoms were reduced from 189 to 145 days whilst annual sick days were reduced from 3.7 to 1.2 days. The 15D-score increased from 0.83 to 0.86 and the EQ-5D-score from 0.70 to 0.77, which indicated an annual gain per patient of 0.03-0.06 QALY. CONCLUSIONS: Allergic patients suffering from rhino-conjunctivitis alone or rhino-conjunctivitis and asthma experience significantly increased HRQoL and they gain 0.03-0.06 QALY, when treated with SCIT for one year. TRIAL REGISTRATION: The study was registered at ClinicalTrials.gov with the identifier: NCT01486498. World Allergy Organization 2013-09-09 /pmc/articles/PMC3846409/ /pubmed/24229439 http://dx.doi.org/10.1186/1939-4551-6-15 Text en Copyright © 2013 Petersen 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 Original Research
Petersen, Karin D
Kronborg, Christian
Larsen, Jørgen N
Dahl, Ronald
Gyrd-Hansen, Dorte
Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days
title Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days
title_full Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days
title_fullStr Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days
title_full_unstemmed Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days
title_short Patient related outcomes in a real life prospective follow up study: Allergen immunotherapy increase quality of life and reduce sick days
title_sort patient related outcomes in a real life prospective follow up study: allergen immunotherapy increase quality of life and reduce sick days
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846409/
https://www.ncbi.nlm.nih.gov/pubmed/24229439
http://dx.doi.org/10.1186/1939-4551-6-15
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