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Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review
BACKGROUND: Oral corticosteroid use increases the risk of systemic adverse effects including osteoporosis, bone fractures, diabetes, ocular disorders and respiratory infections. We sought to understand if inhaled corticosteroid (ICS) use in asthma is also associated with increased risk of systemic e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713222/ https://www.ncbi.nlm.nih.gov/pubmed/33268342 http://dx.doi.org/10.1136/bmjresp-2020-000756 |
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author | Patel, Roshni Naqvi, Sumrah A Griffiths, Chris Bloom, Chloe I |
author_facet | Patel, Roshni Naqvi, Sumrah A Griffiths, Chris Bloom, Chloe I |
author_sort | Patel, Roshni |
collection | PubMed |
description | BACKGROUND: Oral corticosteroid use increases the risk of systemic adverse effects including osteoporosis, bone fractures, diabetes, ocular disorders and respiratory infections. We sought to understand if inhaled corticosteroid (ICS) use in asthma is also associated with increased risk of systemic effects. METHODS: MEDLINE and Embase databases were searched to identify studies that were designed to investigate ICS-related systemic adverse effects in people with asthma. Studies were grouped by outcome: bone mineral density (BMD), respiratory infection (pneumonia or mycobacterial infection), diabetes and ocular disorder (glaucoma or cataracts). Study information was extracted using the PICO checklist. Risk of bias was assessed using the Cochrane Risk of Bias tool (randomised controlled trials) and Risk of Bias In Non-randomised Studies of Interventions-I tool (observational studies). A narrative synthesis was carried out due to the low number of studies reporting each outcome. RESULTS: Thirteen studies met the inclusion criteria, 2 trials and 11 observational studies. Study numbers by outcome were: six BMD, six respiratory infections (four pneumonia, one tuberculosis (TB), one non-TB mycobacteria), one ocular disorder (cataracts) and no diabetes. BMD studies found conflicting results (three found loss of BMD and three found no loss), but were limited by study size, short follow-up and lack of generalisability. Studies addressing infection risk generally found positive associations but suffered from a lack of power, misclassification and selection bias. The one study which assessed ocular disorders found an increased risk of cataracts. Most studies were not able to fully adjust for known confounders, including oral corticosteroids. CONCLUSION: There is a paucity of studies assessing systemic adverse effects associated with ICS use in asthma. Those studies that have been carried out present conflicting findings and are limited by multiple biases and residual confounding. Further appropriately designed studies are needed to quantify the magnitude of the risk for ICS-related systemic effects in people with asthma. |
format | Online Article Text |
id | pubmed-7713222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-77132222020-12-04 Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review Patel, Roshni Naqvi, Sumrah A Griffiths, Chris Bloom, Chloe I BMJ Open Respir Res Asthma BACKGROUND: Oral corticosteroid use increases the risk of systemic adverse effects including osteoporosis, bone fractures, diabetes, ocular disorders and respiratory infections. We sought to understand if inhaled corticosteroid (ICS) use in asthma is also associated with increased risk of systemic effects. METHODS: MEDLINE and Embase databases were searched to identify studies that were designed to investigate ICS-related systemic adverse effects in people with asthma. Studies were grouped by outcome: bone mineral density (BMD), respiratory infection (pneumonia or mycobacterial infection), diabetes and ocular disorder (glaucoma or cataracts). Study information was extracted using the PICO checklist. Risk of bias was assessed using the Cochrane Risk of Bias tool (randomised controlled trials) and Risk of Bias In Non-randomised Studies of Interventions-I tool (observational studies). A narrative synthesis was carried out due to the low number of studies reporting each outcome. RESULTS: Thirteen studies met the inclusion criteria, 2 trials and 11 observational studies. Study numbers by outcome were: six BMD, six respiratory infections (four pneumonia, one tuberculosis (TB), one non-TB mycobacteria), one ocular disorder (cataracts) and no diabetes. BMD studies found conflicting results (three found loss of BMD and three found no loss), but were limited by study size, short follow-up and lack of generalisability. Studies addressing infection risk generally found positive associations but suffered from a lack of power, misclassification and selection bias. The one study which assessed ocular disorders found an increased risk of cataracts. Most studies were not able to fully adjust for known confounders, including oral corticosteroids. CONCLUSION: There is a paucity of studies assessing systemic adverse effects associated with ICS use in asthma. Those studies that have been carried out present conflicting findings and are limited by multiple biases and residual confounding. Further appropriately designed studies are needed to quantify the magnitude of the risk for ICS-related systemic effects in people with asthma. BMJ Publishing Group 2020-12-02 /pmc/articles/PMC7713222/ /pubmed/33268342 http://dx.doi.org/10.1136/bmjresp-2020-000756 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Asthma Patel, Roshni Naqvi, Sumrah A Griffiths, Chris Bloom, Chloe I Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review |
title | Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review |
title_full | Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review |
title_fullStr | Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review |
title_full_unstemmed | Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review |
title_short | Systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review |
title_sort | systemic adverse effects from inhaled corticosteroid use in asthma: a systematic review |
topic | Asthma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713222/ https://www.ncbi.nlm.nih.gov/pubmed/33268342 http://dx.doi.org/10.1136/bmjresp-2020-000756 |
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