Publication:
Adverse effects associated with influenza vaccination in patients with COPD: A randomized controlled study

dc.contributor.authorPhunsup Wongsurakiaten_US
dc.contributor.authorKhun Nanta Maranetraen_US
dc.contributor.authorPenpun Gulprasutdilogen_US
dc.contributor.authorMonchai Aksorninten_US
dc.contributor.authorWichian Srilumen_US
dc.contributor.authorChairat Ruengjamen_US
dc.contributor.authorWichean Sateden_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:46:57Z
dc.date.available2018-07-24T03:46:57Z
dc.date.issued2004-11-01en_US
dc.description.abstractObjective: The aim of this study was to assess the frequency and type of adverse reactions following influenza vaccination and its effects on lung function, dyspnoeic symptoms, exercise capacity, and clinical acute respiratory illness (ARI) in patients with COPD, and the relationship of these adverse effects to the degree of airflow obstruction. Methodology: A stratified, randomized, double-blind placebo-controlled study was conducted over an 18-month period at a single university hospital. In total, 125 patients with COPD were randomized to the vaccine group (62 patients who received purified trivalent split-virus vaccine injections) or the placebo group (63 patients). Local and systemic symptoms during the week following the injections were evaluated. Clinical ARI, lung function tests, dyspnoeic symptoms (assessed using a visual analogue scale), and a 6-min walking test were evaluated before and at 1 week and 4 weeks following vaccination. Results: The frequency of local adverse reactions was 27% in the vaccine group and 6% in the placebo group (P = 0.002). There was no significant difference in systemic adverse reactions between the vaccine and placebo groups (76% vs. 81%; P = 0.5). No difference was observed in the incidence of ARI between the vaccine and placebo groups during the first week (6.4% vs. 6.3%; P = 1) and the first 4 weeks (24.2% vs. 31.7%; P = 0.5) following vaccination. There was no significant change in lung function, dyspnoeic symptoms, and exercise capacity of the patients in both groups, at 1 week and 4 weeks following vaccination, regardless of the severity of COPD. Conclusion: Influenza vaccination is associated with minimal local adverse reactions in patients with COPD. Vaccination does not cause systemic adverse reactions, induce clinical exacerbations or adversely affect lung function, dyspnoeic symptoms and exercise capacity in patients with COPD, regardless of the severity of airflow obstruction.en_US
dc.identifier.citationRespirology. Vol.9, No.4 (2004), 550-556en_US
dc.identifier.doi10.1111/j.1440-1843.2004.00616.xen_US
dc.identifier.issn13237799en_US
dc.identifier.other2-s2.0-13144256700en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/21496
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=13144256700&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleAdverse effects associated with influenza vaccination in patients with COPD: A randomized controlled studyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=13144256700&origin=inwarden_US

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