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Infection

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Inhaled corticosteroids and risk of upper respiratory tract infection in patients with asthma: a meta-analysis

  • Mingjin Yang
  • Yan Zhang
  • Hong Chen
  • Jiachen Lin
  • Jiatao Zeng
  • Zhibo Xu
Original Paper
  • 65 Downloads

Abstract

Background

Recent studies have suggested a possible association between respiratory infection and the use of inhaled corticosteroids (ICS). We aimed to ascertain the risk of upper respiratory tract infection (URTI) with long-term inhaled corticosteroid use among patients with asthma.

Methods

Through a comprehensive literature search of PubMed, Cochrane Library, EMBASE, and Google Scholar from inception to May 2018, we included randomized controlled trials of any ICS vs. a control treatment for asthma, with reporting of URTI as an adverse event. We conducted meta-analyses by the Peto approaches to generate summary estimates comparing ICS with non-ICS treatment on the risk of URTI.

Results

Seventeen trials (15,336 subjects) were included. Compared with non-ICS treatment, ICSs were associated with a significantly increased risk of URTI (Peto OR, 1.24; 95% CI 1.08–1.42; I2 = 5%, p = 0.002). Subgroup analyses were performed for different dose, both high- and low-dose ICSs were associated with a significantly increased risk of URTI (high dose: Peto OR, 1.46; 95% CI 1.05–2.03; I2 = 0%; p = 0.03) (low dose: Peto OR, 1.20; 95% CI 1.04–1.39; I2 = 25%; p = 0.01). Moreover, fluticasone was observed with an increased risk of URTI (Peto OR, 1.18; 95% CI 1.02–1.38; p = 0.03; heterogeneity: I2 = 21%) but not budesonide, low-dose fluticasone treatment was associated with a significantly higher risk of URTI but not high dose.

Conclusions

This study raises safety concerns about the risk of URTI associated with ICS use in patients with asthma, but it should be further investigated.

Keywords

Inhaled corticosteroids (ICS) Asthma Upper respiratory tract infection (URTI) Risk Meta-analysis 

Notes

Acknowledgements

All authors contributed substantially to the study design, data analysis and interpretation, and the writing of the manuscript. The authors are indebted to all members of the Respiratory Diseases Laboratory of Chengdu Second People’s Hospital. Financial Support: Natural Science Foundation of China, Project Grant Numbers: 81650003. Chengdu Health Bureau Science and Technology Research Fund, Project Number: 20140735. Chengdu Science and Technology Project, Project Application Numbers: 2015-HM0100621-SF. The funding bodies had no role in the study design, manuscript writing, or decision to submit the manuscript for publication.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  • Mingjin Yang
    • 1
  • Yan Zhang
    • 2
  • Hong Chen
    • 1
  • Jiachen Lin
    • 1
  • Jiatao Zeng
    • 1
  • Zhibo Xu
    • 1
  1. 1.Respiratory Diseases LaboratoryChengdu Second People’s HospitalChengduChina
  2. 2.Digestive System DepartmentChengdu Second People’s HospitalChengduChina

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