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      Adverse outcomes from initiation of systemic corticosteroids for asthma: long-term observational study

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          Abstract

          Purpose

          Prior work suggests a threshold of four courses/year of systemic corticosteroid (SCS) therapy is associated with adverse consequences. The objective of this study was to investigate the onset of adverse outcomes beginning at SCS initiation in a broad asthma population.

          Patients and methods

          This historical matched cohort study utilized anonymized, longitudinal medical record data (1984–2017) of patients (≥18 years) with active asthma. Matched patients with first SCS prescription (SCS arm) and no SCS exposure (non-SCS arm) were followed until first outcome event. Associations between time-varying exposure measures and onset of 17 SCS-associated adverse outcomes were estimated using Cox proportional hazard regression, adjusting for confounders, in separate models.

          Results

          We matched 24,117 pairs of patients with median record availability before SCS initiation of 9.9 and 8.7 years and median follow-up 7.4 and 6.4 years in SCS and non-SCS arms, respectively. Compared with patients in the non-SCS arm, patients prescribed SCS had significantly increased risk of osteoporosis/osteoporotic fracture (adjusted hazard ratio 3.11; 95% CI 1.87–5.19), pneumonia (2.68; 2.30–3.11), cardio-/cerebrovascular diseases (1.53; 1.36–1.72), cataract (1.50; 1.31–1.73), sleep apnea (1.40; 1.04–1.86), renal impairment (1.36; 1.26–1.47), depression/anxiety (1.31; 1.21–1.41), type 2 diabetes (1.26; 1.15–1.37), and weight gain (1.14; 1.10–1.18). A dose-response relationship for cumulative SCS exposure with most adverse outcomes began at cumulative exposures of 1.0–<2.5 g and for some outcomes at cumulative exposures of only 0.5–<1 g (vs >0–<0.5 g reference), equivalent to four lifetime SCS courses.

          Conclusion

          Our findings suggest urgent need for reappraisal of when patients need specialist care and consideration of nonsteroid therapy.

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          Most cited references18

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          The impact of confounder selection criteria on effect estimation.

          Much controversy exists regarding proper methods for the selection of variables in confounder control. Many authors condemn any use of significance testing, some encourage such testing, and other propose a mixed approach. This paper presents the results of a Monte Carlo simulation of several confounder selection criteria, including change-in-estimate and collapsibility test criteria. The methods are compared with respect to their impact on inferences regarding the study factor's effect, as measured by test size and power, bias, mean-squared error, and confidence interval coverage rates. In situations in which the best decision (of whether or not to adjust) is not always obvious, the change-in-estimate criterion tends to be superior, though significance testing methods can perform acceptably if their significance levels are set much higher than conventional levels (to values of 0.20 or more).
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            Comorbidity in severe asthma requiring systemic corticosteroid therapy: cross-sectional data from the Optimum Patient Care Research Database and the British Thoracic Difficult Asthma Registry.

            To determine the prevalence of systemic corticosteroid-induced morbidity in severe asthma.
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              • Record: found
              • Abstract: found
              • Article: not found

              Oral corticosteroid exposure and adverse effects in asthmatic patients.

              Significant adverse effects (AEs) have been associated with continuous exposure to oral corticosteroids (OCSs). The potential association with intermittent exposure is unknown.
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                Author and article information

                Journal
                J Asthma Allergy
                J Asthma Allergy
                Journal of Asthma and Allergy
                Journal of Asthma and Allergy
                Dove Medical Press
                1178-6965
                2018
                29 August 2018
                : 11
                : 193-204
                Affiliations
                [1 ]Observational and Pragmatic Research Institute, Singapore, Singapore, dprice@ 123456opri.sg
                [2 ]Academic Primary Care, Division of Applied Health Sciences, University of Aberdeen, Aberdeen, UK, dprice@ 123456opri.sg
                [3 ]Medical Affairs, AstraZeneca, Wilmington, DE, USA
                [4 ]Global Payer Evidence and Pricing, AstraZeneca, Gaithersburg, MD, USA
                [5 ]Medical Evidence and Observational Research, AstraZeneca, Gaithersburg, MD, USA
                Author notes
                Correspondence: David B Price, Academic Primary Care, Division of Applied Health Sciences, University of Aberdeen, Polwarth Building, Foresterhill, Aberdeen AB25 2ZD, UK, Tel +65 6 802 9724, Email dprice@ 123456opri.sg
                Article
                jaa-11-193
                10.2147/JAA.S176026
                6121746
                f6bd3d18-0b60-4417-b81b-eaa3b963a28b
                © 2018 Price et al. This work is published and licensed by Dove Medical Press Limited

                The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.

                History
                Categories
                Original Research

                Immunology
                adverse outcomes,asthma,cumulative exposure,oral corticosteroids,systemic corticosteroids

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