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      Use of systemic corticosteroids for atopic dermatitis: International Eczema Council consensus statement

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          Summary

          Background

          Guidelines discourage the use of systemic corticosteroids for atopic dermatitis ( AD), but their use remains widespread.

          Objectives

          To reach consensus among an international group of AD experts on the use of systemic corticosteroids for AD.

          Methods

          A survey consisting of statements accompanied by visual analogue scales ranging from ‘strongly disagree’ to ‘neutral’ to ‘strongly agree’ was distributed to the International Eczema Council ( IEC). Consensus was reached in agreement on a statement if < 30% of respondents marked to the left of ‘neutral’ towards ‘strongly disagree’.

          Results

          Sixty of 77 (78%) IEC members participated. Consensus was reached on 12 statements, including that systemic corticosteroids should generally be avoided but can be used rarely for severe AD under certain circumstances, including a lack of other treatment options, as a bridge to other systemic therapies or phototherapy, during acute flares in need of immediate relief, in anticipation of a major life event or in the most severe cases. If used, treatment should be limited to the short term. Most respondents agreed that systemic corticosteroids should never be used in children, but consensus was not reached on that statement. The conclusions of our expert group are limited by a dearth of high‐quality published evidence. If more stringent consensus criteria were applied (e.g. requiring < 20% of respondents marking towards ‘strongly disagree’), consensus would have been reached on fewer statements.

          Conclusions

          Based on expert opinion from the IEC, routine use of systemic corticosteroids for AD is generally discouraged and should be reserved for special circumstances.

          Abstract

          What's already known about this topic?

          • Despite recommendations against their use in practice guidelines, systemic corticosteroids are commonly used for atopic dermatitis (AD).

          What does this study add?

          • The International Eczema Council reached consensus on circumstances in which systemic corticosteroids can be used for AD, including a lack of other treatment options, as a bridge to other systemic therapies or phototherapy, during acute flares in need of immediate relief, in anticipation of a major life event, or in the most severe cases.

          • Clinicians should limit the use of systemic corticosteroids for severe AD to those circumstances.

          https://doi.org/10.1111/bjd.16385 available online

          https://goo.gl/Uqv3dl

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          Most cited references31

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          Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

          Research electronic data capture (REDCap) is a novel workflow methodology and software solution designed for rapid development and deployment of electronic data capture tools to support clinical and translational research. We present: (1) a brief description of the REDCap metadata-driven software toolset; (2) detail concerning the capture and use of study-related metadata from scientific research teams; (3) measures of impact for REDCap; (4) details concerning a consortium network of domestic and international institutions collaborating on the project; and (5) strengths and limitations of the REDCap system. REDCap is currently supporting 286 translational research projects in a growing collaborative network including 27 active partner institutions.
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            Short term use of oral corticosteroids and related harms among adults in the United States: population based cohort study

            Objective To determine the frequency of prescriptions for short term use of oral corticosteroids, and adverse events (sepsis, venous thromboembolism, fractures) associated with their use. Design Retrospective cohort study and self controlled case series. Setting Nationwide dataset of private insurance claims. Participants Adults aged 18 to 64 years who were continuously enrolled from 2012 to 2014. Main outcome measures Rates of short term use of oral corticosteroids defined as less than 30 days duration. Incidence rates of adverse events in corticosteroid users and non-users. Incidence rate ratios for adverse events within 30 day and 31-90 day risk periods after drug initiation. Results Of 1 548 945 adults, 327 452 (21.1%) received at least one outpatient prescription for short term use of oral corticosteroids over the three year period. Use was more frequent among older patients, women, and white adults, with significant regional variation (all P<0.001). The most common indications for use were upper respiratory tract infections, spinal conditions, and allergies. Prescriptions were provided by a diverse range of specialties. Within 30 days of drug initiation, there was an increase in rates of sepsis (incidence rate ratio 5.30, 95% confidence interval 3.80 to 7.41), venous thromboembolism (3.33, 2.78 to 3.99), and fracture (1.87, 1.69 to 2.07), which diminished over the subsequent 31-90 days. The increased risk persisted at prednisone equivalent doses of less than 20 mg/day (incidence rate ratio 4.02 for sepsis, 3.61 for venous thromboembolism, and 1.83 for fracture; all P<0.001). Conclusion One in five American adults in a commercially insured plan were given prescriptions for short term use of oral corticosteroids during a three year period, with an associated increased risk of adverse events.
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              Guidelines of care for the management of atopic dermatitis: section 3. Management and treatment with phototherapy and systemic agents.

              Atopic dermatitis is a chronic, pruritic inflammatory dermatosis that affects up to 25% of children and 2% to 3% of adults. This guideline addresses important clinical questions that arise in atopic dermatitis management and care, providing recommendations based on the available evidence. In this third of 4 sections, treatment of atopic dermatitis with phototherapy and systemic immunomodulators, antimicrobials, and antihistamines is reviewed, including indications for use and the risk-benefit profile of each treatment option.
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                Author and article information

                Contributors
                aaron.drucker@wchospital.ca
                Journal
                Br J Dermatol
                Br. J. Dermatol
                10.1111/(ISSN)1365-2133
                BJD
                The British Journal of Dermatology
                John Wiley and Sons Inc. (Hoboken )
                0007-0963
                1365-2133
                28 January 2018
                March 2018
                : 178
                : 3 ( doiID: 10.1111/bjd.2018.178.issue-3 )
                : 768-775
                Affiliations
                [ 1 ] Department of Dermatology Alpert Medical School of Brown University and Rhode Island Hospital Providence RI U.S.A.
                [ 2 ] Division of Dermatology Department of Medicine University of Toronto Toronto Canada
                [ 3 ] Division of Dermatology Department of Medicine and Women's College Research Institute Women's College Hospital Toronto Canada
                [ 4 ] Department of Dermatology and Allergy Technical University of Munich Munich Germany
                [ 5 ] National Expertise Center for Atopic Dermatitis Department of Dermatology and Allergology University Medical Center Utrecht Utrecht the Netherlands
                [ 6 ] Department of Dermatology and Allergy Herlev‐Gentofte Hospital University of Copenhagen Hellerup Denmark
                [ 7 ] Department of Dermatology Academic Medical Centre Amsterdam the Netherlands
                [ 8 ] Trinity College Dublin National Children's Research Centre Paediatric Dermatology, Our Lady's Children's Hospital Dublin Ireland
                [ 9 ] Department of Medicine Section of Dermatology University of Verona Verona Italy
                [ 10 ] Department of Pediatric Dermatology Institute of Child Health Kolkata India
                [ 11 ] Unit for Population‐Based Dermatology Research St John's Institute of Dermatology King's College London and Guy's & St Thomas’ NHS Foundation Trust London U.K.
                [ 12 ] Faculty of Medicine University of Sydney Sydney NSW Australia
                [ 13 ] Departments of Dermatology and Pediatrics Northwestern University Feinberg School of Medicine Chicago IL U.S.A.
                [ 14 ] Department of Dermatology Icahn School of Medicine at Mount Sinai Medical Center New York NY U.S.A.
                Author notes
                [*] Correspondence

                Aaron M. Drucker.

                E‐mail: aaron.drucker@ 123456wchospital.ca

                Author information
                http://orcid.org/0000-0002-7388-9475
                http://orcid.org/0000-0002-1249-6993
                http://orcid.org/0000-0003-2971-0199
                http://orcid.org/0000-0002-9363-324X
                Article
                BJD15928
                10.1111/bjd.15928
                5901393
                28865094
                7b5c1a64-cd9e-4ba1-a407-e826f57de4f3
                © 2017 The Authors. British Journal of Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 17 August 2017
                Page count
                Figures: 0, Tables: 2, Pages: 8, Words: 5924
                Funding
                Funded by: National Institute for Health Research
                Award ID: CDF‐2014‐07‐037
                Categories
                General Dermatology
                Original Articles
                General Dermatology
                Custom metadata
                2.0
                bjd15928
                March 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.4 mode:remove_FC converted:16.04.2018

                Dermatology
                Dermatology

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