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      Over-prescription of short-acting β 2-agonists and asthma management in the Gulf region: a multicountry observational study

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          Abstract

          Background

          The overuse of short-acting β 2-agonists (SABA) is associated with poor asthma control. However, data on SABA use in the Gulf region are limited. Herein, we describe SABA prescription practices and clinical outcomes in patients with asthma from the Gulf cohort of the SABA use IN Asthma (SABINA) III study.

          Methods

          In this cross-sectional study conducted at 16 sites across Kuwait, Oman, and the United Arab Emirates, eligible patients (aged ≥ 12 years) with asthma were classified based on investigator-defined disease severity guided by the 2017 Global Initiative for Asthma report and by practice type, i.e., respiratory specialist or primary care physician. Data on demographics, disease characteristics, and prescribed asthma treatments, including SABA, in the 12 months prior to a single, prospective, study visit were transcribed onto electronic case report forms (eCRFs). All analyses were descriptive in nature. Continuous variables were summarized by the number of non-missing values, given as mean (standard deviation [SD]) and median (range). Categorical variables were summarized by frequency counts and percentages.

          Results

          This study analyzed data from 301 patients with asthma, 54.5% of whom were treated by respiratory specialists. Most patients were female (61.8%), with a mean age of 43.9 years, and 84.4% were classified with moderate-to-severe disease, with a mean (SD) asthma duration of 14.8 (10.8) years. Asthma was partly controlled or uncontrolled in 51.2% of patients, with 41.9% experiencing ≥ 1 severe exacerbation in the 12 months preceding their study visit. Overall, 58.5% of patients were prescribed ≥ 3 SABA canisters, 19.3% were prescribed ≥ 10 canisters, and 13.3% purchased SABA over-the-counter (OTC) in the 12 months before the study visit. Most patients who purchased OTC SABA (92.5%) also received SABA prescriptions. Inhaled corticosteroid/long-acting β 2-agonist combinations and oral corticosteroid bursts were prescribed to 87.7% and 22.6% of patients, respectively.

          Conclusions

          SABA over-prescription was highly prevalent in the Gulf region, compounded by purchases of nonprescription SABA and suboptimal asthma-related outcomes. Increased awareness among policymakers and healthcare practitioners is needed to ensure implementation of current, evidence-based, treatment recommendations to optimize asthma management in this region.

          Trial registration

          NCT03857178 (ClinicalTrials.gov).

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s40733-022-00085-5.

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          Most cited references44

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          An official American Thoracic Society/European Respiratory Society statement: asthma control and exacerbations: standardizing endpoints for clinical asthma trials and clinical practice.

          The assessment of asthma control is pivotal to the evaluation of treatment response in individuals and in clinical trials. Previously, asthma control, severity, and exacerbations were defined and assessed in many different ways. The Task Force was established to provide recommendations about standardization of outcomes relating to asthma control, severity, and exacerbations in clinical trials and clinical practice, for adults and children aged 6 years or older. A narrative literature review was conducted to evaluate the measurement properties and strengths/weaknesses of outcome measures relevant to asthma control and exacerbations. The review focused on diary variables, physiologic measurements, composite scores, biomarkers, quality of life questionnaires, and indirect measures. The Task Force developed new definitions for asthma control, severity, and exacerbations, based on current treatment principles and clinical and research relevance. In view of current knowledge about the multiple domains of asthma and asthma control, no single outcome measure can adequately assess asthma control. Its assessment in clinical trials and in clinical practice should include components relevant to both of the goals of asthma treatment, namely achievement of best possible clinical control and reduction of future risk of adverse outcomes. Recommendations are provided for the assessment of asthma control in clinical trials and clinical practice, both at baseline and in the assessment of treatment response. The Task Force recommendations provide a basis for a multicomponent assessment of asthma by clinicians, researchers, and other relevant groups in the design, conduct, and evaluation of clinical trials, and in clinical practice.
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            The global burden of asthma: executive summary of the GINA Dissemination Committee report.

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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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                Author and article information

                Contributors
                ashrafalzaabi@hotmail.com
                Journal
                Asthma Res Pract
                Asthma Res Pract
                Asthma Research and Practice
                BioMed Central (London )
                2054-7064
                7 July 2022
                7 July 2022
                2022
                : 8
                : 3
                Affiliations
                [1 ]GRID grid.417387.e, ISNI 0000 0004 1796 6389, Pulmonology Department, , Zayed Military Hospital, ; Abu Dhabi, United Arab Emirates
                [2 ]GRID grid.416132.3, ISNI 0000 0004 1772 5665, Pulmonology Medicine Department, , Royal Hospital, ; Muscat, Sultanate of Oman
                [3 ]GRID grid.415691.e, ISNI 0000 0004 1796 6338, Pulmonology Medicine Department, , Rashid Hospital, Dubai Health Authority, ; Dubai, United Arab Emirates
                [4 ]Primary Health Care Department, Emirates Health Services Establishment, Dubai, United Arab Emirates
                [5 ]GRID grid.414167.1, ISNI 0000 0004 1757 0894, Health Affairs Department, , Primary Health Care Services Sector, Dubai Health Authority, ; Dubai, United Arab Emirates
                [6 ]Department of Family Medicine, Ahmadi Hospital, Al Ahmadi, Kuwait
                [7 ]Sabah El-Salem Primary Healthcare Centre, Sabah Al-Salem, Kuwait
                [8 ]Al-Rumaithiya Primary Healthcare Centre, Al-Rumaithiya, Kuwait
                [9 ]GRID grid.413288.4, ISNI 0000 0004 0429 4288, Al Adan Hospital, ; Hadiya, Kuwait
                [10 ]Medical Affairs Department, AstraZeneca, Dubai, United Arab Emirates
                [11 ]GRID grid.476086.b, ISNI 0000 0000 9959 1197, AstraZeneca, ; The Hague, The Netherlands
                Author information
                http://orcid.org/0000-0001-9840-2339
                Article
                85
                10.1186/s40733-022-00085-5
                9260980
                35799290
                7c26d436-8ac1-48e8-9fa3-e6917041556a
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 7 April 2022
                : 8 June 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100004325, AstraZeneca;
                Categories
                Research
                Custom metadata
                © The Author(s) 2022

                asthma,exacerbations,gulf region,over-prescription,sabina,short-acting β2-agonists

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