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Review
. 2023 Feb 8;33(1):7.
doi: 10.1038/s41533-023-00330-1.

Key recommendations for primary care from the 2022 Global Initiative for Asthma (GINA) update

Affiliations
Review

Key recommendations for primary care from the 2022 Global Initiative for Asthma (GINA) update

Mark L Levy et al. NPJ Prim Care Respir Med. .

Abstract

The Global Initiative for Asthma (GINA) was established in 1993 by the World Health Organization and the US National Heart Lung and Blood Institute to improve asthma awareness, prevention and management worldwide. GINA develops and publishes evidence-based, annually updated resources for clinicians. GINA guidance is adopted by national asthma guidelines in many countries, adapted to fit local healthcare systems, practices, and resource availability. GINA is independent of industry, funded by the sale and licensing of its materials. This review summarizes key practical guidance for primary care from the 2022 GINA strategy report. It provides guidance on confirming the diagnosis of asthma using spirometry or peak expiratory flow. GINA recommends that all adults, adolescents and most children with asthma should receive inhaled corticosteroid (ICS)-containing therapy to reduce the risk of severe exacerbations, either taken regularly, or (for adults and adolescents with "mild" asthma) as combination ICS-formoterol taken as needed for symptom relief. For patients with moderate-severe asthma, the preferred regimen is maintenance-and-reliever therapy (MART) with ICS-formoterol. Asthma treatment is not "one size fits all"; GINA recommends individualized assessment, adjustment, and review of treatment. As many patients with difficult-to-treat or severe asthma are not referred early for specialist review, we provide updated guidance for primary care on diagnosis, further investigation, optimization and treatment of severe asthma across secondary and tertiary care. While the GINA strategy has global relevance, we recognize that there are special considerations for its adoption in low- and middle-income countries, particularly the current poor access to inhaled medications.

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Conflict of interest statement

J.D. declares no competing interests. The other authors report the following conflicting interests (including financial and non-financial): M.L.L. has received consultancy fees from Clement Clarke International, Boehringer Ingelheim, AstraZeneca, GSK, Orion, TEVA pharmaceuticals, Menarini, NSHI, Chiesi Pharmaceuticals, Novartis, Aspire, Respiri Ltd (Australia), and Smart Respiratory Products Ltd, speaker fees from TEVA, Novartis, Orion, AstraZeneca, NAPP, Chiesi, and NSHI, and honoraria from ADMIT Group - Consorzio Ferrara Ricerche. M.L.L. is Editor Emeritus of npj Primary Care Respiratory Medicine, but was not involved in the journal’s review of, or decisions related to, this manuscript. L.B.B. has received grants from NIH/NIAID and NHLBI, personal fees from GlaxoSmithKline Genentech/Novartis, DBV Technologies, Teva, Boehringer Ingelheim, AstraZeneca, WebMD/Medscape, Sanofi, Regeneron, Vectura, Circassia, Kinaset, Vertex, and OM Pharma, and royalties from Elsevier outside the submitted work. E.B. has received speaker honoraria from AstraZeneca, Boehringer Ingelheim, Cipla, Chiesi, Hikma pharma, Menarini, Novartis, Sanofi Genzyme, and Regeneron, and consulting fees from AstraZeneca, Sanofi Genzyme, Regeneron, and Novartis. L.-P.B. has received research grants for participation in multicenter studies from Amgen, AstraZeneca, GlaxoSmithKline, Merck, Novartis, Sanofi-Regeneron, and BioHaven, research funding for projects introduced by the investigator from AstraZeneca, GlaxoSmithKline, and Merck, consulting and advisory board fees from Astra Zeneca, Novartis, GlaxoSmithKline, Merck, and Sanofi-Regeneron, lecture fees from AstraZeneca, Covis, Cipla, GlaxoSmithKline, Novartis and Merck, and Sanofi, and non-profit grants to produce educational materials from AstraZeneca, Covis, GlaxoSmithKline, Merck, and Novartis. C.B. has received consultancy fees or grants (paid to Institution) from GSK, AZ, BI, Novartis, Chiesi, Genentech, Roche, Sanofi, Regeneron, Mologic, and 4DPharma. G.B. has received speaker fees and advisory board fees from Astra Zeneca, Boehringer-Ingelheim, Chiesi, GSK, Merck Sharp & Dohme, Novartis, and Sanofi Regeneron. R.B. has received consulting fees or honoraria for lectures from ALK, AstraZeneca, Berlin-Chemie, Boehringer-Ingelheim, Chiesi, Cipla, GSK, Novartis, Roche, Sanofi, and TEVA, and grants to Mainz University Hospital for research or clinical trials, or both from Boehringer Ingelheim, GSK, Novartis, and Roche. A.A.C. has received consultancy and speaker fees from Abdi-Ibrahim, AstraZeneca, Boehringer-Ingelheim, Chiesi, Eurofarma, Glennmark, GSK, Novartis, and Sanofi. A.C.C. is a member of the Planning Group of the Global Alliance against Chronic Respiratory Diseases (GARD)/WHO, and the Executive Director of ProAR Foundation – Brazil. L.D. has received grants from the European Union Horizon 2020 research and innovation program (LIFECYCLE, grant agreement No 733206, 2016; EUCAN-Connect grant agreement No 824989; ATHLETE, grant agreement No 874583) and Stichting Vrienden van Sophia, and speaker fee (paid to institute) from Hong Kong University. L.D. is Vice chair of the Dutch Pediatric Respiratory Society. L.F. has received personal fees from Novartis, Astra Zeneca, and Sanofi, outside the submitted work. H.I. has received speaker and advisory board fees from Astellas, AstraZeneca, Boehringer-Ingelheim, Fukuda-Denshi, GSK, Kracie, Kyorin, Novartis, Omron, Pfizer, and Sanofi, and research grants and support (paid to university) from Asahi-Kasei Pharma, AstraZeneca, Boehringer-Ingelheim, Chugai, GlaxoSmithKline, Kyorin, Otsuka, Teijin, Taiho, and Ono. F.W.S.K. has received funding for conducting multi-center research on asthma from the Hong Kong Thoracic Society (which was supported by AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, and Novartis) with all fees paid directly to the institution. J.A.K. has received consulting fees from GlaxoSmithKline, AstraZeneca, and BData, Inc., and grants and contract fees from Regeneron (COVID-19 clinical trial), Sergey Bring Family Foundation (COVID-19 cohort study), Patient-Centered Outcomes Research Institute (research studies in asthma, COPD, insomnia), National Institutes of Health (research studies in asthma, COPD, acute COVID-19, and post-acute sequelae of SARS-CoV-2), and American Lung Association (asthma and COPD research). K.M. has received advisory board fees from AstraZeneca. P.M.P. has received consultancy and speaker fees from AstraZeneca, GSK, Novartis, Boehringer Ingelheim, Novartis, and Sanofi. A.S. has advised AstraZeneca on an unremunerated basis and has received a research grant from GSK (COVID-19 therapeutics). A.S. is editor emeritus of npj PCRM but was not involved in the journal’s review of, or decisions related to, this manuscript. A.Y. has received consultancy and speaker honoraria from Astra-Zeneca, Novartis, GSK, Chiesi, DEVA, and Abdi İbrahim. A.Y. is Chair of GARD. A.Y. is an editor for npj Primary Care Respiratory Medicine but was not involved in the journal’s review of, or decisions related to, this manuscript. H.K.R. has received honoraria for participation in advisory boards for AstraZeneca, Chiesi, GlaxoSmithKline, Novartis, and Sanofi-Genzyme; and from AstraZeneca, Boehringer Ingelheim, Chiesi, Getz, GlaxoSmithKline, Sanofi, and Teva Pharmaceuticals for independent medical educational presentations; she has received independent research funding from AstraZeneca, GlaxoSmithKline, and Novartis; and consulting fees from AstraZeneca and Novartis. L.P.B. (Chair), E.B., G.B., A.A.C., H.I., J.K., M.L.L., H.K.R., and A.Y. are members of Global Initiative for Asthma (GINA) Board of Directors. L.B., E.B., L.P.B., C.B., G.B., R.B., J.D., L.D., L.F., H.I., F.K., K.M., P.M.P., H.K.R. (Chair), A.S., and A.Y. are members of the GINA Science Committee. L.P.B., A.A.C., H.I., M.L.L. (Chair), and A.Y. are members of GINA Dissemination and Implementation Task Group.

Figures

Fig. 1
Fig. 1. The GINA diagnostic flowchart 2022.
PEF peak expiratory flow. Source: Box 1–1 in GINA report 2022. Box numbers within the figure refer to the GINA 2022 report. Reproduced with permission from ref. .
Fig. 2
Fig. 2. Investigating poor symptom control and/or exacerbations despite treatment.
ICS inhaled corticosteroid, NSAID nonsteroidal anti-inflammatory drug, GERD gastro-esophageal reflux disease. Reproduced with permission from ref. .
Fig. 3
Fig. 3. Approach to initial treatment in patients with asthma and/or COPD.
GOLD Global Initiative for Obstructive Lung Disease, ICS inhaled corticosteroid, LABA long-acting β2 agonist; LAMA long-acting muscarinic antagonist. A summary of differentiating and diagnostic features in people with Asthma, COPD and Asthma + COPD. Source: Box 5–2 in GINA 2022. Reproduced with permission from ref. .
Fig. 4
Fig. 4. Two-track options for personalized management of asthma for adults and adolescents, to control symptoms and minimize future risk.
HDM house dust mite, ICS inhaled corticosteroid, LABA long-acting beta2 agonist, LAMA long-acting muscarinic antagonist, LTRA leukotriene receptor antagonist, OCS oral corticosteroids, SABA short-acting beta2 agonist, SLIT sublingual immunotherapy. Box number refers to the GINA 2022 report. Before starting, stepping up or down or switching between tracks, patients should be assessed using the “assess, adjust, review” cycle shown at the top of the figure. Refer to the GINA report for more information about Step 5 options, including biologic therapies for patients with severe asthma. Source: Box 3–5A in GINA report 2022. Reproduced with permission from ref. .
Fig. 5
Fig. 5. Initial medications for adults and adolescents diagnosed with asthma.
ICS inhaled corticosteroid, LABA long-acting beta2 agonist, LAMA long-acting muscarinic antagonist, MART maintenance and reliever therapy with ICS–formoterol, OCS oral corticosteroids, SABA short-acting beta2 agonist. Initial medications for adults and adolescents diagnosed with asthma, with guidance on initial levels of medication for each treatment track based on symptoms and lung function where appropriate. Refer to the GINA report for other treatment components, including treatment of modifiable risk factors and comorbidities, non-pharmacologic strategies, and education and skills training. Source: Box 3.4Bi in GINA report 2022. Reproduced with permission from ref. .
Fig. 6
Fig. 6. Initial medications for children aged 6–11 years diagnosed with asthma.
BUD-FORM budesonide–formoterol, ICS inhaled corticosteroid, LABA long-acting beta2 agonist, LTRA leukotriene receptor antagonist, MART maintenance and reliever therapy with ICS–formoterol, OCS oral corticosteroids, SABA short-acting beta2 agonist. Initial treatment for children aged 6–11 years diagnosed with asthma, with guidance on initial levels of medication for each treatment track based on symptoms and lung function where appropriate. Source: Box 3–4Di in GINA report 2022. Refer to the GINA report for other treatment components, including treatment of modifiable risk factors and comorbidities, non-pharmacologic strategies, and education and skills training. Reproduced with permission from ref. .
Fig. 7
Fig. 7. Investigating and managing difficult-to-treat asthma in adult and adolescent patients.
ICS inhaled corticosteroid, LABA long-acting beta2 agonist, LAMA long-acting muscarinic antagonist, LTRA leukotriene receptor antagonists, SABA short-acting beta2 agoinst, OCS oral corticosteroid. The GINA strategy includes a decision tree about the management of difficult-to-treat and severe asthma spanning primary through tertiary care. The section of the flow diagram applicable to generalists in primary and secondary care is shown here. Source: Box 3–16A in GINA report 2022. Reproduced with permission from ref. .
Fig. 8
Fig. 8. Proportion of adults with difficult-to-treat or severe asthma.
Severe asthma is a subset of those with “difficult-to-treat” asthma. Source: Box 3–15 in GINA report 2022, data from Hekking et al.. Reproduced with permission from ref. .

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