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Review
. 2021 Dec 11;22(1):244.
doi: 10.1186/s12875-021-01583-w.

COPD - do the right thing

Affiliations
Review

COPD - do the right thing

Hanna Sandelowsky et al. BMC Fam Pract. .

Abstract

A gap exists between guidelines and real-world clinical practice for the management and treatment of chronic obstructive pulmonary disease (COPD). Although this has narrowed in the last decade, there is room for improvement in detection rates, treatment choices and disease monitoring. In practical terms, primary care practitioners need to become aware of the huge impact of COPD on patients, have non-judgemental views of smoking and of COPD as a chronic disease, use a holistic consultation approach and actively motivate patients to adhere to treatment.This article is based on discussions at a virtual meeting of leading Nordic experts in COPD (the authors) who were developing an educational programme for COPD primary care in the Nordic region. The article aims to describe the diagnosis and lifelong management cycle of COPD, with a strong focus on providing a hands-on, practical approach for medical professionals to optimise patient outcomes in COPD primary care.

Keywords: Chronic obstructive; Primary health care; Pulmonary disease; Referral and consultation general practice.

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Conflict of interest statement

HS has served on an advisory board or participated in educational activities arranged by AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline and Novartis.

UMW has served on an advisory board, as a speaker and/or participated in educational activities arranged by AstraZeneca, Boehringer Ingelheim, Chiesi, Fisher and Paykel Healthcare, GlaxoSmithKline, Novartis, Orion Pharma, Pfizer and Teva. In addition, UMW has received travel grants from Fisher and Paykel Healthcare.

BBA has served on an advisory board, as a speaker and/or participated in educational activities arranged by AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Novartis and Sanofi-Aventis.

JS has served as a speaker and/or participated in educational activities arranged by AstraZeneca, Boehringer Ingelheim, Chiesi and Novartis.

KH has served on an advisory board, as a speaker and/or participated in educational activities arranged by ALK, AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Novartis, Orion Pharma, Sanofi-Aventis and Teva.

GS is a full-time employee of AstraZeneca.

AL has served on an advisory board, as a speaker, as principal investigator and/or participated in educational activities arranged by AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Novartis, Orion Pharma, Pfizer and Teva. Additionally, AL has received unrestricted research grants from Boehringer Ingelheim, Chiesi and Pfizer.

CJa has received honoraria for educational activities and lectures from AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, Novartis and Orion and has served on advisory boards arranged by AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline and Novartis.

CJe has served on an advisory board, as a speaker and/or participated in educational activities arranged by AstraZeneca, Boehringer Ingelheim, Chiesi, Novartis and Sanofi-Aventis.

KL has served on an advisory board, as a speaker and/or participated in educational activities arranged by AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Novartis, Orion, Sanofi and Teva.

Figures

Fig. 1
Fig. 1
The pathophysiological background to dyspnoea. Alveolar wall destruction leads to loss of elastic ‘passive’ recoil of the alveoli and support for the bronchiole is lost, leading to bronchiole collapse, which in turn results in air trapping, static hyperinflation and increased functional residual capacity [, –43]
Fig. 2
Fig. 2
The pathophysiology of COPD exacerbations. Reproduced with permission from: Wedzicha JA, Seemungal TAR. COPD exacerbations: defining their cause and prevention. Lancet. 2007;370(9589):786–96. Copyright © Elsevier 2007. COPD chronic obstructive pulmonary disease
Fig. 3
Fig. 3
Proportion of exacerbations under-reported in different studies. From references [, –100]
Fig. 4
Fig. 4
Disease characteristics and initial pharmacological treatment algorithm. aConsider if highly symptomatic (e.g. CAT > 20). bConsider if EOS ≥0.3 × 109 cells/L (≥300 cells/mm3). Reproduced with permission from: Global Initiative for Chronic Obstructive Lung Disease 2021 Report; Figure 4.2. Available from https://goldcopd.org/wp-content/uploads/2020/11/GOLD-REPORT-2021-v1.0-16Nov20_WMV.pdf, accessed 18 November 2020. CAT COPD assessment test, COPD chronic obstructive pulmonary disease, EOS eosinophil count, ICS inhaled corticosteroids, LABA long-acting β2-agonist, LAMA long-acting muscarinic antagonist, mMRC modified Medical Research Council dyspnoea scale
Fig. 5
Fig. 5
Treatment algorithm for patients with a) dyspnoea or b) exacerbations at review. aConsider if EOS ≥0.3 × 109 cells/L (≥300 cells/mm3) or EOS ≥0.1 × 109 cells/L (≥100 cells/mm3) AND ≥ 2 moderate exacerbations/1 hospitalisation. bConsider de-escalation of ICS or switch in response to pneumonia, inappropriate original indication or lack of response to ICS. Reproduced with permission from: Global Initiative for Chronic Obstructive Lung Disease 2021 Report; Figure 4.4. Available from https://goldcopd.org/wp-content/uploads/2020/11/GOLD-REPORT-2021-v1.0-16Nov20_WMV.pdf, accessed 18 November 2020. EOS eosinophil count, FEV1 forced expiratory volume in 1 s, ICS inhaled corticosteroid, LABA long-acting β2-agonist, LAMA long-acting muscarinic antagonist

References

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