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. 2022 Aug 11;60(2):2102760. doi: 10.1183/13993003.02760-2021

The carbon footprint of respiratory treatments in Europe and Canada: an observational study from the CARBON programme

Christer Janson 1,, Ekaterina Maslova 2, Alexander Wilkinson 3, Erika Penz 4,5, Alberto Papi 6, Nigel Budgen 7, Claus F Vogelmeier 8, Maciej Kupczyk 9,10, John Bell 2, Andrew Menzies-Gow 11
PMCID: PMC9363844  PMID: 35777767

Climate change represents a global challenge and nations are increasingly looking to decarbonise their economies by developing roadmaps for reducing greenhouse gas (GHG) emissions in accordance with international treaties, such as the Paris Agreement [1]. As the healthcare sector remains a key contributor to GHG emissions [2], an examination of the global carbon footprint of its operations and treatment pathways is essential to identify targets for decarbonisation.

Short abstract

Relievers account for the majority of inhaler use and associated GHG emissions. Implementing treatment guidelines can reduce the unmet need in respiratory care by improving disease control and reducing reliever overuse and the overall carbon footprint. https://bit.ly/3zh3c2B


To the Editor:

Climate change represents a global challenge and nations are increasingly looking to decarbonise their economies by developing roadmaps for reducing greenhouse gas (GHG) emissions in accordance with international treaties, such as the Paris Agreement [1]. As the healthcare sector remains a key contributor to GHG emissions [2], an examination of the global carbon footprint of its operations and treatment pathways is essential to identify targets for decarbonisation.

In respiratory treatment, the environmental impact of controller inhalers has received considerable attention due to the hydrofluorocarbon propellants used in metered-dose inhalers (MDIs), which have global warming potential [3]. In the United Kingdom (UK), where MDIs represented ∼3% of health and social care system carbon emissions [4] and 13.1% of emissions related to the delivery of care in 2019 [2], targets are in place to reduce total emissions by 80% by 2036–2039, including those from MDIs [5]. However, the focus on controller inhalers omits other contributors, such as the impact of short-acting β2-agonists (SABAs), presenting an incomplete picture of the carbon footprint of respiratory treatments for both asthma and COPD.

Patients with mild asthma, who represent approximately half of the European asthma population [6], are commonly prescribed SABA-only treatment [7], placing them at increased risk of poor outcomes [8]. Additionally, findings from the real-world SABA use in Asthma (SABINA) programme revealed that approximately one-third of patients with asthma across Europe overuse SABA (prescription/dispensing of three or more canisters per year) [9], which is associated with an increased risk of exacerbations and healthcare resource use [10, 11]. Moreover, increased healthcare resource use in respiratory treatment, whether associated with poor disease control of asthma [12] or progression of COPD [13], carries an additional carbon burden [14].

We considered that suboptimal care of patients with asthma or COPD may drive a higher, yet potentially modifiable, contribution to global GHG emissions, and developed the Healthcare-based Carbon Cost of Treatment (CARBON) programme, an evolving healthcare sustainability scheme to better understand the carbon footprint of respiratory disease control and progression [15]. As part of the CARBON programme, the SABA CARBON Europe and Canada observational cohort study quantified the carbon footprint associated with 1) the use of both reliever and controller inhalers in 20 European countries and in Canada and 2) SABA overuse (prescription/dispensing of three or more canisters per year) in five European countries and two Canadian provinces (Alberta and Nova Scotia) from the SABINA programme.

Inhaler sales data, as a surrogate for inhaler use, for SABA and controller medications (MDIs and dry powder inhalers (DPIs)), across all respiratory uses, were obtained from the IQVIA quarterly MIDAS database Q3 2019 (September 2018 to September 2019), accessed and analysed via the AstraZeneca in-house STAR system. This analysis included patients treated for any respiratory condition. Controller treatments included inhaled corticosteroid-containing drugs, long-acting β2-agonists (LABA), long-acting muscarinic antagonists (LAMA) and LAMA/LABA combinations.

SABA overuse in patients with asthma (aged ≥12 years) of any severity was assessed using prescription/dispensing data from the SABINA programme (2006–2019) [10, 1619].

Data were compared by dose, preventing confounding from inhaler actuation count differences. A 1:1 equivalence of actuation and dose was assumed for SABAs and controller medication delivered via a DPI, whereas a 2:1 ratio for actuation to dose was assumed for controller medication delivered via a MDI. Both analyses were descriptive in nature and annual GHG emissions were expressed as carbon dioxide equivalent (CO2e) and quantified using published data [3, 20] and internal AstraZeneca estimates. Per capita inhaler usage and associated carbon footprint were calculated using the national population for IQVIA sales data and using the study populations for the SABINA data.

SABA use was common across 20 countries in Europe and in Canada (table 1). Although SABAs were mostly administered via MDIs, this varied across countries, ranging from 28.2% in Sweden to 100% in Italy. Per capita SABA use ranged from 98 770 (Poland) to 1 033 535 (UK) doses per 10 000 persons per year. Compared with SABA use, per capita controller medication use was lower, ranging from 58 506 (Romania) to 437 945 (UK) doses per 10 000 persons per year.

TABLE 1.

Greenhouse gas (GHG) emissions related to short-acting β2-agonist (SABAs) versus controller medication in 21 countries, and SABA overuse among patients with asthma from the seven SABA use in Asthma (SABINA) datasets and associated GHG emissions

Per capita SABA use, doses per 10 000 persons per year Per capita controller medication use, doses per 10 000 persons per year SABA versus total inhaler use, % GHG emissions from SABA, tonnes CO2e GHG emissions from controller medication, tonnes CO2e SABA versus total inhaler GHG emissions, % Per capita GHG emissions from SABA, tonnes CO2e per 10 000 persons per year Per capita GHG emissions from controller medication, tonnes CO2e per 10 000 persons per year Total patients in SABINA database (GINA equivalent steps 1–2–3–5) Volume of SABA prescriptions (GINA equivalent steps 1–2–3–5) SABA prescriptions received by patients potentially overusing SABA reliever (GINA equivalent steps 1–2–3–5), % Total GHG emissions from SABA overuse, tonnes CO2e within this cohort Per capita GHG emission from SABA overuse, tonnes CO2e per 10 000 persons
Belgium 131047 267567 33 19672 17422 53 17 15
Bulgaria 125630 141248 47 11959 6949 63 17 10
Canada# 543796 224999 71 193356 73898 72 55 21
 Alberta 107444 274175 81 4303 401
 Nova Scotia 8034 34677 94 694 864
Croatia 126186 111056 53 7253 4175 64 17 10
Czech Republic 125088 210556 37 17563 18485 49 17 17
Denmark 281377 284622 50 10889 8017 58 19 14
Finland 278298 337388 45 10963 11563 49 20 21
France 383001 229696 63 334716 126131 73 50 19
Germany 275899 234476 54 293638 144077 67 36 18 13030 39643 74 540 415
Greece 237510 288218 45 34223 20988 62 32 19
Hungary 182449 144174 56 22597 12560 64 23 13
Ireland 743424 300928 71 48986 16782 75 98 34
Italy 125516 144659 46 104503 86040 55 17 14 22102 17866 69 240 108
The Netherlands 256961 288783 47 46559 52922 47 27 31
Norway 285983 279637 51 14776 10188 59 28 19
Poland 98770 166863 37 49893 43738 53 13 11 98876 135424 74 1928 195
Romania 126896 58506 68 36749 9371 80 17 4
Spain 318751 222311 59 195771 86977 69 40 18
Sweden+ 238512 349211 41 11632 12895 47 12 13 365324 794589 69 2844 78
Switzerland 154456 150331 51 16067 6174 72 20 8
UK 1033535 437945 70 862685 415345 68 134 65 516606 1753804 85 28052 543

GHG emissions associated with medication use were quantified using SimaPro life cycle assessment software modelling resource and energy consumption data, in addition to Ecoinvent datasets and certified published studies. Per capita GHG emissions were calculated to allow comparisons across countries/datasets. CO2e: carbon dioxide equivalent; GINA: Global Initiative for Asthma. #: data from Alberta and Nova Scotia from the SABINA datasets were analysed separately to compare SABA overuse and associated emissions across the two provinces; : patients with zero SABA use could not be categorised across GINA steps; +: 8061 patients from Sweden could not be categorised according to GINA steps.

As a proportion of total inhaler use, SABA inhalers ranged from 33% (Belgium) to 71% (Canada and Ireland), with SABA GHG emissions ranging from 47% (Netherlands and Sweden) to 80% (Romania). Compared with per capita GHG emissions from SABA, which ranged from 12 (Sweden) to 134 (UK) tonnes CO2e per 10 000 persons per year, per capita GHG emissions from controller medication use were lower and ranged from 4 (Romania) to 65 (UK) tonnes CO2e per 10 000 persons per year. Total GHG emissions from the use of SABA and controller medications were approximately 2 and 1 million tonnes CO2e, respectively, with SABA use accounting for 66% of the total GHG emissions from inhalers.

Across the seven SABINA datasets comprising 1 131 416 patients with asthma (table 1), most SABA prescriptions were received by patients who were overusing SABA (three or more canisters per year), ranging from 69% (Italy and Sweden) to 94% (Canada (Nova Scotia)). SABA overuse contributed to excess per capita GHG emissions, ranging from 78 (Sweden) to 864 (Canada (Nova Scotia)) tonnes CO2e per 10 000 persons per year. Per capita GHG emissions from SABA overuse in Canada (Nova Scotia) were 1.6- to 11.1-fold higher versus the UK and Sweden, respectively. As an example, SABA overuse when scaled to the national asthma population of ∼5.4 million in the UK translated to an excess carbon footprint of 293 227 tonnes CO2e. Across the two Canadian provinces, both SABA overuse and the associated per capita emissions were higher in Nova Scotia compared with Alberta.

Although inhaler sales and prescriptions/dispensing data may not reflect actual medication use and final disposal (together accounting for ∼90% of the GHG emissions) [3], this study provides an understanding of how high SABA use, a marker of poor disease control and suboptimal disease management [8], drives the associated carbon footprint of respiratory treatment.

Overall, our findings reveal that suboptimal respiratory treatment, in the form of high SABA use across Europe and Canada, remains widespread, representing approximately two-thirds of total GHG emissions. These findings highlight the importance of assessing the contribution of SABAs to the carbon footprint of respiratory treatment, which in many countries were commonly used and administered by MDIs, thereby explaining higher GHG emissions associated with SABA versus controller inhaler use. Furthermore, an analysis of SABINA datasets demonstrated that SABA overuse, as defined by the threshold of three or more canisters per year [8], drives the majority of SABA prescriptions/dispensing in asthma, suggesting suboptimal disease management in a high proportion of patients who are at increased risk of asthma exacerbations and exacerbation-related healthcare resource use, thereby further contributing to the total carbon footprint.

In most countries, SABAs represented the majority of respiratory-related inhaler use, indicating suboptimal disease control in these populations. The highest per capita use of both SABA and controller inhalers was observed in the UK. SABA overuse in asthma was prevalent despite the different healthcare and reimbursement policies of each country, a finding consistent with previous studies [911, 17, 18, 21, 22]. Across all SABINA datasets, SABA prescribing/dispensing was primarily driven by patients who were potentially overusing SABA relievers. However, these findings should be interpreted in light of diverse asthma management practices and differences in healthcare delivery systems and socioeconomic status across the individual datasets, particularly in relation to access to medications [19]. For example, in Germany and Sweden, SABA is a prescription-only medicine [9], while in Italy, SABA is available without a prescription [17]. Thus, actual SABA use in Italy may have been higher than observed. SABA prescribing/dispensing patterns in Poland may be attributable to underfunding of the healthcare system, leading to relatively high out-of-pocket spending [23]. Variations in SABA overuse between the two Canadian provinces may be due, in part, to differences in socioeconomic status [24] that may have influenced access to recommended asthma medications. However, further research is needed to verify these findings.

Although global asthma guidelines no longer recommend as-needed SABA use alone due to safety concerns [8] and an inconsistent evidence base, asthma management practices have not yet caught up with current evidence-based recommendations, and SABA overuse therefore continues to drive the majority of GHG emissions across countries. Consequently, implementation of clinical guidelines, adherence to asthma action plans, and delivery of personalised care along with a focus on the management of modifiable risk factors for poor disease control, such as SABA overuse, poor medication adherence and incorrect inhaler technique should be prioritised to improve patient outcomes [8]. This approach will subsequently reduce SABA reliever use and additional healthcare resource use, thereby benefiting patients and realising carbon savings that go beyond the reduction in SABA use alone. As suboptimal disease management continues to be an unacceptable unmet need in respiratory treatment, this is a call to action for healthcare professionals and policymakers to ensure that treatment-related decisions are guided by current evidence-based recommendations and tailored to patient needs, thereby reducing SABA use and associated carbon emissions in respiratory treatment, without risking improvements in patient outcomes or causing harm.

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Acknowledgements

The authors thank Dorota Brzostek (AstraZeneca, Poland), Gunilla Telg (AstraZeneca, Sweden), Silvia Boarino (AstraZeneca, Italy), Ingo Mokros (AstraZeneca, Germany) and Stephen Noorduyn (AstraZeneca, Canada) for their assistance in coordinating data collection. Writing and editorial support was provided by Praveen Kaul and Frances Gambling, of Cactus Life Sciences (part of Cactus Communications, Mumbai, India) in accordance with Good Publication Practice (GPP3) guidelines (http://www.ismpp.org/gpp3) and fully funded by AstraZeneca.

Footnotes

IQVIA did not provide any support for the analysis or interpretation of the data.

Author contributions: J. Bell and E. Maslova conceptualised the study design. E. Maslova, N. Budgen and J. Bell performed the data analysis. All authors contributed to data collection, data interpretation and writing.

Conflict of interest: C. Janson reports personal fees from AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline PLC, Novartis and Teva, outside the submitted work. A. Wilkinson is a member of the Montreal protocol Medical and Chemical Technical Options Committee and has made unpaid contributions to publications on the carbon footprint of inhalers and respiratory treatment which were sponsored by GlaxoSmithKline and AstraZeneca. E. Penz has received honoraria and consulting fees from AstraZeneca, GlaxoSmithKline, Sanofi Genzyme, International Centre for Evidence-Based Medicine in Canada and Boehringer Ingelheim. A. Papi reports grants and personal fees from GlaxoSmithKline, AstraZeneca, Boehringer Ingelheim, Chiesi Farmaceutici, Menarini and Sanofi/Regeneron; personal fees from Mundipharma, Zambon, Novartis, Edmond Pharma and Roche; and grants from Fondazione Maugeri and Fondazione Chiesi. C.F. Vogelmeier has delivered presentations at symposia and/or served on scientific advisory boards sponsored by Aerogen, AstraZeneca, Boehringer Ingelheim, CSL Behring, Chiesi, GlaxoSmithKline, Grifols, Menarini, Novartis, Nuvaira and MedUpdate. M. Kupczyk reports grants from AstraZeneca and personal fees from AstraZeneca, Chiesi, GlaxoSmithKline, Novartis, Lekam, Alvogen, Emma, Nexter and Berlin Chemie. E. Maslova, N. Budgen and J. Bell are employees of AstraZeneca. A. Menzies-Gow has attended advisory boards for GlaxoSmithKline, Novartis, AstraZeneca, Sanofi and Teva; received speaker fees from Novartis, AstraZeneca, Vectura, Teva and Roche; participated in research with AstraZeneca; attended international conferences with Teva; and has consultancy agreements with AstraZeneca, Vectura and Sanofi.

Support statement: AstraZeneca funded the CARBON and SABINA studies and was involved in designing the study, developing the study protocol, conducting the study and performing the analyses. AstraZeneca was given the opportunity to review the manuscript before submission. Funding information for this article has been deposited with the Crossref Funder Registry.

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