
Medicine sustainability interventions
Outpatient care
Climate-aware prescription of inhalation medication
Inhalation medications are used in the treatment of asthma and COPD. In the Netherlands, more than 1.4 million people use inhalation medications every year, including bronchodilators, such as short- and long-acting β2 sympathomimetics and parasympatholytics, and inhaled corticosteroids (1). There are various types of inhalers available, including dose aerosols, powder inhalers, and soft mist inhalers. These vary greatly in environmental impact because dose aerosols contain propellants, such as HFA-134a, which has a 1500 times stronger greenhouse effect than CO₂ (2).
In some countries, powder inhalers are already prescribed more often. For example, the proportion of dose aerosols is lowest in Sweden (± 10%), highest in England (± 70%) and around 50% in the Netherlands (2, 3). If the Netherlands were to follow the Swedish example, a significant amount of CO₂ emissions could be prevented (2, 3). This is feasible because powder inhalers and soft mist inhalers are an effective alternative for most adult asthma and COPD patients, provided the inhalation technique is used correctly (4). In addition, more and more dose aerosols based on more sustainable propellants will come on the market in the coming years. This can also reduce the greenhouse gas emissions of inhalation medication.
To encourage doctors and pharmacists to prescribe climate-friendly inhalation medication, the Tranmural guideline for climate-aware prescribing of inhalation medication was developed by the Health Institute in collaboration with GPs, pulmonologists, paediatricians, pharmacists and the Lung Fund (4). To make a real impact, the guideline still requires inclusion in local formularies, so that the large-scale, unnecessary use of environmentally harmful inhalation medications can be reduced.
Intervention
Give preference to climate-friendly inhalation medication (powder inhaler, soft mist inhaler or dose aerosol based on a more sustainable propellant) when starting therapy, or switch from a traditional dose aerosol to a climate-friendly inhaler*1.
Environmental impact
Measured in CO2-emissions by reducing the proportion (traditional*)2) dose aerosols back compared to climate-conscious inhalers, such as powder and soft mist inhalers or a dose aerosol based on a more sustainable propellant.
Working method
1. Determine the population and formulate a goal
- Inventory current policies in selected department/for selected patient group (s):
- Check to what extent local protocols and/or formularies already take sustainability into account.
- Use outpatient prescribing data from the EPD to evaluate what proportion of prescriptions a climate-friendly inhaler contains (inhaler toolkit (NL))?
- Formulate SMART goals together with (the green team of) the relevant department (s). For example, within six months, at least 70% of adult asthma patients will start using a climate-aware inhaler.
- The literature shows that Sweden has a low proportion of dose aerosols: this was only 13% in 2017 (2.3). In the Netherlands, this is approximately 50%, with a slightly higher proportion of dose aerosols being prescribed for the first time since 2024 (5). This can serve as a reference for setting achievable goals.
- Starting with a climate-friendly inhaler is preferred as the first step, as it presents fewer risks than changing well-adjusted patients.
- Keep in mind that within certain target groups, such as pediatrics, there is more often an indication for dose aerosols.
- The literature shows that Sweden has a low proportion of dose aerosols: this was only 13% in 2017 (2.3). In the Netherlands, this is approximately 50%, with a slightly higher proportion of dose aerosols being prescribed for the first time since 2024 (5). This can serve as a reference for setting achievable goals.

2. Implementation
This intervention can be performed in several ways depending on the hospital's preference (Table 1). A combination of different methods is also possible.
- During an outpatient consultation
- Presentation of climate-aware prescribing of inhalation medication, possibly in combination with a climate-aware month, in which you regularly remind colleagues in transmission of climate-conscious prescription of inhalation medication.
- Involve lung nurses as they often do the inhalation check and can thus assess which inhaler someone can use.
- If a switch is chosen, important points of attention (see also recommendations in the Climate-Aware Prescribing Guidelines for Inhalation Medication (NL):
- Asthma or COPD is stable
- The patient is well informed and motivated. Explain to patients the choice of a climate-aware inhaler, including the benefits for the environment and health, for example with the patient flyer.
- Good inhalation instruction and guidance by the (hospital and outpatient) pharmacy and lung nurses to ensure adherence and proper use.
2. Formulary
- Discuss the local prescribing policy and the place of more sustainable inhalers in the formulary committee.
- To support:
- Adjust the formulary where necessary so that climate-aware inhalers are preferred.
- Record preferred resources in the EPD, for example via order sets or preference lists, so that prescribers are automatically directed to climate-aware options.
- To support:
- Inform the prescribers and pharmacists of the department concerned and, if necessary, the Medicines Committee about the change, for example by briefly explaining the change during transfers and/or team meetings.
3. Monitoring and Evaluation
- Monitor implementation using (polyclinic) clinical prescriptions, see “How to evaluate a drug intervention” Hand inhaler toolkit. Discuss (interim) results regularly, for example (twice) monthly, during transfers, team meetings and/or teaching.
- Reflect on results in relation to the set goal, obstructing and promoting factors. Adjust interventions if necessary.
- At the end of the follow-up period, evaluate whether the goal (s) is/have been achieved and how the change is secured.
Provide (interim) results back to the implementation supervisor.
How is this measured?
The environmental impact of the intervention can be determined by an increase in the proportion of climate-friendly inhalation medications based on outpatient (starting) regulations, see “How to evaluate a drug intervention” Hand inhaler toolkit.
When successfully implemented?
Based on the reduction in the proportion of prescriptions of (traditional) dose aerosols compared to climate-friendly alternatives, as described in the previous section, determine when the implementation is considered successful, and reflect on the set goal.
Footnotes
*1: Various pharmaceutical companies are working to develop dose aerosols with more sustainable propellants (HFA-152a and HFO-1234ze) (6). Recently, the first new formulations for Trixeo Aerosphere (formoterol/glycopyrronium/budesonide combination therapy) and Riltrava Aerosphere (budesonide/glycopyrronium bromide/formoterol) for the treatment of COPD (7) came on the market; more are expected to follow. The list of more sustainable dose aerosols can be used for an up-to-date overview of dose aerosols based on more sustainable propellants.
Resources
- Foundation for Pharmaceutical Key Figures (SFK). 180,000 people use multiple types of inhalers. Pharmaceutical Weekly. 2021; PW51/52.
- Wichers IM, Pieters LI. Environmental impact of inhalers in the Netherlands and worldwide. Dutch Journal of Medicine. 2022; 166:E6718.
- Veldkamp R. Inhalation medication and environmental impact considerations in general practice. Utrecht: Level; 2022.
- Zorginstituut Nederland, CAHAG, De Groene Lung Doctor, KNMP, Lung Fund, NHG, NVALT, NVK. Trans-mural guideline for climate-aware prescribing of inhalation medication. April 9, 2025. Available at: https://www.zorginstituutnederland.nl/documenten/2025/04/09/transmurale-leidraad-klimaatbewust-voorschrijven-van-inhalatiemedicatie
- SFK. Shift from aerosol to powder inhaler. Pharmaceutisch Weekblad. 2025; 26. Available at: https://www.sfk.nl/publicatie/2025/farmacie-cijfers/verschuiving-van-aerosol-naar-poederinhalator.
- Drug Review Board. Environmental impact medicines. Pharmacotherapeutic Compass. [Internet]. Utrecht: Health Institute Netherlands. Accessed on: Aug 7, 2025. Available from: https://www.farmacotherapeutischkompas.nl/farmacologie/milieu-impact-geneesmiddelen
- European Medicines Agency (EMA). First reformulation of an inhaled medicine with an environmentally friendly gas propellant. Amsterdam: EMA; 2024 Feb 23. Accessed on: Aug 7, 2025. Available from: https://www.ema.europa.eu/en/news/first-reformulation-inhaled-medicine-environmentally-friendly-gas-propellant
Attachments
- Inhaler toolkit for environmental impact assessment — to follow
View our other interventions
Clinical care and outpatient care
Restrictive opioid prescribing with indication and intended treatment duration
The most commonly used, high-acting opioids are morphine, fentanyl, oxycodone, and buprenorphine (1). In 2024, more than 1.1 million people received an opioid through the public pharmacy (2). Although the total number of benefits in kind fell slightly compared to 2023, the number of prescriptions from the hospital actually increased slightly (3). A first dose of a high-acting opioid included an average of 9 days of medication in 2024 (3), while acute pain due to trauma or surgery often requires only 48 hours of strong opioid pain relief (4). Prescribing opioids for too long increases the risk of dependence and also leads to unnecessary environmental impact.
Research shows that the amount of opioids that patients receive at discharge influences their actual use (5). As recovery progresses, the need for opioids decreases rapidly; four days are sufficient for most patients. This is in line with international recommendations that recommend a duration of 3 - 7 days (6-8). The guideline of the Dutch Association of Anesthesiology (NVA) also recommends appropriate use of opioids through restrictive prescribing (up to 7 days) tailored to the pain experienced (9).
Another bottleneck is that the intended treatment duration and indication of opioids at discharge or outpatient dispensing are not always explicitly stated or shared with patients and primary care providers. As a result, GPs and pharmacists often lack crucial information to continue treatment responsibly or to phase it out in time. This increases the risk of unnecessarily long use, and thus unnecessary environmental impact and risk of dependency.
Clinical care
Paracetamol should be administered orally instead of intravenously
To treat postoperative pain, intravenous (IV) acetaminophen is usually administered. However, research shows that oral (PO) administration is equally effective and more sustainable in most patients. A systematic review of 14 studies shows that there is no convincing difference in the analgesic effect between IV and oral acetaminophen at different times after surgery (1). However, the environmental impact varies considerably: CO2 emissions from IV administration are up to 16x higher (2). Where an oral administration of 1 gram of acetaminophen from a blister results in the emission of approximately 38 grams of CO₂ eq., this can be up to 628 grams when administered IV, depending on the packaging and administration material (2).
In most patients, acetaminophen can be administered orally, as described in the NVZA Monograph 'Paracetamol' (3). The paracetamol challenge demonstrated that IV acetaminophen administration can be reduced by at least 25%, saving staff time, costs and environmental impact (4). These results underline deployment at a larger scale.
Clinical care and outpatient care
Targeted prescribing of proton pump inhibitors (as stomach protection)
Proton pump inhibitors (PPIs) are antacids that are frequently used. Pantoprazole (1.3 million users) and (es) omeprazole (1.2 million users) were among the top 3 most used medicines in 2023 (1). However, it appears that a large number of these drug users have no indication for PPI use (anymore) (2). With short-term use, more than half of the patients appeared to have no indication (3). Part of this is caused by starting PPIs as stomach protection without indication.
The NHG guideline “Prevention of stomach complications due to drug use (NL)” and the knowledge document proton pump inhibitors (NL) indicate that a PPI is indicated as stomach protection based on risk factors, such as age, ulcer or history of stomach complications, NSAID dosing, co-medication with an increased risk of stomach complications and comorbidities, such as rheumatoid arthritis, heart failure or diabetes (4 - 6). By prescribing PPIs based on risk factors for stomach protection, unnecessary PPI use can be reduced, thereby preventing environmental impact.
Clinical care
Treatment with oral antibiotics when bioavailability is good
Based on a recent opinion article This intervention has been selected in the NTvG by Kaal et al. This article recommends that there is more room for oral antibiotic initiation, but does not describe clinically tested interventions. This intervention will therefore be further developed on the basis of available scientific literature and will follow at a later date.