
Medicine sustainability interventions
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.
Intervention
Administer paracetamol orally instead of intravenously unless there is a specific indication for intravenous administration.
Environmental impact
Measured in CO2-emissions by reducing the number of intravenous acetaminophen prescriptions compared to oral administration.
Working method
1. Determine the population and formulate a goal
- Inventory current policies in selected department/for selected patient group (s):
- Using administration data from the EPD, evaluate the proportion of patients receiving paracetamol intravenously (toolkit iv/enterally)?
- Formulate SMART goals together with (the green team of) the relevant department (s). For example: within three months, a 25% reduction in IV paracetamol use in postoperative pain medication in orthopedics.
2. Implementation
- Adjust protocol and predefined medication orders (if necessary).
- 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. To do this, the poster be used.
3. Monitoring and Evaluation
- Using the iv/enterally toolkit, check the proportion of IV compared to PO administrations, see ''Evaluation of a drug intervention' method. 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 reducing IV administrations compared to PO administrations based on administration records before and after implementation with the iv/enteral toolkit. See 'Method of evaluating a drug intervention'.
When successfully implemented?
Based on the reduction in the proportion of IV compared to PO acetaminophen administrations, as described in the previous section, determine when the implementation is considered successful, and reflect on the set goal.
Resources
- Mallama M, Valencia A, Rice K, Rietdijk WJR, Klimek M, Calvache JA. A systematic review and trial sequential analysis of intravenous vs. oral peri-operative acetaminophen. Anaesthesia 2020; 76:270—6.
- Davies JF, McAlister S, Eckelman MJ, McGain F, Seglenieks R, Gutman EN, Groome J, Palipane N, Latoff K, Nielsen D, Sherman JD; TRA2SH, GASP and WAREN collaborators. Environmental and financial impacts of perioperative paracetamol use: a multicentre international life-cycle assessment. Br J Anaesth. 2024 Dec; 133 (6) :1439-1448.
- NVZA Sustainability Committee/Drug Waste Working Group. Paracetamol monograph. Version 06-08-2025.
- Hunfeld N, Tibboel D, Gommers D. The paracetamol challenge in intensive care: going green with acetaminophen. Intensive Care Med. 2024 Oct 28; 50 (12) :2182—2184.
Attachments
- Video from infusion to tablet: the paracetamol challenge is a real win-win-win
- Hunfeld N, Tibboel D, Gommers D. The paracetamol challenge in intensive care: going green with paracetamol. Intensive Care Med. 2024 Oct 28; 50 (12) :2182—2184.
View our other interventions
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.
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 and outpatient care
Discontinuation of proton pump inhibitors without a current indication
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 (2). In short-term use, more than half of the patients appeared to have no indication (3); in chronic use, this figure is even 87% (4). Overtreatment with PPIs risks side effects, such as an increased risk of bone fractures and vitamin B12 deficiency, but also leads to unnecessary costs and environmental impact (2).
The NHG 'Stomach Disease (NL)' guideline and the NVMDL guideline 'Gastroesophageal Reflux Disease (NL)' provide recommendations to prevent overtreatment with PPIs (5.6). These guidelines recommend that patients with stomach problems or disorders with a temporary indication for PPIs should reduce a PPI within three months. Only patients with grade C and D4 reflux esophagitis, Barrett's oesophagus and Zollinger-Ellison syndrome should use a PPI for life (5 - 7). A PPI for stomach protection should be stopped when a patient stops taking the medication for which it was prescribed (8).
The Proton Pump Inhibitors Knowledge Paper (NL) explains the consideration for reducing or discontinuing proton pump inhibitors when using PPIs chronically (7). Reducing appears to be successful in approximately 40 - 70% of the patients, depending on the intervention that is chosen (9). In this way, any long-term side effects of PPIs can be prevented and costs and environmental impact can be saved (5 - 7).
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.