The Role of Pull Incentives in Addressing Antimicrobial Resistance
By Staff Writer
June 26, 2024
Introduction
Antimicrobial resistance (AMR) is a growing global health threat. According to recent estimates, AMR was responsible for 1.27 million deaths in 2019. This issue extends beyond human health, affecting animals, food, and the environment. The impact of AMR is also seen in the clinical and economic dimensions of global health. In order to manage AMR effectively, a comprehensive, multi-sectoral approach aligned with the One Health strategy is required. A recent study analysed the role of pull incentives in pricing, procurement, and reimbursement policies to encourage the development and market entry of novel antibiotics and AMR health products.
Understanding Pull Incentives
Pull incentives are financial rewards linked to research and development (R&D) results. Unlike push incentives, which provide direct funding and grants, pull incentives aim to stimulate market entry by making the market environment more attractive for suppliers. These incentives are crucial for AMR health products, given the high costs and uncertainties associated with developing novel antibiotics and diagnostics. In this study ten countries were selected for investigation: Australia, Brazil, France, Germany, Italy, Saudi Arabia, South Africa, South Korea, Spain, and Türkiye.
Figure 1. Graphical Abstract of Study by Vogler et al 2024
Current Policy Landscape
Some countries outside the selected countries have implemented innovative policies to address AMR. For instance, England introduced a “commercial model” in 2019, offering pharmaceutical companies a fixed annual fee of up to £10 million for novel antibiotics. For this a new cost-effectiveness evaluation methodology was developed by National Institute for Health and Care Excellence (NICE) to conduct health technology assessments (HTAs). Similarly, Sweden piloted a subscription-based model in 2020, granting companies a fixed annual revenue for specific low-volume antibiotics. These models aim to ensure the availability of essential antibiotics while encouraging their judicious use.
Transferability of Non-AMR Policies
Many non-AMR health products share characteristics with antibiotics, such as high prices, low volumes, and limited clinical evidence. These include examples such as oncology and orphan drugs. Policies successful in non-AMR contexts could be adapted for AMR health products. For example, orphan medicines often receive incentives to compensate for low volumes. Similar strategies could be applied to novel antibiotics, which may be produced in small quantities but have significant societal value.
Challenges and Future Directions
Implementing pull incentives comes with challenges. Financial incentives can strain public budgets and may require substantial policy modifications. Policymakers must balance the need to incentivise market entry with maintaining financial sustainability. Interestingly, they found more evidence for medicines than medical devices, suggesting a lower policy implementation level for medical devices. Future research needs to evaluate these policies’ effectiveness. We should also focus on developing indicators to measure their impact on health outcomes.
Conclusion
Addressing AMR requires a multi-faceted approach, including innovative pull incentives in pricing, procurement, and reimbursement policies. While these incentives can encourage the market entry of novel antibiotics, careful consideration of their financial and systemic impacts is essential. Policymakers must navigate these challenges to ensure sustainable and effective solutions for combating AMR.
🚀 Are pharmaceutical companies’ DTC telehealth partnerships reshaping healthcare for better or worse?
Recent findings from the “DTC Investigation 2025” report reveal key insights into the high prescription rates and potential risks of these digital platforms operated by giants like Pfizer and Eli Lilly. Alarmingly, inadequate clinical safeguards raise questions about patient safety, prescribing practices, and cost implications.
Dive into this critical discussion about the intersection of digital health and pharmaceutical practices, and explore what it means for the future of patient care.
🌟 How can personalized medicine transform breast cancer treatment in Spain?
The recent rollout of the MAF Test breast cancer in leading Spanish hospitals is set to revolutionize patient care by enabling targeted treatment strategies. This innovative molecular assay not only identifies patients who will benefit from bisphosphonates but also spares those for whom the treatment may be harmful, ultimately improving outcomes for thousands.
Dive into the article to discover how this approach aligns with global trends in oncology and enhances healthcare resource allocation.
🌟 Are we on the brink of transforming breast cancer treatment?
NICE’s latest guidance endorsing ribociclib in combination with an aromatase inhibitor marks a significant advancement for adults facing high-risk early breast cancer. This decision not only promises enhanced survival outcomes but also expands treatment options for patients historically limited to conventional therapies.
Dive into the details of this important development and learn how it may revolutionize patient care in the oncology landscape.
When you partner with Syenza, it’s like a Nuclear Fusion.
Our expertise are combined with yours, and we contribute clinical expertise and advanced degrees in
health policy, health economics, systems analysis, public finance, business, and project management. You’ll also feel our high-impact global and local perspectives with cultural intelligence.