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A Policy Call to Address Rare Kidney Disease in Health Care Plans
Raymond Vanholder1,2, Rosanna Coppo3, Willem J W Bos4,5
1European Kidney Health Alliance (EKHA), Brussels, Belgium.
Insights
Rare kidney diseases need targeted research and policy for better patient outcomes. This study offers policy recommendations to improve diagnosis, treatment, and patient quality of life for these uncommon conditions.
Area of Science:
- Nephrology
- Public Health Policy
- Rare Diseases Research
Background:
- Rare kidney diseases affect many globally but lack dedicated research and policy focus.
- Current approaches often generalize chronic kidney disease (CKD) management, neglecting specific rare causes.
- Suboptimal treatment of rare kidney diseases negatively impacts patient health, quality of life, and healthcare costs.
Purpose of the Study:
- To highlight the need for increased scientific and policy attention on rare kidney diseases.
- To propose specific policy recommendations for improving the care of rare kidney diseases.
- To advocate for a holistic approach to rare kidney disease management, from diagnosis to therapeutic innovation.
Main Methods:
- Review and analysis of current challenges in rare kidney disease care.
- Development of policy recommendations across key areas: awareness, diagnosis, management, and innovation.
- Emphasis on a collaborative, multi-stakeholder approach involving patients.
Main Results:
- Identified critical gaps in awareness, diagnosis acceleration, and therapeutic advancement for rare kidney diseases.
- Proposed actionable policies to address these gaps, aiming for targeted and effective interventions.
- Highlighted the necessity of patient partnership in developing and implementing solutions.
Conclusions:
- Specific policy interventions are crucial to improve outcomes for patients with rare kidney diseases.
- A coordinated effort involving researchers, policymakers, healthcare providers, and patients is essential.
- Implementing these recommendations can enhance health outcomes, reduce economic burdens, and benefit society.
Abstract:
Despite a large number of people globally being affected by rare kidney diseases, research support and health care policy programs usually focus on the management of the broad spectrum of CKD without particular attention to rare causes that would require a targeted approach for proper cure. Hence, specific curative approaches for rare kidney diseases are scarce, and these diseases are not treated optimally, with implications on the patients' health and quality of life, on the cost for the health care system, and society. There is therefore a need for rare kidney diseases and their mechanisms to receive the appropriate scientific, political, and policy attention to develop specific corrective approaches. A wide range of policies are required to address the various challenges that target care for rare kidney diseases, including the need to increase awareness, improve and accelerate diagnosis, support and implement therapeutic advances, and inform the management of the diseases. In this article, we provide specific policy recommendations to address the challenges hindering the provision of targeted care for rare kidney diseases, focusing on awareness and prioritization, diagnosis, management, and therapeutic innovation. In combination, the recommendations provide a holistic approach aiming for all aspects of rare kidney disease care to improve health outcomes, reduce the economic effect, and deliver benefits to society. Greater commitment from all the key stakeholders is now needed, and a central role should be assigned to patients with rare kidney disease to partner in the design and implementation of potential solutions.
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