The Heart Failure Policy Network
HPP acts as secretariat to the Heart Failure Policy Network, which has recently launched a major call to action for European institutions to address the growing burden of heart failure.
Heart failure is a chronic syndrome where the heart is too weak or stiff to pump enough blood to support the needs of other organs in the body.
It is a challenging condition to manage, placing a heavy physical and psychological toll on those who live with the syndrome, along with their carers and families. Despite its significant cost to society, it is largely forgotten, with poor public awareness and understanding.
Heart failure is the most frequent cause of hospitalisation in people aged over 65, so the effect of an ageing population will make the disease burden even greater. Of people hospitalised with heart failure, one in four is readmitted to hospital within one month, and one in three will die within one year.
One in five people can expect to be diagnosed with heart failure at some point in their lives. Yet few governments have recognised its strategic significance, and health outcomes for people living with heart failure are unacceptable.
Heart failure and COVID-19
This report explores the emerging evidence around links between heart failure and COVID-19.Find out more
Heart failure policy and practice in Europe
Along with the pan-European report, country profiles explore the national picture of heart failure care in 11 countries.Find out more
A series of reports on topics at the forefront of debates and challenges in the future of heart failure care.Find out more
Understanding heart failure guidelines
A collection of seven lay summaries of key principles in leading European guidelines.Find out more
What we’ve achieved
HPP acts as secretariat to the Heart Failure Policy Network, which was launched in 2015. We have been instrumental leading the Network’s publications, meetings and political campaigns.
In 2015, Heart Failure Policy Network members and supporters gathered at the European Parliament on World Heart Day (29 September), to launch the Network’s Call to Action and the Heart Failure Policy Toolkit.
In 2016/17, the Network led a European Parliament Written Declaration on Heart Failure (WD 110/2016). Gaining 236 signatures, it was one of the largest ever political campaigns on heart failure. During 2017, the Network published summaries on the state of play in heart failure in 12 countries across Europe.
In 2018, the Network built on its previous work to produce The handbook of multidisciplinary and integrated heart failure care. It is designed to provide an accessible, action-oriented view of best practice, highlighting practical tools and models for change management aimed at patient advocates, healthcare professionals and decision-makers. It showcases examples of service innovation from across Europe and offers a starting point for policy discussions.
The handbook was launched at the European Parliament on 5 September 2018, along with five extended ‘pressure point’ documents published online. The handbook was originally published in English, with translations later published in Spanish (2019) and French (2021). A 10-page summary of the handbook is available in English, French, Italian, Polish and Spanish.
In 2019, the Network published a seven-part collection called Understanding heart failure guidelines, which offer an accessible overview of what key European guidelines say about important areas of heart failure. The guides focus on prevention, diagnosis, the multidisciplinary team, clinical management, comorbidities, patient empowerment and self-care, and advance care planning. In 2020, the Network launched the Spotlight series of reports focusing on topics at the forefront of debates and challenges in the future of heart failure care.
The Network published a landmark project in 2020: Heart failure policy and practice in Europe. Comprising a pan-European report and 11 country profiles, the project was developed to equip and empower national advocates across Europe with a clear picture of central leadership and overall performance in terms of major pillars of health services, treatment and care.
The Network has also published a report on heart failure and COVID-19, exploring the effect of the pandemic on heart failure care. Early in 2021, the Network developed a case study on reducing hospitalisations in heart failure, which was presented at the first global summit of the Partnership for Health System Sustainability and Resilience.
In 2021–23, the Network will continue raising awareness of unmet needs surrounding heart failure and will support advocates in securing high-level policy commitments for the syndrome at the national and European level. In September 2021, it launched the Action Statement on Heart Failure, arguably the most detailed call to action on heart failure yet directed at European institutions.
To find out more, please see the Heart Failure Policy Network website.
Key partners and stakeholders
The Heart Failure Policy Network is an independent, multidisciplinary group working to improve the lives of people living with heart failure by raising awareness of unmet needs. Its members and supporters include healthcare professionals, patient advocacy groups, policymakers and other stakeholders from across Europe. All members donate their time for free.
For full membership details, please see the Heart Failure Policy Network website.
The Heart Failure Policy Network is made possible with financial support from AstraZeneca, Vifor Pharma and Novartis Pharma. For details of past or project-specific funding, please visit the Network’s website.