25in25 倡议:在未来 25 年内将心力衰竭导致的死亡率降低 25% 的新型变革项目

IF 16.9 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS European Journal of Heart Failure Pub Date : 2024-10-25 DOI:10.1002/ejhf.3496
Henry Oluwasefunmi Savage, Kyle McBeath, Janine Hogan, Lynn MacKay-Thomas, Lisa Anderson, Andy Smith, Joanne Bateman, Poppy Brooks, Antoni Bayes-Genis, Amanda Vest, John Teerlink, Giuseppe Rosano, Roy S. Gardner
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Gardner","doi":"10.1002/ejhf.3496","DOIUrl":null,"url":null,"abstract":"<p>We are at a crucial point in time for those with cardiovascular diseases such as heart failure (HF).</p><p>An estimated 64.3 million people are living with HF worldwide.<span><sup>1</sup></span> In developed countries, the prevalence of diagnosed HF is estimated at 1–2% of the adult population,<span><sup>2, 3</sup></span> and with factors such as our expanding ageing population, figures are set to double by 2040 (<i>Figure</i> 1).</p><p>Heart failure is a final common pathway for almost all cardiovascular diseases, but also a significant cause of mortality across the wider cardio-renal-metabolic spectrum. Over 90% of those who are diagnosed with HF are living with at least one other long-term condition<span><sup>4</sup></span> such as diabetes, kidney disease, high blood pressure, chronic obstructive pulmonary disease and depression. From epidemiology to pathophysiology, there is a large multi-specialty and multi-disciplinary overlap.</p><p>Diagnosing HF, however, remains a challenge. Eighty per cent of patients receive their diagnosis during an emergency admission.<span><sup>5</sup></span> This is even though up to 40% of these patients had symptoms many months prior to that admission which should have triggered an earlier assessment.<span><sup>5</sup></span> Delayed diagnosis has a significant impact on mortality and spending. One in three of these patients do not survive up to 1 year and inpatient costs are a significant driver of expenditure for HF care, which itself accounts for almost 2% (€2.3 billion) of the entire National Health Service (NHS) budget.<span><sup>6</sup></span></p><p>Many patients with HF remain undetected and undiagnosed. In the UK alone, it is estimated that around 400 000 people who have HF remain without a documented diagnosis. These patients are disproportionately at risk of socioeconomic deprivation and associated worse outcomes, including more frequent exacerbations, repeated hospital admissions and increased HF mortality.<span><sup>7</sup></span> The undetected and undiagnosed are deprived of life-preserving HF treatments. The human and economic costs are huge. It is time for action.</p><p>The primary aim of the 25in25 initiative is to reduce HF mortality in the first year after diagnosis by 25% in the next 25 years. This equates to five fewer deaths for every 100 patients newly diagnosed with HF every year, translating to over 10 000 lives saved annually.</p><p>Secondary aims include: (i) the development of a robust ambulatory HF database from a community focal point, with dynamic data modelling and the opportunity for future research; (ii) to educate, encourage and facilitate engagement from the broader spectrum of clinicians in specialties intersecting with HF care to make every contact count; and (iii) to make HF a national priority by influencing thought leaders, policymakers, and politicians to prioritize HF.</p><p>The British Society for Heart Failure (BSH) recognized the internationally shared concern of increasing HF caseload and realized that as a specialty, we are under resourced and therefore less able to face the growing unmet need of HF care, alone. Spearheaded by the BSH a Summit was called in March 2023, to bring together ~60 organizations (online supplementary <i>Appendix</i> <i>S1</i>) across a broad spectrum of specialties that intersect with HF care, including clinicians, patients and policy groups. These selected organizations brought specialist knowledge and expertise to the discussion, which ended with signing the ‘25in25 declaration’—to change the trajectory of HF and become part of the 25in25 Collaborative (<i>Figure</i> 2).</p><p>The 25in25 Collaborative agreed to implement/test a Fast-Track Communities (FTC) approach, successfully deployed for HIV as the model for implementation.<span><sup>8</sup></span></p><p>Risk identification (prevention), early diagnosis, early treatment and patient empowerment (such as quality of life (QOL)/mental health and wellbeing measures) were agreed as priority areas for data collection and indicators to prevent avoidable deaths due to HF. As a result of the Summit, the Collaborative finalized a roadmap to guide implementation and the 25in25 initiative was launched as a novel transformative quality improvement project to reduce mortality due to HF by 25% in the next 25 years.</p><p>The 25in25 implementation programme targets this significant public health issue with a long-term strategy: lowering the 1-year mortality rate following a HF diagnosis by 25% within 25 years by identifying the key areas of improvement across a locality and community. By risk factor identification (prevention), early detection, diagnosis, treatment, and improving QOL, the focus is on developing collaborative solutions to methodically prioritize and address them.</p><p>The 25in25 pilot programme, which relies on systematic case-finding of currently undetected HF, is underway in five locations across the UK. Data are being collected through specified searches from patient records on general practitioner systems aligned to a national strategy of reducing mortality and morbidity. Local system searches will identify citizens that need intervention or monitoring across the community, with aggregated, anonymized data uploaded and benchmarked on a national platform to observe the national picture.</p><p>The extracts of data collected will be analysed locally and potential areas for quality improvement identified. Solutions will be developed and supported across the community, involving all stakeholders across care settings providing holistic support, including social and community advocates. Benchmarked data would be utilized to monitor impact over time and enhance HF management.</p><p>By focusing on prevention, early detection, accurate diagnosis, appropriate treatment and empowering not just the clinicians but citizens and communities, the 25in25 initiative will transform population health outcomes related to HF and its comorbidities and reduce the burden on the health service. The initiative underscores the importance of a collaborative, community-based approach to tackling HF, ensuring that health improvements start within the communities and extend to a national scale.</p><p>We have started work with pilot sites regarding data collection and intelligence needed to build the dashboard. Early analysis to identify potential areas for quality improvement has begun as a dynamic process for change. Solutions will be developed and supported across the community and benchmarked data would be utilized to monitor impact over time and enhance HF management.</p><p>Furthermore, we are establishing engagement strategies with health and care boards and local health authorities to support these pilot programmes. And we intend to create cross-stakeholder agreements in these pilot sites, on priority factors to address future challenges in cardiovascular outcomes.</p><p>The 25in25 initiative will support informed care and improved outcomes in patients with long-term conditions leading to HF, and address health inequalities by tackling disparities of access, experience, and outcomes in under-served patient groups.</p><p>By focusing on prevention, early detection, accurate diagnosis, appropriate treatment and empowering citizens and communities, the 25in25 initiative aims to significantly improve population health outcomes related to HF and reduce the burden on health services. 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From epidemiology to pathophysiology, there is a large multi-specialty and multi-disciplinary overlap.</p><p>Diagnosing HF, however, remains a challenge. Eighty per cent of patients receive their diagnosis during an emergency admission.<span><sup>5</sup></span> This is even though up to 40% of these patients had symptoms many months prior to that admission which should have triggered an earlier assessment.<span><sup>5</sup></span> Delayed diagnosis has a significant impact on mortality and spending. One in three of these patients do not survive up to 1 year and inpatient costs are a significant driver of expenditure for HF care, which itself accounts for almost 2% (€2.3 billion) of the entire National Health Service (NHS) budget.<span><sup>6</sup></span></p><p>Many patients with HF remain undetected and undiagnosed. In the UK alone, it is estimated that around 400 000 people who have HF remain without a documented diagnosis. These patients are disproportionately at risk of socioeconomic deprivation and associated worse outcomes, including more frequent exacerbations, repeated hospital admissions and increased HF mortality.<span><sup>7</sup></span> The undetected and undiagnosed are deprived of life-preserving HF treatments. The human and economic costs are huge. It is time for action.</p><p>The primary aim of the 25in25 initiative is to reduce HF mortality in the first year after diagnosis by 25% in the next 25 years. This equates to five fewer deaths for every 100 patients newly diagnosed with HF every year, translating to over 10 000 lives saved annually.</p><p>Secondary aims include: (i) the development of a robust ambulatory HF database from a community focal point, with dynamic data modelling and the opportunity for future research; (ii) to educate, encourage and facilitate engagement from the broader spectrum of clinicians in specialties intersecting with HF care to make every contact count; and (iii) to make HF a national priority by influencing thought leaders, policymakers, and politicians to prioritize HF.</p><p>The British Society for Heart Failure (BSH) recognized the internationally shared concern of increasing HF caseload and realized that as a specialty, we are under resourced and therefore less able to face the growing unmet need of HF care, alone. 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引用次数: 0

摘要

导言 对于心血管疾病(如心力衰竭)患者来说,我们正处于一个关键时刻。据估计,全球有 6430 万人患有心力衰竭。在发达国家,确诊的心力衰竭患病率估计占成年人口的 1-2%,2, 3 而随着人口老龄化等因素的加剧,到 2040 年,这一数字将翻一番(图 1)。图 1在图形浏览器中打开PowerPoint2019 年,英格兰和 2040 年预测的对 30 岁及以上人群医疗保健使用和死亡率影响最大的 10 种疾病的确诊病例总数,包括人口变化。资料来源:健康基金会 REAL 中心。13 REAL 中心和利物浦大学对关联的医疗记录和死亡率数据进行了分析。红色阴影条代表不确定区间。心力衰竭是几乎所有心血管疾病的最终常见途径,同时也是导致心肾代谢疾病死亡的重要原因。超过 90% 的心力衰竭患者至少还患有其他一种长期疾病4 ,如糖尿病、肾病、高血压、慢性阻塞性肺病和抑郁症。从流行病学到病理生理学,存在大量的多专业和多学科重叠。80% 的患者在急诊入院时得到诊断。5 尽管其中高达 40% 的患者在入院前数月就已出现症状,本应更早进行评估。5 诊断延误对死亡率和医疗支出都有重大影响。三分之一的患者无法存活 1 年,住院费用是心房颤动医疗支出的主要驱动因素,而心房颤动医疗支出本身就占整个国民健康服务(NHS)预算的近 2%(23 亿欧元)。据估计,仅在英国就有约 40 万心房颤动患者仍未得到确诊。这些患者面临着极大的社会经济贫困和相关不良后果的风险,包括更频繁的病情加重、反复入院和更高的心房颤动死亡率。这将造成巨大的人力和经济损失。现在是采取行动的时候了。
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The 25in25 initiative: A novel transformative project to reduce mortality due to heart failure by 25% in the next 25 years

We are at a crucial point in time for those with cardiovascular diseases such as heart failure (HF).

An estimated 64.3 million people are living with HF worldwide.1 In developed countries, the prevalence of diagnosed HF is estimated at 1–2% of the adult population,2, 3 and with factors such as our expanding ageing population, figures are set to double by 2040 (Figure 1).

Heart failure is a final common pathway for almost all cardiovascular diseases, but also a significant cause of mortality across the wider cardio-renal-metabolic spectrum. Over 90% of those who are diagnosed with HF are living with at least one other long-term condition4 such as diabetes, kidney disease, high blood pressure, chronic obstructive pulmonary disease and depression. From epidemiology to pathophysiology, there is a large multi-specialty and multi-disciplinary overlap.

Diagnosing HF, however, remains a challenge. Eighty per cent of patients receive their diagnosis during an emergency admission.5 This is even though up to 40% of these patients had symptoms many months prior to that admission which should have triggered an earlier assessment.5 Delayed diagnosis has a significant impact on mortality and spending. One in three of these patients do not survive up to 1 year and inpatient costs are a significant driver of expenditure for HF care, which itself accounts for almost 2% (€2.3 billion) of the entire National Health Service (NHS) budget.6

Many patients with HF remain undetected and undiagnosed. In the UK alone, it is estimated that around 400 000 people who have HF remain without a documented diagnosis. These patients are disproportionately at risk of socioeconomic deprivation and associated worse outcomes, including more frequent exacerbations, repeated hospital admissions and increased HF mortality.7 The undetected and undiagnosed are deprived of life-preserving HF treatments. The human and economic costs are huge. It is time for action.

The primary aim of the 25in25 initiative is to reduce HF mortality in the first year after diagnosis by 25% in the next 25 years. This equates to five fewer deaths for every 100 patients newly diagnosed with HF every year, translating to over 10 000 lives saved annually.

Secondary aims include: (i) the development of a robust ambulatory HF database from a community focal point, with dynamic data modelling and the opportunity for future research; (ii) to educate, encourage and facilitate engagement from the broader spectrum of clinicians in specialties intersecting with HF care to make every contact count; and (iii) to make HF a national priority by influencing thought leaders, policymakers, and politicians to prioritize HF.

The British Society for Heart Failure (BSH) recognized the internationally shared concern of increasing HF caseload and realized that as a specialty, we are under resourced and therefore less able to face the growing unmet need of HF care, alone. Spearheaded by the BSH a Summit was called in March 2023, to bring together ~60 organizations (online supplementary Appendix S1) across a broad spectrum of specialties that intersect with HF care, including clinicians, patients and policy groups. These selected organizations brought specialist knowledge and expertise to the discussion, which ended with signing the ‘25in25 declaration’—to change the trajectory of HF and become part of the 25in25 Collaborative (Figure 2).

The 25in25 Collaborative agreed to implement/test a Fast-Track Communities (FTC) approach, successfully deployed for HIV as the model for implementation.8

Risk identification (prevention), early diagnosis, early treatment and patient empowerment (such as quality of life (QOL)/mental health and wellbeing measures) were agreed as priority areas for data collection and indicators to prevent avoidable deaths due to HF. As a result of the Summit, the Collaborative finalized a roadmap to guide implementation and the 25in25 initiative was launched as a novel transformative quality improvement project to reduce mortality due to HF by 25% in the next 25 years.

The 25in25 implementation programme targets this significant public health issue with a long-term strategy: lowering the 1-year mortality rate following a HF diagnosis by 25% within 25 years by identifying the key areas of improvement across a locality and community. By risk factor identification (prevention), early detection, diagnosis, treatment, and improving QOL, the focus is on developing collaborative solutions to methodically prioritize and address them.

The 25in25 pilot programme, which relies on systematic case-finding of currently undetected HF, is underway in five locations across the UK. Data are being collected through specified searches from patient records on general practitioner systems aligned to a national strategy of reducing mortality and morbidity. Local system searches will identify citizens that need intervention or monitoring across the community, with aggregated, anonymized data uploaded and benchmarked on a national platform to observe the national picture.

The extracts of data collected will be analysed locally and potential areas for quality improvement identified. Solutions will be developed and supported across the community, involving all stakeholders across care settings providing holistic support, including social and community advocates. Benchmarked data would be utilized to monitor impact over time and enhance HF management.

By focusing on prevention, early detection, accurate diagnosis, appropriate treatment and empowering not just the clinicians but citizens and communities, the 25in25 initiative will transform population health outcomes related to HF and its comorbidities and reduce the burden on the health service. The initiative underscores the importance of a collaborative, community-based approach to tackling HF, ensuring that health improvements start within the communities and extend to a national scale.

We have started work with pilot sites regarding data collection and intelligence needed to build the dashboard. Early analysis to identify potential areas for quality improvement has begun as a dynamic process for change. Solutions will be developed and supported across the community and benchmarked data would be utilized to monitor impact over time and enhance HF management.

Furthermore, we are establishing engagement strategies with health and care boards and local health authorities to support these pilot programmes. And we intend to create cross-stakeholder agreements in these pilot sites, on priority factors to address future challenges in cardiovascular outcomes.

The 25in25 initiative will support informed care and improved outcomes in patients with long-term conditions leading to HF, and address health inequalities by tackling disparities of access, experience, and outcomes in under-served patient groups.

By focusing on prevention, early detection, accurate diagnosis, appropriate treatment and empowering citizens and communities, the 25in25 initiative aims to significantly improve population health outcomes related to HF and reduce the burden on health services. The initiative underscores the importance of a collaborative, community-based approach and locally designed solutions, ensuring that health improvements start within the communities and trends observed nationally.

The 25in25 initiative will leverage its reach, infrastructure, and human capacity to build a more equitable, inclusive, prosperous, and sustainable future for all those in danger of premature mortality from HF, regardless of age, gender, ethnicity, and social and economic circumstances.

We believe that this strategy is viable, cost-effective and has a transferrable methodology to improve the care of patients with HF across diverse healthcare systems.

Conflict of interest: none declared.

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来源期刊
European Journal of Heart Failure
European Journal of Heart Failure 医学-心血管系统
CiteScore
27.30
自引率
11.50%
发文量
365
审稿时长
1 months
期刊介绍: European Journal of Heart Failure is an international journal dedicated to advancing knowledge in the field of heart failure management. The journal publishes reviews and editorials aimed at improving understanding, prevention, investigation, and treatment of heart failure. It covers various disciplines such as molecular and cellular biology, pathology, physiology, electrophysiology, pharmacology, clinical sciences, social sciences, and population sciences. The journal welcomes submissions of manuscripts on basic, clinical, and population sciences, as well as original contributions on nursing, care of the elderly, primary care, health economics, and other related specialist fields. It is published monthly and has a readership that includes cardiologists, emergency room physicians, intensivists, internists, general physicians, cardiac nurses, diabetologists, epidemiologists, basic scientists focusing on cardiovascular research, and those working in rehabilitation. The journal is abstracted and indexed in various databases such as Academic Search, Embase, MEDLINE/PubMed, and Science Citation Index.
期刊最新文献
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