家庭癌症护理的未来:来自美国癌症协会峰会的发现

IF 503.1 1区 医学 Q1 ONCOLOGY CA: A Cancer Journal for Clinicians Pub Date : 2023-05-24 DOI:10.3322/caac.21784
Arif H. Kamal MD, MBA, MHS, Paul P. Thienprayoon MBA, MS, Marco H. M. Janssen MSc, PhD, Lisa A. Lacasse MBA, William L. Dahut MD, Justin E. Bekelman MD
{"title":"家庭癌症护理的未来:来自美国癌症协会峰会的发现","authors":"Arif H. Kamal MD, MBA, MHS,&nbsp;Paul P. Thienprayoon MBA, MS,&nbsp;Marco H. M. Janssen MSc, PhD,&nbsp;Lisa A. Lacasse MBA,&nbsp;William L. Dahut MD,&nbsp;Justin E. Bekelman MD","doi":"10.3322/caac.21784","DOIUrl":null,"url":null,"abstract":"<p>In February 2022, the White House announced the reignition of the Cancer Moonshot Initiative with the goals of reducing the death rate from cancer by at least 50% over the next 25 years and improving the experience of people and their families living with and surviving cancer. A core component of the Cancer Moonshot Initiative is the facilitation of multisector partnerships to solve the compelling challenges faced in cancer care delivery. The American Cancer Society (ACS) has a longstanding tradition of convening partners across the cancer landscape, most notably through conferences, partner meetings, advocacy coalitions, and coalescing of thought leaders through roundtables. For example, the ACS and several patient advocacy organizations, scientific organizations, and pharmaceutical partners came together in October 2022 to launch the new ACS National Breast Cancer Roundtable and the ACS National Cervical Cancer Roundtable as “all-hands-on-deck” coalitions to reshape cancer care.<span><sup>1</sup></span> These Roundtables aim to both (1) identify the leading challenges in detection and treatment within these cancers and (2) provide expert guidance to providers, patients, payers, and policy makers regarding evolutions needed to increase access and patient centricity of cancer care. Beyond disease-specific issues, the ACS and its partners have also explored topics that span the cancer care continuum.</p><p>Currently, much of the attention given to innovation in oncology is centered upon creating and delivering a rapidly expanding armamentarium of anticancer treatments. Efforts to develop more novel, personalized, and targeted therapies have been fruitful but also continue to further highlight issues related to access. How treatments are selected and delivered and how outcomes are monitored require additional focus. Furthermore, how such efforts align with increasing calls for patient centricity, meeting patients where they are both figuratively and literally, requires a national discussion. Herein, we describe the findings from the first effort of the ACS in convening national leaders across multiple stakeholders, including the provider, payer, government, and technology communities, to discuss cancer care delivery at home.</p><p>This ACS Cancer Care at Home Summit convened in Cambridge, Massachusetts, on October 26, 2022, using a “design-thinking” framework to identify the major issues in decentralized cancer care delivery and plan for the next steps forward. The Summit convened 30 national leaders at the Philips North America campus using Chatham House rules during which participants were guided in building a shared mental model, framing the challenges and ideating around barriers, defining opportunities, and sharing findings with each other to determine next steps. To ensure that the ACS optimally used the time dedicated by these senior leaders, untapping the immense potential of the combination of participants in the room, and really getting to actionable outcomes, the ACS invited the Philips Experience Design Team to facilitate the Summit. The Experience Design Team had experience in guiding discussions in this area, leveraging a recent effort in developing a Caregiver Journey Map for Veteran caregivers in partnership with the Elizabeth Dole Foundation and the Veterans Administration. Together, the ACS and the Experience Design Team used conversations with national leaders in cancer care delivered at home to identify four major challenges along with issues that underly barriers: (1) logistics/supply chain, (2) finance/payment, (3) patient acceptance, and (4) regulatory. The participants also identified issues that affect all four of those areas and must be included when ideating around solutions such as health equity and social determinants of health, care-provider acceptance, and data interoperability and ecosystem implications. Participants were split into four preselected groupings to provide the right balance between domain knowledge and “out-of-the-box” thinking in each area.</p><p>Each group was led by an Experience Design facilitator who fostered communication and captured points as the discussions occurred. Conversations operated under Chatham House rules.<span><sup>2</sup></span> Facilitators homed in on common themes from the group discussions, and themes were organized (or <i>framed</i>) into multiple “how might we” statements, allowing for the groups to decide which areas were the most critical or needed to be prioritized to successfully create cancer care delivery at home. From there, the group participants focused on solutions that would help solve the selected issue, which would then allow for easier ability to approach the other “how might we” areas.</p><p>Finally, to realize change, leaders must be willing to challenge the status quo. This recommendation provides a goal to help simplify the multitude of appointments needed by optimizing care plans according to standard care pathways, introduce patient preference for their conversations, and flag opportunities for more streamlined appointment coordination. Together, this vision combines the human touch of patient navigation with optimized workflows that have ardent efficiency.</p><p>The group chose to further drill down on the two more critical groupings of the three, provide new “how might we” questions, and provide solutions to those barrier themes:</p><p>The workgroup used two questions to build a solution around redefining questions: “how might we understand the real costs of cancer care at home relative to outpatient, office, or hospital care?” and “how might we identify benefits and risks to the patients and to the providers associated with cancer care at home?” To do this, the group recommended that the first solution to financial barriers was <i>to ensure information dissemination</i>. This would require all stakeholders to make available to patients and caregivers out-of-pocket expenses and other financial costs associated with care at home relative to care in office, outpatient, or hospital settings. In further detail, leaders need to publish barriers to financially viable models. In addition, those models would be augmented with stories of successful implementation and alignment of incentives. Finally, the group called on the ACS to lead cancer plan decision mapping and criteria for success of cancer care at home programs.</p><p>To guide solution design, for the total cost of care, the group answered two questions: “how might we, as a nation, finance nonreimbursed patient support services?” and “how might we share cost savings with patients, caregivers, and providers?” The second solution would require leaders <i>to explore, test and validate new financial benefit programs and products</i>. This would include programs for direct financial reimbursement to caregivers delivering home care, home care insurance policy products, and test those benefit programs with the Center for Medicare and Medicaid Innovation and the Centers for Medicare and Medicaid Services. Continuing with the total cost of care, the group provided two additional questions to guide the third solution: “how might we optimize payer models for care at home?” and “how might we redefine incentives to match optimal care models?”</p><p>From these concepts, the <i>gains</i> the national cancer population could and needs to affect are improved health equity along with improved patient, provider, and caregiver experience. In addition, it is expected to garner increased patient satisfaction, improved care, and lower costs across all stakeholders. These <i>gains</i> became the catalyst for the group's opportunity build statement: “How might we stand up an innovation laboratory to enable cross-collaboration with community-based health systems, payers, and patients?”</p><p>The two “how might we” statements that the group chose to work on were: “how might we drive change to enable more care to be delivered across state lines” and “how might we rethink reimbursements?” For driving change across state lines, the group found that many of the <i>changes that were implemented in response to COVID would enable cancer care at home and should be extended in order for cancer care at home to be successful</i>. Specifically looking at licensing acceptance on a national basis, having a standard set across state lines allows for cancer care at home to be better implemented for all patients as opposed to different requirements in each state. Together, both approaches allow for more scalable use of expert resources for patients, caregivers, and care providers. In addition, telehealth programs to support home care can be more effectively delivered. Finally, these measures are foundational for <i>at home</i> or <i>out-of-hospital</i> care. The second statement, “how might we rethink reimbursements,” called on national leaders to look for more incentives, and regulations to support those incentives, for more out-of-hospital care with a new reimbursement model that would reflect this new cancer care delivery approach. This would also have to include changes to regulations that enable increased patient preference in how and where they receive care. Finally, these regulatory changes will stimulate innovative delivery practices and the data that support them.</p><p>The successful delivery of cancer care, spanning from prevention through early detection, treatment, and survivorship, as well as clinical trials outside traditional medical facilities, represents a potential seismic shift in oncology. Complementing the recent unprecedented expansion of cancer treatment options, cancer care in the place a patient calls home could help address some longstanding barriers to equitable access to care, particularly for populations marginalized because of geography, travel requirements to get to care providers, proximity to clinical trials, and overall financial burdens of cancer care. We look forward to continuing to build partnerships and further discussions to explore the potential of, barriers to, and solutions to achieve a paradigm shift where appropriate to bring cancer care to the patient rather than requiring the patient to go to cancer care.</p><p>Arif H. Kamal reports personal fees from Homebase Medical outside the submitted work and is chief executive officer of Prepped Health. Justin E. Bekelman reports personal fees from AstraZeneca, Healthcare Foundry, Reimagine Care, and United Healthcare outside the submitted work. The remaining authors declared no conflicts of interest.</p>","PeriodicalId":137,"journal":{"name":"CA: A Cancer Journal for Clinicians","volume":null,"pages":null},"PeriodicalIF":503.1000,"publicationDate":"2023-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.3322/caac.21784","citationCount":"0","resultStr":"{\"title\":\"The future of cancer care at home: Findings from an American Cancer Society summit\",\"authors\":\"Arif H. Kamal MD, MBA, MHS,&nbsp;Paul P. Thienprayoon MBA, MS,&nbsp;Marco H. M. Janssen MSc, PhD,&nbsp;Lisa A. Lacasse MBA,&nbsp;William L. Dahut MD,&nbsp;Justin E. Bekelman MD\",\"doi\":\"10.3322/caac.21784\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In February 2022, the White House announced the reignition of the Cancer Moonshot Initiative with the goals of reducing the death rate from cancer by at least 50% over the next 25 years and improving the experience of people and their families living with and surviving cancer. A core component of the Cancer Moonshot Initiative is the facilitation of multisector partnerships to solve the compelling challenges faced in cancer care delivery. The American Cancer Society (ACS) has a longstanding tradition of convening partners across the cancer landscape, most notably through conferences, partner meetings, advocacy coalitions, and coalescing of thought leaders through roundtables. For example, the ACS and several patient advocacy organizations, scientific organizations, and pharmaceutical partners came together in October 2022 to launch the new ACS National Breast Cancer Roundtable and the ACS National Cervical Cancer Roundtable as “all-hands-on-deck” coalitions to reshape cancer care.<span><sup>1</sup></span> These Roundtables aim to both (1) identify the leading challenges in detection and treatment within these cancers and (2) provide expert guidance to providers, patients, payers, and policy makers regarding evolutions needed to increase access and patient centricity of cancer care. Beyond disease-specific issues, the ACS and its partners have also explored topics that span the cancer care continuum.</p><p>Currently, much of the attention given to innovation in oncology is centered upon creating and delivering a rapidly expanding armamentarium of anticancer treatments. Efforts to develop more novel, personalized, and targeted therapies have been fruitful but also continue to further highlight issues related to access. How treatments are selected and delivered and how outcomes are monitored require additional focus. Furthermore, how such efforts align with increasing calls for patient centricity, meeting patients where they are both figuratively and literally, requires a national discussion. Herein, we describe the findings from the first effort of the ACS in convening national leaders across multiple stakeholders, including the provider, payer, government, and technology communities, to discuss cancer care delivery at home.</p><p>This ACS Cancer Care at Home Summit convened in Cambridge, Massachusetts, on October 26, 2022, using a “design-thinking” framework to identify the major issues in decentralized cancer care delivery and plan for the next steps forward. The Summit convened 30 national leaders at the Philips North America campus using Chatham House rules during which participants were guided in building a shared mental model, framing the challenges and ideating around barriers, defining opportunities, and sharing findings with each other to determine next steps. To ensure that the ACS optimally used the time dedicated by these senior leaders, untapping the immense potential of the combination of participants in the room, and really getting to actionable outcomes, the ACS invited the Philips Experience Design Team to facilitate the Summit. The Experience Design Team had experience in guiding discussions in this area, leveraging a recent effort in developing a Caregiver Journey Map for Veteran caregivers in partnership with the Elizabeth Dole Foundation and the Veterans Administration. Together, the ACS and the Experience Design Team used conversations with national leaders in cancer care delivered at home to identify four major challenges along with issues that underly barriers: (1) logistics/supply chain, (2) finance/payment, (3) patient acceptance, and (4) regulatory. The participants also identified issues that affect all four of those areas and must be included when ideating around solutions such as health equity and social determinants of health, care-provider acceptance, and data interoperability and ecosystem implications. Participants were split into four preselected groupings to provide the right balance between domain knowledge and “out-of-the-box” thinking in each area.</p><p>Each group was led by an Experience Design facilitator who fostered communication and captured points as the discussions occurred. Conversations operated under Chatham House rules.<span><sup>2</sup></span> Facilitators homed in on common themes from the group discussions, and themes were organized (or <i>framed</i>) into multiple “how might we” statements, allowing for the groups to decide which areas were the most critical or needed to be prioritized to successfully create cancer care delivery at home. From there, the group participants focused on solutions that would help solve the selected issue, which would then allow for easier ability to approach the other “how might we” areas.</p><p>Finally, to realize change, leaders must be willing to challenge the status quo. This recommendation provides a goal to help simplify the multitude of appointments needed by optimizing care plans according to standard care pathways, introduce patient preference for their conversations, and flag opportunities for more streamlined appointment coordination. Together, this vision combines the human touch of patient navigation with optimized workflows that have ardent efficiency.</p><p>The group chose to further drill down on the two more critical groupings of the three, provide new “how might we” questions, and provide solutions to those barrier themes:</p><p>The workgroup used two questions to build a solution around redefining questions: “how might we understand the real costs of cancer care at home relative to outpatient, office, or hospital care?” and “how might we identify benefits and risks to the patients and to the providers associated with cancer care at home?” To do this, the group recommended that the first solution to financial barriers was <i>to ensure information dissemination</i>. This would require all stakeholders to make available to patients and caregivers out-of-pocket expenses and other financial costs associated with care at home relative to care in office, outpatient, or hospital settings. In further detail, leaders need to publish barriers to financially viable models. In addition, those models would be augmented with stories of successful implementation and alignment of incentives. Finally, the group called on the ACS to lead cancer plan decision mapping and criteria for success of cancer care at home programs.</p><p>To guide solution design, for the total cost of care, the group answered two questions: “how might we, as a nation, finance nonreimbursed patient support services?” and “how might we share cost savings with patients, caregivers, and providers?” The second solution would require leaders <i>to explore, test and validate new financial benefit programs and products</i>. This would include programs for direct financial reimbursement to caregivers delivering home care, home care insurance policy products, and test those benefit programs with the Center for Medicare and Medicaid Innovation and the Centers for Medicare and Medicaid Services. Continuing with the total cost of care, the group provided two additional questions to guide the third solution: “how might we optimize payer models for care at home?” and “how might we redefine incentives to match optimal care models?”</p><p>From these concepts, the <i>gains</i> the national cancer population could and needs to affect are improved health equity along with improved patient, provider, and caregiver experience. In addition, it is expected to garner increased patient satisfaction, improved care, and lower costs across all stakeholders. These <i>gains</i> became the catalyst for the group's opportunity build statement: “How might we stand up an innovation laboratory to enable cross-collaboration with community-based health systems, payers, and patients?”</p><p>The two “how might we” statements that the group chose to work on were: “how might we drive change to enable more care to be delivered across state lines” and “how might we rethink reimbursements?” For driving change across state lines, the group found that many of the <i>changes that were implemented in response to COVID would enable cancer care at home and should be extended in order for cancer care at home to be successful</i>. Specifically looking at licensing acceptance on a national basis, having a standard set across state lines allows for cancer care at home to be better implemented for all patients as opposed to different requirements in each state. Together, both approaches allow for more scalable use of expert resources for patients, caregivers, and care providers. In addition, telehealth programs to support home care can be more effectively delivered. Finally, these measures are foundational for <i>at home</i> or <i>out-of-hospital</i> care. The second statement, “how might we rethink reimbursements,” called on national leaders to look for more incentives, and regulations to support those incentives, for more out-of-hospital care with a new reimbursement model that would reflect this new cancer care delivery approach. This would also have to include changes to regulations that enable increased patient preference in how and where they receive care. Finally, these regulatory changes will stimulate innovative delivery practices and the data that support them.</p><p>The successful delivery of cancer care, spanning from prevention through early detection, treatment, and survivorship, as well as clinical trials outside traditional medical facilities, represents a potential seismic shift in oncology. Complementing the recent unprecedented expansion of cancer treatment options, cancer care in the place a patient calls home could help address some longstanding barriers to equitable access to care, particularly for populations marginalized because of geography, travel requirements to get to care providers, proximity to clinical trials, and overall financial burdens of cancer care. We look forward to continuing to build partnerships and further discussions to explore the potential of, barriers to, and solutions to achieve a paradigm shift where appropriate to bring cancer care to the patient rather than requiring the patient to go to cancer care.</p><p>Arif H. Kamal reports personal fees from Homebase Medical outside the submitted work and is chief executive officer of Prepped Health. Justin E. Bekelman reports personal fees from AstraZeneca, Healthcare Foundry, Reimagine Care, and United Healthcare outside the submitted work. The remaining authors declared no conflicts of interest.</p>\",\"PeriodicalId\":137,\"journal\":{\"name\":\"CA: A Cancer Journal for Clinicians\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":503.1000,\"publicationDate\":\"2023-05-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.3322/caac.21784\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CA: A Cancer Journal for Clinicians\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.3322/caac.21784\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"CA: A Cancer Journal for Clinicians","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.3322/caac.21784","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
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摘要

2022年2月,白宫宣布重新启动癌症登月计划,目标是在未来25年内将癌症死亡率降低至少50%,并改善癌症患者及其家人的生活和生存体验。癌症登月计划的一个核心组成部分是促进多部门合作,以解决癌症护理服务面临的紧迫挑战。美国癌症协会(ACS)在召集癌症领域的合作伙伴方面有着悠久的传统,最显著的是通过会议、合作伙伴会议、倡导联盟,以及通过圆桌会议凝聚思想领袖。例如,ACS和几个患者倡导组织、科学组织和制药合作伙伴于2022年10月共同发起了新的ACS国家乳腺癌圆桌会议和ACS国家宫颈癌圆桌会议,作为重塑癌症护理的“全体参与”联盟这些圆桌会议旨在(1)确定这些癌症检测和治疗方面的主要挑战,(2)为提供者、患者、支付方和政策制定者提供专家指导,以增加癌症治疗的可及性和以患者为中心所需的发展。除了特定疾病的问题,美国癌症学会及其合作伙伴还探索了跨越癌症治疗连续体的主题。目前,对肿瘤学创新的大部分关注集中在创造和提供快速扩展的抗癌治疗手段上。开发更新颖、更个性化和更有针对性的治疗方法的努力取得了丰硕成果,但也继续进一步突出与获取相关的问题。如何选择和提供治疗以及如何监测结果需要额外的关注。此外,这些努力如何与日益增长的以患者为中心的呼吁相一致,在象征性和字面意义上满足患者,需要全国讨论。在此,我们描述了ACS在召集多个利益相关者(包括提供者、付款人、政府和技术社区)的国家领导人讨论家庭癌症护理交付方面的首次努力的结果。本次ACS家庭癌症护理峰会于2022年10月26日在马萨诸塞州剑桥市召开,使用“设计思维”框架确定分散式癌症护理交付中的主要问题,并为下一步制定计划。峰会在飞利浦北美校区召集了30位国家领导人,使用查塔姆研究所的规则,指导与会者建立共同的思维模式,制定挑战,围绕障碍进行构思,确定机会,并相互分享研究结果,以确定下一步行动。为了确保ACS充分利用这些高层领导的宝贵时间,挖掘与会者的巨大潜力,并取得切实可行的成果,ACS邀请了飞利浦体验设计团队为峰会提供便利。体验设计团队在指导这一领域的讨论方面有经验,利用最近与伊丽莎白多尔基金会和退伍军人管理局合作开发的退伍军人护理人员旅程地图。ACS和体验设计团队通过与国内癌症护理领导者的对话,确定了四大主要挑战以及潜在障碍的问题:(1)物流/供应链,(2)财务/支付,(3)患者接受程度,(4)监管。与会者还确定了影响所有这四个领域的问题,在围绕诸如卫生公平和卫生的社会决定因素、保健提供者接受度以及数据互操作性和生态系统影响等解决方案进行构想时必须将这些问题包括在内。参与者被分成四个预先选定的小组,以便在领域知识和每个领域的“开箱即用”思维之间提供适当的平衡。每个小组都由一名体验设计协调员领导,他负责促进交流,并在讨论过程中捕捉要点。谈话是按照查塔姆研究所的规定进行的主持人从小组讨论中找到共同的主题,这些主题被组织(或框架)成多个“我们如何做”的陈述,允许小组决定哪些领域是最关键的或需要优先考虑的,以成功地在家中创建癌症护理服务。在此基础上,小组参与者将重点放在有助于解决选定问题的解决方案上,这样就可以更容易地接近其他“我们如何做”的领域。最后,要实现变革,领导者必须愿意挑战现状。 该建议提供了一个目标,通过根据标准护理途径优化护理计划,介绍患者对他们的谈话的偏好,并为更精简的预约协调提供机会,从而帮助简化所需的众多预约。总之,这个愿景结合了人性化的病人导航和优化的工作流程,具有热情的效率。该小组选择进一步深入研究三个问题中两个更关键的分组,提出新的“我们如何才能”的问题,并为这些障碍主题提供解决方案:工作组使用两个问题围绕重新定义的问题构建解决方案:“我们如何理解家庭癌症护理相对于门诊、办公室或医院护理的实际成本?”以及“我们如何确定与家庭癌症护理相关的患者和提供者的利益和风险?”为此,工作组建议解决财政障碍的第一个办法是确保信息的传播。这将要求所有利益相关者向患者和护理人员提供与在家护理相关的自付费用和其他财务费用,而不是在办公室、门诊或医院环境中进行护理。更详细地说,领导者需要公布经济上可行模式的障碍。此外,这些模型将被成功实施的故事和激励的一致性所增强。最后,该组织呼吁美国癌症学会领导癌症计划决策绘图和家庭癌症护理项目成功的标准。为了指导解决方案的设计,对于护理的总成本,该小组回答了两个问题:“作为一个国家,我们如何为不报销的患者支持服务提供资金?”以及“我们如何与患者、护理人员和提供者分享节省下来的成本?”第二个解决方案要求领导者探索、测试和验证新的经济效益计划和产品。这将包括向提供家庭护理的护理人员提供直接财务补偿的项目,家庭护理保险政策产品,并与医疗保险和医疗补助创新中心以及医疗保险和医疗补助服务中心一起测试这些福利项目。继续讨论护理总成本,该小组提出了两个额外的问题来指导第三个解决方案:“我们如何优化家庭护理的付款人模式?”以及“我们如何重新定义激励机制,以匹配最佳护理模式?”从这些概念中,国家癌症人口可以并且需要影响的收益是改善健康公平以及改善患者、提供者和护理人员的经验。此外,它有望提高患者满意度,改善护理,并降低所有利益相关者的成本。这些成果促成了该小组的机会构建声明:“我们如何建立一个创新实验室,以实现与社区卫生系统、付款人和患者的交叉合作?”该小组选择的两个“我们如何才能”的陈述是:“我们如何才能推动变革,使更多的医疗服务跨越州界”和“我们如何才能重新考虑报销?”为了推动跨州的变革,该小组发现,为应对COVID而实施的许多变革将使家庭癌症护理成为可能,为了使家庭癌症护理取得成功,应该扩大这些变革。具体来看全国范围内的许可接受情况,跨州制定标准可以更好地为所有患者实施家庭癌症护理,而不是每个州有不同的要求。这两种方法结合在一起,可以为患者、护理人员和护理提供者提供更可扩展的专家资源。此外,可以更有效地提供支持家庭护理的远程医疗方案。最后,这些措施是家庭或院外护理的基础。第二份声明,“我们应该如何重新考虑报销”,呼吁国家领导人寻找更多的激励措施,并制定法规来支持这些激励措施,以一种新的报销模式来提供更多的院外护理,这种模式将反映这种新的癌症护理方式。这还必须包括对法规的修改,以提高患者对接受治疗的方式和地点的偏好。最后,这些监管变化将刺激创新的交付实践和支持它们的数据。从预防到早期发现、治疗和生存,以及传统医疗机构之外的临床试验,癌症护理的成功提供代表了肿瘤学领域潜在的巨大转变。
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The future of cancer care at home: Findings from an American Cancer Society summit

In February 2022, the White House announced the reignition of the Cancer Moonshot Initiative with the goals of reducing the death rate from cancer by at least 50% over the next 25 years and improving the experience of people and their families living with and surviving cancer. A core component of the Cancer Moonshot Initiative is the facilitation of multisector partnerships to solve the compelling challenges faced in cancer care delivery. The American Cancer Society (ACS) has a longstanding tradition of convening partners across the cancer landscape, most notably through conferences, partner meetings, advocacy coalitions, and coalescing of thought leaders through roundtables. For example, the ACS and several patient advocacy organizations, scientific organizations, and pharmaceutical partners came together in October 2022 to launch the new ACS National Breast Cancer Roundtable and the ACS National Cervical Cancer Roundtable as “all-hands-on-deck” coalitions to reshape cancer care.1 These Roundtables aim to both (1) identify the leading challenges in detection and treatment within these cancers and (2) provide expert guidance to providers, patients, payers, and policy makers regarding evolutions needed to increase access and patient centricity of cancer care. Beyond disease-specific issues, the ACS and its partners have also explored topics that span the cancer care continuum.

Currently, much of the attention given to innovation in oncology is centered upon creating and delivering a rapidly expanding armamentarium of anticancer treatments. Efforts to develop more novel, personalized, and targeted therapies have been fruitful but also continue to further highlight issues related to access. How treatments are selected and delivered and how outcomes are monitored require additional focus. Furthermore, how such efforts align with increasing calls for patient centricity, meeting patients where they are both figuratively and literally, requires a national discussion. Herein, we describe the findings from the first effort of the ACS in convening national leaders across multiple stakeholders, including the provider, payer, government, and technology communities, to discuss cancer care delivery at home.

This ACS Cancer Care at Home Summit convened in Cambridge, Massachusetts, on October 26, 2022, using a “design-thinking” framework to identify the major issues in decentralized cancer care delivery and plan for the next steps forward. The Summit convened 30 national leaders at the Philips North America campus using Chatham House rules during which participants were guided in building a shared mental model, framing the challenges and ideating around barriers, defining opportunities, and sharing findings with each other to determine next steps. To ensure that the ACS optimally used the time dedicated by these senior leaders, untapping the immense potential of the combination of participants in the room, and really getting to actionable outcomes, the ACS invited the Philips Experience Design Team to facilitate the Summit. The Experience Design Team had experience in guiding discussions in this area, leveraging a recent effort in developing a Caregiver Journey Map for Veteran caregivers in partnership with the Elizabeth Dole Foundation and the Veterans Administration. Together, the ACS and the Experience Design Team used conversations with national leaders in cancer care delivered at home to identify four major challenges along with issues that underly barriers: (1) logistics/supply chain, (2) finance/payment, (3) patient acceptance, and (4) regulatory. The participants also identified issues that affect all four of those areas and must be included when ideating around solutions such as health equity and social determinants of health, care-provider acceptance, and data interoperability and ecosystem implications. Participants were split into four preselected groupings to provide the right balance between domain knowledge and “out-of-the-box” thinking in each area.

Each group was led by an Experience Design facilitator who fostered communication and captured points as the discussions occurred. Conversations operated under Chatham House rules.2 Facilitators homed in on common themes from the group discussions, and themes were organized (or framed) into multiple “how might we” statements, allowing for the groups to decide which areas were the most critical or needed to be prioritized to successfully create cancer care delivery at home. From there, the group participants focused on solutions that would help solve the selected issue, which would then allow for easier ability to approach the other “how might we” areas.

Finally, to realize change, leaders must be willing to challenge the status quo. This recommendation provides a goal to help simplify the multitude of appointments needed by optimizing care plans according to standard care pathways, introduce patient preference for their conversations, and flag opportunities for more streamlined appointment coordination. Together, this vision combines the human touch of patient navigation with optimized workflows that have ardent efficiency.

The group chose to further drill down on the two more critical groupings of the three, provide new “how might we” questions, and provide solutions to those barrier themes:

The workgroup used two questions to build a solution around redefining questions: “how might we understand the real costs of cancer care at home relative to outpatient, office, or hospital care?” and “how might we identify benefits and risks to the patients and to the providers associated with cancer care at home?” To do this, the group recommended that the first solution to financial barriers was to ensure information dissemination. This would require all stakeholders to make available to patients and caregivers out-of-pocket expenses and other financial costs associated with care at home relative to care in office, outpatient, or hospital settings. In further detail, leaders need to publish barriers to financially viable models. In addition, those models would be augmented with stories of successful implementation and alignment of incentives. Finally, the group called on the ACS to lead cancer plan decision mapping and criteria for success of cancer care at home programs.

To guide solution design, for the total cost of care, the group answered two questions: “how might we, as a nation, finance nonreimbursed patient support services?” and “how might we share cost savings with patients, caregivers, and providers?” The second solution would require leaders to explore, test and validate new financial benefit programs and products. This would include programs for direct financial reimbursement to caregivers delivering home care, home care insurance policy products, and test those benefit programs with the Center for Medicare and Medicaid Innovation and the Centers for Medicare and Medicaid Services. Continuing with the total cost of care, the group provided two additional questions to guide the third solution: “how might we optimize payer models for care at home?” and “how might we redefine incentives to match optimal care models?”

From these concepts, the gains the national cancer population could and needs to affect are improved health equity along with improved patient, provider, and caregiver experience. In addition, it is expected to garner increased patient satisfaction, improved care, and lower costs across all stakeholders. These gains became the catalyst for the group's opportunity build statement: “How might we stand up an innovation laboratory to enable cross-collaboration with community-based health systems, payers, and patients?”

The two “how might we” statements that the group chose to work on were: “how might we drive change to enable more care to be delivered across state lines” and “how might we rethink reimbursements?” For driving change across state lines, the group found that many of the changes that were implemented in response to COVID would enable cancer care at home and should be extended in order for cancer care at home to be successful. Specifically looking at licensing acceptance on a national basis, having a standard set across state lines allows for cancer care at home to be better implemented for all patients as opposed to different requirements in each state. Together, both approaches allow for more scalable use of expert resources for patients, caregivers, and care providers. In addition, telehealth programs to support home care can be more effectively delivered. Finally, these measures are foundational for at home or out-of-hospital care. The second statement, “how might we rethink reimbursements,” called on national leaders to look for more incentives, and regulations to support those incentives, for more out-of-hospital care with a new reimbursement model that would reflect this new cancer care delivery approach. This would also have to include changes to regulations that enable increased patient preference in how and where they receive care. Finally, these regulatory changes will stimulate innovative delivery practices and the data that support them.

The successful delivery of cancer care, spanning from prevention through early detection, treatment, and survivorship, as well as clinical trials outside traditional medical facilities, represents a potential seismic shift in oncology. Complementing the recent unprecedented expansion of cancer treatment options, cancer care in the place a patient calls home could help address some longstanding barriers to equitable access to care, particularly for populations marginalized because of geography, travel requirements to get to care providers, proximity to clinical trials, and overall financial burdens of cancer care. We look forward to continuing to build partnerships and further discussions to explore the potential of, barriers to, and solutions to achieve a paradigm shift where appropriate to bring cancer care to the patient rather than requiring the patient to go to cancer care.

Arif H. Kamal reports personal fees from Homebase Medical outside the submitted work and is chief executive officer of Prepped Health. Justin E. Bekelman reports personal fees from AstraZeneca, Healthcare Foundry, Reimagine Care, and United Healthcare outside the submitted work. The remaining authors declared no conflicts of interest.

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来源期刊
CiteScore
873.20
自引率
0.10%
发文量
51
审稿时长
1 months
期刊介绍: CA: A Cancer Journal for Clinicians" has been published by the American Cancer Society since 1950, making it one of the oldest peer-reviewed journals in oncology. It maintains the highest impact factor among all ISI-ranked journals. The journal effectively reaches a broad and diverse audience of health professionals, offering a unique platform to disseminate information on cancer prevention, early detection, various treatment modalities, palliative care, advocacy matters, quality-of-life topics, and more. As the premier journal of the American Cancer Society, it publishes mission-driven content that significantly influences patient care.
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