S Mattke, A Gustavsson, L Jacobs, S Kern, S Palmqvist, M Eriksdotter, I Skoog, B Winblad, A Wimo, L Jönsson
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We calculate the investment requirements for Sweden to achieve this target over a timeframe of 20 years.</p><p><strong>Design: </strong>Desk research to identify data for population, mortality, disease burden, cost of services and current capacity, expert consultation to inform assumptions about patient journey, and use of a Markov model to predict waiting times. The model simulates the patients' journey through different evaluation stages: initial evaluation by a primary care specialist, neurocognitive testing by an AD specialist, and confirmatory biomarker testing with PET scanning or cerebrospinal fluid (CSF) testing. The model assumes specialist appointments and PET scans are capacity constrained, and patients progress from cognitively normal to MCI and from MCI to dementia in the resulting waiting times.</p><p><strong>Measurements: </strong>Projected waiting times for diagnosis of eligibility for disease-modifying Alzheimer's treatment from 2023 to 2042 assuming current capacity, assuming 20% of Swedish residents aged 60 years and above would seek an evaluation for cognitive decline. Investments required to scale capacity up to reach target of providing diagnosis within six months on average.</p><p><strong>Results: </strong>Initial average waiting times for AD specialist appointments would be around 21 months in 2023 and remain around 55 months through 2042, as demand would continue to outstrip supply throughout the 20-year model horizon. Waiting times for biomarker testing would be stable at less than four weeks, as patients would be held up in the queue for their first specialist consultations, and use of CSF testing is widely accepted in Sweden. An additional 25% of AD specialists would have to be added above the current growth trend to reduce waiting times to less than 6 months at an average annual cost of approximately 805 million SEK. The increased cost of volume of biomarker testing would amount to about 106 million SEK per year.</p><p><strong>Conclusions: </strong>At current capacity, the Swedish healthcare system is unable to provide timely diagnosis of patients eligible for disease-modifying AD treatment. Although future diagnostic technologies, such as digital cognitive assessments and blood tests for the AD pathology, might decrease demand for capacity-constrained services, substantial investments will be required to meet a target of less than six months of waiting time for a diagnosis.</p>","PeriodicalId":48606,"journal":{"name":"Jpad-Journal of Prevention of Alzheimers Disease","volume":"1 1","pages":"155-161"},"PeriodicalIF":8.5000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10995070/pdf/","citationCount":"0","resultStr":"{\"title\":\"Estimates of Current Capacity for Diagnosing Alzheimer's Disease in Sweden and the Need to Expand Specialist Numbers.\",\"authors\":\"S Mattke, A Gustavsson, L Jacobs, S Kern, S Palmqvist, M Eriksdotter, I Skoog, B Winblad, A Wimo, L Jönsson\",\"doi\":\"10.14283/jpad.2023.94\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The emergence of disease-modifying Alzheimer's (AD) treatments provides new hope to patients and families but concerns have been raised about the preparedness of healthcare systems to provide timely access to such treatments because of a combination of a complex diagnostic process and a large prevalent pool.</p><p><strong>Objectives: </strong>We assess the preparedness of Sweden, a high-income country known for its dementia-friendly policies, to diagnose AD patients eligible for treatment within a six-month window, given current capacity for specialist evaluations and biomarker testing. We calculate the investment requirements for Sweden to achieve this target over a timeframe of 20 years.</p><p><strong>Design: </strong>Desk research to identify data for population, mortality, disease burden, cost of services and current capacity, expert consultation to inform assumptions about patient journey, and use of a Markov model to predict waiting times. The model simulates the patients' journey through different evaluation stages: initial evaluation by a primary care specialist, neurocognitive testing by an AD specialist, and confirmatory biomarker testing with PET scanning or cerebrospinal fluid (CSF) testing. The model assumes specialist appointments and PET scans are capacity constrained, and patients progress from cognitively normal to MCI and from MCI to dementia in the resulting waiting times.</p><p><strong>Measurements: </strong>Projected waiting times for diagnosis of eligibility for disease-modifying Alzheimer's treatment from 2023 to 2042 assuming current capacity, assuming 20% of Swedish residents aged 60 years and above would seek an evaluation for cognitive decline. Investments required to scale capacity up to reach target of providing diagnosis within six months on average.</p><p><strong>Results: </strong>Initial average waiting times for AD specialist appointments would be around 21 months in 2023 and remain around 55 months through 2042, as demand would continue to outstrip supply throughout the 20-year model horizon. 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引用次数: 0
摘要
背景:改变病情的阿尔茨海默氏症(AD)治疗方法的出现为患者和家属带来了新的希望,但由于诊断过程复杂、患病人数众多,人们对医疗系统是否做好了及时提供此类治疗的准备表示担忧:我们评估了瑞典(一个以痴呆症友好政策而闻名的高收入国家)在目前的专家评估和生物标记物检测能力下,在六个月的时间内诊断出符合治疗条件的注意力缺失症患者的准备情况。我们计算了瑞典在 20 年内实现这一目标所需的投资:设计:进行案头研究,以确定人口、死亡率、疾病负担、服务成本和现有能力等方面的数据;咨询专家,以了解有关患者旅程的假设;使用马尔可夫模型预测等待时间。该模型模拟了患者经历不同评估阶段的过程:初级保健专家的初步评估、AD 专家的神经认知测试以及 PET 扫描或脑脊液 (CSF) 测试的确证生物标记物测试。该模型假设专家预约和 PET 扫描的容量受到限制,患者在由此产生的等待时间内从认知正常发展到 MCI,再从 MCI 发展到痴呆:假定 20% 的 60 岁及以上瑞典居民会寻求认知能力衰退评估,假定目前的治疗能力,2023 年至 2042 年阿尔茨海默病治疗资格诊断的预计等待时间。为达到平均在 6 个月内提供诊断所需的投资:由于在整个20年的模型范围内,AD专科预约的最初平均等候时间将继续供不应求,因此2023年的平均等候时间约为21个月,到2042年将保持在55个月左右。生物标志物检测的等待时间将稳定在四周以内,因为患者在首次专家会诊时会排队等候,而且脑脊液检测的使用在瑞典已被广泛接受。若要将等待时间缩短至 6 个月以内,则必须在当前增长趋势的基础上再增加 25% 的 AD 专家,年均成本约为 8.05 亿瑞典克朗。生物标志物检测量增加的成本将达到每年约1.06亿瑞典克朗:以目前的能力,瑞典医疗系统无法及时诊断出符合接受改变病情的注意力缺失症治疗条件的患者。尽管未来的诊断技术,如数字化认知评估和AD病理血液检测,可能会减少对能力有限的服务的需求,但要实现诊断等待时间少于6个月的目标,还需要大量投资。
Estimates of Current Capacity for Diagnosing Alzheimer's Disease in Sweden and the Need to Expand Specialist Numbers.
Background: The emergence of disease-modifying Alzheimer's (AD) treatments provides new hope to patients and families but concerns have been raised about the preparedness of healthcare systems to provide timely access to such treatments because of a combination of a complex diagnostic process and a large prevalent pool.
Objectives: We assess the preparedness of Sweden, a high-income country known for its dementia-friendly policies, to diagnose AD patients eligible for treatment within a six-month window, given current capacity for specialist evaluations and biomarker testing. We calculate the investment requirements for Sweden to achieve this target over a timeframe of 20 years.
Design: Desk research to identify data for population, mortality, disease burden, cost of services and current capacity, expert consultation to inform assumptions about patient journey, and use of a Markov model to predict waiting times. The model simulates the patients' journey through different evaluation stages: initial evaluation by a primary care specialist, neurocognitive testing by an AD specialist, and confirmatory biomarker testing with PET scanning or cerebrospinal fluid (CSF) testing. The model assumes specialist appointments and PET scans are capacity constrained, and patients progress from cognitively normal to MCI and from MCI to dementia in the resulting waiting times.
Measurements: Projected waiting times for diagnosis of eligibility for disease-modifying Alzheimer's treatment from 2023 to 2042 assuming current capacity, assuming 20% of Swedish residents aged 60 years and above would seek an evaluation for cognitive decline. Investments required to scale capacity up to reach target of providing diagnosis within six months on average.
Results: Initial average waiting times for AD specialist appointments would be around 21 months in 2023 and remain around 55 months through 2042, as demand would continue to outstrip supply throughout the 20-year model horizon. Waiting times for biomarker testing would be stable at less than four weeks, as patients would be held up in the queue for their first specialist consultations, and use of CSF testing is widely accepted in Sweden. An additional 25% of AD specialists would have to be added above the current growth trend to reduce waiting times to less than 6 months at an average annual cost of approximately 805 million SEK. The increased cost of volume of biomarker testing would amount to about 106 million SEK per year.
Conclusions: At current capacity, the Swedish healthcare system is unable to provide timely diagnosis of patients eligible for disease-modifying AD treatment. Although future diagnostic technologies, such as digital cognitive assessments and blood tests for the AD pathology, might decrease demand for capacity-constrained services, substantial investments will be required to meet a target of less than six months of waiting time for a diagnosis.
期刊介绍:
The JPAD « Journal of Prevention of Alzheimer’Disease » will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including : neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.
JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.