The USC Brain Health Observatory, USC Dornsife, Los Angeles, CA, USA.
Department of Geriatrics, University Medical Center Goettingen, Goettingen, Germany.
J Alzheimers Dis. 2024;101(4):1249-1259. doi: 10.3233/JAD-240728.
Amyloid-targeting therapies for Alzheimer's disease (AD) might become available in Germany soon. The combination of a large pool of prevalent cases and a complex diagnostic process to determine eligibility for these treatments is likely to challenge health systems' capacity.
To analyze Germany's healthcare system capacity to identify treatment-eligible patients in a timely and equitable manner.
We modeled patients' diagnostic journey and projects wait times due to capacity constraints for AD specialist visits and PET scans from 2024 to 2043. Model parameters were derived from published data and expert input.
Wait times would be ∼50 months over the model horizon, if patients were referred to specialists based on a brief cognitive assessment in primary care. Wait times for patients with social health insurance are projected to be 1.9 times those of patients with private insurance, with peak wait times of around 76 and 40 months, respectively. Adding a blood test for the AD pathology as additional triage step would reduce wait times to below 24 months.
In spite of having a well-resourced health system, Germany is projected to be unable to cope with the demand for biomarker-based AD diagnosis, if a disease-modifying AD treatment were introduced. As these treatments might become available by the end of 2024, decisive action, in particular dissemination of high-performing AD blood tests for triage in primary care, will be needed to prevent delays in access and potentially avoidable and inequitable disease progression.
治疗阿尔茨海默病(AD)的淀粉样蛋白靶向疗法可能很快在德国上市。大量的常见病例和确定这些治疗方法资格的复杂诊断过程可能会对卫生系统的能力构成挑战。
分析德国医疗保健系统及时公平地确定有资格接受治疗的患者的能力。
我们对 2024 年至 2043 年期间 AD 专家就诊和 PET 扫描的能力限制导致的等待时间进行建模。该模型利用患者的诊断过程和项目,利用已发表的数据和专家意见得出模型参数。
如果根据初级保健中的简要认知评估将患者转介给专家,那么在模型期间内,等待时间将约为 50 个月。社会健康保险患者的等待时间预计将是私人保险患者的 1.9 倍,分别为 76 个月和 40 个月左右。添加用于 AD 病理的血液检测作为额外的分诊步骤将使等待时间缩短至 24 个月以下。
尽管德国拥有资源充足的医疗体系,但如果引入针对 AD 的疾病修饰治疗方法,预计该国将无法应对基于生物标志物的 AD 诊断的需求。由于这些治疗方法可能会在 2024 年底上市,因此需要采取果断行动,特别是在初级保健中推广用于分诊的高性能 AD 血液检测,以防止出现延误,并避免潜在的不可避免的和不公平的疾病进展。