Background: With the emergence of disease-modifying therapies (DMTs) for early Alzheimer's disease (AD), evolution of healthcare infrastructure is needed to identify patients eligible for treatment with an AD DMT, and to adequately treat and monitor patients throughout. Our research aimed to assess current practices and available infrastructure, to identify bottlenecks, and to propose solutions to increase patient access to AD DMTs in the EU4+UK.
Methods: We searched publicly available information (to August 2023) to derive a foundational understanding of the current level of healthcare infrastructure in each country. Subsequent primary research with 11 neurologists and 39 hospital administrators across the 5 countries informed an assessment of AD diagnostic, infusion, and monitoring capacity.
Results: Magnetic resonance imaging (MRI) is recommended for differential dementia diagnoses and will be required for monitoring patients throughout treatment with an AD DMT. However, in most countries, capacity is expected to bottleneck due to shortages in MRI machinery, trained staff, and limited allocation of scans to AD. Optimizing the use of MRI will be key to expanding patient access to AD DMTs. Confirming amyloid positivity via cerebrospinal fluid testing/ lumbar puncture or positron emission tomography (PET) is recommended for AD diagnoses and a requirement for AD DMT eligibility. Amyloid PET is not widely conducted due to a lack of dedicated centers and/or reimbursement in some countries, whereas lumbar puncture is not expected to be associated with major access challenges. AD DMTs require administration via infusion; however, current neurology units are adapted for infusions of DMTs for multiple sclerosis. Infusion capacity may also be limited by trained staff shortages and lack of dedicated outpatient infusion units for AD. There is potential to repurpose some infusion capacity to AD.
Conclusions: European healthcare system infrastructure can adapt to improve access to AD DMTs. Establishing and/or expanding country-wide networks of accredited hospitals and external/private partnerships could allow patients greater access to services across multiple locations and individual hospitals to better leverage external resources. At an organizational level, more resources can be allocated towards AD and efficient resource planning can help to optimize healthcare for patients with early AD.
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http://dx.doi.org/10.1002/alz.094773 | DOI Listing |
Alzheimers Dement
December 2024
Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, Amsterdam, Netherlands.
Background: The increasing dementia prevalence and potential introduction of disease-modifying therapies (DMTs) highlight the need for efficient diagnostic pathways. Clear recommendations to guide the choice of diagnostic tests are lacking and may vary depending on different clinical scenarios. We used a data-driven approach to identify efficient and effective stepwise diagnostic testing for three clinical scenarios: 1) syndrome diagnosis, 2) etiological diagnosis, 3) potential eligibility for DMT.
View Article and Find Full Text PDFBackground: With the emergence of disease-modifying therapies (DMTs) for early Alzheimer's disease (AD), evolution of healthcare infrastructure is needed to identify patients eligible for treatment with an AD DMT, and to adequately treat and monitor patients throughout. Our research aimed to assess current practices and available infrastructure, to identify bottlenecks, and to propose solutions to increase patient access to AD DMTs in the EU4+UK.
Methods: We searched publicly available information (to August 2023) to derive a foundational understanding of the current level of healthcare infrastructure in each country.
Real-world data on the uptake, effectiveness and safety of new diagnostics and disease-modifying (DMT) treatments for Alzheimer's Disease (AD) are imperative. This can be achieved through patient registries. A major challenge is how to embed registry data capture into routine clinical practice.
View Article and Find Full Text PDFCureus
December 2024
Department of Neurology, Cheikh Khalifa International University Hospital, Faculty of Medicine, Mohamed VI University of Health Sciences (UM6SS), Casablanca, MAR.
Multiple sclerosis (MS) is the most prevalent long-term inflammatory condition affecting the central nervous system in adults. However, seizures are rarely described as the first presentation of MS or as a sole manifestation of radiologically isolated syndrome (RIS) or clinically isolated syndrome (CIS). The diagnosis of MS typically requires clinical evidence of neurological deficits and supportive radiological findings; however, RIS is characterized by incidental magnetic resonance imaging (MRI) findings suggestive of MS in the absence of clinical symptoms.
View Article and Find Full Text PDFFront Neurol
December 2024
Optimax Access Ltd, Southampton, United Kingdom.
Background: Relapsing multiple sclerosis (RMS) is a chronic, inflammatory disease of the central nervous system. Ublituximab, an anti-CD20 monoclonal antibody (mAb), is indicated for the treatment of RMS. We performed a systematic literature review (SLR) to identify randomized trials reporting the clinical efficacy and tolerability of ublituximab or comparator disease-modifying therapies (DMTs) for treatment of RMS, and assessed their comparative effects using network meta-analysis (NMA).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!