Generating real-world evidence in Alzheimer's disease: Considerations for establishing a core dataset
Ongoing assessment of patients with Alzheimer's disease (AD) in postapproval studies is important for mapping disease progression and evaluating real-world treatment effectiveness and safety. However, interpreting outcomes in the real world is challenging owing to variation in data collected ac...
- Autores:
-
Galvin, James E.
Cummings, Jeffrey L.
Levitchi Benea, Mihaela
de Moor, Carl
Allegri, Ricardo Francisco
Atri, Alireza
Chertkow, Howard
Paquet, Claire
Porter, Verna R.
Ritchie, Craig W.
Sikkes, Sietske A. M.
Smith, Michael R.
Grassi, Christina Marsica
Rubino, Ivana
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2024
- Institución:
- Corporación Universidad de la Costa
- Repositorio:
- REDICUC - Repositorio CUC
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.cuc.edu.co:11323/14084
- Acceso en línea:
- https://hdl.handle.net/11323/14084
https://repositorio.cuc.edu.co/
- Palabra clave:
- Alzheimer's disease
Core outcomes
Data collection
Population
Real-world evidence
Study aims
- Rights
- openAccess
- License
- Atribución 4.0 Internacional (CC BY 4.0)
Summary: | Ongoing assessment of patients with Alzheimer's disease (AD) in postapproval studies is important for mapping disease progression and evaluating real-world treatment effectiveness and safety. However, interpreting outcomes in the real world is challenging owing to variation in data collected across centers and specialties and greater heterogeneity of patients compared with trial participants. Here, we share considerations for observational postapproval studies designed to collect harmonized longitudinal data from individuals with mild cognitive impairment or mild dementia stage of disease who receive therapies targeting the underlying pathological processes of AD in routine practice. This paper considers key study design parameters, including proposed aims and objectives, study populations, approaches to data collection, and measures of cognition, functional abilities, neuropsychiatric status, quality of life, health economics, safety, and drug utilization. Postapproval studies that capture these considerations will be important to provide standardized data on AD treatment effectiveness and safety in real-world settings. |
---|