TY - JOUR
T1 - Public Health
AU - Porras, Maria Lazo
AU - Serruto, Francisco Tateishi
AU - Butler, Christopher R.
AU - Cuba, María Sofía
AU - Vilchez, Daniela Rossini
AU - Quinoso, Silvana Perez León
AU - Flores, Miriam Lucar
AU - Miranda, Jaime
AU - Bernabe, Antonio
AU - Canseco, Francisco Diez
AU - Moore, Graham
AU - Landeiro, Filipa
AU - Cardenas, Maria Kathia
AU - Tudela, Carlos Vera
AU - Calvo, Rafael A.
AU - Whiteley, William
AU - Hawkins, Jemma
N1 - Publisher Copyright:
© 2025 The Alzheimer's Association. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
PY - 2025/12/1
Y1 - 2025/12/1
N2 - BACKGROUND: Dementia is a high burden condition in many low- and middle- income countries (LMIC). However, data are limited in terms of the patients' journey to receive a dementia diagnosis and treatment. There is also a lack of guidance on how to conduct this kind of research. This is the first study of its kind in Peru, providing a patient-centered approach to understand the patient journey of people with dementia (PWD) and their carers. Understanding this journey is essential for improving healthcare practices that address the unique challenges faced in this context METHOD: This qualitative study used in-depth interviews to map the patient journey of PWD. Participants included PWD, carers, and healthcare workers. A draft of the journey map was shared with a sub-sample of participants for validation, involving individual and group discussions at each site. Participants reflected on their experiences, identifying missing steps, emotions, touch points, timelines, and actors involved. RESULT: We interviewed 39 participants: 4 PWD (2 female, 2 male), 18 carers (15 female, 3 male), and 17 healthcare workers (12 female, 5 male). Mapping the patient journey revealed that PWD and carers navigate more steps than healthcare professionals perceive. They often make logistical decisions, engaging with multiple health systems before obtaining a diagnosis and treatment. The validation process highlighted missing details in the initial map. Participants offered valuable feedback, enriching the map to better reflect the fragmented pathways to dementia care in Peru. Additionally, these sessions provided a supportive environment for carers and healthcare workers to share experiences, fostering a sense of community and engagement with the research process. CONCLUSION: Mapping the experiences of PWD and carers revealed longer, more complex journeys than previously recognised by healthcare professionals. The validation process further enriched the findings, providing key insights into navigating the Peruvian health system for dementia care and highlighting the importance of patient-centred approaches in improving healthcare delivery.
AB - BACKGROUND: Dementia is a high burden condition in many low- and middle- income countries (LMIC). However, data are limited in terms of the patients' journey to receive a dementia diagnosis and treatment. There is also a lack of guidance on how to conduct this kind of research. This is the first study of its kind in Peru, providing a patient-centered approach to understand the patient journey of people with dementia (PWD) and their carers. Understanding this journey is essential for improving healthcare practices that address the unique challenges faced in this context METHOD: This qualitative study used in-depth interviews to map the patient journey of PWD. Participants included PWD, carers, and healthcare workers. A draft of the journey map was shared with a sub-sample of participants for validation, involving individual and group discussions at each site. Participants reflected on their experiences, identifying missing steps, emotions, touch points, timelines, and actors involved. RESULT: We interviewed 39 participants: 4 PWD (2 female, 2 male), 18 carers (15 female, 3 male), and 17 healthcare workers (12 female, 5 male). Mapping the patient journey revealed that PWD and carers navigate more steps than healthcare professionals perceive. They often make logistical decisions, engaging with multiple health systems before obtaining a diagnosis and treatment. The validation process highlighted missing details in the initial map. Participants offered valuable feedback, enriching the map to better reflect the fragmented pathways to dementia care in Peru. Additionally, these sessions provided a supportive environment for carers and healthcare workers to share experiences, fostering a sense of community and engagement with the research process. CONCLUSION: Mapping the experiences of PWD and carers revealed longer, more complex journeys than previously recognised by healthcare professionals. The validation process further enriched the findings, providing key insights into navigating the Peruvian health system for dementia care and highlighting the importance of patient-centred approaches in improving healthcare delivery.
UR - https://www.scopus.com/pages/publications/105025737348
U2 - 10.1002/alz70860_103153
DO - 10.1002/alz70860_103153
M3 - Artículo
C2 - 41433971
AN - SCOPUS:105025737348
SN - 1552-5279
VL - 21
SP - e103153
JO - Alzheimer's & dementia : the journal of the Alzheimer's Association
JF - Alzheimer's & dementia : the journal of the Alzheimer's Association
ER -