Evidence map›Paper›PMID 41820958›Full record

ArticleBMC health services research2026

The patient's voice: real-world experiences of a transthyretin amyloidosis focus group.

Mónica Angélica López, Tomás Ripoll-Vera, Teresa Sevilla, Prado Salamanca-Bautista, Inmaculada Mediavilla, José Francisco Soto, CARABELA-ATTR Scientific Committee

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Article in BMC health services research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mónica Angélica LópezDepartment of Internal Medicine, Hospital Universitario Ramón y Cajal, IRYCIS, M-607, Km. 9, 100, Fuencarral-El Pardo, Madrid, 28034, Spain. monicaa.lopez@salud.madrid.org.
Tomás Ripoll-VeraDepartment of Cardiology, Hospital Universitario Son Llatzer, IdISBa, Palma de Mallorca, Spain.
Teresa SevillaDepartment of Neurology, Hospital Universitari i Politècnic La Fe & IIS La Fe, Valencia, Spain.
Prado Salamanca-BautistaDepartment of Internal Medicine, Hospital Universitario Virgen de la Macarena, Universidad de Sevilla, Seville, Spain.
Inmaculada MediavillaPrimary Care Management of SERMAS, Madrid, Spain.
José Francisco SotoFundación Hospital Instituto San José, Madrid, Spain.
CARABELA-ATTR Scientific Committee

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransthyretin amyloidosis (ATTR) is a progressive, multisystemic disorder that severely impacts patient quality of life. Despite therapeutic advancements, significant delays in diagnosis and care persist, often due to insufficient awareness among healthcare professionals. We aimed to highlight the experiences of patients living with ATTR in Spain in order to understand their daily challenges within the healthcare system.

methodsAs part of the CARABELA-ATTR initiative, we conducted a focus group discussion with six patients with confirmed ATTR from different regions of Spain. The discussions explored three main areas: (1) communication and coordination between healthcare professionals and patients; (2) patient education, focusing on awareness, knowledge, and engagement; and (3) emotions, quality of life, and living with the disease, which explored the physical and emotional impacts of ATTR.

resultsParticipants reported significant challenges, including diagnosis and treatment delays, fragmented care due to poor coordination between specialists, and barriers to accessing treatments and care, both financial and administrative. The physical and psychological toll of the disease was explored. Patients who received multidisciplinary care at specialized centres reported more positive experiences, emphasizing the importance of coordinated care and timely interventions.

conclusionsThis study amplifies patients’ voices to underscore their unmet needs in the current ATTR care pathway, including increased awareness, earlier diagnosis, enhanced coordination among specialists, and equitable access to specialized care. Integrating mental health support and patient education into care plans is critical for improving the well-being of ATTR patients. These findings advocate for a more patient-centred, comprehensive approach to ATTR care.

Indexed as

Amyloid Neuropathies, FamilialAgedAged, 80 and overFemaleFocus GroupsHumansMaleMiddle AgedPatient Education as TopicQuality of LifeSpainATTRCARABELAHealthcareInterviewsPatientsQuality of lifeTransthyretin amyloidosis

Identifiers

PMID41820958
PMCPMC13097830

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.