Publications
The material below is provided to support scientific exchange. Any content about investigational therapeutics or investigational uses of locally approved products does not establish the safety or efficacy of these therapeutics or uses, and there is no guarantee of local regulatory approval.
For questions beyond a product’s authorized indications or for information not available here, please contact Alnylam Medical Information.
Best Practices and Key Barriers for Amyloidosis Patient Care at US Specialized Amyloidosis Centers: An Analysis by ARC-ASPIRE
Publication Details
Clinical Medicine Insights: Cardiology
April 2026
Author(s)
Jose Nativi-Nicolau1, Johana Fajardo2, Alyssa Galloway3 4, Sami Khella5, Nisith Kumar4 6, Michaela Liedtke7, Isabelle Lousada8, Tiffany Patrick 4 9, Colleen Moffitt4 9, Lori Klein10, Gabriela Tamariz4 9, Karthikeyan Veeraraghavalu4 11, Alexandra Haddad-Angulo4 6
Affiliations
1Mayo Clinic, FL, USA; 2Duke University Hospital, NC, USA; 3BridgeBio, CA, USA; 4Amyloidosis Reserach Consortium (ARC) - Amyloidosis Stakeholder Partnerships for Impact, Reach & Equity (ASPIRE), MA, USA; 5University of Pennsylvania School of Medicine, PA, USA; 6Pfizer Inc, NY, USA; 7Stanford Health Care, CA, USA; 8Amyloidosis Research Consortium (ARC), MA, USA; 9Alnylam Pharmaceuticals, MA, USA; 10Putnam Associates, MA, USA; 11Prothena Biosciences Inc, CA, USA
Abstract
Objectives:
Amyloidosis is a group of rare diseases that often manifest in multi-organ symptoms requiring an effective multidisciplinary team of care providers to manage. This study aimed to identify the best practices and key barriers to patient-centric care at US specialized amyloidosis centers (SACs) which have emerged as central hubs for multidisciplinary amyloidosis care.
Methods:
We conducted and analyzed interviews with 77 stakeholders of amyloidosis diseases, including specialist physicians from 17 SACs across the US, patients, patient advocacy group representatives, and referring physicians.
Results:
The most commonly mentioned best practices were patient-centric multidisciplinary care, timely intake of new high-risk patients, and responsiveness to patient questions. Expanding local physician education was noted as critical to earlier diagnosis. Fifteen out of 17 SACs are actively involved in clinical trials for amyloidosis treatments. Key barriers to care identified were patient distance to SACs, limited medical records and data sharing, and insurance hurdles. Most SACs keep track of metrics, such as patient volume, patient demographics, time to first appointment, as part of internal or in external registries to measure progress.
Conclusions:
These findings offer practical insights for optimizing amyloidosis care and highlight the structural and informational gaps that must be addressed to improve access and outcomes.
PMID
42077643
DOI
10.1177/11795468261444669
Publication Materials
Visit website/URL/link
Related Materials
Transthyretin Amyloidosis (ATTR)
Société Francophone du Nerf Périphérique (SFNP) 2025
Transthyretin Amyloidosis (ATTR)
Worsening of Heart Failure in Outpatients With Transthyretin Amyloidosis and Cardiomyopathy in the APOLLO-B Trial
Journal of the American College of Cardiology
Author(s)
Marianna Fontana, Mathew S. Maurer, Julian D. Gillmore, et al
January 2025
Transthyretin Amyloidosis (ATTR)
Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy
JAMA Neurology
Author(s)
David Adams, Jonas Wixner, Michael Polydefkis, et al
January 2025
Transthyretin Amyloidosis (ATTR)
International Society for Pharmacoeconomics and Outcomes Research (ISPOR) Europe 2024
Transthyretin Amyloidosis (ATTR), Cardiovascular (CV)
American Heart Association (AHA) 2024
Transthyretin Amyloidosis (ATTR)
The journey to diagnosis of wild-type transthyretin-mediated (ATTRwt) amyloidosis: a path with multisystem involvement
Orphanet Journal of Rare Diseases
Author(s)
Chafic Karam, Colleen Moffit, Catherine Summers, et al
November 2024
