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Enhancing Equitable Access to Rare Disease Diagnosis and Treatment around the World: A Review of Evidence, Policies, and Challenges
Indexado
Scopus SCOPUS_ID:85151660479
DOI 10.3390/IJERPH20064732
Año 2023
Tipo

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



This document provides a comprehensive summary of evidence on the current situation of rare diseases (RDs) globally and regionally, including conditions, practices, policies, and regulations, as well as the challenges and barriers faced by RD patients, their families, and caregivers. The document builds on a review of academic literature and policies and a process of validation and feedback by a group of seven experts from across the globe. Panelists were selected based on their academic merit, expertise, and knowledge regarding the RD environment. The document is divided into five main sections: (1) methodology and objective; (2) background and context; (3) overview of the current situation and key challenges related to RDs covering six dimensions: burden of disease, patient journey, social impact, disease management, RD-related policies, and research and development; (4) recommendations; and (5) conclusions. The recommendations are derived from the discussion undertaken by the experts on the findings of this review and provide a set of actionable solutions to the challenges and barriers to improving access to RD diagnosis and treatment around the world. The recommendations can support critical decision-making, guiding efforts by a broad range of RDs stakeholders, including governments, international organizations, manufacturers, researchers, and patient advocacy groups.

Métricas Externas



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Disciplinas de Investigación



WOS
Public, Environmental & Occupational Health
Environmental Sciences
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Adachi, Takeya - Keio University School of Medicine - Japón
Graduate School of Medical Science - Japón
United Japanese-Researchers Around-the-World (UJA) - Japón
2 El-Hattab, Ayman W. - College of Medicine - Emiratos Árabes Unidos
MENA (Middle East and North Africa) Organization for Rare Diseases - Emiratos Árabes Unidos
University Hospital Sharjah - Emiratos Árabes Unidos
3 Jain, Ritu - Dystrophic Epidermolysis Bullosa Research Association (DEBRA) - Singapur
Asia Pacific Alliance of Rare Disease Organisations - Singapur
School of Humanities - Singapur
4 Nogales Crespo, Katya A. Mujer Policy Wisdom LLC - Puerto Rico
PolicyWisdom LLC - Puerto Rico
5 Quirland, Camila Mujer Fundación Arturo López Pérez - Chile
Universitat Autònoma de Barcelona - España
Universidad de Chile - Chile
6 Scarpa, Maurizio Hombre European Reference Network for Hereditary Metabolic Disorders (MetabERN) - Italia
Policlinico Universitario, Udine - Italia
Brains for Brain Foundation - Italia
MetabERN: European Reference Network for Hereditary Metabolic Disorders - Italia
7 Summar, Marshall - National Institutes of Health (NIH) - Estados Unidos
Childrens National Health System - Estados Unidos
National Organization for Rare Disorders - Estados Unidos
The George Washington University - Estados Unidos
The National Organization for Rare Disorders, Inc. - Estados Unidos
The George Washington University School of Medicine and Health Sciences - Estados Unidos
8 Wattanasirichaigoon, Duangrurdee - Thai Rare Disease Foundation (ThaiRDF) - Tailandia
Ramathibodi Hospital - Tailandia
National Health Security Office - Tailandia
The Food and Drug Administration, Thailand Ministry of Public Health - Tailandia
Genetics Society of Thailand - Tailandia
Thailand Medical Genetics and Genomics Association (TMGGA) - Tailandia
Asia Pacific Society of Human Genetics (APSHG) - Singapur

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Financiamiento



Fuente
Takeda Pharmaceutical Company

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Agradecimientos



Agradecimiento
The authors disclose receipt of financial support from Takeda Pharmaceutical Company Limited for the research and the discussion process that was part of developing this document. The authors independently drafted the manuscript’s contents and recommendations, and this manuscript is their product.

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