Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators.
GPD; developing nations; rare diseases; survey; undiagnosed diseases; Public Health, Environmental and Occupational Health
Abstract :
[en] [en] BACKGROUND: Patients, families, the healthcare system, and society as a whole are all significantly impacted by rare diseases (RDs). According to various classifications, there are currently up to 9,000 different rare diseases that have been recognized, and new diseases are discovered every month. Although very few people are affected by each uncommon disease individually, millions of people are thought to be impacted globally when all these conditions are considered. Therefore, RDs represent an important public health concern. Although crucial for clinical care, early and correct diagnosis is still difficult to achieve in many nations, especially those with low and middle incomes. Consequently, a sizeable amount of the overall burden of RD is attributable to undiagnosed RD (URD). Existing barriers and policy aspects impacting the care of patients with RD and URD remain to be investigated.
METHODS: To identify unmet needs and opportunities for patients with URD, the Developing Nations Working Group of the Undiagnosed Diseases Network International (DNWG-UDNI) conducted a survey among its members, who were from 20 different nations. The survey used a mix of multiple choice and dedicated open questions covering a variety of topics. To explore reported needs and analyze them in relation to national healthcare economical aspects, publicly available data on (a) World Bank ranking; (b) Current health expenditure per capita; (c) GDP per capita; (d) Domestic general government health expenditure (% of GDP); and (e) Life expectancy at birth, total (years) were incorporated in our study.
RESULTS: This study provides an in-depth evaluation of the unmet needs for 20 countries: low-income (3), middle-income (10), and high-income (7). When analyzing reported unmet needs, almost all countries (N = 19) indicated that major barriers still exist when attempting to improve the care of patients with UR and/or URD; most countries report unmet needs related to the availability of specialized care and dedicated facilities. However, while the countries ranked as low income by the World Bank showed the highest prevalence of referred unmet needs across the different domains, no specific trend appeared when comparing the high, upper, and low-middle income nations. No overt trend was observed when separating countries by current health expenditure per capita, GDP per capita, domestic general government health expenditure (% of GDP) and life expectancy at birth, total (years). Conversely, both the GDP and domestic general government health expenditure for each country impacted the presence of ongoing research.
CONCLUSION: We found that policy characteristics varied greatly with the type of health system and country. No overall pattern in terms of referral for unmet needs when separating countries by main economic or health indicators were observed. Our findings highlight the importance of identifying actionable points (e.g., implemented orphan drug acts or registries where not available) in order to improve the care and diagnosis of RDs and URDs on a global scale.
Disciplines :
Public health, health care sciences & services
Author, co-author :
Sciascia, Savino; Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) With Nephrology and Dialysis Unit, San Giovanni Bosco Hub Hospital, ASL Città di Torino and University of Turin, Turin, Italy
Roccatello, Dario; Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) With Nephrology and Dialysis Unit, San Giovanni Bosco Hub Hospital, ASL Città di Torino and University of Turin, Turin, Italy
Salvatore, Marco; National Center for Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, Rome, Italy
Carta, Claudio; National Center for Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, Rome, Italy
Cellai, Laura L; National Center for Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, Rome, Italy
Ferrari, Gianluca; National Center for Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, Rome, Italy
Lumaka Zola, Aimé ; Université de Liège - ULiège > GIGA > GIGA Cancer - Human Genetics ; Centre Hospitalier Universitaire de Liège - CHU > > Service de génétique
Groft, Stephen; National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, United States
Alanay, Yasemin; ACURARE-Rare and Undiagnosed Diseases Center, Acibadem University, Istanbul, Türkiye
Azam, Maleeha; COMSATS University Islamabad, Islamabad, Pakistan
Baynam, Gareth; Rare Care, Clinical Center of Expertise for Rare and Undiagnosed Diseases, Perth Children's Hospital, Perth, WA, Australia
Cederroth, Helene; Wilhelm Foundation, Stockholm, Sweden
Cutiongco-de la Paz, Eva Maria; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, Manila, Philippines
Dissanayake, Vajira Harshadeva Weerabaddana; Department of Anatomy, Genetics and Biomedical Informatics, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka
Giugliani, Roberto; House of Rares, Medical Genetics Service, HCPA, Department Genetics UFRGS and DASA, Porto Alegre, Brazil
Gonzaga-Jauregui, Claudia; International Laboratory for Human Genome Research, Universidad Nacional Autonoma de Mexico, Juriquilla, Queretaro, Mexico
Hettiarachchi, Dineshani; Department of Anatomy, Genetics and Biomedical Informatics, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka
Kvlividze, Oleg; Georgian Foundation for Genetic and Rare Diseases (GeRaD), School of Medicine, New Vision University, Tbilisi, Georgia
Landoure, Guida; Faculté de Médecine et d'Odontostomatologie, l'Université des Sciences, des Techniques et des Technologies de Bamako, Bamako, Mali
Makay, Prince; Reference Center for Rare and Undiagnosed Diseases, University of Kinshasa, Kinshasa, Democratic Republic of Congo
Melegh, Béla; Department of Medical Genetics, School of Medicine, University of Pécs, Pécs, Hungary
Ozbek, Ugur; ACURARE-Rare and Undiagnosed Diseases Center, Acibadem University, Istanbul, Türkiye
Puri, Ratna Dua; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India
Romero, Vanessa I; School of Medicine, Universidad San Francisco de Quito, Quito, Ecuador
Scaria, Vinod; CSIR Institute of Genomics and Integrative Biology, New Delhi, India
Jamuar, Saumya S; Genetics Service, Department of Pediatrics, KK Women's and Children's Hospital and Pediatric ACP, Duke-NUS Medical School, Singapore, Singapore ; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore
Shotelersuk, Vorasuk; Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, King Chulalongkorn Memorial Hospital and Chulalongkorn University, Bangkok, Thailand
Gahl, William A; National Institutes of Health, National Human Genome Research Institute, Bethesda, MD, United States
Wiafe, Samuel A; Rare Disease Ghana Initiative, Accra, Ghana
Bodamer, Olaf; Division of Genetics and Genomics, Harvard Medical School, Boston Children's Hospital, Boston, MA, United States
Posada, Manuel; Rare Diseases Research Institute (IIER), SpainUDP, Instituto de Salud Carlos III (ISCIII), Madrid, Spain
Taruscio, Domenica; National Center for Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, Rome, Italy
Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators.
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