Evidence map›Paper›PMID 41883813›Full record

ReviewTherapeutic advances in rare disease

Challenges and opportunities for the use of telehealth in rare disease diagnosis, treatment, research, and education: key opinion leader interviews by the IRDiRC telehealth task force.

Melissa A Parisi, Adam L Hartman, Mary Catherine V Letinturier, Elena-Alexandra Tataru, Victoria Antoniadou, Gareth Baynam, Lara Bloom, Marco Crimi, Maria G Della Rocca, Giuseppe Didato and 10 more

Abstract readReview
In one paragraph

Review in Therapeutic advances in rare disease. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Melissa A ParisiEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), 6710B Rockledge Dr., Bethesda, MD 20817, USA.ORCID https://orcid.org/0000-0001-6707-1004
Adam L HartmanNational Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH), USA.
Mary Catherine V LetinturierIRDiRC Scientific Secretariat, French National Institute of Health and Medical Research (Inserm), France.
Elena-Alexandra TataruIRDiRC Scientific Secretariat, French National Institute of Health and Medical Research (Inserm), France.
Victoria AntoniadouCyprus Alliance for Rare Disorders, Cyprus.
Gareth BaynamRare Care Centre, Perth Children's Hospital and Western Australian Register of Developmental Anomalies, King Edward Memorial Hospital, Australia.
Lara BloomThe Ehlers-Danlos Society, UK & USA.
Marco CrimiKaleidos SCS, and Net Medicare SRL, Italy.
Maria G Della RoccaGlobal Genes, Rockville, MD, USA.
Giuseppe DidatoEpilepsy Unit, Sleep Disorders Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Sofia Douzgou HougeDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Anneliene H JonkerHealth Technologies and Services Research, TechMed Centre, University of Twente, Twente, The Netherlands.ORCID https://orcid.org/0000-0001-5883-7610
Martina KawomeSally Mugabe Central Hospital, Zimbabwe.
Friederike MuellerDepartment of Child and Youth Psychiatry, Psychosomatics and Psychotherapy, Asklepios Hospital Luebben, Germany.ORCID https://orcid.org/0000-0001-8525-308X
James O'BrienInternational Prader Willi Syndrome Organisation (IPWSO), UK.
Ratna Dua PuriInstitute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, India.
Nuala RyanNCBRS (Nicolaides-Baraitser Syndrome) Worldwide Foundation, UK.
Meow-Keong ThongGenetics and Metabolism Unit, Department of Paediatrics, Faculty of Medicine, University of Malaya, Malaysia and M. Kandiah Faculty of Medicine and Health Sciences, Universiti Tunku Abdul Rahman, Malaysia.
Birutė TumienėVilnius University, Faculty of Medicine, Institute of Biomedical Sciences; Vilnius University Hospital Santaros Klinikos, Lithuania.
Faye H ChenNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institutes of Health (NIH), 6701 Democracy Boulevard, Bethesda, MD 20817, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The International Rare Diseases Research Consortium (IRDiRC) Telehealth (TH) Task Force explored the use of TH for improving diagnosis, care, research, and education for rare diseases (RDs) worldwide. The Task Force members interviewed 23 key opinion leaders (KOLs), providing perspectives from experts in the use of TH for the diagnosis, treatment, and prevention of RDs (10 KOLs); for research and evaluation in RDs (7); and for the continuing education of health care providers (HCPs) in RDs (6). The KOLs represented a broad array of diverse perspectives with regard to both geographic regions, including Europe, United States, Sub-Saharan Africa, and Asia, and professional expertise, including rare disease patients and family members, RD association spokespersons, TH association representatives, physicians, researchers, and regulatory authorities. The Task Force solicited KOL opinions to identify factors that influence TH in improving access to diagnosis, care, prevention, and research experiences for RD patients and providers as well as continuing education and peer mentoring for HCPs. This manuscript represents a synthesis of those interviews and some common themes that emerged, along with identification of evidence and knowledge gaps that will benefit from future research efforts to help advance and expand the use of TH for RD care, research, and education. KOLs agreed on the unique elements of RD medical care that could benefit from TH approaches and recognized the increasing role that remote assessments can play in supporting RD research. They identified models for health care provider education afforded by TH that can enhance care for RD patients and broaden the pool of experts in these conditions. While recognizing that barriers to broad implementation exist, they agreed that TH provides a unique tool to provide greater access to care for RD patients worldwide.

Indexed as

decentralized clinical trialeHealthIRDiRCkey opinion leaderpeer mentoringrare diseaserare disease carerare disease educationrare disease researchteleconsultationtelehealthtelemedicine

Identifiers

PMID41883813
PMCPMC13009623

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.