Evidence map›Paper›PMID 32514667›Full record

ReviewCurrent osteoporosis reports2020

The Rare Bone Disease TeleECHO Program: Leveraging Telehealth to Improve Rare Bone Disease Care.

Laura L Tosi, Elmer N Rajah, Michael H Stewart, Austin P Gillies, Tracy S Hart, E Michael Lewiecki

Open access · hybridAbstract readReview
In one paragraph

Review in Current osteoporosis reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Bridging the knowledge gap in rare bone disorders: insights from the APCO Asia-Pacific Rare Bone Disorders Engagement (ASPIRE) survey.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
    Article
  6. Review
  7. Review
  8. Article
  9. Rare genetic skeletal disorders: Evolving terminology, therapies, education and advocacy.Journal of the Pediatric Orthopaedic Society of North America · 2024
    Article
  10. Article
  11. Improving care pathways for people living with rare bone diseases (RBDs): outcomes from the first RBD Summit.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2023
    Article
  12. Review
  13. Three-year progress report of Bone Health TeleECHO Moscow: a strategy to improve the care of patients with osteoporosis and other metabolic skeletal diseases in underserved communities of Russia.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2022
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Proceedings of the 2023 Santa Fe Bone Symposium: Progress and Controversies in the Management of Patients with Skeletal Diseases.Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry
    Review
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

6 authors at 3 institutions in 1 country.

Laura L TosiDivision of Orthopaedics & Sports Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA. ltosi@childrensnational.org.ORCID 0000-0001-8827-9883
Elmer N RajahDivision of Orthopaedics & Sports Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA.
Michael H StewartOsteogenesis Imperfecta Foundation, 804 W Diamond Ave #210, Gaithersburg, MD, 20878, USA.
Austin P GilliesDivision of Orthopaedics & Sports Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA.
Tracy S HartOsteogenesis Imperfecta Foundation, 804 W Diamond Ave #210, Gaithersburg, MD, 20878, USA.
E Michael LewieckiNew Mexico Clinical Research & Osteoporosis Center, 300 Oak St NE, Albuquerque, NM, 87106, USA.
Children's National · USOsteogenesis Imperfecta Foundation · USNew Mexico Clinical Research & Osteoporosis Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewRare bone diseases constitute ~ 5% of all known rare diseases and can require complex, multidisciplinary care. Advancing access to current medical knowledge is an important strategy for improving care for rare bone diseases throughout the world. To support this goal, the Rare Bone Disease Alliance launched the Rare Bone Disease TeleECHO in 2019. RECENT

findingsThe Rare Bone Disease TeleECHO is a monthly video teleconference that fosters a collegial community of practice and opportunities for active learning through interactive case-based learning. TeleECHO relies on a hub-and-spoke model, where medical professionals at the "hub" provide support and expertise for other healthcare providers, or the "spokes". Evidence of the global reach of the program as well as qualitative feedback from registrants supports the need for rare bone disease education and the value of the TeleECHO model. The Rare Bone Disease TeleECHO helps meet the challenge of disseminating rapidly expanding rare bone disease knowledge by leveraging telehealth.

Indexed as

Bone DiseasesProgram DevelopmentRare DiseasesVideoconferencingEducation, Medical, ContinuingHumansInformation DisseminationTelemedicineCommunity of practiceForce multiplierTelementoring

Identifiers

PMID32514667
PMCPMC7419447
OpenAlexW3033813239

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.