Evidence map›Paper›PMID 30697974›Full record

ArticleMolecular genetics & genomic medicine2019

A multidisciplinary approach to the clinical management of Prader-Willi syndrome.

Jessica Duis, Pieter J van Wattum, Ann Scheimann, Parisa Salehi, Elly Brokamp, Laura Fairbrother, Anna Childers, Althea Robinson Shelton, Nathan C Bingham, Ashley H Shoemaker and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
10.4field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Article
  4. Article
  5. JCEM case reports · 2026
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  19. Review
  20. Clinical Trials in Prader-Willi Syndrome: A Review.International journal of molecular sciences · 2023
    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

11 authors at 5 institutions in 1 country.

Jessica DuisDivision of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.ORCID 0000-0001-6605-1028
Pieter J van WattumDepartment of Psychiatry, Child Study Center, Yale School of Medicine, New Haven, Connecticut.
Ann ScheimannPediatric Gastroenterology, Johns Hopkins Children's Center, Baltimore, Maryland.
Parisa SalehiDivision of Endocrinology and Diabetes, Seattle Children's, University of Washington, Seattle, Washington.
Elly BrokampDivision of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Laura FairbrotherDivision of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Anna ChildersDivision of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Althea Robinson SheltonNeuro-Sleep Division, Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tennessee.
Nathan C BinghamDivision of Pediatric Endocrinology, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Ashley H ShoemakerDivision of Pediatric Endocrinology, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Jennifer L MillerPediatric Endocrinology, University of Florida, Gainesville, Florida.
Vanderbilt University · USJohns Hopkins University · USSeattle Children's Hospital · USUniversity of Florida Health · USYale University · US

Funding

Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DYKENS, ELISABETH MAY · 2015 to 2019
$7.1M
Early Onset Obesity and Cognitive Impairment in PseudohypoparathyroidismK23DK101689 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SHOEMAKER, ASHLEY HALL · 2014 to 2018
$778k
NICHD NIH HHS U54 HD083211NIDDK NIH HHS K23 DK101689
6 · The paper itself

Abstract

backgroundPrader-Willi syndrome (PWS) is a complex neuroendocrine disorder affecting approximately 1/15,000-1/30,000 people. Unmet medical needs of individuals with PWS make it a rare disease that models the importance of multidisciplinary approaches to care with collaboration between academic centers, medical homes, industry, and parent organizations. Multidisciplinary clinics support comprehensive, patient-centered care for individuals with complex genetic disorders and their families. Value comes from improved communication and focuses on quality family-centered care.

methodsInterviews with medical professionals, scientists, managed care experts, parents, and individuals with PWS were conducted from July 1 to December 1, 2016. Review of the literature was used to provide support.

resultsData are presented based on consensus from these interviews by specialty focusing on unique aspects of care, research, and management. We have also defined the Center of Excellence beyond the multidisciplinary clinic.

conclusionEstablishment of clinics motivates collaboration to provide evidence-based new standards of care, increases the knowledge base including through randomized controlled trials, and offers an additional resource for the community. They have a role in global telemedicine, including to rural areas with few resources, and create opportunities for clinical work to inform basic and translational research. As a care team, we are currently charged with understanding the molecular basis of PWS beyond the known genetic cause; developing appropriate clinical outcome measures and biomarkers; bringing new therapies to change the natural history of disease; improving daily patient struggles, access to care, and caregiver burden; and decreasing healthcare load. Based on experience to date with a PWS multidisciplinary clinic, we propose a design for this approach and emphasize the development of "Centers of Excellence." We highlight the dearth of evidence for management approaches creating huge gaps in care practices as a means to illustrate the importance of the collaborative environment and translational approaches.

Indexed as

Disease ManagementInterdisciplinary CommunicationHealth Knowledge, Attitudes, PracticeHealth PersonnelHumansPrader-Willi SyndromeSurveys and Questionnairesgenomic imprintinginterdisciplinary communicationoutcome and process assessment (health care)Prader-Willi syndrometelemedicinetranslational medical research

Identifiers

PMID30697974
PMCPMC6418440
OpenAlexW2913687538

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.