Evidence map›Paper›PMID 41767010›Full record

ArticleFrontiers in neurology

Unlocking the potential of multidisciplinary clinics to transform rare epilepsies care, insights, and research.

Carole Bakhos, Christal G Delagrammatikas, Scott Demarest, Yssa DeWoody, Tuesdi Dyer, Ilene Penn Miller, Amanda Moore, Ashley Fortney Point, Charlene Son Rigby, Jackie Steinberg and 2 more

Abstract read
In one paragraph

Article in Frontiers in neurology. 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

12 authors.

Carole BakhosJordan's Guardian Angels, Sacramento, CA, United States.
Christal G DelagrammatikasMalan Syndrome Foundation, Old Bridge, NJ, United States.
Scott DemarestDepartment of Pediatrics and Neurology, Precision Medicine Institute, Children's Hospital of Colorado, University of Colorado, Aurora, CO, United States.
Yssa DeWoodyRing14, USA, Midland, TX, United States.
Tuesdi DyerCardio-Facio-Cutaneous Syndrome & RASopathies Network, Lake Worth, TX, United States.
Ilene Penn MillerRare Epilepsy Network, Bethesda, MD, United States.
Amanda MooreAngelman Syndrome Foundation, Aurora, IL, United States.
Ashley Fortney PointKoolen-de Vries Syndrome Foundation, Wilmington, NC, United States.
Charlene Son RigbySTXBP1 Foundation, Holly Springs, NC, United States.
Jackie SteinbergSTXBP1 Foundation, Holly Springs, NC, United States.
Vanessa Vogel-FarleyRare Epilepsy Network, Cedarburg, WI, United States.
Kimberly WiltroutBoston's Children's Hospital, Boston, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Multidisciplinary clinics (MDCs) improve care for patients with complex, comorbid conditions through coordinated, team-based care. Despite their potential, MDCs remain underutilized and understudied in pediatric neurology, particularly for individuals with rare, chronic epilepsies. Observations: The subject of MDCs in pediatric epilepsy was explored through two workshops and surveys of caregivers and clinicians. MDC models vary widely-from general clinics (e.g., neurology, genetics, and neuropsychology) to disorder-specific clinics with multisystemic specialists. Caregivers identified key barriers, including geographical distance, personal expense, and insurance prior authorization requirements, yet overall reported positive experiences-citing valuable opportunities to participate in research and meaningful changes to clinical care. Although the findings reflect responses from a predominantly white, higher-income, English-speaking group of caregivers recruited through patient advocacy networks-and may therefore carry certain biases-their perspectives remain broadly generalizable to prospective patients across diverse socioeconomic settings. Similarly, physicians identified funding and space as the primary barriers to establishing multidisciplinary clinics, yet a majority recognized the importance of advancing research, translational studies, and clinical trials. Conclusions and relevance: MDCs can improve care for patients with medically complex rare epilepsies by integrating the management of comorbidities. These clinics bring value to both rare patients and physicians by providing a setting for synergistic activities between clinical care, clinical trials, and research. To expand their impact, we recommend: (1) establishing more MDCs using sustainable models; (2) improving access to extend the reach of MDCs; (3) including key specialists for integrated care; (4) sharing disorder-specific expertise through collaboration and training; and (5) tracking standardized success measures to validate and scale these efforts.

Indexed as

care coordinationclinical research and trialsDevelopmental and Epileptic Encephalopathies (DEEs)integrated care modelsmedically complex caremultidisciplinary clinicspediatric epilepsyrare epilepsies

Identifiers

PMID41767010
PMCPMC12935687

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Registered trials

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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.