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

**Authors:** Carole Bakhos, Christal G. Delagrammatikas, Scott Demarest, Yssa DeWoody, Tuesdi Dyer, Ilene Penn Miller, Amanda Moore, Ashley Fortney Point, Charlene Son Rigby, Jackie Steinberg, Vanessa Vogel-Farley, Kimberly Wiltrout

PMC · DOI: 10.3389/fneur.2026.1619219 · Frontiers in Neurology · 2026-02-12

## TL;DR

Multidisciplinary clinics can improve care for children with rare epilepsies by integrating specialists and addressing barriers like cost and access.

## Contribution

The paper provides insights into the structure, benefits, and challenges of multidisciplinary clinics for rare epilepsies based on caregiver and clinician feedback.

## Key findings

- Caregivers reported positive experiences with MDCs despite barriers like cost and distance.
- Physicians identified funding and space as main obstacles to establishing MDCs.
- Recommendations include expanding MDCs and tracking success measures to improve care and research.

## Abstract

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.

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.

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.

## Full-text entities

- **Genes:** SCN2A (sodium voltage-gated channel alpha subunit 2) [NCBI Gene 6326] {aka BFIC3, BFIS3, BFNIS, DEE11, EA9, EIEE11}, CACNA1A (calcium voltage-gated channel subunit alpha1 A) [NCBI Gene 773] {aka APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2}, SCN8A (sodium voltage-gated channel alpha subunit 8) [NCBI Gene 6334] {aka BFIS5, CERIII, CIAT, DEE13, EIEE13, MED}
- **Diseases:** chronic epilepsies (MESH:D002908), channelopathies (MESH:D053447), Prader-Willi syndrome (MESH:D011218), anxiety (MESH:D001007), DEEs (MESH:C562695), movement disorders (MESH:D009069), autism (MESH:D001321), Leverage disorder (MESH:D009358), COVID-19 (MESH:D000086382), neuromuscular disorders (MESH:D009468), Tuberous Sclerosis Complex (MESH:D014402), CD (MESH:D003424), Neurological Disorders &amp; Stroke (MESH:D009461), Related Disorders (MESH:D019973), MDCs (MESH:D000075902), Duchenne Muscular Dystrophy (MESH:D020388), seizure (MESH:D012640), inherited metabolic diseases (MESH:D030342), stroke (MESH:D020521), Malan Syndrome (MESH:D013577), Rare (MESH:D035583), refractory epilepsy (MESH:D000069279), sleep disorders (MESH:D012893), Rett Syndrome (MESH:D015518), TSC (MESH:C565346), CVI (MESH:D014786), TD (MESH:D004409), Beckwith-Wiedmann Syndrome (MESH:D001506), Epilepsies (MESH:D004827), multi-disorder (MESH:D015161)
- **Species:** Homo sapiens (human, species) [taxon 9606], Crohivirus B (no rank) [taxon 2169854]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935687/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935687/full.md

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Source: https://tomesphere.com/paper/PMC12935687