# Prevalence, severity, frequency and healthcare resource use of epilepsy among individuals with Rett Syndrome: analysis of data from a Rett Center of Excellence

**Authors:** Nazia Rashid, Charles Ruetsch, Emily M. LaFrance, Jonathan D. Darer

PMC · DOI: 10.3389/fneur.2025.1634105 · Frontiers in Neurology · 2025-10-10

## TL;DR

This study shows that individuals with Rett Syndrome who have severe epilepsy experience more frequent seizures and higher healthcare use compared to those with non-severe epilepsy.

## Contribution

The study provides real-world data on epilepsy-related healthcare utilization in Rett Syndrome using electronic health records.

## Key findings

- Severe epilepsy in Rett Syndrome is associated with significantly higher rates of ED visits and inpatient admissions.
- Over half of individuals with non-severe epilepsy experience no seizures.
- Up to one-fourth of individuals with epilepsy experience daily seizures.

## Abstract

Individuals with Rett Syndrome (RTT) frequently experience comorbid epilepsy. Few studies have examined the impact of epilepsy healthcare utilization using real-world datasets among RTT. The objective of this study was to examine all-cause and epilepsy-related healthcare utilization among individuals with RTT using electronic health record (EHR) data and chart notes.

A retrospective comparative cohort analysis was performed among RTT individuals with and without epilepsy using EHR structured and abstracted clinical notes data. Epilepsy cases were stratified into severe (associated with prolonged or intractable seizures) and non-severe. RTT individuals with no epilepsy, non-severe epilepsy, and severe epilepsy were compared on seizure frequency and healthcare utilization.

In this analysis, 98 individuals with RTT were included: 71 (72%) had epilepsy of which 33 (46%) had severe epilepsy. Individuals with severe epilepsy (n = 33) vs. non-severe epilepsy [experienced daily seizures (53.8% vs. 11.1%), weekly (23.1% vs. 14.8%), or monthly (23.1% vs. 22.2%)], respectively; however, more than half (51.9%) experienced no seizures among the non-severe group. The prevalence of ED visits was significantly higher among those with severe epilepsy compared to those with non-severe epilepsy (27% vs. 7%, p < 0.05). Inpatient admissions were significantly more prevalent among those with severe epilepsy vs. non-severe epilepsy (37% vs. 14%, p < 0.05).

Rates of epilepsy among individuals with RTT are at increased risk for healthcare utilization, especially those with severe epilepsy described as prolonged or intractable seizures. Of individuals with epilepsy, up to one-fourth experience daily seizures. It is important to educate health professionals of the high rate of concomitant epilepsy among RTT syndrome and how it can represent a substantial burden to patients and families with RTT. The frequency of seizures is more common among those with severe epilepsy.

## Linked entities

- **Diseases:** Rett Syndrome (MONDO:0010726), epilepsy (MONDO:0005027)

## Full-text entities

- **Diseases:** seizure (MESH:D012640), Epilepsy (MESH:D004827), RTT (MESH:D015518)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12549289/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12549289/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12549289/full.md

---
Source: https://tomesphere.com/paper/PMC12549289