Volume 55, Issue 12 pp. 1996-2002
Full-Length Original Research

Vagus nerve stimulation reduces cardiac electrical instability assessed by quantitative T-wave alternans analysis in patients with drug-resistant focal epilepsy

Andrew C. Schomer

Andrew C. Schomer

Department of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, U.S.A

Harvard Medical School, Boston, Massa-chusetts, U.S.A

Search for more papers by this author
Bruce D. Nearing

Bruce D. Nearing

Harvard Medical School, Boston, Massa-chusetts, U.S.A

Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, U.S.A

Search for more papers by this author
Steven C. Schachter

Steven C. Schachter

Department of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, U.S.A

Harvard Medical School, Boston, Massa-chusetts, U.S.A

Search for more papers by this author
Richard L. Verrier

Corresponding Author

Richard L. Verrier

Harvard Medical School, Boston, Massa-chusetts, U.S.A

Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, U.S.A

Address correspondence to Richard L. Verrier, Division of Cardiovascular Medicine, Department of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center, Harvard-Thorndike Electrophysiology Institute, 99 Brookline Avenue, RN-301, Boston, MA 02215-3908, U.S.A. E-mail: [email protected]Search for more papers by this author
First published: 03 December 2014
Citations: 76

Summary

Objective

The cardiac component of risk for sudden unexpected death in epilepsy (SUDEP) and alterations in cardiac risk by vagus nerve stimulation (VNS) are not well understood. We determined changes in T-wave alternans (TWA), a proven noninvasive marker of risk for sudden cardiac death in patients with cardiovascular disease, and heart rate variability (HRV), an indicator of autonomic function, in association with VNS in patients with drug-resistant focal epilepsy.

Methods

Ambulatory 24-h electrocardiograms (N = 9: ages 29–63, six males) were analyzed.

Results

Mean TWA during the interictal period was 37 ± 3.1 μV (mean ± SEM) in lead V1 for nine patients monitored following implantation of the VNS system (n = 7) or battery change (n = 2). Of these, six patients also monitored prior to implantation (n = 5) or battery change (n = 1) showed abnormally high TWA levels pre-VNS (60.0 ± 4.3 μV), which were significantly reduced by 24.3 μV (to 35.7 ± 4.8 μV, p = 0.02) after VNS settings were adjusted for desired clinical response. TWA in four (67%) of the six patients was reduced in association with VNS to levels below the 47-μV cut point of abnormality. The decrease in TWA was correlated with VNS intensity (r = 0.88, p < 0.02). In addition, low-frequency HRV was reduced by 60% (805.61 ± 253.96 to 323.49 ± 102.74 msec2, p = 0.05) and low-to high-frequency HRV ratio by 32% (3.34 ± 0.57 to 2.26 ± 0.31, p = 0.025), indicating a change in autonomic balance in favor of parasympathetic dominance.

Significance

This is the first report that elevated levels of TWA in patients with drug-refractory partial-onset seizures were reduced in association with VNS, potentially by improving sympathetic/parasympathetic balance. VNS may have a cardioprotective role at stimulation settings typically used for seizure control. These findings indicate the utility of TWA for tracking improvement in cardiac status in this population.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.

click me