
==== Front
Cureus
Cureus
2168-8184
Cureus
2168-8184
Cureus Palo Alto (CA)

10.7759/cureus.67402
Neurology
Refractory Obstructive Sleep Apnea Secondary to Vagal Nerve Stimulation
Muacevic Alexander
Adler John R
Coburn Ryan P 1
Lipford Melissa C 2
1 Department of Neurology, Mayo Clinic, Rochester, USA
2 Department of Neurology, Division of Pulmonary and Critical Care, Center for Sleep Medicine, Mayo Clinic, Rochester, USA
Ryan P. Coburn coburn.ryan@mayo.edu
21 8 2024
8 2024
16 8 e6740220 8 2024
Copyright © 2024, Coburn et al.
2024
Coburn et al.
https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This article is available from https://www.cureus.com/articles/267081-refractory-obstructive-sleep-apnea-secondary-to-vagal-nerve-stimulation
Vagal nerve stimulator (VNS) devices are commonly used as a non-pharmacologic option for improved seizure control in patients with refractory epilepsy. However, a side effect associated with VNS device placement includes sleep-disordered breathing, which is complicated by the fact that a significant minority of patients with epilepsy have sleep-disordered breathing. We describe a patient with iatrogenically worsened refractory obstructive sleep apnea (OSA) secondary to VNS device placement, which resolved upon turning off the VNS device. This case highlights the need to screen for OSA in patients who are candidates for VNS device placement, as iatrogenic sleep-disordered breathing could place the patient at risk for adverse clinical outcomes, as well as paradoxically worsen seizure control due to poor quality sleep.

obstructive sleep apnea
worsening obstructive sleep apnea (osa)
iatrogenic obstructive sleep apnea
vagal nerve stimulator
obstructive sleep apnea (osa)
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pmcIntroduction

Drug-resistant epilepsy (DRE) poses a significant challenge for providers, with an estimated one-third of patients with inadequate seizure control despite two anti-seizure medications (ASMs) at therapeutic doses [1]. Additional medications are unlikely to lead to seizure freedom and may instead result in medication side effects [2]. With additional ASMs unlikely to be effective, non-pharmacologic options for seizure control are considered in the Neurologist’s armamentarium. Such options include the ketogenic or low glycemic index diet, surgical intervention such as resection of a structural lesion, or a neurostimulatory method such as a vagal nerve stimulator (VNS) [3].

The mechanism by which vagal nerve stimulation reduces seizure burden is not yet well elucidated. Proposed mechanisms include release of inhibitory neurotransmitters, desynchronization of cortical hypersynchronization during seizure activity, and increased blood flow to limbic and cortical brain regions, among others [4].

Side effects related to vagal stimulation commonly include hoarse voice, cough, and paresthesia [5]. More significant side effects are related to cardiovagal function; thus, cardiac conduction disorders serve as a contraindication to VNS placement, as increased vagal efferent firing could lead to symptomatic arrhythmia. A relative contraindication to placement includes a history of obstructive sleep apnea (OSA), as VNS devices have been shown to worsen or even cause iatrogenic obstructive and central sleep apnea [6]. 

We present a case of a woman with intractable epilepsy who upon VNS placement developed OSA which was refractory to continuous positive airway pressure (CPAP) and completely abated with the VNS device turned off.

Case presentation

The patient is a left-handed female in her 60s with relevant comorbidities that include intellectual disability, severe OSA, and intractable multifocal epilepsy. 

The patient was diagnosed with epilepsy at the age of six months which was felt to be due to multiple intracranial vascular malformations. She had multiple seizure semiologies, including generalized tonic clonic, tonic, and atonic. Many ASMs were trialed at varying doses and combinations, including lamotrigine, carbamazepine, phenobarbital, felbamate, topiramate, valproate, and levetiracetam, with continued unacceptably high seizure burden. She underwent a partial corpus callosotomy at the age of 38. 

OSA was initially diagnosed at the age of 39. The patient had symptoms of daytime hypersomnolence and observed apneas in sleep, prompting further evaluation. A polysomnography study demonstrated very severe OSA with an apnea-hypopnea index (AHI) of 83 per hour (83/h). Disordered breathing events were eliminated by CPAP with a pressure of 9 cm water (H2O). 

Several years later, the patient underwent VNS implantation at the age of 49 due to continued high seizure burden. She experienced significant reduction in seizure frequency with VNS settings of current 1.5 milliamperes (mA), on time of 30 seconds, off time of 1.1 minutes, signal frequency of 25 Hertz (Hz), and pulse width of 250 micro-seconds (µsec).

She returned to the sleep clinic four years after VNS placement in the setting of losing her CPAP device and gaining 30 pounds. She was restarted on auto-titrating CPAP with a pressure window of 6-12 cm H2O. At a follow-up appointment, her CPAP device indicated persistent OSA, despite regular usage of CPAP. The estimated residual AHI was 20.2/h. Her auto-titrating settings were subsequently increased to 11-20 cm H20, and she was asked to return with an overnight oximetry study performed on CPAP (Figure 1A). This study showed an oxygen desaturation index of 36/h (suggesting severe residual OSA). This was followed by overnight polysomnography (Figure 2A) which confirmed persistent OSA that did not respond to increasing CPAP pressures.

Figure 1 Patient Overnight Oximetry

The patient’s overnight oximetry studies before (A) and after (B) the VNS stimulator was turned off are shown.  In (A), time is represented on the x-axis, with each dash representing 15 minutes.  Oxygen saturation and pulse are located on the y-axis (left and right side of the axis, respectively), with oxygen saturation in black and pulse in light grey.  In (B), oxygen saturation is located on the y-axis of the top graph and pulse is located on the y-axis of the bottom graph. The initial study (A) showed an oxygen desaturation index of 36/h, with the subsequent study once the VNS device was turned off (B) revealing a marked improvement to 2.4/h.  The figure was used with permission of Mayo Foundation for Medical Education and Research. All rights reserved.

VNS: Vagal nerve stimulator; ODI: oxygen desaturation index

Figure 2 Patient Polysomnogram

The patient’s polysomnogram prior to having their VNS turned off is shown.  In (A), an apneic event is seen, signified by the red highlighted portion of the study.  In (B), time is further compressed on the x-axis.  This allows for the ability to see multiple apneic events, again highlighted in red, which correspond to the VNS signal “on” time.  Return of respirations is seen during the “off” time.  The figure was used with permission of Mayo Foundation for Medical Education and Research. All rights reserved.

VNS: Vagal nerve stimulator

The fixed timing of her obstructive events matched with her VNS on cycle time, thus demonstrating the VNS device activating at the start of each obstructive apnea (Figure 2B). In consultation with her epilepsy physician, the VNS device was turned off overnight and a repeat overnight oximetry study was performed on CPAP (Figure 1B). This demonstrated a normal oxygen desaturation index of 2.4/h, indicating resolution of OSA.

Discussion

The case we describe is an example of a patient with severe OSA previously well controlled with use of CPAP, who developed CPAP-refractory OSA following implantation of the VNS device. 

VNS device placement has been associated with worsening of underlying OSA and even de novo iatrogenic sleep-disordered breathing [7-9]. As available literature is predominantly small case series and case reports, true prevalence of sleep-disordered breathing following VNS placement is uncertain, but one meta-analysis estimates 31.9% in the adult population [10]. Apneas and hypopneas, as seen in our patient, are more frequent during VNS activation. 

Several mechanisms by which vagal nerve stimulation causes OSA have been proposed. Vagal afferent stimulation activates the dorsal motor nucleus of the vagal nerve, altering neuromuscular transmission to airway muscles of the pharynx and larynx, leading to pharyngeal closure. An alternative explanation is stimulation of vagal afferent projections to brainstem respiratory centers may influence breathing patterns [11]. The mechanism underlying vagal nerve stimulation and central sleep apnea is poorly elucidated [12]. 

An estimated 33.4% of patients with epilepsy have comorbid OSA [13]. As sleep is a well-recognized modifiable risk factor in seizure control, there is significant importance in treatment of underlying OSA, with positive pressure therapy shown to reduce seizure frequency over time [14]. Thus, the interplay between VNS placement and OSA represents a complicated dynamic. Screening for OSA before and after VNS placement should therefore be considered. 

The management of OSA following VNS placement should be managed in a multidisciplinary manner, with Neurology and Sleep Medicine providers optimizing VNS and CPAP settings, respectively. Adjustments to VNS settings to mitigate this effect include reducing stimulus intensity or frequency, decreasing pulse width, or increasing time off [12]. A programmable device that allows adjustments of the above settings during a specific time of day, or turning the device off overnight, represents an additional option. Trials of higher CPAP pressures may be necessary. However, as shown in our case, apneas may remain refractory to CPAP therapy. 

Conclusions

We describe a case of CPAP-refractory OSA due to VNS device placement. This case highlights the importance of screening for OSA both before and after device placement, as proper management of OSA and improved sleep quality play an important role in seizure control. Adjustments to VNS settings or titration of CPAP pressures may be necessary, although some cases may remain refractory, and alternative solutions such as a programmable device may be required.

Disclosures

Author Contributions

Human subjects: Consent was obtained or waived by all participants in this study.

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following:

Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work.

Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work.

Intellectual property info: Permission was granted by the Mayo Foundation for Medical Education and Research to include the attached figures, in print and electronic format of the new work on the condition attribution is cited as follows: “Used with permission of Mayo Foundation for Medical Education and Research. All rights reserved.”.

Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Concept and design:  Ryan P. Coburn, Melissa C. Lipford

Drafting of the manuscript:  Ryan P. Coburn

Acquisition, analysis, or interpretation of data:  Melissa C. Lipford

Critical review of the manuscript for important intellectual content:  Melissa C. Lipford

Supervision:  Melissa C. Lipford
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