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Vagus nerve stimulation: predictors of seizure freedom
  1. J Janszky,
  2. M Hoppe,
  3. F Behne,
  4. I Tuxhorn,
  5. H W Pannek,
  6. A Ebner
  1. Bethel Epilepsy Centre, Bielefeld, Germany
  1. Correspondence to:
 Dr Alois Ebner
 Epilepsie-Zentrum Bethel, Mara Krankenhaus, Maraweg 21, Bielefeld 33617, Germany; aemara.de

Abstract

Objectives: To identify predictive factors for the seizure-free outcome of vagus nerve stimulation (VNS).

Methods: All 47 patients who had undergone VNS implantation at one centre and had at least one year of follow up were studied. They underwent complete presurgical evaluation including detailed clinical history, magnetic resonance imaging, and long term video-EEG with ictal and interictal recordings. After implantation, adjustment of stimulation parameters and concomitant antiepileptic drugs were at the discretion of the treating physician.

Results: Mean (SD) age of the patients was 22.7 (11.6) years (range 7 to 53). Six patients (13%) became seizure-free after the VNS implantation. Only two variables showed a significant association with the seizure-free outcome: absence of bilateral interictal epileptiform discharges (IED) and presence of malformation of cortical development (MCD). Epilepsy duration showed a non-significant trend towards a negative association with outcome. By logistic regression analysis, only absence of bilateral IED correlated independently with successful VNS treatment (p<0.01, odds ratio = 29.2 (95% confidence interval, 2.4 to 353)). Bilateral IED (independent or bilateral synchronous) was found in one of six seizure-free patients and in 33 of 41 non-seizure-free patients. When bilateral IED were absent, the sensitivity for seizure-free outcome was 0.83 (0.44 to 0.97), and the specificity was 0.80 (0.66 to 0.90).

Conclusions: Bilateral IED was independently associated with the outcome of VNS. These results are preliminary because they were based on a small patient population. They may facilitate prospective VNS studies enrolling larger numbers of patients to confirm the results.

  • HQOL, health related quality of life
  • IED, interictal epileptiform discharge
  • MCD, malformation of cortical development
  • VNS, vagus nerve stimulation
  • vagus nerve stimulation
  • interictal epileptiform discharges
  • malformation of cortical development

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Vagus nerve stimulation (VNS) has been shown to be effective treatment for drug resistant epilepsy in two randomised, double blind studies.1,2 During recent years VNS has become an accepted method of treating patients with refractory epilepsy who are not candidates for epilepsy surgery or in whom surgery resulted in no benefit. From the experience of centres using VNS, one third of patients have a reduction in seizure frequency of at least 50%, another third have a worthwhile seizure reduction, while in the remaining third there is little or no effect.3 There is only limited information on patients who become seizure-free.3 The rate of seizure freedom shows a large variation across the studies which have provided any information at all about it, and ranged from 0% to 24%.4,5,6,7,8,9,10,11,12,13

Despite increasing amounts of clinical data, it is still not possible to predict which patients will profit from VNS.14 Determining prognostic factors is important in predicting seizure outcome of VNS and in counselling patients. Moreover, because of the invasive nature of the procedure, the possible hazards of chronic implantation, and the relatively high cost of the treatment, factors indicating a poor prognosis could favour other treatment options including the newer antiepileptic drugs, palliative epilepsy surgery, non-surgical non-pharmacological treatment, or a ketogenic diet. The identification of prognostic factors could also improve our general understanding of the physiological mechanisms of the effect of VNS on seizures.

In two studies focusing on epilepsy duration it was found that patients with a longer duration of epilepsy had a significantly smaller chance of being seizure-free on VNS treatment than those with epilepsy duration of less than six years.7,15 In contrast, in a study involving a search of the VNS outcome treatment registry—a database created by participating prescribing physicians who voluntarily submit baseline information on patient treatment to a centralised data storage site10—it was found that VNS responsiveness was associated with older age, longer epilepsy duration, and epilepsy syndromes other than Lennox-Gastaut syndrome.10 Some other studies have unsuccessfully tried to identify prognostic factors for a seizure reduction of more than 50% by VNS treatment.12,13 Moreover, in all studies analysing the efficacy of VNS, a 50–75% reduction or percentage change in seizure frequency rather than seizure freedom has been the dominant end point.1,2,12,16–18 Conversely, health related quality of life (HQOL) is primarily related to seizure freedom and not to seizure reduction. In a study evaluating the relation of seizure improvement to HQOL after introducing a new antiepileptic drug, HQOL improvement was consistently evident only among patients achieving seizure freedom and not in those who had a 50–75% or 75–99% seizure reduction.19 Although epilepsy patients experience significant impairment in their HQOL, seizure-free patients can have HQOL levels comparable to those of the general population, which supports striving for seizure freedom as an epilepsy care goal.20

Most studies investigating the outcome of VNS do not require complete presurgical evaluation. A recent study reported that four of 11 patients who were referred for VNS because of “drug resistant epilepsy” without presurgical evaluation actually had no epilepsy at all or had been good candidates for epilepsy surgery, which was obvious only after a presurgical evaluation that included video-EEG monitoring.21 Moreover, more detailed data provided by presurgical evaluation may lead to greater insight into the predictors of VNS success. Our study was aimed at identifying predictive factors for seizure-free outcome after VNS in 47 patients who had undergone extensive presurgical evaluation including magnetic resonance imaging (MRI) and long term video-EEG.

METHODS

Patient selection

For this retrospective study we included all patients in whom VNS implantation had been carried out in our centre between 1 January 2000 and 31 October 2002, and who had at least one year of follow up. Neither our centre nor our patients had participated in previous double blind randomised studies. All patients were referred to our centre for presurgical evaluation because of chronic drug resistant epilepsy and were selected for VNS on the basis of their prognosis for resective brain surgery. We selected only those patients who had undergone a complete presurgical evaluation including a detailed clinical history, MRI, and long term video-EEG with ictal and interictal recordings.

Presurgical evaluation at the epilepsy surgery department of the Bethel epilepsy centre

As the observed variables were based on presurgical evaluation of epileptic patients, we shall describe our protocol briefly. In patients who were to be considered possible candidates for epilepsy surgery, a detailed neurological history was taken. Resistance to first line antiepileptic drugs was evaluated. A high resolution MRI was carried out in all patients. In those with negative MRI, a second and more detailed MRI investigation was undertaken, focusing more on the region where the epileptogenic lesion was thought to be located, based on the presurgical evaluation. (the technical details of MRI investigation are described below). Patients underwent continuous video-EEG monitoring lasting two to 10 days. In all patients except small children, psychiatric and neuropsychological examination and a social assessment were undertaken. Findings of the presurgical evaluation were discussed at a multidisciplinary case conference, where decisions were made about the possibility and type of brain surgery or VNS, and on the need for further investigations.

Vagus nerve stimulation

Stimulation of the left vagal nerve was carried out using the NCP system (Cyberonics Inc, Houston, Texas, USA). The system and surgical procedure have been described elsewhere previously.6,22 Stimulation was initiated in the immediate postoperative period, using the following parameters: current 0.25 mA, frequency 30 Hz, pulse width 500 μs, 30 s signal on time, 5 min signal off time. Patients in whom a vagus nerve stimulator had been implanted were usually examined every one to three months. At every follow up visit seizure frequency, seizure type, antiepileptic drug regimen change, and any side effects of the treatment were assessed. On these subsequent visits the current was gradually increased by 0.25 to 0.5 mA per visit until the individual patient’s tolerance, seizure freedom, or a maximum of 3.5 mA were reached. The other device parameters usually remained unchanged except for the signal on and off time. Patients who had no seizure reducing effect 0.5 to 1.5 years after implantation by changing the output current were offered the “rapid cycle mode” which consisted of on/off periods of 7 s/14 s. No restrictions were placed on changes of the concomitant antiepileptic drug. The adjustment of stimulation parameters and concomitant antiepileptic drug were at the discretion of the treating physician. The patients were also provided with a magnet allowing additional stimulation to be commanded by the patient or a caregiver in the case of an aura or seizure. The magnet output current was programmed at 0.25 mA, higher than the automatically delivered stimulation, with a pulse width of 500 μs for a period of 60 seconds.

Data collection

We investigated the following groups of variables: general data, seizure semiology, EEG and neuroimaging data, and epilepsy syndrome. General data were obtained from the clinical history and medical records. The list of variables is presented in table 1. The variables of seizure semiology were based on video-EEG recordings, while aura, the presence of secondarily generalised tonic-clonic seizures (SGTCS), number of seizure types, and seizure frequency were obtained from the clinical history (see list of variables in table 2). EEG data (table 3) were determined from non-invasive continuous video-EEG monitoring. Preoperative 32–64 channel EEG recordings were used; electrodes were placed according to the 10-10 system,23 the number of electrodes and their placement being varied individually according to the suspected epileptogenic region and side. The location and frequency of interictal epileptiform discharges (IED) were assessed by visual analysis of interictal EEG samples of two minutes duration per hour.

Table 1

 General data

Table 2

 Seizure characteristics

Table 3

 EEG data

Structural MRI investigations

MRI scanning was carried out on a 1.5 T scanner equipped with ultra gradients, a standard head coil, and vacuum cushions to reduce patient movement (Siemens Magnetom Symphony, Erlangen, Germany). The MRI investigation for epilepsy consisted of coronal and axial FLAIR datasets (time of repetition (TR) = 9000 ms, time of echo (TE) = 110 ms, inversion time (TI) = 2500 ms, slice thickness 5 mm, field of view (FOV) 201×230, matrix 220×256); coronal proton density and T2 weighted images (TR = 3075 ms, TE = 14/85 ms, slice thickness 5 mm, FOV 201×230, matrix 210×256); axial T2 weighted images (TR = 5401 ms, TE = 90 ms, slice thickness 5 mm, FOV 230×230, matrix 270×512); and a T1 weighted coronal three dimensional sequence (MPRAGE, TR = 11.1 ms, TE = 4.3 ms, slice thickness 1.5 mm, FOV 201×230 mm, matrix 224×256). T2 relaxometry or proton MR spectroscopy was undertaken in many patients; however, the results of these investigations were not evaluated in the present study.

Outcome assessment

Outcome was assessed at regular postoperative visits. We only evaluated the seizure outcome, and psychiatric, social, and neuropsychological outcomes were ignored. For this study we divided the patients into the two categories, seizure-free and non-seizure-free. Patients who had non-disabling auras exclusively were considered to be seizure-free. Seizure freedom was defined if the patient was seizure-free more than three months before the last postoperative visit. If seizures reappeared in an initially seizure-free patient, the outcome was defined as non-seizure-free.

Statistical methods

For the single predictive variable analyses using categorical variables, χ2, Fisher’s exact, and binomial tests were used. The Mann–Whitney U test was employed for comparisons of continuous variables. The non-parametric tests were used because variables were not distributed normally. To identify which variables could predict the outcome independently, we carried out a logistic regression for variables showing a significant effect in single predictive variable analyses. Two tailed error probabilities smaller than p<0.05 were considered significant.

RESULTS

Three patients were excluded because they had no video-EEG monitoring before VNS implantation and 47 patients met the inclusion criteria (25 women and 22 men). Their mean (SD) age was 22.7 (11.6) years (range 7 to 53). Mean age at disease onset was 4.9 (4.6) years (range 0 to 18). Fourteen patients had previously had unsuccessful epilepsy surgery. Table 2 presents the seizure characteristics of the patient population. Complex partial seizures were the most common seizure type. Secondary generalisation of seizures was present in 43%. Table 3 shows the EEG data. In 72% of patients, bilateral independent or bilateral synchronous IED were present. Table 4 shows the MRI data. In 26% of the patients no structural abnormalities were detected. The most common abnormalities were malformations of cortical development (MCD), occurring in 34% of patients, while hippocampal sclerosis was present in 11%; perinatal stroke, tuberous sclerosis, and hypothalamic hamartoma occurred in 6% of the patients. Most patients had extratemporal focal epilepsy (see table 5).

Table 4

 MRI data

Table 5

 Epilepsy syndrome

Six of 47 patients (13%) became seizure-free after the VNS implantation. None of the three patients who were previously excluded owing to lack of video-EEG monitoring became seizure-free. The mean (SD) follow up time was 22 (7) months (range 12 months to 3 years). In the seizure-free patients, the mean follow up time was 27 (5) months; in the non-seizure-free it was 21 (7) months. This difference showed a non-significant trend (p = 0.08). In the seizure-free patients the mean current output was 1.5 (0.6) mA (range 0.5 to 2); in non-seizure-free patients it was 1.9 (0.6) mA (range 0.75 to 3.5), p = 0.3. At the time of the evaluation, all the six seizure-free patients had been seizure-free for more than six months (mean 11 months, range 6 to 20). There were no patients who initially became seizure-free (that is, more than three months of seizure freedom) and later experienced a seizure recurrence. The time for achieving seizure freedom ranged from 0 to 21 months (mean 16 months).

In 23 patients, we changed the standard cycle parameters to rapid cycle parameters and three became seizure-free; three of the 24 patients who did not receive rapid cycle stimuli also became seizure-free (p = 1.0).

Single predictive variable analyses

Only two variables showed a significant association with the seizure-free outcome (see tables 1–5): absence of bilateral IED and presence of MCD. Concerning the absence of bilateral IED, the sensitivity for a seizure-free outcome was 0.83 (95% confidence interval (CI), 0.44 to 0.97); while the specificity was 0.8 (0.66 to 0.9). In the case of MCD, the sensitivity for a seizure-free outcome was 0.83 (0.44 to 0.97), while the specificity was 0.73 (0.58 to 0.84). The duration of illness showed a non-significant trend towards a negative association with outcome. It is important to note that owing to the relatively small number of patients the sensitivity and specificity data provide only limited information, and further data will be needed to get really reliable estimates.

The possible effect of new antiepileptic drug

During the follow up, new antiepileptic drugs were added in 11 patients (23%)—in two of six patients who became seizure-free and in nine of the remaining patients (p = 0.6). In both seizure-free patients, the new add-on antiepileptic drug was levetiracetam. In the first case, the 35 year old male patient was initially seizure-free on 0.75 mA current output during VNS. Two months later the seizures returned and increasing the current output resulted in no further benefit. Levetiracetam was added and the patient then became seizure-free. In the second case, the nine year old girl suffering from intractable temporal lobe epilepsy had a >50% seizure reduction during VNS treatment with the standard cycle mode. After introduction of a rapid cycle mode, a slight further improvement was seen. One year later, however, there was no more change in the seizure situation; thus levetiracetam was added as a new antiepileptic drug and this resulted in seizure freedom. Conversely, there were four other patients who did not become seizure-free and who received levetiracetam as a new antiepileptic drug. The possible positive effect of the newly introduced levetiracetam on the seizure-free outcome was not significant (p = 0.16).

Concerning those 35 patients in whom MRI abnormalities were visualised, seven had bilateral abnormalities and none became seizure-free, while five of the remaining 28 patients with unilateral pathology became seizure-free (table 4). This difference, however, was not statistically significant (p = 0.6). Of those 28 patients with unilateral pathology on MRI, four of 14 patients with left sided and one of 14 with right sided abnormalities achieved seizure freedom (p = 0.3).

Independence of variables and logistic regression analysis

Stepwise logistic regression was undertaken to investigate the two factors that were found to be significant in single predictive variable analyses. Only the absence of bilateral IED correlated independently with successful VNS treatment (p<0.01, odds ratio 29.2 (95% CI, 2.4 to 353); the presence of MCD did not.

DISCUSSION

In our study, the absence of bilateral spike focus and malformation of cortical development on MRI were associated with successful VNS treatment according to the single predictive variable analysis. However, logistic regression analysis showed that only the absence of bilateral interictal epileptiform discharges was independently associated with the outcome of VNS; the presence of cortical malformations was not. Age at epilepsy onset, duration of epilepsy, seizure type, seizure frequency, epilepsy syndrome, or other MRI abnormalities showed no significant association with the outcome of VNS treatment. However, our patient population was relatively small, so some infrequent clinical phenomena might have had no chance of reaching statistical significance. Interestingly, our results are in agreement with epilepsy surgery studies showing that EEG is a reliable tool for assessing outcome prognosis.24–27

Some studies have shown that patients with bitemporal epilepsy (such as bitemporal independent seizure onset in one patient) may benefit from VNS treatment; however, no seizure-free patients were reported.28,29 In our study, none of the patients who had bilateral independent seizures became seizure-free. However, this result was not statistically significant (table 3). Conversely, we found that the absence of bilateral (independent and bilateral synchronous) IED showed an association with a favourable outcome of VNS treatment. Interestingly, absence of bilateral IED is also a good prognostic factor for resective epilepsy surgery according to previous studies. Bilateral independent IED are associated with worse surgical outcome after temporal lobectomy compared with unitemporal spike foci.24,25 The reason for this could be that they represent an extended epileptogenic region or a greater epileptogenicity, as they are more often associated not only with a worse surgical outcome but also with bilateral seizure onset zone, bilateral seizure propagation, and greater seizure frequency.30,31 Some studies have found that patients with generalised epilepsies (which are typically associated with generalised IED) may obtain some benefit from VNS treatment, although seizure freedom was infrequently reported.8,9,11,12,32,33 On the other hand, Labar found that Lennox-Gastaut syndrome might be associated with unresponsiveness to VNS treatment.10

Although only four of our patients had symptomatic generalised epilepsy, generalised IED occurred in 14 other patients with focal epilepsy. Generalised (bilateral synchronous) IED in focal epilepsy is termed secondary bilateral synchrony.34 Some studies found them related to worse surgical outcome in frontal26 and temporal35,36 epilepsy. The pathomechanism of bilateral synchronous IED in focal epilepsy is not clear, but it is likely that discharges from the primary focus spread through the thalamus or through the corpus callosum to the corresponding contralateral area, producing a nearly synchronised discharge.37,38 An alternative explanation is that bilateral synchronous IED arise from an interaction of multiple active foci.39 Our findings of a correlation between lack of bilateral (independent and dependent) IED and favourable VNS outcome support the assumption that bilateral IED represent a higher degree of epileptogenicity.

Two large multicentre studies showed that patients with a long duration of epilepsy had less chance of being seizure-free on VNS treatment.7,15 On the other hand, another study found that VNS responsiveness was associated with a longer duration of epilepsy.10 Although the epilepsy duration in our study showed no significant influence on the outcome, we found a non-significant trend towards a negative association between longer illness duration and VNS outcome.

One may speculate that the intrinsic epileptogenicity of MCD—which is accompanied by altered functional properties40,41 different from other epileptogenic lesions—might be associated with altered pharmacology or response to VNS. In the single predictive variable analyses, we found that the presence of MCD was associated with favourable VNS outcome; however, the logistic regression analysis did not confirm this result.

A relatively large number of our patients became seizure-free compared with other studies in this field. One explanation for this may be that the outcome results of long term and open VNS studies have tended to be better than in controlled and short term investigations.3,4,5,6,7,8,9,10,11,12,13 Another possibility is that there was a large number of patients with lesional epilepsy in our study compared with other studies. This might explain the better outcome. Indeed, abnormal MRI predicts a better outcome in epilepsy surgery.24,26 Conversely, the epilepsies with most frequent aetiologies found in our study, such as MCD and hippocampal sclerosis, are poorly controlled by antiepileptic drugs compared with epilepsies with normal MRI findings.42

In two patients, seizure freedom was achieved after introducing levetiracetam. In both patients the VNS initially resulted in a benefit (the first patient had >50% seizure reduction, the second a two month initial seizure freedom), but final seizure freedom was only achieved directly after the introduction of levetiracetam. The possible positive effect of the newly introduced drug levetiracetam on seizure-free outcome was not significant owing to the limited statistical power of this study, which precluded adequate analysis of the effect of new antiepileptic drugs. In another reported patient receiving VNS treatment, seizure freedom occurred after adding lamotrigin.5 Further studies are required to determine whether there are some specific VNS antiepileptic drug synergistic effects.

Our results may have been influenced by the fact that there were no restrictions on changes in concomitant antiepileptic drugs, and adjustments of concomitant drugs were at the discretion of the treating physician. This is one of the limitations of our study. Conversely, in long term outcome studies it is impossible to stabilise the antiepileptic drug regime. This is true for long term studies investigating surgical43,44 or VNS5,13,15 outcomes. Fixing the antiepileptic regimen would not only be a clinical but also a theoretical failure because it would have resulted in excluding patients who needed a change in their antiepileptic drug treatment. The effectiveness of VNS, however, improves over time.3 Thus some patients with long term improvement would have been excluded. The way to address this issue is to compare a group of patients receiving medical treatment only with a group of VNS patients, as was done in the study that proved the effectiveness of temporal lobectomy.45 The retrospective nature of our study, however, did not make it possible to include such a control group.

Our results are preliminary because they were based on a relatively small patient population. However, with respect to other single centre VNS studies, only one included more patients with long term outcome data.12 The relatively small number of patients resulted in limited statistical power. Thus some variables such as bilateral independent seizure pattern (table 3), tuberous sclerosis, perinatal stroke, or hypothalamic hamartoma (table 4) did not occur with a great enough frequency to reach statistical significance, although all of these occurred only in non-seizure-free patients. Our study may facilitate other prospective investigations enrolling larger numbers of patients.

Acknowledgments

This work was supported by a grant from the Deutsche Forschungsgemeinschaft (DFG-Eb 111/2-2)

REFERENCES

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Footnotes

  • Competing interests: none declared

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