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Vagus nerve stimulation for pediatric patients with intractable epilepsy between 3 and 6 years of age: study protocol for a double-blind, randomized control trial

  • Taoyun Ji
  • Zhao Yang
  • Qingzhu Liu
  • Jianxiang Liao
  • Fei Yin
  • Yanhui Chen
  • Liping Zou
  • Baomin Li
  • Yuxing Gao
  • Xiaomei Shu
  • Shaoping Huang
  • Feng Gao
  • Jianmin Liang
  • Su Fang Lin
  • Jing Peng
  • Shiwei Song
  • Jing Wang
  • Chao Che
  • Wenxiu Sun
  • Maoqiang Tian
  • Lin Yang
  • Yi Hua
  • Yunpeng Hao
  • Lixin CaiEmail author
  • Luming LiEmail author
  • Yuwu JiangEmail author
Open Access
Study protocol
  • 68 Downloads

Abstract

Background

Recent clinical observations have reported the potential benefit of vagus nerve stimulation (VNS) as an adjunctive therapy for pediatric epilepsy. Preliminary evidence suggests that VNS treatment is effective for seizure reduction and mental development in young participants between 3 and 6 years of age who suffer from intractable epilepsy. However, robust clinical evidence for quantifying the difference of the efficacy and safety of VNS treatment in this specific patient population has yet to be reported.

Methods/design

A two-armed, multicenter, randomized, double-blind, prospective trial will be carried out to evaluate whether VNS is beneficial and safe for pediatric epilepsy. Pediatric participants aged between 3 to 6 years old with intractable epilepsy will be recruited and randomly assigned to experimental and control groups with a 1:1 allocation using a computer-generating randomization schedule. Before enrollment, informed consent will be signed by the parents of the participants and the study researchers. Participants in the experimental group will receive electrical stimulation over 24 weeks under standard stimulation parameters. Participants in the control group will not receive any stimulation during the 12 weeks of the double-blind period. The guardians of the participants are required to keep a detailed diary to record seizure activity. Outcome assessments including seizure frequency, Gesell Mental Developmental Scale scores, use of antiepileptic drugs and dosages, and adverse events will be collected at baseline, 6, 12, 18 and/or 24 weeks after electrical stimulation is initiated. The effects of treatment will be analyzed with time and treatment group comparisons.

Discussion

This trial will evaluate quantitative differences in efficacy and safety with/without VNS treatment for pediatric participants aged between 3 to 6 years with intractable epilepsy and will explore whether the current age range of VNS therapy can be expanded.

Trial registration

ClinicalTrials.gov, ID: NCT03062514, Registered on 23 February 2017.

Keywords

Pediatric intractable epilepsy Vagus nerve stimulation Efficacy Safety 

Abbreviations

AE

Adverse event

AED

Antiepileptic drugs

CFDA

Chinese Food and Drug Administration

CG

Control group

CRA

Clinical research associate

CRF

Case report form

ECG

Electrocardiograph

EEG

Electroencephalograph

EG

Experimental group

FDA

Food and Drug Administration

IPG

Implantable pulse generator

MRI

Magnetic resonance imaging

QOL

Quality of life

SAE

Serious adverse event

SOP

Standard operating procedure

VNS

Vagus nerve stimulation

Background

Epilepsy is a brain disorder with symptomatic manifestation of uncontrolled seizures affecting patients of all ages [1]. Over 65 million people worldwide are estimated to have epilepsy, including approximately 10.5 million patients of which are children [1, 2]. Around one third of patients are resistant to antiepileptic drugs (AEDs) resulting in morbidity and high mortality, with a similar proportion being found in both adults and children [3]. Pediatric patients with drug-resistant epilepsy demonstrate age-related seizure expression but the reasons for such an occurrence are not fully understood [2]. Recurrent seizures in children have a high negative impact on physical growth, mental development, sleep and contribute to a heightened rate of behavior disturbances and psychiatric disorders (such as depression, anxiety, psychosis, suicide) later in life, bringing a heavy burden to families and care givers [2, 3, 4, 5, 6, 7, 8, 9].

In 1997, the US Food and Drug Administration (FDA) approved VNS as an adjuvant treatment for patients with refractory epilepsy aged ≥ 12 years, who were poor candidates or had failed to gain curative effects by various therapeutic approaches such as ketogenic diet, resection surgery, and palliative surgery [10, 11, 12, 13]. The commonly used VNS system (Cyberonics, Inc., Houston, TX, USA) was recently approved by the FDA (2017) for use in patients over 4 years of age who exhibit partial-onset seizures, who are refractory to antiepileptic medications based on retrospective analysis [14]. Indeed, many clinical studies suggest that VNS therapy is as effective in children as it is in adult patients [15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27]. A retrospective study using a large sample size in children (N = 347) has shown that VNS reduces the frequency of seizures and is well tolerated for over 2-years’ follow-up [26]. More specifically, 40–50% pediatric patients had reached > 50% reduction compared to baseline seizure frequency of the predominant seizure type. Several studies have found similar levels of efficacy for VNS treatment in pediatric patients with refractory epilepsy during 1–10 years of treatment [10, 15, 20, 21, 22, 24, 27, 28, 29, 30, 31, 32, 33]. Interestingly, age may be an important factor affecting the efficacy of VNS in children, as previous data have shown that younger participants demonstrate greater improvements following VNS intervention [26, 34]. In China, the domestic vagus nerve stimulator (G112, PINS Medical, Ltd., Beijing, China) has so far been implanted in 283 epileptic patients, with 32 participants being within the age range of 1–6 years. For these 32 pediatric participants, 8 participants showed adverse effects (25%, 8/32) including onset of coughing and notable voice change. However, all adverse reactions disappeared following changes to stimulation parameters. Furthermore, seizure frequency of 20 pediatric participants was reduced by > 50% (data not published).

Intractable epilepsy is associated with negative impact on development in children such as in cognition [6, 35], social behavior and maturation, academic achievements, language processing, and psychology, which causes a worsening of quality of life (QOL) [35, 36, 37, 38, 39]. Early and more effective seizure control is suggested to improve cognitive outcomes and QOL in children, which has been reported in several retrospective studies investigating the effects of epileptic surgery [40, 41]. It is well recognized that some AEDs often exert a negative impact on cognition and psychological development [4, 5], while VNS has not been associated with such adverse effects on cognitive developments. Indeed, most studies have observed stable cognitive function during VNS treatment, with some studies reporting mild positive effects on verbal performance, memory and/or mental state in children independent of seizure control [10, 11, 25, 35, 40].

According to the definition of drug-resistant epilepsy [42], Chinese clinical physicians always observe more than 2 years to before a diagnose of intractable epilepsy. Thus, the minimum age, 3 years old, in this trial could possibly be enough time to be examined and satisfy the inclusion criteria. In the largest sample size study of VNS in children, 46 participants (of 347,13.3%) aged < 6 years were enrolled but no specific outcomes were reported for this specific age range [26]. Lowering the age range for VNS treatment requires further clinical evidence. In this paper, we plan to conduct a multicenter, double-blind, prospective, randomized control study (VNS-PIE trial) in children with intractable epilepsy. The aim of this study is to quantitatively evaluate efficacy and safety of VNS treatment. The VNS-PIE trial is the first pilot study with children between 3 and 6 years of age with intractable epilepsy. Employing a randomized control trial (RCT) design, we assigned the first 12 weeks for double-blind comparisons from 2 weeks post VNS implantation. The latter 12 weeks were used to study the effects of treatment.

Methods/design

Type of trial

The VNS-PIE study is designed as a two-armed, randomized, double-blinded, multicenter prospective study. According to the trial flow chart (Fig. 1), pediatric participants with intractable epilepsy will be screened strictly based on the inclusion and exclusion criteria. A total of seven follow-up surveys are scheduled as shown in Fig. 2. For follow-ups V3–V7, participants will receive VNS treatment according to the group. The clinical measurements of the two groups will be examined based on Fig. 2. Prior to implantation, all participants will undergo baseline seizure evaluation, Gesell Mental Development Scale assessment and other clinical measures, including physical examination; blood, urine, stool routine analyses, blood biochemistry and coagulation, as well as electrocardiograph (ECG) examinations. At 2 weeks following operation, a total of 84 participants will be randomized (1:1) to one of two arms; the experimental group (EG) or the control group (CG) (n = 42 participants per arm). The participants in the EG will receive VNS therapy at 2 weeks post implantation until the end of the trial. The implantable pulse generator (IPG) of participants in the CG will not be switched on from the 2nd to the 14th weeks post operation. The outcomes will be calculated by blinded statisticians appointed by the Clinical Research Institute of Peking University following the end of the trial.
Fig. 1

Flow chart of the VNS-PIE trial

Fig. 2

Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) Figure for the VNS-PIE trial

The VNS-PIE trial protocol was written in accordance with the Standard Protocol Items: Recommendations for Interventional Trials Statement (SPIRIT). A SPIRIT Checklist is included in Additional file 1. The trial will be carried out according to the principles of the Declaration of Helsinki (Edinburgh Version, 2000).

Study setting

A total of 11 centers will participate in the VNS-PIE study. These include Peking University First Hospital (principal unit), Chinese PLA General Hospital, Shenzhen Children’s Hospital, Qilu Hospital of Shandong University, Shandong Province Hospital, the First Hospital of Jilin University, the Second Affiliated Hospital of Xi’an Jiaotong University, Xiangya Hospital Central South University, the Children’s Hospital Zhejiang University School of Medical, Fujian Medical University Union Hospital, and the Affiliated Hospital of Zunyi Medical College. The RCT design of this trial will allow for observations of safety and efficacy in the EG and CG, from the blinded and unblinded periods. The participants in the CG will not receive VNS treatment until 12 weeks after the EG begins receiving VNS treatment. One study reported that average seizure frequency reduction in very young group (< 8 years old) was nearly 50% after 3 and 6 months of VNS. However, The percentage of responders (seizure frequency reduction of 50% or more) increased with implantation time [2]. Thus, on the one hand, 24-week follow-up was considered adequate to observe the possible efficacy and safety difference between the EG and the CG and balance the blinding and unblinding stages. On the other hand, longer follow-up time for this RCT would be harder to be conducted considering participants’ compliance. Since protocol version 1.0 was first submitted to the Research Ethics Committee in September 2016, the Ethical Committee reviews have provided several rounds of review comments concerning to background, inclusion standard, comparator, clinical assessments, exit criteria, follow-up frequency, remedial measures, and other details. And the protocol was updated to version 3.0 in November 2016. In July 2017, all researchers and the sponsor held a meeting to discuss further amendments to the protocol with the mental development scale mainly changed. Protocol version 3.0 was finally updated to 3.1. The final version has been approved by the Clinical Trial Ethics Committee of Peking University First Hospital (Protocol number: G112 L31101; date: 31 July 2017) and registered at ClinicalTrials.gov protocol system (Clinical Trials Identifier: NCT03062514).

Recruitment of participants

The target population for the VNS-PIE study is children aged between 3 to 6 years old who do not have any history of a vagus nerve lesion. Participants will be recruited by Internet advertisement and directly through the hospitals.

Inclusion criteria

Inclusion criteria are shown in Table 1.
Table 1

Inclusion criteria of the VNS-PIE trial

Inclusion criteria

 1. Age 3–6

 2. At least 6 seizures per month

 3. Refractory epilepsy

 4. In good health except for epilepsy

 5. Family members of participants can understand the method and sign the informed consent

 6. Participants with good compliance and can complete post-operative follow-up

Exclusion criteria

Exclusion criteria are shown in Table 2.
Table 2

Exclusion criteria of the VNS-PIE trial

Exclusion criteria

 1. Results of magnetic resonance imaging (MRI) show that epilepsy is caused by intracranial space-occupying lesions

 2. Tumor, cardiopulmonary anomaly, heart failure, progressive neurological diseases, asthma, mental disease, peptic ulcer, diabetes, poor health, and other contraindications to surgery

 3. Vagus nerve lesion or damage

 4. Cannot write the epilepsy diary

 5. Participating in another clinical trial

 6. Cannot complete the operation

 7. Cannot complete the post-operative follow-up

 8. Cannot complete the programming

Sample size

We adopted a pilot study design to evaluate efficacy and to primarily quantify the frequency of seizure reduction between the EG and the CG at 12 weeks’ follow-up after VNS treatment. It has been estimated that the variation of seizure frequency in the EG (VNS + AEDs) will be conservatively higher (25%) than the CG (AEDs only). The standard deviation of the two groups is set at 35%. Therefore, the sample size calculation formula is:
$$ n=\frac{2{\left({\mu}_{\alpha /2}+{\mu}_{1-\beta}\right)}^2{\sigma}^2}{{\left({x}_T-{x}_C\right)}^2}, $$
(1)
where xT is the expected curative effect of the EG, xC is the expected curative effect of the CG, σ is the standard deviation of the two groups (35%), μ is the quantile of the standard normal distribution, α is the first-class error level for statistical test (0.025, here for unilateral test; 0.05 for bilateral test if need), and β is the second-class error level for statistical test (0.2, here). The calculated sample size per group through this calculation is 38. Considering that the maximum possible loss rate is 10%, the final sample size is 42 pairs (N = 84) [43, 44, 45] .

Screening and enrollment

Research staff will check the medical history of participants (mainly the seizure and treatment history), perform a detailed physical examination and assess the participant’s auxiliary status (brain magnetic resonance imaging (MRI), electroencephalogram (EEG)) for eligibility. Once eligibility is confirmed, parents of participants are required to provide informed consent to researchers that specifies the possible risks and benefits of this trial. Researchers and parents should both sign their own names and date in handwritten form on the informed consent in duplicate copies. One copy will be given to the parents. In cases where the participant is not able to provide consent at the time of screening, the preoperative clinical measurements will not be arranged until the participants and their parents are able to give consent. Participants are numbered according to the registration sequence. Once participants are enrolled into the study, parents are required to record and keep daily diaries for occurrence of epileptic seizures.

Randomization

The study participants will be randomly assigned to either the EG or the CG at a ratio of 1:1 at 2 weeks post surgery, according to the “random number table” generated by the BlueBALLANCE clinical trial central randomization system of the third party (Blue Balloons, Ltd., Beijing, China). There are two kinds of balancing factors: intra-block balance and systematic stochastic balance. Firstly, based on SAS software, each block has four ordered participants’ random numbers, randomly generated (two EG and two CG) to satisfy intra-block balance. Secondly, each time a participant registration number is entered into the BlueBALLANCE clinical trial central randomization system, a block placeholder is generated automatically on the stratification factor: medical center to which the participant belongs. Following the rules of the competitive block, if the current placeholder belongs to a block that has been occupied and has spare random number(s), the next spare random number in this occupied block is sequentially taken and assigned to the participant. Otherwise, a new block is occupied and the first random number inside this block is given to the participant. This operation ensures the random balance of the system. Each center designates a unique researcher to have a random system account and password. When a participant in one center needs their random number, the appointed researcher in this center enters the patient’s trial number into the system and obtains the unique random number of this participant from the computer operations, which then assigns the participant to the EG or the CG.

Blinding

The study will be carried out under double-blind conditions with both investigator and participants (and their parents) being blind to the treatment given. Several approaches will be adopted to ensure that the blinded conditions of the clinical trial remain for assessing test treatment. i.e., stimulation intervention [46]. Researchers involved in this study will also be divided into two groups: blind and unblind. Researchers assigned to modulate the stimulation parameters and operate the randomized system will be unblinded. Other researchers, especially the evaluators, will be blind to treatment conditions until the end of the open-label period. Researchers blind to conditions will be trained to obey the experimental rules and not enquire into the randomized results. Normally, at 14 weeks’ follow-up after implantation surgery, participants in both the EG and the CG should be unblinded and the designated researcher will inform the random results to the participants and other researchers. During the double-blind stage, if one of two following specific circumstances occurs, participants can be unblinded. The first type is that there is an unacceptable deterioration and/or security issues that jeopardize the participant, especially in the CG. The unblinding process must be conducted after informing the sponsor or the sponsor’s authorized representative, with the consent of the participant, researchers, and sponsor. Stimulation parameters may be adjusted to a more reasonable treatment intensity by the researcher. As for participants in the CG, receiving stimulation during the double-blind stage means completely unblinding. The second circumstance is that the participant decides to withdraw from the trial during blinding and, therefore, the unblinded process will be executed immediately by the researcher. The time of unblinding, reasons for executing this process and operations need to be documented in hospital medical records and CRFs (case report forms) by the recording researcher. Accidental unblinding of participants also need to continue with follow-up observations. In such cases, their efficacy outcome after unblinding will not be included into the analysis of this trial. However, their safety outcome will still be included.

Intervention phase

Following baseline and preoperative assessments, researchers will confirm the results collected within a normal clinical range and clinical significance. All participants will receive surgery for implantation of the VNS system (G112, PINS Medical, Ltd., Beijing, China). Participants will be observed for at least 2 days after surgery before being hospital discharged. For the first 12 weeks of VNS treatment, the recommended stimulation parameters for the EG will be as follows: frequency = 20–30 Hz; duration = 250–500 μs; stimulation cycle = 30 s; rest cycle = 5 min, electrical intensity = 0–1.5 mA and no magnetic stimulation. In the CG, no stimulation will be provided during the first 12 weeks. For the latter 12 weeks of treatment, personalized optimal stimulation parameters will be employed in the two groups. The pursuits of personal parameter adjustment are the alleviation of the seizures as much as possible, as well as nonoccurrence of adverse events (AEs) of the participants. The prescribed AEDs are not expected to be modified during this trial. Researchers may modulate the electrical intensity in gradual incremental steps of 0.1–0.5 mA for each parameter. If participants show symptoms of maladjustment at higher parameters, reduction will be recommended based on the researcher’s professional advice. For changes of any kind to the dose or type of AED, researchers are required to keep detailed records.

Outcome measures

Efficacy outcomes

Following 12 weeks of VNS treatment, seizure frequency will be compared between the EG and the CG. This will be calculated as the primary measurement according to participant diaries and CRFs. Seizure outcomes will be expressed with a modified Engel scale [47].

For secondary outcomes of efficacy, change in seizure frequency, the modified Engel scale description, number of antiepileptic drugs used and Gesell Mental Development Scale scores will also be calculated and compared to baseline across the various time points of 6, 12, 18, and 24 weeks.

Safety outcomes

The occurrence rate of AEs/SAEs (serious adverse events) at distinct stages during the perioperative, double-blind, and open-label period will be used to evaluate the safety of treatment. If an adverse reaction occurs, the researcher will decide to take the necessary measures based on the health status of the participant. If a SAE occurs, the clinician will immediately turn off the IPG and assess the participant’s vital signs before providing appropriate symptomatic treatment. These events will be reported to the trial manager within 24 h. In extreme cases, the VNS system may be removed and the participant will be given post-trial care.

Quality control and trial monitoring

Prior to the initiation of this clinical study, the primary investigator has formulated several documents including an investigator’s brochure, standard operating procedures (SOP), and a detailed research plan. All the staff involved in this clinical trial have participated in special training, including sessions on enrolling participants, completing the CRF and using the VNS system. To help avoid subjective differences in the grading between experimenters, researchers who are due to carry out the Gesell Mental Development Scale assessment have passed the consistency training course and been awarded graduation certificated by Peking University First Hospital.

In the VNS-PIE trial, clinical assessments, intervention parameters, and AE/SAE cases are documented on the CRFs. Each center has authorized researchers to finish data entry on the CRFs. If documented data are doubted, the major investigator gives clinical judgment and reasons for accepting or rejecting data. The researchers then make corresponding records or modifications on the CRFs. All the data in this trial will be kept in a special document cabinet by authorized researchers in each hospital. The files include the raw records, CRFs, and electronic documents. These data will be removed from hospitals only after the sponsor informs the clinical trial facility and researchers that it no longer needs the data. Before this, no data will be removed.

Data monitors, who are professional certificated clinical research associates (CRAs) from the sponsor (PINS Medical, Ltd., Beijing, China), will conduct monthly checks on contents of CRFs and the status of trial completion of each participation. Such reports will contain trial progress, discovered violation issues, historical records of issues resolved and revised, and the inspection results the center’s quality control organization. Each center’s quality control organization, independent from investigators and the sponsor, should inspect the trial’s quality and data management according to the trial plan and schedule (a minimum of three times). This includes, but is not limited to: when the first case is enrolled, when half of the enrollments have been completed and at the end of the trial.

Participants who do not complete the study or withdraw at any time in the trial will be noted. Reasons for withdrawal so will be fully documented. The trial sponsor will have full access to all datasets of the trial.

The final report will follow the Consolidated Standards of Reporting Trials (CONSORT) extension guidelines for non-pharmaceutical interventions. In order to minimize 6-month attrition, the first step will be to enroll participants whose guardians are aware of the beneficial effects of VNS therapy and who can understand the mechanisms of VNS. Secondly, in the consent form, the participant and their guardian will be informed that the participants can receive physician consultations throughout the whole study period. Moreover, participants will receive physical examination (Gesell Mental Development Scale), the VNS system and modulation of parameters free of charge if they complete the study. The physician will remain in contact for the participants’ medical needs throughout the study.

Guidelines for stopping treatment

The trial may be ended prematurely by the Ethical Committee, medical supervision department and the sponsor if there are concerns of safety, or if there is evidence of harm in the study. The treatment in the trial can be interdictory when the researchers identify a SAE or if side effects occur under the regular increase of electrical stimulation parameters.

Statistical analysis

To compare treatment efficacy and safety parameters between the EG and the CG, as well as within-group comparisons to baseline, data will be analyzed with t tests and χ2 tests for continuous variables and categorical variables, respectively. The Kolmogorov-Smirnov test or parametric tests will be used for analysis of data with normal distributions. Non-parametric data will be analyzed by a rank-sum test. The factors that impact curative effects will be analyzed with a multinomial logistic regression method. A p value < 0.05 will be considered as statistically significant. All analyses will be conducted using SAS 9.4 or higher version software.

Confidentiality

All data generated in this study will be treated as confidential information belonging to the sponsor. With the exception of Chinese Food and Drug Administration (CFDA) procedures and compliance to relevant laws, researchers will be information confidential to any third parties and use such information only to the extent agreed, unless written consent has been granted.

The investigators must ensure that the privacy of the participant is maintained during and after the whole trial. Among all submissions, the identity of the potential and actual participant can only be determined by the abbreviation of their name and registration number.

Discussion

The currently proposed, randomized controlled, double-blind clinical trial aims to quantify the efficacy and safety of VNS treatment in drug-resistant epileptic patients between 3 and 6 years of age. The results of this study may extend the age range of VNS therapy for clinical use.

Frequency and severity of seizures are the main parameters that are measured to illustrate the efficacy of VNS therapy in participants. Therefore, parents are required to document the observed frequency and average duration of daily seizures during this trial.

Early studies have demonstrated that children and adults have a similar extent of seizure reduction after VNS treatment following several months [15, 48, 49]. Orosz and colleagues have previously assessed change in seizure frequency following adjunctive VNS therapy in 347 children with drug-resistant epilepsy, with patients aged between 6 months to 17.9 years at the time of VNS implantation [26]. Data from this study showed that seizure frequency was reduced (32.5, 37.6 and 43.8%; at 6, 12, and 24 months, respectively) over a 2-year follow-up period. However, the findings of this study are limited in certain respects, such as lack of subgroup analysis based on age, which would be useful for separating patients on different stages of physiological development. While the number of participants aged < 6 years old in Orosz’s study was 46, the efficacy of VNS in patients was not released. It is important to note that age may be an important factor for the efficacy of VNS. This is indicated by a higher reduction of seizures in younger patients (< 12 years at implantation) than older patients (> 12 years at implantation), with the most beneficial patient group being children aged 0–6 years [19]. However, not all studies to date have shown differences in the efficacy of VNS between age groups [18, 22, 24, 28]. Interestingly, the age of seizure onset may be relevant to the clinical response. The earlier the age of seizure onset, the worse the VNS response may be because of the cumulative damage of epilepsy itself [27]. Therefore, implantation of VNS in children may be an effective means of controlling seizures at an early stage. Furthermore, VNS may reduce the severity of seizures in children with refractory epilepsy based on NHS3 scale measurements (baseline 9.5; endpoint:8.3; p < 0.001) [50, 51, 52]. Currently, in China, the CFDA approves VNS therapy in patients between the age of 6–60 years old. Few studies have been conducted in pediatric patients of an age range of 3–6 years old, which is an important period for growth and development in children [53]. Moreover, there are many types of epileptic syndromes in childhood according to classifications based on the age of seizure onset [53]. Interestingly, VNS treatment has shown a more curative response in certain epileptic syndromes (Dravet syndrome or Lennox-Gastaut syndrome) [26]. Considering this, we note that there is a need for a similar distribution of disease characteristics between the CG and the EG for this study.

Previous studies exploring VNS have reported stable outcomes or improvements in (subscales of) QOL [17, 33, 54, 55]. However, the QOL scale is not applicable to patients of 3–6 years of age. In comparison to commonly used drug treatments (such as phenobarbital, phenytoin, carbamazepine, and valproate) [56], VNS has no negative effects on cognitive and social ability. Participants with VNS treatment have demonstrated mood, attention, language, and memory improvements [25, 57].

Childhood development from birth to the age of 6 years old is essential for gross motor, fine motor, language, cognition, and social/emotional learning [58]. With the importance of measuring developments in a specific age range in children, the Gesell Mental Development Scale has been chosen for this trial [59, 60, 61, 62]. This is because it is designed to provide relevance to the mental development in children aged between 3 and 6 years old [60, 62].

The adverse reactions of VNS treatment are mainly (80%) caused by the transient response induced by electrical stimulation. These AEs include voice change, dysphagia, and coughing, all of which are commonly alleviated following several hours of stimulation [15, 20, 63, 64]. More rare complications caused by VNS therapy includes respiratory sinus arrhythmia, which can reduce oxygen transport to brain tissue, aggravate the brain tissue injury of epileptic patients [30, 65]. During VNS treatment, sleep apnea can occur infrequently, but is especially dangerous for patients with obstructive breathing [66]. Equipment-related complications, electrode fracture (3%) or IPG malfunction (4%, such as power depletion, accidental power-off, too large/low impedance and unprogrammed electrical stimulation) [32], may also arise in patients. For younger patients, adolescent body growth and development may cause electrode fracture, which is the main complication that has been reported in previous studies [32, 67]. Complications associated with the VNS implantation operation are infrequent, with the most common issue being wound infection after surgery. The superficial infection can be controlled by antibiotics, while severe infections may require removal of the vagus nerve stimulator [27, 67, 68]. Stimulation, equipment and surgery-related AEs will be recorded on CRFs in order to assess the safety of VNS treatment for pediatric epilepsy.

It is important to note that this study has several potential limitations. Firstly, all the outcome measures of efficacy are self-assessments taken from a seizure diary. While objective measures of seizures can be made from an epilepsy-recording bracelet, this will not be used in this study because of the age of the patients and specificity of equipment to seizures (i.e., generalized tonic-clonic seizures) [69]. Here we will utilize daily diaries to assess changes in seizure frequency and severity, which have been a common method in RCTs for epilepsy. Another potential limitation of this clinical trial is the time duration of 24 weeks for follow-up. We note that longer follow-ups for assessing chronic VNS treatment over 1–2 years are valuable [27, 70].

Trial status

Enrollment of participants into this study started in March 2017 and was completed in May 2018. Target enrollment for this study is 84 participants.

Notes

Acknowledgements

We would like to thank the entire team of researchers for their work, professional skills, enthusiasm and great efforts. This includes all the nurses and staff at the 11 hospitals.

Funding

Funding for this study is provided by PINS Medical Ltd.

Sponser: PINS Medical Ltd

Central contact person: Fumin Jia, PhD

Email address: pins_medical@163.com

Telephone number: +8601060736388

Availability of data and materials

Data from this study are unavailable before the end of this trial. Obtaining data and materials requires the consent of the sponsor.

Authors’ contributions

All authors have made substantial contributions to the design and concept of this study. TyJ and ZY drafted the paper under supervision of YwJ, QzL, LxC, and LmL. All authors critically revised the manuscript. TyJ, JxL, FY, YhC, LpZ, BmL, YxG, XmS, SpH, FG, JmL, QC, and HW were involved in collection and analyses of the data. YwJ and LxC will supervise the therapist involved in the study. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The VNS-PIE study received ethical approval from the Clinical Trial Ethics Committee of Peking University First Hospital, covering all participating sites. Important changes to the protocol will be submitted to the Ethics Committee for review. Informed consent will be obtained from all participants in the trial.

Consent for publication

Consent forms for the trial include consent for publication of results in peer-reviewed journals.

Competing interests

Salary and grant supports in this trial are supported by the sponsor. No additional reporting is allowed until the final report of the trial is completed, with the exception of consent by the sponsor. Information on the sponsor’s and investigator’s publishing policies will be described in their clinical trial contract.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary material

13063_2018_3087_MOESM1_ESM.doc (124 kb)
Additional file 1: Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) 2013 Checklist: recommended items to address in this clinical trial protocol and related documents. It is strongly recommended that this checklist is read in conjunction with the SPIRIT 2013 Explanation and Elaboration for important clarification on the items. Amendments to the protocol should be tracked and dated. The SPIRIT Checklist is copyrighted by the SPIRIT Group under the Creative Commons “Attribution-NonCommercialNoDerivs 3.0 Unported ” license. (DOC 124 kb)

References

  1. 1.
    Moshé SL, et al. Epilepsy: new advances. Lancet. 2015;385(9971):884–98.PubMedGoogle Scholar
  2. 2.
    Guerrini R. Epilepsy in children. Lancet. 2006;367(9509):499–524.PubMedGoogle Scholar
  3. 3.
    Fisher RS, et al. Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE). Epilepsia. 2005;46(4):470–2.PubMedGoogle Scholar
  4. 4.
    Helmstaedter C, et al. Chronic epilepsy and cognition: a longitudinal study in temporal lobe epilepsy. Ann Neurol. 2003;54(4):425–32.PubMedGoogle Scholar
  5. 5.
    Hirsch E, Schmitz B, Carreno M. Epilepsy, antiepileptic drugs (AEDs) and cognition. Acta Neurol Scand. 2003;108(s180):23–32.Google Scholar
  6. 6.
    Jones JE, et al. Cognition, academic achievement, language, and psychopathology in pediatric chronic epilepsy: short-term outcomes. Epilepsy Behav. 2010;18(3):211–7.PubMedPubMedCentralGoogle Scholar
  7. 7.
    Hansen BH, et al. Sleep problems in children and adolescents with epilepsy: associations with psychiatric comorbidity. Epilepsy Behav. 2016;62:14–9.PubMedGoogle Scholar
  8. 8.
    Austin Joan K, Caplan R. Behavioral and psychiatric comorbidities in pediatric epilepsy: toward an integrative model. Epilepsia. 2007;48(9):1639–51.PubMedGoogle Scholar
  9. 9.
    Agrawal N, Govender S. Epilepsy and neuropsychiatric comorbidities. Adv Psychiatr Treat. 2018;17(1):44–53.Google Scholar
  10. 10.
    Bodin E, et al. Vagus nerve stimulation in the treatment of drug-resistant epilepsy in 29 children. Eur J Paediatric Neurol. 2016;20(3):346–51.Google Scholar
  11. 11.
    Gurbani S, et al. Neuromodulation therapy with vagus nerve stimulation for intractable epilepsy: a 2-year efficacy analysis study in patients under 12 years of age. Epilepsy Res Treatment. 2016;2016:9709056.Google Scholar
  12. 12.
    García-Pallero MA, et al. Effectiveness of vagal nerve stimulation in medication-resistant epilepsy. Comparison between patients with and without medication changes. Acta Neurochir. 2017;159(1):131–6.PubMedGoogle Scholar
  13. 13.
    Schachter SC. Vagus nerve stimulation therapy summary five years after FDA approval. Neurology. 2002;59(6 suppl 4):S15–29.PubMedGoogle Scholar
  14. 14.
  15. 15.
    Murphy JV. Left vagal nerve stimulation in children with medically refractory epilepsy. J Pediatr. 1999;134(5):563–6.PubMedGoogle Scholar
  16. 16.
    Patwardhan RV, et al. Efficacy of vagal nerve stimulation in children with medically refractory epilepsy. Neurosurgery. 2000;47(6):1353–7 discussion 1357-8.PubMedGoogle Scholar
  17. 17.
    Helmers SL, et al. Vagus nerve stimulation therapy in pediatric patients with refractory epilepsy: retrospective study. J Child Neurol. 2001;16(11):843–8.PubMedGoogle Scholar
  18. 18.
    Wheless JW, Maggio V. Vagus nerve stimulation therapy in patients younger than 18 years. Neurology. 2002;59(6 Suppl 4):S21–5.PubMedGoogle Scholar
  19. 19.
    Alexopoulos AV, et al. Long-term results with vagus nerve stimulation in children with pharmacoresistant epilepsy. Seizure. 2006;15(7):491–503.PubMedGoogle Scholar
  20. 20.
    Rossignol E, et al. Vagus nerve stimulation in pediatric epileptic syndromes. Seizure. 2009;18(1):34–7.PubMedGoogle Scholar
  21. 21.
    Shahwan A, et al. Vagus nerve stimulation for refractory epilepsy in children: more to VNS than seizure frequency reduction. Epilepsia. 2009;50(5):1220–8.PubMedGoogle Scholar
  22. 22.
    Elliott RE, et al. Vagus nerve stimulation for children with treatment-resistant epilepsy: a consecutive series of 141 cases. J Neurosurg Pediatr. 2011;7(5):491–500.PubMedGoogle Scholar
  23. 23.
    Chen C-Y, et al. Short-term results of vagus nerve stimulation in pediatric patients with refractory epilepsy. Pediatr Neonatol. 2012;53(3):184–7.PubMedGoogle Scholar
  24. 24.
    Thompson EM, et al. Vagus nerve stimulation for partial and generalized epilepsy from infancy to adolescence. J Neurosurg Pediatr. 2012;10(3):200–5.PubMedGoogle Scholar
  25. 25.
    Klinkenberg S, et al. Behavioural and cognitive effects during vagus nerve stimulation in children with intractable epilepsy—a randomized controlled trial. Eur J Paediatr Neurol. 2013;17(1):82–90.PubMedGoogle Scholar
  26. 26.
    Orosz I, et al. Vagus nerve stimulation for drug-resistant epilepsy: a European long-term study up to 24 months in 347 children. Epilepsia. 2014;55(10):1576–84.PubMedGoogle Scholar
  27. 27.
    Serdaroglu A, et al. Long term effect of vagus nerve stimulation in pediatric intractable epilepsy: an extended follow-up. Child’s Nervous Syst. 2016;32(4):641–6.Google Scholar
  28. 28.
    Murphy JV, et al. Vagal nerve stimulation in refractory epilepsy: the first 100 patients receiving vagal nerve stimulation at a pediatric epilepsy center. Arch Pediatrics Adolesc Med. 2003;157(6):560–4.Google Scholar
  29. 29.
    Benifla M, et al. Vagal nerve stimulation for refractory epilepsy in children: indications and experience at The Hospital for Sick Children. Child’s Nervous Syst. 2006;22(8):1018–26.Google Scholar
  30. 30.
    Zaaimi B, et al. Vagus nerve stimulation induces changes in respiratory sinus arrhythmia of epileptic children during sleep. Epilepsia. 2009;50(11):2473–80.PubMedGoogle Scholar
  31. 31.
    Connor DE Jr, et al. Vagal nerve stimulation for the treatment of medically refractory epilepsy: a review of the current literature. Neurosurg Focus. 2012;32(3):E12.PubMedGoogle Scholar
  32. 32.
    Klinkenberg S. VNS in children: more than just seizure reduction. Netherlands: Maastricht University; 2015.Google Scholar
  33. 33.
    Ulate-Campos A, et al. Vagus nerve stimulator implantation for epilepsy in a paediatric hospital: outcomes and effect on quality of life. Neurol (English Edition). 2015;30(8):465–71.Google Scholar
  34. 34.
    Colicchio G, et al. Vagal nerve stimulation for drug-resistant epilepsies in different age, aetiology and duration. Childs Nerv Syst. 2010;26(6):811–9.PubMedGoogle Scholar
  35. 35.
    Marques CM, et al. Cognitive decline in temporal lobe epilepsy due to unilateral hippocampal sclerosis. Epilepsy Behav. 2007;10(3):477–85.PubMedGoogle Scholar
  36. 36.
    Caplan R, et al. Childhood absence epilepsy: behavioral, cognitive, and linguistic comorbidities. Epilepsia. 2008;49(11):1838–46.PubMedGoogle Scholar
  37. 37.
    Høie B, et al. The combined burden of cognitive, executive function, and psychosocial problems in children with epilepsy: a population-based study. Dev Med Child Neurol. 2008;50(7):530–6.PubMedGoogle Scholar
  38. 38.
    Verrotti A, et al. Neuropsychological impairment in childhood absence epilepsy: review of the literature. J Neurol Sci. 2015;359(1):59–66.PubMedGoogle Scholar
  39. 39.
    Hermann BP, et al. Cognitive phenotypes in childhood idiopathic epilepsies. Epilepsy Behav. 2016;61:269–74.PubMedPubMedCentralGoogle Scholar
  40. 40.
    Sabaz M, et al. The impact of epilepsy surgery on quality of life in children. Neurology. 2006;66(4):557–61.PubMedGoogle Scholar
  41. 41.
    Spencer SS, et al. Initial outcomes in the multicenter study of epilepsy surgery. Neurology. 2003;61(12):1680–5.PubMedGoogle Scholar
  42. 42.
    Kwan P, et al. Definition of drug resistant epilepsy: consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies. Epilepsia. 2010;51(6):1069–77.PubMedGoogle Scholar
  43. 43.
    Elliott RE, et al. Efficacy of vagus nerve stimulation over time: review of 65 consecutive patients with treatment-resistant epilepsy treated with VNS > 10 years. Epilepsy & Behavior. 2011;20(3):478–83.Google Scholar
  44. 44.
    Amar AP, Apuzzo MLJ, Liu CY. Vagus nerve stimulation therapy after failed cranial surgery for intractable epilepsy: results from the Vagus Nerve Stimulation Therapy Patient Outcome Registry. Neurosurgery. 2004;55(5):1086–93.PubMedGoogle Scholar
  45. 45.
    Fisher R, et al. Electrical stimulation of the anterior nucleus of thalamus for treatment of refractory epilepsy. Epilepsia. 2010;51(5):899–908.PubMedGoogle Scholar
  46. 46.
    Boutron I, et al. Reporting methods of blinding in randomized trials assessing nonpharmacological treatments. PLoS Med. 2007;4(2):e61.PubMedPubMedCentralGoogle Scholar
  47. 47.
    Montavont A, et al. Efficacité de la stimulation intermittente du nerf vague dans les épilepsies pharmaco-résistantes non chirurgicales de l’adolescent et de l’adulte. Rev Neurol. 2007;163(12):1169–77.PubMedGoogle Scholar
  48. 48.
    Murphy JV, Hornig G, Schallert G. Left vagal nerve stimulation in children with refractory epilepsy. Preliminary observations. Arch Neurol. 1995;52(9):886–9.PubMedGoogle Scholar
  49. 49.
    Hornig GW, et al. Left vagus nerve stimulation in children with refractory epilepsy: an update. South Med J. 1997;90(5):484–8.PubMedGoogle Scholar
  50. 50.
    Lundgren J, et al. Vagus nerve stimulation in 16 children with refractory epilepsy. Epilepsia. 1998;39(8):809–13.PubMedGoogle Scholar
  51. 51.
    Majoie HJM, et al. Vagus nerve stimulation in patients with catastrophic childhood epilepsy, a 2-year follow-up study. Seizure. 2005;14(1):10–8.PubMedGoogle Scholar
  52. 52.
    Klinkenberg S, et al. Vagus nerve stimulation in children with intractable epilepsy: a randomized controlled trial. Dev Med Child Neurol. 2012;54(9):855–61.PubMedGoogle Scholar
  53. 53.
    Klenberg L, Korkman M, Lahti-Nuuttila P. Differential development of attention and executive functions in 3-to 12-year-old Finnish children. Dev Neuropsychol. 2001;20(1):407–28.PubMedGoogle Scholar
  54. 54.
    Handforth A, et al. Vagus nerve stimulation therapy for partial-onset seizures: a randomized active-control trial. Neurology. 1998;51(1):48–55.PubMedGoogle Scholar
  55. 55.
    You SJ, et al. Vagus nerve stimulation in intractable childhood epilepsy: a Korean multicenter experience. J Korean Med Sci. 2007;22(3):442–5.PubMedPubMedCentralGoogle Scholar
  56. 56.
    Lagae L. Cognitive side effects of anti-epileptic drugs. Seizure-Eur J Epilepsy. 2006;15(4):235–41.Google Scholar
  57. 57.
    Terra VC, et al. Vagus nerve stimulation in pediatric patients: is it really worthwhile? Epilepsy Behav. 2014;31:329–33.PubMedGoogle Scholar
  58. 58.
    Childhood Development. 2018. Available from: https://www.msdmanuals.com/professional/pediatrics/growth-and-development/childhood-development. Accessed 2 Jan 2019.
  59. 59.
    Li B-M, et al. Autism in Dravet syndrome: prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation. Epilepsy Behav. 2011;21(3):291–5.PubMedGoogle Scholar
  60. 60.
    Liu SY, et al. Surgical treatment for epilepsy in 17 children with tuberous sclerosis-related West syndrome. Epilepsy Res. 2012;101(1–2):36–45.PubMedGoogle Scholar
  61. 61.
    Zhu DN, et al. Therapeutic effect of ketogenic diet for refractory epilepsy in children: a prospective observational study. Chinese J Contemp Pediatrics. 2014;16(5):513–7.Google Scholar
  62. 62.
    Xiang S, Li X, Feng X. Effects of focal interictal epileptiform discharges on cognitive development in children with cerebral palsy. Chinese J Rehabil Med. 2015;30(1):22–5.Google Scholar
  63. 63.
    Nagarajan L, et al. VNS therapy in clinical practice in children with refractory epilepsy. Acta Neurol Scand. 2002;105(1):13–7.PubMedGoogle Scholar
  64. 64.
    Ardesch J, et al. Vagus nerve stimulation for epilepsy activates the vocal folds maximally at therapeutic levels. Epilepsy Res. 2010;89(2–3):227–31.PubMedGoogle Scholar
  65. 65.
    Malow B, et al. Effects of vagus nerve stimulation on respiration during sleep. A pilot study. Neurology. 2000;55(10):1450–4.PubMedGoogle Scholar
  66. 66.
    Hsieh T, et al. Sleep-related breathing disorder in children with vagal nerve stimulators. Pediatr Neurol. 2008;38(2):99–103.PubMedGoogle Scholar
  67. 67.
    Murphy JV, et al. Adverse events in children receiving intermittent left vagal nerve stimulation. Pediatr Neurol. 1998;19(1):42–4.PubMedGoogle Scholar
  68. 68.
    Spuck S, et al. Operative and technical complications of vagus nerve stimulator implantation. Operat Neurosurg. 2010;67(uppl_2):ons489–94.Google Scholar
  69. 69.
    Sarkis RA, et al. Autonomic changes following generalized tonic clonic seizures: an analysis of adult and pediatric patients with epilepsy. Epilepsy Res. 2015;115:113–8.PubMedGoogle Scholar
  70. 70.
    Morris GL, et al. Evidence-based guideline update: vagus nerve stimulation for the treatment of epilepsy Report of the Guideline Development Subcommittee of the American Academy of Neurology. Neurology. 2013;81(16):1453–9.PubMedPubMedCentralGoogle Scholar

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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors and Affiliations

  • Taoyun Ji
    • 1
    • 2
  • Zhao Yang
    • 3
  • Qingzhu Liu
    • 2
  • Jianxiang Liao
    • 4
  • Fei Yin
    • 5
    • 6
  • Yanhui Chen
    • 7
    • 8
  • Liping Zou
    • 9
  • Baomin Li
    • 10
  • Yuxing Gao
    • 11
  • Xiaomei Shu
    • 12
  • Shaoping Huang
    • 13
  • Feng Gao
    • 14
  • Jianmin Liang
    • 15
    • 16
  • Su Fang Lin
    • 4
  • Jing Peng
    • 5
    • 6
  • Shiwei Song
    • 8
    • 17
  • Jing Wang
    • 9
  • Chao Che
    • 10
  • Wenxiu Sun
    • 11
  • Maoqiang Tian
    • 12
  • Lin Yang
    • 13
  • Yi Hua
    • 14
  • Yunpeng Hao
    • 15
  • Lixin Cai
    • 2
    Email author
  • Luming Li
    • 3
    • 18
    • 19
    • 20
    Email author
  • Yuwu Jiang
    • 1
    • 2
    Email author return OK on get
  1. 1.Division of Pediatric Neurology, Pediatrics DepartmentPeking University First HospitalBeijingChina
  2. 2.Department of Pediatric Epilepsy CenterPeking University First HospitalBeijingChina
  3. 3.National Engineering Laboratory for Neuromodulation, School of Aerospace Engineering, Tsinghua UniversityBeijingChina
  4. 4.Department of NeurologyShenzhen Children’s HospitalShenzhenChina
  5. 5.Department of PediatricsXiangya Hospital of Central South UniversityChangshaChina
  6. 6.Hunan Intellectual and Developmental Disabilities Research Center of ChildrenChangshaChina
  7. 7.Division of Pediatric Neurology, Pediatrics DepartmentFujian Medical University Union HospitalFuzhouChina
  8. 8.Department of Epilepsy CenterFujian Medical University Union HospitalFuzhouChina
  9. 9.Department of PediatricChinese PLA General HospitalBeijingChina
  10. 10.Pediatics DepartmentQilu Hospital of Shandong UniversityJinanChina
  11. 11.Division of Pediatrics NeurologyProvincial Hospital Affiliated to Shandong UniversityJinanChina
  12. 12.Department of PediatricsAffiliated Hospital of Zunyi Medical CollegeZunyiChina
  13. 13.Department of PediatricsThe Second Affiliated Hospital of Xi’an Jiaotong UniversityXi’anChina
  14. 14.Department of NeurologyThe Children’s Hospital, ZheJiang University School of MedicineHangzhouChina
  15. 15.Department of Pediatric NeurologyFirst Bethune Hospital, Jilin UniversityChangchunChina
  16. 16.Research Center of NeuroscienceFirst Bethune Hospital, Jilin UniversityChangchunChina
  17. 17.Department of NeurosurgeryFujian Medical University Union HospitalFuzhouChina
  18. 18.Man-Machine-Environment Engineering Institute, School of Aerospace EngineeringTsinghua UniversityBeijingChina
  19. 19.Precision Medicine and Healthcare Research CenterTsinghua-Berkeley Shenzhen InstituteShenzhenChina
  20. 20.Center of Epilepsy, Beijing Institute for Brain DisordersBeijingChina

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