- Review article
- Open Access
Therapeutic efficacy and safety of Botulinum Toxin A Therapy in Trigeminal Neuralgia: a systematic review and meta-analysis of randomized controlled trials
- Mostafa Ebraheem Morra†1,
- Ahmed Elgebaly†1,
- Ahmed Elmaraezy†1,
- Adham M. Khalil†2,
- Ahmed M. A. Altibi3,
- Tran Le-Huy Vu4,
- Mostafa Reda Mostafa5,
- Nguyen Tien Huy6, 7Email authorView ORCID ID profile and
- Kenji Hirayama8Email author
© The Author(s). 2016
- Received: 28 March 2016
- Accepted: 17 June 2016
- Published: 5 July 2016
Several different interventions have been examined to alleviate pain and reduce frequency of trigeminal neuralgia (TN) paroxysms. However, some patients continue to have persistent or recurrent painful attacks. Using a systematic review and meta-analysis approach, we aimed to synthesize evidence from published randomized controlled trials (RCTs) regarding safety and efficacy of botulinum toxin type A (BTX-A) as a possible emerging choice of treatment for TN.
We conducted an electronic search in 10 databases/electronic search engines to access relevant publications. All articles in all languages reporting RCTs on the efficacy and safety of BTX-A in the treatment of TN were included for systematic review and meta-analysis.
A total of four RCTs (n = 178) were identified for final meta-analysis. The overall effect favored BTX-A versus placebo in terms of proportion of responders (risk ratio RR = 2.87, 95 % confidence interval CI [1.76, 4.69], p <0.0001) with no significant detected heterogeneity (p = 0.31; I2 = 4 %). Paroxysms frequency per day was significantly lower for BTX-A group (mean difference MD = -29.79, 95 % CI [-38.50,–21.08], p <0.00001) with no significant heterogeneity (p = 0.21; I2 = 36 %).
Despite limited data, our results suggest that BTX-A may be an effective and safe treatment option for patients with TN. Further larger and well-designed RCTs are encouraged to translate these findings into better clinical outcome and better quality of life for TN patients.
- Trigeminal neuralgia
- Clinical trials
- Systematic review
Trigeminal neuralgia (TN) is a characteristic pain along the distribution of one or more branches of the trigeminal nerve. The pain is usually unilateral and described as severe, sharp, and stabbing electric shock-like pain. Consequently, quality of life of TN patients is profoundly worsened due to impairment of daily life activities, thus patients are at a high risk of depression and other psychiatric disorders [1–3]. Epidemiological studies showed that approximately 4 to 28.9/100,000 persons worldwide experience TN [4, 5]. Moreover, a recent large retrospective cohort study reported increased risk of depression and anxiety disorders in TN patients . To date, the mechanisms underlying the pathogenesis of TN are still controversial; however, the microvascular compression is the most common hypothesis [7, 8].
Recently, therapeutic and surgical approaches have been evolved to alleviate the neuropathic pain and improve quality of life in TN patients. Oral antiepileptic drugs, including carbamazepine, remain the first line of treatment . Yet, 25–50 % of cases became refractory to the drug therapy . Invasive operations such as neurovascular decompression , gamma knife radiosurgery , partial sensory rhizotomy, and percutaneous radiofrequency thermo-coagulation  may be required in some intractable cases. Then again, Surgical interventions occasionally effect severe and often untreatable complications that might be even worse than the primary TN . Moreover, a study reported recurrence of the pain in about half of the patients within 2 years of percutaneous radiofrequency rhizotomy . Recently, a cross specialty management program for TN patients was implemented in a tertiary referral center for headache and pain . The program involved collaboration between neurologists, neuroradiologists, and neurosurgeons and showed promising in terms of feasibility and utility in management of TN .
In light of the evidence currently available, it seems fair to argue that there is an overwhelming need for developing much safer, better tolerated, and efficacious treatment for TN. Botulinum toxin type A (BTX-A) is a neurotoxin derived from Clostridium botulinum . It acts via inhibiting release of acetylcholine at neuromuscular junctions, causing relaxation of the muscle [18, 19]. BTX-A has been shown to be a promising option for treatment of headache [20, 21]. It was further approved by the US Food and Drug Administration (FDA) for prevention of headache in adults suffering from chronic migraine.
In 2002, Micheli and colleagues  reported successful relief of twitching and pain in a patient with TN-associated hemifacial spasm. Since then, several clinical trials have been investigating the safety and efficacy of BTX-A in TN. The drug showed favorable effects in many reports. Having said that, the majority of studies were at a high risk of bias, aside from the small sample size included in each trial. This necessitates a confirmatory evidence to be released asserting the notion that BTX-A may be safe and effective option for management of TN.
The aim of this study is to provide a clear-cut evidence regarding safety and efficacy of botulinum toxin type A in trigeminal neuralgia from published randomized controlled trials in a systematic review and meta-analysis approach.
The study strictly followed the recommendation of Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement (Additional file 1: Table S1). During September and October, we established the protocol and registered our study with PROSPERO, University of York (CRD42015026861). Ten electronic search engines/libraries were systematically searched for relevant publications, including PubMed, Scopus, Web of Science, Google Scholar, Virtual Health Library (VHL), WHO Global Health Library (GHL), ClinicalTrials, POPLINE, System for Information on Grey Literature in Europe (SIGLE), and the New York Academy of Medicine (NYAM). Except for Google Scholar, the search term for all other libraries was as follows: (botulinum OR onabotulinumtoxinA OR onabotulinum OR botox OR botulinus) AND ((trigeminal neuralgia) OR prosopalgia OR (Fothergill's disease) OR (tic doloureux)). For Google Scholar, we used the advanced setting in which “trigeminal neuralgia” was filled in “with all of the words” and “botulinum botulinus botox onabotulinum toxin A onabotulinum” for “with at least one of the words”. Additionally, we conducted a manual search by reviewing the citations within the included publications and reviewing the related references presented in PubMed.
Selection criteria and title and abstract screening
Search results from the ten aforementioned search engines/libraries were imported into Endnote X7 (Thompson Reuter, CA, USA) for duplicates deletion. Two reviewers independently screened the references using the predetermined eligibility criteria. The inclusion criteria were: (i) randomized-controlled trials (RCTs) reporting efficacy and safety of botulinum toxin in treatment of trigeminal neuralgia and (ii) no restriction on language, area, publication year, and age of patients. The exclusion criteria were: (i) unreliably extracted data; (ii) over-lapped data sets; (iii) book chapters, abstract articles only, conference papers, reviews, theses, and posters; and (iv) in vitro or animal studies. Any different decision in screening step was discussed between two reviewers to reach a consensus. Consultation from supervisor (NTH and KH) was acquired if necessary. The full texts of included references were then retrieved through the Library of Nagasaki University, and full text screening was subsequently conducted to identify relevant references for data extraction.
All patients’ outcomes were considered to analyze the efficacy and safety of botulinum toxin in the treatment of trigeminal neuralgia: (1) proportion of respondents – defined as patients with >50 % reduction in mean pain score from baseline to endpoint; (2) mean paroxysms frequency per day; (3) mean visual analog scale (VAS) score at the end of follow up; and (4) adverse events and complications of BTX A treatment.
The standardized template was developed through a pilot extraction with the two most relevant references. Two researchers then independently extracted the data into the template. Extracted data included: authors, publication year, journal, country of authors, country of patients, source of BTX-A, active drug types and their doses, control types and their doses, number and site of injection, characteristics of patients (gender and age), duration of treatment, duration of follow up, year of neuralgia, affected branch, surgical procedures, efficacy point, proportion of responders, relapse, visual analog scale, number of paroxysms per day, quality of life, anxiety scale, and depression scale .
Statistical analysis was carried out using RevMan version 5.3 (The Cochrane Collaboration, Oxford, United Kingdom). Continuous data were pooled as mean difference (MD), while pooled risk ratio (RR) was combined for dichotomous data using Mantel-Haenszel (M-H) method. Fixed effect model was adopted in all analyses. We performed a sensitivity analysis to: (1) investigate the effect of the model assumed on the overall effect size, by running the analysis under the random effects model and observing if a difference exists (2) explore the effect of the study quality on the summary effect estimate, by omitting studies rated as "high risk of bias" for both random sequence generation and allocation concealment. Heterogeneity was assessed by visual inspection of the forest plots and measured by I-square and Chi-square tests. P-values reported in this paper are not adjusted for multiplicity; however, adequate randomization and blinding was achieved by most included studies, ensuring appropriate control for confounders. P-value < 0.05 was considered statistically significant.
The methodological quality of each RCT was independently assessed by two reviewers using "The Cochrane Collaboration's tool for assessing risk of bias". It is a two-part tool, addressing seven specific domains, including: sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective outcome reporting, and other sources of bias. The judgment of each reviewer on each domain was categorized as ‘low risk,’ ‘high risk,’ or ‘unclear risk’ of bias. Any disagreement was resolved by discussion between two reviewers and by consultation from a supervisor to reach a consensus.
Baseline characteristics of included RCTs
No. of patients
Mean age (year)
Mean duration before treatment (year)
Frequency of attacks per day before treatment (SD)
Pain severity before treatment, VAS Mean (SD)
Mean follow up (week)
Mean duration of effect (week)
Zhang et al. 
25 Group1: 25U
28 Group2: 75U
Shehata et al. 
Wu et al. 
Zúñiga et al. 
Injection protocol of BTX-A
Type of BTX-A
Source of BTX-A
Amount of BTX-A
No. of injection
Rout of injection
Zhang et al. 
Botulinum toxin type A (BTX-A)
Lanzhou Bioproduction Institute, Lanzhou, China
Group 1:25u Group 2:75u
Dermatome and/or mucosa
Intradermal and submucosal
Shehata et al. 
Botulinum toxin type A (Botox®)
Wu et al. 
BTX-A (100U of Clostridium botulinum type-A neurotoxin complex, 5 mg gelatin, 25 mg dextran, and 25 mg saccharose)
Lanzhou Biological Products Institute, China
Zúñiga et al. 
Onabotulinum toxin A (Botox)
Various sites, 1 cm apart from one another
Three patients’ therapeutic outcomes include: (1) proportion of respondents – defined as patients with >50 % reduction in mean pain score from baseline to endpoint; (2) mean paroxysms frequency per day; and (3) mean visual analog scale (VAS) score at the end of follow up.
Adverse events for all patients in included RCTs
Treatment of TN continues to present a clinical appeal to both patients and health care providers. Medications (such as antiepileptic drugs) were poorly tolerated. They effected central nervous system adverse events in a substantial proportion of patients . As such, refractory cases were approached by alternative surgical interventions, which yielded marked improvement in about 63–94 % of cases . Nonetheless, serious complications of invasive surgery (including aseptic meningitis and hearing loss) rendered further sufferings to TN patients .
Thus safer, well tolerated, and more effective alternative is imperative for TN. The evidence from this systematic review suggests that botulinum toxin type A (BTX-A) has a clinically significant benefit in treatment of trigeminal neuralgia when compared to placebo in terms of proportion of responders, the mean paroxysms frequency per day, and the VAS score at the end of follow up. These overall outcomes consistently favored BTX-A compared with placebo across studies.
The duration of effect for BTX-A seems to be of relatively long duration (at least 3 months). In Wu et al.  trial, BTX-A was effective within a median follow-up duration of 90 days. Also, Zuniga et al.  showed that BTX-A was effective during the 3 months follow-up period. However, a conclusion cannot be made on how long the effect of BTX-A lasts, and how often recurrent injections are needed. This raises the need for further studies with extended follow-up duration that implement chronic pain measurement scales. A point of variation is the dosage of BTX-A; the used dosage of BTX-A in the analyzed RCTs ranged from 25 to 100 U. Zhang et al.  found that lower dose (25 U) and higher dose (75 U) were similar in efficacy on short-term assessment. Moreover, a dramatic response to BTX-A was also reported in an open-label trial  at a much lower dose of BTX-A (6.45–9.11 U).
The treatment mechanism of BTX-A in TN remains unclear. Previous preclinical studies suggested that it acts locally or on the trigeminal ganglia [30, 31]. Conversely, Matak et al. reported a central antinociceptive effect of BTX-A in a rat model of TN [32, 33]. Wu et al. recently asserted this notion and proved that peripherally applied BTX-A exerts antinociceptive function via reducing central sensitization and inhibiting high expression of nociceptors .
It is noteworthy to mention that Yong Hu et al.  approached the same topic with our study, but they mostly included open-label trials, which potentially weakened their conclusion. Furthermore, by combining one randomized, double-blind, placebo control trial with five open-label trials, the previous study possibly introduced some heterogeneity into their review.
One limitation of the current systematic review was the small number of trials that investigated the safety and efficacy of BTX-A in trigeminal neuralgia. Therefore, we cannot explore the publication bias using Egger's test for funnel plot asymmetry, we rather searched clinical trial registries and grey literature and found only two protocols of ongoing studies. No completed unpublished studies were retrieved. Missing data (mean baseline age in Shehata et al. and length of follow up in Zhang et al.) could not be used to adjust for possible biases in the aforementioned studies. More double-blinded RCTs are required to elaborate more on (1) optimal dose of BTX-A, (2) optimal duration of treatment, and (3) optimal route of administration. In addition, further research is needed to explore more on the mechanism of action of BTX-A to relieve pain in trigeminal neuralgia.
In conclusion, our systematic review suggests that BTX-A is a promising alternative treatment option that might spare the need for surgical interventions for refractory cases of trigeminal neuralgia in the future. Evidence from larger and well-designed RCTs is still required to assert upon these findings.
➢ RCTs reporting the efficacy and safety of BTX-A in the treatment of TN were included for systematic review and meta-analysis.
➢ BTX-A is an effective and safe treatment option for patients with trigeminal neuralgia.
➢ No serious adverse events or systemic reaction of BTX-A have been reported.
This study was supported by the Japan Initiative for Global Research Network on Infectious Diseases (J-GRID). The funders had no role in the study design, data collection and analysis, decision to publish or preparation of the manuscript.
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