Open Access
CC BY 4.0 · Arch Plast Surg 2026; 53(01): 060-071
DOI: 10.1055/a-2707-0408
Pediatric/Craniomaxillofacial/Head & Neck
Review Article

Postoperative Outcomes of Masseteric Nerve Transposition versus Cross-Facial Nerve Graft in Facial Reanimation: A Systematic Review and Meta-Analysis

Authors

  • Indri Lakshmi Putri

    1   Department of Plastic Reconstructive and Aesthetic Surgery, Faculty of Medicine, Airlangga University, Surabaya, Indonesia
    2   Plastic Reconstructive and Aesthetic Surgery Unit, Airlangga University Hospital, Surabaya, Indonesia
  • Klarina Elsa Siti Sarah

    2   Plastic Reconstructive and Aesthetic Surgery Unit, Airlangga University Hospital, Surabaya, Indonesia
  • Imaniar Fitri Aisyah

    3   Department of Mechanical Engineering, Institut Teknologi Sepuluh Nopember, Surabaya, Indonesia
  • Rachmaniar Pramanasari

    2   Plastic Reconstructive and Aesthetic Surgery Unit, Airlangga University Hospital, Surabaya, Indonesia
  • Citrawati Dyah Kencono Wungu

    4   Department of Physiology and Medical Biochemistry, Faculty of Medicine, Airlangga University, Surabaya, Indonesia
    5   Institute of Tropical Disease, Airlangga University, Surabaya, Indonesia

Funding Information None.
 

Abstract

Facial reanimation surgery offers various approaches, with the choice of method influenced by numerous factors. Masseteric nerve transposition (MNT) has become a preferred neural source, often compared with cross-face nerve graft (CFNG) for its respective advantages. This systematic review and meta-analysis aim to compare postoperative outcomes between MNT and CFNG in facial reanimation surgery for patients with facial nerve paralysis sequelae.

A comprehensive electronic search was conducted using databases such as PubMed/Medline, Scopus, ScienceDirect, EBSCO, Web of Science, and Cochrane Library, along with gray literature sources like Scopus Preprints and MedRxiv. Statistical analyses were performed using Review Manager version 5.4.1, with the quality of included studies assessed using the Newcastle–Ottawa Scale.

Results showed that MNT provided statistically significant improvements in commissural excursion (CE; mean difference [MD] = 2.36 mm) and commissural contraction velocity (CCV; MD = 7.01 mm/s) compared with CFNG. Additionally, MNT had a higher recovery percentage for CE (MD = 26.86%) and CCV (MD = 13.00%). Superior outcomes were also noted for static and dynamic smile symmetry, quality of life, and patient satisfaction.

This meta-analysis underscores the advantages of MNT over CFNG in the majority of parameters in the analysis, at once highlighting the need for further research with larger sample sizes for more precise comparisons.


Introduction

Reanimation of the paralyzed face depends on several key factors, with denervation time being one of the most critical determinants.[1] [2] Prolonged denervation is associated with a higher likelihood of unsuccessful outcomes.[3] [4] For instance, in patients with short-term facial paralysis (ranging from 3 months to 2 years), the facial musculature remains viable, making nerve transposition a favorable option.[5] [6] In contrast, for long-standing paralysis where the facial muscles are no longer viable, a new muscle unit must be introduced to restore motion.[1] [7]

There is considerable variation in expert recommendations regarding the optimal nerve source for reanimation.[8] Common neurotization options include the cross-facial nerve graft (CFNG), as well as the masseteric, hypoglossal, accessory, and phrenic nerves.[6] [9] [10] [11] Historically, the CFNG has been considered one of the most effective choices for facial reanimation, primarily due to its ability to facilitate spontaneous contraction.[11] [12] [13] [14] However, the procedure can be limited by factors such as reduced oral commissure excursion, which results from a lower axonal count, a longer nerve regeneration distance, and a higher incidence of donor site morbidity.[15]

Masseteric nerve transposition (MNT) has recently become one of the most frequently used neural sources for enhancing facial function due to its high axonal density[8] [16] and favorable anatomical position.[11] [13] [17] [18] It has emerged as a standard option for patients who are not suitable candidates for CFNG.[19] [20] MNT offers several advantages, including improved muscle contraction strength and an expanded window for restoring facial nerve function, with minimal impairment at the donor site.[20] [21] The key benefits of MNT include reduced morbidity,[5] proximity to the facial nerve, a robust motor impulse, reliability, and rapid reinnervation, making it a viable option for most patients.[16] [18] [22] [23] This technique is applicable to both chronic and acute facial palsy (within 24 months).[7] [24]

Previous studies comparing MNT and CFNG have often been limited in scope, focusing on the specific muscle used for reanimation, employing a single assessment tool, or constrained by the nature of the cases studied. Therefore, it is essential to determine which reanimation technique provides the best outcomes across different contexts. This study aims to offer a comprehensive comparison of MNT and CFNG, with an emphasis on specific functional outcomes in both adult and pediatric populations. The comparison includes multiple etiologies, regardless of which muscle is involved, and covers cases of complete or incomplete paralysis, as well as unilateral or bilateral facial palsy.

Facial reanimation surgery aims to restore both static and dynamic facial symmetry, achieve oral competence, enable eye closure,[21] [25] promote voluntary facial movement, and facilitate effortless, spontaneous expression without synkinesis, all while minimizing functional loss at the donor site. Clinical experience and research suggest that asymmetry of the smile is often the primary concern for individuals with facial paralysis,[26] as facial symmetry plays a crucial role in perceived attractiveness.[27] [28] [29] The effectiveness of these interventions can be evaluated using a range of techniques, metrics, and methodologies.[24] [25] [30] [31] [32]


Methods

Search Strategy

A comprehensive database search was conducted by the first author in April 2024 across Scopus, PubMed, ScienceDirect, EBSCO, Web of Science, the Cochrane Central Register of Controlled Trials (CENTRAL), medRxiv, Scopus Preprints, and SSRN. Additionally, the reference lists of identified articles were manually reviewed. The detailed search strategy can be found in [Supplementary Table S1] (available in the online version only). The first author conducted an initial screening of titles, abstracts, and full texts to assess their relevance and eligibility for inclusion in this paper. This process was collaboratively reviewed by the other authors, ensuring a thorough and systematic approach to the research.


Study Selection

The retrieved studies were initially screened based on the relevance of their titles and abstracts. Articles were included if they reported outcomes using either MNT or CFNG techniques. Studies in non-English languages and those involving animal subjects were excluded. Additionally, case series, case reports, literature reviews, and previous meta-analyses were not considered for inclusion. There were no restrictions on the date of publication. The PICO (Participants, Intervention, Comparison, and Outcomes) criteria used for this review are detailed in [Table 1]. This systematic review adhered to the 2020 Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, and the study protocol was preregistered in the International Prospective Register of Systematic Reviews (PROSPERO) database (ID: CRD42024576631). A search of PROSPERO confirmed that no other protocols addressing this topic had been registered.

Table 1

PICO criteria for the systematic review

Participants

Patients with facial nerve paralysis, both complete/incomplete and bilateral/unilateral.

Intervention

Masseteric nerve transposition

Comparison

Cross-facial nerve graft

Outcomes

Commissural excursion

Commissural contraction velocity

Recovery percentage

Static lip symmetry

 • MNT versus CFNG: Static lip angle symmetry (in degrees)

 • MNT versus CFNG: Static lip length symmetry (in mm)

Dynamic lip symmetry

 • MNT versus CFNG: Dynamic lip angle symmetry (in degrees)

 • MNT versus CFNG: Dynamic lip length symmetry (in mm)

Total smile improvement

Quality of life

Satisfaction

Abbreviations: CFNG, cross-facial nerve graft; MNT, masseteric nerve transposition.



Data Collection and Quality Assessment

Full-text articles meeting the eligibility criteria were independently retrieved and evaluated based on predefined selection parameters. Data from the included studies were carefully extracted and organized in Excel spreadsheets to ensure accuracy and completeness. This process was conducted by two authors (I.L.P. and R.P.), and any discrepancies were resolved through discussion until consensus was reached. The following baseline information was extracted from each study: “author name,” “publication year,” “study design,” “type of centre,” and “surgical approach.” Cohort characteristics such as patient demographics (sample size, age, sex, cause of paralysis, and denervation time) were also recorded. Data on continuous variables, including postoperative outcomes such as commissural excursion (CE), commissural contraction velocity (CCV), static and dynamic lip symmetry, and overall smile improvement on the reanimated side, were collected and expressed as means and standard deviations. For postoperative complications, dichotomous data were extracted, and qualitative analysis would have been performed if the data were heterogeneous.

Each study's methodological quality was independently assessed by two authors (K.E.S.S. and C.D.K.W.) using the Newcastle–Ottawa Scale (NOS).[33] Any disagreements were resolved through discussion or, if necessary, by consulting a third author (I.F.A.). Studies were rated as very good quality (7–9 stars), good quality (5–6 stars), satisfactory quality (3–4 stars), or unsatisfactory quality (0–2 stars).


Statistical Analysis

Any relevant results from research that directly compare MNT and CFNG approaches will be subjected to a pairwise meta-analysis. Mean differences (MDs) will be utilized for continuous variables. Meta-analysis results will be presented in forest plots, with summary estimates, 95% confidence intervals (CIs), and relative study weights indicated by the midpoint, horizontal line, and square size, respectively. A diamond shape's midpoint and width, representing the mean and 95% CI, will serve as the overall summary statistic. When data are insufficient for meta-analysis, pooled summary cohort characteristics for each outcome of interest will be reported for both operative techniques. Statistical heterogeneity between studies will be evaluated using the I 2 statistic, with values above 50% suggesting substantial heterogeneity. In this analysis, the effects model is chosen depending on the similarity of the data, including factors such as tools, units of measurement, and the presence of heterogeneity. All statistical analyses will be performed employing Review Manager version 5.4.1 (Cochrane Collaboration, Software Update, Oxford, United Kingdom).



Results

Study Characteristics

A total of 1,684 articles were identified through the literature search, with 665 duplicates being removed. After an initial screening of titles and abstracts, 104 articles were deemed relevant and underwent a full-text evaluation based on the established inclusion and exclusion criteria. Following this assessment, seven articles met the criteria for inclusion in the quantitative analysis. Additionally, two more eligible articles were identified through screening the reference lists of the included studies. Ultimately, 11 studies were included in the final quantitative and qualitative synthesis ([Fig. 1]). All of the included studies were retrospective cohort studies (n = 11), with the majority conducted in the United States (n = 5). The remaining studies were from Spain (n = 2), Canada (n = 2), India (n = 1), and China (n = 1). All studies were conducted in single-center settings. The quality of the studies was rated as good (n = 2) to very good (n = 9; [Supplementary Table S2] [available in the online version only]).

Zoom
Fig. 1 PRISMA flow diagram data added to the PRISMA template (from Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ. 2021;372: n71) under the terms of the Creative Commons Attribution License. PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses. *Consider, if feasible to do so, reporting the number of records identified from each database or register searched (rather than the total number across all databases/registers).

Cohort Description

The studies included a total of 569 patients, of whom 173 underwent MNT procedures. The age range of patients was broad, from 4 to 80 years. Nine studies reported sex distribution, with 41.5% (267/643) of the patients being male. In most studies (n = 6), tumors were the primary cause of facial paralysis, followed by other etiologies such as Bell's palsy (n = 3), congenital paralysis (n = 1), and trauma (n = 1). Five studies reported cases of long-standing paralysis, with a denervation time exceeding 24 months. Complete paralysis was predominant in most studies (n = 8), while three studies reported cases of incomplete paralysis. The outcomes analyzed across the studies were as follows: CE (n = 9), CCV (n = 2), recovery percentage (n = 2), static lip symmetry (n = 2), dynamic lip symmetry (n = 2), and total smile improvement (n = 2; [Table 2]).

Table 2

Demographic data and sample characteristics

Number

Study, year, country

Title

Single/Multicenter

Study design

Surgical technique

Patient population

Denervation time

Follow-up (months)

Outcome

Evaluation tools

Intervention

Control

n [a]

Age (years)

Sex

Cause

1

Hontanilla et al (2018),

Spain[37]

Cross-face nerve grafting versus masseteric-to- facial nerve transposition for reanimation of incomplete facial paralysis: A comparative study using the FACIAL CLIMA evaluating system.

Single center

Cohort retrospective

MNT

CFNG

28

MNT (16–43) CFNG (19–58)

M:F MNT (5:13) CFNG (3:7)

The main cause was Bell's palsy

MNT (23–60) CFNG (26–56) months

MNT (25–44) CFNG (24–47) months

CD (in mm), CCV (in mm/s), satisfaction %, spontaneous %

FACIAL CLIMA software

2

Hontanilla et al (2013),

Spain[1]

Facial reanimation with gracilis muscle transfer neurotised to cross-facial nerve graft versus masseteric nerve: A comparative study using the FACIAL CLIMA evaluating system.

Single center

Cohort retrospective

FGMT to CFNG

FGMT to MNT

47

MNT (40.7 ± 13.8) CFNG (42.4 ± 10.1)

MNT (12:15) CFNG (7:13)

The main cause was acoustic neurinoma

MNT (108.4 ± 152.4) CFNG (121.7 ± 157.8) months

MNT (33.2 ± 12.2) CFNG (38.4 ± 15.7)

CD (in mm), CCV (in mm/s)

FACIAL CLIMA software

3

Alison K. Snyder-Warwick et al (2015),

Canada[54]

The degree of facial movement following microvascular muscle transfer in pediatric facial reanimation depends on donor motor nerve axonal density.

Multicenter

Cohort retrospective

FGMT to MNT

FGMT to CFNG

34

MNT (9.5) CFNG (10.2)

Commissural excursion (in mm), average myelinated axons

SMILE software

4

Kalra et al (2022),

India[38]

Facial reanimation using free functional muscle transfer: Lessons learnt from a long-term experience comparing innervation with cross facial nerve graft and masseter nerve.

Single center

Cohort retrospective

FFMT to CFNG

FFMT to MNT

205

4–62 years

93:112

The main cause was Bell's palsy

(1–48) years

Commissural excursion (in mm), satisfaction %, desc acute complication

5

Liang et al

(2024), China[48]

Comparison of outcomes of facial reanimation between the use of cross-facial nerve graft and the masseteric nerve as the donor nerve for reinnervation of gracilis muscle flap transfer.

Single center

Cohort retrospective

FGMT to MNT

FGMT to CFNG

21

MNT (48.9 ± 6.2) CFNG (19.6 ± 4.6)

MNT (6:4) CFNG (5:6)

The main cause was trauma

MNT (5.7 ± 2.8) CFNG (11.3 ± 6.1) months

MNT (24.1 ± 12.4) CFNG (37.1 ± 18.3)

Commissural excursion (mm), static and dynamic lip symmetry angle (degrees)

Standardized lateral photographs after surgery

6

Bhama et al

(2014), United States[50]

Objective outcomes analysis following microvascular gracilis transfer for facial reanimation a review of 10 years' experience.

Single center

Cohort retrospective

GFTT to CFNG

GGFT to MNT

78

35 ± 18 (6–80)

52:72

The main cause was tumors (intracranial neoplasm and vestibular schwannoma)

128 ± 183

Commissural excursion (mm), static and dynamic lip symmetry angle (degrees and mm)

FACE Gram

7

Lindsay et al

(2014), United States[34]

The success of free gracilis muscle transfer to restore smile in patients with nonflaccid facial paralysis.

Single center

Cohort retrospective

Gracilis to MNT

Gracilis to CFNG

20

37.75 ± 15.93

04.16

The main cause was vestibular schwannoma and Bell's palsy

Commissural excursion (mm), static and dynamic lip symmetry angle (degrees and mm), FaCE score determining quality of life (synkinesis)

FACE Gram/FGS, FaCE score

8

Bae et al (2006),

Canada[30]

A comparison of commissure excursion following gracilis muscle transplantation for facial paralysis using a cross-face nerve graft versus the motor nerve to the masseter nerve.

Single center

Cohort retrospective

FFMT to CFNG

FFMT to MNT

36

Mean age: MNT (8.7) CFNG (9.9) years

MNT (21:29) CFNG (29:41)

The main cause was congenital

Long-standing (congenital)

Operation time (hours), circumference of muscle (%), lengths of muscle used (cm), commissural excursion

Measurement using standardized photographs

9

Lindsay et al

(2014), United States[35]

Quality-of-life improvement after free gracilis muscle transfer for smile restoration in patients with facial paralysis.

Single center

Cohort retrospective

FGMT to MNT

FGMT to CFNG

72

40.1 ± 16.7 (20 patients; <14 years)

25;41

The main cause was brain tumors

FaCE score determining Quality of Life (synkinesis)

FaCE Score

10

Faris C. et al (2017),

United States[55]

Free-gracilis muscle transfer for smile reanimation after treatment for advanced parotid malignancy.

Single center

Cohort retrospective

MNT

CFNG

11

27–67

5;7

The main cause was tumors

12–204 months

Commissural excursion (in mm)

FACE, SaCE score

11

Hadlock et al (2011),

United States[36]

Free gracilis transfer for smile in children: The Massachusetts Eye and Ear Infirmary experience in excursion and quality-of-life changes.

Single center

Cohort retrospective

MNT (trigeminal)

CFNG

17

4–18 years

?

The main cause was brain tumors

FaCE score determining Quality of Life (synkinesis)

FaCE score

Abbreviations: CFNG, cross-facial nerve graft; FGMT, free gracilis muscle transfer; MNT, masseteric nerve transposition; GFTT, gracilis free tissue transfer; FFMT, free functional muscle transfer.


a n stands for total patients.



Meta-Analysis

Primary Outcomes

Commissural Excursion

The smile excursion results were summarized in [Table 2]. Nine studies (n = 478) compared CE in facial reanimation using MNT versus CFNG as the donor nerve. MNT was shown to have a considerably higher CE, indicating more similarity to the healthy score (if the disparities between the two sides were ignored, the most symmetrical smile would be taken into consideration). There was no heterogeneity between the studies with I 2 < 50%. The analysis showed significantly different outcomes between MNT versus CFNG in the CE (in mm; pooled MD = 2.36, 95% CI = 1.74–2.99, p < 0.00001; [Fig. 2]).

Zoom
Fig. 2 (A) Forest plot of the commissural excursion in the MNT versus the CFNG procedure. (B) Funnel plot of the commissural excursion in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MD, mean difference; MNT, masseteric nerve transposition; SD, standard deviation.

Commissural Contraction Velocity

Two studies (n = 75) compared CCV in facial reanimation using MNT versus CFNG as the donor nerve. MNT was shown to have considerably higher CCV than CFNG, indicating more similarity to the healthy score (if the disparities between the two sides were ignored, the most symmetrical smile would be taken into consideration). There was no heterogeneity between the studies with I 2 <50%. The analysis showed a significant difference between MNT and CFNG (pooled MD = 7.01, 95% CI = 3.61–10.41, p < 0.0001; [Fig. 3]).

Zoom
Fig. 3 The commissural contraction velocity in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.

Recovery Percentage

Two studies (n = 75) compared recovery percentages in facial reanimation using MNT versus CFNG as the donor nerve. It was found that MNT had a much higher percentage of CCV than CFNG. A higher percentage (up to 100%) means the technique is more effective and closer to the healthy side score. There was no heterogeneity between the studies with I 2 < 50%. The study of the MNT recovery rate in CE showed a much better result than in CFNG (pooled MD = 26.86, 95% CI = 19.89–33.83, p < 0.00001; [Fig. 4A]). Similarly, the MNT group showed a significantly higher recovery percentage in CCV (pooled MD = 13.00, 95% CI = 5.63–20.38, p = 0.0005; [Fig. 4B]).

Zoom
Fig. 4 (A) Recovery percentage of the commissural excursion in the MNT versus the CFNG procedure. (B) Recovery percentage of the commissural contraction velocity in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.

Static Lip Symmetry

A total of 119 people (n = 119) from all three studies were looked at to see how the static lip angle symmetry changed when MNT or CFNG nerves were used as the donor. The angle symmetry was measured between the vertical midline of the lower lip and the oral commissure. There was no heterogeneity between the studies with I 2 < 50% ([Fig. 5A]). The analysis showed non-significant association between MNT and static lip symmetry angle (pooled MD = −0.19, 95% CI = −1.27–0.89, p = 0.73; [Fig. 5A]). When comparing lip length symmetry (in mm), we obtained two studies (n = 98) Similarly, the MNT group showed no significant difference between the two interventions in static lip symmetry length (in mm; pooled MD = 0.65, 95% CI = −0.89–2.18, p = 0.41); there was no heterogeneity between the studies with I 2 < 50% ([Fig. 5B]).

Zoom
Fig. 5 (A) Static lip angle symmetry in the MNT versus the CFNG procedure. (B) Static lip length symmetry in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.

Dynamic Lip Symmetry

Three studies with 119 people (n = 119) looked at the dynamic lip angle symmetry (in degrees) between the vertical midline of the lower lip and the oral commissure. The donor nerves used in these studies were either MNT or CFNG. There was heterogeneity between the studies with I 2 > 50% ([Fig. 5A]). The analysis showed no significant difference between MNT and dynamic lip angle symmetry (pooled MD = 0.21, 95% CI = −2.22–2.65, p = 0.86; [Fig. 6A]). When comparing dynamic lip length symmetry (in mm), we obtained two studies (n = 98). Similarly, the MNT group showed no significant difference between MNT versus CFNG in dynamic lip symmetry length (in mm; pooled MD = −0.42, 95% CI = −2.81–1.96, p = 0.73). There was heterogeneity between the studies with I 2 > 50% ([Fig. 6B]).

Zoom
Fig. 6 (A) Dynamic lip angle symmetry in the MNT versus the CFNG procedure. (B) Dynamic lip length symmetry in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.

Total Smile Improvement

Two studies (n = 98) were included to compare smile improvement in facial reanimation using MNT versus CFNG as the donor nerve. MNT was shown to have considerably higher improvement than CFNG. There was no heterogeneity between the studies with I 2 < 50%. The analysis showed no significant difference between MNT and total smile improvement (pooled MD = −1.96, 95% CI −4.12–0.19, p = 0.07; [Fig. 7]).

Zoom
Fig. 7 Total smile improvement in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.


Secondary Outcomes

Quality of Life

Three retrospective studies (n = 99) assessed improvements in quality of life (QOL) following facial reanimation using the Face Clinimetric Evaluation (FaCE) instrument.[34] [35] [36] Patients who underwent free gracilis muscle transfer (FGMT) innervated by CFNG showed no statistically significant difference in FaCE score improvements compared with the MNT group.[35] In one study, 13 pediatric patients completed FaCE surveys, with preintervention and postintervention scores improving from 51.3 to 65.7, reflecting a statistically significant improvement. The average FaCE score improvement was 12.9 for CFNG and 17.7 for MNT.[36] Based on these studies, all three suggested that the QOL associated with the MNT procedure was generally higher than with CFNG, although two studies did not reach statistical significance. Thus, it can be concluded that MNT tends to be more favorable than CFNG in improving QOL.


Satisfaction

Two studies (n = 233) reported patient satisfaction scores following reanimation surgery.[37] [38] The masseter nerve gracilis transfer demonstrated favorable outcomes within the briefest recovery timeframe. In the CFNG group, five patients (2.8%, 3.1 ± 0.64) were unsatisfied and reported unsuccessful outcomes, while in the MNT group, one patient (5%, 3.45 ± 0.81) experienced failed results.[38] Another study by Hontanilla et al[37] reported that 16 patients (88.8%) were satisfied with MNT, while 8 patients (80%) were satisfied in the CFNG group. These studies suggest that satisfaction rates are generally higher with MNT compared with CFNG, with a lower incidence of dissatisfaction among MNT patients. However, one study noted a relatively higher rate of dissatisfaction in the MNT cohort, which may be due to differences in preoperative complexity.





Discussion

Facial nerve paralysis is a severe disorder marked by partial or full loss of facial nerve function, resulting in facial asymmetry, deformity, and functional impairment.[19] One of the most important decisions in managing this condition is deciding which motor nerve to supply the paralyzed side.[19] In bilateral paralysis cases, where both facial nerves lack functionality, alternative cranial nerves have been evaluated for reinnervation.[30] Recently, MNT has gained prominence as the preferred technique for facial reanimation.[8] [16] [22] MNT uses the masseter nerve's descending branch while leaving the proximal branches intact, preventing masseter muscle atrophy.[39]

The masseter nerve, the largest pure motor branch of the trigeminal nerve,[30] innervates the masseter muscle, which plays a crucial role in mastication. Its consistent anatomical structure, sufficient length, and proximity to the facial nerve branches[39] make it an ideal motor source for facial reanimation surgery.[11] [23] [24] [39] The motor branch innervating the masseter muscle lies on the muscle's undersurface, generally extending vertically downward along the posterior margin, positioned just beneath the zygomatic arch. The nerve is found approximately 11 mm below the zygomatic arch, 38 mm anterior to the tragus, and 13 mm deep within the masseter muscle.[4] [19] [40] Prior research indicates that the mean distance from the coronoid notch to the entrance of the masseter nerve is 32 mm.[39] During surgery, the masseter nerve is carefully dissected to achieve the necessary length for reinnervation.[38]

In contrast to MNT, the CFNG procedure involves connecting the motor branch of the facial nerve from the healthy, non-paralyzed side to a sural nerve graft. This technique carries the inherent risk of compromising facial nerve function on the unaffected side.[41] Additionally, CFNG is typically a multistage procedure, which increases the risk of failure.[14] The facial nerve's primary role is to provide motor innervation to the muscles responsible for facial expression. To identify the facial nerve branches on the paralyzed side, a periauricular incision is made, extending toward the modiolus until the desired branch is located,[1] usually found at the anterior border of the parotid gland.[42] The buccal or zygomatic branches are often chosen for coaptation with the cross-face sural nerve graft, although they can be challenging to distinguish anatomically.[30]

The surgical durations of both MNT and CFNG vary depending on their complexity and the surgeon's expertise. Data from previous studies show that the CFNG procedure takes approximately 80 to 90 minutes for the first stage and 150 to 180 minutes for the second stage. In contrast, the MNT procedure, performed in a single stage, typically requires 170 to 200 minutes. This suggests that MNT, while taking longer in a single session, may be more time-efficient overall compared with the multistage CFNG.[38] However, no significant differences were observed in total operative time when comparing the muscle transplantation component of both techniques.[30]

In a study by Snyder-Warwick et al, the masseteric nerve demonstrated an average of 5,289 myelinated fibers per square millimeter, compared with the 1,647 axons per square millimeter found in the CFNG, representing a 76% reduction in fiber density from the donor facial nerve. Neurotization using the masseteric nerve has proven to be a reliable technique for smile reanimation, producing robust, symmetrical,[28] and natural smiles with significant functional recovery.[18] These findings are in-line with our comprehensive comparison of both interventions, as summarized in this report ([Table 3]).

Table 3

Comprehensive summary of outcomes derived from the forest plot analysis

Outcomes

Pooled MD (95% CI)

I 2

p-Value

Commissural excursion

2.36 (1.74–2.99)

43%

<0.00001

Commissural contraction velocity

7.01 (3.61–10.41)

0%

<0.0001

Recovery percentage

 • CE recovery percentage

 • CCV recovery percentage

26.86 (19.89–33.83)

13.00 (5.63–20.38)

0%

12%

<0.00001

0.0005

Static lip symmetry

 • By angle

 • By length

−0.19 (−1.27–0.89)

0.65 (−0.89–2.18)

0%

0%

0.73

0.41

Dynamic lip symmetry

 • By angle

 • By length

0.21 (−2.22–2.65)

−0.42 (−2.81–1.96)

75%

51%

0.86

0.73

Total smile improvement

−1.96 (−4.12–0.19)

0%

0.07

Abbreviations: CCV, commissural contraction velocity; CE, commissural excursion; CI, confidence interval; MD, mean difference.


Previous research indicates that smile asymmetry is often a primary concern for patients with facial paralysis, as symmetry is a crucial determinant of facial attractiveness. The masseter nerve transfer has been shown to improve both facial symmetry and oral commissure excursion[22] due to its strong motor input.[13] Studies by Bianchi et al have established that the normal range of commissural movement is between 7 and 22 mm, with a mean of 14 mm.[43] Clinical observations suggest that muscles innervated by the masseter nerve exhibit greater excursion[16] [44] compared with those utilizing CFNG. For instance, Roy et al reported that the masseter nerve transfer resulted in a greater smile excursion (10.0 mm) than CFNG (6.8 mm).[26] Additionally, quantitative assessments using tools such as FACEGram[12] [35] and FACIAL CLIMA[31] have shown that over 75% of patients undergoing masseter nerve transfer experience significant improvements in commissural excursion and velocity.[22] This finding supports our current study, which demonstrates the advantages of masseter nerve transfer in enhancing CE. Notably, the oral commissure movement on the side treated with CFNG was significantly less than that on the healthy side and the masseter nerve transfer group. However, some studies suggest that the CFNG procedure may facilitate a degree of spontaneous movement that is not achievable with the masseter nerve.

CCV is another important parameter for assessing facial symmetry[45] and is evaluated alongside CE[17] [42] [46] in tools like FACIAL CLIMA.[31] A recent study by Hontanilla et al (2018) compared MNT and CFNG, reporting mean CCV values of 35.0 ± 4.5 for MNT and 33.6 ± 5.4 for CFNG.[37] A closer alignment of the CCV on the reanimated side to that of the healthy side indicates a higher likelihood of surgical success. Our analysis corroborates this, revealing that the CCV on the reanimated side following MNT is statistically significantly higher than that observed in the CFNG group. Furthermore, in a separate analysis of CCV, the healthy side and the reanimated side using masseter-innervated nerve transfer showed no significant difference (23.8 vs. 31.3, p = 0.29). This suggests that successful outcomes are associated with the reanimated side achieving results that closely resemble those of the healthy side.

CE and CCV values were converted into recovery percentages to evaluate the improvement rates of each technique based on the paralyzed side's recovery relative to the healthy side.[22] [42] This study revealed that the MNT group exhibited significantly higher recovery rates for both commissural displacement and contraction velocity. An optimal smile is characterized by minimal differences between the reanimated and healthy sides; conversely, substantial discrepancies indicate asymmetrical movement.

Achieving symmetry in both static and dynamic facial expressions poses a considerable challenge in the reconstruction of facial nerve paralysis. Changes in oral commissural symmetry can be assessed through both horizontal and vertical dimensions, which collectively define the angle. A previous study demonstrated that gracilis free muscle transfer, powered by the masseteric nerve, led to significant improvements in horizontal length symmetry during both rest and smiling.[47] Symmetry was quantified by the ratio of oral commissure movement on the affected side compared with the healthy side, with significant enhancements noted during smiling.[12] Patients in the MNT group exhibited more substantial enhancements in static angle symmetry compared with those in the CFNG group. Furthermore, comparisons of dynamic angle differences in both groups indicated impressive improvements, with the masseter-innervated group achieving a larger angle. This group also demonstrated superior improvements in angle symmetry during both rest and smiling.[47] It has been suggested that a satisfactory smile is indicated when postoperative static and dynamic angles approach 90 degrees, and the smile excursion on the affected side closely approximates that of the healthy side.[48] However, it is unfortunate that the comparison of the two procedures in terms of static and dynamic lip symmetry did not reach statistical significance. This lack of significance may be attributed to various factors, including the patient's condition (unilateral or bilateral abnormalities), denervation time,[9] and the high level of dependence on the operator, who plays a critical role in determining the expected outcomes.

Facial paralysis is a serious condition that adversely affects patients' QoL and is linked to depression, making it an important issue in facial reanimation surgery.[2] [49] Patient-reported outcome measures, including the Facial Clinimetric Evaluation (FaCE) Scale, offer clinically significant insights into QoL enhancements and have been widely employed in the literature.[35] [50] The FaCE Scale serves multiple important clinical purposes, including assessing the natural progression of facial disability from the acute phase of paralysis through various recovery stages caused by different underlying factors. This tool enhances our understanding of patients' needs and their responses to various treatment modalities. Furthermore, the FaCE Scale complements clinician-administered instruments designed to quantify facial impairment.[25] [51]

In this study, patients who underwent the CFNG procedure did not show a statistically significant difference in FaCE scores compared with those who received MNT. One potential explanation for this finding is that the mean age of the MNT group was significantly higher than that of the CFNG group,[35] which is relevant since age can influence axonal density.[14] CFNG is considered an ideal choice for those patients who have a sufficiently strong contralateral facial nerve.[19] Previous research indicates that younger patients with severe facial paralysis tend to benefit more from early MNT, particularly in cases of traumatic injury.[25] However, other studies have suggested that patient age at the time of surgery does not significantly impact aesthetic or functional outcomes.[52]

This is an important aspect to consider the possibility of complication when comparing different techniques of facial reanimation. In fact, from previous studies, complication rates were not significantly different between groups. Some mild to severe complications might happen postoperatively and during the healing phase. These complications vary, including postoperative bleeding, hematoma, wound infections, the risk of wound dehiscence, muscle atrophy, and flap failure.[4] [47] [53] In the CFNG procedure, there is always the risk of damage to the function of the facial nerve, weakness of the smile on the nonparalyzed side, once the branch of the zygomatic or buccal nerve is transected for anastomosis. There will be numbness on the lateral aspect of the foot from the sural nerve harvest. If the deep peroneal nerve is accidentally transected, foot drop remains a possibility.[41] Whereas in the MNT procedure, minor synkinesis was also observed in the masseter nerve transfer group.[44] A previous study stated that there have been no reports of donor site morbidity related to loss of masseter muscle function and masseter muscle atrophy.[4] Although there is a possibility of various complications occurring, with good postoperative care, these complaints can be resolved, and rehabilitation is very important to begin around 6 weeks postoperatively, including massage, smile training or induction exercise, and muscle stimulation. Smile training in front of the mirror is quite important.[38]

This study has several limitations, including a small sample size and an unbalanced distribution of outcome parameters, which may affect the statistical significance of the results. This meta-analysis includes two studies[34] [35] with a potential overlap in patient cohorts, representing a minor limitation concerning the independence of data points. Nonetheless, the impact is anticipated to be minimal. Additionally, conducting head-to-head comparisons proved challenging during data collection with the predominance of retrospective studies, resulting in potential bias and limited ability to access broader outcomes such as axonal improvement and spontaneous smiles. Therefore, further comparative studies with larger sample sizes are necessary to provide more robust evidence regarding the benefits of the MNT procedure. Future research is expected to address the gaps identified in this review, particularly in areas where the findings were non-significant, by including a diverse patient population and employing standardized outcome measures to strengthen the evidence supporting the efficacy of MNT in facial reanimation surgery. Additionally, outcomes should be evaluated using reliable and standardized assessment parameters to ensure the validity of future studies.


Conclusion

In conclusion, various facial nerve reconstruction techniques are viable options for facial reanimation, considering the individual patient's circumstances and preoperative conditions. This meta-analysis highlights the significant advantages of MNT over CFNG procedures. Improvements in lip movement and smile functionality, as measured by critical parameters such as CE, CCV, and both static and dynamic symmetry, demonstrate that MNT is a highly preferred approach for facial reanimation. Additionally, secondary outcomes suggest that MNT may further benefit facial reanimation. However, more comprehensive data are needed to analyze these secondary outcomes in-depth.



Conflict of Interest

The authors declare that they have no conflict of interest.

Acknowledgment

We would like to thank all authors whose studies are included in our systematic review and meta-analysis.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.


Contributors' Statement

I.L.P.: Conceptualization; formal analysis; methodology; supervision; validation; writing—review and editing.


K.E.S.S.: Data curation; investigation; software; writing—original draft.


I.F.A.: Project administration; resources; visualization; writing—review and editing; writing—original draft.


R.P.: Formal analysis; investigation; supervision; writing—review and editing.


C.D.K.W.: Formal analysis; methodology; software; supervision; writing—review and editing.


Ethical Approval

This article does not contain any studies with human or animal participants.


Informed Consent

Not applicable.



Correspondence

Indri Lakshmi Putri, MD, PhD
Kampus A UNAIR - Mayjen Prof. Dr. Moestopo 47, Surabaya, 60131
Indonesia   

Publication History

Received: 19 October 2024

Accepted: 19 September 2025

Article published online:
30 January 2026

© 2026. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA


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Fig. 1 PRISMA flow diagram data added to the PRISMA template (from Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ. 2021;372: n71) under the terms of the Creative Commons Attribution License. PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses. *Consider, if feasible to do so, reporting the number of records identified from each database or register searched (rather than the total number across all databases/registers).
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Fig. 2 (A) Forest plot of the commissural excursion in the MNT versus the CFNG procedure. (B) Funnel plot of the commissural excursion in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MD, mean difference; MNT, masseteric nerve transposition; SD, standard deviation.
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Fig. 3 The commissural contraction velocity in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.
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Fig. 4 (A) Recovery percentage of the commissural excursion in the MNT versus the CFNG procedure. (B) Recovery percentage of the commissural contraction velocity in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.
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Fig. 5 (A) Static lip angle symmetry in the MNT versus the CFNG procedure. (B) Static lip length symmetry in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.
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Fig. 6 (A) Dynamic lip angle symmetry in the MNT versus the CFNG procedure. (B) Dynamic lip length symmetry in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.
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Fig. 7 Total smile improvement in the MNT versus the CFNG procedure. CFNG, cross-facial nerve graft; CI, confidence interval; MNT, masseteric nerve transposition; SD, standard deviation.