Literature DB >> 32104052

The Long-Term Outcomes and Predictors of Microvascular Decompression with or without Partial Sensory Rhizotomy for Trigeminal Neuralgia.

Ruiquan Liu1,2, Zhu Deng1,2, Li Zhang1,2, Yin Liu2,3, Zheng Wang2,3, Yanbing Yu1,2.   

Abstract

PURPOSE: Microvascular decompression (MVD) and MVD combined with partial sensory rhizotomy (PSR) are effective surgical treatments for idiopathic trigeminal neuralgia (TN). The aim of this study was to compare the long-term outcomes of both MVD and MVD+PSR for the treatment of TN and to identify the factors that may influence the long-term outcomes after MVD or MVD+PSR. PATIENTS AND METHODS: From March 2009 to December 2017, 99 patients with idiopathic TN who underwent MVD or MVD+PSR in our hospital (40 MVD, 59 MVD+PSR) were included in the study. The indications for MVD+PSR were as follows: vessels only contacted the nerve root, absence of arterial conflict, or failing to completely decompress from the arteries or veins. All patients were treated by one neurosurgeon and were followed up for at least 1 year. The outcomes were assessed with the Barrow Neurological Institute (BNI) Pain Intensity Scale.
RESULTS: The average follow-up duration was 63.0 months (range, 13.2-118.8 months). Patients in the MVD group were younger than those in the MVD+PSR group (55.1 years and 60.5 years, respectively, P=0.012). A total of 62.5% of the patients in the MVD group and 69.5% of the patients in the MVD+PSR group had favorable long-term outcomes. The Kaplan-Meier survival analysis showed no significant difference in long-term outcomes between the two groups (P=0.202). No factors were associated with long-term outcomes after MVD. For MVD+PSR, a long duration of the disease (odds ratio (OR) 6.967, P=0.016) was associated with unfavorable long-term outcomes, whereas pure arterial compression (OR 0.131, P=0.013) was associated with favorable long-term outcomes.
CONCLUSION: For patients who are not suitable to undergo pure MVD, MVD+PSR can be used as an effective alternative. For MVD+PSR, patients with a long duration of symptoms may have poor long-term outcomes, while patients with pure arterial compression may have favorable long-term outcomes.
© 2020 Liu et al.

Entities:  

Keywords:  factors; long-term outcome; microvascular decompression; partial sensory rhizotomy; trigeminal neuralgia

Year:  2020        PMID: 32104052      PMCID: PMC7014959          DOI: 10.2147/JPR.S225188

Source DB:  PubMed          Journal:  J Pain Res        ISSN: 1178-7090            Impact factor:   3.133


Introduction

Trigeminal neuralgia (TN) is a disorder characterized by recurrent, brief, abrupt-onset and termination, electric shock-like pains, which are limited to the distribution of one or more divisions of the trigeminal nerve and triggered by innocuous stimuli.1 After being diagnosed with TN, patients are routinely treated with anticonvulsant drugs, such as carbamazepine. However, some patients who have medically refractory pain or cannot tolerate the adverse effects of drugs need surgical treatment. Surgical treatment for TN includes microvascular decompression (MVD), partial sensory rhizotomy (PSR), gamma knife radiosurgery (GKRS), percutaneous balloon compression, radiofrequency thermocoagulation and so on. Since first proposed by Jannetta2 and after years of development, MVD has become the most effective surgical method for treating TN.3 However, there are still some patients who cannot achieve favorable long-term outcomes after receiving pure MVD. Because of the high incidence of postoperative facial dysesthesia and the high recurrence rate of TN, pure PSR has been used in recent years for patients without obvious intraoperative vascular compression.4,5 Although many neurosurgeons have performed MVD combined with PSR (MVD+PSR) on some TN patients who are not suitable to undergo pure MVD,5–7 only a few studies have reported the differences in postoperative outcomes between MVD and MVD+PSR.5 In addition, while many studies have reported the prognostic factors associated with long-term outcomes after MVD,8–19 few reports have reported the prognostic factors associated with long-term outcomes after MVD+PSR. We followed up patients who underwent MVD or MVD+PSR at the Department of Neurosurgery of our hospital from March 2009 to December 2017 and collected their data. The purpose of this retrospective study is to provide valuable information for improving the postoperative outcomes of TN patients by comparing the long-term outcomes of both MVD and MVD+PSR in treating TN and to identify the prognostic factors associated with the long-term outcomes after MVD or MVD+PSR.

Methods

Subjects

The subjects were selected from a group of TN patients who underwent surgery at the Department of Neurosurgery, China-Japan Friendship Hospital from March 2009 to December 2017.20 A total of 181 patients with medically refractory TN underwent microneurosurgery via a retrosigmoid approach. All operations were performed by one neurosurgeon. Because the number of patients who underwent pure PSR was small (n=7), this study only included patients who underwent MVD and MVD+PSR. The inclusion criteria were as follows: idiopathic TN according to the diagnostic criteria of the International Classification of Headache Disorders, 3rd edition;1 no previous MVD or PSR; sufficient clinical data; and follow-up duration >1 year. The exclusion criteria were as follows: had secondary TN; had concurrent cranial nerve disorder, such as glossopharyngeal neuralgia; and did not agree to be followed up. All patients underwent magnetic resonance imaging (MRI) to evaluate neurovascular compression (NVC) before the operation. Based on previous studies, we divided the MRI findings of NVC into three categories: no vascular compression, only contact (the vessel touches the nerve without visible alteration of the nerve, and the cerebrospinal fluid cannot be seen between the nerve and the vessel), and obvious compression (nerve root has displacement, distortion, or indentation).21,22 We also judged the type of offending vessel on MRI. The patients were not randomly treated with the three surgical procedures (MVD, MVD+PSR, PSR). Before surgery, we informed each patient about the advantages and disadvantages of the various surgical procedures. The general principles for selecting the surgical procedure were as follows: Patients with obvious compression (nerve root has displacement, distortion, or indentation) on MRI were recommended for pure MVD [Figure 1A and B]. MVD+PSR was recommended for patients who met the following conditions: vessels only contacted the trigeminal nerve root [Figure 1C], and pure venous compression[Figure 1D]. Before the operation, we informed patients that if conditions we found during operation were not consistent with the preoperative MRI assessment, we might change the surgical plan according to their specific conditions identified during the operation and patients’ wishes. For example, if we were unable to completely decompress arteries or the veins due to technical difficulties (there were still offending vessels, such as veins that affect the brainstem blood flow, or some perforating vessels) or the degree of vascular compression was found intraoperatively to be less severe (only contact) than that of preoperative MRI, patients were recommended to receive MVD+PSR. However, due to the high incidence of facial dysesthesia after PSR, we performed pure MVD for patients who did not want to endure facial dysesthesia. On the other hand, if we found intraoperatively that vessels obviously compress the nerve root, rather than just contacting the nerve root as indicated by preoperative MRI assessment, we would perform pure MVD. Pure PSR was only used for patients without vascular compression.
Figure 1

Preoperative magnetic resonance imaging (MRI) images under different neurovascular compression. (A) The left basilar artery (BA; white arrow) obviously compresses the trigeminal nerve (black arrow) and causes the nerve root to displacement. Note that the trigeminal nerve on the right (red arrow) has no vascular compression and no displacement. (B) The left superior cerebellar artery (SCA; white arrow) obviously compresses the trigeminal nerve (black arrow). (C) The SCA (white arrow) only contacts the trigeminal nerve (black arrow). Note that there is no cerebrospinal fluid visualized between the nerve and the artery. No deformity of the nerve is observed. (D) Only the vein (white arrow) compresses the right trigeminal nerve (black arrow).

Preoperative magnetic resonance imaging (MRI) images under different neurovascular compression. (A) The left basilar artery (BA; white arrow) obviously compresses the trigeminal nerve (black arrow) and causes the nerve root to displacement. Note that the trigeminal nerve on the right (red arrow) has no vascular compression and no displacement. (B) The left superior cerebellar artery (SCA; white arrow) obviously compresses the trigeminal nerve (black arrow). (C) The SCA (white arrow) only contacts the trigeminal nerve (black arrow). Note that there is no cerebrospinal fluid visualized between the nerve and the artery. No deformity of the nerve is observed. (D) Only the vein (white arrow) compresses the right trigeminal nerve (black arrow). A total of 99 patients met the inclusion criteria of the study: 40 patients underwent MVD, and 59 patients underwent MVD+PSR (Figure 2). The patients signed informed consent forms before undergoing surgery. The study was approved by the Ethics Committee of the China-Japan Friendship Hospital and all patients who participated in the study signed informed consent. This manuscript follows the STROBE reporting guidelines.
Figure 2

Flowchart showing the inclusion and exclusion criteria of patients in the study.

Abbreviations: TN, trigeminal neuralgia; MVD, microvascular decompression; PSR, partial sensory rhizotomy.

Flowchart showing the inclusion and exclusion criteria of patients in the study. Abbreviations: TN, trigeminal neuralgia; MVD, microvascular decompression; PSR, partial sensory rhizotomy.

Data Collection and Outcome Measures

When the TN patient underwent surgical treatment at our hospital, the demographic and clinical data of the patient were recorded, including sex, age, duration of disease, affected side, distribution of pain, type of TN (typical or atypical TN), and history of previous ablative procedures (such as percutaneous balloon compression, radiofrequency thermocoagulation, or GRKS). Previous literature has reported that patients older than 60 years had better long-term outcomes after MVD than patients younger than 60 years,9 while patients with a long duration of the disease had unfavorable outcomes after MVD.15 Therefore, the patients were stratified by age (< 60 years or ≥ 60 years) and duration of disease (< 5 years or ≥ 5 years). Atypical TN was characterized by concomitant continuous or near-continuous pain between attacks in the affected trigeminal distribution.1 The intraoperative data of the patient were also recorded, including the posterior fossa volume (normal or small), presence of arachnoid thickening adhesion, type of offending vessel, and decompression degree. Some researchers believe that the small posterior fossa is a risk factor for NVC and may cause TN.23 We assessed the size of the posterior fossa volume (the posterior fossa volume was defined as the region bordered by the tentorium of the cerebellum, the occipital bone, the clivus, and the pyramidal bones24) based on previously reported MRI assessment methods25 or intraoperative conditions. If the posterior fossa volume measured by linear measurement was less than 500 cm3 or if the platybasia or basilar invagination was found during surgery, we considered that the posterior fossa was small. The literature reports that patients with pure arterial compression have better outcomes after MVD than patients without pure arterial compression,8,18 so we divided the type of offending vessel into the following two subgroups: pure arterial compression (only artery) and nonpure arterial compression (artery + vein, pure vein). We classified the intraoperative decompression degree into two categories: complete decompression from arteries or veins (no offending vessels) and incomplete decompression from arteries or veins (there were still offending vessels). The demographic, clinical and intraoperative variables above may be predictors associated with long-term outcomes after surgery. An independent observer followed up all patients with outpatient visits and by telephone. The data collected during the follow-up visits included TN pain description, complications, the impact of facial dysesthesia on life, medication use, and other treatments received. All patients were followed up for at least 1 year. We used the Barrow Neurological Institute (BNI) Pain Intensity Scale26 to assess the postoperative outcomes (Table 1). According to whether the patient needed medication after surgery, the postoperative outcomes of patients were divided into the following two categories: favorable (BNI score I-II) and unfavorable (BNI score III-V).9 We assessed the immediate outcomes at 1 week after the operation and assessed the long-term outcomes at the last follow-up.
Table 1

Barrow Neurological Institute (BNI) Pain Intensity Scale

ScoreDescription
INo pain, no medication
IIOccasional pain, not requiring medication
IIISome pain, adequately controlled with medication
IVSome pain, not adequately controlled with medication
VSevere pain/no pain relief

Note: Reproduced with permission from Rogers CL, Shetter AG, Fiedler JA, Smith KA, Han PP, Speiser BL. Gamma knife radiosurgery for trigeminal neuralgia: the initial experience of The Barrow Neurological Institute. Int J Radiat Oncol Biol Phys. 2000;47(4):1013–1019. © 2000 Elsevier Science Inc. Published by Elsevier Inc. All rights reserved.26

Barrow Neurological Institute (BNI) Pain Intensity Scale Note: Reproduced with permission from Rogers CL, Shetter AG, Fiedler JA, Smith KA, Han PP, Speiser BL. Gamma knife radiosurgery for trigeminal neuralgia: the initial experience of The Barrow Neurological Institute. Int J Radiat Oncol Biol Phys. 2000;47(4):1013–1019. © 2000 Elsevier Science Inc. Published by Elsevier Inc. All rights reserved.26

Surgical Methods

All operations were performed by one neurosurgeon. After general anesthesia, the patients were placed in the lateral decubitus position with the affected side facing upward. The suboccipital retrosigmoid approach was used for all operations. The diameter of the bone window was approximately 2 cm. After opening the dura mater, part of the cerebrospinal fluid was suctioned out, and the arachnoid surrounding the trigeminal nerve was carefully separated. The position of the patient’s head and the angle of the microscope were adjusted, and the full length of the trigeminal nerve root was carefully explored to identify the compressive vessels. Different surgical procedures were selected according to the preoperative MRI assessment, patient’s wishes, and the specific conditions identified during the operation. If pure MVD treatment was performed, the compressive vessel was separated, and polyester pads were placed between the vessel and the brainstem. If MVD was combined with PSR treatment, 1/3-2/3 of the trigeminal sensory root was cut according to the distribution of pain (if the pain only affected the V3 division, we cut off 1/3 of the sensory root; if the pain affected the V1 or V2 division, not only the V3 division, we cut off 2/3 of the sensory root). The dura mater was sutured, and the skull defect was repaired. Finally, the muscles and skin were sutured.

Statistical Analysis

All statistical analyses were performed using SPSS version 24.0 (IBM, Armonk, New York, USA). All analyses compared the MVD and MVD+PSR only. The categorical variables are presented as numbers and percentages, and the continuous variables are presented as the mean ± standard deviation. After the continuous variables were tested for normality by the Shapiro–Wilk test, a Student’s t-test or Mann–Whitney U-test was used to compare the continuous variables between the two groups. Categorical variables were compared with Pearson’s χ2 test or Fisher’s exact test. Kaplan-Meier survival analysis was used to assess the outcomes of the two surgical procedures, and the Log rank test was used to compare the long-term outcomes between the two groups. Based on our experience and previous literature, we included the following factors in our study: sex, age, duration of disease, affected side, distribution of pain, type of TN, history of previous ablative procedures, posterior fossa volume, arachnoid thickening adhesion, type of offending vessel, decompression degree, and immediate postoperative outcomes. Univariate analysis was performed using Pearson’s χ2 test or Fisher’s exact test. Multivariate analysis was then performed using binary logistic regression to further assess the association between the prognostic factors and long-term outcome. The association strength was assessed using odds ratios (ORs) and 95% confidence intervals (95% CI). Only factors with a P-value < 0.2 from the univariate analysis were included in the multivariate analysis. In addition, previous literature reported that the duration of disease, the type of offending vessel and the immediate postoperative outcome were factors associated with the long-term outcome,8,15,18 so these three factors were also included in the multivariate analysis. A P-value ≤ 0.05 was considered statistically significant.

Results

In this study, a total of 181 patients with TN underwent surgical treatment. Among these patients, 7 patients underwent pure PSR, 8 patients had secondary TN, 24 patients had concurrent cranial nerve disorders, and 44 patients were followed up for less than 1 year (Figure 2). After excluding the above patients, a total of 99 patients were included in the study to comprise the MVD group (n = 40) and the MVD+PSR group (n = 59). The follow-up duration was 13.2 to 118.8 months, with an average of 63.0 months. The demographic and clinical data of the patients are shown in Table 2. The data showed that the patients in the MVD group (mean age, 55.1 ± 10.7 years) were younger (P = 0.012) than those in the MVD + PSR group (mean age, 60.5 ± 10.1 years). In total, 25 (62.5%) patients in the MVD group were <60 years old, and 24 (40.7%) patients in the MVD+PSR group were <60 years old. In addition, the proportion of patients with complete decompression from arteries or veins in the MVD group was higher than that in the MVD+PSR group (P=0.001). There were no significant differences in sex, duration of disease, affected side, distribution of pain, type of TN, history of previous ablative procedures, posterior fossa volume, presence of arachnoid thickening adhesion, and type of offending vessel between the two groups (P>0.05).
Table 2

Demographic and Clinical Data of Patients in the MVD and MVD+PSR Groups

VariableMVDMVD+PSRP value
Sex, n (%)0.402a
 Male14(35%)16(27.1%)
 Female26(65%)43(72.9%)
Age (years), mean±SD55.1±10.760.5±10.10.012b
Age (years), n (%)0.033a
 <6025(62.5%)24(40.7%)
 ≥6015(37.5%)35(59.3%)
Duration of disease (years), n (%)0.369a
 <516(40.0%)29(49.2%)
 ≥524(60.0%)30(50.8%)
Affected side, n (%)0.551a
 Left18(45.0%)23(39.0%)
 Right22(55.0%)36(61.0%)
Distribution of pain, n (%)0.802a
 V11(2.5%)0(0.0%)
 V214(35.0%)18(30.5%)
 V34(10.0%)8(13.6%)
 V1+V26(15.0%)6(10.2%)
 V2+V313(32.5%)23(39.0%)
 V1+V2+V32(5%)4(6.8%)
Type of TN, n (%)1.000a
 Typical38(95.0%)57(96.6%)
 Atypical2(5.0%)2(3.4%)
History of previous ablative procedures, n (%)1.000a
 Yes5(12.5%)7(11.9%)
 No35(87.5%)52(88.1%)
Posterior fossa volume, n (%)0.877a
 Normal17(42.5%)26(44.1%)
 Small23(57.5%)33(55.9%)
Presence of arachnoid thickening adhesion, n (%)0.359a
 Yes31(77.5%)50(84.7%)
 No9(22.5%)9(15.3%)
Type of offending vessel, n (%)0.367a
 Pure artery compression22(55.0%)27(45.8%)
 Nonpure artery compression18(45.0%)32(54.2%)
Decompression degree, n (%)0.001a
 Complete decompression from arteries or veins38(95.0%)39(66.1%)
 Incomplete decompression from arteries or veins2(5.0%)20(33.9%)

Notes: aP value, Pearson’s χ2 test or Fisher’s exact test; bP value, Student’s t-test.

Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy, TN, trigeminal neuralgia; V1, the first division of the trigeminal nerve; V2, the second division of the trigeminal nerve; V3, the third division of the trigeminal nerve.

Demographic and Clinical Data of Patients in the MVD and MVD+PSR Groups Notes: aP value, Pearson’s χ2 test or Fisher’s exact test; bP value, Student’s t-test. Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy, TN, trigeminal neuralgia; V1, the first division of the trigeminal nerve; V2, the second division of the trigeminal nerve; V3, the third division of the trigeminal nerve. The most common offending vessels were the superior cerebellar artery (SCA) in 71 cases (71.7%, MVD: 33 cases, MVD+PSR: 38 cases), followed by the superior petrosal vein (SPV) in 50 cases (50.5%, MVD: 18 cases, MVD+PSR: 32 cases) and the anterior inferior cerebellar artery (AICA) in 36 cases (36.4%, MVD: 13 cases, MVD+PSR: 23 cases). A total of 56.6% of patients were found to have two or more offending vessels during surgery (60.0% in the MVD group and 54.2% in the MVD+PSR group) (Table 3).
Table 3

Type of Offending Vessel

VesselAllMVDMVD+PSR
SCA, n (%)71(71.7%)33(82.5%)38(64.4%)
AICA, n (%)36(36.4%)13(32.5%)23(39.0%)
PICA, n (%)1(1.0%)1(2.5%)0(0.0%)
BA, n (%)5(5.1%)2(5.0%)3(5.1%)
SPV, n (%)50(50.5%)18(45.0%)32(54.2%)
Multiple offending vessels, n (%)56(56.6%)24(60.0%)32(54.2%)

Abbreviations: SCA, superior cerebellar artery; AICA, anterior inferior cerebellar artery; PICA, posterior inferior cerebellar artery; BA, basilar artery; SPV, super petrosal vein.

Type of Offending Vessel Abbreviations: SCA, superior cerebellar artery; AICA, anterior inferior cerebellar artery; PICA, posterior inferior cerebellar artery; BA, basilar artery; SPV, super petrosal vein.

Postoperative Outcomes

One week after the operation, 34 (85%) patients in the MVD group achieved favorable outcomes, and 55 (93.2%) patients in the MVD+PSR group achieved favorable outcomes. There was no significant difference between the two groups (P=0.321). The average follow-up duration was 48.4 months (13.2–118.8 months) in the MVD group and 72.9 months (16.8–118.8 months) in the MVD+PSR group. There was a statistically significant difference between the two groups (P<0.001). At the last follow-up, 25 (62.5%) of the patients who underwent MVD achieved favorable long-term outcomes, and 15 (37.5%) had unfavorable long-term outcomes. In the MVD+PSR group, 41 (69.5%) patients achieved favorable long-term outcomes, and 18 (30.5%) patients had unfavorable long-term outcomes. To compare the differences in long-term outcomes between the two groups, we performed a Kaplan-Meier survival analysis (Figure 3). The duration of favorable outcomes in the MVD group was 74.2 ± 9.0 months, and the duration of favorable outcomes in the MVD + PSR group was 86.0 ± 6.5 months. However, the Log rank test showed no significant difference in long-term outcomes between the two groups (P=0.202).
Figure 3

Postoperative outcomes: MVD versus MVD+PSR. The Kaplan-Meier survival curves for the MVD and MVD+PSR groups are shown.

Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy.

Postoperative outcomes: MVD versus MVD+PSR. The Kaplan-Meier survival curves for the MVD and MVD+PSR groups are shown. Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy.

Factors Influencing the Postoperative Outcomes

We analyzed the association between the following factors and long-term outcomes after MVD or MVD+PSR: sex, age, duration of disease, affected side, distribution of pain, type of TN, history of previous ablative procedures, posterior fossa volume, arachnoid thickening adhesion, type of offending vessel, decompression degree, and immediate postoperative outcomes. In the MVD group, the univariate analysis showed no significant associations between any of the above factors and the long-term outcomes after MVD (Table 4). Because no factors met the criteria of P < 0.2, we only included the duration of disease (P=0.505), type of offending vessel (P=0.870) and immediate postoperative outcomes (P=0.253). The multivariate analysis showed that the duration of disease (OR 1.212, 95% CI 0.295–4.972, P=0.790), type of offending vessel (OR 0.663, 95% CI 0.166–2.652, P=0.561) and immediate postoperative outcomes (OR 4.853, 95% CI 0.707–33.299, P=0.108) were not significantly associated with the long-term outcomes of patients.
Table 4

The Univariate Analysis of Factors Associated with Long-Term Outcomes in MVD Group

VariableBNI Score 1-2BNI Score 3-5P value
Sex, n (%)0.608
 Male8(32.0%)6(40.0%).
 Female17(68.0%)9(60.0%)
Age (years), n (%)0.800
 <6016(64.0%)9(60.0%)
 ≥609(36.0%)6(40.0%)
Duration of disease (years), n (%)0.505
 <511(44.0%)5(33.3%)
 ≥514(56.0%)10(66.7%)
Affected side, n (%)0.412
 Left10(40.0%)8(53.3%)
 Right15(60.0%)7(46.7%)
Distribution of pain, n (%)0.498
 V10(0.0%)1(6.7%)
 V27(28.0%)7(46.7%)
 V33(12.0%)1(6.7%)
 V1+V25(20.0%)1(6.7%)
 V2+V38(32.0%)5(33.3%)
 V1+V2+V32(8.0%)0(0.0%)
Type of TN, n (%)1.000
 Typical24(96.0%)14(93.3%)
 Atypical1(4.0%)1(6.7%)
History of previous ablative procedures, n (%)0.711
 Yes4(16.0%)1(6.7%)
 No21(84.0%)14(93.3%)
Posterior fossa volume, n (%)0.804
 Normal11(44.0%)6(40.0%)
 Small14(56.0%)9(60.0%)
Presence of arachnoid thickening adhesion, n (%)0.494
 Yes18(72.0%)13(86.7%)
 No7(28.0%)2(13.3%)
Type of offending vessel, n (%)0.870
 Pure artery compression14(56.0%)8(53.3%)
 Nonpure artery compression11(44.0%)7(46.7%)
Decompression degree, n (%)1.000
 Complete decompression from arteries or veins24(96.0%)14(93.3%)
 Incomplete decompression from arteries or veins1(4.0%)1(6.7%)
Immediate postoperative outcomes, n (%)0.253
 Favorable23(92.0%)11(73.3%)
 Unfavorable2(8.0%)4(26.7%)

Note: p values: Pearson’s χ2 test or Fisher’s exact test.

Abbreviations: MVD, microvascular decompression; TN, trigeminal neuralgia; V1, the first division of the trigeminal nerve; V2, the second division of the trigeminal nerve; V3, the third division of the trigeminal nerve; BNI, Barrow Neurological Institute.

The Univariate Analysis of Factors Associated with Long-Term Outcomes in MVD Group Note: p values: Pearson’s χ2 test or Fisher’s exact test. Abbreviations: MVD, microvascular decompression; TN, trigeminal neuralgia; V1, the first division of the trigeminal nerve; V2, the second division of the trigeminal nerve; V3, the third division of the trigeminal nerve; BNI, Barrow Neurological Institute. We also analyzed the effects of the above factors on the long-term outcomes of MVD+PSR patients. The univariate analysis showed that the duration of disease (P=0.001), posterior fossa volume (P=0. 025) and type of offending vessel (P=0. 016) were associated with long-term outcomes (Table 5). To further evaluate the impact of these factors on the long-term outcomes, we included these three variables and the immediate postoperative outcomes (P=0.150) in a binary logistic regression for multivariate analysis. The multivariate analysis showed that a duration of disease ≥ 5 years (OR 6.967, 95% CI 1.444–33.626, P=0.016) was significantly associated with unfavorable postoperative long-term outcomes (Table 6), while pure arterial compression (OR 0.131, 95% CI 0.026–0. 647, P=0. 013) was significantly associated with favorable long-term outcomes.
Table 5

The Univariate Analysis of Factors Associated with Long-Term Outcomes in MVD+PSR Group

VariableBNI Score 1-2BNI Score 3-5P value
Sex, n (%)1.000
 Male11(26.8%)5(27.8%)
 Female30(73.2%)13(72.2%)
Age (years), n (%)0.334
 <6015(36.6%)9(50.0%)
 ≥6026(63.4%)9(50.0%)
Duration of disease (years), n (%)0.001
 <526(63.4%)3(16.7%)
 ≥515(36.6%)15(83.3%)
Affected side, n (%)0.569
 Left15(36.6%)8(44.4%)
 Right26(63.4%)10(55.6%)
Distribution of pain, n (%)0.988
 V10(0.0%)0(0.0%)
 V213(31.7%)5(27.8%)
 V36(14.6%)2(11.1%)
 V1+V24(9.8%)2(11.1%)
 V2+V315(36.6%)8(44.4%)
 V1+V2+V33(7.3%)1(5.6%)
Type of TN, n (%)1.000
 Typical39(95.1%)18(100.0%)
 Atypical2(4.9%)0(0.0%)
History of previous ablative procedures, n (%)0.233
 Yes3(7.3%)4(22.2%)
 No38(92.7%)14(77.8%)
Posterior fossa volume, n (%)0.025
 Normal22(53.7%)4(22.2%)
 Small19(46.3%)14(77.8%)
Presence of arachnoid thickening adhesion, n (%)0.847
 Yes34(82.9%)16(88.9%)
 No7(17.1%)2(11.1%)
Type of offending vessel, n (%)0.016
 Pure artery compression23(56.1%)4(22.2%)
 Nonpure artery compression18(43.9%)14(77.8%)
Decompression degree, n (%)0.592
 Complete decompression from arteries or veins28(68.3%)11(61.1%)
 Incomplete decompression from arteries or veins13(31.7%)7(38.9%)
Immediate postoperative outcomes, n (%)0.150
 Favorable40(97.6%)15(83.3%)
 Unfavorable1(2.4%)3(16.7%)

Note: p values: Pearson’s χ2 test or Fisher’s exact test.

Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy, TN, trigeminal neuralgia; V1, the first division of the trigeminal nerve; V2, the second division of the trigeminal nerve; V3, the third division of the trigeminal nerve; BNI, Barrow Neurological Institute.

Table 6

The Binary Logistic Regression Analysis of Factors Associated with Long-Term Outcomes in MVD+PSR Group

VariableOR (95% CI)P value
Duration of disease (years)
 <51
 ≥56.967(1.444–33.626)0.016
Posterior fossa volume
 Normal1
 Small3.703(0.724–18.938)0.116
Type of offending vessel
 Nonpure artery compression1
 Pure artery compression0.131 (0.026–0.647)0.013
Immediate postoperative outcomes
 Favorable1
 Unfavorable29.692(0.905–974.694)0.057

Note: All the factors were analyzed by binary logistic regression analysis, including the duration of disease, posterior fossa volume, type of the offending vessel and the immediate postoperative outcomes.

Abbreviations: OR, odds ratio; CI, confidence interval.

The Univariate Analysis of Factors Associated with Long-Term Outcomes in MVD+PSR Group Note: p values: Pearson’s χ2 test or Fisher’s exact test. Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy, TN, trigeminal neuralgia; V1, the first division of the trigeminal nerve; V2, the second division of the trigeminal nerve; V3, the third division of the trigeminal nerve; BNI, Barrow Neurological Institute. The Binary Logistic Regression Analysis of Factors Associated with Long-Term Outcomes in MVD+PSR Group Note: All the factors were analyzed by binary logistic regression analysis, including the duration of disease, posterior fossa volume, type of the offending vessel and the immediate postoperative outcomes. Abbreviations: OR, odds ratio; CI, confidence interval.

Postoperative Complications

The postoperative complications of the two groups of patients are shown in Table 7. In MVD group, complications included facial dysesthesia in 3 cases, intracranial infection in 4 cases, hearing loss in 2 cases, and intracranial bleeding in 1 case. In MVD+PSR group, complications included facial dysesthesia in 48 cases, intracranial infection in 2 cases, hearing loss in 4 cases, facial continuous pain in 3 cases, facial paresis in 1 case, wound infection in 1 case, and dizziness in 2 cases. There were no perioperative deaths in either group. There were no significant differences in postoperative complications between the two groups, except for facial dysesthesia. For the impact of facial dysesthesia on life, only 1 of the 4 people with facial dysesthesia in the MVD group thought that facial dysesthesia had an impact on life. In MVD+PSR group, only 2 of the 48 people with facial dysesthesia considered that facial dysesthesia had an impact on life.
Table 7

Postoperative Complications of Patients in the MVD and MVD+PSR Groups

Postoperative ComplicationsMVDMVD+PSRP value
Facial dysesthesia3(7.5%)48(81.4%)<0.001
Intracranial infection4(10.0%)2(3.4%)0.356
Hearing loss2(5.0%)4(6.8%)1.000
Intracranial bleeding1(2.5%)0(0.0%)0.404
Facial continuous pain0(%)3(5.1%)0.395
Facial paresis0(%)1(1.7%)1.000
Wound infection0(%)1(1.7%)1.000
Dizziness0(%)2(3.4%)0.514

Note: p values: Pearson’s χ2 test or Fisher’s exact test.

Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy.

Postoperative Complications of Patients in the MVD and MVD+PSR Groups Note: p values: Pearson’s χ2 test or Fisher’s exact test. Abbreviations: MVD, microvascular decompression; PSR, partial sensory rhizotomy.

Discussion

We retrospectively analyzed 99 patients who underwent MVD or MVD+PSR and found no statistically significant difference in long-term outcomes between the two groups. In addition, we found that no factors were associated with long-term outcomes after MVD. For patients who underwent MVD+PSR, a long duration of the disease (≥5 years) was an independent predictor of unfavorable long-term outcomes, while pure arterial compression was an independent predictor of favorable long-term outcomes. We evaluated the postoperative outcomes with the BNI Pain Intensity Scale. The postoperative outcomes were divided into the following two categories according to whether the patients needed to take medication after surgery: favorable (BNI score I-II) and unfavorable (BNI score III-V).9 Among patients who underwent MVD, 62.5% of the patients maintained favorable outcomes at the last follow-up. This result was similar to the MVD outcomes reported in many other studies.3,8,14,17 For MVD+PSR, 69.5% of the patients had favorable long-term outcomes. In the study by Zhang et al5 after 2 years of follow-up, the pain-free rate in the MVD+PSR group was 95.7%. The longer follow-up duration (an average of 6.1 years) in this study may be the cause of the above differences. According to our experiences and previous literature,8,10–12,16,18 pure MVD leads to poor outcomes in patients who had the following conditions: vessels only contacted the trigeminal nerve root, pure venous compression, and incomplete decompression from arteries or veins. Therefore, we recommend that these patients receive MVD+PSR treatment. Patients who underwent MVD+PSR in this study were older than those who underwent MVD, and we thought it might be because older patients were more likely to accept postoperative facial dysesthesia, so they were willing to choose MVD+PSR. In our study, although the average follow-up duration in the MVD+PSR group was significantly longer than that in the MVD group, the proportion of patients with favorable long-term outcomes in the MVD+PSR group was slightly higher than that in the MVD group, but there was no statistically significant difference. Therefore, the long-term outcomes of MVD+PSR on patients who had the above conditions and can tolerate postoperative facial dysesthesia are positive. For patients without clear vascular compression, there are other alternative surgical treatments in addition to PSR, such as GKRS and internal neurolysis (IN). For GKRS, in one previous study, the patients with NVC had better responses to GKRS than those without NVC.27 In another study, after long-term follow-up, although the proportion of patients with NVC who had good outcomes was higher than that of patients without NVC, there was no statistical difference between the two groups (86.4% and 68.0%,respectively).28 Chang et al29 found that there was no significant difference in successful pain control rates (BNI score I-III) among patients with different NVC conditions after GKRS treatment (successful pain control rate, no NVC 85%, small vessel NVC 75%, large vessel NVC 88%, respectively). However, a large proportion of patients will experience facial numbness after receiving GKRS.17,30 For IN, it is also a safe and effective option for the treatment of TN without vascular compression. Jie et al31 found that IN has better efficacy in patients without vascular compression than patients with vascular compression. As reported in previous studies, for patients without NVC, 47%–72.7% of patients receiving IN can achieve good long-term results, but the incidence of facial dysesthesia and numbness after IN is 76.5%-96%.32,33 However, there is currently no study comparing the efficacy of PSR, IN, and GKRS in the treatment of TN without clear NVC. Some studies have noted that a long duration of TN had an adverse effect on the long-term outcomes of MVD. A study by Barker et al8 reported that patients who had TN for less than 8 years were more likely to have good long-term outcomes. Sarsam et al15 found that the risk of recurrence after MVD increased by 0.3% for each additional month of preoperative pain. However, many studies have shown that the duration of TN was not associated with long-term outcomes after MVD.9,14,16,18,19 Our study also found that the duration of the disease was not associated with long-term outcomes after MVD; however, for patients who underwent MVD+PSR, patients with a longer duration of disease are less likely to obtain favorable long-term outcomes. We believe that the reason for the above results is as follows: patients with a longer duration of the disease have more severe nerve damage. For patients who are suitable to undergo pure MVD, vascular compression may be the only cause of nerve damage. After complete decompression, nerve function can be gradually recovered. However, for the above patients who are not suitable to undergo pure MVD, vascular compression may not be the only cause of pain. MVD+PSR cannot solve other potential pathological mechanisms, and patients with a longer duration of the disease have more severe nerve damage. Therefore, the postoperative outcomes of this population of patients are poor. The literature reports that patients with pure arterial compression can achieve favorable long-term outcomes after MVD.8,18 In our study, there was no significant difference in the long-term outcomes between patients with pure arterial compression and patients with nonpure arterial compression (artery+vein, pure vein) after MVD treatment. However, in the MVD+PSR group, patients with pure artery compression were more likely to have good long-term outcomes after the operation than those with nonpure arterial compression. Compared to decompressing arteries, decompressing veins is more difficult, because the risk of bleeding is higher, and it is not possible to perform electrocoagulation or other decompression operations on parts of offending veins that affect the brainstem blood flow. Therefore, it is more difficult to perform complete decompression in patients with venous compression than in those with pure arterial compression. Moreover, because we mostly performed MVD+PSR on patients who could not be completely decompressed, there were more patients in the MVD+PSR group than in the MVD group who could not be decompressed completely due to nonpure arterial compression. This may be why the results of our study are different from those of previous studies. In addition, 50.5% of the patients in our study had venous compression, which was consistent with the venous involvement rates (17.5%–68%) reported in other studies.8,19,34,35 We believe that the adverse effect of venous compression on the long-term outcomes may be caused by incomplete decompression, so careful intraoperative exploration should be performed to avoid missing veins, and patients should be treated with MVD or MVD+PSR according to the degree of intraoperative decompression. Many studies have reported some prognostic factors associated with long-term outcomes after MVD, but the conclusions are different. These factors included sex,8,9 age,9,15,18 distribution of pain,9 types of TN,13,15,18,19 history of previous ablative procedures,12 and immediate postoperative outcomes.8 However, in our study, we did not find that these factors were associated with long-term outcomes after MVD or MVD+PSR. Patients who underwent MVD+PSR had a significantly higher probability of facial dysesthesia than patients who underwent pure MVD, but only a few people thought that facial dysesthesia had an impact on life.

Limitations

There are several limitations to our study. First, this study was a retrospective study, which forces us to exclude patients with incomplete follow-up data. Second, the patients in this study were not randomly assigned to the different treatment groups (MVD or MVD+PSR) so their treatment choice was subject to bias. We cannot rule out the possibility that the differences in the observed outcomes in this study were due to differences in the baseline characteristics between the two groups. Third, the sample size of this study was small, and we hope to conduct a study with a larger sample size in the future. Finally, our study only included patients with primary TN, so our results are not applicable to patients with secondary TN and patients with concurrent cranial nerve disorders.

Conclusion

In our study, some patients who were not suitable to undergo pure MVD were treated with MVD+PSR, and these patients were able to achieve similar outcomes to the patients who underwent MVD. No factors were associated with long-term outcomes after MVD. For MVD+PSR, patients with a long duration of symptoms may have poor long-term outcomes, while patients with pure arterial compression may have favorable long-term outcomes. We suggest that the appropriate surgical procedure should be selected based on the opinions of the patients, preoperative MRI evaluation and the specific conditions identified during the operation. For patients who are not suitable to undergo pure MVD, MVD+PSR can be considered an effective alternative.
  35 in total

1.  The efficacy and safety of nerve combing for trigeminal neuralgia without neurovascular compression.

Authors:  De-Bao Yang; Zhi-Min Wang
Journal:  Acta Neurol Belg       Date:  2019-03-06       Impact factor: 2.396

2.  The long-term outcome predictors of pure microvascular decompression for primary trigeminal neuralgia.

Authors:  Heng Zhang; Ding Lei; Chao You; Bo-Yong Mao; Bo Wu; Yuan Fang
Journal:  World Neurosurg       Date:  2012-01-26       Impact factor: 2.104

3.  Microvascular decompression surgery: surgical principles and technical nuances based on 4000 cases.

Authors:  Jun Zhong; Jin Zhu; Hui Sun; Ning-Ning Dou; Yong-Nan Wang; Ting-Ting Ying; Lei Xia; Ming-Xin Liu; Bang-Bao Tao; Shi-Ting Li
Journal:  Neurol Res       Date:  2014-03-05       Impact factor: 2.448

4.  Microvascular Decompression for Treatment of Trigeminal Neuralgia: Factors That Predict Complete Pain Relief and Study of Efficacy and Safety in Older Patients.

Authors:  Sarun Nunta-Aree; Kasemsak Patiwech; Bunpot Sitthinamsuwan
Journal:  World Neurosurg       Date:  2017-12-02       Impact factor: 2.104

5.  Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition.

Authors: 
Journal:  Cephalalgia       Date:  2018-01       Impact factor: 6.292

6.  Long-term efficacy and safety of internal neurolysis for trigeminal neuralgia without neurovascular compression.

Authors:  Andrew L Ko; Alp Ozpinar; Albert Lee; Ahmed M Raslan; Shirley McCartney; Kim J Burchiel
Journal:  J Neurosurg       Date:  2015-02-13       Impact factor: 5.115

7.  Association between neurovascular contact on MRI and response to gamma knife radiosurgery in trigeminal neuralgia.

Authors:  Sami H Erbay; Rafeeque A Bhadelia; Ron Riesenburger; Punita Gupta; Mark O'Callaghan; Eric Yun; Steven Oljeski
Journal:  Neuroradiology       Date:  2005-10-20       Impact factor: 2.804

8.  Predictors of long-term success after microvascular decompression for trigeminal neuralgia.

Authors:  Jonathan P Miller; Stephen T Magill; Feridun Acar; Kim J Burchiel
Journal:  J Neurosurg       Date:  2009-04       Impact factor: 5.115

9.  Partial sensory trigeminal rhizotomy at the pons for trigeminal neuralgia.

Authors:  J N Young; R H Wilkins
Journal:  J Neurosurg       Date:  1993-11       Impact factor: 5.115

10.  The long-term outcome of microvascular decompression for trigeminal neuralgia.

Authors:  F G Barker; P J Jannetta; D J Bissonette; M V Larkins; H D Jho
Journal:  N Engl J Med       Date:  1996-04-25       Impact factor: 91.245

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  2 in total

1.  Value of Partial Sensory Rhizotomy in the Microsurgical Treatment of Trigeminal Neuralgia Through Retrosigmoid Approach.

Authors:  Yin Liu; Yanbing Yu; Zheng Wang; Zhu Deng; Ruiquan Liu; Na Luo; Li Zhang
Journal:  J Pain Res       Date:  2020-12-01       Impact factor: 3.133

Review 2.  Treatment of redo-microvascular decompression or internal neurolysis plus microvascular decompression for recurrent trigeminal neuralgia: a review of long-term effectiveness and safety.

Authors:  Baisheng Wang; Li Zhang; Yanbing Yu
Journal:  J Int Med Res       Date:  2022-03       Impact factor: 1.671

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