Literature DB >> 29951637

Influence of neural monitoring during thyroid surgery on nerve integrity and postoperative vocal function.

A F Engelsman1, S Warhurst2, S Fraser1, D Novakovic2, S B Sidhu1.   

Abstract

BACKGROUND: Integrity of the recurrent laryngeal nerve (RLN) and the external branch of the superior laryngeal nerve (EBSLN) can be checked by intraoperative nerve monitoring (IONM) after visualization. The aim of this study was to determine the prevalence and nature of voice dysfunction following thyroid surgery with routine IONM.
METHODS: Thyroidectomies were performed with routine division of strap muscles and nerve monitoring to confirm integrity of the RLN and EBSLN following dissection. Patients were assessed for vocal function before surgery and at 1 and 3 months after operation. Assessment included use of the Voice Handicap Index (VHI) 10, maximum phonation time, fundamental frequency, pitch range, harmonic to noise ratio, cepstral peak prominence and smoothed cepstral peak prominence.
RESULTS: A total of 172 nerves at risk were analysed in 102 consecutive patients undergoing elective thyroid surgery. In 23·3 per cent of EBSLNs and 0·6 per cent of RLNs nerve identification required the assistance of IONM in addition to visualization. Nerve integrity was confirmed during surgery for 98·8 per cent of EBSLNs and 98·3 per cent of RLNs. There were no differences between preoperative and postoperative VHI-10 scores. Acoustic voice assessment showed small changes in maximum phonation time at 1 and 3 months after surgery.
CONCLUSION: Where there is routine division of strap muscles, thyroidectomy using nerve monitoring confirmation of RLN and EBSLN function following dissection results in no clinically significant voice change.

Entities:  

Year:  2018        PMID: 29951637      PMCID: PMC5989980          DOI: 10.1002/bjs5.50

Source DB:  PubMed          Journal:  BJS Open        ISSN: 2474-9842


Introduction

Thyroidectomy is the most frequently performed endocrine operation in the world. One of the significant complications is vocal fold paralysis from recurrent laryngeal nerve (RLN) injury, although vocal fold paresis resulting from partial loss of nerve function can also cause postoperative dysphonia. The standard to avoid vocal fold paresis is direct visualization, dissection and protection of the RLN1. Using this technique, nerve injury rates have been low, with a temporary RLN palsy rate of 3–8 per cent and a permanent rate of 0·3–3 per cent reported2. The reported prevalence of external branch of the superior laryngeal nerve (EBSLN) damage is higher. EBSLN damage produces changes in voice that are heterogeneous and difficult to diagnose. A lesion of the EBSLN impairs motor function of the cricothyroid muscle, affecting the production of high tones, limiting pitch range and voice projection, and leading to phonatory fatigue3 4. The rate of EBSLN injury has been reported to be as high as 28 per cent5. Intraoperative nerve monitoring (IONM) was developed to reduce the incidence of these problems, and in one RCT6 decreased the rate of temporary RLN palsy from 5·0 to 2·7 per cent (P = 0·007). Owing to the low RLN injury rate, most studies are, however, underpowered to detect statistically significant differences and, as a result, the routine use of IONM remains controversial. In response to variations in practice and conflicting data, a consensus statement in 2011 by the International Neural Monitoring Study Group7 emphasized the importance of standardizing the use of IONM in RLN identification as an adjunct to visualization. When used in a standard fashion during thyroid surgery, nerve monitoring has been shown to improve identification of both the EBSLN and RLN compared with visualization alone8. This is especially the case for the EBSLN. An RCT9 found significantly less severe impairment of the voice handicap score in monitored patients than in those who had direct visualization alone (2·6 versus 11·2 per cent respectively; P = 0·021). In addition, reports suggest that damage to the strap muscles can lead to voice impairment10, although no causal relation between voice changes and transection of the strap muscles has been established. The aim of the present study was to determine the prevalence and nature of voice dysfunction following thyroid surgery with IONM and routine strap muscle division.

Methods

A cohort of consecutive patients undergoing thyroidectomy who completed informed consent and preoperative and postoperative vocal function assessment were included in the study. Operations were performed by the same single surgeon. Data were held in a specific database approved by the Northern Sydney Area ethics committee. Videostroboscopy and voice assessment were performed on all patients before surgery and at 1 and 3 months after surgery by an independent laryngologist and speech–language therapist. Demographics, type of operation, pathology, visualization of EBSLN and RLN, findings at IONM, EBSLN subtype classification11 and complications were recorded. The Voice Handicap Index (VHI) 10 questionnaire result was used as the primary outcome measure. Secondary outcome measurements were based on objective acoustic analysis of recorded voice samples. The preoperative voice outcome assessment functioned as the control for postoperative tests.

Voice Handicap Index‐10

The VHI‐10 is a validated short version of the 30‐item VHI questionnaire consisting of the ten most robust items12. This questionnaire is used to assess the patient's voice‐related quality of life before surgery and 1 and 3 months after surgery.

Acoustic analysis

Standardized voice recordings were taken in a quiet room with background noise minimized to less than 50 dB and captured with a Quad‐Capture USB sound card (Roland Corporation, Nakagawa, Japan) and an AKG C540 head‐mounted cardioid microphone (Harman International, Stamford, Connecticut, USA), positioned 5 cm from the edge of the lips. The recordings were captured with WavePad audio software 2015 (NCH Software, Greenwood Village, Colorado, USA) at 44 100 Hz, 16‐bit sample rate, and saved as a .wav file. The text and sentences were standardized (Appendix S1, supporting information). Participants were asked to read the Rainbow Passage as a connected speech sample, to produce an /a/ vowel for as long as they could and produce a pitch glide task on /i/. The recordings were analysed for fundamental frequency of connected speech (f0), harmonic to noise ratio on a 4‐s segment of prolonged /a/ vowel (HNR), and minimum and maximum frequency (on the pitch glide task) using the Praat speech tool version 5.3.7513. The speech tool was used for the cepstral peak prominence (CPP) and smoothed cepstral peak prominence (CPPS) analyses, performed on the connected speech sample14. Maximum phonation time (MPT) was taken from the longest /a/ vowel produced in three attempts and was measured in seconds in WavePad once the recording was complete.

Surgical protocol

Thyroidectomy was performed in a standard fashion under general anaesthesia and cervical block; intubation was with the TriVantage® EMG endotracheal tube (Medtronic, Jacksonville, Florida, USA). The patient was positioned supine with a shoulder roll providing neck extension. A cervical incision in a skin crease was performed and the strap muscles were routinely transected, preserving innervation by the ansa cervicalis, and resuturing with a 3/0 polyglactin suture (Vicryl™; Ethicon, Somerville, New Jersey, USA) at the conclusion of the procedure. The LigaSure™ (Medtronic) thermal sealing system was used for dissection and ligation. IONM was performed with the NIM® 3.0 system (Medtronic). Before dissection of the thyroid, the system was checked by vagal response. Visual identification of the EBSLN was carried out as reported previously15 and confirmed using the nerve monitor. A positive result was recorded when strong and simultaneous contraction of the pars recta and pars oblique components of the cricothyroid muscle was observed. The RLN was also identified and dissected over the course of the nerve, with monitoring again used to confirm nerve function. In all patients with loss of signal, contralateral stimulation of the vagus nerve was performed to exclude equipment failure and palpation for a cricopharyngeal twitch on ipsilateral stimulation of the RLN and vagus nerve. Failure to confirm the integrity of the nerve after dissection was recorded.

Statistical analysis

Statistical analysis was performed using SPSS® version 24.0 (IBM, Armonk, New York, USA) data analysis software. Baseline characteristics were described as mean(s.d.) or median (range) values for continuous variables, and as counts with percentages for categorical variables. For continuous variables, differences between groups per time point were calculated with ANOVA for independent samples. The Kruskal–Wallis test was used to compare medians between all groups per time point. The significance of change over time per outcome for continuous variables was determined with the generalized linear mixed model for paired data. VHI‐10 outcomes are ordinal and thus P values were calculated using a generalized estimating equation model for repeated measures. Outcomes with incomplete data over time were excluded from analysis. P < 0·050 was considered significant.

Results

Of 102 patients, 70 (69 per cent) underwent total thyroidectomy and 32 (31 per cent) had a hemithyroidectomy, resulting in a total of 172 EBSLNs and RLNs at risk (Tables 1 and 2). All nerves at risk were identified during surgery, but 23·3 per cent of EBSLNs and 0·6 per cent of RLNs required the assistance of IONM as well as visualization. Nerve integrity was confirmed during surgery for 98·8 per cent of EBSLNs and 98·3 per cent of RLNs. There were no significant differences between median preoperative and postoperative VHI‐10 scores, or in objective outcome measures over the three different time points for all patients combined (Table 3).
Table 1

Baseline characteristics of patients and nerves at risk

No. of patients (n = 102)
Age (years)* 54·5 (21–84)
Sex ratio (F : M)85 : 17
Type of surgery
Total thyroidectomy70 (68·6)
Hemithyroidectomy32 (31·4)
Lymph node dissection15 (14·7)
Indication for surgery
Risk of malignancy43 (42·2)
Goitre43 (42·2)
Thyrotoxicosis14 (13·7)
Other2 (2·0)
Histopathology
Goitre54 (52·9)
Thyroiditis4 (3·9)
Other benign22 (21·6)
Carcinoma22 (21·6)

Values in parentheses are percentages unless indicated otherwise;

values are median (range).

Table 2

Baseline characteristics of nerves at risk

No. of nerves at risk
Right side (n = 82)Left side (n = 90)Total (n = 172)
EBSLN
Cernea classification11
Type 123 (28)44 (49)67 (39·0)
Type 2a42 (51)27 (30)69 (40·1)
Type 2b10 (12)8 (9)18 (10·5)
Missing7 (9)11 (12)18 (10·5)
IONM‐assisted identification20 (24)20 (22)40 (23·3)
Loss of signal1 (1)1 (1)2 (1·2)
RLN
IONM‐assisted identification0 (0)1 (1)1 (0·6)
Not identified0 (0)1 (1)1 (0·6)
Missing2 (2)2 (2)4 (2·3)
Loss of signal3 (4)0 (0)3 (1·7)

Values in parentheses are percentages. EBLSN, external branch of the superior laryngeal nerve; IONM, intraoperative nerve monitoring; RLN, recurrent laryngeal nerve.

Table 3

Results of the objective patient‐reported outcome according to the Voice Handicap Index‐10 over time

Voice Handicap Index‐10 score*
Before surgery P 1 month P 3 months P
Total thyroidectomy0·0150·4640·221
No5·5 (0–29)3·0 (0–29)2·0 (0–19)
Yes1·0 (0–21)2·0 (0–34)1·5 (0–23)
Lymph node dissection0·0220·6500·515
No2·0 (0–29)2·0 (0–34)2·0 (0–23)
Yes0·0 (0–5)3·0 (0–17)1·5 (0–11)
Loss of signal0·4560·5380·888
No1·0 (0–29)2·0 (0–29)2·0 (0–23)
Yes2·0 (0–21)2·0 (0–34)1·0 (0–11)
Cancer0·1750·8050·898
No2·0 (0–29)2·0 (0–34)2·0 (0–23)
Yes0·5 (0–13)4·0 (0–17)2·0 (0–13)

Values are median (range).

Kruskal–Wallis test.

Baseline characteristics of patients and nerves at risk Values in parentheses are percentages unless indicated otherwise; values are median (range). Baseline characteristics of nerves at risk Values in parentheses are percentages. EBLSN, external branch of the superior laryngeal nerve; IONM, intraoperative nerve monitoring; RLN, recurrent laryngeal nerve. Results of the objective patient‐reported outcome according to the Voice Handicap Index‐10 over time Values are median (range). Kruskal–Wallis test. Type of thyroidectomy did not influence objective voice outcomes (Table 3). The preoperative VHI‐10 score was significantly higher in patients who had a hemithyroidectomy or no lymph node dissection. The VHI‐10 score did not change after 1 and 3 months with respect to the different predictors (Table 3). Intraoperative loss of signal in either nerve seemed to be a significant predictor of postoperative change in the VHI‐10 score, although median VHI‐10 changes in patients with and without intraoperative loss of signal showed no clinically relevant differences (Table 3). Patients had a significantly lower f0 (highest) value at 1 month after surgery compared with the preoperative value (461·3 versus 515·2 Hz respectively; P = 0·005) (Table 4). After 3 months there was complete recovery. Overall, all objective voice outcomes showed no changes 3 months after surgery compared with preoperative values (Table 4). Patients who underwent total thyroidectomy had significantly lower f0 (highest) values before surgery and at 1 month compared with those having a hemithyroidectomy. This difference tended to disappear at 3 months (Table 5). There were no differences in acoustic outcomes between patients who underwent lymph node dissection and those who did not (Table 6). MPT was significantly reduced 1 month after surgery in patients who had loss of signal during surgery, but it returned to the preoperative baseline after 3 months (Table 7). CPP and CPPS were significantly lower after 3 months in patients who had loss of signal during operation (Table 7). Histopathological findings were stratified by benign or malignant outcome. Malignant outcome included all cancer subtypes and sizes, with a mean of 22 (range 4–80) mm. Histopathological findings did not influence objective voice outcome measures (Table 8).
Table 4

Overall changes in objective outcome measurements over time

After surgery*
n Before surgery* 1 month3 months P
MPT (s)9917·1(7·1)15·2(6·7)13·4(7·2)0·854  
f0 (Hz)85190·4(51·6)194·6(49·8)194·4(43·4)0·418  
f0 (lowest) (Hz)82128·9(33·1)125·8(38·6)128·3(31·1)0·782  
f0 (highest) (Hz)82515·2(218·9)461·3(200·1)505·5(202·2)0·654  
HNR (Hz)8320·4(3·7)20·3(4·2)20·5(3·8)0·774  
CPP (dB)8012·3(0·8)12·2(0·8)12·3(0·8)0·957  
CPPS (dB)794·2(0·5)4·1(0·5)4·2(0·5)0·307  
VHI‐10992·0 (0–6) 2·0 (0–8) 2·0 (0–6) 0·326§

Values are mean(s.d.) unless indicated otherwise;

values are median (i.q.r.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence; VHI, Voice Handicap Index.

Generalized linear mixed model, except

generalized estimating equation.

Table 5

Objective voice outcome measures for each time point, stratified for type of thyroidectomy (hemithyroidectomy versus total thyroidectomy)

After surgery
Total thyroidectomyBefore surgery* P 1 month* P 3 months* P
MPT (s)0·2640·2280·183
No18·3(7·3)16·5(6·2)15·0(6·6)
Yes16·6(7·0)14·8(7·0)12·9(7·5)
f0 (Hz)0·2740·8650·312
No177·5(66·1)196·0(57·0)187·6(44·6)
Yes190·5(49·6)194·1(48·8)197·4(41·7)
f0 (lowest) (Hz)0·7590·8530·407
No128·5(35·7)125·4(46·4)124·1(34·2)
Yes126·2(33·7)126·9(33·6)130·0(30·1)
f0 (highest) (Hz)0·0400·0260·055
No572·8(250·0)524·1(225·8)567·0(213·1)
Yes478·2(185·9)431·7(193·0)479·7(190·8)
HNR (Hz)0·5130·1570·314
No20·6(2·9)19·5(3·9)20·0(4·1)
Yes20·0(4·7)20·8(4·1)20·1(3·8)
CPP (dB)0·3110·7970·506
No12·1(0·8)12·2(0·8)12·3(0·7)
Yes12·3(0·8)12·2(0·8)12·2(0·8)
CPPS (dB)0·2220·5100·722
No4·1(0·5)4·1(0·6)4·2(0·6)
Yes4·2(0·6)4·2(0·6)4·2(0·6)

Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence.

ANOVA.

Table 6

Objective voice outcome measures for each time point, stratified for lymph node dissection

After surgery*
Lymph node dissectionBefore surgery* P 1 month P 3 months P
MPT (s)0·5470·2120·119
No16·9(6·3)15·0(6·3)13·1(6·9)
Yes18·2(11·3)17·4(9·4)16·4(8·7)
f0 (Hz)0·8360·3500·957
No186·8(53·6)192·8(51·9)194·0(43·2)
Yes183·5(67·4)207·2(47·3)194·7(41·6)
f0 (lowest) (Hz)0·3330·6190·375
No128·2(32·3)125·7(38·3)126·8(31·6)
Yes118·3(45·8)131·6(37·6)135·9(31·7)
f0 (highest) (Hz)0·0140·9900·490
No527·5(211·7)462·4(201·5)515·5(212·0)
Yes374·0(154·0)463·1(123·4)470·2(106·5)
HNR (Hz)0·0500·8510·637
No20·5(4·1)20·3(4·1)20·6(3·9)
Yes18·1(4·1)20·5(3·9)20·1(3·1)
CPP (dB)0·7780·5140·771
No12·2(0·8)12·2(0·8)12·3(0·8)
Yes12·3(0·9)12·1(1·2)12·3(1·0)
CPPS (dB)0·9300·7110·987
No4·2(0·6)4·2(0·5)4·2(0·6)
Yes4·2(0·6)4·1(0·6)4·2(0·6)

Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence.

ANOVA.

Table 7

Objective voice outcome measures for each time point, stratified for intraoperative loss of signal of any nerve

After surgery*
Loss of signalBefore surgery* P 1 month P 3 months P
MPT (s)0·6710·0060·887
No17·2(7·3)15·7(6·6)13·6(7·4)
Yes15·8(2·6)7·2(6·7)13·1(2·1)
f0 (Hz)0·8940·5700·694
No186·2(56·5)194·2(51·8)194·5(43·6)
Yes189·6(27·5)211·4(33·1)186·7(25·9)
f0 (lowest) (Hz)0·4400·9480·472
No126·3(34·6)126·5(38·7)128·6(31·3)
Yes138·5(26·4)125·0(5·9)118·1(37·9)
f0 (highest) (Hz)0·9950·2530·395
No507·1(215·2)466·6(194·6)514·4(204·9)
Yes507·7(116·0)336·7(49·8)434·7(136·2)
HNR (Hz)0·0020·9000·563
No20·5(3·7)20·3(4·0)20·5(3·8)
Yes14·5(8·7)20·6(6·2)21·5(2·1)
CPP (dB)0·1720·1100·039
No12·3(0·8)12·2(0·8)12·3(0·8)
Yes11·8(0·8)11·4(0·8)11·6(1·0)
CPPS (dB)0·1730·4480·039
No4·2(0·6)4·2(0·6)4·2(0·5)
Yes3·9(0·6)3·9(0·3)3·7(1·0)

Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence.

ANOVA.

Table 8

Objective voice outcome measures for each time point, stratified for histopathology outcome

After surgery*
PathologyBefore surgery* P 1 month P 3 months P
MPT (s)0·2340·1970·178
Benign16·7(6·1)14·9(6·4)13·0(6·8)
Malignant18·8(10·1)17·0(8·0)15·4(8·4)
f0 (Hz)0·7150·7330·631
Benign187·4(54·4)193·8(51·9)195·2(43·9)
Malignant182·5(59·9)198·1(50·4)189·9(38·8)
f0 (lowest) (Hz)0·0960·3280·738
Benign129·9(32·2)128·4(36·2)128·6(31·8)
Malignant115·9(39·9)119·0(44·8)125·8(31·1)
f0 (highest) (Hz)0·0670·9440·842
Benign527·5(205·8)461·8(190·9)512·0(217·6)
Malignant432·5(217·7)465·2(209·3)501·3(129·2)
HNR (Hz)0·2430·6140·283
Benign20·5(4·1)20·4(4·1)20·8(3·8)
Malignant19·2(4·4)19·9(4·1)19·8(3·7)
CPP (dB)0·5740·5870·968
Benign12·3(0·8)12·2(0·8)12·3(0·8)
Malignant12·2(0·8)12·1(0·9)12·3(0·8)
CPPS (dB)0·1150·3060·428
Benign4·3(0·6)4·2(0·6)4·2(0·6)
Malignant4·0(0·6)4·1(0·6)4·2(0·6)

Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence.

ANOVA.

Overall changes in objective outcome measurements over time Values are mean(s.d.) unless indicated otherwise; values are median (i.q.r.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence; VHI, Voice Handicap Index. Generalized linear mixed model, except generalized estimating equation. Objective voice outcome measures for each time point, stratified for type of thyroidectomy (hemithyroidectomy versus total thyroidectomy) Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence. ANOVA. Objective voice outcome measures for each time point, stratified for lymph node dissection Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence. ANOVA. Objective voice outcome measures for each time point, stratified for intraoperative loss of signal of any nerve Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence. ANOVA. Objective voice outcome measures for each time point, stratified for histopathology outcome Values are mean(s.d.). MPT, maximum phonation time; f0, fundamental frequency; HNR, harmonic to noise ratio; CPP, cepstral peak prominence; CPPS, smoothed cepstral peak prominence. ANOVA.

Discussion

IONM during thyroid surgery is widely used, frequently employing the standards set by the International Neural Monitoring Study Group7 16. The present study has shown that IONM contributed to reliable identification of the RLN and EBSLN in 0·6 and 23·3 per cent of nerves respectively. The impact of reliable identification of the RLN and EBSLN with IONM correlated with clinical preservation of voice outcome after thyroid surgery. In this cohort, transection of the strap muscles while preserving the ansa cervicalis was routine. The results showed that this element of the surgery did not impair voice outcome. Overall, there were no clinically relevant changes in voice‐related quality of life in the study group regarding patient‐reported outcomes, with a stable median VHI‐10 score of 2·0 before and after surgery, whereas the normal score is less than 7. Objective measurements performed by an independent laryngologist and speech–language therapist also showed no clinically relevant changes in all six variables after surgery. The VHI‐10 score represents the patient's experience of voice changes. Of all clinical factors tested for their influence on VHI‐10 outcomes, none resulted in a prolonged reduction of voice outcome. In contrast to a previous report17 concluding that strap muscle division impairs voice outcome, the present results show that meticulous identification of all nerves is the main contributor to maintaining vocal outcome. Subgroup analyses assessing the influence of lymph node dissection, total thyroidectomy, histopathological outcome and intraoperative loss of signal found no clinically significant changes in voice outcome, despite some reaching statistical significance. None of these, however, appeared to reflect clinically significant or long‐term impairment of vocal function. Nonetheless, CPP and CPPS were significantly lower after 3 months in patients who had loss of signal during operation. This was not the case at 1 month and could not be explained by a mutual reduction after 1 month in combination with lack of recovery for patients with loss of signal. This may be a late result of intraoperative loss of signal. The main limitation of this study was the lack of a control group for direct comparison of the effect of nerve monitoring on voice outcome. The studied cohort was also small. The rare nature of nerve damage means that very large numbers of patients would be needed to generate sufficient power for the study. Cricothyroid electromyography was not performed in this study, although the rate of EBSLN injury was assessed by identification of cricothyroid twitch and indirectly during follow‐up by videostroboscopy. Thyroidectomy with IONM confirmation of postdissection RLN and EBSLN function and routine division of strap muscles resulted in no clinically significant voice change as measured in an independent laryngology clinic.

Disclosure

The authors declare no conflict of interest. Appendix S1 Standardized voice recording/assessment protocol Click here for additional data file.
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Review 1.  External branch of the superior laryngeal nerve monitoring during thyroid and parathyroid surgery: International Neural Monitoring Study Group standards guideline statement.

Authors:  Marcin Barczyński; Gregory W Randolph; Claudio R Cernea; Henning Dralle; Gianlorenzo Dionigi; Piero F Alesina; Radu Mihai; Camille Finck; Davide Lombardi; Dana M Hartl; Akira Miyauchi; Jonathan Serpell; Samuel Snyder; Erivelto Volpi; Gayle Woodson; Jean Louis Kraimps; Abdullah N Hisham
Journal:  Laryngoscope       Date:  2013-09       Impact factor: 3.325

2.  Neuromonitoring of the external branch of the superior laryngeal nerve during thyroid surgery.

Authors:  J Jonas; R Bähr
Journal:  Am J Surg       Date:  2000-03       Impact factor: 2.565

3.  Prospective randomized study on injury of the external branch of the superior laryngeal nerve during thyroidectomy comparing intraoperative nerve monitoring and a conventional technique.

Authors:  Hiroo Masuoka; Akira Miyauchi; Takuya Higashiyama; Tomonori Yabuta; Mitsuhiro Fukushima; Yasuhiro Ito; Minoru Kihara; Kaoru Kobayashi; Osamu Yamada; Ayako Nakayama; Akihiro Miya
Journal:  Head Neck       Date:  2014-10-29       Impact factor: 3.147

4.  Prospective evaluation of the utility of routine neuromonitoring for an established thyroid surgical practice.

Authors:  Jane Lee; Sheila Fraser; Anthony Glover; Stan Sidhu
Journal:  ANZ J Surg       Date:  2016-04-18       Impact factor: 1.872

5.  Voice changes after thyroidectomy: role of the external laryngeal nerve.

Authors:  A E Kark; M W Kissin; R Auerbach; M Meikle
Journal:  Br Med J (Clin Res Ed)       Date:  1984-11-24

6.  Randomized clinical trial of visualization versus neuromonitoring of recurrent laryngeal nerves during thyroidectomy.

Authors:  M Barczyński; A Konturek; S Cichoń
Journal:  Br J Surg       Date:  2009-03       Impact factor: 6.939

7.  Development and validation of the voice handicap index-10.

Authors:  Clark A Rosen; Annie S Lee; Jamie Osborne; Thomas Zullo; Thomas Murry
Journal:  Laryngoscope       Date:  2004-09       Impact factor: 3.325

8.  Identification of the external branch of the superior laryngeal nerve (EBSLN) in large goiters.

Authors:  C R Cernea; S Nishio; F C Hojaij
Journal:  Am J Otolaryngol       Date:  1995 Sep-Oct       Impact factor: 1.808

9.  Neuromonitoring of the external branch of the superior laryngeal nerve during minimally invasive thyroid surgery under local anesthesia: a prospective study of 10 patients.

Authors:  William B Inabnet; Thomas Murry; Shamly Dhiman; Jonathan Aviv; Jean-Christophe Lifante
Journal:  Laryngoscope       Date:  2009-03       Impact factor: 3.325

10.  Randomized controlled trial of visualization versus neuromonitoring of the external branch of the superior laryngeal nerve during thyroidectomy.

Authors:  Marcin Barczyński; Aleksander Konturek; Małgorzata Stopa; Agnieszka Honowska; Wojciech Nowak
Journal:  World J Surg       Date:  2012-06       Impact factor: 3.352

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Review 1.  Improving classification of the external branch of the superior laryngeal nerve with neural monitoring: a research appraisal and narrative review.

Authors:  Yishen Zhao; Zihan Zhao; Daqi Zhang; Yujia Han; Gianlorenzo Dionigi; Hui Sun
Journal:  Gland Surg       Date:  2021-09

2.  Visual and electrophysiological identification of the external branch of superior laryngeal nerve in redo thyroid surgery compared with primary thyroid surgery.

Authors:  Emin Gurleyik; Sami Dogan; Fuat Cetin; Gunay Gurleyik
Journal:  Ann Surg Treat Res       Date:  2019-05-29       Impact factor: 1.859

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