Vessel Sealing Device in Parotid Gland Surgery: Clinical and Pathological Study

Isao Uemaetomari1, Tetsuro Wada1, Bungo Nishimura1, Shuho Tanaka1, Masahiro Nakayama1, Kei Ashizawa1, Keiji Tabuchi1, Yuko Minami2 and Akira Hara1

1Department of Otolaryngology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

2Department of Pathology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

Academic Editor: Vassilios A. Lachanas

Cite this Article as:

Isao Uemaetomari, Tetsuro Wada, Bungo Nishimura, Shuho Tanaka, Masahiro Nakayama, Kei Ashizawa, Keiji Tabuchi, Yuko Minami and Akira Hara (2013), "Vessel Sealing Device in Parotid Gland Surgery: Clinical and Pathological Study," Advances in Cancer Research & Treatment, Vol. 2013 (2013), Article ID 992721, DOI: 10.5171/2013.992721

Copyright © 2013 Isao Uemaetomari, Tetsuro Wada, Bungo Nishimura, Shuho Tanaka, Masahiro Nakayama, Kei Ashizawa, Keiji Tabuchi, Yuko Minami and Akira Hara. Distributed under Creative Commons CC-BY 3.0

Abstract

Facial palsy, salivary leakage and postoperative bleeding are the main complications in parotid gland surgery. To find ways to reduce the occurrence of these complications, we compare traditional methods using the hand-tie ligation technique with a bipolar electrode knife against LigaSureTM Small Jaw, a newly developed vessel sealing device, in parotid gland operations. Eighteen parotid gland tumour cases were retrospectively evaluated. All patients were treated in the University of Tsukuba Hospital, Ibaraki, Japan between January, 2011 and October, 2012. The patient groups were randomly allocated. Surgery was performed in eight cases with LigaSureTM Small Jaw, and ten consecutive cases were done with the conventional dissection technique. The clinical records and histopathological findings were reviewed for each group.In this study we could not find any difference between the two groups in clinical issues. However, difference in histological damage was revealed at the cut edges of the connective tissue, nerve and salivary gland, i.e., less damage to the nerve was observed in the LigaSureTM Small Jaw group. These findings indicated that LigaSureTM Small Jaw was a safe and useful device for parotid gland surgery.

Keywords: Parotid gland, operation, LigaSureTM Small Jaw

Introduction

The LigaSureTM vessel-sealing device (Covidien, Mansfield, MA, USA) is comparatively new equipment, featuring a computer-based, temperature-controlled bipolar electrocoagulation system. So far, LigaSureTM has been mainly applied to chest, gynecological, gastroenterological, and urological surgery (Levy and Emery, 2003; Leonardo et al., 2005; Tsunezuka et al., 2010; Gehrig et al., 2011). LigaSureTM can consistently, reliably and permanently seal off vessels and connective tissue. Thus, it is reported to save operation time by reducing sutures in thyroid surgery (Schiphorst et al., 2012). Although the conventional dissection technique using the hand-tie ligation technique and a bipolar electrode knife has been usual practice, some reports have described use of LigaSure PreciseTM, an earlier model of LigaSureTM Small Jaw, in parotid gland surgery (Prokopakis et al., 2005; Colella et al., 2005; Colella and Giudice, 2006) Shortening of the operative time and decrease in risk of facial nerve damage were reported for using LigaSurePreciseTM (Prokopakis et al., 2005; Colella et al., 2005).The difference between LigaSurePreciseTM and LigaSureTM Small Jaw, which debuted in 2007, is the addition of a cutter. The basic mechanism is considered to be the same, although it is said that performance, such as sealing time, is improved in the new model. LigaSureTM Small Jaw has not been reported as far as we could find.  

Materials and Methods

Eighteen parotid gland tumor cases were retrospectively evaluated. All patients were treated in the University of Tsukuba Hospital, Ibaraki, Japan between January, 2011 and October, 2012. The patient groups were randomly allocated. The operation was performed in eight cases with LigaSureTM Small Jaw (Fig. 1), and ten consecutive cases were done with the conventional dissection technique.

Figure1. LigaSureTM Small Jaw

The clinical records and histopathological findings were reviewed for the nine cases using LigaSureTM Small Jaw and ten cases using traditional methods with respect to complications, operative time, quantities of operative haemorrhage and histological evaluation of the excision stump.

Results

The average patient age in the parotidgland tumor cases using LigaSureTM Small Jaw was 54.5 years. Histologically, pleomorphic adenoma (including deep lobe tumour of the parotid gland) and Warthintumour were included; the mean tumour size was 34 mm. Mean operative time, mean amount of bleeding and mean drain custody period were 140 minutes, 41 ml and3.0 days, respectively. No patient developed complications except for a malignant case with facial paralysis, in which the facial nerve was intended to be sacrificed. On the other hand, the average age of the 10 patients that underwent traditional methods was 50.4 years. Histologically, nine cases of pleomorphic adenoma and one case of Warthintumour were included. Mean operative time, mean amount of bleeding and mean drain custody period were 165 minutes, 15 .6 ml and 3.2 days, respectively (Table 1). One case developed postoperative salivary leakage in this group.

The histological evaluation under hematoxylin and eosin staining of the excision stump of the salivary gland and connective tissue of the two groups revealed that in the LigaSureTM Small Jaw group damage to the tissue was limited to around 1mm and there tended to be less thermal denaturation (Fig. 2A). In addition, in the one malignant tumour case in which a tumour was removed with the facial nerve, it was recognized that histological damage from the stump to the facial nerve was less than approximately 1mm (Fig. 2B). On the other hand, in the traditional methods group the histological damage at the excision stump was slightly more severe than in the LigaSureTM Small Jaw group, and the extension of the damage from the excision stump was over 1.5mm (Fig. 3A). Moreover, in the LigaSureTM Small Jaw group, the excision stump of the salivary gland was shielded from all surroundings with degeneration (Fig. 2C).

Figure 2 A, B, C. Histological Findings of the Surgical Stump of LigaSureTM Small Jaw. Damage to the Tissue was Limited to around 1mm (Arrows) (A). Histological Damage from Stump to the Facial Nerve was Approximately less than 1mm (Arrows) (B). The Salivary Gland was Shielded against all Surroundings with Degeneration (Arrows) (C). HE, bar = 1000μm.

Similarly, degeneration was observed around a suture thread in the traditional methods group, and the degeneration was particularly severe at the site of the inside side of the thread where the pressure of the ligature applied (Fig. 3B).

Figure 3 A, B. Histological Findings about the Surgical Stump in the Traditional Methods Group. Extension of Damage from the Excision Stump was over 1.5mm (Arrows) (A). Degeneration was Particularly Severe at the Inside of the Thread where the Pressure of the Ligature Applied (arrows) (B). HE, bar = 1000μm.

Discussion

Recently, supersonic wave coagulation cutting devices and new energy devices such as LigaSureTM have been used for many operations. However, so far traditional methods like the hand ligation technique and the bipolar electrode knife have mainly been used in parotid gland surgery to avoid facial nerve damage. Therefore, the operation is lengthy, and there are risks such as postoperative bleeding and salivary fistulas when the ligations become loosened. Moreover, ligature left inside the body can pose a risk of postoperative infection. Also, the electrode knife used during parotid gland surgery is well known for its potential to cause nerve damage by heat and direct electric current. Moreover, the possibility of heat damage from the ultrasonic wave surgical knife has also been pointed out (Kim et al., 2008). LigaSureTM Small Jaw could be used instead of hand ligation, because it was reported that heat damage was comparatively slight (Seehofer et al., 2012).

LigaSureTM Small Jaw is called a vessel sealing system. Collagen and elastin are denatured, and then the intravascular lumen is occluded; it fuses the vessel walls, and the blood stream is intercepted. First of all, LigaSureTM Small Jaw senses the tissue at the point of the device, and the best pressure is applied; the main body of LigaSureTM measures the tissue impedance, and an appropriate energy setting is selected. In addition, feedback control and high frequency energy is supplied, and the output is adjusted automatically. The output also automatically stops when the seal is completed, and the tissue is cut with the attached surgical knife by the surgeon’s hand. Generally, heat damage to tissue is believed to spread wide if the voltage is high, like with the electrode knife, and the current is low. Inversely, it is supposed that protein will fuse and integrate in a short time and scorching is suppressed because of the high current and the decreased voltage in LigaSureTM Small Jaw. A lot of experiences of the efficacy of LigaSureTM have been reported in chest, gynecological, gastroenterological, urological surgeryand so on (Levy and Emery, 2003; Leonardo et al, 2005; Tsunezuka et al., 2010; Gehrig et al., 2011).Recently, the number of reports about using ultrasonic wave coagulation cutting devices and an advanced bipolar device such as LigaSureTM has increased for thyroid surgery in the head and neck region (Prokopakis et al., 2010). As for LigaSureTM Small Jaw used in parotid gland surgery, no report has been made until now as far as we could find. We have clinically and histologically examined the effect of using LigaSureTM Small Jaw in parotid gland surgery.

As a comparison with parotid gland surgery using LigaSureTM Small Jaw, ten consecutive cases of parotid benign tumour surgery in our department using the hand ligation technique were examined. The average operation time was 165 minutes, the average amount of bleeding was 15.6ml, and the average drain custody period was 3.2 days with this conventional method. On the other hand, the average operation time was 140 minutes, the average amount of bleeding was 41 ml, and the average drain custody period was 3.0 days using LigaSureTM Small Jaw. Although the cases were limited in number, there was no significant difference between the two groups. However, shortened operation time using LigaSurePreciseTM compared with the traditional methods has been reported. It was considered that because bigger and deeper lobes of parotid gland tumour were included in the LigaSureTM Small Jaw group, therefore excessive blood loss was experienced in these cases compared with the traditional method cases. On the other hand, less bleeding has been reported when using LigaSurePreciseTM than the traditional methods, especially in patient who are at risk of haemorrhage (Prokopakis et al., 2005; Colella et al., 2005). The United States FDA (US Food and Drug Administration) authorizes LigaSureTM for cutting blood vessels and lymphatic vessels up to 7mm in diameter, and the resisting pressure is reported to be three times or more than usual arterial pressure (Kennedy et al., 1998; Heniford et al., 2001; Harold et al., 2003; Dubuc-Lissoir, 2003).Therefore, it was suggested that less bleeding was accomplished. Secure sealing of the salivary duct was also expected in the same way. We had one case of salivary fistula among the ten traditional method cases. Therefore, it was thought that a further investigation would be required concerning salivary fistulain parotid gland surgery using LigaSureTM Small Jaw.

It was mentioned in previous reports (Kennedy et al., 1998; Heniford et al., 200; Harold et al., 2003; Dubuc-Lissoir, 2003) on LigaSureTM use that heat was transmitted from the device to the surrounding structures to the extent of about 1.5-3.3mm. Cell denaturation was limited to about 1mm of the surrounding tissues in our investigation of damage by LigaSureTM Small Jaw to the cutting stump. Preservation of the facial nerve was thought to be possible, if there was a distance of 1mm or more between the cutting edge and the facial nerve. It was reported that facial palsy was also a rare complication after parotid gland surgery using LigaSurePreciseTM (Prokopakis et al., 2005; Colella et al., 2005).

Previous reports said the operation time with LigaSurePreciseTM was shortened. This was supposed to be due to the omission of hand ligation time. Similar to the previous report, in our cases operation time with LigaSureTM had a tendency to be shorter, although the difference was not significant because of the limited number of cases.

Although there were no clinical or histology investigations about its use in parotid gland surgery so far, LigaSureTM Small Jaw was thought to be as a useful  device as LigaSurePreciseTM was reported to be in the past. Regarding complications of parotid gland surgery using LigaSureTM Small Jaw and damage to near organs, coexisting complications such as facial palsy, salivary fistulas and postoperative bleedings were not identified in our study, but the number of cases was limited. According to past reports on LigaSurePreciseTM and our study, LigaSureTM Small Jaw has the potential to reduce complications and shorten operation time. Further research is necessary to investigate the cost-effectiveness of LigaSureTM Small Jaw.  

Conclusion

In this study, complications of parotid gland surgery using LigaSureTM Small Jaw are not identified, though the number of cases is limited. Moreover, histological examination reveals less damage to the nerve at the cut edge of the connective tissue, nerve and salivary gland in the LigaSureTM Small Jaw group. Our findings indicate that LigaSureTM Small Jaw is a safe and useful device for parotid gland surgery.

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