Methods: Newly sacrificed six sheep hemithoraces were studied between August 2016 and October 2016. Thoracic sympathectomy was performed by clipping at T2, T3, T4, and T5 sympathetic chain levels and their branches. Electrophysiological studies were performed with an electromyography device and the filter range was 1 Hz with 20 ?V/D amplification. Signals were processed digitally; bipolar subdermal needle electrodes were used as stimulation and recording electrodes (Ø 0.75 mm); and the ground electrode was placed in the intercostal muscle where the thoracic sympathectomy procedure would be performed.
Results: Electrophysiological evaluations showed that clips placed on the main sympathetic chain branches and sympathetic nerve trunk prevented collateral impulse conduction and stimulated potentials were not recorded. However, sympathetic conduction continued at the same intensity after removal of the clips.
Conclusion: Clipping of different regions of the sympathetic nerve provides electrophysiological blockage of the sympathetic nerve, and conduction continues after removal of the clips. However, the shortand long-term postoperative electrophysiological results after removal of the clips over the sympathetic nerve is still a question mark.
Thoracic sympathectomy is performed as resection, ablation or division of the thoracic sympathetic chain to prevent adrenergic effect of the arms.[1,2,5,11-14] In recent years, for the treatment of hyperhidrosis, the application of metal clips to the sympathetic chain has become widespread.[15-18] Compensatory sweating is the most common complication of TS.[4,5,7,8] If the complication occurs, the metal clips should be removed and nerve conduction should be restored.[6,8,17]
In the present study, we aimed to examine the efficacy of clipping in TS based on electrophysiological evaluation and to investigate whether nerve conduction could be formed by collateral nerve extensions as a result of the clipping procedure to different levels of sympathetic nerve.
After a median sternotomy, the visibility of both hemithoraces was achieved, and care was taken not to damage the nerves and ganglia of the sympathetic system during removal of the other thoracic organs. Following dissection of the parietal pleura, TS was performed by applying a single titanium clip at the T2, T3, T4, and T5 levels of the sympathetic chain with the aid of a right-angled, U-shaped endoscopic multiple clip applier.
Thoracic sympathectomy was applied to the first cadaver by clipping from T2 and T3 levels in the right hemithorax and T3 in the left hemithorax. The clips were, then, applied on the right hemithorax of the second cadaver at the level of T4 and T5 and at the level of the lower branch sympathetic chain of the left hemithorax. In the third cadaver, the clips were applied at the T3 level of the right hemithorax and at the T3 level lower branch sympathetic chain in the left hemithorax (Figure 1).
Electrophysiological studies of all sympathetic nerves were performed using the Medtronic Keypoint 4 (Medtronic Inc., MN, USA) electromyography device. The filter range was 1 Hz with 20 ?V amplification. In addition, the signals were processed digitally to minimize artifact. Bipolar subdermal needle electrodes were used as stimulation and recording electrodes (Ø 0.75 mm). The ground electrode was placed in the intercostal muscle where the TS procedure would be performed. To evaluate the different levels of sympathetic nerve activity in each hemithorax, a disposable bipolar needle electrode was placed on the nerve branch in the direct sympathetic chain through an invasive method to stimulate the nerve. Stimulated potentials from the caudal end of the nerve were recorded by stimulating at a current intensity of 10.4 to 10.6 mA and 1 ms from the cranial end of the sympathetic nerve branch. The sympathetic nerve was tested with the same stimulation technique for the presence of conduction before, after, and after removal of the clip. Observation of stimulated potentials after stimulation was interpreted as conduction, and the absence of potentials was interpreted as non-conduction. The sympathetic nerve stimulation study is given schematically in Figure 1.
In the left hemithorax, stimulation was continued after the clip was placed on the lower branch of the sympathetic nerve at the T3 level. After the second clip was placed on the sympathetic nerve trunk, the nerve conduction was not continued despite stimulation at the same intensity. When the clip placed on the main branch was removed, the nerve conduction continued.
The second cadaver
In the right hemithorax, before TS, the sympathetic
nerve was stimulated with 10.6 mA intensity and
recording was obtained. The clips were applied to
the T4 and T5 sympathetic nerve levels, which were
used for the treatment of axillary hyperhidrosis. After
the clip was placed on the main nerve branch, the
stimulated potentials of the same intensity could not
be recorded. In direct nerve stimulation after removal
of the clip, evoked potentials were evident and the
conduction was maintained (Figure 2).
In the left hemithorax, when the clip was placed on one of the lower sympathetic branch of the T4 ganglion and stimulated with 10.6 mA stimulus, the clipping process did not block the conduction and the conduction continued. However, after the second clip was placed on the sympathetic nerve body, the nerve conduction did not persist despite stimulation of the same intensity. When the clip placed on the main branch was removed, the conduction continued.
The third cadaver
In the right hemithorax, before TS, the sympathetic
nerve was stimulated at 10.4 mA and recordings were
obtained. The clips were placed in the main branch
of the sympathetic nerve originating from the T3
ganglion, which was used in the treatment of palmar
hyperhidrosis, and the conduction discontinued. After
removal of the clip, the conduction continued.
In the left hemithorax, the stimulation continued, when the clip was placed on the lower nerve branch of the T3 ganglion. After removal of the clip from the main nerve branch, the evoked potentials could not be recorded from the caudal parts of the clipping nerve.
The localization of the clips on the sympathetic chain and the electrophysiological findings of the efficacy of the clipping on sympathetic chain are given in Table 1.
Table 1: Clip localization on sympathetic chain and electrophysiological findings of clipping
In the treatment of primary hyperhidrosis, the nerve is clipped with titanium clips to prevent the conduction of sympathetic nerve stimulation.[6,7,11] In a study, although 11% of patients had relapse over a five-year period, the clinical outcomes were similar to resection (sympathectomy) or sympathetic chain transection (sympatheticotomy).[17] It is well documented that the use of metal clips is preferred over other methods, since it is theoretically thought that nerve stimulation can be achieved by removing the clips, when undesirable side effects develop.[11,17,18] Considering its widespread use in surgery and favorable results reported in the literature, we performed sympathectomy with clips. Sympathectomy by clipping allows nerve blockage without traumatizing the nerves. In another study, nerve conduction was shown to be prevented with a pressure of 44 g on the nerve and the pressure applied by the clips was about 150 g.[18] However, whether the nerve conduction can be restored after the removal of the clip is still controversial.[17]
Previous studies have demonstrated that the application of clips in the rabbit sympathetic nerve causes degeneration of the nerve after 48 hand that the nerve degenerative process continues after the removal of the clip.[18] However, it has been suggested that if the clip is removed within two weeks following application, conduction can continue successfully.[8] In this electrophysiological study, we observed that the transmission of stimulation in the sympathetic nerve occurred again shortly after removal of the clip. In addition, in the histological results of our previous study,[6] the regenerative histological process and nerve conduction continued after the removal of the clip.
Surgical intervention to T2 sympathetic nerve ganglion is widely used in the treatment of palmar hyperhidrosis.[1,5] However, since T3 and T4 nerves provide branches to the T2 ganglion, surgical interventions involving T3 and T4 are also recommended to prevent axillary and palmar hyperhidrosis.[18] In a TS study, sympathetic chain ablation from the T3 level was reported to be the optimal procedure for palmar hyperhidrosis.[14] In the present study, the clip applied to any side branches of the sympathetic chain did not block the sympathetic conduction alone and that the clip should be applied on the sympathetic chain. In addition, since the present study was ex-vivo, there was no clinical evaluation of whether the sympathetic nerve locations selected for clipping were suitable for recurrence and compensatory hyperhidrosis.
Since the current data regarding sympathetic nerve surgery includes subjective results, more useful comparisons cannot be made between the studies.[12] To illustrate, it has been reported that the nerve conduction study in the sympathetic truncus cannot reveal reproducible evoked potentials, although nerve conduction in the phrenic and sural nerves is measured using the same stimulation technique.[17] This finding indicates that cadaveric sympathetic nerve conduction study may lead to non-invasive electrophysiology evaluation of conduction presence during and after sympathectomy with clips.
In conclusion, clipping of different regions of the sympathetic nerve provides electrophysiological blockage of the sympathetic nerve, and conduction continues after removal of the clips. However, the short- and long-term postoperative electrophysiological results after removal of the clips over the sympathetic nerve is still a matter of debate.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
This study was supported by the Scientific Research Project
grant of Bursa Uludag University, Faculty of Veterinary Medicine
(Project no: BUAP(V)-2015/3).
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