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130
A manual of basic microsurgical techniques
using the angle of incision, the size and grouping of the fascicles and the epineural vascular topography as visual guides to matching.
The epineurium should not be stripped from the nerve segments, as this is important to the vascular supply of the anastomosed nerve.
Grasp the epifascicular epineurium with forceps working under 6–10× magnicaon
and pass a 9/0 or 10/0 suture at the 120° posion. Take 1 mm bites out of the epineurium and pass the needle so that it lies parallel with the surface just beneath the epineurium, not into the perineurium, and taking care not to transx any of the fascicles.
Secure with a double and two single throws, leaving the proximal end long. Repeat
at the opposite 120° point (Figure 14.5).
Figure 14.5 Stay suture placement.
Place the third and fourth sutures between the two stays, tying a simple square
knot and cung both ends short. All subsequent sutures should be simple square knots (Figure 14.6).
The nerve is now rotated about its longitudinal axis using the stay sutures, the long
ends of which are aached to single Acland clamps to hold the nerve in posion (Figure 14.7).
Before suturing the posterior wall, aenon must be paid to the axoplasm. Unlike human nerves, the axoplasm is exuded connuously from the proximal nerve stump and can make the anastomosis dicult to complete. To alleviate this, a few millimetres of the proximal and distal axoplasm are resected, creang an empty epineural ‘pocket’ in which to place the exuding proximal axoplasm. This is not necessary in humans, as the axoplasm does not protrude.
Peripheral nerve repair
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131
Figure 14.6 Anterior wall.
Figure 14.7 Posterior wall.
Care should be taken when tying subsequent sutures that the epineural walls are brought together without involving the neuroplasm. This should be gently ‘tucked’ into the distal pocket as the stches are brought together.
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A manual of basic microsurgical techniques
The h suture is placed at the midpoint posion and the proximal end le long.
The single clamp is removed and placed onto this midpoint suture to ensure ten-
sion; this rotates the nerve and allows placement of the sixth and seventh sutures (Figure 14.8).
The Acland clamp is then moved to the le, sll aached to the midpoint suture;
this then rotates the nerve to the le and allows placement of the eighth and ninth sutures (Figure 14.9).
Figure 14.8 Clamp repositioned.
Figure 14.9 Nerve rotated.
Peripheral nerve repair
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Once the anastomosis is complete, the Acland clamps are removed and the nerve rotated to its original posion. The stay sutures are then cut short, the background material removed and the area irrigated (Figure 14.10).
133
Figure 14.10 Completed nerve anastomosis.
Interpositional nerve grafts
To mimic the clinical situaon in which interposional nerve gras are used to join damaged nerves without undue tension, the rat sciac nerve is removed from one leg via the standard surgical approach and graed onto the opposite limb.
It is possible to harvest between 1.0 and 1.2 cm of donor nerve. With the chicken nerve, 1 cm can be removed, reversed and then anastomosed into the gap.
Excise 0.5 cm of nerve from the recipient side. The nerve stumps will spring back
and create a gap to be bridged of at least 1.0 cm.
The gra is then sutured in posion using the standard epineural anastomosis
described earlier (Figure 14.11).
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A manual of basic microsurgical techniques
Figure 14.11 Nerve graft.
Interfasicular repair
This repair is no longer used in the clinical situaon due to excessive brosis occur­ring within the nerve; however, it is a useful exercise for dissecon and anastomoc purposes, parcularly when wanng to repair nerves at the supramicrosurgical level.
This exercise can also be performed using the chicken nerve.
The sciac nerve is exposed and dissected clear for a sucient length to allow tran-
secon 5 mm proximal to its division into bial, sural and peroneal nerves.
Using the microscope at 10× magnicaon, dissect and roll back the peripheral epi-
neurium for a distance of about 1 mm, then separate each fascicle gently, teasing apart the interfascicular epineurium.
Transect each fascicle.
It is possible to place two sutures 180° apart in the two smaller fascicles, passing the needle (9/0 or 10/0) through the perineurium only. In the larger fascicle, it may be possible to place three sutures (Figure 14.12).
Figure 14.12 Fascicular anastomosis.
15
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This exercise ulises rat testes and the vas anastomosed end to end using a two-layer technique. The same exercise could be carried out on abaoir specimens obtainable from farm animals if available.
Vasovasostomy can be performed in rats as a model for training and research, although the rat vas lacks the thick musculature characteriscs of the human vas.
In man, the vasovasostomy can also be completed either by a single layer of inter­rupted sutures through the whole wall of the vas or by two layers of sutures, one join­ing mucosa to mucosa and the other seromusculature to seromusculature.
The suture used throughout is a 10/0 nylon for the rat and in man 9/0 nylon on a micropoint needle.
The method described is the modied two-layer technique, though other techniques are described in the literature.
Rat vasovasostomy
Vasovasostomy clamps
When aempng a vasovasostomy, it is best to use specially designed double clamps; these will make the operaon that much easier but are expensive to pur­chase (Figure 15.1).
Figure 15.1 Vasovasostomy clamps.
DOI: 10.1201/9781003413080-15
136
A manual of basic microsurgical techniques
Advantages:
Reduces operang me
Ends clamp slippage with the use of at-pped, non-penetrang steel spikes
Gentle to mucosa
Two-direconal fold that facilitates anterior and posterior wall anastomosis
Adjustable and lockable
Easily stabilised by aaching a haemostat
The vasovasostomy described in the rat utilises two single clamps instead of the approximator clamp, as some units may not have them due to availability or cost.
Rat dissection
A vercal incision over the scrotum is carefully deepened unl the tess, epididy­mis and straight poron of the vas are revealed. The whole structure is elevated and placed onto a damp swab to hold it in posion (Figure 15.2).
Figure 15.2 Vas dissection.
Rat vasovasostomy
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Exposing the whole length of the vas gives room for pracsing mulple anastomoses (Figure 15.3).
Anatomy
137
Figure 15.3 Anatomy.
Vasovasostomy: Two-layer method
There are a few dierent techniques described in the literature; the most common is the two-layer or modied two-layer method. Either method can be used for prac­ce; the method used here for training purposes is the modied two layer. This diers from the standard two layer, as the rst two or three stches are placed through the full thickness of the vas deferens, not just the mucosal layer.
Vasovasostomy modied two-layer method
With this method, four (in the rat) to six (in man) sutures are placed through the full thickness of the vas. These sutures ensure that the lumens on both sides of the vas are correctly aligned.
Stches are then placed in the outer layer of the two ends to prevent sperm leakage and potenal scarring or breakdown.
The thick walls of the vas can prevent adequate alignment if anastomosed by the sero­muscular layer alone.
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A manual of basic microsurgical techniques
Vasovasostomy preparation
It is important that the area is kept irrigated throughout the procedure to alleviate dehiscence and to prevent later adhesions.
The advena is gently freed from around the vas (Figure 15.4).
Figure 15.4 Adventitia removal.
The main vessel (artery of the vas deferens) underlying the vas is carefully dissected
free and preserved (Figure 15.5).
Figure 15.5 Preservation of the artery of the vas deferens.
Rat vasovasostomy
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It is important that before the vas is divided any possible bleeding is controlled, as any oozing will obscure the transected end of the vas and make anastomosis more dicult.
The smaller vessel can also be dissected free and preserved (in man) or be ligated
or cauterised in the rat model.
Once the possibility of any bleeding is alleviated, the vas can be placed over a piece
of background material and then divided.
The rst suture is placed at the 10 o’clock posion through the seromuscular layer
and into the lumen on both sides, leaving the stch uned unl the 2 o’clock suture is in posion (Figure 15.6).
139
Figure 15.6 First stitch placement.
Once in posion, the stches are ed and cut.
Due to the thickness of the vas wall, the stches should consist of a double throw
followed by two single throws.
The ends of the vas are again aligned with two 10/0 sutures, this me through the
seromuscular layer at 180°. These are secured, leaving one end of the stch long in each case. These help to manipulate the vessel and place subsequent sutures.