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140
A manual of basic microsurgical techniques
The next stch is placed equidistant to these two on the anterior wall and the gaps
between lled with two to three more stches (Figure 15.7).
Figure 15.7 Completed anterior wall.
On compleon of the anterior wall, the vas is ipped over (this is easy if a double
clamp is used), or alternavely, if this clamp is not available, single clamps can be applied to the long suture ends. These act as weights and help to keep the vas in place for the posterior anastomosis (Figure 15.8).
As before, two sutures are placed at 10 o’clock and 2 o’clock into the vas lumen and
not ed unl both are in place.
Figure 15.8 Posterior wall exposure.
Rat vasovasostomy
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The next stch is placed in the middle of the posterior wall into the seromuscular
layer, leaving one end long. Another one to two sutures are placed alongside this.
To reach the last quadrant, a single clamp can be removed and placed onto the cen-
tral posterior stch. This rotates the vas and makes it easier to place the last one to two sutures (Figure 15.9).
Figure 15.9 Rotating to stitch the last quadrant.
141
On completion, make sure the vas is not twisted and remove the background
material (Figure 15.10).
Figure 15.10 Completed vasovasostomy.
16
The inial dissecon is the same as the for the vasovasostomy. The suture used throughout is 10/0 nylon for the rat and 9/0 for man on a micropoint needle.
Double-armed needles are available that make the anastomosis much easier but are expensive, so for pracce purposes and as some units do not have access to them, single needles are ulised.
In this module the exercise ulises rat testes and the vas is anastomosed using an intussuscepon two-suture transverse technique (modied for pracce in the rat).
Rat epididymovasostomy
Epididymovasostomy clamps
When aempng an epididymovasostomy, it is best to use specially designed double clamps; as menoned, these will make the operaon that much easier but are expen­sive to purchase (Figure 16.1).
Figure 16.1 Epididymovasostomy clamp example.
Advantages:
Reduces operang me
Ends clamp slippage with the use of at-pped, non-penetrang steel spikes
Gentle to mucosa
DOI: 10.1201/9781003413080-16
Rat epididymovasostomy
Данная книга находится в списке для перевода на русский язык сайта https://meduniver.com/
Two-direconal fold that facilitates anterior and posterior wall anastomosis
Adjustable and lockable
Easily stabilised by aaching a haemostat
The epididymovasostomy described here in the rat does not use these clamps, as some units may not have them due to availability or cost.
Various methods are described in the literature, and any of these could be used for training purposes. The method utilised for this exercise is an intussusception two-suture transverse technique. The transverse technique has been chosen, as the epididymis transection is easier to perform on the rat than with a longitudinal incision.
Epididymovasostomy dissection
Normally in man the caput epididymis is used, but in the rat exercise, the cauda is ulised, as the caput is too fragile (Figure 16.2).
143
Figure 16.2 Anatomy.
144
A manual of basic microsurgical techniques
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 16.3).
Figure 16.3 Adventitia removal.
The main vessel underlying the vas can be carefully dissected free, doubly ligated
and cut (Figure 16.4).
Figure 16.4 Dividing the artery of the vas deferens.
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.
Rat epididymovasostomy
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The vas is then transected, leaving a longer ‘stump’ on the vas side (Figure 16.5).
Figure 16.5 Dividing the vas.
145
The vas is then placed adjacent to the cauda.
With scissors, an incision is made in the caudal sac equal to the outside diameter
of the vas (Figure 16.6).
Figure 16.6 Incising the caudal sac.
146
A manual of basic microsurgical techniques
The epididymis tubule is gently freed by blunt dissecon (in man, sharp dissecon
is needed, as the ssue is much tougher) (Figure 16.7).
Two 8/0 monolament nylon sutures are placed on either side of the vas lumen and
ed to secure the vas in place, ensuring there is no tension (Figure 16.8).
Figure 16.7 Exposing the tubule. Figure 16.8 Securing with 8/0.
The end of the vas is then resected to healthy, vascularised ssue and the vas lumen
exposed (Figure 16.9).
Figure 16.9 Exposing the vas lumen.
Rat epididymovasostomy
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Insert one 10/0 suture ~3 mm from the vas end from outside of the vas to the
inside. Bring the needle through to the external vas opening and then transversely into the tubule. Leave the suture uned. Repeat for the other side (Figure 16.10).
Figure 16.10 Insertion of rst two sutures.
Transversely, incise the tubule between the sutures with Vannas scissors, making
the smallest cut possible (Figure 16.11).
147
1
Figure 16.11 Incising the tubule transversely.
Take the needles back into the vas and exit at the original entrance point. Double-e
each stch, ensuring the tubule is invaginated into the vas (Figure 16.12).
Figure 16.12 Invaginating the tubule.
148
A manual of basic microsurgical techniques
With 10/0 sutures placed into the vas muscularis, secure the vas to the caudal sac
along the anterior wall (Figure 16.13).
Figure 16.13 Securing the vas muscularis on the anterior wall.
Complete the posterior wall with 10/0 interrupted sutures to secure the vas to the
caudal sac.
Posion the vas so there is no tension present (Figure 16.14).
Figure 16.14 Completed epididymovasostomy.
Note
1 In man, the suture is normally placed into tubule rst and then out through the vas. This
puts unnecessary strain on a rat tubule, so the preference is to do it the other way a round.
17
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Key points:
Properly maintained instruments are crical to success.
Microvascular transfer has major surgical stress to the paent. Perioperave assess-
ment is important.
High blood ow into and out of the free ssue transfer is the key to success. Vessel
selecon is crical in ensuring success. When possible, use large-calibre vessels.
Seng up the posion of the microscope and the ergonomics of the chair are
important.
Postoperave support for blood pressure, intravascular volume and cardiac support
is important in maintaining good ow through the free ssue transfer.
The rate of successful salvage is inversely proporonal to the elapsed me between
the onset of ischaemia and clinical recognion. Postoperave monitoring is an essenal element of microsurgery.
Clinical practice
Preoperative
Free ssue transfer is a major surgical procedure, with signicant surgical stress. Fluid loss, hypothermia and length of procedure all have signicant eects on suc­cess. Paents must be crically assessed for cardiac, pulmonary and renal status and opmised.
Microsurgical instruments
Operating microscope
The operang microscope should have good opcs, a wide eld of view with a good depth and a strong light source. Other desirable features include binocular tube assemblies with an adjustable angle of inclinaon, an X-Y unit with a wide range of movement in both planes and independent focus and zoom controls for the surgeon and the assistant. An addional useful feature is an aached video camera that allows the scrub nurses and other surgical team members to view the anastomoses for teach­ing and training.
DOI: 10.1201/9781003413080-17