Porcine As a Training Module for Head and Neck Microvascular Reconstruction

Summary

Here we present a protocol for the use of the pig superior epigastric artery perforator flap as a learning module for head and neck microvascular reconstruction.

Abstract

Live models that resemble surgical conditions of humans are needed for training free-flap harvesting and anastomosis. Animal models for training purposes have been available for years in many surgical fields. We used the female (because they are easy to handle for the procedure) Yorkshire pigs for the head and neck reconstruction by harvesting the deep inferior epigastric artery perforator or the superior epigastric artery perforator flap. The anastomosis site (neck skin defect or tracheal wall defect) was prepared via the dissection of the common carotid artery and the internal jugular vein, in which 3.5× loupe magnification was used for anastomosis as we use on human cases in real life. This procedure demonstrates a new training method using a reliable learning model and provides a detailed anatomy in a live scenario. We focused on the ischemia time, harvesting, vessel anastomosis, and designing the flap to fit the defect site. This model improves tissue handling and with the use of proper instruments can be repeated many times so that the surgeon is fully confident before starting the surgery on humans.

Introduction

Reconstruction following surgery for the head and neck malignant diseases is a difficult procedure associated with significant morbidity. Microvascular free-flap reconstruction has been well established as the standard approach to reconstruction for over 20 years^1,2,3. Free-flap transfer plays a significant role in improving the head and neck management in cancer patients and in post-traumatic injuries thereby pushing the boundaries of surgical excision of disease beyond previous techniques, resulting in greater patient quality of life and longer survival rates^1,2,3. The various flaps for reconstruction include rotational, graft, and free flaps.

The role of free flaps in the head and neck reconstruction has expanded. It is the most difficult flap to work with, requiring skilled and delicate handling. Flap failure is a catastrophic event, with significant morbidity^4,5. Thus, considerable training time is required to develop the precision necessary for the successful surgical outcomes^{3,4,5,6,7,8,9}. The steep learning curve associated with such a surgery can influence the outcome for patients and affect treatment management^{3,4,5,6,7,8,9}. To reduce the training time and learning curve for new surgeons, a training model is needed that mimics human biology and provides similar surgical field conditions⁸.

The goal of this study is to show the visibility of Porcine as a good training module for the head and neck microvascular reconstruction resembling the human case with improved skills in the active fashion.

This study investigated the use of a porcine model for training new colleagues in the head and neck microvascular reconstruction for free-flap transfer to provide a cost-effective and less stressful supplement to the clinical field training with reliably similar features for free-flap procedures. Pigs have been used for many studies and as teaching models for various surgical reconstructions, e.g., breast reconstruction;⁵ however, pigs have never been used for head and neck reconstruction except in our study for tracheal reconstruction due to tracheal stenosis¹⁰.

The idea was started after Frederic Bodin⁷, who describe the similar flap for breast reconstruction. The main advantage for the study over the other module of microvascular training is the active livening module with a real immediate result of the procedure.

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Protocol

This study was guided and approved by the Department of Laboratory Animal Resources, Yonsei Biomedical Research Institute, Yonsei University College of Medicine, accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International. This study followed the guidelines for the Care and Use of Laboratory Animals of the Institute of Laboratory Animal Resources Commission on Life Sciences National Research Council. All Pigs were acclimated for One week before the operation.

1. Preparation

1. Keep the pigs without food for over 12 h before general anesthesia with free access to water.
   Note: Six female Yorkshire pigs were used weighing 25–30 kg each.
2. Use a 16 Gauge Needle of 1 cm length to intramuscularly inject alfaxan (1 mg/kg), xylazine (2 mg/kg), and azaperone (2 mg/kg) behind and below the ear to initiate anesthesia.
3. Shave the anterior midline of the neck and the abdominal wall of the pig using a surgical hair removal shaver.
4. Secure an intravenous (IV) route through central or marginal ear vein on the posterior side of the auricle with a 22-G needle. Inject Ketorolac (1 mg/kg) via an IV line.
5. Then inject atropine (0.04 mg/kg) intramuscularly as described in 1.2. Inject cefazolin (30 mg/kg) intramuscularly as described in 1.2.
6. Put the pig lying down in a supine position over the Operating room table.
7. Allow the pig to breath 2 L of oxygen with 5% of isoflurane through Swine anesthesia mask spontaneously.
8. Expose the vocal cords through the mouth by using a laryngoscope and spray them with two puffs of 2% Lidocaine topical solution to prevent intubation-induced laryngospasm.
9. Intubate with a 6.5 mm tube, inflate the tube cuff with 3-5 mL of air using a syringe without a needle attached to it.
   Note: Perform capnometry to ensure that the tracheal tube, which is a part of the anesthesia machine, is in proper position and there is CO₂ back to the machine as an indication of proper oxygenation.
10. Maintain the anesthesia after the intubation with 2% isoflurane.
11. Use the vet ointment on pig’s eyes and close it with an eye cover patch.

2. Procedure: Reception Site

1. Disinfect the neck and the abdominal wall with the iodine-based scrub solution 1%.
2. Start a vertical midline incision in the anterior neck using blade No. 23 up to the sternum.
3. Dissect the strap muscles and retract it laterally using Kelly tissue scissor and Lahey retractor.
4. Expose the trachea from the first ring to the thoracic inlet.
5. Then, expose the common carotid artery and the internal jugular vein for the anastomosis.
6. Create a window in the second or third tracheal cartilage, ~1 cm in width using blade no. 11.
7. Look for the endotracheal tube through the tracheal defect created, and make sure the aeration through the tube is continued using the ventilator without a leak.

3. Procedure: Flap Site

Note: The superior epigastric artery perforator (SEAP) flap harvest can be performed, according to the method described by Frederic Bodin⁷.

1. Design a flap on the upper abdomen by a surgical marker pen (Figure 1A).
2. Create an elliptical Skin incision 4 x 3 cm using a No. 23 scalpel to the anterior sheath of the abdominal wall on the medial side of the drawn flap (Figure 1B).
3. Elevate (peel) the Flap from the rectus abdominis muscle sheath looking for the perforators going to the skin flap while holding the fascia by the allis.
4. Perform the intramuscular dissection and follow the perforators to the superior epigastric vessels (Figure 1B)
5. Now perform the lateral skin incision on the designed flap (Figure 1A) using a No. 23 scalpel (Figure 1C)
6. Clamp the superior epigastric vessels and venae comitantes with the hemostat superiorly and use Kelly tissue scissors to cut below the hemostat and ligate the vessel above the hemostat by 3-0 suture. Then take off the hemostat.

4. Anastomosis and Closure

1. Put on a surgical loupe.
2. Clamp the Carotid artery using two hemostats with 1-2 cm distance between them.
3. Use micro-scissors to cut between the carotid artery and tie the superior part by double suture insure no oozing.
4. Use the double clamp without the frame between the carotid artery and flap artery.
5. Start anastomosis by using 10-0 suture simple full thickness interpreted.
6. Place the first two stay sutures approximately 120 degrees apart on the vessel’s circumference then in between place 2-3 stitches.
7. Release the clamp. If there is blood oozing do the similar suture at the oozing site.
8. Look for the venous back flow from venae comitantes.
9. Perform anastomosis as described in step 4.1 to 4.7 for the internal jugular vein and venae comitantes (Figure 1D).
10. Use a syringe needle size 18 to prick the skin to ensure flap viability by seeing a blood drop.
11. Close the tracheal window and suture it with the muscle fascia of the SEAP flap using 3-0 suture.
12. Exteriorize and suture a skin paddle of the SEAP flap to the cervical midline skin incision (Figure 2A).
13. Close the abdominal skin incision (Figure 2B).

5. Post-operative Care

1. Get the pig back into the prone position.
2. Stop the isoflurane and wean the pig from the ventilator.
3. Allow the pig to recover in the animal cage and monitor it closely to ensure its smooth recovery from the procedure.
4. Look for the flap at reconstruction site after healing (Figure 2C).
5. Look at the donor site in the animal after healing (Figure 2D).
6. Start Ringer's lactate at the rate of 150 mL/h until full recovery and administer 0.3 mg buprenorphine for analgesia.
7. Following extubation, monitor the pig closely until it has regained sufficient consciousness to maintain position and breathing and is able to drink spontaneously.
8. Keep the post-surgery pigs in separated place from no operated animals.
9. Start intramuscular amoxicillin–clavulanate (14 mg/kg) for 1 week.
10. Start intramuscular Meloxicam (0.2 mg/kg) for 1 week.

6. Euthanasia

1. Start anesthesia for the pig by injecting propofol through i.v. (5-10 mL) and maintain it with isoflurane 5%.
2. Intubate the pig as described on step (1.1, 1.2, 1.6-1.10).
3. Induce the cardiac arrest by intravenous injection of 40 mmol KCl.

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Results

We performed the procedure on six pigs: cervical skin defect reconstruction on two pigs, tracheal reconstruction on two pigs, and free flap to test vascular anastomosis device in two pigs. The pigs were monitored for 3 months and there was no clinical sign of neurological deficit.

The mean time for ischemia was 50 min (range, 35-80 min); the time decreased as the procedure was repeated. The mean harvest time of the six pigs was ...

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Discussion

Significant morbidity and defects can occur in head and neck malignancy patients during surgical management. Microvascular free tissue transfer has become essential for reconstruction in most cases. The viability of the flap is a critical issue, requiring steadiness, precise handling of the pedicle, tactile sensation, visuospatial ability, and excellent operative flow from the surgeon⁸. To develop these skills, one needs extensive practice with a training model^3,...

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Materials

Name	Company	Catalog Number	Comments
Pigs XP Bio, Seoul, South Korea
Surgical Hair Removal shaver	3M
22 gage catheter	B.BRAUN
syring with needle size 18	Jung Rim Medical
Intramuscular alfaxan	Careside		10ml/VAL
Intramuscularxylazine	Bayer
Intramuscular azaperone	Sigma-aldrich		34223
Intramuscular atropine	Daewon		0.5mg/A
Intramuscular cefazolin	Yuhan		1g
intravenous Ketorolac	Hana Pharm		30mg
Swine ansthesia mask	DRE		1392
endotracheal cuff tube 6.5 mm	SMITH medical		100/150/065
ansthesia Machine	Dräger		PRIMUS IE
2% lidocaine topical solution	Taejoon
vet ointment	Pfizer		terramycin
eye cover patch	Innomed		S-universal010S
betadine solution 1%.	Korea Pharma
gauze 4*4	First Medical		22*30CM 320S
blade No. 23	Paragon		23
lahey retractor	V.Mueller		SU3960
kelly tissue scissors	SOLCO		05-1990
blade No. 11	Paragon		11
surgical marking pen	Aspen Surgical		Regular #2750
allis	V.Mueller		SU4055
tie suture	Covidein		non-needle
3.5× surgical loupe	zeiss		eyemag smart
double clamp without frame	V.Mueller		CH7155
microscissors	AESCULAP		FD038R
Ringer's lactate	Daehan		500ml/1bag
amoxicillin–clavulanate	Ilsung		0.6g/V
Meloxicam	Samil		7.5mg
propofol	Dong Kook		120mg/V
intravenous KCl solution	Daehan		20ml/50P
mosquito curved	SOLCO		013-0111
mosquito straight	SOLCO		05-1050
ethilone 10-0 suture	ethicone		10/0W1756
Vicryl 3-0.	ethicone		3/0W9890
buprenorphine	Hanlim		0.3mg