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25 Transanal Minimally Invasive Surgery (TAMIS): Operative Technique, Pitfalls, and Tips
287
Fig. 25.6 The tumor is cauterized in the full-thickness plane. The trac­tion applied to allow easy cauterization of the tissue is well demonstrated
Fig. 25.9 Continued full-thickness dissection on the inferior aspect of the lesion. Notice the excellent hemostasis
Fig. 25.7 Dissection continues on the medial side. Notice the full­thickness dissection
Fig. 25.8 As the dissection continues in the full-thickness plane, trac­tion allow excellent visualization
Specimen extraction should be performed at completion of resection and prior to closure to maintain specimen integrity and avoid accidental proximal migration. The specimen is then pinned in place or marked per surgeon and pathologist preference (Figs.
25.12 and 25.13 ). The majority of plat-
forms accommodate extraction by allowing removal of the faceplate; however, some ports require removal of the entire
Fig. 25.10 Dissection continues in the previously marked lateral boundary to complete the resection
Fig. 25.11 The size of the defect can be appreciated in this defect. It was approximately 40 % of the circumference of the rectum
device with reinsertion for closure. Irrigation of the excision bed with dilute betadine, presumably for its tumoricidal and bactericidal effects, is a common practice. However, no evi­dence-based literature exists to support this technique.
For tumors that are extremely low, in the distal rectum and even abutting the dentate line, a hybrid technique can maintain all the benefi ts of TAMIS and facilitate a superior resection.
288
F. Quinteros et al.
Fig. 25.12 A full-thickness specimen after extraction. The mesorectal fat is evident on the portion of the specimen that was not anterior
Fig. 25.13 Notice the perirectal fat on the posterior aspect of the tumor to confi rm full-thickness resection
Although these can be performed with traditional anorectal retractors to avoid additional expense, we believe that use of a transanal port is extremely advantageous in bulky friable vil­lous tumors, circumferential or near circumferential tumors, or lesions that extend more proximally into the rectum. The distal incision is made prior to port insertion with dissection carried proximally a short distance. This is followed by port deployment and standard excision once the mass is above the anorectal ring, where the port will be seated.
Closure is performed by placing a suture for traction at the midportion of the proximal rectal wall followed by port removal and replacement with an anorectal retractor. Easy closure is permitted with perfect alignment of the rectal wall. There is no consensus as to whether it is necessary to close the remaining mural defect in the rectal wall. Certainly, this can be the most diffi cult component of the operation.
Fig. 25.14 The defect is fi rst re-approximated at the midportion using an absorbable stitch
Extraperitoneal full-thickness resections can be left to heal without closure of the defect. This technique almost certainly arose from the amount of diffi culty and time it took to close a defect with conventional transanal surgery, as well as the common belief that wound dehiscence and abscess are a regular occurrence. Aside from the aesthetic pleasure, the authors recommend closure of all defects with a 2-0 or 3-0 absorbable sutures for postoperative hemostasis. In addition to minimizing bleeding complications, the wound usually remains closed at postoperative offi ce proctoscopy, and this facilitates quicker healing.
Laparoscopic suturing with traditional laparoscopic nee­dle holders is challenging due to the ergonomic diffi culties of suturing within a confi ned space. Wound closure can be performed using interrupted, fi gure-of-eight, or running sutures. Initially, decreasing the insuffl ator pressure by 3–5 mmHg can “shrink” a seemingly daunting defect to one that is more manageable. Defects should be closed from proximal to distal and not side to side to avoid narrowing of the lumen. Given the compliance of the rectal wall, it is uncommon to have to mobilize the proximal rectum to oppose the wound. Dividing the defect into two sections by re-approximating the midportion of the defect can be helpful (Fig. 25.14 ). Intracorporeal knot tying is time consuming and diffi cult and can be avoided using a standard 25 cm lapa­roscopic knot pusher or an automated suture tying device. Alternatively, performing a continuous sutured closure with a barbed suture avoids the need to tie altogether. The use of modern laparoscopic suture devices endoluminally to close defects can dramatically shorten the learning curve and improve precision of closure, but requires increased procedural costs (Endostitch, Ethicon, Cincinnati, OH; LSI, Covidien, CT). With practice, given the minimal increase in operative time and technical diffi culty, the authors feel that closure is warranted to minimize any complications (Fig.
25.15 ).
Entry into the peritoneal cavity is not an uncommon occurrence with anterior-based tumors, especially in women where the peritoneal refl ection is lower and is surrounded by
25 Transanal Minimally Invasive Surgery (TAMIS): Operative Technique, Pitfalls, and Tips
289
Fig. 25.15 The wound is shown nearly closed, with only the last suture requiring a tie. The lumen is clearly visible and is not narrowed with the closure
Fig. 25.16 An anterior rectal mass leading to entry into the peritoneal cavity is shown from an abdominal perspective. The loss of pneumorec­tum made closure not possible transanally and required placement of laparoscopic trocars. The peritoneal wound was closed with interrupted sutures, and the rectum was then re-insuffl ated and closed with inter­rupted sutures as well
less perirectal fat (Fig. 25.16 ). This should be anticipated by tumor localization on preoperative proctoscopic evaluation and appropriate precautions and discussion with the patient. During the early history of TEM, this commonly necessi­tated conversion to laparotomy with the need for resection and frequently colostomy. In addition, the potential for trans­peritoneal seeding in the setting of malignancy was a com­mon concern. More recently, Gavagan demonstrated this to be a low-risk event, which does not mandate conversion [ 21 ]. Obviously, a secure closure becomes mandatory. A two- layer closure of outer peritoneum fi rst followed by full- thickness closure of the rectal wall is recommended. In this scenario, some surgeons have suggested a water-soluble contrast study the following morning prior to discharge. In our experience with peritoneal entry during TAMIS, we have had two cases where insuffl ation failed to maintain distention of the rectum to permit adequate closure. In both of these instances, lapa­roscopy with suture closure of the peritoneal defect from the abdominal side allowed reestablishment of the pneumorectum
Fig. 25.17 The instruments are positioned at a comfortable height
with completion of the closure endoluminally. These patients were discharged the following day without further studies.
Minimal postoperative care with same-day discharge can be accomplished in most patients, except those with exces­sive comorbidities. No postoperative antibiotics are required and patients may resume normal diet and activity immedi­ately. Postoperative surveillance of adenomas over the initial postoperative year can be performed with proctoscopy at regular intervals. Small recurrences can often be removed with endoscopic techniques. Patients with malignancy should be followed by standard NCCN or locoregional guidelines with quarterly follow-up and CEA levels. Serial MRI or endoscopic ultrasound has been advocated for early detection of mural and mesorectal recurrences that tend to occur following local excision; however, no standard guide­lines currently exist. If “salvage” operation is required for patients with more advanced lesions than suspected preop­eratively or with later fi ndings of nodal disease, no negative prognosis has thus far been associated with the initial TAMIS approach followed by abdominal surgical resection in our experience.

Pearls and Pitfalls

• Select your patients wisely, especially at the beginning.
Posterior, <3 cm, mid-rectal lesions are often the best can-
didates. Even if they can be performed by traditional
transanal methods, use TAMIS for increased visualization
and better instrumentation.
• Position the patient and set up the room to maximize
ergonomics. These are complex operations, but will only
become harder if you are uncomfortable with the instru-
mentation and straining (Figs.
25.17 , 25.18 , and 25.19 ).
290
F. Quinteros et al.
Fig. 25.18 An experienced assistant or surgeon is invaluable
• Immediately prior to transecting the fi nal attachments on
the specimen, ensure you have proper orientation prior to
removal to assist in marking the boundaries for pathology.
A grasper placed on the anterior (i.e., distal) midline facil-
itates this process.
• Attempt intracorporeal suturing in easy cases, but don’t
waste time, effort, and frustration—use one of the described
methods above to make things much easier.
• Preoperatively discuss with your patient the potential for
an inability to complete the case purely via TAMIS and
the possibility of abdominal exploration if peritoneal
entry occurs.

Conclusion

Transanal minimally invasive surgery is a feasible technique that has maximized the advantages introduced by minimally invasive techniques and evolving laparoscopic instrumenta­tion. The improved access to the rectum enhances visualiza­tion, improves resection, and extends the upper limits of resection in comparison to traditional transanal excision. TAMIS should be a part of every colorectal specialist’s armamentarium.
Fig. 25.19 Creating space between the different instrumentations pro­vides clear visualization while avoiding collisions
• Ensure you have adequate margins. Marking your bound­aries of resection closer to 1 cm at the onset of the case, especially in your early experience, and ensuring you have a full-thickness excision are imperative. Although the defect will be slightly larger, it is better than the alter­native of positive margins.
• It is imperative that your anesthesiology team has com­pletely paralyzed the patient and continues to re-dose during the procedure as needed. Failure to ensure this is done will compromise your visualization.
• Take care of the troublesome bleeding right away. Don’t let small nuisance bleeding obstruct your visualization.
• Although the lesion is fi xed, be active in changing angles of the camera and of changing which ports your instru­ments and cameras use. Impossible angles typically become very easy when the perspectives are changed.
Disclosures Dr. Quinteros and Dr. Thiruppathy have no disclosures. Dr. Albert is a paid speaker, program director, and consultant for Applied Medical and is a speaker for Lifecell.

References

1. Buess G, Theiss R, Gunther M, Hutterer F, Pichlmaier H. [Transanal endoscopic microsurgery]. Leber Magen Darm. 1985;15(6): 271–9.
2. Atallah S, Albert M, Larach S. Transanal minimally invasive sur­gery: a giant leap forward. Surg Endosc. 2010;24(9):2200–5.
3. Matz J, Matz A. Use of a SILS port in transanal endoscopic micro­surgery in the setting of a community hospital. J Laparoendosc Adv Surg Tech A. 2012;22(1):93–6.
4. Albert MR, Atallah SB, deBeche-Adams TC, Izfar S, Larach SW. Transanal minimally invasive surgery (TAMIS) for local exci­sion of benign neoplasms and early-stage rectal cancer: effi cacy and outcomes in the fi rst 50 patients. Dis Colon Rectum. 2013; 56(3):301–7.
5. Atallah SB, Albert MR. Transanal minimally invasive surgery (TAMIS) versus transanal endoscopic microsurgery (TEM): Is one better than the other? Surg Endosc. 2013;27(12):4750–1.
6. Allaix ME, Arezzo A, Caldart M, Festa F, Morino M. Transanal endoscopic microsurgery for rectal neoplasms: experience of 300 consecutive cases. Dis Colon Rectum. 2009;52(11):1831–6.
7. de Lacy AM, Rattner DW, Adelsdorfer C, Tasende MM, Fernandez M, Delgado S, et al. Transanal natural orifi ce transluminal endo­scopic surgery (NOTES) rectal resection: “down-to-up” total mesorectal excision (TME)-short-term outcomes in the fi rst 20 cases. Surg Endosc. 2013;27(9):3165–72.
8. Marks J, Nassif G, Schoonyoung H, Denittis A, Zeger E, Mohiuddin M, et al. Sphincter-sparing surgery for adenocarcinoma of the distal
25 Transanal Minimally Invasive Surgery (TAMIS): Operative Technique, Pitfalls, and Tips
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3 cm of the true rectum: results after neoadjuvant therapy and minimally invasive radical surgery or local excision. Surg Endosc. 2013;27(12):4469–77.
9. Lee TG, Lee SJ. Transanal single-port microsurgery for rectal tumors: minimal invasive surgery under spinal anesthesia. Surg Endosc. 2013;28(1):271–80.
10. Heald RJ, Moran BJ, Ryall RD, Sexton R, MacFarlane JK. Rectal cancer: the Basingstoke experience of total mesorectal excision, 1978-1997. Arch Surg. 1998;133(8):894–9.
11. MacFarlane JK, Ryall RD, Heald RJ. Mesorectal excision for rectal cancer. Lancet. 1993;341(8843):457–60.
12. Morino M, Parini U, Giraudo G, Salval M, Brachet CR, Garrone C. Laparoscopic total mesorectal excision: a consecutive series of 100 patients. Ann Surg. 2003;237(3):335–42.
13. Hendren SK, O’Connor BI, Liu M, Asano T, Cohen Z, Swallow CJ, et al. Prevalence of male and female sexual dysfunction is high fol­lowing surgery for rectal cancer. Ann Surg. 2005;242(2):212–23.
14. Morino M, Arezzo A, Allaix ME. Transanal endoscopic microsur­gery. Tech Coloproctol. 2013;17 Suppl 1:S55–61.
15. Habr-Gama A, Perez RO, Nadalin W, Sabbaga J, Ribeiro Jr U, Silva E, et al. Operative versus nonoperative treatment for stage 0 distal
rectal cancer following chemoradiation therapy: long-term results. Ann Surg. 2004;240(4):711–7.
16. Zmora O, Dasilva GM, Gurland B, Pfeffer R, Koller M, Nogueras JJ, et al. Does rectal wall tumor eradication with preoperative chemoradiation permit a change in the operative strategy? Dis Colon Rectum. 2004;47(10):1607–12.
17. Salerno GV, Daniels IR, Moran BJ, Heald RJ, Thomas K, Brown G. Magnetic resonance imaging prediction of an involved surgical resection margin in low rectal cancer. Dis Colon Rectum. 2009; 52(4):632–9.
18. Shihab OC, Moran BJ, Heald RJ, Quirke P, Brown G. MRI staging of low rectal cancer. Eur Radiol. 2009;19(3):643–50.
19. Brown G. Thin section MRI in multidisciplinary pre-operative decision making for patients with rectal cancer. Br J Radiol. 2005;78(Spec No. 2):S117–27.
20. McLemore EC, Coker A, Jacobsen G, Talamini MA, Horgan S. eTAMIS: endoscopic visualization for transanal minimally invasive surgery. Surg Endosc. 2013;27(5):1842–5.
21. Gavagan JA, Whiteford MH, Swanstrom LL. Full-thickness intra­peritoneal excision by transanal endoscopic microsurgery does not increase short-term complications. Am J Surg. 2004;187(5):630–4.

Combined Endo-Laparoscopic Surgery (CELS)

Kelly A. Garrett and Sang W. Lee
K e y P o i n t s
• The technique of combined endo-laparoscopic surgery is for patients with benign colon polyps that cannot be removed endoscopically.
• Colonoscopy report and pathology results should be reviewed at initial consultation.
• CO
colonoscopy should be employed in order for this
2
technique to be more often successful.
• The polyp should be localized fi rst endoscopically and its location marked using dilute indigo carmine solution.
• The colon wall adjacent to the polyp can be manipulated laparoscopically to facilitate snare polypectomy.
• If a repair of the colon wall is performed, repair should be leak-tested with the colonoscope.
• Endoscopic-assisted laparoscopic wall excision may be necessary in some locations.
• If there are features of malignancy, the procedure can be converted to laparoscopic colectomy.
• If CELS is successful, but fi nal pathology reveals malig­nancy, patients may go on to require colectomy in the postoperative period.
Electronic supplementary material: Supplementary material is available in the online version of this chapter at Videos can also be accessed at
978-1-4939-1580-4
K. A. Garrett , M.D., F.A.C.S., F.A.S.C.R.S Division of Colorectal Surgery, Department of Surgery , NY Presbyterian Hospital, Weill Cornell Medical College , 525 East 68th Street , Box 172 , New York , NY 10065 , USA
S. W. Lee , M.D., F.A.C.S., F.A.S.C.R.S. ( Division of Colon and Rectal Surgery, Department of Surgery , Weill-Cornell Medical College, New York Presbyterian Hospital, New York , NY , USA
sal2013@med.cornell.edu
e-mail:
.
10.1007/978-1-4939-1581-1_26 .
http://www.springerimages.com/videos/
*)
26

Background

Large colon polyps and those on or behind a haustral fold can be very challenging to remove endoscopically. Although endoscopic mucosal resection (EMR) and submucosal dis­section (ESD) have been performed for these polyps, this technique is not widely available and does not provide a solution for certain polyps [ 1 , 2 ]. For this reason, the most common recommendation for these patients who cannot have their polyps removed through endoscopic means has traditionally been segmental colectomy. There are many studies that demonstrate that laparoscopic colectomy has quicker recovery rates, faster return of bowel function, and earlier return to normal activities in comparison with open colectomy. However, while the laparoscopic approach can minimize the morbidity associated with colectomy, only a minority of the colon resections performed in the United States are being performed laparoscopically [ 3 ]. Furthermore, even if a minimally invasive approach is employed, it still entails a major abdominal operation with the potential for associated morbidities. In place of resec­tion, combined endo-laparoscopic surgery (CELS) removal of the polyps has been described as an alternative in select patients [ 310 ].
The technique of laparoscopic-assisted polypectomy was fi rst described in 1993 as a means to avoid the morbidities asso­ciated with a major bowel resection [ 4 ]. Larger retrospective studies have since been published indicating that the technique is safe and effective [ 3 , 6 , 7 , 1012 ]. The benefi ts of CELS include mobilization of the colon to make the polyp easier to resect with the colonoscope, the ability to directly observe the wall of the colon laparoscopically to ensure there is not a full­thickness defect, the capacity to repair an injury if there is one, and the option of converting directly to a laparoscopic resection if the polyp cannot be resected endoscopically or there are fi nd­ings suspicious for malignancy (Fig. 26.1 ). Many different techniques and approaches have been described including lap­aroscopic-assisted colonoscopic resection, endoscopic-assisted
H.M. Ross et al. (eds.), Minimally Invasive Approaches to Colon and Rectal Disease: Technique and Best Practices, DOI 10.1007/978-1-4939-1581-1_26, © Springer Science+Business Media New York 2015
293
294
K.A. Garrett and S.W. Lee
Fig. 26.1 Combined endo-laparoscopic polypectomy. Laparoscopic manipulation of the bowel wall allows invagination of the bowel wall ( right ) facilitating polypectomy
laparoscopic wedge resection, and endoscopic-assisted laparoscopic resection [ 1315 ]. The largest study to date was performed by Franklin et al., which included long-term fol­low-up of 160 patients with 209 polyps. At a median follow-up of 65 months (range 6–196 months), there were no recurrences of completely resected polyps [ 16 ].

Indications

Current indications for CELS include large benign colon polyps or polyps in a diffi cult anatomic location that are unable to be removed by colonoscopic snare polypectomy. In addition, a similar polyp that has been incompletely removed via traditional endoscopic techniques may be considered for CELS. Patients should have a preoperative colonoscopic biopsy that is benign, although polyps with high-grade dysplasia can be included. If patients have other polyps, they should be able to be removed colonoscopically or with CELS technique. CELS should not be performed on patients with a known polyposis syndrome. Finally, relative contraindications for CELS would include a history of mul­tiple previous abdominal surgeries or polyps that are too close to the ileocecal valve.
elsewhere, it is important to obtain both the colonoscopy and pathology report, and frequently the pathology slides them­selves for internal review. If the polyp is on the left side, it is often useful to evaluate the area in the offi ce with a fl exible sigmoidoscope to determine the exact location, polyp char­acteristics, and feasibility of CELS.
Patients should undergo a preoperative workup as they would for any other abdominal procedure including blood work, electrocardiogram, and chest X-ray. Patients should receive a full mechanical bowel preparation the day prior to the procedure in order to aid in visualization of the polyp. When discussing the procedure, the patient should be informed that colonoscopic polypectomy would be attempted; however, if the polyp cannot be resected endo­scopically or if there are fi ndings suspicious for malignancy, then laparoscopic colectomy will need to be performed. In addition, patients should be made aware that even if CELS is successful in completely removing the polyp, it is possible that the fi nal pathology may reveal a malignancy and that they may require a bowel resection at a later date.

Procedure (Video 26.1 )

Setup

Preoperative Planning

A complete history and physical examination should be done including past medical and surgical history. If the patient has a history of multiple abdominal operations, then CELS may not be feasible. Generally, if the colonoscopy has been done
After the induction of general anesthesia, Venodyne boots, a nasogastric tube, and a Foley catheter are placed. The patient is positioned in modifi ed lithotomy, ensuring the legs are abducted and placed in padded yellow fi n stirrups to facilitate the insertion and manipulation of the colonoscope during the operation. Both arms are tucked at the sides, and the hands
26 Combined Endo-Laparoscopic Surgery (CELS)
295
Table 26.1 Equipment needed for CELS
Adult or pediatric colonoscope with monitor (CO 2 insuffl ation if available) Indigo carmine diluted 50 % with injectable saline Endoscopic injector needle Endoscopic snare Endoscopic Roth net Suction trap Bovie cautery Laparoscopic monitors High-defi nition, fl exible-tip laparoscope Trocars: 5 mm × 4, 10 mm × 1, and 12 mm × 1 Laparoscopic bowel graspers and scissors Laparoscopic needle driver Laparoscopic energy device (surgeon preference) Micro-laparoscopic (3 mm) instruments if available Laparoscopic linear stapler (with appropriate loads) Endo Catch bag (Covidien, Norwalk, CT) Wound protector Polysorb or vicryl sutures
CELS combined endo-laparoscopic surgery
®
(US Endoscopy, Mentor, OH)
and wrists are padded. All equipment should be available to perform colonoscopic polypectomy as well as laparoscopic and open colectomy (though only opened as needed) (Table 26.1 ). Subcutaneous heparin and intravenous antibiot- ics are given prior to incision.
Laparoscopic monitors will be placed depending on the location of the lesion. For right colon polyps, monitors are placed on the patient’s right side and toward the head of the bed (Fig. 26.2 ). For left colon lesions, the monitors are placed at the patient’s left and toward the foot of the bed. For transverse colon or fl exure lesions, the monitors are placed at the head of the bed as the surgeon may stand between the patient’s legs (as will the endoscopist).
Endoscopic equipment may vary. Surgeons may prefer to use pediatric versus an adult colonoscope. In addition, we feel it is a prerequisite to have CO 2 colonoscopy available in the operating room. Simultaneous performance of laparos­copy and colonoscopy with room air can present technical challenges. Insuffl ation using room air can signifi cantly obscure the laparoscopic view and compromise exposure. For institutions where this is not possible, a technique of laparoscopically clamping the terminal ileum to minimize bowel distention during laparoscopy has been described, but we have found that colonic distention alone still is a major impediment to this method [
3 , 4 ]. Since 2003, our group has
been performing colonoscopy with the use of CO 2 insuffl a­tion during laparoscopy. Because the bowel absorbs CO 2 gas approximately 150 times faster than room air, there is mini­mal unwanted dilation of the colon and excellent simultane­ous endoscopic and laparoscopic visualization. We have previously demonstrated that intraoperative CO 2 colonos­copy is safe during laparoscopy and can be used to avoid excessive bowel dilation during CELS procedures [ 9 , 17 ].
Therefore, if available, it is preferred to have CO
for
2
insuffl ation during colonoscopy.
Procedure Steps
Endoscopy
• After the abdomen is prepped and draped in a sterile fashion, CO 2 colonoscopy is performed to locate the lesion (Fig. 26.3 ). We then use dilute indigo carmine solution (50 % dilution of indigo carmine with injectable saline solution) to mark the area directly under and surrounding the polyp.
Port Placement
Initial access : A periumbilical incision is made and the fascia is entered sharply. A 5 mm port is placed and pneu­moperitoneum is established. A 5 mm, high-defi nition, fl exible-tip laparoscope is preferred for better visuali­zation. The abdomen is explored and the site that was previously marked is located.
Secondary trocars : Depending on the location of the lesion, typically two 5 mm trocars may be placed. For right colon lesions, trocars can be placed in the left lower quad­rant and suprapubically. For left colon lesions, trocars can be placed in the right lower quadrant and suprapubically. For transverse colon lesions, trocars can be placed on both sides in both the lower and upper quadrants. If available, micro-laparoscopic (3 mm) instruments are used.
Optional trocars : A 5–12 mm port may be needed for a stapler if a colonoscopic-assisted laparoscopic wall exci­sion is anticipated.
GelPort : For CELS, a hand port is not necessary. However, if converting to a segmental or formal colectomy, then some may elect to place a GelPort™ for hand-assisted laparoscopy.
Mobilization
• For laparoscopic-assisted colonoscopic polypectomy, the lesion is located by the endoscopist, and its position is confi rmed by laparoscopic visualization with the use of transillumination and/or by endoscopic visualization dur­ing laparoscopic manipulation of the colon (Fig. 26.4 ). This maneuver can also expose areas that were not previ­ously visualized because of mucosal folds or segmental kinks of the colon. The location of the polyp in relation to the peritoneum is important. Polyps that are located on the retroperitoneal side or mesenteric side require lateral mobilization of the colon for adequate exposure.
• If the polyp is in a diffi cult location (i.e., at a fl exure or near the mesenteric border of the colon) and this area can­not be manipulated, the colon will need to be mobilized. This is done as in any laparoscopic procedure. We prefer to use an energy device along the line of Toldt and carried in the native planes. Once the colon is mobilized ade­quately, the polyp can then be manipulated.
296
Fig. 26.2 Patient positioning and room setup for a right-sided CELS procedure
K.A. Garrett and S.W. Lee
Fig. 26.3 CO 2 colonoscopy to determine lesion location. With permis­sion from Yuko Tonohira
Fig. 26.4 Laparoscopic manipulation of the bowel wall helps to put the polyp in ideal position for endoscopic removal. With permission from Yuko Tonohira
Fig. 26.5 Endoscopic snare is placed around the polyp while the wall is invaginated laparoscopically. With permission from Yuko Tonohira
Polypectomy
• As stated previously, the polyp is lifted with dilute indigo carmine solution. This aids in visualizing the polyp in comparison to the normal surrounding mucosa and also aids in seeing the location of the polyp laparoscopically. It also provides a “buffer” zone to facilitate endoscopic resection without causing a full-thickness injury.
• Polypectomy is performed using an electrosurgical snare. This can be done using a single attempt or in a piecemeal fashion. For polyps that are either fl at or situated in tough location, laparoscopic manipulation of the polyp during snare polypectomy can facilitate delivery of the polyp into the snare (Fig. 26.5 ).
• During polypectomy, the serosal aspect of the colon should be monitored closely. If there is any subtle change to the area, this can be immediately recognized and then
26 Combined Endo-Laparoscopic Surgery (CELS)
Fig. 26.6 Laparoscopic closure of the bowel wall. With permission from Yuko Tonohira
297
oversewn if needed (Fig. 26.6 ). Typically, seromuscular sutures are placed if a full-thickness thermal injury or per­foration is noted. If there is some evidence of blanching or deterioration of muscle layers, the area can also be rein­forced to avoid the evolution of partial-thickness to full­thickness injuries in the postoperative period. The ability to laparoscopically repair potential damage allows for a more aggressive polypectomy.
Colonoscopic-Assisted Laparoscopic Wall Excision
• For polyps that are located in the cecum where the wall of the colon is the thinnest, one may elect for a laparoscopic sleeve excision of the polyp.
• Colonoscopy is used to locate the lesion and monitor ade­quate surgical margins. It should be noted if polyps are located very close to the ileocecal valve in order to avoid injury to this structure. This can be monitored with the colonoscope.
• Sleeve resection is performed using a laparoscopic linear stapler through a 12 mm port (Fig. 26.7 ). Once the speci- men is removed, it can be placed within an Endo Catch bag (Covidien, Norwalk, CT) and brought out through the 12 mm port site. The specimen can be opened in the oper­ating room to make sure there is a clear margin.
• Oversewing of the staple line can be performed laparo­scopically as needed.
Fig. 26.7 Sleeve resection of a polyp using CELS. With permission from Yuko Tonohira
Leak Test
• A leak test using CO 2 insuffl ation with the colonoscope and immersion of the bowel segment under saline (using gravity to make the correct area dependent) should be performed.