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412 Part III Esophagus
30. Mathisen DJ, Grillo HC, Wilkins EW, Jr, Moncure AC, Hilgenberg AD. Transthoracic esophagectomy: a safe approach to carcinoma of the esophagus. Ann orac Surg. 1988;45:137.
31. Orringer M, Marshall B, lannetioni M. Transhiatal esophagectomy: clinical experience and renements. Ann Surg. 1999;230:392–403.
32. Patil P, Patel S, Desai P. Cancer of the esophagus: esophagogastric anastomotic leak—a retrospective study of predisposing factors. Surg On- col. 1992;49:163–167.
33. Law S, Fok M, Chu KM, Wong J. Comparison of hand-sewn and sta­pled esophagogastric anastomosis after esophageal resection for cancer. A prospective randomized controlled trial. Ann Surg. 1997;226:169–173.
34. Urschel J. Esophagogastrostomy anastomotic leaks complicating esophagectomy: a review. Am J Surg. 1995;169:634–639.
35. Honkoop P, Siersema PD, Tilanus HW, et al. Benign anastomotic strictures after transhiatal esophagectomy and cervical esophagogastrostomy: risk fac­tors and management. J orac Cardiovasc Surg. 1996;111:1141–1146.
36. Swanson SJ, Batirel HF, Bueno R, et al. Transthoracic esophagectomy with radical mediastinal and abdominal lymph node dissection and cervical esophagogastrostomy for esophageal carcinoma. Ann orac Surg. 2001;72:1918–1925.
37. Orringer MB, Marshall B, Chang AC, et al. Two thousand transhiatal esophagectomies: changing trends, lessons learned. Ann Surg. 2007;246(3): 363–372; discussion 372–374.
38. Cope C, Kaiser L. Management of unremitting chylothorax by percutane­ous embolization and blockage of retroperitoneal lymphatic vessels in 42 patients. J Vase Intervent Radiol. 2002;13:1139–1148.
39. Fok M, Cheng S, Wong J. Pyloroplasty versus no drainage in gastric replacement of the esophagus. Am. J Surg. 1991;162:447–452.
40. Bemelman W, Taat C, Slors F. Delayed postoperative emptying after esoph­ageal resection is dependent on the size of the gastric substitute. J Am Coll Surg. 1995;180:461–464.
41. Luketich JD, Alvelo-Rivera M, Buenaventura PO, et al. Minimally invasive esophagectomy: outcomes in 222 patients. Ann Surg. 2003;238(4):486–494; discussion 494–495.
42. Birkmeyer JD, Stukel TA, Siewers AE, et al. Surgeon volume and operative mortality in the United States. N Engl J Med. 2003;349(22): 2117–2127.
43. Dimick JB, Wainess RM, Upchurch GR, Jr, et al. National trends in out­comes for esophageal resection. Ann orac Surg. 2005;79(1):212–216; discussion 217–218.

VIDEO-ASSISTED THORACIC SURGERY OF THE ESOPHAGUS

Ryan M. Levy • James D. Luketich
INTRODUCTION
Since the initial description of laparoscopic fundoplication in 1991, invasive approaches to esophageal disease. While proponents of minimally invasive surgery claim decreases in perioperative pain and length of stay, critics often express concerns over compromised outcomes, prolonged operating times, and increased cost. However, numerous reports have documented that for both gastroesophageal (GE) re ux and achalasia, the laparoscopic approach o ers equal e cacy and safety as well as decreased recovery times compared with traditional open surgery.  ese reports and the bene ts of minimally invasive surgery perceived by the general public have increased referrals to surgeons who o er these approaches to esopha­geal disorders, even though alternative medical therapies are available.
conditions involving the distal esophagus and GE junction are now standard of care, this is not necessarily the case for minimally invasive approaches to the thoracic esophagus.  is is particularly true for esophageal cancer. Concerns regarding the high degree of technical complexity, signi cant operator learning curves, reproducibility of outcomes in lower-volume centers, and equivalence of oncologic outcomes are at the forefront of the discussion. Despite evolving techniques and improvements in both the transhiatal and Ivor Lewis surgi­cal approaches, esophagectomies are complex operations that are associated with signi cant morbidity and mortality. Fur­thermore, surgical candidates are often elderly patients with coexisting medical comorbidities, including respiratory and cardiovascular diseases. Nationwide, the mortality rates from esophagectomies range from 8% in high-volume centers to as high as 23% in low-volume centers.
cases may o er several potential bene ts. First, open esopha­gectomy, even in experienced centers, continues to be associ­ated with a signi cant morbidity, lengthy hospital stay, and
1
there has been continued interest in minimally
2,
4,
5
Although laparoscopic approaches for many benign
6
 e application of minimally invasive surgery to complex
delay in returning to preoperative activities. plication rate along with the disappointing 25% 5-year sur­vival rate after esophagectomy has led to ongoing concern over the role of surgery in the treatment of esophageal cancer. Consequently, for some patients, alternative approaches such as de nitive chemoradiation alone, palliative photodynamic therapy, or stents may be chosen by health care providers. Min­imally invasive approaches to esophagectomy that promise to decrease perioperative morbidity and allow for faster postoper­ative recovery are, therefore, appealing to patients and referring
3
physicians.  e caveat, however, is that the minimally invasive approach should not compromise operative technique or onco­logic and functional outcomes.
 ere has been a signi cant evolution in technique since the initial descriptions of hybrid approaches to esophagectomy that employed thoracoscopic esophageal mobilization with a laparotomy. domized studies of minimally invasive esophagectomy (MIE) have been performed, experience in our  rst 222 patients has suggested that MIE is associated with a com­plication rate and mortality lower than most reports of open esophagectomy. invasive approach reduces postoperative pain and pulmo­nary complications while comparing favorably to the best published open series with regard to morbidity, mortality, and oncologic outcomes. In addition, we and others have shown that minimally invasive staging of esophageal cancer patients is superior to conventional staging by computed tomography (CT) and endoscopic ultrasound (EUS) and may allow for a better selection of patients to receive combined modality therapy. In this chapter, we review our experience with minimally invasive surgery for esophageal cancer, as well as detail surgical techniques for several other diseases of the thoracic esophagus, such as resection of benign esophageal tumors and thoracoscopic treatment of esophageal dysmotility. Laparoscopic approaches to other complex esophageal operations, including achalasia and paraesophageal hernia, are covered in Chapters 14 and 15.
19
7
 is high com-
8–10
Although no ran-
11
In our experience, a minimally
413
12
414 Part III Esophagus
ESOPHAGEAL CANCER
e optimal management of patients with potentially resectable esophageal cancer is still evolving. Although sur­gery remains the standard of care for early disease, several studies have suggested that denitive chemoradiation may be an acceptable alternative. is position is supported by the results of a randomized, prospective trial conducted by the Radiation erapy Oncology Group (RTOG 8501), which compared denitive chemoradiation versus radiation therapy alone for patients with locally advanced esophageal
13
cancer, who were not considered surgical candidates.
e study was closed after accrual of 121 patients, due to a clear survival benet in the combined treatment group. e sur­prising nding in this study was that the 5-year survival in the chemoradiation group was 27%, a rate not appreciably dier­ent from the survival rates following esophagectomy alone.
14
Additional support for the use of chemoradiation for esoph­ageal cancer comes from the results of two, large prospective European studies. In these studies, chemoradiation followed
15,16
by surgery was compared to chemoradiation alone.
In both studies, overall survival was equivalent between the two treatment arms. Chemoradiation with surgery decreased locoregional recurrence within 2 years of surgery. However, with chemoradiation alone, treatment-related mortality was decreased and hospital stays were shorter.
15,16
ese reports have led some clinicians to recommend nonoperative therapy for marginal surgical candidates, such as the elderly or those with multiple comorbidities. Indeed, the National Comprehensive Cancer Network now considers denitive chemoradiation to be an acceptable alternative to
17
esophagectomy in their recent guidelines.
It is incumbent upon esophageal surgeons, therefore, to continue to rene the technique of esophagectomy, in order to oer therapy with either lower morbidity, improved survival, or both compared to traditional esophagectomy and other approaches.
Staging for Esophageal Cancer
Unlike lung cancer, in which mediastinoscopy is an accepted and proven staging technique, no invasive modality is con­sidered standard for staging patients with esophageal cancer. However, to date none of the noninvasive staging techniques currently available, such as CT, EUS, or positron emission tomography (PET), has proven accurate enough to preclude the need for invasive staging. A recent evidence-based review concluded that there exists a benet for laparoscopic staging of esophageal cancer based on level 2 evidence, showing a sensitivity of 71 and 78% for detection of peritoneal and nodal metastasis, respectively. and exceeded sensitivities for endoscopic ultrasound and CT imaging.
e current noninvasive technology suers from several, well-described limitations. CT, often the initial staging test per­formed for patients with esophageal cancer, is an appropriate
18
is compared favorably
tool to screen for distant disease, such as pulmonary or liver metastases. However, even in this role, occult metastatic dis­ease is missed by CT scans in up to 15–20% of patients.
19
Furthermore, CT is clearly unable to provide sucient ana­tomic detail to either accurately stage the depth of invasion of the esophageal wall or determine the presence of local nodal involvement. Indeed, the accuracy of CT scanning for nodal disease is only 45–60% in most series.
20,21
PET scanning is a recently introduced technology that is based on imaging the dierential uptake of radio-labeled glucose by malignant and normal cells. PET scanning has been extensively studied in the context of both lung and esophageal cancer. Indeed in some centers, PET scanning has become a routine component of the preoperative evalu­ation of lung cancer patients. is practice is justied by several meta- analyses that have demonstrated the superiority of PET over CT in staging nodal disease in the mediasti-
22,23
num.
However, equal ecacy for PET scanning has not been demonstrated for esophageal cancer patients. We have found the accuracy of PET scanning to assess locoregional lymph nodes in patients with esophageal cancer to be only
24
about 50%.
e specicity is improved, compared to CT, but the sensitivity remains poor. In our experience PET scan­ning has been more useful in detecting distant metastatic disease. In a series of 100 consecutive patients with poten­tially resectable esophageal cancer staged at our institution by PET and CT, PET identied metastatic disease in 16%
25
of patients missed by CT.
e false-negative rate for PET in this series was only 10% and usually occurred in cases of subcentimeter disease that was below the detection threshold of PET scans.
Another staging tool available in specialized centers is EUS. Although EUS is operator dependent, in experienced hands its accuracy for assessing T stage is greater than 90%, and it
26
has an image resolution of 0.2 mm.
e accuracy of deter­mining T stage increases with penetration of the esophageal wall: the accuracy for T1 tumors is 80%, T2 tumors 90%,
27
and T3/4 tumors 95%.
However, the accuracy of EUS to determine nodal status is far lower than its ability to deter­mine tumor depth and has been reported to be 65–86%.
12,28
Technique of Minimally Invasive Surgical Staging
Currently, all patients at the University of Pittsburgh with a diagnosis of esophageal cancer undergo noninvasive staging with CT scans, PET scanning, and EUS. If any of these studies indicates metastatic disease or nodal involvement (in the case of EUS), a needle biopsy is performed. If distant metastatic disease is proven, palliative options are generally pursued. For patients without proven metastatic disease and GE junction tumors, we then, generally, proceed to laparoscopic staging. Laparoscopic staging is performed with the patient in a steep reverse Trendelenburg position with thesurgeon standing on the patient’s right side.
Chapter 19 Video-Assisted oracic Surgery of the Esophagus 415
OPERATIVE STEPS OF MINIMALLY INVASIVE STAGING—LAPAROSCOPY
1. An initial 10-mm blunt trocar is placed via an open, cut-down technique in the right epigastrium. e loca­tion of this port is approximately 3 cm to the right of the junction between the lower and middle third of a line connecting the xiphoid and umbilicus. After the rst port is placed, a visual assessment is made of the liver and peritoneal surfaces, and, if obvious metastatic disease is present, biopsy conrmation is obtained and the staging is complete. If no metastatic disease is seen on this initial survey, a more thorough staging is performed with place­ment of additional port sites. ese are placed in the same locations utilized for MIE.
2. e ve ports generally include one 10-mm blunt cut-down port just to the patient’s right of midline, midway between the xiphoid and umbilicus (for the surgeon’s right hand instruments), one 10-mm port at the same level to the left of midline for the laparoscope, two additional 5-mm ports along the right costal margin (for liver retraction and dis­section), and one 5-mm port on the left costal margin for countertraction by the assistant (Fig. 19-1). e liver sur­faces are carefully examined and any abnormalities biopsied.
Ultrasound examination of the liver may then be performed, although in our experience, the yield of ultrasound examina­tion in patients who do not have some visual evidence of liver metastases is low.
19
3. e stomach is carefully assessed for gastric extension of the tumor to determine the suitability of the stomach for gastric pull-up.
4. Nodal assessment is initiated by incising the gastrohe­patic ligament. e lesser sac is entered, and nodes along the lesser curve and at the base of the celiac artery are sampled.
5. We have been evaluating preoperative “conditioning” of the esophagus. is may be performed at the time of laparoscopic staging and includes lymph node dissec­tion of the left gastric artery and vein and division with an Autosuture Endo GIA stapler (Covidien, Manseld, MA) with a vascular load. We also divide the short gastric vessels from the left crus to the right gastroepiploic arcade.
6. At the conclusion of the staging procedure, a laparoscopic feeding tube may be placed. However, we have found that, in most cases, dysphagia will respond to chemotherapy, rendering a feeding tube unnecessary. If chemotherapy is planned, an Infusaport is placed at the time of staging.
If the patient has no metastatic disease and minimal or
no nodal disease is apparent on laparoscopy, we proceed to MIE. We have not found routine thoracoscopic staging to be very benecial for most adenocarcinomas of the distal esophagus. oracoscopy is used selectively for tumors of the midthoracic esophagus, once laparoscopic staging has excluded gross intra-abdominal disease. is practice is based on our prospective series of 53 patients all of whom under­went both laparoscopic and thoracoscopic staging. Of the 36 patients with adenocarcinoma of the GE junction, those who were identied as node-positive using minimally invasive
12
staging, 31 were identied by laparoscopy.
If thoracoscopy is indicated, the approach is normally through the right chest, although a left-sided approach may be appropriate if suspi­cious pulmonary lesions are identied on that side.
5 mm
10 mm
5 mm
FIGURE 19-1 Abdominal port placement for staging laparoscopy
and totally minimally invasive Ivor Lewis esophagectomy.
5 mm
10 mm
OPERATIVE STEPS OF MINIMALLY INVASIVE STAGING—THORACOSCOPY
1. Five ports are used for access and placed as depicted
inFig. 19-2.
2. e initial step is to mobilize the inferior pulmonary
ligament and to sample the level 9 nodes.
3. Next, the pleura overlying the lower third of the esophagus
is opened. Once this plane is developed, nodes from the periesophageal (level 8) and subcarinal stations (level 7) may be harvested. Lymph node dissection is continued until a positive node is found or an adequate sampling indicates benign nodes only.
Two large, prospective studies have investigated the benets of minimally invasive staging for esophageal cancer. e rst, from our institution, showed signicant advantages
416 Part III Esophagus
10 mm
5 mm
5 mm
10 mm
10 mm
FIGURE 19-2 oracoscopic port placement for staging and totally
minimally invasive Ivor Lewis esophagectomy.
for minimally invasive staging compared with more standard modalities. and concurrent laparoscopy and thoracoscopy. Forty-seven patients also underwent endoscopic ultrasound. e sensitivities of CT and EUS to document nodal metastases were only 33 and 63%, respectively. Even when these two modalities were combined, inaccuracies in staging were seen in 32% of cases, compared with minimally invasive staging. Only two complications were seen in this series: a prolonged air leakand a port site hernia that was repaired on the rst postoperative day.
e second study, comprising 134 patients, was a multi­institution, National Cancer Institute (NCI)–sponsored study designed to determine the feasibility of minimally invasive staging. as documentation of T4 or M1 disease, the procurement of at least one abdominal and three thoracic lymph nodes, or one node that documented metastatic disease. Minimally invasive staging was successful in 73% of patients and was performed with no mortality and only minimal morbidity. Noninvasive tests, such as CT and EUS, failed to identify positive lymph nodes documented by minimally invasive staging in 20% of patients. Unfortunately, the true sensitivity of minimally invasive staging was not determined by this study because
12
All 53 patients in this report underwent CT
29
Successful minimally invasive staging was dened
the majority of patients underwent induction chemotherapy prior to resection.
Ultimately the role of minimally invasive staging should be claried by clinical trials that demonstrate a survival advantage for patients with node-positive disease who receive induction therapy. To date, most randomized trials have had signicant limitations and demonstrated
30
marginal benets for preoperative chemoradiation.
How­ever, the poor survival obtained after surgery alone ensures that the neoadjuvant approach will continue to be inves­tigated. We believe that a signicant limitation of the studies performed to date is that patients have not been accurately staged prior to undergoing combined modality therapy. Accurate staging may identify a subpopulation of patients who would benet from such aggressive treatment, and studies not designed for subgroup analysis may report false-negative conclusions.
Molecular Staging of Esophageal Cancer
It is estimated that between 30 and 50% of patients who are staged as node-negative by routine histological evalua­tion following esophagectomy will develop a recurrence of
31
their disease.
is suggests that these patients harbored micrometastatic disease that was undetected by routine histology. In an attempt to improve the staging of these patients, we have used minimally invasive staging to obtain lymph nodes that are evaluated with molecular biology techniques, such as reverse transcription polymerase chain reaction (RT-PCR), to determine the presence of micro-
32
metastases. were histologically staged as node-negative.
We evaluated nodes from 30 patients who
33
Of these 30 patients, 11 were identied by RT-PCR as harboring micrometastatic disease. Furthermore, the quantitative expression of carcinoembryonic antigen by RT-PCR was a powerful, independent predictor of disease recurrence and death. We believe that these techniques may identify patients with early-stage disease who have a high risk of recurrence and may benet from additional therapy.
Minimally Invasive Esophagectomy
e technique of minimally invasive esophagectomy (MIE) that has evolved as our experience with other minimally invasive foregut procedures, such as laparoscopic Heller’s myotomy, repair of giant paraesophageal hernia, and staging for esophageal cancer, has grown. At present, minimally inva­sive techniques for esophagectomy include laparoscopic tran­shiatal, laparoscopic-thoracoscopic three-hole (McKeown), and laparoscopic-thoracoscopic (Ivor Lewis) esophagectomy. Each of these can be performed with lymph node sampling or a more complete lymph node dissection. While the choice between approaches is to a large degree based on surgeon pref­erence, the operative approach is at times dictated by anatomic location of the tumor margins.
Chapter 19 Video-Assisted oracic Surgery of the Esophagus 417
Initial attempts at MIE were hybrid operations combining traditional open surgery with minimally invasive techniques. One of the rst reports by Collard et al in 1993 included 12 patients who underwent thoracoscopic mobilization of the esophagus followed by laparotomy and preparation of
9
the gastric conduit.
In that series, two patients required conversion to thoracotomy for bleeding. Several subsequent reports have demonstrated the feasibility of this approach; however no denitive benet has been shown compared to open esophagectomy.
34–36
A completely laparoscopic transhiatal esophagectomy
has also been described. e largest series, published by
37
DePaula et al in 1995,
described 48 patients who required esophagectomy predominantly for end-stage achalasia sec­ondary to Chagas’ disease. Only two patients required con­version to laparotomy. Early experience with MIE in the United States was reported in 1997, when Swanstrom and Hansen described a carefully selected group of nine patients with small tumors, benign strictures, and Barrett’s disease.
38
Eight of these patients had a totally laparoscopic transhiatal
video-assisted thoracoscopic surgery (VATS) procedure.
Similar to these early reports, our initial eorts at MIE were with the transhiatal approach. Advantages of a totally laparoscopic approach include single patient positioning and no need for single-lung ventilation. However, we found that the disadvantages of this approach were signicant. e small working space through the hiatus allowed limited access to the middle and upper third of the esophagus and made any thoracic lymph node dissection extremely di­cult. Because of this, we added a right VATS to mobilize the thoracic esophagus followed by laparoscopy to prepare the gastric tube. To date, we have performed over 1000 MIEs at the University of Pittsburgh Medical Center. For the majority of our initial experience, we utilized a three-hole laparoscopic-thoracoscopic approach. In our earlier publica­tions with this technique, we demonstrated that MIE could be performed safely with equivalent stage-specic survival as compared to the larger open series in the existing literature.
11
ough technically demanding and associated with a signi­cant operator learning curve, data from our series revealed a decrease in operative blood loss, length of stay, pulmo­nary complications, and narcotic requirements. In both our own experience and publications elsewhere, concerns arose regarding an increased incidence of technical complications associated with cervical esophagogastric anastomosis, includ­ing anastomotic leak, stricture, recurrent laryngeal nerve injury, and pharyngoesophageal swallowing dysfunction.
39–41
In light of these concerns and the dominance of GE junc­tion cancers in our current referral pattern, our technique has evolved to a completely laparoscopic-thoracoscopic (Ivor Lewis) esophagectomy with complete lymph node dissec­tion. Unless contraindicated by tumor location or previous thoracic surgery, we presently favor the totally minimally invasive Ivor Lewis approach.
e main criteria favoring the Ivor Lewis approach include the following: (1) e surgical margin aorded by the Ivor
Lewis approach is adequate for almost all GE junction tumors. (2) e technical experience of most training programs in thoracic and general surgery residencies is in the abdomen and chest and not in the neck. (3) e morbidity of recur­rent laryngeal nerve injury is as high as 20–30% with neck anastomosis. (4) e length of gastric conduit needed to reach the neck may be up to 10 cm longer than that needed for an intrathoracic esophagogastric anastomosis. (5) Although easier management of leaks through the neck incision may be considered an advantage of cervical anastomoses, leaks from the neck may still drain into the chest after laparoscopic­thoracoscopic three-hole (McKeown) techniques especially when a narrow gastric conduit is constructed.
Early in our experience, MIE was only oered to patients with Barrett’s disease and early-stage tumors; however, we now oer MIE to patients with more advanced disease. Patients found to have bulky celiac nodal metastases by CT or staging laparoscopy are not felt to be immediate candidates for MIE, and consideration is given to an open operation, a neoadju­vant protocol, or denitive chemoradiation.
Operative Technique
As previously mentioned, our preferred approach has evolved to a totally minimally invasive laparoscopic-thoracoscopic (Ivor Lewis) esophagectomy. e patient is positioned supine on the operating room table with a foot board in place. A double-lumen endotracheal tube is placed for single-lung ven­tilation during the thoracoscopic portion of the procedure. e laparoscopic portion of the procedure is performed rst.
LAPAROSCOPIC PHASE
1. e initial step of MIE is an on-table esophagogas-
troduodenoscopy (EGD) to conrm the precise loca­tion of the tumor, evaluate proximal and distal extent with careful attention to involvement of the cardia, and assess the suitability of the stomach as a conduit for reconstruction. It is important to minimize insuf­ation during the endoscopy as overdistention of the small bowel can complicate the laparoscopic phase of the procedure.
2. e laparoscopic portion of the procedure is then
initiated. e surgeon stands on the right side and the assistant on the left. Five ports (three of 5 mm and two of 10 mm) are placed, similar to the staging procedure (see Fig. 19-1). Initially, we place the 10-mm port via a cut-down technique approximately 3 cm to the right of the junction between the lower and middle third of a line connecting the xiphoid and umbilicus. Carbon dioxide insuation is utilized for pneumoperitoneum to a pres­sure of 15 mm Hg. e remaining ports are then placed: 5cm to the left of the operating port (30-degree camera port), subcostal on the right and left midclavicular lines (tissue grasper ports), and in the right ank (liver retrac­tor port). If clinically indicated, we then perform laparo-
418 Part III Esophagus
Division of gastrohepatic &
Division of
phrenoesophageal ligaments
FIGURE 19-3 Initial dissection, division of gastrohepatic ligament
and crura, hiatal mobilization.
scopic staging as described previously. is lower position of the ports may make the hiatal dissection somewhat dicult but greatly facilitates the mobilization of the gas­tric tube. is emphasizes the importance of completely mobilizing the esophagus and any hiatal hernia sac cir­cumferentially during the thoracoscopic dissection.
3. e gastrohepatic ligament (lesser omentum) is rst divided and the right and left crura of the diaphragm are dissected to mobilize the lateral wall of the esopha­gus (Fig. 19-3). Care is taken not to divide the phreno­esophageal membrane at this point so as to prevent loss of pneumoperitoneum into the chest cavity. e left gastric artery/vein pedicle is identied, and by tracing its course proximally the celiac lymph nodes are then examined. A complete lymph node dissection is carried out to include the celiac nodes, sweeping all nodal and fatty tissue with the specimen; the nodal dissection is later continued along the splenic artery and the superior border of the pancreas during gastric mobilization. is plane continues cephalad toward the right and left crus, continuous with the preaortic dissection plane into the lower thoracic cavity. All lymph nodes are removed, and any lymph nodes suspicious for metastatic involvement are dissected and sent for frozen-section analysis.
4. Gastric mobilization (Fig. 19-4). e dissection is then carried anteriorly and superiorly over the esophagus to nally expose the anterior hiatus. As the dissection is continued toward the left crus, the fundus of the stom­ach begins to be mobilized. e medial border of the right crus is dissected inferiorly until the decussation of the right and left crural bers, thereby exposing a retroesophageal window and completing the mobiliza­tion of the superior portion of the lesser curvature and GE junction. e greater curvature of the stomach is
gastrosplenic lig
& short gastric
vessels
FIGURE 19-4 Gastric mobilization. (Modied from Tsai WS, Levy RM,
Luketich JD. Technique of minimally invasive Ivor Lewis esophagectomy. Op Techn orac Cardiovasc Surg. 2009;14:176–192. Copyright 2009, with permission from
Elsevier.)
then mobilized by rst dividing the short gastric vessels, followed by division of the gastrocolic omentum while carefully preserving the right gastroepiploic arcade (see Fig. 19-4). We utilize either the ultrasonic shears such as Autosonix (Covidien, Manseld, MA) or the LigaS­ure device (Valleylab, Boulder, CO). Occasionally, clips will be required during division of large-diameter, short gastric vessels. Recently, on the basis of published data
42
and personal communication (Dr Earl Wilkins), we have selectively utilized an omental pedicle wrap of the intrathoracic esophagogastric anastomosis. At this point in the operation, we mobilize a long, narrow tongue of omentum from the middle to upper third of the greater curvature. We attempt to base this omental pedicle o of two feeding vessels to ensure viability (Fig. 19-5). After the gastrocolic omentum is identied, the antrum of the stomach is retracted and a window is created in the greater omentum, thus allowing access to the lesser sac. Dissection is carried along the greater curve of the stomach until the end of the gastroepiploic arcade is reached. During this mobilization, it is important to be constantly mindful of the location of the right gastro­epiploic vessel.
5. e mobilized stomach is retracted superiorly, and any remaining adhesions between the posterior wall of the stomach and the pancreas are divided as well. e left gastric vessels are then identied, dissected, and
Chapter 19 Video-Assisted oracic Surgery of the Esophagus 419
Pyloroplasty
ere are often signicant adhesions in the retroantral and periduodenal regions that also need to be dissected to allow for adequate mobilization of the inferior portion of the stomach. Particular attention to mobilization of the pyloric antral area is needed in patients who have had prior cholecystectomy. Adequate mobilization is evident when the pylorus can be gently lifted up to the level of the right crus in a tension-free manner. is may require a partial or complete Kocher maneuver. Two traction sutures are placed at the edges of the pylorus with the 2-0 Endo Stitch (US Surgical, Norwalk, CT). e pyloroplasty is performed by incising the pylorus longitudinally with the
FIGURE 19-5 Creation of omental pedicle ap.
ultrasonic shears and closing it transversely with inter­rupted sutures using the Endo Stitch device in a Heineke­Mikulicz fashion. is usually requires four to ve sutures. Prior to completing the abdominal portion of the proce-
divided with a vascular load of the stapler. is is done by approaching the pedicle from the lesser curve. Prior to division, a complete celiac lymph node dissection is performed, continuing along the superior border of the splenic artery and pancreas toward the splenic hilum. Adherence to oncologic principles is important at this step, so the pedicle should be dissected com­pletely clean with all celiac and left gastric nodes swept up into the specimen.
6. Attention is then turned to mobilization of the pyloric antral area and subsequent pyloroplasty (Fig. 19-6).
dure, a tongue of omentum is mobilized to fashion an omental patch that is sutured to the pyloroplasty site.
7. Creation of the gastric tube. All tubes previously in the stomach or esophagus are pulled back. A 4- to 5-cm-diameter gastric conduit is then constructed using multiple res of the stapler (4.8 mm) beginning from the lesser curve antral area, just proximal to the pylo­rus and heading toward the angle of His (Figs. 19-7 and 19-8). It is essential to avoid excessive manipulation and resulting trauma to the gastric conduit during all steps. To facilitate exposure, staple alignment, and conduit
incision
Pyloroplasty closed
transversely with
auto suture device
Pyloroplasty
A B
FIGURE 19-6 Creation of the laparoscopic pyloroplasty.
420 Part III Esophagus
Surgical
Tumor
specimen
Gentle traction
Divided
left gastric
Gentle traction
5 cm
Creation of gastric tube
Division parallel to greater curvature
FIGURE 19-7 A vascular stapler is red across the lesser curvature near the incisura to begin formation of the gastric tube.
Pyloroplasty
FIGURE 19-8 Completion of gastric tube construction.
Surgical
specimen
Gastric tube
Chapter 19 Video-Assisted oracic Surgery of the Esophagus 421
30 cm distal
length during this step, we have found it helpful to have the assistant gently lift the greater curve of the stomach, along the line of the proximal short gastric arteries and retract gently toward the spleen. Simultaneously, another assistant grasps the antrum and retracts inferiorly. is is accomplished through an additional 12-mm port placed in the right lower quadrant to assist with the creation of the gastrictube. is essentially elongates the entire stomach and provides the alignment necessary to con­struct a consistent diameter gastric conduit without spi­raling. e rst stapler used for this is a vascular load to control bleeding from the adipose tissue and vessels along the lesser curve. e stapler is placed just up to, but not onto, the gastric antrum as this tends to be thicker tissue. e initial 12-mm right midclavicular port is changed to a 15-mm port to allow for the placement of a 4.8-mm Endo GIA stapler. Creation of the gastric tube is then started by dividing the stomach at the lower end of the lesser curve near the incisura using a vascular load (2.5­mm) stapler, with care being taken to preserve the main right gastric vessels and one or two of the rst branches entering the antral area. e stomach is rst divided across the antrum with 4.8-mm staple loads. Because this region of the stomach is generally quite thick and muscular, larger staples are required to secure its closure. Early in our experience, we discovered that very narrow gastric conduits (2–3 cm in diameter) were associated with increased gastric tip necrosis and anastomotic leaks, and therefore we now construct wider conduits measur­ing about 4–5 cm in diameter. Once the thicker antrum has been divided, the operating port is changed back to an 11-mm port and the fundus is divided using a 3.5­mm stapler. As the fundus is divided, the graspers are readjusted to keep the stomach constantly stretched. If
there is extension of tumor onto the gastric cardia, a wider margin is left in this region.
8. Feeding jejunostomy. Under direct vision, a jejunostomy catheter (10F) is then placed using the Seldinger technique as depicted in Fig. 19-9. e patient is placed in the Tren­delenburg position with the transverse colon and greater omentum retracted cranially. e 12-mm, previously placed, right lower quadrant port is used as the operating port while the right upper quadrant epigastric port is used for the camera to facilitate this maneuver. e ligament of Treitz is identied, and approximately 30cm distal to this point, a suitable limb of proximal jejunum is tacked to the lateral, anterior abdominal wall in the left midquadrant with a single 2-0 Endo Stitch. Under direct visualization, a jejunostomy catheter (Compat Biosystems, Minneapolis, MN) is then placed, with intraluminal position conrmed by distending the jejunum with 10 mL of air insuated via the catheter. e jejunum is then securely tacked to the abdominal wall at the catheter entry site with a purse-string type circumferential tacking stitch using a 2-0 Surgidac Endo Stitch. A second simple 2-0 Surgidac Endo Stitch is placed 3 cm distal to the catheter insertion site so as to prevent torsion and possible strangulation around a single xed point (see Fig. 19-9).
9. e tip of the gastric conduit is then secured to the speci­men with 2-0 Endo Stitch (Fig 19-10). During this step, care is taken to maintain alignment so that subsequent retrieval of the specimen through the hiatus into the chest does not lead to any rotation and maintains perfect ana­tomic alignment of the gastric conduit with the short gas­trics facing the direction of the spleen and the lesser curve staple line facing the right chest. With our recent use of omental pedicles, we have also started tacking the omental pedicle wrap to the proximal end of the conduit so as to
FIGURE 19-9 Feeding jejunostomy.
to ligament of
Treitz
One additional
suture placed
into peritoneal wall
20 cm distance
into jejunum