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- •Contents
- •Contributors
- •Preface
- •1. A Focused History of Surgery
- •2. Preoperative and Postoperative Management
- •3. Endoscopy and Endoscopic Intervention
- •4. Fundamentals of Laparoscopic Surgery
- •5. Laparoscopic Staging and Approaches to Cancer
- •6. Incisions, Closures, and Management of the Abdominal Wound
- •7. Hernias
- •9. Intestinal Stomas
- •10. Abdominal Abscess and Enteric Fistulae
- •11. Gastrointestinal Bleeding
- •12. Management of Abdominal Trauma
- •13. Abdominal Vascular Emergencies
- •14. Benign Esophageal Disorders
- •15. Gastroesophageal Reflux Disease and Hiatal Hernia (Including Paraesophageal)
- •16. Perspective on Benign Esophageal Disease
- •17. Cancer of the Esophagus
- •18. Surgical Procedures to Resect and Replace the Esophagus
- •19. Video-Assisted Thoracic Surgery of the Esophagus
- •20. Perspective on Malignant Esophageal Disease
- •21. Benign Gastric Disorders
- •22. Gastric Adenocarcinoma and Other Gastric Neoplasms (Except Gastrointestinal Stromal Tumors)

92 Part I Introduction
A laparoscopically assisted method is suitable in thin
patients. Two stay sutures are placed on either side of the
anastomotic defect. ese sutures are cut long. e 12-mm
trocar is removed, and the incision is enlarged to 20 mm.
Using retraction on the stay sutures, the newly created biliary-enteric anastomosis can be exteriorized and the enterotomy closed in a standard fashion. When this is completed,
the bowel is returned to the abdominal cavity, and the wound
is closed. e abdomen is reinsuated and the anastomosis inspected. is technique allows for the construction of
a 2.5-cm cholecystojejunal anastomosis without any bowel
narrowing. No intra-abdominal drains are used.
e technique for fashioning a gastrojejunostomy is
similar. In this case, a proximal loop of jejunum is brought
in an antecolic position to the stomach. e left upper
quadrant 5-mm laparoscopic trocar is converted to a 12-mm
trocar. Two 3-0 coated, braided lactomer sutures (Polysorb,
US Surgical) are used to approximate the jejunum to the
stomach. Enterotomies are made in both stomach and jejunum. In cases in which there has been a signicant period of
gastric obstruction, the gastric wall may be hypertrophied,
making creation of the gastrotomy dicult. Conrmation
that one is inside the stomach is required before placement
of the stapler. When this is achieved, a 30-mm linear stapler is inserted through the 12-mm left upper quadrant port
and manipulated into both enterotomies. e instrument is
positioned and red. e stapler is removed and reloaded,
returned into the anastomosis, and rered. is creates an
anastomosis approximately 5 cm in length. e anterior
defect can be closed in a fashion similar to the cholecystojejunostomy (Fig. 5-19). Any defects in the anastomosis can
be repaired with individual 3-0 sutures.
e ideal palliative procedure for biliary or gastric obstruction should be eective in relieving jaundice or GOO, have
minimal morbidity, be associated with a short hospital stay,
have a low symptomatic recurrence, and maintain quality of
life. Laparoscopic procedures have the potential to achieve
FIGURE 5-19 Laparoscopic gastrojejunostomy.
these goals, although data do not support prophylactic
bypass procedures in patients who do not otherwise require
surgery.
SUMMARY
Laparoscopy is no longer a tool of limited use and now has
widespread indications within surgical oncologic practice.
Despite improvements in noninvasive imaging, there is still
an added value to use LS in selected patients with upper
gastrointestinal cancers. In the future, the combination of
NOTES technology and MIS techniques oers further exciting potential to enhance staging of these patients.
REFERENCES
1. Samee A, Moorthy K, Jaipersad T, et al. Evaluation of the role of
l aparoscopic ultrasonography in the staging of oesophagogastric cancers.
Surg Endosc. 2009;23(9):2061–2065.
2. Muntean V, Mihailov A, Iancu C, et al. Staging laparoscopy in gastric
cancer. Accuracy and impact on therapy. J Gastrointestin Liver Dis.
2009;18(2):189–195.
3. De Gra GW, Ayantunde AA, Parsons SL, Duy JP, Welch NT. e role
of staging laparoscopy in oesophagogastric cancers. Eur J Surg Oncol.
2007;33(8):988–992.
4. Hemming AW, Nagy AG, Scudmore CH, et al. Laparoscopic staging of
intra-abdominal malignancy. Surg Endosc. 1995;9:325–328.
5. Van Delden OM, De Wit LT, Bemelman WA, et al. Laparoscopic ultrasonography for abdominal tumor staging: technical aspects and imaging
ndings. Abdom Imaging. 1997;22:125–131.
6. Buyske J. Role of videoscopic-assisted techniques in staging malignant
diseases. Surg Clin North Am. 2000;80:495–503.
7. Pratt Bl, Greene FL. Role of laparoscopy in the staging of malignant
disease. Surg Clin North Am. 2000;80:1111–1126.
8. Schoonderwoerd L, Swank DJ. e role of optical access trocars in
laparoscopic surgery. Surg Technol Int. 2005;14:61–67.
9. Kamangar F, Dores GM, Anderson WF. Patterns of cancer incidence,
mortality, and prevalence across ve continents: dening priorities
to reduce cancer disparities in different geographic regions of the
world. J Clin Oncol. 2006;24(14):2137–2150.
10. Jemal A, Siegel R, Ward E, et al. Cancer statistics. CA Cancer J Clin.
2008;58(2):71–96.
11. Aibe T, Fuji T, Okita K, et al. A fundamental study of normal layer
structure of the gastrointestinal wall visualised by endoscopic ultrasonography. Scand J Gastroenterol. 1986;21:6–15.
12. Tio TL, Tytgat GNJ. Endoscopic ultrasonography of normal and
pathologic upper gastrointestinal wall structure: comparison of studies in
vivo and in vitro with histology. Scand J Gastroenterol. 1986;21:27–33.
13. Dittler HJ, Siewert JR. Role of endoscopic ultrasonography in esophageal
carcinoma. Endoscopy. 1993;25:156–161.
14. Lea JW 4th, Prager RL, Bender HW Jr. e questionable role of computed
tomography in preoperative staging of esophageal cancer. Ann orac Surg.
1984;38:479–481.
15. van Vliet EPM, Heijenbrok-Kal MH, Hunink MGM, Kuipers EJ,
Siersema PD. Staging investigations for oesophageal cancer: a metaanalysis. BJC. 2008;98:547–557.
16. van Vliet EPM, Hermans JJ, De Wever W, et al. Radiologist experience and CT examination quality determine metastasis detection in
patients with esophageal or gastric cardia cancer. European Radiology.
2008;18(11):2475–2484.
17. Kimmey MB, Martin RW, Haggit RC, et al. Histologic correlates of
gastrointestinal ultrasound images. Gastroenterology. 1989;96:433–441.
18. Aibe T, Ito T, Yoshida T. Endoscopic ultrasonography of lymph nodes
surrounding the upper GI tract. Scand J Gastroenterol. 1986;21:
164–169.

Chapter 5 Laparoscopic Staging and Approaches to Cancer 93
19. Tio TL, Cohen P, Coene PP, et al. Endosonography and computed
tomography of esophageal carcinoma: pre-operative classication
compared to the new TNM system. Gastroenterology. 1989;96:
1478–1486.
20. Rosch T, Lorenz R, Zenker K, et al. Local staging and assessment of
resectability in carcinoma of esophagus, stomach, and duodenum by
endoscopic ultrasonography. Gastrointest Endosc. 1992;38:460–467.
21. Harewood GC, Wiersema MJ. A cost analysis of endoscopic ultrasound in the evaluation of esophageal cancer. Am J Gastroenterol.
2002;97:452–458.
22. de Graaf GW, Ayantunde AA, Parsons SL, Duy JP, Welch NT. e role
of staging laparoscopy in oesophagogastric cancers. Euro J Surg Oncol.
2007;33(8):988–992.
23. Morris JM, Suzuki H, McKernan M, Stephen M, Stuart RC, Stanley AJ.
Impact of EUS-FNA in the management of patients with oesophageal
cancer. Scottish Med J. 2009;54(2):30–33.
24. Puli SR, Reddy JBK, Bechtold ML, Antillon D, Ibdah JA, Antillon MR. Staging accuracy of esophageal cancer by endoscopic ultrasound: a meta-analysis and systematic review. World J Gastroenterol.
2008;14(10);1479–1490.
25. Maple JT, Peifer KJ, Edmundowicz SA, et al. e impact of endoscopic
ultrasonography with ne needle aspiration (EUS-FNA) on esophageal
cancer staging: a survey of thoracic surgeons and gastroenterologists.
Dis Esoph. 2008;21(6):480–487.
26. Pfau PR, Perlman SB, Stanko P. e role and clinical value of EUS in
a multimodality esophageal carcinoma staging program with CT and
positron emission tomography. Gastrointest Endosc. 2007;65:377–384.
27. Salahudeen HM, Balan A, Naik K. Impact of the introduction of integrated PET-CT into the preoperative staging pathway of
patients with potentially operable oesophageal carcinoma. Clin Radiol.
2008;63:765–773.
28. Kato H, Kimura H, Nakajima M. e additional value of integrated
PET/CT over PET in initial lymph node staging of esophageal cancer.
Oncol Rep. 2008;20:857–862.
29. Block MI, Patterson GA, Sundaresan RS. Improvement in staging of
esophageal cancer with the addition of positron emission tomography.
Ann orac Surg. 1997;64:770–776.
30. Kato H, Miyazaki T, Nakajima M. e incremental eect of positron
emission tomography on diagnostic accuracy in the initial staging of
esophageal carcinoma. Cancer. 2005;103:148–156.
31. Kato H, Kuwano H, Nakajima M. Comparison between positron emission tomography and computed tomography in the use of the assessment
of esophageal carcinoma. Cancer. 2002;94:921–928.
32. Flamen P, Lerut A, Van Cutsem E. Utility of positron emission tomography for the staging of patients with potentially operable esophageal
carcinoma. J Clin Oncol. 2000;18:3202–3210.
33. Monjazeb AM, Riedlinger G, Aklilu M, et al. Outcomes of patients with
esophageal cancer staged with [1F]uorodeoxyglucose positron emission
tomography (FDG- PET): can postchemoradiotherapy FDG- PET predict the utility of resection? J clin Oncol. 2010;28(31):4714–4721.
34. Flanagan FL, Dehdashti F, Siegal BA, et al. Staging of esophageal
cancer with 18F-uordexyglucose positron emission tomography. AJR.
1997;168:417–424.
35. Block MI, Patterson GA, Sundaresan RS, et al. Improvement in staging
of esophageal cancer with addition of positron emission tomography.
Ann orac Surg. 1997;64:770–776.
36. Weber WA, Ott K, Becker K, et al. Prediction of response to preoperative chemotherapy in adenocarcinoma of the esophagogastric junction
by metabolic imaging. J Clin Oncol. 2001;19:3058–3065.
37. Christina TM, Jannet CB, Jan P, et al. A systematic review on the
role of FDG-PET/CT in tumour delineation and radiotherapy planning in patients with esophageal cancer. Radiotherapy and Oncology.
2010;97(2):165–171.
38. Neeraj K, Asif K, Debra B, James L, Kevin M. Endoscopic ultrasound
compared with laparoscopy for staging esophageal cancer. Ann oracic
Surg. 2007;83(6):2000–2002.
39. De Graaf GW, Ayantunde AA, Parsons SL, Duy JP, Welch NT. e role
of staging laparoscopy in oesophagogastric cancers. Euro J Surg Oncol
(EJSO). 2007;33(8):988–992.
40. Watt I, Stewart I, Anderson D, Bell G, Anderson JR. Laparoscopy,
ultrasound and computed tomography in cancer of the oesophagus and
gastric cardia: a prospective comparison for detecting intra-abdominal
metastases. Br J Surg. 1989;76:1036–1039.
41. O’Brien MG, Fitzgerald FF, Lee G, Crowley M, Shanahan F, O’Sullivan
GC. A prospective comparison of laparoscopy and imaging in the
staging of oesophageal cancer before surgery. Am J Gastroenterol.
1995;90:2191–2194.
42. Samee A, Moorthy K, Jaipersad T, et al. Evaluation of the role of laparoscopic ultrasonography in the staging of oesophagogastric cancers. Surg
Endosc Other Interven Tech. 2009;23(9):2061–2065.
43. Mortensen MB, Fristrup C, Ainsworth A, Nielsen HO, Pless T, Hovendal C. Combined pretherapeutic endoscopic and laparoscopic ultrasonography may predict survival of patients with upper gastrointestinal
tract cancer. Surg Endoscopy. 2011;43:596–603.
44. Dagnini G, Caldironi MW, Marian G, et al. Laparoscopy in abdominal
staging of esophageal carcinoma: report of 369 cases. Gastrointest Endosc.
1986;32:400–402.
45. Stein HJ, Kraemer SJ, Freussner H, et al. Clinical value of diagnostic
laparoscopy with laparoscopic ultrasound in patients with cancer of the
esophagous or cardia. J Gastrointest Surg. 1997;1:167–173.
46. Ferlay J, Autier P, Boniol M, et al. Estimates of the cancer incidence and
mortality in Europe in 2006. Ann Oncol. 2007;18:581–592.
47. Crew KD, Neugut AI. Epidemiology of gastric cancer. World J Gastroen-
terol. 2006;12(3):354–362.
48. Hartgrink HH, Jansen EP, van Grieken NC, van de Velde CJ. Gastric
cancer. Lancet. 2009;374(9688):477–490.
49. Karpeh MS Jr, Brennan MF. Gastric carcinoma. Ann Surg Oncol.
1998;5:650–656.
50. Brennan MF, Karpeh MS Jr. Surgery for gastric cancer: the American
view. Ann Surg Oncol. 1996;23:352–359.
51. Pye JK, Crumplin MK, Charles J, et al. Hospital clinicians in Wales:
one-year survey of carcinoma of the oesophagus and stomach in Wales.
Br J Surg. 2001;88:278–285.
52. Lordick F, Siewert JR. Recent advances in multimodal treatment for gastric cancer: a review. Gastric Ca. 2005;8(2):78–85.
53. Davies AR, Deans DAC, Penman I, et al. e multidisciplinary team
meeting improves staging accuracy and treatment selection for gastroesophageal cancer. Diseases of the Esophagus. 2006;19(6):496–503.
54. Burke EC, Karpeh MS Jr, Conlon KC, et al. Laparoscopy in the management of gastric adenocarcinoma. Ann Surg. 1997;225:262–267.
55. Wakelin SJ, Deans C, Crofts PL, et al. A comparison of computerised
tomography, laparoscopic ultrasound and endoscopic ultrasound in
the preoperative staging of oesphago-gastric carcinoma. Eur J Radiol.
2002;41:161–167.
56. Finch M, John T, Garden OJ, et al. Laparoscopic ultra-sonography for
staging gastroesophageal cancer. Surgery. 1997;121:10–17.
57. Stell DA, Carter Cr, Stewart I, Anderson JR. Prospective comparison of
laparoscopy, ultrasonography and computed tomography in the staging
of gastric cancer. Br J Surg. 1996;83:1260–1262.
58. Muntean V, Mihailov A, Iancu C, et al. Staging laparoscopy in gastric cancer: accuracy and impact on therapy. J Gastrointest Liver Dis.
2009;18(2):189–195.
59. Sotiropoulos GC, Kaiser GM, Lang H, et al. Staging laparoscopy in gastric cancer. Eur J Medical Res. 2005;10(2):88–91.
60. Kim SJ, Kim HH, Kim YH, et al. Peritoneal metastasis: detection with
16- or 64-detector row CT in patients undergoing surgery for gastric
cancer. Radiology. 2009;253(2):407–415.
61. Chen CY, Hsu JS, Wu DC, et al. Gastric cancer: preoperative local staging with 3D multi-detector row CT: correlation with surgical and histopathologic results. Radiology. 2007;242(2):472–482.
62. Mezhir JJ, Shah MA, Jacks LM, Brennan MF, Coit DG, Strong VE.
Positive peritoneal cytology in patients with gastric cancer: natural history and outcome of 291 patients. Ann Surg Oncol. 2010 Jun 29. [Epub
ahead of print].
63. Bentrem D, Wilton A, Mazumdar M, Brennan M, Coit D. e
value of peritoneal cytology as a preoperative predictor in patients with
gastric carcinoma undergoing a curative resection. Ann Surg Oncol.
2005;12(5):1–7.
64. La Torre M, Ferri M, Giovagnoli MR, et al. Peritoneal wash cytology in
gastric carcinoma: prognostic signicance and therapeutic consequences.
Eur J Surg Oncol. 2010;36(10):982–986.
65. Hiroki S, Hiroshi I, Katsuya O, et al. Usefulness of staging laparoscopy
for advanced gastric cancer. Surg Today. 2010;40(2):119–124.
66. Wong J, Schulman A, Kelly K, Zamarin D, Palese P, Fong Y. Detection
of free peritoneal cancer cells in gastric cancer using cancer-specic Newcastle disease virus. J Gastrointest Surg. 2010;14(1):7–14.

94 Part I Introduction
67. Dalal KM, Woo Y, Kelly K, et al. Detection of micrometastases in peritoneal
washings of gastric cancer patients by the reverse transcriptase polymerase
chain reaction. Gastric Ca. 2008;11(4):206–213.
68. Kitagawa Y, Fujii H, Mukai M, et al. Current status and future prospects
of sentinel node navigational surgery for gastrointestinal cancers. Ann
Surg Oncol. 2004;11:242S–244S.
69. Fortner JG, Silva JS, Cox EB, et al. Multivariate analysis of a personal
series of 247 patients with liver metastases from colorectal cancer: treatment by intrahepatic chemotherapy. Ann Surg. 1984;199:317–324.
70. Jarnagin WR, Bodniewicz J, Dougherty E, et al. A prospective analysis of
staging laparoscopy in patients with primary and secondary hepatobiliary malignancies. J Gastrointest Surg. 2000;4:24–43.
71. Lo CM, Lai E, Liu CL, et al. Laparoscopy and laparoscopic ultrasonography avoid exploratory laparotomy in patients with hepatocellular carcinoma. Ann Surg. 1998;227:527–532.
72. John TG, Greig JD, Crosbie JL, et al. Superior staging of liver tumors
with laparoscopy and laparoscopic ultrasound. Ann Surg. 1994;220:
711–719.
73. Callery MP, Strasberg SM, Doherty GM, et al. Staging laparoscopy with
laparoscopic ultrasonography: optimizing resectability in hepatobiliary
and pancreatic malignancy. J Am Coll Surg. 1997;185:33–39.
74. D’Angelica M, Fong Y, Weber S, et al. e role of laparoscopy in hepatobiliary malignancy: prospective analysis of 401 cases. Ann Surg Oncol.
2003;10:183–189.
75. Jarnagin WR, Conlon K, Bodniewicz J, et al. A clinical scoring system
predicts the yield of diagnostic laparoscopy in patients with potentially
resectable hepatic colorectal metastases. Cancer. 2001;91:1121–1128.
76. Grobmyer SR, Fong Y, D’Angelica M, et al. Diagnostic laparoscopy
prior to planned hepatic resection for colorectal metastases. Arch Surg.
2004;139:1326–1330.
77. Mann CD, Neal CP, Metcalfe MS, Pattenden CJ, Dennison AR, Berry
DP. Br J Surg. 2007;94:855–859.
78. Shah AJ, Phull J, Finch-Jones MD. Clinical risk score can be used to
select patients for staging laparoscopy and laparoscopic ultrasound for
colorectal metastases. World J Surg. 2010;34:2141–2145.
79. Rahusen FD, Cuesta MA, Borgstein PJ, et al. Selection of patients for
resection of colorectal metastases to the liver using diagnostic laparoscopy and laparoscopic ultrasonography. Ann Surg. 1999;230:31–37.
80. de Castro SM, Tilleman EH, Busch OR, et al. Diagnostic laparoscopy for
primary and secondary liver malignancies: impact of improved imaging
and changed criteria for resection. Ann Surg Oncol. 2004;11:522–529.
81. Koea J, Rodgers M, ompson P, et al. Laparoscopy in the management of colorectal cancer metastatic to the liver. ANZ J Surg. 2004;74:
1056–1059.
82. aler K, Kanneganti S, Khajanchee Y, et al. e evolving role of staging
laparoscopy in the treatment of colorectal hepatic metastases. Arch Surg.
2005;140:727–734.
83. Foroutani A, Garland AM, Berber E. Laparoscopic ultrasound versus
triphasic computed tomography for detecting liver tumors. Arch Surg.
2000;135:953–958.
84. Metcalfe MS, Close JS, Iswariah H, et al. e value of laparoscopic
staging for patients with colorectal metastases. Arch Surg. 2003;138:
770–772.
85. Berber E, Garland AM, Engle KL, et al. Laproscopic ultrasonography
and biopsy of hepatic tumors in 310 patients. Am J Surg. 2004;187:
213–218.
86. Mortensen MB, Fristrup C, Ainsworth A, et al. Laparoscopic ultrasound-guided biopsy in upper gastrointestinal tract cancer patients. Surg
Endosc. 2009;23:2738–2742.
87. Hartley JE, Kumar H, Drew PJ, et al. Laparoscopic ultrasound for the
detection of hepatic metastases during laparoscopic colorectal cancer surgery. Dis Colon Rectum. 2000;43:320–324.
88. Lightdale CJ. Laparoscopy and biopsy in malignant liver disease. Cancer.
1982;50:2672–2675.
89. Jeers L, Spieglman G, Reddy R, et al. Laparoscopically directed ne
needle aspiration for the diagnosis of hepatocellular carcinoma: a safe
and accurate technique. Gastrointest Endosc. 1988;34:235–237.
90. Lai EC, Tang CN, Ha JP, Tsui DK, Li MK. e evolving inuence of
laparoscopy and laparoscopic ultrasonography on patients with hepatocellular carcinoma. Am J Surg. 2008;196:736–740.
91. Casaccia M, Andorno E, Nardi I, et al. Laparoscopic staging and radiofrequency of hepatocellular carcinoma in liver cirrhosis: a “bridge” treatment to liver transplantation. Hepatogastroenterology. 2009;56:793–797.
92. D’Angelica MD, Jarnagin WR, Dematteo RP, et al. Staging laparoscopy
for potentially resectable non-colorectal nonendocrine liver metastases.
Ann Surg Oncol. 2003;9:204–209.
93. Agrawal S, Sonawane RN, Behari A, et al. Dig Surgery. 2005;22:440–445.
94. Goere D, Wagholikar GD, Pessaux P, et al. Utility of staging laparoscopy
in subsets of biliary cancers. Surg Endosc. 2006;20:721–725.
95. Jemal A, Tiwari RC, Murray T, et al. Cancer statistics. CA Cancer J Clin.
2004;54:8–29.
96. Bernheim BM. Organoscopy. Ann Surg. 1911;53:764–767.
97. Warshaw AL, Gu ZY, Wittenberg J, et al. Preoperative staging and assessment of resectability of pancreatic cancer. Arch Surg. 1990;125:230–233.
98. Warshaw AL, Tepper JE, Shipley WU. Laparoscopy in the staging and
planning therapy for pancreatic cancer. Am J Surg. 1986;151:76–80.
99. Cuschieri A, Hall AW, Clark J. Value of laparoscopy in the diagnosis and
management of pancreatic carcinoma. Gut. 1978;19:672–677.
100. Cuschieri A. Laparoscopy for pancreatic cancer: does it benet the patient?
Eur J Surg Oncol. 1988;14:41–44.
101. Pisters PW, Lee JE, Vauthey JN, et al. Laparoscopy in the staging of
pancreatic cancer. Br J Surg. 2001;88:325–337.
102. Conlon KC, Dougherty E, Klimstra DS, et al. e value of minimal
access surgery in the staging of patients with potentially resectable peripancreatic malignancy. Ann Surg. 1996;223:134–140.
103. John TG, Greig JD, Carter DC, et al. Carcinoma of the pancreatic head
and periampullary region: tumor staging with laparoscopy and laparoscopic ultrasonography. Ann Surg. 1995;221:156–164.
104. Bemelman WA, de Wit LT, van Delden OM, et al. Diagnostic laparoscopy combined with laparoscopic ultrasonography in staging of cancer
of the pancreatic head region. Br J Surg. 1995;82:820–824.
105. Fernandez-del Castillo C, Rattner DW, Warshaw AL. Further experience
with laparoscopy and peritoneal cytology in the staging of pancreatic
cancer. Br J Surg. 1995;82:1127–1129.
106. Reddy KR, Levi J, Livingstone A, et al. Experience with staging laparoscopy in pancreatic malignancy. Gastrointest Endosc. 1999;49:498–503.
107. Yoshida T, Matsumoto T, Morii Y, et al. Staging with helical computed
tomography and laparoscopy in pancreatic head cancer. Hepatogastroen-
terology. 2002;49:1428–1431.
108. Conlon KC, Brennan MF. Laparoscopy for staging abdominal malignancies. Adv Surg. 2000;34:331–350.
109. White R, Winston C, Gonen M, et al. Current utility of staging laparoscopy for pancreatic and peripancreatic neoplasms. J Am Coll Surg.
2008;206:445–450.
110. Doran HE, Bosonnet L, Connor S, et al. Laparoscopy and laparoscopic
ultrasound in the evaluation of pancreatic and periampullary tumors.
Dig Surg. 2004;21:305–313.
111. Halloran C, Ghaneh P, Connor S, Sutton R, Neoptolemos J, Raraty
MGT. Carboihydrate antigen 19-9 accurately selects patients for laparoscopic assessment to determine respectability of pancreatic malignancy.
Br J Surg. 2008;95:453–459.
112. Maithel SK, Maloney S, Winston C, et al. Preoperative Ca 19-9 and the
yield of staging laparoscopy in patients with radiographically resectable
pancreatic adenocarcinoma. Ann Surg Oncol. 2008;15;3512–3520.
113. Mayo SC, Austin DF, Sheppard Bc, Mori M, Shipley DK, Billingsley KG.
Evolving preoperative evaluation of patients with pancreatic cancer: does
laparoscopy have a role in the current era? J Am Coll Surg. 2009;208:87–95.
114. Cuesta MA, Meijer S, Borgstein PJ, et al. Laparoscopic ultrasonography for hepatobiliary and pancreatic malignancy. Br J Surg. 1993;80:
1571–1574.
115. Ascher SM, Evans SR, Zeman RK. Laparoscopic cholecystectomy: intraoperative ultrasound of the extrahepatic biliary tree and the natural
history of postoperative transabdominal ultrasound ndings. Semin
Ultrasound CT MR. 1993;14:331–337.
116. John TG, Wright A, Allan PL, et al. Laparoscopy with laparoscopic ultrasonography in the TNM staging of pancreatic carcinoma. World J Surg.
1999;23:870–881.
117. Minnard EA, Conlon KC, Hoos A, et al. Laparoscopic ultrasound enhances standard laparoscopy in the staging of pancreatic cancer. Ann
Surg. 1998;228:182–187.
118. Pietrabissa A, Caramella D, Di Candio G, et al. Laparoscopy and laparoscopic ultrasonography for staging pancreatic cancer: critical appraisal.
World J Surg. 1999;23:998–1002.
119. Murugiah M, Paterson-Brown S, Windsor JA, et al. Early experience
of laparoscopic ultrasonography in the management of pancreatic carcinoma. Surg Endosc. 1993;7:177–181.

Chapter 5 Laparoscopic Staging and Approaches to Cancer 95
120. Schachter PP, Avni Y, Shimonov M, Gvirtz G, Rosen A, Czerniak A.
e impact of laparoscopy and laparoscopic ultrasonography on the
management of pancreatic cancer. Arch Surg. 2000;135:1303–1307.
121. Catheline J, Turner R, Rizk N. e use of diagnostic laparoscopy supported by laparoscopic ultrasonongraphy in the assessment of pancreatic
cancer. Surg Endoscopy. 1999;13:239–245.
122. Vollmer CM, Drebin JA, Middleton WD, et al. Utility of staging laparoscopy in subsets of peripancreatic and biliary malignancies. Ann Surg.
2002;235:1–7.
123. Merchant NB, Conlon KC, Saigo P, et al. Positive peritoneal cytology
predicts unresectability of pancreatic adenocarcinoma. J Am Coll Surg.
1999;188:421–426.
124. Loyer EM, David CL, Dubrow RA, Evans DB, Charnsangavej C. Vascular involvement in pancreatic adenocarcinoma: reassessment by thinsection CT. Abdom Imaging. 1996;21:202–206.
125. omson BNJ, Parks RW, Redhead DN, et al. Rening the role of laparoscopy and laparoscopic ultrasound in the staging of presumed pancreatic head and ampullary tumours. Br J Cancer. 2006;94:213–217.
126. Hariharan D, Constantinides VA, Froeling FEM, Tekkis PP, Kocher
HM. EJSO. 2010;36:941–948.
127. Jimenez RE, Warshaw AL, Fernandez-del Castillo C. Laparoscopy and
peritoneal cytology in the staging of pancreatic cancer. J Hepatobil Pan-
creat Surg. 2000;7:15–20.
128. Fernandez-del Castillo CL, Warshaw AL. Pancreatic cancer: laparoscopic
staging and peritoneal cytology. Surg Oncol Clin North Am. 1998;7:
135–142.
129. Leach SD, Rose JA, Lowy AM, et al. Signicance of peritoneal cytology
in patients with potentially resectable adenocarcinoma of the pancreatic
head. Surgery. 1995;118:472–478.
130. Dalal KM, Woo Y, Galanis C, et al. Detection of micrometastases in
peritoneal washings of pancreatic cancer patients by the reverse transcriptase polymerase chain reaction. J Gastrointest Surg. 2007;11:1598–1601.
131. Abdalla EK, Barnett CC, Pisters PW, et al. Subaquatic laparoscopy for
staging of intraabdominal malignancy. J Am Coll Surg. 2003;196:155–158.
132. Spitz FR, Abbruzzese JL, Lee JE, et al. Preoperative and postoperative
chemoradiation strategies in patients treated with pancreaticoduodenectomy for adenocarcinoma of the pancreas. J Clin Oncol. 1997;15:928–937.
133. Obertop H, Gouma DJ. Essentials in biliopancreatic staging: a decision
analysis. Ann Oncol. 1999;10:150–152.
134. Nieveen van Dijkum EJ, Romijn MG, Terwee CB, et al. Laparoscopic
staging and subsequent palliation in patients with peripancreatic carcinoma. Ann Surg. 2003;237:66–73.
135. Shoup M, Winston C, Brennan MF, et al. Is there a role for staging
laparoscopy in patients with locally advanced unresectable pancreatic
adenocarcinoma? J Gastrointest Surg. 2004;8:1068–1071.
136. Liu RC, Traverso W. Diagnostic laparoscopy improves staging of pancreatic cancer deemed locally unresectable by computed tomography. Surg
Endosc. 2005;19:638–642.
137. Morak MJM, Hermans JJ, Smeenk Hg, et al. Staging for locally
advanced pancreatic cancer. EJSO. 2009;35:963–968.
138. Hochwald SN, Weiser MR, Colleoni R, et al. Laparoscopy predicts metastatic disease and spares laparotomy in selected patients with pancreatic
non-functioning islet cell tumors. Ann Surg Oncol. 2001;8:249–253.
139. Brooks AD, Mallis MJ, Brennan MF, et al. e value of laparoscopy
in the management of ampullary, duodenal, and distal bile duct tumors.
J Gastrointest Surg. 2002;6:139–145.
140. Rodgers MS, Windsor JA, Koea JB, McCall JL. Laparoscopic staging of
upper gastrointestinal malignancy. ANZ J Surg. 2003;73(10):806–810.
141. Dobronte Z, Wittmann T, Karacsony G. Rapid development of
malignant metastases in the abdominal wall after laparoscopy. Endoscopy.
1978;10:127–130.
142. Nieveen van Dijkum EJ, de Wit LT, van Delden OM, et al. Staging laparoscopy and laparoscopic ultrasonography in more than
400 patients with upper gastrointestinal carcinoma. J Am Coll Surg.
1999;189:459–465.
143. Pearlstone DB, Manseld PF, Curley SA, et al. Laparoscopy in 533 patients
with abdominal malignancy. Surgery. 1999;125:67–72.
144. Shoup M, Brennan MF, Karpeh MS, et al. Port site metastasis after
diagnostic laparoscopy for upper gastrointestinal tract malignancies: an
uncommon entity. Ann Surg Oncol. 2002;9:632–636.
145. Hughes ES, McDermott FT, Polglase AL, et al. Tumor recurrence in the
abdominal wall scar tissue after large-bowel cancer surgery. Dis Colon Rec-
tum. 1983;26:571–572.
146. Velanovich V. e eects of staging laparoscopy on trocar site and
peritoneal recurrence of pancreatic cancer. Surg Endosc. 2004;18:
310–313.
147. Bouvy ND, Marquet RL, Jeekel H, et al. Impact of gas(less) laparoscopy
and laparotomy on peritoneal tumor growth and abdominal wall metastases. Ann Surg. 1996;224:694–700; discussion 700–701.
148. Jones DB, Guo LW, Reinhard MK, et al. Impact of pneumoperitoneum
on trocar site implantation of colon cancer in hamster model. Dis Colon
Rectum. 1995;38:1182–1188.
149. Yamaguchi K, Hirabayashi Y, Shiromizu A, et al. Enhancement of port
site metastasis by hyaluronic acid under CO2 pneumoperitoneum in a
murine model. Surg Endosc. 2001;15:504–507.
150. Curet MJ. Port site metastases. Am J Surg. 2004;187:705–712.
151. Rhodes M, Nathanson L, Fielding G. Laparoscopic biliary and gastric
bypass: a useful adjunct in the treatment of carcinoma of the pancreas.
Gut. 1995;36:778–780.
152. Rothlin MA, Schob O, Weber M. Laparoscopic gastroand hepaticojejunostomy for palliation of pancreatic cancer: a case-controlled study.
Surg Endosc. 1999;13:1065–1069.
153. Choi YB. Laparoscopic gastrojejunostomy for palliation of gastric outlet obstruction in unresectable gastric cancer. Surg Endosc.
2002;16:1620–1626.
154. Navarra G, Musolino C, Venneri A, deMarco ML, Bartolotta M. Palliative antecolic isoperistaltic gastrojejunostomy: a randomized controlled trial comparing open and laparoscopic approaches. Surg Endosc.
2006;20:1831–1834.
155. Bucher P, Pugin F, Morel P. Transumbilical single-incision laparoscopic
intracorporal anastomosis for gastrojejunostomy: a case report. Surg
Endosc. 2009;1667–1670.
156. Espat NJ, Brennan MF, Conlon KC. Patients with laparoscopically staged
unresectable pancreatic adenocarcinoma do not require subsequent
surgical biliary or gastric bypass. J Am Coll Surg. 1999;188:649–657.
157. Sohn TA, Lillemoe KD, Cameron JL, et al. Surgical palliation of unresectable periampullary adenocarcinoma in the 1990s. J Am Coll Surg.
1999;188:658–669.
158. Molinari M, Helton WS, Espat NJ. Palliative strategies for locally advanced unresectable and metastatic pancreatic cancer. Surg Clin North
Am. 2002;81:651–666.
159. Casaccia M, Diviacco P, Molinello P, et al. Laparoscopic palliation
of unresectable pancreatic cancers: preliminary results. Eur J Surg.
1999;165:556–559.
160. Yim HB, Jacobson BC, Saltzman JR, et al. Clinical outcome of the use of
enteral stents for palliation of patients with malignant upper GI obstruction. Gastrointest Endosc. 2001;53:329–332.
161. DiMango EP, Reber HA, Tempero MA. AGA technical review on the
epidemiology, diagnosis, and treatment of pancreatic ductal adenocarcinoma. Gastroenterology. 1999;117:1464–1484.
162. Nagy A, Brosseuk D, Hemming A, et al. Laparoscopic gastroenterostomy for duodenal obstruction. Am J Surg. 1995;165:539–542.

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ABDOMINAL WALL
II

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INCISIONS, CLOSURES, AND MANAGEMENT OF THE ABDOMINAL WOUND
Robert E. Roses • Jon B. Morris
6
INCISIONS
e impact that the planning, execution, and closure of
an incision has on the outcome of an abdominal operation
should not be underestimated. e high combined incidence
of surgical site infection (SSI), wound dehiscence, and hernia formation suggests a dominant contribution of wound
complications to surgical morbidity. Moreover, the quality
of exposure provided by an incision in uences the ease and
safety with which an operation can be undertaken and the
outcome in ways which defy easy quanti cation.
An incision must provide access to the site of abdominal
pathology and allow easy extension if greater exposure than
originally anticipated is required. Indeed, the adequacy of an
incision is determined above all else by the safety with which
an operation can be undertaken. Nothing should compromise this and a larger incision or even, on occasion, a second
incision should be created without hesitation if exposure is
inadequate. Notwithstanding this, the incision should be
executed in a fashion that anticipates a secure wound closure
and interferes as little as possible with the function and cosmesis of the abdominal wall. ese principles apply to both
open and laparoscopic incisions. While the vertical midline
incision remains most popular, and is, perhaps the most exible, a variety of other incisions may have distinct advantages
in speci c settings.
Choice of Incision
Abdominal incisions can be vertically, transversely, or obliquely
oriented. e avascular linea alba a ords the vertical midline
its superior exibility. Indeed, when optimal exposure of the
abdominal cavity is necessary (eg, exploration for abdominal
trauma), the vertical midline incision is preferred and can
be extended superiorly to the xiphoid process and inferiorly
to the symphysis pubis. Alternatively, vertical incisions may
be placed in a paramedian position, an approach that was
previously more popular than it is today but continues to
have its proponents. Transverse and oblique incisions can be
placed in any of the four quadrants of the abdomen depending on the site of pathology. Common examples include the
Kocher subcostal incision for biliary surgery, the Pfannenstiel infraumbilical incision for gynecologic surgery, and the
McBurney and Rockey-Davis incisions for appendectomy.
A bilateral subcostal incision a ords excellent exposure of
the upper abdomen. Alternatively, when superior exposure of
upper abdominal organs (eg, the esophagogastric junction) is
required, thoracoabdominal incisions may be used.
e relative merit of vertical versus transverse incisions
remains a topic of active debate. Proponents of transverse
incisions argue that they anticipate a more secure closure
than do vertical incisions, a hypothesis supported by anatomic and surgical principle. e fascial bers of the anterior abdominal wall are oriented transversely or obliquely.
erefore, transverse incisions parallel the direction of the
fascial bers and allow for ready reapproximation with
sutures placed perpendicular to these bers. In contrast,
vertical incisions disrupt fascial bers and must be reapproximated with sutures placed between bers.
ter case, the absence of an anatomic barrier may predispose
such sutures to pull through tissue resulting in dehiscence
or hernia formation. Despite these concerns, little evidence
supports a substantial bene t of transverse incisions. A
number of retrospective clinical studies and a meta-analysis
do suggest that transverse incisions are superior to vertical
incisions with regard to long-term and short-term outcomes
(eg, postoperative pain, pulmonary complications, and frequencies of incisional hernia and dehiscence).
data has been less de nitive, however. One randomized controlled trial compared vertical and transverse incisions with
regards to the frequency of evisceration; no signi cant difference in outcome was observed with either technique.
a more recent prospective randomized trial, no signi cant
di erences in 30-day mortality, pulmonary complications,
median length of hospital stay, median time to tolerate
1
In the lat-
1
Prospective
2
In
99

100 Part II Abdominal Wall
solid food, and incisional hernia formation at 1 year were
observed. More wound infections were seen with transverse
incisions.
3
Likewise, some controversy persists regarding the relative
advantages of midline versus paramedian incisions. e theoretical advantage of a paramedian over a midline incision is
a diminished risk of wound dehiscence and incisional hernia
owing to the presence of rectus muscle interposed between
layers of divided fascia. In practice, when these incisions are
reopened, the medial edge of the rectus muscle is frequently
found to be adherent to the posterior sheath incision and
does not eectively buttress the wound. e potential advantages of the paramedian incision have also been investigated
in prospective randomized trials which fail to demonstrate
any advantage with regards to wound failure rates when
4
compared to midline or transverse incisions.
A “lateral
paramedian incision” refers to a vertical incision created
several centimeters lateral to the location of the traditional
5
paramedian incision.
One randomized prospective study
suggested a statistically signicant decrease in the incidence
incisions (0%) compared to medial paramedian incisions
6
(14.9%)
and midline incisions (6.9%).7 A disadvantage of
the paramedian incision is the greater length of time needed
to create the wound, which increases with the distance from
the midline.
In the patient who has had prior abdominal surgery, the
cosmetic advantages of re-entering the abdomen through a
preexisting scar must be balanced against the challenges associated with dissection in a reoperative eld. Close proximity
of a new incision to an old one should be avoided in order
to minimize the risk of ischemic necrosis of intervening skin
and fascial bridges.
Preparation of the Surgical Site
Incisions: Technical Considerations
VERTICAL INCISIONS
Midline Incision. e midline incision allows rapid access to,
and adequate exposure of, almost every region of the abdominal cavity and retroperitoneum. It is typically associated with
little blood loss and does not require transection of muscle
bers or nerves. e upper midline incision (ie, above the
umbilicus) may be used to expose the esophageal hiatus,
abdominal esophagus and vagus nerves, stomach, duodenum,
gallbladder, pancreas, and spleen (Fig. 6-1). e lower midline incision (ie, below the umbilicus) provides exposure of
lower abdominal and pelvic organs. When broad exposure is
required, as in an exploration for trauma, the midline incision
can be extended to the xiphoid process superiorly and to the
pubic symphysis inferiorly.
In creating a midline incision, the operating surgeon and
assistant apply opposing traction to the skin on both sides of
the abdomen. e skin is then incised with a scalpel. Gauze
pads are applied to the skin edges to tamponade bleeding
cutaneous vessels and lateral traction is placed on the subcutaneous fat on both sides of the incision. e incision is
then carried down to the linea alba using either electrocautery or a scalpel; the decussation of fascial bers in the upper
abdomen serves as an important landmark for the midline.
e linea alba, extraperitoneal fat, and peritoneum are then
divided sequentially. If exposure of both the upper and lower
peritoneal cavities is required, the incision is carried around
the umbilicus in a curvilinear fashion. e peritoneum itself
is best divided with scissors or scalpel to avoid coagulation
injury to underlying intraabdominal organs. Additionally, safe entry may be facilitated by picking up a fold of
peritoneum, palpating it to ensure that no bowel hasbeen
drawn up, and sharply incising the raised fold. e falciform ligament is best avoided by entering the peritoneum
to the left or right of the midline in the upper abdomen.
Prior to incision, the surgical eld is prepared with antiseptic
solution and draped in order to reduce skin bacterial counts
and the likelihood of subsequent wound infection. Shaving
prior to operation has been associated with an increased
rate of SSI and should, therefore, be avoided. If hair at the
surgical site will interfere with accurate wound closure or
precludes thorough application of the sterile preparation,
8
the use of clippers is preferred to a razor.
A variety of antiseptic solutions are commonly used to prepare the skin,
including povidone-iodine, alcohol, and chlorhexidene.
e ecacy of povidine-iodine depends on the release of the
active iodine from a carrier molecule. e solution should,
therefore, be applied several minutes prior to incision to
maximize its ecacy. e use of chlorhexidine gluconate
has been associated with greater reductions in skin bacterial
counts and lower rates of SSI when compared to povidine-
6,9,10
iodine in a number of studies
and is emerging as the
preferred skin antiseptic.
FIGURE 6-1 Epigastric midline incision: surface markings.

Chapter 6 Incisions, Closures, and Management of the Abdominal Wound 101
FIGURE 6-3 Upper paramedian incision: surface markings.
Additional exposure can be obtained by sloping the upper portion of
the incision upward toward the xiphoid process.
FIGURE 6-2 Vertical midline incision: the linea alba and peritoneum
are divided.
Toavoid injuries to the bladder, the peritoneum is entered
in the upper portion of the incision. After a small opening
is created in the midline, it is enlarged to accommodate two
ngers that are then used to protect the underlying viscera
as the peritoneum is further divided along the length of the
wound (Fig. 6-2).
Paramedian Incision. Paramedian incisions are vertical inci-
sions placed either to the right or the left of the midline on the
abdominal wall. Like midline incisions, paramedian incisions
obviate division of nerves and the rectus muscle and may be
made in the upper or lower abdomen. Superiorly, additional
access can be obtained by curving the upper portion of the
incision along the costal margin toward the xiphoid process
(Fig. 6-3). e anterior border of the rectus sheath is exposed
and incised across the entire length of the wound. e medial
aspect of the anterior rectus sheath is then dissected away from
the rectus muscle to its medial edge (Fig. 6-4). Particular care
must be taken during this dissection in the upper abdomen
where tendinous inscriptions that attach the rectus muscle to
the anterior fascia are associated with segmental vessels. ese
vessels should be clipped or ligated when encountered to avoid
signicant bleeding. Once free, the rectus muscle is retracted
laterally. e posterior sheath (above the arcuate line) and
peritoneum are then incised to gain entry into the abdomen.
During creation of a paramedian incision in the lower abdomen, the inferior epigastric vessels may be encountered and
must be ligated prior to division (Fig. 6-5).
Vertical Muscle-Splitting Incision. e vertical muscle-
splitting incision is made in much the same way as the
traditional paramedian incision except that the rectus muscle is
split, rather than retracted laterally. is wound can be opened
and closed quickly and is of particular value in reopening a previous paramedian incision where dissection of the rectus muscle
away from the rectus sheath can be dicult. Longer incisions
should be avoided, however, because they result in signicantly
more bleeding and sacrice of nerves that may lead to weakening of the corresponding area of the abdominal wall.
TRANSVERSE AND OBLIQUE INCISIONS
Transverse and oblique incisions generally follow Langer’s
lines of tension and usually allow a more cosmetic closure
than do vertical incisions. Importantly, the rectus muscle has a
segmental nerve supply derived from intercostal nerves, which
enter the rectus sheath laterally. Transverse or slightly oblique
incisions through the rectus most often spare these nerves.
Provided that the anterior and posterior sheaths are closed,
the rectus muscle can therefore be divided transversely without signicantly compromising the integrity of the abdominal
wall. Although properly placed transverse incisions can provide exposure of specic organs, they may be limiting when
pathology is located in both the upper and lower abdomen.
Kocher Subcostal Incision. A right subcostal incision is
used commonly for operations in which exposure of the gallbladder and biliary tree is necessary. e left-sided subcostal
incision is used less often, mainly for splenectomy. A bilateral
subcostal incision provides excellent exposure of the upper
abdomen and can be employed for hepatic resections, liver
transplantation, total gastrectomy, and for anterior access to
both adrenal glands.
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