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386
S. Ross et al.

Duodenojejunostomy

• The jejunum distal to the hepaticojejunostomy is brought up in an antecolic fash­ion to the duodenal staple line.
• Using the scissors, we remove the duodenal staple line to expose the lumen. A generous incision is made with scissors on the anti-mesenteric aspect of the jeju­nal limb to expose the lumen.
• The duodenojejunostomy is undertaken in a similar fashion to the hepaticojeju­nostomy, this time using two running 3-0 non-absorbable V-Loc™ sutures (Figs.21.21, 21.22, 21.23, and 21.24).
• Arm #4 is used to retract the stomach in the cephalad and ventral direction by grasping the stapler line.
• We run the dorsal and ventral layers of the anastomosis from the 9-o’clock to 3-o’clock positions, with knots tied on the extra-luminal surface at the 3-o’ clock position. On the ventral layer, a Gambee technique allows inversion of the sero­sal surfaces and prevents mucosal perturbance.
Fig. 21.21 Duodenojejunostomy
21 Robotic Pancreatoduodenectomy
Fig. 21.22 Duodenojejunostomy
387
Fig. 21.23 Duodenojejunostomy
388
Fig. 21.24 Duodenojejunostomy, completed
S. Ross et al.
Drainage andClosure
• Using the energized scissors, a falciform ligament ap is developed and placed over the hepaticojejunostomy and the GDA stump for reinforcement.
• An omental ap is placed over the pancreatojejunostomy and duodenojejunos­tomy to minimize leaks.
• A closed suction Jackson-Pratt drain is placed next to the hepaticojejunostomy and pancreatojejunostomy anastomosis.
• The robot is undocked, and the diaphragm is irrigated with bupivacaine to mini­mize postoperative pain.
• The fascia for all working ports is closed using an absorbable monolament suture. The skin is closed with 4-0 Vicryl Brunswick, NJ, USA).
®
sutures (Johnson & Johnson, New

References

1. Whipple AO, Parsons WB, Mullins CR.Treatment of carcinoma of the ampulla of Vater. Ann Surg. 1935;102:763–79.
2. Newhook TE, LaPar DJ, Lindberg JM, Bauer TW, Adams RB, Zaydfudim VM.Morbidity and mortality of pancreatoduodenectomy for benign and premalignant pancreatic neoplasms. J Gastrointest Surg. 2015;19:1072–7.
3. Luu AM, Braumann C, Belyaev O, etal. Long-term survival after pancreatoduodenectomy in patients with ductal adenocarcinoma of the pancreatic head. Hepatobiliary Pancreat Dis Int. 2021;20:271–8.
4. Gagner M, Pomp A.Laparoscopic pylorus-preserving pancreatoduodenectomy. Surg Endosc. 1994;8:408–10.
21 Robotic Pancreatoduodenectomy
5. Wang M, Peng B, Liu J, etal. Practice patterns and perioperative outcomes of laparoscopic pancreatoduodenectomy in China: a retrospective multicenter analysis of 1029 patients. Ann Surg. 2021;273(1):145–53.
6. Kuroki T, Fujioka H. Training for laparoscopic pancreatoduodenectomy. Surg Today. 2019;49(2):103–7.
7. Nickel F, Haney CM, Kowalewski KF, et al. Laparoscopic versus open pancreatoduode­nectomy: a systematic review and meta-analysis of randomized controlled trials. Ann Surg. 2020;271:54–66.
8. van Hilst J, de Rooij T, Bosscha K, etal. Laparoscopic versus open pancreatoduodenectomy for pancreatic or periampullary tumours (LEOPARD-2): a multicentre, patient-blinded, ran­domised controlled phase 2/3 trial. Lancet Gastroenterol Hepatol. 2019;4:199–207.
9. Leal Ghezzi T, Campos Corleta O. 30 years of robotic surgery. World J Surg. 2016;40(10):2550–7.
10. Ross SB, Downs D, Sucandy I, Rosemurgy AS.Robotic pylorus-preserving pancreatoduode­nectomy. In: Fong Y, Woo Y, Hyung W, Lau C, Strong V, editors. The SAGES atlas of robotic surgery. Cham: Springer; 2018. p.319–34.
11. Rosemurgy A, Ross S, Luberice K, Browning H, Sucandy I.Robotic pancreatic surgery for solid, cystic, and mixed lesions. Surg Clin North Am. 2020;100:303–36.
12. Ross S, Rosemurgy A, Wecowski J, Bourdeau T, Sucandy I.Robotic pylorus-preserving pan­creatoduodenectomy and cholecystectomy. Robotic general surgery. In: Atlas of robotic gen­eral surgery. Elsevier; 2021. p.309–22.
13. Ross S, Rayman S, Sucandy I, Syblis C, Rosemurgy A.Whipple’s operation and distal pan­createctomy. In: Costello T, editor. Principles and practice of robotic surgery. Elsevier; 2023.
14. Rosemurgy A, Ross S, Bourdeau T, etal. Cost analysis of pancreatoduodenectomy at a high­volume robotic hepatopancreaticobiliary surgery program. J Am Coll Surg. 2021;232:461–9.
15. Rosemurgy A, Ross S, Espeut A, etal. Survival and robotic approach for pancreatoduodenec­tomy: a propensity score-match study. J Am Coll Surg. 2022;234:677–84.
16. Rice MK, Hodges JC, Bellon J, etal. Association of mentorship and a formal robotic pro­ciency skills curriculum with subsequent generations’ learning curve and safety for robotic pancreatoduodenectomy. JAMA Surg. 2020;155:607–15.
17. Rosemurgy A, Ross S, Bourdeau T, etal. Robotic pancreatoduodenectomy is the future: here and now. J Am Coll Surg. 2019;228(4):613–24.
18. Ouyang L, Zhang J, Feng Q, Zhang Z, Ma H, Zhang G.Robotic versus laparoscopic pancreato­duodenectomy: an up-to-date system review and meta-analysis. Front Oncol. 2022;12:834382.
19. Fogel EL, Shahda S, Sandrasegaran K, etal. A multidisciplinary approach to pancreas cancer in 2016: a review. Am J Gastroenterol. 2017;112(4):537–54.
20. National Comprehensive Cancer Network. Pancreatic adenocarcinoma (version 1.2022). Available from: https://www.nccn.org/professionals/physician_gls/pdf/pancreatic.pdf
21. Wiltberger G, Muhl B, Benzing C, etal. Preoperative risk stratication for major compli­cations following pancreatoduodenectomy: identication of high-risk patients. Int J Surg. 2016;31:33–9.
22. Liang Y, Zhao L, Jiang C, etal. Laparoscopic pancreatoduodenectomy in elderly patients. Surg Endosc. 2020;34:2028–34.
23. Mogal H, Vermilion SA, Dodson R, etal. Modied frailty index predicts morbidity and mortal­ity after pancreatoduodenectomy. Ann Surg Oncol. 2017;24(6):1714–21.
24. Melloul E, Lassen K, Roulin D, et al. Guidelines for perioperative care for pancreatoduo­denectomy: enhanced recovery after surgery (ERAS) recommendations 2019. World J Surg. 2020;44(7):2056–84.
25. Zhang L, Sanagapalli S, Stoita A. Challenges in diagnosis of pancreatic cancer. World J Gastroenterol. 2018;24(19):2047–60.
26. Bispo M, Marques S, Rio-Tinto R, Fidalgo P, Devière J. The role of endoscopic ultrasound in pancreatic cancer staging in the era of neoadjuvant therapy and personalised medicine. GE Port J Gastroenterol. 2021;28(2):111–20.
389
Part VI
Surgical Technique—Distal
Pancreatectomy
Chapter 22
Open Distal Pancreatectomy
AndrewJ.Sinnamon andPamelaJ.Hodul

Introduction

First reported attempts at open distal pancreatectomy date back to the 1880s, with Trendelenburg’s resection of a pancreatic tail sarcoma in 1882, and Billroth per­forming resections of both the pancreatic head and tail in 1884 [1]. Sadly, Trendelenburg’s initial foray into a distal pancreatic resection did not end well, as the patient reportedly died on postoperative day 1. Distal pancreatic resection was subsequently accomplished by the likes of Finney and Mayo at the turn of the cen­tury, but in general, signicant gains in pancreatic resection were limited due to the three observations made by Mickulicz: (1) the pancreas being “exceedingly difcult to reach,” (2) the notoriously difcult diagnosis of pancreatic disease, and (3) the “overwhelming physiological pitfalls” of surgery itself [13]. However, with the discovery of tumors of the endocrine pancreas in the late 1920s, enthusiasm for attempts at pancreatic resection returned, with a burst of activity by pancreatic sur­geons including Mayo, Roscoe, and Whipple, during which time the technique for the distal pancreatectomy was rened [1, 4].
Following the establishment of pancreatic resection by these founders of surgery, modern surgical methodology generally favored a retrograde approach to distal pan­createctomy. This has classically been described and taught utilizing a lateral-to­medial operative ow. In this way, the spleen is mobilized rst and retracted medially to gain exposure to the distal pancreas and lift it from the retroperitoneum. The popularity of this method is perhaps related to the ease of controlling the pancreas once the spleen is mobilized and manipulated with the left hand of the operating surgeon. However, this maneuver poses obvious risk of bleeding and may not place due focus on lymphadenectomy or resection margins in cases of malignancy.
A. J. Sinnamon (*) · P. J. Hodul Moftt Cancer Center, Tampa, FL, USA e-mail: Andrew.Sinnamon@moftt.org; Pamela.Hodul@moftt.org
Switzerland AG 2025 E. P. Ceppa et al. (eds.), The SAGES Manual of Evolving Techniques in Pancreatic Surgery, https://doi.org/10.1007/978-3-031-78409-5_22
393© The Author(s), under exclusive license to Springer Nature
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A. J. Sinnamon and P. J. Hodul
As emphasis on oncologic principles over trauma principles grew for elective resections, a transition to an antegrade approach gradually took hold in the surgical school of thought. The most referenced technique for an antegrade operative approach was described by Strasberg, Drebin, and Linehan in 2003 and termed the radical antegrade modular pancreatosplenectomy (RAMPS) [5]. The rationale for the RAMPS approach was to utilize a medial-to-lateral dissection to provide early vascular control and optimize lymphadenectomy (the “antegrade” aspect of RAMPS) and to achieve negative tangential margins by tailoring dissection to the appropriate retroperitoneal fascial plane by adjusting as needed (“modular”). By “modulating” the dissection, one may perform an anterior RAMPS by removing the anterior renal fascia while preserving the left adrenal gland or, alternatively, per­form a posterior RAMPS by removing the adrenal en bloc with the retroperitoneal dissection. Modern high-quality cross-sectional imaging allows for careful preop­erative planning to plan between the two. Initial experience with RAMPS showed good lymph node retrieval rate with median of 15 nodes removed as well as over 90% negative tangential margins in cases of adenocarcinoma, which was conrmed in a subsequent follow-up study [6, 7]. While prospective comparison of RAMPS to standard retrograde distal pancreatectomy is limited, growing retrospective data suggests a higher lymph node retrieval rate and more frequent R0 resection for oncologic resections [811]. Differences in intraoperative blood loss and operative time remain unclear [8, 11].
Since lymphadenectomy and clear retroperitoneal margins were the intended goals of the RAMPS technique, it is most appropriate for oncologic resections. However, because of the advantages of early vascular control with an antegrade approach, the technique has been applied to other indications for distal pancreatic resection as well. As a result, RAMPS has steadily become a preferred approach among many surgeons for open distal pancreatectomy and splenectomy and has subsequently been adapted for minimally invasive approaches, not to be discussed in this chapter.
With the rise of laparoscopy and robotic platforms, minimally invasive approaches have become preferable for many distal pancreatic resections using either antegrade or retrograde approach. However, open distal pancreatectomy remains the safest option in many cases. This is particularly so for patients with signicant past surgi­cal history, pancreatitis, and locally invasive malignancy. Borderline resectable pan­creatic adenocarcinoma is often best approached in an open manner for vascular involvement or need for en bloc resection of adjacent organs. When approaching these cases, the surgeon should be comfortable with both retrograde and antegrade approach so they may adapt to the case at hand. As such, both will be described in this chapter.
22 Open Distal Pancreatectomy
395

Preoperative Planning

Appropriate preoperative imaging to guide operative planning is critical. Pancreatic protocol CT scan is the preferred imaging modality in most cases, including thin section cuts at least <3mm in thickness and preferably 0.5–1mm [12]. Intravenous contrast should be used with imaging acquisition to include pancreatic parenchymal and arterial phase as well as delayed portal venous phase. If a specic pancreatic protocol is not available, a CT of the abdomen and pelvis with as thin as cuts as possible with arterial and venous phase may be an acceptable alternative. MRI with MRCP may be additionally helpful in cases with pancreatic cystic neoplasms where the relationship between cyst and pancreatic duct is of importance.
Open distal pancreatectomy is often performed for the specic reason that vas­cular involvement by a pathologic process makes a minimally invasive approach unsafe. For this reason, preoperative planning must include careful review of pancreas- dedicated imaging with attention to vascular anatomy. A potential site to divide the splenic artery must be identied that is free of disease pathology. This includes the absence of tumor encasement or abutment, but also in vasculopathic patients, this site must also be free of signicant calcications to be compliant for safe ligation. If there is no site for margin-negative division of the splenic artery due to tumor involvement up to and including the celiac trunk, en bloc resection of the celiac trunk (Appleby procedure) may be required. En bloc celiac resection with distal pancreatectomy will be thoroughly discussed in a subsequent chapter. In addi­tion to identifying a suitable site for division, the course of the splenic artery should also be noted preoperatively to minimize any possibility of disastrously mistaking the common hepatic artery for the splenic during the operation.
An understanding of the portal venous anatomy is also mandatory for preopera­tive planning. It should be known if the inferior mesenteric vein (IMV) drains into the splenic vein as this would be necessarily divided during the resection. Similarly, the drainage of the left gastric vein should be noted as it may be preferable to leave this intact for improved gastric venous outow. Identication of a proper site for ligation and division of the splenic vein is critical. For pancreatic cancer cases, thrombosis of the splenic vein is relatively common and may propagate to the level of the junction with the superior mesenteric vein (SMV). Occlusion of the splenic vein due to thrombosis or tumor encasement may result in left-sided portal hyper­tension. The presence of large varices, collaterals, or splenomegaly should be noted to prepare for safe resection while avoiding hemorrhage.
Based on preoperative imaging review, a general operative strategy may be planned. Depending on the site of disease, one may decide whether to divide the pancreas at the surgical neck (i.e., a subtotal pancreatectomy) versus transection at a point more distally. A more distal resection spares exocrine and endocrine func­tion but also typically involves dividing a thicker pancreas. Transection of the body appears to result in a higher rate of postoperative pancreatic stula but no difference in clinically signicant stulae [1315]. Operative planning must also consider the possibility of resection of adjacent structures, most commonly the splenic exure of
396
A. J. Sinnamon and P. J. Hodul
colon, posterior stomach, or left adrenal gland. The possibility of splenic preserva­tion will be discussed in detail in a subsequent chapter. If partial colectomy is planned, appropriate bowel preparation is warranted if not routinely performed for pancreatectomy. Surgical planning should consider whether an antegrade or retro­grade approach is most suitable given the anatomy. Lastly, the retroperitoneal mar­gin should be examined for an oncologic resection; if the posterior margin appears threatened with a standard resection plane, an anterior or posterior RAMPS (en bloc adrenalectomy) should be considered depending on the depth of invasion.
Other preoperative planning to consider for open distal pancreatectomy includes splenic immunization, thromboprophylaxis, consideration of bowel preparation, preoperative antibiotics, and relevant medications for an Enhanced Recovery After Surgery (ERAS) protocol. For planned splenectomy, vaccination against S. pneu- moniae, N. meningitidis, and H. inuenzae should ideally be started 10–12weeks preoperatively, if possible, for completion of all vaccines 2weeks prior to surgery. If not possible, vaccine series may be safely resumed 14days postoperatively [16,
17]. Thromboprophylaxis should be considered according to a patient’s calculated
risk for venous thromboembolism. Bowel preparation should be performed if con­sidering partial colectomy as noted above. However, the use of routine preparation for distal pancreatectomy is not standard; among 23 surveyed European centers performing distal pancreatectomy, routine bowel preparation was standard in only 8 [18]. Antibiotic prophylaxis should be administered within 1 h of incision and redosed accordingly during surgery. The use of ERAS protocols for pancreatec­tomy, potentially utilizing epidural anesthesia, will be discussed in a subsequent chapter, but may be an important piece of preoperative planning for open distal pancreatectomy.
Operative Setup andSteps
After induction of general anesthesia and placement of appropriate monitoring lines and urinary catheter, the patient is placed in the supine position with arms out. The abdomen is shaved, and sterile skin prep is applied. Open distal pancreatectomy may be performed using a variety of incisions, most commonly either a midline or transverse subcostal incision, and is per the operating surgeon’s preference. Appropriate incision may be tailored according to patient body habitus and intraab­dominal anatomy based on imaging review. A transverse incision is more benecial than midline for distal pancreatectomy according to one survey of pancreatic sur­geons [18]. Furthermore, a Cochrane review pooling data from different operations to compare midline versus transverse incision concluded that there is no difference in infection rate for elective operations and a lower rate of incisional hernia for transverse incision, and possibly less pain [19]. A left subcostal incision approxi­mately two ngerbreadths inferior to and in a parallel orientation with the costal margin is most appropriate and may be extended across the midline as needed. It is our preference in many cases to use a bilateral subcostal incision for optimal
22 Open Distal Pancreatectomy
exposure, providing ample visualization of both the medial aspect of vascular dis­section and the lateral peri-splenic dissection, both sites of potential unwanted nui­sance bleeding. We prefer to use the Thompson retractor system for open distal pancreatectomy.
397
Diagnostic Laparoscopy
Regardless of the preferred open incision, diagnostic laparoscopy is valuable prior to entering the abdomen as it may spare a considerable proportion of patients a nontherapeutic laparotomy. This is particularly the case when operating for pancre­atic adenocarcinoma. Older data suggests that diagnostic laparoscopy at the outset of a planned pancreatic resection for adenocarcinoma may change management in up to 44% of cases [20]. More contemporary data from the Dutch PREOPANC trial found that staging laparoscopy identied occult peritoneal metastatic disease in 11–12% of cases [21]. Laparoscopy may be rapidly performed using a single cam­era port, with placement of additional ports as needed for visualization and/or biopsy of suspicious lesions. Ports may be placed that will be incorporated into the open incision, but this is not mandatory; a supraumbilical camera port is typically most appropriate for staging purposes and will obviously not lie in a subcostal inci­sion. When operating for malignancy, laparoscopy should include thorough exami­nation of the liver surface, omentum, peritoneal surface, and pelvis. Any suspicious lesions are biopsied and sent for frozen pathologic examination.
Open Exposure ofthePancreas
Once the decision is made to proceed with laparotomy, the abdomen is entered via the preferred incision. Care should be taken during this step to spare the falciform ligament so that it may be used later for ap coverage of the transected pancreas. Exposure of the pancreas may be rst obtained by dividing the gastrocolic ligament to enter the lesser sac. Dissection is continued up the greater curvature of the stom­ach dividing the gastrocolic and gastrosplenic ligaments containing the short gastric vessels all the way to the left crura. Bipolar energy devices are useful for efcient hemostasis at this step. The gastroepiploic pedicle should be spared for gastric per­fusion. Once the superior-most short gastric vessels are divided, it can be helpful to turn laterally to dissect just superior to the spleen in order to simplify completion of the dissection at a later point. Division of the gastrocolic ligament is then continued medially toward the pylorus. Dissection in this direction can proceed as far toward the patient’s right as necessary to provide adequate exposure. In cases with a history of pancreatitis, the gastrocolic ligament may be found to be fused to the transverse mesocolon, or the posterior stomach may be densely adhered to the anterior pancre­atic body. Careful dissection at this time should be undertaken to avoid entering the