Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1260_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
15.09.2026
Размер:
15 Мб
Скачать
☆
Robotic hepatopancreatic surgery 139
7 Venkat R, Edil BH, Schulick RD, et al. Laparoscopic distal
pancreatectomy is associated with significantly less overall morbidity compared to the open technique: a systematic review and meta–analysis. Ann Surg 2012; 255:1048–1059.
8 Simillis C, Constantinides VA, Tekkis PP, et al. Laparoscopic
versus open hepatic resections for benign and malignant neoplasms – a meta-analysis. Surgery 2007; 141:203–211.
9 Kendrick ML, Cusati D. Total laparoscopic pancreaticoduo-
denectomy: feasibility and outcome in an early experience. Arch Surg 2010; 145:19–23.
10 Sarpel U, Hefti MM, Wisnievsky JP, et al. Outcome for patients
treated with laparoscopic versus open resection of hepato­cellular carcinoma: case-matched analysis. Ann Surg Oncol 2009; 16:1572–1577.
11 Castaing D, Vibert E, Ricca L, et al. Oncologic results of
laparoscopic versus open hepatectomy for colorectal liver metastases in two specialized centers. Ann Surg 2009; 250: 849–855.
12 Daouadi M, Zureikat AH, Zenati MS, et al. Robot-assisted
minimally invasive distal pancreatectomy is superior to the laparoscopic technique. Ann Surg 2013; 257:128–132.
13 Prasad SM, Prasad SM, Maniar HS, et al. Surgical robotics:
impact of motion scaling on task performance. J Am Coll Surg 2004; 199:863–868.
14 Giulianotti PC, Sbrana F, Bianco FM, et al. Robot-assisted
laparoscopic pancreatic surgery: single-surgeon experience. Surg Endosc 2010; 24:1646–1657.
15 Buell JF, Cherqui D, Geller DA, et al. The international
position on laparoscopic liver surgery: The Louisville State­ment, 2008. Ann Surg 2009; 250:825–830.
16 Nguyen KT, Gamblin TC, Geller DA. World review of laparo-
scopic liver resection –2,804 patients. Ann Surg 2009; 250:831–841.
17 Giulianotti PC, Coratti A, Angelini M, et al. Robotics in general
surgery: personal experience in a large community hospital. Arch Surg 2003; 138:777–784.
18 Vibert E, Denet C, Gayet B. Major digestive surgery using a
remote-controlled robot: the next revolution. Arch Surg 2003; 138:1002–1006.
19 Giulianotti PC, Coratti A, Sbrana F, et al. Robotic liver surgery:
results for 70 resections. Surgery 2011; 149:29–39.
20 Tsung A, Geller DA, Sukato DC, et al. Robotic versus laparo-
scopic hepatectomy: a matched comparison. Ann Surg 2014; 249:549–555. Lai EC, Yang GP, Tang CN. Robot-assisted laparoscopic liver
21
resection for hepatocellular carcinoma: short-term outcome. Am J Surg 2013; 205:697–702.
22 Troisi RI, Patriti A, Montalti R, et al. Robot assistance in liver
surgery: a real advantage over a fully laparoscopic approach? Results of a comparative bi-institutional analysis. Int J Med Robot 2013; 9:160–166.
23 Choi GH, Choi SH, Kim SH, et al. Robotic liver resection:
technique and results of 30 consecutive procedures. Surg Endosc 2012; 26:2247–2258.
24 Ji WB, Wang HG, Zhao ZM, et al. Robotic-assisted laparoscopic
anatomic hepatectomy in China: initial experience. Ann Surg 2011; 253:342–348.
25 Berber E, Akyildiz HY, Aucejo F, et al. Robotic versus laparo-
scopic resection of liver tumours. HPB (Oxford) 2010; 12: 583–586.
26 Abood GJ, Tsung A. Robot-assisted surgery: improved tool for
major liver resections? J Hepatobiliary Pancreat Sci 2013; 20:151–156.
27 Kendrick ML, Sclabas GM. Major venous resection during
total laparoscopic pancreaticoduodenectomy. HPB (Oxford) 2011; 13:454–458.
28 Gumbs AA, Rodriguez Rivera AM, Milone L, et al. Laparo-
scopic pancreatoduodenectomy: a review of 285 published cases. Ann Surg Oncol 2011; 18:1335–1341.
29 Tran Cao HS, Lopez N, Chang DC, et al. Improved perioper-
ative outcomes with minimally invasive distal pancreatec­tomy: results from a population-based analysis. JAMA Surg 2014; 149:237–243.
30 Melvin WS, Needleman BJ, Krause KR, et al. Robotic resec-
tion of pancreatic neuroendocrine tumor. J Laparoendosc Adv Surg Tech A 2003; 13:33–36.
31 Winer J, Can MF, Bartlett DL, et al. The current state of
robotic-assisted pancreatic surgery. Nat Rev Gastroenterol Hepatol 2012; 9:468–476.
32 Milone L, Daskalaki D, Wang X, et al. State of the art in robotic
pancreatic surgery. World J Surg 2013; 37:2761–2770.
33 Strijker M, van Santvoort HC, Besselink MG, et al. Robot-
assisted pancreatic surgery: a systematic review of the litera­ture. HPB (Oxford) 2013; 15:1–10.
34 Zhang J, Wu WM, You L, et al. Robotic versus open pancrea-
tectomy: a systematic review and meta-analysis. Ann Surg Oncol 2013; 20:1774–1780.
35 Zureikat AH, Moser AJ, Boone BA, et al. 250 robotic pancre-
atic resections: safety and feasibility. Ann Surg 2013; 258: 554–559.
36 Giulianotti PC, Sbrana F, Bianco FM, et
laparoscopic pancreatic surgery: single-surgeon experience. Surg Endosc 2010; 24:1646–1657.
37 Chalikonda S, Aguilar-Saavedra JR, Walsh RM. Laparoscopic
robotic-assisted pancreaticoduodenectomy: a case-matched comparison with open resection. Surg Endosc 2012; 26: 2397–2402.
38 Lai EC, Yang GP, Tang CN. Robot-assisted laparoscopic
pancreaticoduodenectomy versus open pancreaticoduode­nectomy – a comparative study. Int J Surg 2012; 10: 475–479.
39 Zhou NX, Chen JZ, Liu Q, et al. Outcomes of pancreatoduo-
denectomy with robotic surgery versus open surgery. Int J Med Robot 2011; 7:131–137.
40 Kang CM, Kim DH, Lee WJ, et al. Initial experiences using
robot-assisted central pancreatectomy with pancreaticogas­trostomy: a potential way to advanced laparoscopic pancrea­tectomy. Surg Endosc 2011; 25:1101–1106.
al. Robot-assisted
140 Chapter 8
41 Giulianotti PC, Sbrana F, Blanco FM, et al. Robot-assisted
laparoscopic middle pancreatectomy. J Laparoendosc Adv Surg Tech A 2010; 20:135–139.
42 Hwang HK, Kang CM, Chung YE, et al. Robot-assisted spleen-
preserving distal pancreatectomy: a single surgeon’s experi­ences and proposal of clinical application. Surg Endosc 2013; 27:774–781.
43 Waters JA, Canal DF, Wiebke EA, et al. Robotic distal
pancreatectomy: cost effective? Surgery 2010; 148: 814–823.
44 Fernandes E, Giulianotti PC. Robotic-assisted pancreatic sur-
gery. J Hepatobiliary Pancreat Sci 2013; 20:583–589.
45 Buchs NC, Addeo P, Bianco FM, et al. Robotic versus open
pancreaticoduodenectomy: a comparative study at a single institution. World J Surg 2011; 35:2739–2746.
46 Daouadi M, Zureikat AH, Zenati MS, et al. Robot-assisted
minimally invasive distal pancreatectomy is superior to the laparoscopic technique. Ann Surg 2013; 257:128–132.
47 Kang CM, Kim DH, Lee WJ, et al. Conventional laparoscopic
and robot-assisted spleen-preserving pancreatectomy: does da Vinci have clinical advantages? Surg Endosc 2011; 25:2004–2009.
48 Baker MS, Bentrem DJ, Ujiki MB, et al. Adding days spent in
readmission to the initial postoperative length of stay limits the perceived benefit of laparoscopic distal pancreatectomy when compared with open distal pancreatectomy. Am J Surg 2011; 201:295–299.
49 Tzeng CW, Tran Cao HS, Lee JE, et al. Treatment sequencing
for resectable pancreatic cancer: influence of early metastases and surgical complications on multimodality therapy com­pletion and survival. J Gastrointest Surg 2014; 18:16–25.
50 Zeh HJ, Zureikat AH, Secrest A, et al. Outcomes after robot-
assisted pancreaticoduodenectomy for periampullary lesions. Ann Surg Oncol 2012; 19:864–870.
51 Tran Cao HS, Kellogg B, Lowy AM, et al. Cystic neoplasms of
the pancreas. Surg Oncol Clin N Am 2010; 19:267–295.
CHAPTER 9
Enhanced recovery after hepatopancreatobiliary surgery
David Fuks,1Thomas A. Aloia,2and Brice Gayet
1
Department of Digestive Diseases, Institut Mutualiste Montsouris, Paris, France
2
Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA
EDITOR COMMENT
In this chapter, the authors provide an overview of the available evidence regarding enhanced recovery after hepatopancreatobiliary surgery. They remind us that optimal recovery for the major procedures we perform in liver and pancreas surgery begins prior to surgery. Meticulous patient selection and optimization of medical comorbidities are key contributors to the goals of any fast-track program, shortening length of stay while lowering perioperative morbidity. During surgery, the surgeon must strive for a transfusion rate of zero, while communicating clearly with the anesthesia team regarding fluid, pain, and analgesic management. While the results of published literature on enhanced and fast-track recovery programs can be difficult to interpret because of variations in protocol adherence, uncontrolled confounders, and nonweighted composite outcome measures, a programmatic approach to optimizing recovery is important. In addition to programmatic policies of early enteral nutrition, early mobilization, and restrictive transfusion policies, excellent communication among the patient, family, nursing, anesthesia, and surgery staff is critical for ensuring optimal recovery with faster discharge. As advanced laparoscopic hepatopancreatobiliary surgeons, we must remind ourselves that low complication rate is the most important component in earlier discharge.
Keywords: enhanced recovery after hepatic surgery, enhanced recovery after hepatopancreatobiliary surgery, enhanced recovery after pancreas surgery, fast-track surgery, length of stay
9.1 Introduction
Major abdominal surgical procedures such as hepatic or pancreatic resections cause a considerable surgical stress reaction and derangements in metabolic and cardio­pulmonary function [1,2]. In past decades, advances in diagnostic and surgical techniques and improved anes­thetic/intensive care management have led to better out­comes after both liver and pancreatic resections. Mortality for the most common liver and pancreatic resection has been reported to be consistently below 5% in specialized centers [3,4]. However, morbidity, especially for pancre­atic surgery, remains high at a rate of 40–60% [3,4]. Complications, such as anastomotic leak, hemorrhage, biliary and pancreatic fistula, delayed gastric emptying
1
(DGE), and intra-abdominal abscess, are the main reasons for delayed recovery and frequently require additional percutaneous or surgical interventions.
In the past decade, fast-track surgery protocols have been used for various types of surgery, to attenuate the stress response to surgical trauma and improve recovery, thereby decreasing postoperative complications and postoperative length of stay (LOS) [5]. The intention is to prevent complications associated with an exagger­ated inflammatory reaction to surgery, such as poor healing, infections, and organ dysfunction [6]. Fast-track surgery incorporating intensive optimization of early patient mobility, intestinal function, and analgesia [7] contributes to expediting recovery and minimizing morbidity [8].
Laparoscopic Liver, Pancreas, and Biliary Surgery: Textbook and Illustrated Video Atlas, First Edition. Edited by Claudius Conrad and Brice Gayet. © 2017 John Wiley & Sons, Ltd. Published 2017 by John Wiley & Sons, Ltd.
141
142 Chapter 9
Table 9.1 Elements included in the fast-track programme applicable to both liver and pancreatic surgery.
Evidence-based factors Probably useful factors
No oral bowel preparation Preoperative counseling Preoperative feeding: carbohydrate loading up to 2 h before surgery Provision of intravenous analgesia No preanaesthetic medication Stimulation of bowel movement with laxatives Antithrombotic prophylaxis Early and scheduled mobilization Single-dose antibiotics Audit Epidural analgesia Prevention of postoperative nausea and vomiting Avoidance of hypothermia No routine drainage of peritoneal cavity Preoperative biliary drainage if total bilirubinemia >250 μmol/L No postoperative nasogastric intubation Optimized fluid balance Removal of urinary catheter on day 1 Normal food at will after surgery from day 1
∗
Specific to liver surgery.
∗∗
Specific to pancreas surgery.
∗
∗∗
Fast-track surgery protocols have gained ground quickly because of the associated cost efficiency derived from the reduction in LOS, an important issue in today’s context of rapidly increasing healthcare costs and the consequent need for optimization. Studies showing fast-track surgery protocols that reduce LOS and morbid­ity rates and improved patient satisfaction have been published for vascular [9], orthopedic [10], gynecologi­cal [11], breast [12], bariatric [13], and prostate surgery [14], as well as other forms of abdominal (includ­ing major) surgery [15]. However, although fast-track surgery protocols have also been implemented in hep­atopancreatobiliary (HPB) surgery, their widespread acceptance remains limited. A summary of fast-track protocols applicable to both liver and pancreas surgery is detailed in Table 9.1.
9.2 Fast-track liver surgery
Liver resection is associated with specific postoperative changes which need to be recognized when optimizing outcomes of patients following liver surgery. The surgical outcomes of liver resection are largely dependent on the complexity of the procedure and the host liver function. To maximize the potential benefit of fast-track liver sur­gery programs, future research needs to aim at establish­ing perioperative care plans specific to liver surgery. We have identified a total of 257 relevant articles on fast-track
liver surgery. These include studies investigating out­comes of open hepatic surgery, including two randomized controlled trials (RCTs) [16,17], two prospective cohort studies [18,19], one retrospective cohort study [20], and two case-control studies [21,22].
The two case–control trials compared outcomes of fast- track surgery protocols with those of conventional care after laparoscopic surgery [23,24]. As expected, fast-track surgery programs in those two studies reduced LOS, a result seen in all studies on fast-track surgery in open liver resection. However, fast-track programs have the ability to reduce not only LOS but also complication rates. Similar to the colorectal literature [5], in hepatic surgery, fast-track programs reduced complication rates: a meta-analysis of two published RCTs [16,17] shows a reduction in overall complication rates. This reduction was not reproduced in non-RCT studies, though this may be due to selection bias or to the methodology of those particular protocols. In the randomized series reported by Ni et al. [17], the selected population was particularly young and fit, and it is possible that better general health in the study populations leads to no difference between fast-track and conventional care with respect to complication rate [16,17].
Compliance with fast-track protocols is an additional factor that has been examined in several studies. Com­pliance with a fast-track program incorporating 19 com­ponents was exceptionally high in the series published by Jones et al. [16]. While only three trials commented on adherence to the protocol, higher rates of compliance are
Enhanced recovery after hepatopancreatobiliary surgery 143
associated with reduced LOS. Further, low compliance is associated with higher readmission rates [16,18,22]. Compliance with fast-track programs is clearly an area which has potential to increase the efficacy of fast-track liver surgery protocols.
Although the rates of general complications were reduced in the two RCTs, no difference in liver-specific surgical complications was observed. Liver resection offers a unique set of postoperative circumstances as a result of liver regeneration, the anatomical complexity of biliary drainage and intraoperative vascular inflow con­trol, and the transient impairment of liver function fol­lowing resection [25]. It is therefore not surprising that a fast-track surgery approach does not reduce liver-specific complications. However, while fast-track surgery proto­cols focus on general pre- and postoperative considera­tions, the liver surgeon must not forget to optimize intraoperative care for best possible outcome. For exam­ple, minimizing blood loss is one area that may reduce liver-specific surgical complications [26–28].
Overload of salt and free water, as well as hypovolemia in the perioperative period, all increase postoperative complication rates [29], suggesting that near-zero fluid balance should be achieved around the time of surgery. Determining the correct amount required is complicated by the use of epidural anesthesia as it causes vaso­dilatation and intravascular depletion with hypotension, often treated with fluid resuscitation. This may result in the administration of unnecessary and large volumes of fluid [30]. Importantly, elevated central venous pressure (CVP) has been shown to be associated with intraoper­ative blood loss during liver resection [31]. Six of the nine trials included a carecomponent based on the reduction of intraoperative fluid, but only two [21,22] commented on titration of intravenous fluid according to CVP. Jones et al. used goal-directed fluid therapy guided by cardiac output monitoring to prevent fluid overload, although they only monitored this in the early postoperative period [16].
Since the successful report of the first laparoscopic liver wedge resection in 1991 [32], laparoscopic liver resection has progressively gained popularity. For minor liver resec­tions, comparative studies of open and laparoscopic proce­dures have shown that laparoscopic liver resection resulted in decreased intraoperative bleeding, fewer complications, and shorter postoperative hospital stays [33–37]. Over the last few years, technological and instrumental improve­ments have resulted in several centers reporting better hemostasis during laparoscopic liver resection [38–41].
Fast-track surgery protocols in liver surgery should incorporate preoperative, intraoperative, and post­operative components to maximize their benefits. Inter­estingly, use of a thoracic epidural was not explored in any of the studies. Although a thoracic epidural is recom­mended in fast-track surgery in the context of colorectal surgery [42], its use has been questioned in liver sur­gery [43]. There is conflicting evidence regarding the impact of epidurals on recovery in liver surgery, and this continues to be an active area of investigation [44,45]. Further evaluation of analgesia in liver surgery within the context of a fast-track surgery program is required to establish optimal practice. Indeed, paracetamol (acet­aminophen) is routinely utilized as the backbone of analgesic regimens [46,47], but in major hepatic resec­tions it is often withheld for fear of inducing liver damage, which increases opiate requirements.
In summary, the level I evidence investigating fast­track surgery protocols following liver surgery is limited and only two RCTS have been conducted. Fast track liver surgery programs seem to reduce complication rates, although surgical morbidity remains high and is currently unaffected by fast-track surgery protocols following liver surgery. Postoperative LOS is reduced in the context of fast-track surgery in comparison with conventional care (Table 9.2). Future research should concentrate on peri­operative care components specific to liver surgery, such as optimal analgesic regimens and intraoperative manip­ulations to reduce blood loss, rather than simply trans­ferring fast-track concepts from colorectal to liver surgery.
9.3 Fast-track pancreas surgery
Most series focusing on fast-track surgery in pancreatic surgery concern pancreatoduodenectomy (PD). No RCTs have been conducted in pancreatic surgery. This is prob­ably due to the fact that RCTs are difficult to organize for multimodal recovery programs under greatly varying conditions (according to the complexity of liver resec­tion). Problems are likely to be encountered with blinding when various interventions and professionals are involved. The incidence of specific complications, such as DGE and pancreatic fistula, tended to be lower in the fast-track surgery group, but meta-analysis in patients undergoing PD did not show statistically significant dif­ferences [48,49]. The included studies were either retro­spective or prospective case series, or comparative studies
144 Chapter 9
Table 9.2 Postoperative outcomes after implementation of a clinical pathway in liver surgery.
Study Length of stay Morbidity % Mortality % Readmissions %
Study vs control Study vs control Study vs control Study vs control group group group group
Lin et al. 2011 [21] 7 vs 11 days Hendry et al. 2010 [62] 3 vs 5 days Stoot et al. 2009 [24] 5 vs 7 days 15 vs 15% 0 vs 0% 0 vs 0% Koea et al. 2009 [44] 4 vs 6 days 19 0 4 Van Dam et al. 2008 [22] 6 vs 8 days MacKay & O ’Dwyer 4 days (2–7) 17 0 0 2008 [63]
∗
Significant difference.
∗
∗
∗
46 vs 43% 1.8 vs 1.6% 7 vs 3% 17 2 5
41 vs 31% 0 vs 2% 13 vs 10%
based on historical controls. Indeed, there seemed to be little replication of methodology in the studies examined. Individual studies used different study protocols incorpo­rating a variety of elements, and some protocols may have included elements that are more conservative than others. For example, postoperative feeding started from postoperative days 1–2 in some studies [50,51], whereas other studies began with liquid intake with a gradual increase from clear to full liquids and solid food from days 3–4 [52–57]. Unfortunately, it is still unclear which elements are important in perioperative care in pancre­atic resections, and therefore we cannot draw definitive conclusions as to the precise benefit of fast-track programs in pancreas surgery.
Similar to liver fast-track programs, most studies on pancreatic fast-track surgery do not investigate compli­ance with the protocol. Therefore, it remains unclear what the actual measurable difference in perioperative
Table 9.3 Postoperative outcomes after implementation of a clinical pathway in pancreatic surgery.
Study Length of stay Morbidity % Mortality % Readmissions %
Study vs control Study vs control Study vs control Study vs control group group group group
care between study and control group is. Policies to improve postoperative protocol adherence, in particular, should be considered. For instance, reorganization of surgical wards and continuous education of nurses and staff [58] may provide helpful information on which portions of a fast-track program have improved out­comes. A study by Ahmed et al. showed that an overall protocol compliance of 77% compared with 88% com­pliance in patients participating in a clinical trial does not negatively affect outcome [59].
The consistency between criteria defining minor and major complications after pancreatic surgery in the included studies is also limited. Only one study reported complications according to a validated classification scheme (Clavien–Dindo classification) [60]. Therefore, comparing morbidity between different centers is diffi­cult, as shown by the variations in leakage rates ranging from 2% to 62% (Table 9.3). A suggestion would be to use
Robertson et al. 2012 [56] 10 days (8–17) 46% 4% 4% Di Sebastiano et al. 2011 [51] 10 days (6–69) 39% 2.7% 6% Kennedy et al. 2009 [57] 7 vs 10 days Balzano et al. 2008 [54] 13 vs 15 days Berberat et al. 2007 [52] 10 days (4–115) 25% 2% 3% Vanounou et al. 2007 [53] 8 vs 8 days 54 vs 62% 1.4 vs 1.6% 9 vs 6% Kennedy et al. 2007 [55] 7 vs 13 days ∗ 37 vs 44% 1.1 vs 2.3% 8 vs 7% Porter et al. 2000 [64] 13 vs 16 days
∗
Significant difference.
∗
∗
∗
16 vs 37% 1.1 vs 2.3% 7 vs 25% 47 vs 59%
24 vs 20% 1 vs 3% 9 vs 10%
∗
3.6 vs 2.8% 7 vs 6%
∗
Enhanced recovery after hepatopancreatobiliary surgery 145
a composite endpoint [61], which would reduce the required sample sizes for studies and improve objectivity and comparability.
In a meta-analysis of fast-track programs for pancreas surgery, readmission rates were not significantly higher in the fast-track surgery group. One s tudy reported a nonsignificant 1% higher mortality rate in the fast­track surgery group [54]. Also, in a meta-analysis of the four studies addressing PDs, mortality was not significantly different. Additionally, hospital costs were si gnificantly lower in three of the four studies that reported a cost-effectiveness analysis. As for liver
surgery, few data on functional recovery or predefined discharge criteria were available, and accordingly, no conclusion could be drawn.
In summary, although the available evidence is still limited, implementation of a fast-track surgery program in pancreatic resections, particularly PD, is feasible. Such programs may contribute to a shorter hospital stay and do not seem to compromise outcome measures, such as morbidity, mortality, and readmissions. Future studies should report on predefined discharge criteria and time to functional recovery to assess whether postoperative recovery is in fact accelerated.
KEY POINTS
• Recognition of specific postoperative changes is associated with optimal outcomes for patients following liver resection. Outcomes are largely dependent on complexity of the procedure and the host liver function.
• Fast-track programs have the ability to reduce LOS and complication rates. Future research in establishing perioperative care plans specific to liver surgery can help maximize the potential benefit of fast-track programs.
• Fast-track surgery protocols in liver surgery should incorporate preoperative, intraoperative, and postoperative components.
• Most studies on pancreatic fast-track surgery have not investigated compliance with protocol. Policies to improve postoperative
protocol adherence should be considered.
• Although available evidence is limited, a fast-track surgery program in pancreatic resections, particularly PD, is feasible. It may contribute to shorter hospital stay without compromising morbidity, mortality, and readmissions.
• Future studies should report predefined discharge criteria and time to functional recovery to assess whether postoperative recovery is in fact accelerated.
References
1 Reissfelder C, Rahbari NN, Koch M, et al. Postoperative
course and clinical significance of biochemical blood tests following hepatic resection. Br J Surg 2011; 98:836–844.
2 Lassen K, Coolsen MME, Slim K, et al. Guidelines for peri-
operative care for pancreaticoduodenectomy: Enhanced Recovery After Surgery (ERAS World J Surg 2013; 37:240–258.
3 Virani S, Michaelson J, Hutter M, et al. Morbidity and mor-
tality after liver resections: results of the patient safety in surgery study. J Am Coll Surg 2007; 204:1248–1292.
4 Sewnath ME, Karsten TM, Prins MH, et al. A metaanalysis on
the efficacy of preoperative biliary drainage for tumors caus­ing obstructive jaundice. Ann Surg 2002; 236:17–27.
5 Varadhan KK, Neal KR, Dejong CH, et al. The enhanced
recovery after surgery (ERAS) pathway for patients under­going major elective open colorectal surgery: a meta-anal­ysis of randomized controlled trials. Clin Nutr 2010; 29:434–440.
®
) Society Recommendations.
6 Holte K, Kehlet H. Epidural anaesthesia and analgesia – effects
on surgical stress response and implications for postoperative nutrition. Clin Nutr 2002; 21:199– 206.
7 Grade M, Quintel M, Ghadimi M. Standard perioperative
management in gastrointestinal surgery. Langenbecks Arch Surg 2011; 396:591–606.
8 Kehlet H. Multimodal approach to control postoperative
pathophysiology and rehabilitation. Br J Anaesth 1997; 78:606–617.
9 Brustia P, Renghi A, Gramaglia L, et al. Mininvasive abdomi-
nal aortic surgery. Early recovery and reduced hospitalization after multidisciplinary approach. J Cardiovasc Surg (Torino) 2003; 44:629–635.
10 Scott N, McDonald D, Campbell J, et al. The use of enhanced
recovery after surgery (ERAS ) principles in Scottish ortho­paedic units – an implementation and follow-up at 1 year, 2010–2011: a report from the Muculoskeletal Audit, Scot­land. Arch Orthop Trauma Surg 2013; 133:117–124.
11 Lv D, Wang X, Shi G. Perioperative enhanced recovery pro-
grammes for gynaecological cancer patients. Cochrane Data­base Syst Rev 2010; 6:CD008239.
146 Chapter 9
12 Arsalani-Zadaeh R, El Fadl D, Yassin N, MacFie J. Evidence-
based review of enhancing postoperative recovery after breast surgery. Br J Surg 2011; 98:181–196.
13 McCarty TM, Arnold DT, Lamont JP, Fisher TL, Kuhn JA.
Optimizing outcomes in bariatric surgery: outpatient laparo­scopic gastric bypass. Ann Surg 2005; 242:494–498; discus­sion 498–501.
14 Kirsh EJ, Worwag EM, Sinner M, Chodak GW. Using out-
come data and patient satisfaction surveys to develop policies regarding minimum length of hospitalization after radical prostatectomy. Urology 2000; 56:101–106; discussion 106–107.
15 Cerfolio RJ, Bryant AS, Bass CS, Alexander JR, Bartolucci AA.
Fast tracking after Ivor Lewis esophagogastrectomy. Chest 2004; 126:1187–1194.
16 Jones C, Kelliher L, Dickinson M, et al. Randomized clinical
trial on enhanced recovery versus standard care following open liver resection. Br J Surg 2013; 100:1015–1024.
17 Ni C, Yang Y, Chang Y, et al. Fast-track surgery improves
postoperative recovery in patients undergoing partial hepa­tectomy for primary liver cancer: a prospective randomized controlled trial. Eur J Surg Oncol 2013; 39:542–547.
18 MacKay G, O’Dwyer P. Early discharge following liver resec-
tion for colorectal metastases. Scott Med J 2008; 53:22–24.
19 Schultz N, Larsen P, Klarskov B, et al. Evaluation of a fast-track
programme for patients undergoing liver resection. Br J Surg 2013; 100:138–143.
20 Connor S, Cross A, Sakowska M, Linscott D, Woods J. Effects
of introducing an enhanced recovery after surgery pro­gramme for patients undergoing open hepatic resection. HPB 2013; 15:294–301.
21 Lin D, Li X, Ye Q, Lin F, Li L, Zhang Q. Implementation of a
fast-track clinical pathway decreases postoperative length of stay and hospital charges for liver resection. Cell Biochem Biophys 2011; 61:413–419.
22 Van Dam R, Hendry P, Coolsen M, et al. on behalf of the
Enhanced Recovery After Surgery (ERAS) Group. Initial experience with a multimodal enhanced recovery pro­gramme in patients undergoing liver resection. Br J Surg 2008; 95:969–975.
23 Sànchez-Pérez B, Aranda-Narvaez J, Suarez-Munoz M, et al.
Fast-track programme in laparoscopic liver surgery: theory of fact. World J Gastrointest Surg 2012; 4:246–250.
24 Stoot J, van Dam R, Busch O, et al. on behalf of the Enhanced
Recovery After Surgery (ERAS) Group. The effect of multi­modal fast-track programme on outcomes in laparoscopic liver surgery: a multicentre pilot study. HPB (Oxford) 2009; 11:140–144.
25 Hughes MJ, McNally S, Wigmore SJ. Enhanced recovery
following liver surgery: a systematic review and meta-analy­sis. HPB (Oxford) 2014; 16(8):699–706.
26 Hammond J, Guha I, Beckingham I, Lobo D. Prediction,
prevention and management of postresection liver failure. Br J Surg 2011; 98:1188–1200.
27 Zimmitti G, Roses R, Andreou A, et
al. Greater complexity of
liver surgery is not associated with an increased incidence of liver-related complications except for bile leak: an experience with 2628 consecutive resections. J Gastrointest Surg 2013; 17:57–64.
28 Poon R, Fan S, Lo C, et al. Improving perioperative outcome
expands the role of hepatectomy in management of benign and malignant hepatobiliary diseases. Analysis of 1222 con­secutive patients from a prospective database. Ann Surg 2004; 240:698–710.
29 Brandstrup B, Tønnesen H, Beier-Holgersen R, et al. Effects of
intravenous fluid restriction on postoperative complications: comparison of two perioperative fluid regimens: a random­ized assessor-blinded multicenter trial. Ann Surg 2003; 238 (5):641–648.
30 Holte K, Foss NB, Svensén C, Lund C, Madsen JL, Kehlet H.
Epidural anesthesia, hypotension, and changes in intra­vascular volume. Anesthesiology 2004; 100(2):281–286.
31 McNally S, Revie E, Massie L, et al. Factors in perioperative
care that determine blood loss in liver surgery. HPB (Oxford) 2012; 14:236–241.
32 Reich H, McGlynn F, DeCaprio J, Budin R. Laparoscopic
excision of benign liver lesions. Obstet Gynecol 1991; 78:956–958.
33 Ito K, Ito H, Are C, et al. Laparoscopic versus open liver
resection: a matched-pair case control study. J Gastrointest Surg 2009; 13:2276–2283.
34 Belli G, Limongelli P, Fantini C, et al. Laparoscopic and open
treatment of hepatocellular carcinoma in patients with cir­rhosis. Br J Surg 2009; 96:1041–1048.
35 Topal B, Fieuws S, Aerts R, et al. Laparoscopic versus open
liver resection of hepatic neoplasms: comparative analysis of short-term results. Surg Endosc 2008; 22:2208–2213.
36 Tranchart H, Di Giuro G, Lainas P, et al. Laparoscopic resection
for hepatocellular carcinoma: a matched-pair comparative study. Surg Endosc 2010; 24:1170–1176.
37 Buell JF, Cherqui D, Geller DA, et al. The international
position on laparoscopic liver surgery: he Louisville State­ment, 2008. Ann Surg 2009; 250:825–830.
38 Gayet B, Cavaliere D, Vibert E, et al. Totally laparoscopic right
hepatectomy. Am J Surg 2007; 194:685–689.
39 Dagher I, O’Rourke N, Geller DA, et al. Laparoscopic major
hepatectomy: an evolution in standard of care. Ann Surg 2009; 250:856–860.
40 Martin RC, Scoggins CR, McMasters KM. Laparoscopic
hepatic lobectomy: advantages of a minimally invasive approach. J Am Coll Surg 2010; 210:627–634. Nitta H, Sasaki A, Fujita T, et al. Laparoscopy-assisted major
41
liver resections employing a hanging technique: the original procedure. Ann Surg 2010; 251:450–453.
42 Lassen K, Soop M, Nygren J, et al. for the Enhanced Recovery
After Surgery (ERAS) Group. Consensus review of optimal perioperative care in colorectal surgery. Arch Surg 2009; 144:961–969.
Enhanced recovery after hepatopancreatobiliary surgery 147
43 Tzimas P, Prout J, Papadopolous G, Mallett S. Epidural anaes-
thesia and analgesia for liver resection. Anaes thesia 2013; 68:628–635.
44 Koea J, Young Y, Gunn K. Fast track liver resection: the effect
of a comprehensive care package and analgesia with single dose intrathecal morphine with gabapentin or continuous epidural analgesia. HPB Surg 2009; 2009:271986
45 Revie E, McKeown D, Wilson J, Garden O, Wigmore S.
Randomized clinical trial of local infiltration plus patient­controlled opiate analgesia vs epidural analgesia following liver resection surgery. HPB (Oxford) 2012; 14:611–618.
46 Galinski M, Delhotal-Lan des B, Lockey D, et al. Reduction of
paracetamol metabolism after hepatic resection. Pharmacol­ogy 2006; 77:161–165.
47 Hoffmann H, Kettelhack C. Fast-track surgery – conditions
and challenges in postsurgical treatment: a review of ele­ments of translational research in enhanced recovery after surgery. Eur Surg Res 2012; 49:24–34.
48 Coolsen MM, van Dam RM, van der Wilt AA, Slim K, Lassen
K, Dejong CH. Systematic review and meta-analysis of enhanced recovery after pancreatic surgery with particular emphasis on pancreaticoduodenectomies. World J Surg 2013; 37(8):1909–1918.
49 Lassen K, Coolsen MM, Slim K, et al. Enhanced Recovery
After Surgery (ERAS) Society for Perioperative Care; Euro­pean Society for Clinical Nutrition and Metabolism (ESPEN); International Association for Surgical Metabolism and Nutri­tion (IASMEN). Guidelines for perioperative care for pan­creaticoduodenectomy: Enhanced Recovery After Surgery
®
) Society recommendations. World J Surg 2013; 37
(ERAS (2):240–258.
50 Maessen J, Dejong C, Kessels A, von Myenfeldt M. Length of
stay: an inappropriate readout of the success of enhanced recovery programmes. World J Surg 2008; 32:971–997.
51 Di Sebastiano P, Festa L, de Bonis A, et al. A modified fast-track
program for pancreatic surgery: a prospective single-center experience. Langenbecks Arch Surg 2011; 396(3):345–351.
52 Berberat PO, Ingold H, Gulbinas A, et al. Fast track – different
implications in pancreatic surgery. J Gastrointest Surg 2007; 11(7):880–887.
53 Vanounou T, Pratt W, Fischer J, et al. Deviation-based cost
modeling: a novel model to evaluate the clinical and eco­nomic impact of clinical pathways. J Am Coll Surg 2007; 204(4):570–579.
54 Balzano G, Zerbi A, Braga M, et al. Fast-track recovery pro-
gramme after pancreatico-duodenectomy reduces delayed gastric emptying. Br J Surg 2008; 95(11):1387–1393.
55 Kennedy EP, Rosato E, Sauter P, et al. Initiation of a critical
pathway for pancreaticoduodenectomy at an academic insti­tution – the first step in multidisciplinary team building. J Am Coll Surg 2007; 204(5):917–923; discussion 923–924.
56 Robertson N, Gallacher P, Peel N, et al. Implementation of an
enhanced recovery programme following pancreaticoduode­nectomy. HPB (Oxford) 2012; 14(10):700–708.
57 Kennedy EP, Grenda T, Sauter P, et al. Implementation of a
critical pathway for distal pancreatectomy at an academic institution. J Gastrointest Surg 2009; 13(5):938–944.
58 Maessen J, Dejong C, Hausel J, et al. A protocol is not enough
to implement an enhanced recovery programme for colorec­tal resection. Br J Surg 2007; 94(2):224–231.
59 Ahmed J, Khan S, Gatt M, et al. Compliance with enhanced
recovery programmes in elective colorectal surgery. Br J Surg 2010; 97:754–758.
60 Dindo D, Demartines N, Clavien PA. Classification of surgical
complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg 2004; 240:205–213.
61 Van den Broek MA, van Dam RM, van Breukelen GJ, et al.
Development of a composite endpoint for randomized controlled trials in liver surgery. Br J Surg 2011; 98 (8):1138–1145.
62 Hendry PO, van Dam RM, Bukkems SF, et al.
Randomized clinical trial of laxatives and oral nutritional supplements within an enhanced recovery after surgery protocol following liver resection. Br J Surg 2010; 97(8):1198–1206.
63 MacKay G, O’Dwyer PJ. Early discharge following liver resec-
tion for colorectal metastases. Scott Med J 2008; 53(2):22–24.
64 Porter GA, Pisters PW, Mansyur C, et al. Cost and utilization
impact of a clinical pathway for patients undergoing pancrea­ticoduodenectomy. Ann Surg Oncol 2000; 7(7):484–489.
SECTION 2 Advanced laparoscopic hepatobiliary surgery
CHAPTER 10
Relevant hepatobiliary anatomy
Tadatoshi Takayama,1Masatoshi Makuuchi,2and Kimitaka Kogure
1
Department of Digestive Surgery, Nihon University School of Medicine, Tokyo, Japan
2
Department of Hepato-Biliary-Pancreatic Surgery, Japanese Red Cross Medical Center, Tokyo, Japan
3
Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Japan
EDITOR COMMENT
This chapter, by world-renowned and pioneering liver surgeons, allows the reader to obtain an important in-depth understanding of liver anatomy. This level of understanding of liver anatomy is the basis for performing advanced laparoscopic liver surgery as shown in the video atlas portion. The chapter details anatomical classifications by Couinaud, Healey, and Schroy and the results of the Brisbane consensus conference on anatomical classification. The authors further detail the anatomy of each liver segment, including a thorough historical and in-depth account of the special anatomy of segment I. This chapter summarizes essential surgical landmarks that should be used in anatomical liver resection. Beautiful anatomical sketches and intraoperative pictures will allow in-depth comprehension of liver anatomy as we know it today.
Keywords: anatomical liver resection, bile duct anatomy, Brisbane classification, Couinaud classification, Healey classification, hepatic artery anatomy, hepatic vein anatomy, liver segmental resection, caudate lobe (segment I), portal vein anatomy
10.1 Introduction
sound devices. This allowed any of Couinaud’sseg-
3
ments to be removed anatomically [3,4]. The technical Since the 1950s, our developing understanding of the surgical anatomy of the liver has enabled safe resection of hepatic malignancy [1]. A major breakthrough was the segmental anatomy proposed by Couinaud (1954), who divided the liver into eight segments based on the map of the portal vein [2]. The modern era of liver resection bl ossomed from this anatomical revolution, shifting from an inabi lity to refer ence vasculature dur­ing surgery to maj or resection following anatomical planes. The credit for the first anatomical right hepa­tectomy with preliminary hilar ligation belongs to Lor­tat-Jacob (1952) in France [1]. In 1985, Makuuchi developed a systematic approach to segmentectomy through the implementation of intraoperative ultra-
revolution of intraoperative ultrasound has allowed
liver resection to become a potential cure for malig-
nancies; it is now performed at high-volume centers
worldwide, with low morbidity and mortality [5–7]. It
is also the basis for a more recent development, lapa-
roscopic liver resection, which in skillful hands is an
alternative to open surgery in selected cases [8,9].
In this chapter, we outline the relevant hepatobiliary anatomy that forms the basis for advanced laparoscopic liver resections, which requires precise knowledge of hepatic division, vascular structures, and surgical land­marks. A clear understanding of these aspects of liver anatomy enables advanced laparoscopic and open liver resections to be performed safely.
Laparoscopic Liver, Pancreas, and Biliary Surgery: Textbook and Illustrated Video Atlas, First Edition. Edited by Claudius Conrad and Brice Gayet. © 2017 John Wiley & Sons, Ltd. Published 2017 by John Wiley & Sons, Ltd.
148