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16 Endoscopic Ultrasound forHepato-Pancreato-Biliary Diseases
137
b
c
nography (CH-EUS) ndings of pancreatic solid lesions. (a) Typical case of hypo-enhancement (a pancreatic cancer). CH-EUS image: CH-EUS (right) shows that the lesion (arrowhead) has a lower intensity echo signal than that of the surrounding pancreatic tissue. (b) Typical case of iso-enhancement (an inammatory mass). CH-EUS image:
CH-EUS (right) shows that the lesion (arrowhead) has signals of iso­intensity compared to that of the surrounding pancreatic tissue. (c) Typical case of hyper- enhancement (a neuroendocrine tumor). CH-EUS image: CH-EUS (right) shows that the lesion (arrowhead) has a higher intensity echo signal than that of the surrounding pancreatic tissue
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a b
(b) Cytology of EUS-FNA sample: Papanicolaou staining revealed
(EUS-FNA) for a small pancreatic lesion. (a) Image during EUS-FNA: EUS-FNA was performed for the diagnosis of small pancreatic lesion of 6mm in size (arrowhead). The arrow indicates the EUS-FNA needle.
adenocarcinoma with high nuclear-to-cytoplasmic ratio and irregular nuclear contours
Y. Yamashita and M. Kitano
staging with EUS in patients with pancreatic cancers [12]. Minaga et al. reported that the diagnostic accuracy of CT, conventional EUS, and CH-EUS for staging metastasis in the left hepatic lobe was 90.6%, 93.4%, and 98.4%, respectively, and showed that the sensitivity and accuracy of CH-EUS for diagnosing metastasis in the left hepatic lobe were signi­cantly higher than those of conventional EUS or CT.In par­ticular, the sensitivity of CH-EUS for the detection of small liver metastasis (<10mm) was considerably higher than that of CT or conventional EUS (P<0.001). In 2.1% of patients, only CH-EUS could detect a single distant metastasis in the left hepatic lobe, thereby upgrading tumor staging and alter­ing clinical management [13]. With respect to resectability, a meta-analysis of eight studies enrolling 4903 patients indi­cated that EUS alone identied unresectable diseases in 19% of patients after they were diagnosed with resectable pancre­atic cancer by CT [14]. Hence, EUS is an important tool for the determination of pancreatic cancer stage.
Mural nodules (MNs) in IPMNs are important factors for the determination of surgical indications and have a positive pre­dictive value of 62.2% for malignancy according to a meta­analysis of 70 studies involving 2297 resected IPMNs. The MN size also has a considerable effect on the prediction of IPMNs with both invasive cancer and high-grade dysplasia, with a standardized mean difference of 0.79. However, no reliable cut-off value for the MN size was identied owing to
the heterogeneity of proposed thresholds. Multivariate anal­ysis revealed that MN was the only independent predictor of invasive cancer and high-grade dysplasia for all IPMN types [15]. Additionally, all studies included in the meta-analysis used CH-EUS for MN assessment. Therefore, CH-EUS is the best tool for characterizing size and has the best accuracy for predicting malignancy in IPMNs.
Kamata etal. followed up 102 patients with branch-duct IPMNs for a median of 42months and concluded that EUS was useful for the early detection of newly developed con­comitant pancreatic carcinomas, reporting 3- and 5-year rates of 4% and 8.8%, respectively. In their study, the sensi­tivity and specicity for pancreatic cancer detection in patients with IPMNs were 100%, 100% on EUS and 39%, 99% on abdominal ultrasound and 56%, 100% on CT and 50%, 100% on MRI, respectively. EUS was signicantly superior to other modalities [16].
EUS-FNA is also performed to diagnose cystic lesions. A meta-analysis of eight studies including a total of 1438 patients evaluated the diagnostic accuracy of EUS-FNA for distinguishing mucinous from non-mucinous cystic lesions with cyst-uid analysis for cytology and carcinoembryonic antigen (CEA). The most promising cystic uid biomarker was CEA level, which was increased in mucinous cysts but was low in serous cystadenomas and benign lesions. The optimum threshold for cyst-uid CEA level was 192ng/mL in this study, indicating high discriminatory accuracy. Furthermore, the pooled sensitivity and specicity were 54% and 93% for cytology and 63% and 88%, for CEA level, respectively [17]. EUS-FNA, when used in conjunction with
16 Endoscopic Ultrasound forHepato-Pancreato-Biliary Diseases
cross-sectional imaging, is a useful diagnostic tool for the correct identication of mucinous cysts.
Ampullary cancers without submucosal or ductal inltration that are conned to the ampulla are considered amenable to endoscopic resection [1822] because neither vascular inva­sion, lymphatic permeation, nor lymph node metastasis is observed in patients when the lesions are restricted to the duo­denal mucosa [22, 23]. A meta-analysis of 14 studies investi­gating ampullary cancer staging by EUS in 422 patients reported a pooled sensitivity and specicity of 77% and 78% for T1 staging, 73% and 76% for T2 staging, 79% and 76% for T3 staging, 84% and 74% for T4 staging, and 70% and 74% for N staging, respectively [24]. Therefore, EUS is important for prognostic prediction and determination of the most appro­priate therapeutic approach for ampullary cancers.
A comparison of different diagnostic tools for the detection of cholangiocellular carcinomas indicated the following accuracy rates: 92% for endoscopic retrograde cholangio­pancreatography (ERCP)/intraductal ultrasound (IDUS), 74% for endoscopic transpapillary forceps biopsy (ETP), 92% for IDUS + ETP, 70% for EUS, and 79% for CT.An analysis of accuracy rates with respect to localization of bile duct stenosis revealed that the accuracy rate of EUS for prox­imal versus distal stenosis was signicantly higher than that for distal stenosis (79% vs. 57%; P<0.0001) [25]. ERCP/ IDUS is superior to EUS and CT in establishing accurate diagnoses of bile duct strictures of uncertain etiology. Hence, multimodal diagnostic imaging is recommended for bile duct cancers.
139
Transpapillary drainage with ERCP is generally performed for malignant biliary obstruction. Nonetheless, some previ­ous studies have reported difculty in biliary cannulation in 15–22% of patients [29, 30], occurrence of post-ERCP pan­creatitis (PEP) in 3–15% of patients [31], and an inaccessible biliary orice due to duodenal stenosis in 7–13% of patients with pancreatic head cancers [32].
Percutaneous transhepatic biliary drainage is convention­ally performed when ERCP fails; however, this procedure has several disadvantages, including tube dislocation, exter­nal drainage, and cosmetic problems. The recently devel­oped EUS-BD is carried out when endoscopic transpapillary drainage fails in patients with distal malignant biliary obstruction. Important advantages of this method over other procedures include internal drainage and prevention of PEP (Fig. 16.4). A meta-analysis of four studies enrolling 302 patients revealed no difference in technical success (risk ratio [RR], 1.00; 95% CI, 0.93–1.08), clinical success (RR,
1.00; 95% CI, 0.94–1.06), and total adverse events (RR,
0.68; 95% CI, 0.31–1.48) between EUS-BD and ERCP drainage as primary treatment for distal malignant biliary obstruction. EUS-BD was associated with lower rates of PEP (RR, 0.12; 95% CI, 0.02–0.62), stent dysfunction (RR, 0.54; 95% CI, 0.32–0.91), and tumor ingrowth and overgrowth (RR, 0.22; 95% CI, 0.07–0.76). No differences in reinterven­tions (RR, 0.59; 95% CI, 0.21–1.69), procedural duration (weighted mean difference, 2.11; 95% CI, −9.51–5.29), stent patency (hazard ratio, 0.61; 95% CI, 0.34–1.11), and overall survival (hazard ratio, 1.00; 95% CI, 0.66–1.51) were observed [33]. With adequate expertise in endoscopy, EUS-BD can show the same efcacy and safety as ERCP for the primary palliation of distal malignant biliary obstruction and exhibits several clinical advantages with respect to complications.
Diagnosis using imaging modalities is important because preoperative pathological diagnosis is difcult in gallbladder cancers. Malignancy diagnosis with conventional EUS and CH-EUS for 36 gallbladder wall thickening lesions had been reported to have an overall sensitivity of 61–87% and 90–97%, specicity of 65–83% and 56–98% (P < 0.001), and accuracy of 73–86% and 94–96%, respectively [2628]. An inhomogeneous enhanced pattern on CH-EUS was a strong predictive factor for malignant gallbladder wall thick­ening. CH-EUS has the potential to improve preoperative diagnostic accuracy in the differential diagnosis of gallblad­der wall thickening.
EUS-PD is considered a feasible alternative to percutaneous drainage (PCD) or surgical drainage when endoscopic retro­grade pancreatography is unsuccessful in patients with pan­creatic ductal obstruction (Fig.16.5). The overall technical and clinical success rates of EUS-PD had been reported to be 85% (339/401; range, 63–100%) and 88% (328/372; range, 76–100%), respectively. Additionally, 25% (102/401) of cases experienced short-term adverse events, including abdominal pain (n=45), acute pancreatitis (n=17), bleeding (n=10), and problems associated with pancreatic juice leak­age such as perigastric or peripancreatic uid collection
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Y. Yamashita and M. Kitano
a
b
showing a guidewire inserted into the dilating bile duct. (c) Fluoroscopic
denostomy. (a) EUS showing a 19-gauge needle (arrows) inserted into the dilating extrahepatic bile duct (arrowhead). (b) Fluoroscopic image
(PFC; n =9) [34]. EUS-PD continues to be a challenging procedure associated with a high risk of adverse events; nonetheless, it is an alternative tool for pancreatic duct drain­age in patients with altered anatomy or selected patients for whom ERCP conducted by experts at high-volume centers is unsuccessful.
image showing stent placement. (d) Endoscopic image showing the fully opened stent in duodenum
were developed to overcome these limitations (Fig.16.6). A meta-analysis that included 15 studies (1746 patients) identi­ed no signicant difference in clinical success between LAMSs and DPPSs (RR, 1.04; 95% CI, 0.99–1.11) or between LAMSs and FCSEMSs (RR, 0.96; 95% CI, 0.91–
1.03). FCSEMSs were superior to DPPSs with respect to clinical success (RR, 1.09; 95% CI, 1.02–1.15). Furthermore, no signicant difference in PFC recurrence was observed
EUS-guided drainage has become a widely accepted treat­ment option for PFC. In the early days, EUS-guided PFC drainage was performed using double-pigtail plastic stents (DPPSs) to minimize migration risk. However, endoscopists eventually recognized the limitations of DPPSs. Consequently, fully covered self-expanding metal stents (FCSEMSs) and lumen-apposing metal stents (LAMSs)
among the groups. As for adverse events, LAMSs exhibited a higher bleeding risk than FCSEMSs (RR, 6.70; 95% CI,
1.77–36.27) and tended to have a higher bleeding risk than DPPSs (RR, 2.67; 95% CI, 0.71–9.28) [35]. LAMSs were considered a breakthrough in the endoscopic management of walled-off necrosis (WON), as their larger drainage diameter was expected to result in effective necrotic material drainage.
16 Endoscopic Ultrasound forHepato-Pancreato-Biliary Diseases
141
a
b
d
c
drainage. (a) EUS showing a 19-gauge needle inserted into the dilating main pancreatic duct (arrows). EUS showing pancreatic stone (arrow head) in main pancreatic duct. (b) Fluoroscopic image showing dilating
Rana et al. reported that LAMSs were associated with a signicantly shorter time to resolution; however, with respect to technical success, the WON resolution and complication rates were similar between patients treated with multiple plastic stents and LAMSs [36]. Moreover, large WON or WON with a high proportion of solid debris may be a good indication for direct endoscopic necrosectomy through LAMS with large inner diameter [37] (Fig.16.7).
POPFC is an important complication following abdominal surgery. While PCD is the traditional mainstay of treatment,
main pancreatic duct and stone (arrowhead). (c) Fluoroscopic image showing stent placement. (d) Endoscopic image showing the plastic stent in stomach
EUS-guided drainage for POPFC has recently been per­formed. EUS and PCD were used in the management of POPFC in 10 (239 patients) and 6 (267 patients) out of 13 studies included in a meta-analysis. The pooled clinical suc­cess rate was signicantly higher with EUS than with PCD (93.2% vs. 79.8%; P= 0.002). Furthermore, the recurrence rate was signicantly lower with EUS than with PCD (9.4% vs. 25.7%) [38]. The pooled technical success and adverse event rates were similar between EUS and PCD.EUS has signicantly better clinical outcomes in terms of clinical suc­cess and disease recurrence than PCD in the management of POPFC.Therefore, EUS-guided drainage plays a role in the management of POPFC.
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Y. Yamashita and M. Kitano
a
b
area. (b) EUS image: EUS shows electrocautery-enhanced delivery sys-
scopic necrosectomy through lumen-apposing metal stent (LAMS) for walled-off necrosis. (a) MDCT showing large walled-off necrosis (WON) with a high proportion of solid debris (arrow) in peripancreatic
tem (arrow) was inserted into WON with a high proportion of solid debris. (c) Fluoroscopic image showing stent placement (arrowhead). (d) Endoscopic image showing the fully opened stent in stomach
eral approach. A meta-analysis extracted data from eight
EUS-CPN is widely employed to reduce pain originating from upper abdominal organs. In particular, EUS-CPN using the central or bilateral approach is accepted as a com­mon pain control measure for patients with pancreatic can­cer and chronic pancreatitis. Some of its advantages include real- time guidance; short puncture distance; use of anterior pathway, thereby avoiding puncture through the posterior diaphragm space; and color Doppler, thus preventing vas­cular damage. Absolute ethanol is injected through the FNA needle at the base of the celiac artery in the central approach and on both sides of the celiac artery in the bilat-
studies (238 patients) evaluating EUS-CPN for the relief of pain due to pancreatic cancer and from nine studies (376 patients) investigating EUS-CPN for the relief of pain due to chronic pancreatitis. Overall, 80.12% of patients with pancreatic cancer (95% CI, 74.47–85.22) and 59.45% of patients with chronic pancreatitis (95% CI, 54.51–64.30) showed pain relief [39]. Wyse etal. reported that the relief of pain due to pancreatic cancer was signicantly greater at three months in the EUS- CPN group than in the morphine group [40]. Hence, EUS- CPN offers a safe alternative tech­nique for pain relief in patients with chronic pancreatitis or pancreatic cancer.
16 Endoscopic Ultrasound forHepato-Pancreato-Biliary Diseases
ab
of necrotic tissue. (b) Necrotic tissues are removed from inside of WON
(LAMS) for walled-off necrosis (WON). (a) Endoscopic image: Endoscopy is inserted into WON via LAMS and shows a large amount
by endoscopic necrosectomy
143
EUS-guided ablation therapy is considered a safe alternative treatment for patients deemed unsuitable to undergo sur­gery. According to a meta-analysis of 14 studies that included 158 patients, the major types of solid pancreatic tumors were nonfunctional pancreatic neuroendocrine tumors (n=78, 49.4%), pancreatic cancers (n=48, 30.4%), and insulinomas (n=26, 16.5%). Overall, the pooled clini­cal success and complication rates were 85.9% (95% CI,
75.4–92.4%) and 29.1% (95% CI, 18.6–42.3%), respec­tively. A subgroup analysis of ablation methods indicated clinical success rates of 83.5% (95% CI, 67.9–92.4%) and
87.9% (95% CI, 66.2–96.4%) and complication rates of
32.2% (95% CI, 19.4–48.4%) and 21.2% (95% CI, 6.8–
49.9%) for radiofrequency ablation and ethanol ablation, respectively [41]. EUS-guided ablation therapy may be an alternative treatment for solid pancreatic tumors, particu­larly neuroendocrine tumors and insulinomas <2 cm with rarely severe complications. Further prospective studies with long-term follow-up are warranted in the future owing to the small number of studies.
EUS plays an important role in the diagnosis and staging of pancreaticobiliary lesions, offers advantages over other imaging methods in the detection of small lesions, and is superior to any other modality with respect to spatial resolu­tion. With a high accuracy rate and a low complication rate,
EUS-FNA can be regarded as the nal tool for decision­making regarding the therapeutic strategy and is extensively applied as treatment for hepato-pancreato-biliary diseases. EUS-guided drainage for PFC is a widely accepted treatment option, and EUS-guided pancreatobiliary duct drainage has become an alternative to conventional drainage in difcult cases. Further studies investigating the role of EUS ablation in solid pancreatic lesions are required in the future.
1. Kitano M, Yoshida T, Itonaga M, Tamura T, Hatamaru K, Yamashita
Y. Impact of endoscopic ultrasonography on diagnosis of pancre­atic cancer. J Gastroenterol. 2019;54:19–32.
2. Kanno A, Masamune A, Hanada K, etal. Multicenter study of early
pancreatic cancer in Japan. Pancreatology. 2018;18:61–7.
3. Krishna SG, Rao BB, Ugbarugba E, etal. Diagnostic performance
of endoscopic ultrasound for detection of pancreatic malignancy following an indeterminate multidetector CT scan: a systemic review and meta-analysis. Surg Endosc. 2017;31:4558–67.
4. Yamashita Y, Shimokawa T, Napoléon B, etal. Value of contrast-
enhanced harmonic endoscopic ultrasonography with enhancement pattern for diagnosis of pancreatic cancer: a meta-analysis. Dig Endosc. 2019;31:125–33.
5. Reddy NK, Ioncica AM, Saftoiu A, etal. Contrast-enhanced endo-
scopic ultrasonography. World J Gastroenterol. 2011;17:42–8.
6. Shiina T, Nitta N, Ueno E, Bamber JC. Real time tissue elastic-
ity imaging using the combined autocorrelation method. J Med Ultrason (2001). 2002;29:119–28.
7. Hirooka Y, Kuwahara T, Irisawa A, etal. JSUM ultrasound elas-
tography practice guidelines: pancreas. J Med Ultrason (2001). 2015;42:151–74.
144
Y. Yamashita and M. Kitano
8. Zhang B, Zhu F, Li P, Yu S, Zhao Y, Li M.Endoscopic ultrasound elastography in the diagnosis of pancreatic masses: a meta-analysis. Pancreatology. 2018;18:833–40.
9. Wang KX, Ben QW, Jin ZD, et al. Assessment of morbidity and mortality associated with EUS-guided FNA: a systematic review. Gastrointest Endosc. 2011;73:283–90.
10. Chen G, Liu S, Zhao Y, Dai M, Zhang T. Diagnostic accuracy of endoscopic ultrasound-guided ne-needle aspiration for pancreatic cancer: a meta-analysis. Pancreatology. 2013;13:298–304.
11. Yane K, Kuwatani M, Yoshida M, etal. Non-negligible rate of nee­dle tract seeding after endoscopic ultrasound-guided ne-needle aspiration for patients undergoing distal pancreatectomy for pan­creatic cancer. Dig Endosc. 2020;32:801–11.
12. Nawaz H, Fan CY, Kloke J, etal. Performance characteristics of endoscopic ultrasound in the staging of pancreatic cancer: a meta­analysis. JOP. 2013;14:484–97.
13. Minaga K, Kitano M, Nakai A, etal. Improved detection of liver metastasis using Kupffer-phase imaging in contrast-enhanced harmonic EUS in patients with pancreatic cancer (with video). Gastrointest Endosc. 2021;93(2):433–41.
14. James PD, Meng ZW, Zhang M, et al. The incremental ben­et of EUS for identifying unresectable disease among adults with pancreatic adenocarcinoma: a meta-analysis. PLoS One. 2017;12:e0173687.
15. Marchegiani G, Andrianello S, Borin A, etal. Systematic review, meta-analysis, and a high-volume center experience support­ing the new role of mural nodules proposed by the updated 2017 international guidelines on IPMN of the pancreas. Surgery. 2018;163:1272–9.
16. Kamata K, Kitano M, Kudo M, etal. Value of EUS in early detec­tion of pancreatic ductal adenocarcinomas in patients with intra­ductal papillary mucinous neoplasms. Endoscopy. 2014;46:22–9.
17. Thornton GD, McPhail MJ, Nayagam S, Hewitt MJ, Vlavianos P, Monahan KJ.Endoscopic ultrasound guided ne needle aspiration for the diagnosis of pancreatic cystic neoplasms: a meta-analysis. Pancreatology. 2013;13:48–57.
18. Norton ID, Gostout CJ, Baron TH, Geller A, Petersen BT, Wiersema MJ.Safety and outcome of endoscopic snare excision of the major duodenal papilla. Gastrointest Endosc. 2002;56:239–43.
19. Catalano MF, Linder JD, Chak A, etal. Endoscopic management of adenoma of the major duodenal papilla. Gastrointest Endosc. 2004;59:225–32.
20. Jung S, Kim MH, Seo DW, Lee SK.Endoscopic snare papillectomy of adenocarcinoma of the major duodenal papilla. Gastrointest Endosc. 2001;54:622.
21. Binmoeller KF, Boaventura S, Ramsperger K, Soehendra N.Endoscopic snare excision of benign adenomas of the papilla of Vater. Gastrointest Endosc. 1993;39:127–31.
22. Wee E, Lakhtakia S, Gupta R, etal. The diagnostic accuracy and strength of agreement between endoscopic ultrasound and histopa­thology in the staging of ampullary tumors. Indian J Gastroenterol. 2012;31:324–32.
23. Ito K, Fujita N, Noda Y, etal. Preoperative evaluation of ampullary neoplasm with EUS and transpapillary intraductal US: a prospec­tive and histopathologically controlled study. Gastrointest Endosc. 2007;66:740–7.
24. Trikudanathan G, Njei B, Attam R, Arain M, Shaukat A. Staging accuracy of ampullary tumors by endoscopic ultrasound: meta­analysis and systematic review. Dig Endosc. 2014;26:617–26.
25. Heinzow HS, Kammerer S, Rammes C, Wessling J, Domagk D, Meister T.Comparative analysis of ERCP, IDUS, EUS and CT in
predicting malignant bile duct strictures. World J Gastroenterol. 2014;20:10495–503.
26. Imazu H, Mori N, Kanazawa K, etal. Contrast-enhanced harmonic endoscopic ultrasonography in the differential diagnosis of gall­bladder wall thickening. Dig Dis Sci. 2014;59:1909–16.
27. Kamata K, Takenaka M, Kitano M, etal. Contrast-enhanced har­monic endoscopic ultrasonography for differential diagnosis of localized gallbladder lesions. Dig Endosc. 2018;30:98–106.
28. Leem G, Chung MJ, Park JY, et al. Clinical value of contrast­enhanced harmonic endoscopic ultrasonography in the differential diagnosis of pancreatic and gallbladder masses. Clin Endosc. 2018;51:80–8.
29. Halttunen J, Meisner S, Aabakken L, etal. Difcult cannulation as dened by a prospective study of the Scandinavian Association for Digestive Endoscopy (SADE) in 907 ERCPs. Scand J Gastroenterol. 2014;49:752–8.
30. Bailey AA, Bourke MJ, Williams SJ, etal. A prospective random­ized trial of cannulation technique in ERCP: effects on technical success and post-ERCP pancreatitis. Endoscopy. 2008;40:296–301.
31. Morales SJ, Sampath K, Gardner TB. A review of prevention of post-ERCP pancreatitis. Gastroenterol Hepatol. 2018;14:286–92.
32. Tuca A, Guell E, Martinez-Losada E, Codorniu N. Malignant bowel obstruction in advanced cancer patients: epidemiology, man­agement, and factors inuencing spontaneous resolution. Cancer Manag Res. 2012;4:159–69.
33. Jin Z, Wei Y, Lin H, et al. Endoscopic ultrasound-guided ver­sus endoscopic retrograde cholangiopancreatography-guided biliary drainage for primary treatment of distal malignant biliary obstruction: a systematic review and meta-analysis. Dig Endosc. 2020;32:16–26.
34. Imoto A, Ogura T, Higuchi K.Endoscopic ultrasound-guided pan­creatic duct drainage: techniques and literature review of transmu­ral stenting. Clin Endosc. 2020;53:525–34.
35. Park CH, Park SW, Nam E, Jung JH, Jo JH.Comparative efcacy of stents in endoscopic ultrasonography-guided peripancreatic uid collection drainage: a systematic review and network meta­analysis. J Gastroenterol Hepatol. 2020;35:941–52.
36. Rana SS, Sharma R, Dhalaria L, Gupta R.Efcacy and safety of plastic versus lumen-apposing metal stents for transmural drain­age of walled-off necrosis: a retrospective single-center study. Ann Gastroenterol. 2020;33:426–32.
37. Rerknimitr R.Endoscopic transmural necrosectomy: timing, indi­cations, and methods. Clin Endosc. 2020;53:49–53.
38. Mohan BP, Shakhatreh M, Dugyala S, et al. EUS versus percu­taneous management of postoperative pancreatic uid collec­tion: a systematic review and meta-analysis. Endosc Ultrasound. 2019;8:298–309.
39. Puli SR, Reddy JB, Bechtold ML, Antillon MR, Brugge WR.EUS­guided celiac plexus neurolysis for pain due to chronic pancreatitis or pancreatic cancer pain: a meta-analysis and systematic review. Dig Dis Sci. 2009;54:2330–7.
40. Wyse JM, Carone M, Paquin SC, Usatii M, Sahai AV.Randomized, double-blind, controlled trial of early endoscopic ultrasound-guided celiac plexus neurolysis to prevent pain progression in patients with newly diagnosed, painful, inoperable pancreatic cancer. J Clin Oncol. 2011;29:3541–6.
41. Zhang L, Tan S, Huang S, etal. The safety and efcacy of endoscopic ultrasound-guided ablation therapy for solid pancreatic tumors: a systematic review. Scand J Gastroenterol. 2020;55:1121–31.
Intraoperative Imaging Techniques inLiver Surgery
FlorinBotea, AlexandruBarcu, andIrinelPopescu
17
Abstract
Despite tremendous development of preoperative imag­ing techniques in liver tumors, the high complexity liver surgery, including techniques to increase resectability and the minimal invasive approach, as well as the signicant intraoperative risk, demand the development and imple­mentation of intraoperative imaging techniques, such as intraoperative cholangiography, intraoperative ultra­sound, intraoperative uorescence, and intraoperative navigation.
Despite tremendous development of preoperative imaging techniques in liver tumors, the high complexity liver surgery, including techniques to increase resectability and the mini­mal invasive approach, as well as the signicant intraopera­tive risk, demand the development and implementation of intraoperative imaging techniques, such as intraoperative cholangiography, intraoperative ultrasound, intraoperative uorescence, and intraoperative navigation.

17.1 Intraoperative Cholangiography

The rst report on depiction of the biliary ducts was pub­lished in 1918 by Reich [1], who used bismuth and petrola­tum to dene a biliary stula. Mirizzi advanced the eld by reporting in 1932 the rst series of routine intraoperative cholangiography (IOC) is using lipiodol during cholecystec­tomy [2]. Berci, Shore, Hamlin, and Morgenstern [3] reported in 1978 a series of patients in whom a C-arm mobile image intensier was used for IOC, obtaining high-denition X-rays.
Intraoperative cholangiography (IOC) is currently the
most frequently used technique for intraoperative assess-
F. Botea (*) · A. Barcu · I. Popescu “Dan Setlacec” Center of General Surgery and Liver Transplantation, Fundeni Clinical Institute, Bucharest, Romania
ment of the biliary anatomy. Being safe, effective, and help­ful in evaluating the biliary anatomy and guiding the surgical procedures that involves the bile ducts.
The diagnostic accuracy of a static X-ray method is 50–70%, but the digitized image intensier uoroscopic method increases the accuracy to 95–100%. The time decreased from 20–30 min for a static cholangiogram to 3–5min with uoroscopic IOC.Dynamic uoroscopy speeds up the IOC and provides high-resolution images that more accurately depict the biliary anatomy [4].
The advantages of IOC are [4]:
– identication of the anatomy and aberrant anatomy of the
extrahepatic bile ducts,
– identication of pathology and injuries of the common
bile duct or Oddi’s sphincter,
– data storage for documentation and review, – landmarks for further surgical dissection.
However, IOC has several drawbacks, preventing the routine use of IOC:
– does not allow 3-dimensional (3D) anatomical viewing; – the spatial relationships between the bile ducts and liver
parenchyma, as well as the location of the bile ducts pass-
ing through the liver, are difcult to understand because
only the bile duct can be imaged [5].
– the caudate bile ducts, that may cause biliary leakage after
bile duct division, are not always clearly delineated;
– poor detection of variants of intrahepatic biliary anatomy
[6],
– risk of false positive results, – risk of iatrogenic bile duct injuries. – time consuming procedure; – a large C-arm uoroscopy device and additional human
resources are required,
– the patient and medical staff are exposed to radiation.
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022 M. Makuuchi et al. (eds.), The IASGO Textbook of Multi-Disciplinary Management of Hepato-Pancreato-Biliary Diseases,
https://doi.org/10.1007/978-981-19-0063-1_17
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However, in the era of laparoscopy and of no tolerance for complications in living donor, IOC is extremely important in case of unclear or aberrant biliary anatomy [4].

17.2 Intraoperative Ultrasound

Intraoperative ultrasonography (IOUS) was introduced in liver surgery in 1980 by Makuuchi [7] and had proven to be fundamental for making a complete diagnosis during liver surgery, but also for guiding the liver resection (LR), with a low rate of intraoperative incidents and postoperative com­plications, while increasing the resectability [8].
IOUS usually uses high-frequency probes (7.5–10MHz), due to the high resolution and, therefore, the highest detection rate, especially in case of small relatively supercial lesions. The low-frequencies probes (3.5–5MHz) may be used for initial exploration, allowing a panoramic view of the liver and the detection of deep located structures and lesion (such as segment 1). They also are used for contrast-enhance IOUS.
It is worth mentioning that IOUS has difculties in detect­ing small subcapsular lesions; however, these are usually easily detected at inspection and palpation. If IOUS is intended to be used for detecting such lesions, especially in case of a brotic liver that impedes lesion palpation, a surgi-
cal glove lled with sterile saline solution can be used as an interface between the probe and the liver surface, making the lesion visible.
IOUS is performed using specic devices, either in open approach or in laparoscopy (Fig.17.1), after partial mobili­zation of the liver by sectioning the round and falciform ligaments, and the triangular and coronary ligaments. It involves four main steps:
1. evaluation of liver anatomy: exploration of vessels and
bile ducts at hilum and intrahepatic levels, establishing the liver segmentation;
2. diagnosis: detection, diagnosis and mapping (according
to liver segmentation and relation to major intrahepatic structures) of all liver lesions; Contrast-enhanced IOUS may detect additional lesions and/or ensure a positive diagnosis of the detected lesions [9]. Additionally, IOUS evaluates the background liver, assessing its impairments, such as cirrhosis and steatosis,
3. guidance of liver resection: resection planning, and real-
time guidance of the transection plane using specic techniques, such as the hooking technique for vessel identication during transection [10],
4. control of post-resection results in terms of tumor clear-
ance, including the control of the specimen for very small
Fig. 17.1 BK 5000
ultrasound machine designed for intraoperative ultrasound. of the liver, with various probes: T-shaped convex intraoperative probe (1); I-shaped convex intraoperative probe (2); biplane convex intraoperative probe (3); laparoscopic 4-way convex probe (4); convex probe for (5)