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Original Article Hepatobiliary scintigraphy of bile excretion after endoscopic ultrasound-guided hepaticogastrostomy for malignant biliary obstruction: a retrospective study in Japan
Masanori Yamadaorcid, Kazuo Hara,orcid, Shin Habaorcid, Takamichi Kuwaharaorcid, Nozomi Okunoorcid, Yasuhiro Kuraishiorcid, Takafumi Yanaidaniorcid, Sho Ishikawaorcid, Tsukasa Yasudaorcid, Toshitaka Fukuiorcid

DOI: https://doi.org/10.5946/ce.2023.291
Published online: August 20, 2024

Department of Gastroenterology, Aichi Cancer Center Hospital, Nagoya, Japan

Correspondence: Kazuo Hara Department of Gastroenterology, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan E-mail: khara@aichi-cc.jp
• Received: November 16, 2023   • Revised: February 21, 2024   • Accepted: February 22, 2024

© 2024 Korean Society of Gastrointestinal Endoscopy

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • Background/Aims
    Hepatobiliary scintigraphy (HBS) is used to evaluate bile excretion. This study aimed to evaluate biliary excretion during endoscopic ultrasound-guided hepaticogastrostomy (EUS-HGS) using HBS.
  • Methods
    We retrospectively evaluated 78 consecutive patients with malignant extrahepatic biliary obstruction, who underwent HBS after EUS-HGS between April 2015 and July 2022. The peak time and decay rate were scored with 0, 1, or 2 points based on thresholds of 20 and 35 minutes, and 10% and 50%, respectively. A total score of 4 or 3 was considered indicative of good bile excretion, whereas scores of 2, 1, or 0 indicated poor bile excretion.
  • Results
    The good and poor bile excretion groups included 40 and 38 cases, respectively. The group with good bile excretion had a significantly longer time to recurrent biliary obstruction compared to the poor bile excretion group (not reached vs. 124 days, p=0.026). Multivariate analysis identified the site of obstruction as a significant factor influencing good bile excretion (odds ratio, 3.39; 95% confidence interval, 1.01–11.4, p=0.049), with superior bile excretion observed in cases involving upper biliary obstruction compared to middle or lower biliary obstruction.
  • Conclusions
    In patients with malignant biliary obstruction who underwent HGS, the site of obstruction is significantly associated with stent patency.
Biliary drainage guided by endoscopic retrograde cholangiopancreatography (ERCP), is the gold standard for treating biliary obstruction.1 However, ERCP may not be feasible in complex cases of duodenal obstruction or surgically altered anatomy. As an alternative, percutaneous transhepatic cholangiography can be used; however, it has several disadvantages, such as external drainage and cosmetic concerns.2,3 Endoscopic ultrasound-guided biliary drainage (EUS-BD) has been developed as an alternative method for failed ERCP or percutaneous transhepatic biliary drainage.4,5 Endoscopic ultrasound-guided hepaticogastrostomy (EUS-HGS) can be performed in cases of duodenal bulb obstruction and surgically altered anatomy.6 Recent developments in medical devices have enabled the performance of HGS without the need for intrahepatic bile duct dilatation, broadening its range of indications.7-9
Hepatobiliary scintigraphy (HBS) is a physiological and non-invasive imaging method used to evaluate liver function, gallbladder function, duodenal papillary function, and bile excretion. 99mTc-pyridoxal-5-methly-triptophan (99mTc-PMT) stands out as an effective radiotracer among 99mTc-pyridoxylaminates, and is used in HBS to diagnose diseases related to hepatobiliary function and system in Japan.10-12 In evaluating bile excretion with HBS using 99mTc-PMT, the peak time, appearance time, decay time, and decay rate for each region are calculated from the time-activity curve (TAC) of the region of interest (ROI) set on the scintigram, facilitating a quantitative evaluation. Although bile excretion in HGS is expected to be non-physiological, it has not yet been studied. Therefore, this study aims to evaluate bile excretion in HGS using HBS.
Study design
This single-center retrospective study was conducted at the Aichi Cancer Center Hospital. This study examined consecutive patients with malignant extrahepatic biliary obstruction who underwent HBS within one month of HGS between April 2015 and July 2022. However, patients with malignant extrahepatic biliary obstruction, in which the right and left hepatic ducts were separated, were excluded because transpapillary right biliary drainage was often performed in such patients in addition to HGS. Further, patients who received plastic stents for HGS stents and those who underwent HGS in conjunction with antegrade stenting were also excluded. Finally, a total of 78 consecutive patients with malignant extrahepatic biliary obstruction who underwent HBS after HGS were examined during the study period. A flowchart of the study is shown in Figure 1. This study was approved by Aichi Cancer Center Hospital (approval number: 2121-0-254). Informed consent was obtained from each patient for both the HGS and HBS procedures.
EUS-HGS procedure
EUS-HGS was performed in all patients under sedation with 5 to 10 mg intravenous midazolam (Astellas) and 35 mg intravenous pethidine hydrochloride (Mitsubishi Tanabe Pharma). EUS was performed using an oblique-viewing echoendoscope (GU-UCT260, Olympus; EG-580UT, EG-740UT, Fujifilm) or a forward-viewing EUS (TGF-UC260J; Olympus). A landmark clip was first placed at the esophagogastric junction to allow easy identification under fluoroscopic guidance and prevent puncture of the esophagus.13 A 22-gauge needle (Expect Slimline; Boston Scientific Co.) was filled with the contrast medium and preloaded with a 0.018-inch guidewire (Fielder 18; Asahi Intecc, Aichi, Japan) using a Rotating Hemostatic Valve 0.096 (Abbott, Tokyo, Japan). A 19-gauge needle (Expect, Boston Scientific Co.; Sono Tip Pro Control, Medi-Globe GmbH; or EZ Shot 3 Plus, Olympus) was filled with contrast medium and preloaded with a 0.025-inch guidewire (VisiGlide 2, Olympus; or M-Through, Asahi Intecc) using a connector (Radifocus Hemostasis Valve II; Terumo). To avoid intervening vessels, the B2 or B3 intrahepatic bile duct was punctured using a 22- or 19-gauge needle under Doppler ultrasound guidance. A preloaded guidewire was inserted into the bile duct and a small amount of contrast medium was injected. The needle track was dilated using a tapered-tip dilator (ES Dilator; Zeon Medical Co.), a balloon catheter (4 mm, REN Biliary Dilation Catheter; Kaneka), an electrocautery dilator (6 Fr, Cysto-Gastro-Set; Endo-Flex Co.), and a drill dilator (Tornus ES; Asahi Intecc). Subsequently, a dilator was exchanged for a biliary catheter (Tandem XL Triple Lumen ERCP Cannula, Boston Scientific Co. or Uneven Double Lumen Cannula, Piolax) to aspirate bile juice and inject contrast medium to outline the biliary tree. Finally, HGS stenting was performed using a fully covered metal stent (6 mm×10 or 12 cm HANAROSTENT, HANAROSTENT Benefit, Boston Scientific Co. or 8 mm×10 or 12 cm Covered Bile Rush Advance, Piolax).
Hepatobiliary scintigraphy
HBS images are shown in Figure 2, and an example of an HBS video is shown in Supplemental Video 1. In all the studied patients, HBS was performed within one week to one month following HGS. The isotope preparation used for HBS was 99mTc-PMT (185 MBq). Patients were required to fast in the morning before the isotopes were administered intravenously, while they lay in a supine position. The examination time was 60 minutes, during which sequential dynamic abdominal images were captured every 30 seconds. A video lasting a total of 6 seconds was compiled from these images (60× speeds). The ROI was set at the hilar bile duct, and a TAC was created. Peak time and decay rate were calculated from the TAC, using a scale to evaluate bile excretion. Peak time was defined as the time of maximum accumulation, and the decay rate was defined as the difference between the maximum and minimum accumulation divided by the maximum value. Peak time is the time required for the existing bile in the bile duct to be excreted and replaced by isotope-labeled bile. A shorter peak time indicated better bile excretion. The decay rate is the ratio of isotope-labeled bile excreted within the test time. A higher decay rate indicated better bile excretion.
The scatter plots and scoring systems based on the peak time and decay rate for the 78 cases derived from biliary scintigraphy are shown in Figure 3. From this scatter plot, the peak time and decay rate were assigned scores of 0, 1, or 2 points based on thresholds of 20 and 35 minutes, and 10% and 50%, respectively. Bile excretion was then evaluated based on the sum of these scores. A total score of 4 or 3 indicates good bile excretion, whereas scores of 2, 1, or 0 indicate poor bile excretion. Examples of biliary scintigraphy findings in HGS cases classified according to the scoring system are shown in Figure 4.
Definitions and statistical analyses
Using computed tomography (CT) and magnetic resonance imaging (MRI), the site of bile duct obstruction was divided into upstream (upper biliary obstruction) and downstream (middle and lower biliary obstruction) areas, bordering the confluence of the cystic duct. Recurrent biliary obstruction (RBO) was defined as cholangitis and jaundice with biliary dilatation in imaging studies. Time to recurrent biliary obstruction (TRBO) was defined as the period between EUS-BD and the onset of RBO.14 Clinical success was defined as a decrease in bilirubin levels to normal or <50% of the pre-drainage level within 14 days following EUS-BD. Bile peritonitis was diagnosed if the patient had a fever, elevated inflammatory markers on blood tests, and abdominal pain within 1 day following EUS-HGS. Bile peritonitis was also diagnosed if CT, obtained the day after EUS-HGS, showed bile leakage or peritonitis around the HGS stent. Acute cholangitis was diagnosed according to the Tokyo Guidelines 2018.15 Other adverse events possibly related to the procedure and occurring after the procedure were described in accordance with the American Society for Gastrointestinal Endoscopy lexicon.16 Continuous variables were analyzed using the Mann–Whitney U test. Categorical variables were analyzed using Fisher’s exact test. The Kaplan–Meier method was used to estimate the TRBO. The log-rank test was used to compare the TRBO between the groups. All statistical analyses were performed using the EZR software (Saitama Medical Center, Jichi Medical University).
This study included 43 male (55.1%) and 35 female (44.9%) participants, with ages ranging from 24 to 85 years (median, 68 years). The primary diseases were all malignant, including pancreatic (41 patients, 52.6%), gastric (12 patients, 15.4%), bile duct (5 patients, 6.4%), duodenal (5 patients, 6.4%), gallbladder (5 patients, 6.4%), papillary (2 patients, 2.6%), and other malignancies (8 patients, 10.3%). The primary indications for undergoing endoscopic EUS-HGS were categorized as either primary and salvage drainages in 53 (67.9%) and 25 (32.1%) patients, respectively. Salvage drainage cases included those converted from attempted percutaneous transhepatic biliary drainage, cases difficult for ERCP and EUS-guided choledochoduodenostomy due to duodenal invasion, and cases of ERCP cannulation failure. Bile duct obstructions were classified based on their location as either upstream (upper biliary obstruction, n=19; 24.4%) or downstream (middle and lower biliary obstruction, n=59; 75.6%) areas, bordering the confluence of the cystic duct, using CT and MRI. Duodenal stents were placed in 16 patients (20.5%) due to duodenal obstruction. Sixteen patients (20.5%) had surgically altered anatomy, including Roux-en-Y (n=7), gastrojejunostomy (n=7), and Billroth II (n=2). Peritoneal dissemination was observed in 20 (25.6%) patients and ascites was observed in 15 patients (19.2%). Six (7.7%) patients had undergone cholecystectomy. The stenting routes were B2 and B3 in 50 (64.1%) and 28 (35.9%) patients, respectively. The clinical success rate was 100%. Early adverse events were observed in four cases, including peritonitis, cholangitis, and cholecystitis in one, two, and one case, respectively. Late adverse events were observed in one case, which was a case of biloma (Table 1).
The TRBO values of the good and poor bile excretion groups are shown in Figure 5. The TRBO in the good bile excretion group was significantly longer than that in the poor bile excretion group (p=0.026); the good excretion group did not reach the median TRBO value, while the median TRBO of the poor bile excretion group was 124 days.
Univariate and multivariate analyses of the clinical factors affecting the rate of good bile excretion, which were evaluated using HBS, are presented in Table 2. The following variables with p<0.2 in the univariate analysis were included in the multivariate analysis: obstruction site, duodenal stent, peritoneal dissemination, and ascites. The multivariate analysis indicated that the site of obstruction was significantly associated with the rate of good bile excretion (odds ratio, 3.39; 95% confidence interval, 1.01–11.4, p=0.049), and upper biliary obstruction was associated with good bile excretion.
In this study, HBS was used to assess bile excretion after HGS. Prior to this research, there had been no studies examining bile excretion post-endoscopic biliary drainage using HBS, highlighting the need to establish evaluation criteria. The evaluation of bile excretion employs both peak time and decay rate, yet each metric has its own limitations. Peak time measures the duration for the bile initially present in the bile duct to be expelled and replaced by isotope-labeled bile, indirectly assessing the excretion of isotope-labeled bile. In contrast, the decay rate is the ratio of isotope-labeled bile excreted within the test time, which directly evaluates the isotope-labeled bile itself. However, given that the examination duration was set to 60 min for all cases, and peak times varied from case to case; the time remaining post peak time was often not consistent. Therefore, cases with prolonged peak times often showed lower decay rates. However, there were also cases with late peak times but high decay rates, as well as cases with early peak times but low decay rates. Hence, a combined assessment of both metrics can enhance the efficacy of the evaluation criteria for HBS. A scoring system, derived from scatter plots based on the peak time and decay rate, was used to categorize patients into either good or poor bile excretion groups.
TRBO was significantly longer in the good bile excretion group, and the evaluation based on the scoring system showed a correlation with stent patency. Multivariate analysis of factors associated with bile excretion, as evaluated using HBS, identified the site of obstruction as the only significant factor. Patients with upper biliary obstruction experienced better bile excretion compared to those with middle or lower biliary obstruction. HBS footage of cases with upper biliary obstruction showed that, in cases with good bile excretion, the amount of isotope-labeled bile flowing into the extrahepatic bile duct was small and excreted from the HGS stent in many cases as shown in Supplemental Video 2. In contrast, HBS videos of cases with middle and lower biliary obstruction show good bile excretion, with little inflow of isotope-labeled bile into the extrahepatic bile duct. However, cases showing poor bile excretion, characterized by reduced bile excretion from the HGS stent, resulted from the inflow and stagnation of isotope-labeled bile into the extrahepatic bile duct, as shown in Supplemental Video 3. In cases of middle and lower biliary obstruction, the extrahepatic bile duct is wide, and in some cases, the bile tends to stagnate, possibly leading to biliary stasis.
This study has several limitations. Firstly, it was a single-center, retrospective study, and there was variability in patient characteristics and the types of biliary stents used. Secondly, our hospital adopts a strategy of periodically replacing plastic stents in patients undergoing chemotherapy. This approach aims to prevent segmental cholangitis, biloma, and secondary stenosis, which can arise from the prolonged use of metal stents and lead to hyperplasia. Therefore, several censored cases were included in this TRBO study. A scoring system was developed to assess bile excretion capability as evaluated by HBS and TRBO; however, this system may be inaccurate to some degree. To develop more accurate criteria for the evaluation of bile excretion by HBS, it is necessary to conduct a prospective study with a larger sample size, consistent patient characteristics, and fewer censored cases.
In conclusion, the site of the obstruction is significantly associated with the stent patency of HGS. Bile excretion from the HGS may be prone to greater bile stagnation and stasis with a wider extrahepatic bile duct. Therefore, in cases of middle and lower biliary obstruction, it may be better to consider HGS with antegrade stenting, or an alternative method to HGS, if feasible. However, further research is necessary to validate this recommendation.
Supplemental Video 1. An example of hepatobiliary scintigraphy is shown. In this case, the peak time and decay rate were 10 minutes (1.0 seconds in the video) and 68.9%, respectively. At 5 minutes (0.5 seconds), bile was excreted into the stomach via hepaticogastrostomy route. At 10 minutes (1.0 seconds in the video), the accumulation in the hilar bile duct was maximal. At 20 minutes (2.0 seconds in the video), accumulation in the hilar bile duct was reduced, and at 60 minutes (6.0 seconds in the video), accumulation in the hilar bile ducts was further reduced, with most of the isotope-labeled bile excreted into the stomach.
Supplemental Video 2. The patient had an upper biliary obstruction with a score of 4. The amount of isotope-labeled bile flowing into the extrahepatic bile duct was small and there was good bile excretion from the hepaticogastrostomy stent.
Supplemental Video 3. The patient had middle and lower biliary obstructions with scores of 0. Inflow and stagnation of isotope-labeled bile into the extrahepatic bile duct occurred, and bile excretion from the hepaticogastrostomy stent was poor.
Supplementary materials related to this article can be found online at https://doi.org/10.5946/ce.2023.291.
Fig. 1.
Study flowchart. Flowchart of 123 consecutive patients with malignant extrahepatic biliary obstruction who underwent hepatobiliary scintigraphy (HBS) within one month of undergoing hepaticogastrostomy (HGS) at Aichi Cancer Center Hospital between April 2015 and July 2022. Nine patients with separated left and right hepatic ducts due to malignant tumors, three patients who underwent HGS using plastic stents, and 33 patients who underwent HGS combined with antegrade stenting were excluded. Finally, a total of 78 consecutive patients with malignant extrahepatic biliary obstruction who underwent HBS after HGS were examined during the study period.
ce-2023-291f1.jpg
Fig. 2.
Hepatobiliary scintigraphy. (A) The region of interest (ROI) set at the hilar bile duct. (B) Time-activity curve (TAC). The peak time and decay rate were calculated from the TAC and used as a scale to evaluate bile excretion. An example of a hepatobiliary scintigraphy is shown. The peak time and decay rate, in this case, are 10 minutes and 68.9%, respectively. (C) Key images at 5, 10, 20, and 60 minutes. At 5 minutes, the bile is excreted into the stomach via the hepaticogastrostomy (HGS) route. At 10 minutes, the accumulation in the hilar bile duct is maximal. At 20 minutes, the accumulation in the hilar bile duct is reduced, and at 60 minutes, the accumulation in the hilar bile ducts is further reduced, with most of the isotope-labeled bile excreted into the stomach. Supplemental Video 1 shows this case.
ce-2023-291f2.jpg
Fig. 3.
Scatter plots and scoring system created based on peak time and decay rate for each case obtained from hepatobiliary scintigraphy. Scatter plots and scoring systems. From this scatter plot, the peak time and decay rate were scored as 0, 1, and 2 points based on 20 and 35 min, and 10% and 50%, respectively, and bile excretion was evaluated based on the sum of these scores. A total score of 4 or 3 was defined as good bile excretion, while scores of 2, 1, or 0 indicated poor bile excretion.
ce-2023-291f3.jpg
Fig. 4.
Examples of biliary scintigraphy in hepaticogastrostomy (HGS) cases classified according to the scoring system. In cases with a total score of 0, isotope-labeled bile stagnates in the bile ducts and excretion from the HGS route is poor. In cases with a total score of 4, the isotope-labeled bile was not stagnant and was excreted through the HGS route early on. In cases with a total score of 2, bile excretion was intermediate, ranging from 0 to 4. Supplemental Videos 2 and 3 show the cases with total scores of 4 and 0, respectively.
ce-2023-291f4.jpg
Fig. 5.
Comparison between the good and poor bile excretion groups concerning the time to recurrent biliary obstruction (TRBO). The TRBO of the good bile excretion group was significantly longer than that of the poor bile excretion group; the good excretion groups did not reach the median TRBO value, while the median TRBO of the poor bile excretion group was 124 days. days (not reached vs. 124 days, p=0.026; log-rank test).
ce-2023-291f5.jpg
ce-2023-291f6.jpg
Table 1.
Patient characteristics of hepaticogastrostomy (n=78)
Characteristic Value
Age (yr) 68 (24–85)
Sex (male) 43 (55.1)
Primary disease
 Pancreatic cancer 41 (52.6)
 Gastric cancer 12 (15.4)
 Bile duct cancer 5 (6.4)
 Duodenal cancer 5 (6.4)
 Gallbladder cancer 5 (6.4)
 Papillary cancer 2 (2.6)
 Others 8 (10.3)
Indication for HGSa)
 Primary drainage 53 (67.9)
 Salvage drainage 25 (32.1)
Site of obstructionb)
 Upper 19 (24.4)
 Middle and lower 59 (75.6)
Duodenal stent 16 (20.5)
Surgically altered anatomy 16 (20.5)
 Roux-en-Y 7 (9.0)
 Gastrojejunostomy 7 (9.0)
 Billroth-Ⅱ 2 (2.6)
Peritoneal dissemination 20 (25.6)
Ascites 15 (19.2)
Post-cholecystectomy 6 (7.7)
HGS route
 B2 50 (64.1)
 B3 28 (35.9)
Clinical success 78 (100.0)
Early (£30 days) adverse event 4 (5.1)
 Peritonitis 1 (moderate)
 Cholangitis 2 (mild)
 Cholecystitis 1 (moderate)
Late (>30 days) adverse event 1 (1.3)
 Biloma 1 (moderate)

Values are presented as median (range) or number (%).

HGS, hepaticogastrostomy.

a) Primary drainage, the first drainage; salvage drainage, conversion from other drainage, or additional drainage using another technique.

b) The site of bile duct obstruction was divided into upstream (upper biliary obstruction) and downstream areas (middle and lower biliary obstruction), bordering the confluence of the cystic duct, using computed tomography and magnetic resonance imaging).

Table 2.
Univariable and multivariable analyses of clinical factors affecting rate of good bile excretion evaluated by hepatobiliary scintigraphy
Variable n/total n (%) Univariate analysis
Multivariate analysis
OR (95% CI) p-value OR (95% CI) p-value
Primary disease
 Pancreatic cancer 21/41 (51.2) 0.994 (0.372–2.654) 1
 Others 19/37 (51.4)
Site of obstruction
 Upper 14/19 (73.7) 3.496 (1.022–14.077) 0.035 3.39 (1.01–11.4) 0.049
 Middle and lower 26/59 (44.1)
Duodenal stent
 No 35/62 (56.6) 0.355 (0.086–1.272) 0.095 0.507 (0.144–1.78) 0.289
 Yes 5/16 (31.3)
Surgically altered anatomy
 No 34/62 (54.8) 0.498 (0.131–1.737) 0.268
 Yes 6/16 (37.5)
Peritoneal dissemination
 No 33/58 (56.9) 0.412 (0.12–1.308) 0.121 0.473 (0.132–1.69) 0.25
 Yes 7/20 (35.0)
Ascites
 No 35/63 (55.6) 0.404 (0.096–1.482) 0.834 0.206 (0.222–3.37) 0.799
 Yes 5/15 (33.3)
Post-cholecystectomy
 No 37/72 (51.4) 1.056 (0.132–8.426) 1
 Yes 3/6 (50.0)

OR, odds ratio; CI, confidence interval.

  • 1. ASGE Standards of Practice Committee, Buxbaum JL, Abbas Fehmi SM, et al. ASGE guideline on the role of endoscopy in the evaluation and management of choledocholithiasis. Gastrointest Endosc 2019;89:1075–1105.ArticlePubMedPMC
  • 2. Hayat U, Bakker C, Dirweesh A, et al. EUS-guided versus percutaneous transhepatic cholangiography biliary drainage for obstructed distal malignant biliary strictures in patients who have failed endoscopic retrograde cholangiopancreatography: a systematic review and meta-analysis. Endosc Ultrasound 2022;11:4–16.ArticlePubMedPMC
  • 3. Hassan Z, Gadour E. Percutaneous transhepatic cholangiography vs endoscopic ultrasound-guided biliary drainage: a systematic review. World J Gastroenterol 2022;28:3514–3523.ArticlePubMedPMC
  • 4. Boulay BR, Lo SK. Endoscopic ultrasound-guided biliary drainage. Gastrointest Endosc Clin N Am 2018;28:171–185.ArticlePubMed
  • 5. Isayama H, Nakai Y, Itoi T, et al. Clinical practice guidelines for safe performance of endoscopic ultrasound/ultrasonography-guided biliary drainage: 2018. J Hepatobiliary Pancreat Sci 2019;26:249–269.ArticlePubMedPMCPDF
  • 6. Ogura T, Higuchi K. Technical review of developments in endoscopic ultrasound-guided hepaticogastrostomy. Clin Endosc 2021;54:651–659.ArticlePubMedPMCPDF
  • 7. Ogura T, Ueno S, Okuda A, et al. Expanding indications for endoscopic ultrasound-guided hepaticogastrostomy for patients with insufficient dilatation of the intrahepatic bile duct using a 22G needle combined with a novel 0.018-inch guidewire (with video). Dig Endosc 2022;34:222–227.ArticlePubMedPDF
  • 8. Okuno N, Hara K, Mizuno N, et al. B2 puncture with forward-viewing EUS simplifies EUS-guided hepaticogastrostomy (with video). Endosc Ultrasound 2022;11:319–324.ArticlePubMedPMC
  • 9. Okuno N, Hara K, Haba S, et al. Novel drill dilator facilitates endoscopic ultrasound-guided hepaticogastrostomy. Dig Endosc 2023;35:389–393.ArticlePubMedPDF
  • 10. Kato-Azuma M. TC-99m(Sn)-N-pyridoxylaminates: a new series of hepatobiliary imaging agents. J Nucl Med 1982;23:517–524.PubMed
  • 11. Narabayashi I, Sugimura K, Ishido N, et al. Quantitative analysis by digital computer of 99mTc-N-pyridoxyl-5-methyltryptophan (99mTc-PMT) hepatogram in diffuse parenchymal liver diseases. Eur J Nucl Med 1987;13:285–287.ArticlePubMedPDF
  • 12. Kobayashi M, Nakanishi T, Nishi K, et al. Transport mechanisms of hepatic uptake and bile excretion in clinical hepatobiliary scintigraphy with 99mTc-N-pyridoxyl-5-methyltryptophan. Nucl Med Biol 2014;41:338–342.ArticlePubMed
  • 13. Okuno N, Hara K, Mizuno N, et al. Risks of transesophageal endoscopic ultrasonography-guided biliary drainage. Gastrointest Interv 2017;6:82–84.Article
  • 14. Isayama H, Hamada T, Yasuda I, et al. TOKYO criteria 2014 for transpapillary biliary stenting. Dig Endosc 2015;27:259–264.ArticlePubMed
  • 15. Yokoe M, Hata J, Takada T, et al. Tokyo Guidelines 2018: diagnostic criteria and severity grading of acute cholecystitis (with videos). J Hepatobiliary Pancreat Sci 2018;25:41–54.ArticlePubMed
  • 16. Cotton PB, Eisen GM, Aabakken L, Baron TH, et al. A lexicon for endoscopic adverse events: report of an ASGE workshop. Gastrointest Endosc 2010;71:446–454.ArticlePubMed

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      Hepatobiliary scintigraphy of bile excretion after endoscopic ultrasound-guided hepaticogastrostomy for malignant biliary obstruction: a retrospective study in Japan
      Image Image Image Image Image Image
      Fig. 1. Study flowchart. Flowchart of 123 consecutive patients with malignant extrahepatic biliary obstruction who underwent hepatobiliary scintigraphy (HBS) within one month of undergoing hepaticogastrostomy (HGS) at Aichi Cancer Center Hospital between April 2015 and July 2022. Nine patients with separated left and right hepatic ducts due to malignant tumors, three patients who underwent HGS using plastic stents, and 33 patients who underwent HGS combined with antegrade stenting were excluded. Finally, a total of 78 consecutive patients with malignant extrahepatic biliary obstruction who underwent HBS after HGS were examined during the study period.
      Fig. 2. Hepatobiliary scintigraphy. (A) The region of interest (ROI) set at the hilar bile duct. (B) Time-activity curve (TAC). The peak time and decay rate were calculated from the TAC and used as a scale to evaluate bile excretion. An example of a hepatobiliary scintigraphy is shown. The peak time and decay rate, in this case, are 10 minutes and 68.9%, respectively. (C) Key images at 5, 10, 20, and 60 minutes. At 5 minutes, the bile is excreted into the stomach via the hepaticogastrostomy (HGS) route. At 10 minutes, the accumulation in the hilar bile duct is maximal. At 20 minutes, the accumulation in the hilar bile duct is reduced, and at 60 minutes, the accumulation in the hilar bile ducts is further reduced, with most of the isotope-labeled bile excreted into the stomach. Supplemental Video 1 shows this case.
      Fig. 3. Scatter plots and scoring system created based on peak time and decay rate for each case obtained from hepatobiliary scintigraphy. Scatter plots and scoring systems. From this scatter plot, the peak time and decay rate were scored as 0, 1, and 2 points based on 20 and 35 min, and 10% and 50%, respectively, and bile excretion was evaluated based on the sum of these scores. A total score of 4 or 3 was defined as good bile excretion, while scores of 2, 1, or 0 indicated poor bile excretion.
      Fig. 4. Examples of biliary scintigraphy in hepaticogastrostomy (HGS) cases classified according to the scoring system. In cases with a total score of 0, isotope-labeled bile stagnates in the bile ducts and excretion from the HGS route is poor. In cases with a total score of 4, the isotope-labeled bile was not stagnant and was excreted through the HGS route early on. In cases with a total score of 2, bile excretion was intermediate, ranging from 0 to 4. Supplemental Videos 2 and 3 show the cases with total scores of 4 and 0, respectively.
      Fig. 5. Comparison between the good and poor bile excretion groups concerning the time to recurrent biliary obstruction (TRBO). The TRBO of the good bile excretion group was significantly longer than that of the poor bile excretion group; the good excretion groups did not reach the median TRBO value, while the median TRBO of the poor bile excretion group was 124 days. days (not reached vs. 124 days, p=0.026; log-rank test).
      Graphical abstract
      Hepatobiliary scintigraphy of bile excretion after endoscopic ultrasound-guided hepaticogastrostomy for malignant biliary obstruction: a retrospective study in Japan
      Characteristic Value
      Age (yr) 68 (24–85)
      Sex (male) 43 (55.1)
      Primary disease
       Pancreatic cancer 41 (52.6)
       Gastric cancer 12 (15.4)
       Bile duct cancer 5 (6.4)
       Duodenal cancer 5 (6.4)
       Gallbladder cancer 5 (6.4)
       Papillary cancer 2 (2.6)
       Others 8 (10.3)
      Indication for HGSa)
       Primary drainage 53 (67.9)
       Salvage drainage 25 (32.1)
      Site of obstructionb)
       Upper 19 (24.4)
       Middle and lower 59 (75.6)
      Duodenal stent 16 (20.5)
      Surgically altered anatomy 16 (20.5)
       Roux-en-Y 7 (9.0)
       Gastrojejunostomy 7 (9.0)
       Billroth-Ⅱ 2 (2.6)
      Peritoneal dissemination 20 (25.6)
      Ascites 15 (19.2)
      Post-cholecystectomy 6 (7.7)
      HGS route
       B2 50 (64.1)
       B3 28 (35.9)
      Clinical success 78 (100.0)
      Early (£30 days) adverse event 4 (5.1)
       Peritonitis 1 (moderate)
       Cholangitis 2 (mild)
       Cholecystitis 1 (moderate)
      Late (>30 days) adverse event 1 (1.3)
       Biloma 1 (moderate)
      Variable n/total n (%) Univariate analysis
      Multivariate analysis
      OR (95% CI) p-value OR (95% CI) p-value
      Primary disease
       Pancreatic cancer 21/41 (51.2) 0.994 (0.372–2.654) 1
       Others 19/37 (51.4)
      Site of obstruction
       Upper 14/19 (73.7) 3.496 (1.022–14.077) 0.035 3.39 (1.01–11.4) 0.049
       Middle and lower 26/59 (44.1)
      Duodenal stent
       No 35/62 (56.6) 0.355 (0.086–1.272) 0.095 0.507 (0.144–1.78) 0.289
       Yes 5/16 (31.3)
      Surgically altered anatomy
       No 34/62 (54.8) 0.498 (0.131–1.737) 0.268
       Yes 6/16 (37.5)
      Peritoneal dissemination
       No 33/58 (56.9) 0.412 (0.12–1.308) 0.121 0.473 (0.132–1.69) 0.25
       Yes 7/20 (35.0)
      Ascites
       No 35/63 (55.6) 0.404 (0.096–1.482) 0.834 0.206 (0.222–3.37) 0.799
       Yes 5/15 (33.3)
      Post-cholecystectomy
       No 37/72 (51.4) 1.056 (0.132–8.426) 1
       Yes 3/6 (50.0)
      Table 1. Patient characteristics of hepaticogastrostomy (n=78)

      Values are presented as median (range) or number (%).

      HGS, hepaticogastrostomy.

      Primary drainage, the first drainage; salvage drainage, conversion from other drainage, or additional drainage using another technique.

      The site of bile duct obstruction was divided into upstream (upper biliary obstruction) and downstream areas (middle and lower biliary obstruction), bordering the confluence of the cystic duct, using computed tomography and magnetic resonance imaging).

      Table 2. Univariable and multivariable analyses of clinical factors affecting rate of good bile excretion evaluated by hepatobiliary scintigraphy

      OR, odds ratio; CI, confidence interval.


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