• Users Online:170
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login 

 Table of Contents  
REVIEW ARTICLE
Year : 2019  |  Volume : 8  |  Issue : 5  |  Page : 310-317

The incremental benefit of EUS for the identification of malignancy in indeterminate extrahepatic biliary strictures: A systematic review and meta-analysis


1 Department of Medicine, McMaster University, Hamilton, Ontario, Canada
2 Department of Medicine, University of Medicine and Health Sciences, Basseterre, The Federation of Saint Kitts and Nevis
3 Department of Medicine, University Health Network, University of Toronto, Toronto, Ontario, Canada

Date of Submission19-Jul-2018
Date of Acceptance25-Mar-2019
Date of Web Publication26-Jun-2019

Correspondence Address:
Paul Damien James
University Health Network, University of Toronto, Toronto, Ontario
Canada
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/eus.eus_24_19

Rights and Permissions
  Abstract 


This systematic review aims to assess the literature to determine the impact of EUS for diagnosing malignancy among indeterminate extrahepatic biliary strictures. A systematic review was performed using MEDLINE, EMBASE, Cochrane, and conference proceedings from inception to July 2016. Pooled results were calculated using random-effects model, and heterogeneity was explored using stratified meta-analysis and meta-regression. The main outcome was the incremental benefit of EUS (IBEUS) for the diagnosis of malignancy among patients who have undergone ERCP with brushing cytology for extrahepatic biliary strictures. Of 3131 identified citations, ten met the inclusion criteria and were included in the final analyses (study periods from 1998 to 2014). Pooled IBEUS estimate with the adjustment for publication bias was 14% (95% confidence interval, 7%–20%). Individual studies demonstrate that the IBEUS is greater for distal biliary strictures or when an extrinsic mass is identified on cross-sectional imaging. EUS increases the identification of malignancy for indeterminate biliary strictures following a nondiagnostic ERCP, particularly those that are distal or related to extrinsic compression.

Keywords: Diagnosis, ERCP, biliary stricture, EUS, EUS-FNA, incremental benefit, malignancy


How to cite this article:
Chiang A, Theriault M, Salim M, James PD. The incremental benefit of EUS for the identification of malignancy in indeterminate extrahepatic biliary strictures: A systematic review and meta-analysis. Endosc Ultrasound 2019;8:310-7

How to cite this URL:
Chiang A, Theriault M, Salim M, James PD. The incremental benefit of EUS for the identification of malignancy in indeterminate extrahepatic biliary strictures: A systematic review and meta-analysis. Endosc Ultrasound [serial online] 2019 [cited 2019 Nov 12];8:310-7. Available from: http://www.eusjournal.com/text.asp?2019/8/5/310/261537




  Introduction Top


It is challenging to differentiate between benign and malignant causes of biliary strictures. Currently, ERCP with brush cytology is the primary investigative modality, enabling diagnosis, and therapeutic benefit with stricture dilation and stent placement.[1] However, as the sensitivity of ERCP brushings is 45%, a large proportion of biliary strictures would remain indeterminate using this approach alone.[2]

EUS with fine-needle aspiration is a highly accurate tool for this purpose, with a sensitivity and specificity of 80% and 97%, respectively.[3] Some studies have shown increased diagnostic yield for malignancy with EUS following nondiagnostic ERCP;[4],[5] however, they vary in design, patient population, and results. To determine the added utility of EUS in diagnosing malignant strictures, it must be examined in the context of current practice protocols for extrahepatic biliary strictures and account for the fact that ERCP will diagnose some cases without the need for EUS. Therefore, this systematic review with meta-analysis aims to review the literature to investigate the incremental benefit of EUS (IBEUS) following a nondiagnostic ERCP with brushing cytology for diagnosing malignancy in adult patients presenting with extrahepatic biliary strictures.


  Methods Top


This systematic review was prospectively registered on the PROSPERO international database, registration number CRD42016043987.[6] It is also reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement.[7]

Search strategy

With the support of an expert medical science librarian, the investigators created a bibliographic database search strategy to determine the use of EUS following ERCP with brushing cytology in patients with extrahepatic biliary strictures. Three major search themes were created. The first theme, malignant extrahepatic biliary stricture, combined the Medical Subject Headings (MeSH) terms such as bile duct disease, biliary tract neoplasm, gallbladder neoplasms, cholangiocarcinoma, cholangiocellular carcinoma, biliary atresia, biliary obstruction, biliary stricture, extrahepatic bile duct, and cholestasis. The second theme, endoscopic retrograde cholangiopancreatography, combined the MeSH terms such as endoscopic retrograde cholangiopancreatography, ERCP, and endoscopic cholangiopancreatography. The third theme, endoscopic ultrasound, combined the MeSH terms such as endosonography, endoscopic ultrasound, interventional ultrasonography, endoscopic ultrasound-guided fine-needle aspiration, and biopsy. All three major search themes with corresponding MeSH terms were subsequently combined using the Boolean operator “AND” [Supplementary Table 1 [Additional file 1]].

A medical librarian then utilized the above search strategy to identify the articles in MEDLINE, EMBASE, Cochrane, and conference proceedings from inception to July 2016. Database searches were supplemented by screening the reference lists of relevant studies.

Study selection

Two reviewers independently reviewed the titles and abstracts to identify the articles for full-text review. Any discrepancies in the inclusion of abstracts between reviewers were reconciled by a third reviewer. The same described method was used to perform a full-text review and select the final studies for data analysis. The following inclusion criteria were used: (1) patients were being evaluated for biliary strictures, (2) each patient underwent at least one ERCP, (3) EUS was performed following ERCP, (4) outcomes measured included diagnosis of malignancy, and (5) observational studies (prospective and retrospective) or randomized controlled trial studies. Studies were excluded if patients were younger than 18 years old, “if” initial study population already had a nondiagnostic ERCP or had insufficient data. Case reports or case series were also excluded. Articles published in all languages were considered.

Data extraction and study outcomes

The first two reviewers independently extracted the data from the final list of articles fulfilling the inclusion criteria using a standardized data collection form. Disagreements were reviewed, and consensus on selection was derived with the guidance of the third reviewer. Primary outcomes of interest were number of patients who received an ERCP for suspected biliary stricture, number of patients who had an EUS following an ERCP, and number of cases where EUS alone detected malignancy (ERCP did not yield a diagnosis of malignancy, but EUS did). These were used to calculate the IBEUS as described below. Other data extracted included study information, study design, sample size, study population demographics, stricture location, whether ERCP and EUS were performed in tandem, and other imaging modalities utilized. Study authors were contacted for unpublished data and in instances of missing data.

The diagnosis of malignancy by EUS alone, following nondiagnostic ERCP, was measured by calculating the IBEUS, which was expressed as IBEUS= (NEUS)/(TERCP), where TERCP is the total number of patients who underwent ERCP with brushings for suspected malignant biliary strictures and NEUS is the number of patients who underwent both an ERCP and EUS (following ERCP), where EUS alone identified malignancy. This formula has been described elsewhere to examine the impact of EUS[8] and highlights the additional diagnostic value of EUS in the context of an existing diagnostic pathway for the investigation of biliary strictures.

Risk of bias

The first two reviewers evaluated the study quality of included studies using the Newcastle–Ottawa Quality Assessment Scale Criteria.[9] This included assessing for (1) description of cohort, (2) selection of controls, (3) report of ERCP as initial investigation, (4) description of patients who underwent EUS, (5) description of biliary stricture location, (6) notation of potential confounders, (7) report of the final diagnosis for all patients, (8) adequate follow-up of all patients, and (9) explanation for nondiagnostic outcomes.

Statistical analyses

The approach to statistical analyses as described in previous studies was used in this systematic review.[8]

IBEUS and its variance were represented using the logit of proportion (lP).[8] For sample size proportional weighting, the standard error of each study was calculated.[8] The lP was summarized across studies using a random effects model and the methods proposed by DerSimonian and Laird.[8],[10] The lP was then converted to the IBEUS and the corresponding 95% confidence interval (CI).[8] Small-study effects and publication bias were evaluated through the visual inspection of funnel plots and Begg's asymmetry test.[8]

Heterogeneity of IBEUS across studies was assessed via the inspection of asymmetry among forest plots and calculation of the I2 inconsistency statistic.[8]

Meta-analyses and meta-regression of the study characteristics were performed to evaluate its effects on pooled estimates of effects. A priori characteristics included study origin, publication form, quality score, study design, use of other imaging modalities, use of tandem EUS and ERCP, and use of EUS for all patients.


  Results Top


The process of identifying articles for the systematic review is summarized in [Figure 1]. Among 3131 citations, nine studies met the inclusion criteria. After contacting the study authors of included abstracts, Kim et al. provided their recent publication in the full text.[11],[12] This resulted in a total of ten studies included in the final analyses. The studies reported original data regarding the use of EUS following ERCP with brushing cytology in patients with extrahepatic biliary strictures. Inter-rater agreement for abstract and full-text review was 0.24 and 0.47, respectively.
Figure 1: Flowchart illustration of study selection for meta-analysis

Click here to view


Study characteristics

The characteristics of the ten studies are shown in [Table 1]. Six were prospective studies and four were retrospective studies. All but one were single-center studies. The average age of the study participants was between 62 and 72 years. The total number of patients included in the studies ranged from 23 to 311, with a total of 1162 patients across all studies. Of these, 314 patients had an EUS following nondiagnostic ERCP. Of note, in three studies, ERCP and EUS were performed during the same session. In two studies, the use of EUS depended on the location of stricture.
Table 1: Characteristics of studies included for meta-analysis

Click here to view


Risk of bias assessment

The study quality and the corresponding summary score according to the Newcastle–Ottawa Scale for each of the ten studies are displayed in [Table 2]. The median quality score was 7 out of 9. Consecutive recruitment was described in four of the studies. In the three studies (as noted above) where ERCP and EUS were performed as paired procedures, it could not be ascertained of whether all patients had a nondiagnostic ERCP before undergoing EUS. However, the results of the first procedure were unavailable to the performers of the second procedure. Stricture location was noted in six of the studies, and possible confounders were noted in five.
Table 2: Quality assessment of studies included in the meta-analysis

Click here to view


Proportion of cases where EUS alone identified malignancy

The pooled IBEUS was 15% (95% CI 9%–24%) [Figure 2]. There was no significant heterogeneity noted across studies (I2 = 0%, P = 0.075). In the stratified analyses based on publication characteristics, the estimate of effect was not significantly influenced by whether EUS was performed on all patients or selectively, whether consecutive recruitment was used in the study, or whether a prospective or retrospective study design was used.
Figure 2: Forest plot of pooled estimate of effect for the incremental benefit of EUS in identifying malignancy after nondiagnostic ERCP. CI: Confidence interval; IBEUS: Incremental benefit of EUS

Click here to view


Studies that were published in full text, from Asia, and included computed tomography (CT) and/or magnetic resonance imaging (MRI) yielded higher estimates of effect. Furthermore, studies where ERCP and EUS were conducted in tandem observed greater estimates of effect as compared to when modalities are performed on separate occasions. The full details are shown in [Table 3].
Table 3: Stratified analysis of pooled incremental benefit of EUS in identifying malignancy after nondiagnostic ERCP

Click here to view


Assessment of evidence of publication bias

Visual inspection of the funnel plot showed asymmetry [Figure 3]. This was confirmed with a Begg's test of P = 0.01. Adjusting for small-study effects and publication bias using the “trim-and-fill method,” the adjusted estimate was 13.6% (95% CI 6.7%–20.4%).
Figure 3: Funnel plot for studies considering the incremental benefit of EUS in identifying malignancy after nondiagnostic ERCP

Click here to view


Individual study analysis

By examining individual reports, two studies yielded noteworthy results. Lee et al. described their prospective recruitment and categorization of biliary strictures according to its location – proximal (suprapancreatic) versus distal (intrapancreatic) common bile duct.[13] For proximal strictures, if a diagnosis of malignancy was not made on initial ERCP, ERCP with brushings was repeated. For distal strictures, EUS with fine-needle aspiration was performed. In total, 78 proximal-type strictures were identified, of which initial ERCP was diagnostic in 54 (69%).[13] Twenty-three patients underwent a second ERCP and malignancy was diagnosed in 22 (96%).[13] Of the 42 distal-type strictures identified, initial ERCP diagnosed malignancy in 23 (55%).[13] Nineteen patients underwent subsequent EUS with fine-needle aspiration and malignancy was diagnosed in 18 (94%) patients.[13] Overall, the diagnostic accuracy for the combination of ERCP with the second ERCP for proximal-type strictures and ERCP followed by EUS with fine-needle aspiration for distal-type strictures was 99% and 98%, respectively.[13]

In a later study by Lee et al., consecutive patients were categorized according to the nature of lesion causing the biliary stricture, intrinsic (within bile duct) versus extrinsic (outside bile duct).[12] For individuals with intrinsic strictures and nondiagnostic initial ERCP, a second ERCP was performed. For individuals with extrinsic-type strictures and nondiagnostic ERCP, an EUS with fine-needle aspiration was performed. In total, 88 intrinsic biliary strictures were detected, of which initial ERCP detected malignancy in 69 patients (79%).[12] Nineteen patients underwent a second ERCP and 13 (69%) were found to be positive for malignancy.[12] Of the 90 extrinsic biliary strictures, 57 (63%) strictures were diagnosed to be malignant after initial ERCP.[12] Thirty-three patients underwent EUS with fine-needle aspiration after nondiagnostic ERCP, and of these, 26 (79%) were found to be positive for malignancy.[12] The overall sensitivity of this approach for identifying malignancy for intrinsic- and extrinsic-type strictures was 97% and 97%, respectively.[12]


  Discussion Top


In this systematic review and meta-analysis, our results demonstrate that EUS increases the detection of malignancy among patients investigated for extrahepatic biliary strictures and an initial nonmalignant diagnosis on ERCP. The adjusted IBEUS was 14%. This means that a malignant diagnosis will be realized in one of every seven patients who undergo EUS following a nondiagnostic ERCP for an extrahepatic biliary stricture.

Our review supports the contention that a multimodal approach for investigating extrahepatic biliary strictures that includes ERCP and EUS in selected cases increases the opportunity for detecting the underlying malignancy. With a sensitivity of 45% for ERCP brushings alone, other diagnostic modalities are necessary to increase the detection of cancers early in the investigative process.[21] When paired with ERCP, our results show that EUS facilitates the identification and cytopathological confirmation of malignancy to enable timely therapy. It is interesting to note that ERCP and EUS procedures done in tandem yield a higher pooled estimate of effect than when the procedures are done separately.

There is evidence suggesting that EUS may be particularly useful for distal strictures as well as strictures caused by extrinsic mass compressions. A recent meta-analysis demonstrated that the pooled sensitivity and specificity of EUS for the diagnosis of malignant biliary strictures were 80% and 97%, respectively, with higher diagnostic sensitivity in distal strictures.[3] In single study analysis within our systematic review, Lee et al. demonstrated that EUS with fine-needle aspiration identified malignancy in 18 out of 19 distal biliary strictures, which were not diagnosed by initial ERCP with brushing cytology.[13] This increased the diagnostic accuracy of ERCP followed by EUS to 98% compared to 60% when ERCP was used alone.[13] In 2017, the same authors demonstrated that a combination approach using ERCP and EUS with fine-needle aspiration increased diagnostic sensitivity for biliary strictures related to extrinsic compression from 68% to 97%.[12] EUS identified malignancy in 26 out of 33 strictures that were not previously diagnosed after an initial ERCP with brushings cytology.[12]

An important consideration is the risk of needle tract seeding leading to metastases. Heimbach et al.[22] have demonstrated peritoneal metastases in 83% (5/6) of patients who underwent fine-needle aspiration of unresectable hilar cholangiocarcinoma. Unfortunately, they did not distinguish between percutaneous and EUS approaches. Few studies have examined the risk of seeding among distal common bile duct malignant strictures. Fifteen case reports since 2003 have described needle tract seeding following EUS with fine-needle aspiration of pancreatic neoplasms.[23] Levy et al.[24] have also identified malignant cells within the gastrointestinal luminal fluid of 11.5% (3/26) of patients who underwent EUS with fine-needle aspiration of their pancreatic cancer. On the other hand, several retrospective studies have shown contrary evidence, where it does not significantly increase the risk of needle tract seeding.[25],[26],[27],[28],[29] The use of EUS with fine-needle aspiration has also not shown to impact overall survival or disease recurrence.[27],[30] Overall, based on the evidence to date, EUS with fine-needle aspiration is not recommended for proximal biliary strictures, whereas the risk associated with distal biliary strictures remains unclear.

Integrating the results of our meta-analysis and concerns for needle tract seeding, we propose a diagnostic approach for patients with suspected malignant biliary strictures, illustrated in [Figure 4]. Patients' extrahepatic biliary strictures are initially evaluated by cross-sectional imaging such as CT scan or MRI. The stricture is characterized in terms of its location and whether there is a tumor causing the stricture either by intrinsic or extrinsic compression. For proximal strictures not related to extrinsic compression, ERCP with brush cytology is the initial diagnostic modality of choice. If this is not diagnostic for malignancy, ERCP with brushings can be reattempted. Cholangioscopy may also be considered in centers with access to this technology. For distal bile duct strictures or those related to extrinsic compression, EUS may be the initial diagnostic modality of choice and can be performed in tandem with ERCP if necessary for diagnostic and therapeutic purposes. Surgical resection and imaging surveillance can be considered as appropriate for biliary strictures where malignancy has not been identified after multimodality evaluation. The complementary role of EUS to aid in the diagnostic workup for distal biliary strictures has recently been suggested in a review by Bowlus et al.[31] Prospective studies are needed to validate this algorithm.
Figure 4: Proposed diagnostic algorithm for the assessment of indeterminate biliary strictures. CT: Computed tomography; MRI: Magnetic resonance imaging

Click here to view


There are some limitations of this study. First, the quality of the studies was variable. Almost half of the included studies were abstracts and half of the studies examined were retrospective and therefore prone to bias. Second, small-study effects were noted. This was addressed by correcting the IBEUS estimate for small-study effects using the trim-and-fill method and performing stratified analyses based on the study size, which yielded more conservative estimates. Third, there was heterogeneity among the studies, which could reflect design diversity, especially with varying procedures to identify stricture location and the role of EUS in the included studies. To address this, a random effects model was utilized for pooled estimate of effect. In addition, stratified analyses were performed to identify sources of heterogeneity and how these characteristics affected the pooled estimate of effect. Finally, some factors that have been shown to influence the diagnostic yield (such as the use of fluorescence in situ hybridization) were not measured in the included studies, and this could influence the impact of EUS. Future research in this area will be needed, including large prospective trials that include the impact of procedural and pathology specimen evaluation protocols.


  Conclusion Top


This systematic review demonstrates that EUS is an invaluable diagnostic tool following ERCP to help identify malignancy in patients with extrahepatic biliary strictures. EUS can help establish a diagnosis in one of every seven cases of indeterminate biliary strictures. This impact is likely even greater for patients with distal strictures or those related to masses causing extrinsic compression. ERCP and EUS performed in tandem may be ideal for patient and resource management if biliary stenting is required. Large prospective studies are needed to establish the efficacy of multimodal approaches in the evaluation of extrahepatic biliary strictures to maximize the diagnostic yield in a timely fashion.

Supplementary materials

Supplementary information is linked to the online version of the paper on the Endoscopic Ultrasound website.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Brandi G, Venturi M, Pantaleo MA, et al. Cholangiocarcinoma: Current opinion on clinical practice diagnostic and therapeutic algorithms: A review of the literature and a long-standing experience of a referral center. Dig Liver Dis 2016;48:231-41.  Back to cited text no. 1
    
2.
Navaneethan U, Njei B, Lourdusamy V, et al. Comparative effectiveness of biliary brush cytology and intraductal biopsy for detection of malignant biliary strictures: A systematic review and meta-analysis. Gastrointest Endosc 2015;81:168-76.  Back to cited text no. 2
    
3.
Sadeghi A, Mohamadnejad M, Islami F, et al. Diagnostic yield of EUS-guided FNA for malignant biliary stricture: A systematic review and meta-analysis. Gastrointest Endosc 2016;83:290-80.  Back to cited text no. 3
    
4.
Eloubeidi MA, Chen VK, Jhala NC, et al. Endoscopic ultrasound-guided fine needle aspiration biopsy of suspected cholangiocarcinoma. Clin Gastroenterol Hepatol 2004;2:209-13.  Back to cited text no. 4
    
5.
Fritscher-Ravens A, Broering DC, Knoefel WT, et al. EUS-guided fine-needle aspiration of suspected hilar cholangiocarcinoma in potentially operable patients with negative brush cytology. Am J Gastroenterol 2004;99:45-51.  Back to cited text no. 5
    
6.
Prospero, International Prospective Register of Systematic Reviews. Available from: https://www.crd.york.ac.uk/prospero/. [Last accessed on 2018 Apr 22].  Back to cited text no. 6
    
7.
Shamseer L, Moher D, Clarke M, et al. Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols (PRISMA-P) 2015: Elaboration and explanation. BMJ 2015;350:g7647.  Back to cited text no. 7
    
8.
James PD, Meng ZW, Zhang M, et al. The incremental benefit of EUS for identifying unresectable disease among adults with pancreatic adenocarcinoma: A meta-analysis. PLoS One 2017;12:e0173687.  Back to cited text no. 8
    
9.
Wells GA, Shea B, O'Connell D, et al. The Newcastle-Otawa Scale (NOS) for assessing the quality of nonrandomized studies in meta-analyses; 2014. Available from: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp. [Last accessed on 2018 Jul 18].  Back to cited text no. 9
    
10.
DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials 1986;7:177-88.  Back to cited text no. 10
    
11.
Kim DC, Moon JH, Choi HJ, et al. The role of EUS-FNA after negative endoscopic transpapillary forceps biopsy in patients with malignant biliary strictures. Gastrointest Endosc 2013;77:AB422.  Back to cited text no. 11
    
12.
Lee YN, Moon JH, Choi HJ, et al. Diagnostic approach using ERCP-guided transpapillary forceps biopsy or EUS-guided fine-needle aspiration biopsy according to the nature of stricture segment for patients with suspected malignant biliary stricture. Cancer Med 2017;6:582-90.  Back to cited text no. 12
    
13.
Lee YN, Moon JH, Choi HJ, et al. Diagnostic approach using peroral cholangioscopy-guided forceps biopsy or EUS-guided fine-needle aspiration biopsy according to the location of stricture for patients with suspected malignant biliary stricture: A prospective comparative study. Gastrointest Endosc 2016;83:AB125-6.  Back to cited text no. 13
    
14.
Hijioka S, Hara K, Mizuno N, et al. Diagnostic yield of endoscopic retrograde cholangiography and of EUS-guided fine needle aspiration sampling in gallbladder carcinomas. J Hepatobiliary Pancreat Sci 2012;19:650-5.  Back to cited text no. 14
    
15.
Lo DY, Howell DA, Wright E, et al. Su1429 frozen section of ERCP Forceps biopsy specimens permits efficient intraprocedural diagnosis. Gastrointest Endosc 2011;73:AB263.  Back to cited text no. 15
    
16.
Ohshima Y, Yasuda I, Kawakami H, et al. EUS-FNA for suspected malignant biliary strictures after negative endoscopic transpapillary brush cytology and forceps biopsy. J Gastroenterol 2011;46:921-8.  Back to cited text no. 16
    
17.
Fargahi S, Lee J, Lin F, et al. Endoscopic retrograde cholangiopancreatography (ERCP) and endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) in the cytologic diagnosis of cholangiocarcinoma – A comparative and morphologic study. Cancer Cytopathol 2010;118:323.  Back to cited text no. 17
    
18.
Oppong K, Raine D, Nayar M, et al. EUS-FNA versus biliary brushings and assessment of simultaneous performance in jaundiced patients with suspected malignant obstruction. JOP 2010;11:560-7.  Back to cited text no. 18
    
19.
Saifuku Y, Yamagata M, Koike T, et al. Endoscopic ultrasonography can diagnose distal biliary strictures without a mass on computed tomography. World J Gastroenterol 2010;16:237-44.  Back to cited text no. 19
    
20.
Rösch T, Hofrichter K, Frimberger E, et al. ERCP or EUS for tissue diagnosis of biliary strictures? A prospective comparative study. Gastrointest Endosc 2004;60:390-6.  Back to cited text no. 20
    
21.
Paranandi B, Oppong KW. Biliary strictures: Endoscopic assessment and management. Frontline Gastroenterol 2017;8:133-7.  Back to cited text no. 21
    
22.
Heimbach JK, Sanchez W, Rosen CB, et al. Trans-peritoneal fine needle aspiration biopsy of hilar cholangiocarcinoma is associated with disease dissemination. HPB (Oxford) 2011;13:356-60.  Back to cited text no. 22
    
23.
Minaga K, Takenaka M, Katanuma A, et al. Needle tract seeding: An overlooked rare complication of endoscopic ultrasound-guided fine-needle aspiration. Oncology 2017;93 Suppl 1:107-12.  Back to cited text no. 23
    
24.
Levy MJ, Gleeson FC, Campion MB, et al. Prospective cytological assessment of gastrointestinal luminal fluid acquired during EUS: A potential source of false-positive FNA and needle tract seeding. Am J Gastroenterol 2010;105:1311-8.  Back to cited text no. 24
    
25.
Ngamruengphong S, Xu C, Woodward TA, et al. Risk of gastric or peritoneal recurrence, and long-term outcomes, following pancreatic cancer resection with preoperative endosonographically guided fine needle aspiration. Endoscopy 2013;45:619-26.  Back to cited text no. 25
    
26.
Ikezawa K, Uehara H, Sakai A, et al. Risk of peritoneal carcinomatosis by endoscopic ultrasound-guided fine needle aspiration for pancreatic cancer. J Gastroenterol 2013;48:966-72.  Back to cited text no. 26
    
27.
El Chafic AH, Dewitt J, Leblanc JK, et al. Impact of preoperative endoscopic ultrasound-guided fine needle aspiration on postoperative recurrence and survival in cholangiocarcinoma patients. Endoscopy 2013;45:883-9.  Back to cited text no. 27
    
28.
Yoon WJ, Daglilar ES, Fernández-del Castillo C, et al. Peritoneal seeding in intraductal papillary mucinous neoplasm of the pancreas patients who underwent endoscopic ultrasound-guided fine-needle aspiration: The PIPE study. Endoscopy 2014;46:382-7.  Back to cited text no. 28
    
29.
Tsutsumi H, Hara K, Mizuno N, et al. Clinical impact of preoperative endoscopic ultrasound-guided fine-needle aspiration for pancreatic ductal adenocarcinoma. Endosc Ultrasound 2016;5:94-100.  Back to cited text no. 29
    
30.
Ngamruengphong S, Swanson KM, Shah ND, et al. Preoperative endoscopic ultrasound-guided fine needle aspiration does not impair survival of patients with resected pancreatic cancer. Gut 2015;64:1105-10.  Back to cited text no. 30
    
31.
Bowlus CL, Olson KA, Gershwin ME. Evaluation of indeterminate biliary strictures. Nat Rev Gastroenterol Hepatol 2016;13:28-37.  Back to cited text no. 31
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
   Abstract
  Introduction
  Methods
  Results
  Discussion
  Conclusion
   References
   Article Figures
   Article Tables

 Article Access Statistics
    Viewed699    
    Printed54    
    Emailed0    
    PDF Downloaded119    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]