Skip to main content
Springer logoLink to Springer
. 2023 Jul 15;58(9):801–833. doi: 10.1007/s00535-023-02014-6

Evidence-based clinical practice guidelines for cholelithiasis 2021

Naotaka Fujita 1,2,, Ichiro Yasuda 1, Itaru Endo 1, Hiroyuki Isayama 1, Takuji Iwashita 1, Toshiharu Ueki 1, Kenichiro Uemura 1, Akiko Umezawa 1, Akio Katanuma 1, Yu Katayose 1, Yutaka Suzuki 1, Junichi Shoda 1, Toshio Tsuyuguchi 1, Toshifumi Wakai 1, Kazuo Inui 1, Michiaki Unno 1, Yoshifumi Takeyama 1, Takao Itoi 1, Kazuhiko Koike 1, Satoshi Mochida 1
PMCID: PMC10423145  PMID: 37452855

Abstract

The Japanese Society of Gastroenterology first published evidence-based clinical practice guidelines for cholelithiasis in 2010, followed by a revision in 2016. Currently, the revised third edition was published to reflect recent evidence on the diagnosis, treatment, and prognosis of cholelithiasis conforming to the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) system. Following this revision, the present English version of the guidelines was updated and published herein. The clinical questions (CQ) in the previous version were reviewed and rearranged into three newly divided categories: background questions (BQ) dealing with basic background knowledge, CQ, and future research questions (FRQ), which refer to issues that require further accumulation of evidence. Finally, 52 questions (29 BQs, 19 CQs, and 4 FRQs) were adopted to cover the epidemiology, pathogenesis, diagnosis, treatment, complications, and prognosis. Based on a literature search using MEDLINE, Cochrane Library, and Igaku Chuo Zasshi databases for the period between 1983 and August 2019, along with a manual search of new information reported over the past 5 years, the level of evidence was evaluated for each CQ. The strengths of recommendations were determined using the Delphi method by the committee members considering the body of evidence, including benefits and harms, patient preference, and cost–benefit balance. A comprehensive flowchart was prepared for the diagnosis and treatment of gallbladder stones, common bile duct stones, and intrahepatic stones, respectively. The current revised guidelines are expected to be of great assistance to gastroenterologists and general physicians in making decisions on contemporary clinical management for cholelithiasis patients.

Keywords: Cholelithiasis, Gallbladder stones, Common bile duct stones, Intrahepatic stones, Endoscopic treatment, Surgical treatment

Introduction

Since the decision made by the Japanese Society of Gastroenterology (JSGE) in 2005 to publish evidence-based guidelines for clinically significant common gastrointestinal disorder, 11 clinical practice guidelines have been published. Cholelithiasis was selected as one of the target diseases, and the first edition of “Clinical practice guidelines for the treatment of cholelithiasis” was published in 2009, based on a literature search using the Igaku Chuo Zasshi, PubMed, and Cochrane library from 1983 to 2007. Some of the recommendations and statements, however, were determined by referring to old data or expert opinions due to the lack of available evidence. In 2016, its revised second edition, titled “Evidence-based clinical practice guidelines for the treatment of cholelithiasis”, was published with the cooperation of the Japan Gastroenterological Endoscopy Society and Japan Biliary Association, including new evidence published between 2007 and June 2012 [1].

Currently, following the JSGE policy of revising the guidelines every 5 years as necessary, the third revision has been issued to cover new insights after the publication of the second edition. This revision was carried out following the Minds Manual for Clinical Practice Development [2].

The committee of clinical practice guidelines for cholelithiasis consists of two subcommittees, namely, the development and evaluation committees, with refined new members. The former prepared and refined the draft and determined the final version by taking the suggestions of the latter into consideration.

In the current edition, the items to deal with are divided into three categories: clinical questions (CQs), core CQs, background questions (BQs), knowledge or practice that has been widely accepted, and future research questions (FRQs) which are questions that lack robust evidence at present and require further research to address a recommendation. Through discussions among committee members, eventually, 52 questions (29 BQs, 19 CQs, and 4 FRQs) were adopted covering the epidemiology, pathogenesis, diagnosis, treatments, complications, and prognosis.

A literature search was performed in the same manner as in the second revision, extending the search period to August 2019. A supplemental manual search was also carried out by each committee member, and some latest articles published after the above-mentioned period were also included in the reference as necessary. Structured abstracts were prepared for the CQs and FRQs, and the quality of evidence for each article was ranked as follows: A, high; B, moderate; C, low; and D, very low. [3]

The strengths of recommendations were determined by assessing the body of evidence using not only the data-driven approach but also patient preferences and cost–benefit balance according to voting by the committee members. Consensus was defined in advance as the acquisition of votes 70% or over [4], and the consensus rate was shown following each recommendation.

The present article summarizes the new guidelines to support gastroenterologists and general physicians in decision-making on the clinical management of cholelithiasis patients providing comprehensive statements for BQs and commentary, along with recommendations/statements for CQs and FRQ.

Epidemiology and pathophysiology

BQ1-1. Is the prevalence of cholelithiasis increasing in Japan?

Statement

There are no data showing recent trends in the prevalence of cholelithiasis in Japan. However, it is assumed to have increased with the increasing obese population, which is a risk factor for cholelithiasis.

– The incidence of intrahepatic stones has decreased in recent years but has been increasing again with the increase in biliary surgery.

These statements were made with reference to the following information and papers [511].

BQ1-2. What are the causes of cholecystolithiasis?

Statement

  • The formation of cholesterol gallstones is associated with the supersaturation of cholesterol in bile, crystallization, and decreased contractility of the gallbladder. Such conditions can be caused by excessive calorie and animal fat intake, hyperlipidemia, oral contraceptive use, prolonged fasting, dieting, decreased intestinal motility, obesity, and so on.

  • The main cause of calcium bilirubinate stones is biliary infection. Cholestasis is also associated with the formation.

  • The formation of black stones is presumed to be due, in part, to an increase in unconjugated bilirubin in bile owing to an excessive supply of bilirubin. Such a condition can be caused by hemolytic diseases such as hereditary spherocytosis and thalassemia, Crohn's disease, and ileal resection. Stones of this kind are also seen in liver cirrhosis.

These statements were made with reference to the following information and papers [1219].

BQ1-3. What are the risk factors for gallbladder stones?

Statement

  • Forty (years of age), female, fatty, fair, and fertile (so-called “5 Fs”) remain strong risk factors. In addition, dyslipidemia, previous upper gastrointestinal surgery and bariatric surgery, and diet are also considered to increase the risk of gallbladder stones.

These statements were made with reference to the following information and paper [15, 2048]

BQ1-4. What is the natural history of gallbladder stones?

Statement

  • Approximately 70% of patients with gallbladder stone disease are found asymptomatic and often remain asymptomatic. In asymptomatic gallstones, the cumulative symptomatic rate over a 10 year period is estimated to be about 10–20%. In addition, there have occasionally been reports of cases in which biliary calculi have disappeared asymptomatically. Since obesity and lifestyle-related diseases are risk factors for gallbladder stones, higher cumulative mortality from cardiovascular disease, cancer, and diabetes has been reported in patients with gallbladder stones.

This statement was made with reference to the following information and papers [4959].

CQ1-1. Is gallbladder stone a risk factor for gallbladder cancer?

Statement

  • There is no clear evidence that gallbladder stones are a risk factor for gallbladder cancer.

(Recommendation: none, 100% agreed, evidence level D).

Commentary

It is well known that patients with gallbladder cancer have gallbladder stones at a high rate (69–96%) [60]. Many case–control studies have been reported on the association between gallbladder stones and gallbladder cancer [6176]. Although the relative risks vary from 2.3 to 34.4, gallbladder stones have been reported to be a risk factor for gallbladder cancer. In particular, patients with large stones [61] [76], numerous stones [71] [73], non-cholesterol stones (mixed stones), symptoms [70], and a long symptomatic period [71] reportedly have a high risk of gallbladder cancer. Three previous cohort studies showed a higher incidence of gallbladder cancer in patients with gallbladder stones than in normal controls (relative risk, 3.01–6.1) with a median follow-up period of 6.1–13.3 years [7779]. A meta-analysis of three cohort studies and seven case–control studies also showed that gallstones were the strongest risk factor for gallstone cancer, with a relative risk of 4.9 [80]. In contrast, a large cohort study of 113,394 patients with a history of gallbladder stones/cholecystitis who were followed-up for 11 years showed a hazard ratio of 1.07, which suggests a negative impact of gallbladder stones on the occurrence of gallbladder cancer [81]. Based on these results, there is no dispute regarding the relationship, in some way, between gallbladder stones and gallbladder cancer. However, it is still difficult to determine whether gallbladder stones are the cause of gallbladder cancer, or whether they are more likely to form during the development of gallbladder cancer because the incidence of gallbladder cancer in patients with gallbladder stones is extremely low, and there is also controversial negative evidence.

Porcelain gallbladder and atrophic gallbladder have been considered high-risk factors for gallbladder cancer. However, a recent systematic review revealed that their roles as risk factors were not as significant as previously suggested [8285].

BQ1-5. Is hepatolithiasis a risk factor for intrahepatic cholangiocarcinoma?

Statement

  • Hepatolithiasis is a strong risk factor for intrahepatic cholangiocarcinomas.

This statement was made with reference to the following information and papers [86116].

Diagnosis

Gallbladder stones (see Fig. 1).

Fig. 1.

Fig. 1

Flowchart for diagnosis of gallbladder stones

BQ2-(1)-1. What are the symptoms of gallbladder stones?

Statement

  • Most cases of gallbladder stones are asymptomatic; however, characteristic abdominal pain, nausea, and vomiting may occur during an attack. Fever is also observed in cases of associated acute cholecystitis.

This statement was made with reference to the following information and papers [56, 117120].

BQ2-(1)-2. How should the diagnosis of gallbladder stones be made?

Statement

  • Abdominal ultrasound (US) and blood tests are performed in cases with symptoms suggestive of gallbladder stones. In cases of poor visualization of the gallbladder or indeterminate US findings, suspected cholangitis/bile duct stones, Mirizzi syndrome, confluence stones, or concomitant gallbladder cancer, abdominal computed tomography (CT), magnetic resonance imaging (MRI)/magnetic resonance cholangiopancreatography (MRCP), and/or endoscopic ultrasonography (EUS) are recommended. (Fig. 1)

This statement was made with reference to the following information and papers [121125].

BQ2-(1)-3. What about the diagnostic process of a patient with acute cholecystitis?

Statement

  • The diagnosis of acute cholecystitis is based on local clinical signs, systemic inflammatory findings, and diagnostic imaging. Severity is assessed based on organ dysfunction and local inflammatory findings. (Fig. 2)

Fig. 2.

Fig. 2

Flowchart for diagnosis of acute cholecystitis

This statement was made with reference to the following information and papers [126141].

Common bile duct stones (CBDS) (see Fig. 3).

Fig. 3.

Fig. 3

Flowchart for diagnosis of common bile duct stones

BQ2-(2)-1. What are the symptoms of CBDS?

Statement

  • Patients with CBDS often present with symptoms such as abdominal pain, back pain, fever, jaundice, and nausea/vomiting but are sometimes asymptomatic.

These statements were made with reference to the following information and papers [10, 142, 143].

BQ2-(2)-2. How are CBDS diagnosed?

Statement

  • In patients with suspected CBDS, abdominal US, abdominal CT, and/or MRI/MRCP are performed as appropriate. When these tests are indeterminate, EUS is suggested. Endoscopic retrograde cholangiopancreatography (ERCP) is recommended if symptoms relevant to acute cholangitis are present. (Fig. 3)

This statement was made based on the following information and papers [142, 144153].

CQ2-(2)-1. Is it recommended to perform EUS prior to ERCP rather than direct ERCP when abdominal US, CT, and/or MRI/MRCP are indeterminate in patients with suspected CBDS?

Recommendation

  • EUS prior to ERCP is suggested in patients with suspected CBDS when other diagnostic images are indeterminate.

(Recommendation: weak, 100% agreed, evidence level B).

Commentary

EUS is known to have a high diagnostic capability for CBDS because of its high spatial resolution. According to a meta-analysis evaluating the diagnostic capability of EUS for CBDS, the sensitivity, and specificity were 0.94 (95% confidence interval [CI] 0.93–0.96) and 0.95 (95% CI 0.94–0.96), respectively [150]. Another meta-analysis compared the diagnostic capability of EUS and MRCP for CBDS, reporting that the sensitivities of EUS and MRCP were 0.97 (95% CI 0.91–0.99) and 0.87 (95% CI 0.80–0.93) (p = 0.006), specificities were 0.90 (95% CI 0.83–0.94) and 0.92 (95% CI 0.87–0.96) (p = 0.42), and the diagnostic odds ratios were 162.5 (95% CI 54.0–489.3) and 79.0 (95% CI 23.8–262.2) (p = 0.008), respectively [154]. Both EUS and MRCP showed a high diagnostic capability for CBDS, but the diagnostic odds ratio was significantly superior with EUS, which was considered to be due to the high sensitivity of EUS in detecting small stones [154]. EUS is also useful in diagnosing CBDS in patients with suspected biliary pancreatitis [155, 156].

A meta-analysis of four randomized controlled trials (RCTs) compared the efficacy of performing EUS prior to ERCP (EUS-first strategy) with direct ERCP (ERCP-first strategy) in patients with suspected CBDS [157], reporting that the EUS-first strategy could omit ERCP in 67.1% of the patients; however, the number of procedures in the EUS-first strategy was significantly higher than that in the ERCP-first approach (relative risk [RR] 2.46, 95% CI 1.34–4.52; p = 0.004) since ERCP was performed after EUS. As for safety, the EUS-first strategy significantly reduced the risks of overall adverse events (RR 0.35, 95% CI 0.20–0.62) and post-procedure pancreatitis (RR 0.21, 95% CI 0.06–0.83). EUS prior to ERCP in patients with suspected CBDS allows for omitting unnecessary ERCP and reduces the risk of adverse events. However, the limited availability of EUS is a problem because of the necessity of an experienced endosonographer.

Column 1: is it possible to differentiate between primary CBDS and secondary stones from the gallbladder?

CBDSs include primary and secondary stones migrating from the gallbladder. It is generally believed that calcium bilirubinate stones are formed in the common bile duct (CBD), while cholesterol and black stones are formed in the gallbladder. However, because stones formed in the gallbladder undergo further modification after migrating into the CBD [158], it is difficult to determine whether CBDSs are formed in the CBD or gallbladder in clinical practice. A study on the correlation between CBDS and CBD diameter showed that the diameter of the CBD was significantly larger in patients with primary stones than in those with secondary stones, but this has not been widely accepted because of the small number of cases in this study.

From a therapeutic point of view, the method of bile duct stone removal is independent of the stone type, whether endoscopic or surgical. It has been pointed out that endoscopic treatment even with small-incision endoscopic sphincterotomy (EST) or balloon dilation may impair papillary function to a certain degree, leading to possible increased retrograde infection from the duodenal papilla and recurrence of common bile duct stones [158, 159]. On the other hand, laparoscopic common bile duct exploration (LCBDE) does not impair papillary function and is considered appropriate, especially for younger patients due to the reduced risk of ascending cholangitis.

Stone diseases are benign, and long-term follow-up is necessary. Accumulation of data on the nature of removed stones and continued follow-up may facilitate making an adequate selection of treatment options.

These statements were made with reference to the following information and papers [158, 159].

Hepatolithiasis (see Fig. 4).

Fig. 4.

Fig. 4

Flowchart for diagnosis of hepatolithiasis

BQ2-(3)-1. What are the symptoms of hepatolithiasis?

Statement

  • Abdominal pain, fever, and jaundice are often observed in patients with hepatolithiasis; however, the number of asymptomatic patients has been increasing.

This statement was made with reference to the following information and papers [160162].

BQ2-(3)-2. How is hepatolithiasis diagnosed?

Statements

  • – When hepatolithiasis is suspected, minimally invasive modalities, including blood examination, US, CT, MRI, and MRCP, are performed. Furthermore, measurement of tumor markers is recommended to assess the risk of intrahepatic cholangiocarcinoma.

  • – If intrahepatic stones are visualized and intrahepatic cholangiocarcinoma is suspected, a detailed examination to diagnose intrahepatic cholangiocarcinoma should be performed.

  • – In symptomatic cases or when intrahepatic stones cannot be visualized, direct cholangiography, bile duct cytology, and cholangioscopy are recommended, considering the comorbidity of intrahepatic cholangiocarcinoma.

These statements were made with reference to the following information and papers [11, 160, 161, 163, 164]. (Fig. 4).

Treatment

Gallbladder stones (see Fig. 5).

Fig. 5.

Fig. 5

Flowchart for treatment of gallbladder stones

BQ3-(1)-1. How should the treatment of patients with acute cholecystitis be applied?

Statement

  • After initial treatment, such as adequate intravenous fluid infusion and administration of antibiotics and analgesics, further treatment should be performed based on the severity of acute cholecystitis.

This statement was made with reference to the following information and papers [165173].

BQ3-(1)-2. What are the nonsurgical treatments for cholecystolithiasis?

Statements

  • Butylscopolamine, flopropione, and nonsteroidal anti-inflammatory drugs are used to treat attacks.

  • Oral ursodeoxycholic acid is an option for prophylaxis against attacks.

  • Extracorporeal shock wave lithotripsy (ESWL) and oral chemical dissolution therapy have been used for the treatment of gallbladder stones but have rarely been performed in recent years.

These statements were made with reference to the following information and papers [119, 174183].

CQ3-(1)-1. Is cholecystectomy recommended over follow-up for asymptomatic patients with cholecystolithiasis?

Recommendation

  • Cholecystectomy should be considered for patients at high risk of gallbladder cancer.

(Recommendation: weak, 100% agreed, evidence level C).

Commentary

Asymptomatic gallbladder stones are increasingly being detected due to the widespread use of medical examinations and advances in diagnostic imaging. It is estimated that 2–4% of asymptomatic gallbladder stones become symptomatic within 1 year of diagnosis [184, 185]. Two-thirds of asymptomatic patients are expected to remain asymptomatic for the remainder of their lives. Asymptomatic gallstones have a 0.3% chance of developing acute cholecystitis, 0.2% risk of leading to obstructive jaundice, and 0.04–1.5% risk of developing acute pancreatitis; however, Development of gallstone ileus is rare [186].

It is well known that the frequency of gallbladder cancer complicated by gallbladder calculus is as high as 40–70% [83]. However, the incidence of gallbladder cancer associated with cholelithiasis is approximately 0.1–0.5%, although the rate varies in available reports [85]. Furthermore, the incidence of gallbladder cancer from asymptomatic gallbladder stones is reported to be rare (0–0.5%) [187]. In addition, a decision analysis model showed that prophylactic cholecystectomy for patients with asymptomatic gallbladder stones did not improve their prognosis, including death from gallbladder cancer [188]. Generally, prophylactic cholecystectomy is in consideration of the possibility of developing gallbladder cancer and is not recommended for patients with asymptomatic gallbladder stones. However, cholecystectomy should be considered in patients at high risk of gallbladder cancer. The high-risk groups for gallbladder cancer include patients with stones larger than 3 cm, polyps larger than 10 mm, porcelain gallbladder, thickened gallbladder walls, and stone-filled gallbladders [50, 83, 85, 186, 189].

During follow-up, it is recommended to explain to the patients the risk of developing symptoms, acute cholecystitis, and gallbladder cancer, and the necessity to perform periodic examinations, such as abdominal US.

FRQ 3-(1)-1. Is cholecystectomy recommended in a case of gallbladder stones with an atrophic gallbladder?

Statement

  • Cholecystectomy should be performed if gallbladder cancer is suspected based on the morphology of the thickened gallbladder wall and the course of the disease. However, it is difficult to distinguish and rule out the presence of gallbladder cancer from images; therefore, the indication for surgery in this condition should be established in future studies.

Commentary

If no gallbladder is visualized or an atrophic gallbladder is found on imaging studies, it may be due to a hypoplastic gallbladder, chronic cholecystitis, or biliary gastrointestinal fistulas [190192].

Chronic cholecystitis and biliary gastrointestinal fistulas are often associated with gallbladder stones, and it has been reported that 5.6% of the patients operated on for asymptomatic gallbladder stones have grossly atrophic gallbladders [193]. In biliary gastrointestinal fistulas, a sudden disappearance of symptoms associated with gallbladder stones (e.g., pain and jaundice) is often observed. In addition to stones, ulcers and malignant tumors of the gallbladder may cause fistulas. On imaging, an atrophic gallbladder is sometimes found to be associated with biliary emphysema [192].

The frequency of gallbladder cancer in patients with atrophic gallbladders is unknown. In a case series, 4.4% of the surgical cases of atrophic gallbladder were reported to have gallbladder cancer [194]. An atrophic gallbladder with stones has been considered an indication for cholecystectomy as a high-risk group for gallbladder cancer because the gallbladder wall is difficult to observe and evaluate entirely due to stones filling the lumen [83, 195]. In contrast, it has been suggested that an atrophic gallbladder is a condition in which the epithelium of the gallbladder has been abolished due to chronic cholecystitis; therefore, it is unlikely to become symptomatic or develop gallbladder cancer [85]. As it is difficult to diagnose or rule out the presence of gallbladder cancer from diagnostic imaging in atrophic gallbladders, cholecystectomy may be considered to rule out malignant tumors based on the degree of thickening of the gallbladder wall and the course of the disease. In general, a wall thickening of 3 mm is considered the upper limit of normal, but localized or diffuse irregular thickening is also included in the indication for surgery [196]. In addition, tumor markers and FDG-PET findings are used in clinical practice to determine the indications for surgery. Increased difficulty in surgery with an atrophic gallbladder or biliary gastrointestinal fistula should be kept in mind [197].

CQ3-(1)-2. Is cholecystectomy recommended over nonoperative treatment for symptomatic gallbladder stones?

Recommendation

  • Laparoscopic cholecystectomy is recommended for symptomatic gallbladder stones.

(Recommendation: strong, 91% agreed, evidence level C).

Commentary

Among patients with symptomatic gallbladder stones, 1–3% of the patients with mild symptoms develop severe symptoms or complications (i.e., acute cholecystitis/acute cholangitis, jaundice, and/or pancreatitis) within 1 year. The annual rate of patients with moderate symptoms who develop severe symptoms and undergo surgery is 6–8%, and this rate has decreased over time [55].

After nonoperative treatment of acute cholecystitis, emergency surgery due to flare-ups of symptoms while waiting for an elective cholecystectomy occurs in 6–23% of the cases [198]. In elderly patients, cholecystectomy is preferable if the patient's general condition is judged to be amenable to surgery because sudden recurrence is not uncommon, sometimes in more severe forms, after a long asymptomatic period. Laparoscopic cholecystectomy is a safe and useful treatment for symptomatic gallbladder stones in the absence of acute cholecystitis [199].

Complications associated with laparoscopic cholecystectomy include bile duct injury, bleeding, and injury to other organs. According to the results of a questionnaire survey by the Japanese Society for Endoscopic Surgery in 2017, bile duct injury, bleeding requiring laparotomy, and injury to other organs occurred in approximately 0.4%, 0.3%, and 0.3% of all laparoscopic cholecystectomies, respectively [200].

In a gastrointestinal quality of life index study of symptomatic patients with gallbladder stones, excluding those with acute cholecystitis, pancreatitis, and common bile duct stones, laparoscopic cholecystectomy was reported to significantly improve the quality of life of patients [201].

CQ3-(1)-3. Is early laparoscopic cholecystectomy for severe acute cholecystitis recommended over conservative treatment, including biliary drainage and administration of antibacterial agents?

Recommendation

Systemic treatment using antibacterial agents should be performed first in cases of severe cholecystitis.

  • Early cholecystectomy by a skilled surgeon is recommended in a tertiary medical institution for patients who have undergone surgery.

(Recommendation: weak, 91% agreed, evidence level B).

  • If a patient cannot withstand emergent/early surgery, early gallbladder drainage is recommended.

(Recommendation: strong, 100% agreed, evidence level A).

Commentary

For severe acute cholecystitis with organ failure, systemic or local treatment alone is not recommended [202]. Biliary drainage or surgery should be performed to control local infection along with systemic treatments, such as the administration of antibacterial agents and supportive care for organ failure, depending on the severity of organ failure.

Early cholecystectomy is recommended if organ failure can be controlled. However, mortality is significantly higher in patients with severe acute cholecystitis and critical organ failure, including central nervous system disorder, respiratory dysfunction, and jaundice [203]. According to the Tokyo guidelines 2018, patients with mild-to-moderate cholecystitis, that is, those with an age-adjusted Charlson’s comorbidity index ≥ 6 points, and American Society of Anesthesiologists Physical Status score ≥ 3 points were included in the high-risk surgery group. Patients with severe acute cholecystitis should be treated at an institute with an intensive care unit. For surgical intervention, laparoscopic cholecystectomy should be performed by skilled endoscopic surgeons.

CQ3-(1)-4. Is endoscopic gallbladder drainage recommended over percutaneous transhepatic gallbladder drainage in acute cholecystitis?

Recommendations

  • Percutaneous transhepatic gallbladder drainage (PTGBD) is recommended in cases of acute cholecystitis.

(Recommendation: strong, 100% agreed, evidence level B).

  • Endoscopic gallbladder drainage is proposed for patients with coagulopathy, patients receiving antithrombotic agents, and those with ascites by a skilled endoscopist.

(Recommendation: weak, 100% agreed, evidence level B).

Commentary

There are several methods for gallbladder drainage for acute cholecystitis, such as PTGBD, percutaneous transhepatic gallbladder aspiration, and endoscopic gallbladder drainage, including transpapillary gallbladder drainage (ETGBD) and EUS-guided gallbladder drainage (EUS-GBD). Table 1 presents the published clinical results for each drainage procedure. PTGBD is recommended for high-surgical risk patients because of its high success rate (technical success, 97–100%; clinical success, 89.3–97.6%) and its safety (complication rate, 3–39.5%) in previously published data and because of the simplicity of the technique [173, 204214]. In contrast, ETGBD has been performed as an alternative treatment at skilled pancreatobiliary endoscopic institutions with a lower success rate (technical: 81–96%, clinical: 75–93%) than PTGBD [173, 211214]. Therefore, ETGBD is considered the treatment of choice for patients with suspected CBDS, coagulation abnormalities, antithrombotic medications, ascites accumulation, and other conditions that make PTGBD difficult to perform, as well as for patients with a high risk of PTGBD-related complications to control acute cholecystitis. There have been few reports on the management of acute cholecystitis with coagulation abnormalities or anticoagulant use. Guidelines on interventional radiology allow the performance of PTGBD with single-agent aspirin when the risk of thromboembolism is high [215]. However, the Japanese DPC data reported that PTGBD is associated with a significantly higher risk of bleeding in patients with cholecystitis who are taking antithrombotic drugs. These data should be kept in mind, and a sufficient explanation about the risk of bleeding should be provided to the patient prior to performing PTGBD [216].

Table 1.

Comparison of percutaneous and endoscopic-transpapillary drainages for cholecystitis

Author Year Study design Procedures Number of cases Technical success (%) Clinical success (%) Adverse events (%)
Siddiqui 2019 Retro ETGBD 124 88 90 2
EUS-GBD 102 94 80 5
PTGBD 146 98 97 20
Jang 2012 RCT EUS-GBD 30 97 100 7
PTGBD 29 97 96 3
Itoi 2010 SR

PTGBA

PTGBD

ENGBD

EGBS

122 93 83 0.8
246 98 90 3.7
194 81 75 3.6
127 96 88 6.3
EUS-GBD 12 100 100 16.7
Khan 2017 SR ETGBD 647 83 93 10
EUS-GBD 162 93 97 13
Mohan 2019 SR ETGBD 1,223 83 88.1 9.6
EUS-GBD 557 95.3 96.7 12.4
PTGBD 13,351 98.7 89.3 15.1

Retro retrospective study; RCT randomized controlled trial; SR systematic review; ETGBD endoscopic transpapillary gallbladder drainage; EUS-GBD endoscopic ultrasound-guided gallbladder drainage; PTGBD percutaneous transhepatic gallbladder drainage; PTGBA percutaneous transhepatic gallbladder aspiration; ENGBD endoscopic naso-gallbladder drainage; EGBS endoscopic gallbladder stenting

Although EUS-GBD is a relatively new technique with reportedly high technical and clinical success rates (90–100%), institutions performing this procedure are limited [173, 211, 212, 214]. Recently, three new systematic reviews of EUS-GBD for acute cholecystitis using a lumen-apposing metal stent reported good results comparable to those of PTGBD in cases of acute cholecystitis [183, 217, 218]. At present, the EUS-GBD technique has not yet been generalized and hence, cannot be included in the recommendation.

CQ3-(1)-5. Is endoscopic treatment recommended over surgery for the Mirizzi syndrome and confluence stone?

Recommendations

  • Surgical treatment is recommended for the Mirizzi syndrome.

(Recommendation: strong, 91% agreed, evidence level D).

  • Endoscopic treatment with oral cholangioscopy at a well-equipped endoscopic institution is suggested for confluence stone.

(Recommendation: weak, 100% agreed, evidence level D).

Commentary

The pathogenesis of Mirizzi syndrome is CBD stricture caused by compression of the common hepatic duct by stone and/or inflammation in the neck of the gallbladder. McSherry et al. classified it as type I without fistula and type II with gallbladder-bile duct fistulas. Csendes et al. classified McSherry type II into three subtypes: type II (fistula occupying 1/3 of the CBD), type III (fistula occupying 2/3 of the CBD), and type IV (fistula occupying the entire CBD width). MRCP is useful for diagnosis (44–82%) [219221], and ERCP is performed not only for diagnosis but also for biliary drainage in cases of cholangitis and jaundice [222].

The standard treatment for Mirizzi syndrome is open surgery, including cholecystectomy and fistula closure. Temporary placement of a T-tube is carried out for small fistulas. The adverse event rate in patients with a fistula is reportedly high [219]. Laparoscopic surgery is difficult and has a higher rate of complications than open surgery [219, 223]. The conversion rate from laparoscopic surgery to open surgery is also high (8–76%) [219221, 224, 225], with a complication rate of 12–19% [221, 224] including fatal cases [223, 224]. Laparoscopic treatment of Mirizzi syndrome should be performed only by skilled surgeons. [225, 226].

Endoscopic treatment is indicated for Mirizzi syndrome type II and confluence stones, which are located at the confluence of the cystic duct, common hepatic duct, and CBD. [227]. Peroral cholangioscopy with electrohydraulic lithotripsy (EHL) or YAG laser has shown a very high complete stone removal rate of 95% (92 of 97 cases) [228230].

In Japan, endoscopic treatment is often performed using ESWL. Although endoscopic treatment of confluence stones is deemed to increase with the development and spread of devices, our recommendation has been weak (proposal) considering the local availability of this technique.

Common bile duct stones (see Fig. 6).

Fig. 6.

Fig. 6

Flowchart for treatment of common bile duct stones

BQ3-(2)-1. What kind of endoscopic treatments do we have for CBDS?

Statements

  • – The standard treatment is endoscopic sphincterotomy (EST) with subsequent endoscopic stone extraction; however, endoscopic papillary balloon dilation (EPBD) is also applicable.

  • In cases of endoscopically difficult stones, endoscopic papillary large balloon dilation (EPLBD), peroral cholangioscopy (POCS), percutaneous transhepatic cholangioscopy (PTCS), balloon endoscopy-assisted techniques, and EUS-guided procedures are also used.

These statements were made with reference to the following information and papers [231233].

BQ3-(2)-2. What are the surgical treatments for CBDS?

Statement

  • Surgical treatments for CBDS include "open surgery (cholecystectomy and choledocholithotomy),” "laparoscopic surgery (cholecystectomy and choledocholithotomy)," and "laparoscopic cholecystectomy and endoscopic removal of common bile duct stones."

This statement was made with reference to the following information and papers [10, 200, 234, 235].

BQ3-(2)-3. What are the treatment options for CBDS associated with gallbladder stones?

Statements

  • There are various treatment options, including (1) surgical cholecystectomy after endoscopic bile duct stone removal and (2) simultaneous surgical cholecystectomy and bile duct stone removal (Table 2).

Table 2.

Therapeutic Procedures for gallbladder stones and common bile duct stones

Single session Multi-session
Category Procedure Category Procedure
Gallbladder stone Surgery Open surgical/ laparoscopic cholecystectomy Combination

Endoscopic/percutaneous transhepatic gallbladder drainage

 → Open surgical/Laparoscopic cholecystectomy

Common bile duct stone without gallbladder stone Endoscopy Endoscopic removal of common bile duct stone Endoscopy

Endoscopic biliary drainage

 → Endoscopic removal of common bile duct stone

IR Percutaneous removal of common bile duct stone Combination

Percutaneous transhepatic biliary drainage

 → Endoscopic/Percutaneous removal of common bile duct stone

Surgery Open surgical/ laparoscopic common bile duct stone exploration with or without cholecystectomy Combination

Percutaneous transhepatic biliary drainage

 → Open surgical/ laparoscopic common bile duct stone exploration with or without cholecystectomy

Gallbladder stone with common bile duct stone Surgery Open surgical/ laparoscopic cholecystectomy and common bile duct stone exploration Combination

Endoscopic/percutaneous removal of common bile duct stone (before surgery)

 → Open surgical/ Laparoscopic cholecystectomy

Combination Laparoscopic cholecystectomy and intraoperative ERCP Combination

Open surgical/ laparoscopic cholecystectomy

 → Endoscopic/percutaneous removal of common bile duct stone (after surgery)

Combination

Endoscopic/Percutaneous transhepatic biliary drainage with or without Endoscopic/ percutaneous transhepatic gallbladder drainage

 → Cholecystectomy → Endoscopic/ percutaneous removal of common bile duct stone

Combination

Endoscopic/Percutaneous transhepatic gallbladder drainage

 → Laparoscopic common bile duct stone exploration with or without cholecystectomy

IR interventional radiology, ERCP endoscopic retrograde cholangiopancreatography

This statement was made with reference to the following information and papers [236243].

BQ3-(2)-4. Is endoscopic CBDS removal plus surgical cholecystectomy (two-stage combined treatment) more beneficial than surgical CBDS removal plus cholecystectomy (one-stage surgical treatment) for CBDS complicated with gallbladder stones?

Statement

  • Endoscopic CBDS removal plus surgical cholecystectomy and surgical CBDS removal plus cholecystectomy are equally effective in complete ductal clearance, the rate of residual stones, mortality, and complications, except for longer hospital stay for endoscopic CBDS removal plus surgical cholecystectomy.

  • In Japan, a two-stage combination treatment of endoscopic CBDS removal followed by surgical cholecystectomy is commonly performed.

These statements were made with reference to the following information and papers [10, 200, 244248].

FRQ3-(2)-1. Does surgical treatment for CBDS, which does not affect the function of the sphincter of Oddi, have a better long-term prognosis compared to that of endoscopic treatment?

Statement

  • A method of assessing the relationship between the prognosis and function of the sphincter of Oddi after treatment of CBDS has not been established. The long-term impact of surgical treatment of CBDS on the stone recurrence rate and quality of life of patients should be investigated.

Commentary

The treatment of CBDSs with gallbladder calculi is generally a two-stage procedure consisting of endoscopic treatment (endoscopic CBDS removal) and laparoscopic cholecystectomy, although surgical one-stage treatment is also used. In Japan, 80% of the CBDSs are treated with the two-stage treatment [200].

One-stage treatment allows preservation of the functions of the sphincter of Oddi. The stone recurrence rate is lower with one-stage treatment than with two-stage treatment and is reportedly 3.5% at 10 years [249]. The correlation between the functionality of the sphincter of Oddi and stone recurrence rate is related to the type of CBDSs and their origin (i.e., primary or secondary) [250]. In particular, one-stage treatment for patients aged < 60 years with secondary or cholesterol stones has a low recurrence rate [251].

On the other hand, the relationship between primary bile duct stones and sphincter of Oddi function with respect to etiology, course, and prognosis is not well understood.

Currently, available methods for evaluating papillary function include endoscopic or constant-flow perfusion biliary pressure measurement, biliary excretion dynamics by biliary scintigraphy, and serial MRCP imaging [252255]. The impact of surgical CBDS removal with preservation of papillary sphincter function on long-term prognosis, such as the stone recurrence rate and patients’ quality of life, should be clarified.

FRQ3-(2)-2. Is laparoscopic surgery recommended over open surgery for one-stage surgical treatment of CBDS with gallbladder stones?

Statement

  • Supportive evidence for the recommendation of laparoscopic one-stage surgery for CBDS with gallbladder stones is insufficient, and further accumulation of data is necessary.

Commentary

The one-stage surgical treatment of CBDSs with gallbladder stones consists of open surgery, which has been conventionally performed, and laparoscopic surgery. Laparoscopic surgery includes "laparoscopic cholecystectomy and choledocholithotomy," and laparoscopic cholecystectomy and intraoperative endoscopic removal of CBDS (rendezvous technique)". In recent years, reports of laparoscopic cholecystectomy and intraoperative endoscopic removal of CBDS have been increasing, mainly in Europe and the United States. In Japan, two-stage treatment is widely used, in which endoscopic removal of CBDS is performed first, followed by laparoscopic cholecystectomy. When one-stage surgical treatment is chosen, it is often difficult to perform endoscopic removal of CBDS for some reason.

According to a 2017 survey on endoscopic surgery by the Japan Society for Endoscopic Surgery, only 20 of the 353 centers (6%) performed laparoscopic choledocholithotomy in all cases, 196 centers (56%) performed laparoscopic choledocholithotomy in some cases, and 137 centers (39%) performed open choledocholithotomy in all cases, which is still a high percentage [200].

An RCT compared one-stage open versus one-stage laparoscopic choledocholithotomy in 256 patients with CBDS and found that there was no statistically significant difference in operative time, stone removal rate, or complication rate. However, laparoscopic choledocholithotomy was significantly better in terms of intraoperative bleeding, postoperative hospital stay, and wound infection rate [256]. As this single-center RCT is the only study to compare one-stage open versus one-stage laparoscopic choledocholithotomy, the evidence for the recommendation of the laparoscopic approach is currently insufficient.

One-stage laparoscopic cholecystectomy and choledocholithotomy should be performed safely, taking each institution's environment and surgeons' skills into account.

CQ3-(2)-1. For patients with CBDS uncomplicated with gallbladder stones or post-cholecystectomy, is endoscopic treatment recommended over surgery?

Recommendation

  • Endoscopic treatment is recommended for CBDS that are uncomplicated by gallstones or with a history of cholecystectomy.

(Recommendation: strong, 100% agreed, evidence level C).

Commentary

No RCTs or meta-analyses have compared endoscopy and surgery for CBDSs with uncomplicated gallbladder stones or previous cholecystectomy. Wang et al. [257] reported a retrospective study comparing endoscopic and laparoscopic treatments for CBDSs with previous cholecystectomy. The complete stone clearance rate after endoscopic treatment was significantly higher than that after laparoscopic surgery (97.7 vs. 87%; p = 0.003). The treatment time of endoscopy was significantly shorter than that of laparoscopy (52.0 ± 15.8 min vs. 102.9 ± 40.1 min, p < 0.001). The complication rate after treatment (endoscopy, 3.4%; laparoscopy, 11.1%, p = 0.15) and hospital stay (endoscopy, 5.5 ± 2.6 days; laparoscopy, 5.9 ± 2.3 min, p = 0.40) were not different.

Japan Biliary Association performed a multi-institutional prospective study on the treatment of CBDSs in 2013 [10]. Endoscopic treatment was most frequently performed for CBDSs without cholecystolithiasis (endoscopy, 71.2%; surgery, 7.6%).

Considering these results, endoscopy may be the first-choice treatment for CBDSs uncomplicated by gallbladder stones or after cholecystectomy.

CQ3-(2)-2. For asymptomatic CBDS, is stone removal recommended over follow-up without treatment?

Recommendation

  • Stone removal is proposed for asymptomatic CBDS because of the risk of cholangitis and other complications.

(Recommendation: weak, 82% agreed, evidence level C).

Commentary

Stone removal is generally performed for CBDSs regardless of the presence or absence of symptoms because of the risk of severe cholangitis and other complications [258]. However, the natural history of asymptomatic CBDSs remains unclear. Previous reports have shown that asymptomatic CBDSs are detected in 10–20% of the patients undergoing cholecystectomy [259261]. Kim et al. reported the results of endoscopic treatment for CBDSs according to the presence or absence of symptoms [262] and reported that the incidence of pancreatitis after ERCP was significantly higher in patients with asymptomatic CBDSs (12.5 vs. 3.9%, p = 0.045). Hakuta et al. [263] reported an observational study of 191 asymptomatic cases of CBDSs: 114 cases in the wait-and-see group and 77 in the intervention group. The cumulative incidence of biliary complications was 6.1% at 1 year, 11% at 3 years, and 17% at 5 years, with no differences between the groups (p = 0.55). Procedure-related adverse events were observed in 22 patients (19%), including 4 (5.2%) with severe pancreatitis in the wait-and-see group and 25 (32%) in the early endoscopic removal group. They concluded that a wait-and-see strategy is an option, considering the incidence of procedure-related complications of endoscopic intervention for asymptomatic patients. At present, asymptomatic CBDSs are often treated endoscopically; however, the benefits and disadvantages of endoscopic treatment should be carefully evaluated, especially in the elderly, patients with poor activity of daily living (ADL), and those with serious underlying diseases.

CQ3-(2)-3. Is single-session stone removal recommended in cases of bile duct stones with acute cholangitis?

Recommendation

  • Single-session stone removal can be safely performed in patients with CBDSs and acute cholangitis. Bile duct drainage only in the first session and scheduled stone removal are suggested depending on the patient's condition.

(Recommendation: strong, 100% agreed, evidence level C).

Commentary

For patients with common duct stones associated with acute cholangitis, there are two treatment options: (1) removal of stones in a single session and (2) performing biliary drainage only in the first session and waiting for the improvement of cholangitis before performing stone removal. In cases of severe acute cholangitis, short-term biliary drainage with stent placement (endoscopic biliary stenting (EBS) or endoscopic nasobiliary drainage (ENBD)) is recommended [264]. It is also safer to treat cholangitis with EBS alone without EST and to perform scheduled stone removal after the resolution of acute cholangitis, although the length of hospital stay is prolonged [265]. When complete stone removal is achieved, biliary drainage, such as EBS or ENBD, is not always necessary [266]. Eto et al. reported excellent results for single-session stone removal in 50 patients [267]. However, it should be noted that this study did not include patients with severe cholangitis or poor general condition. In addition, patients with a bleeding tendency or those undergoing antithrombotic treatment may be at risk of bleeding during/following endoscopic procedures, such as EST. The size and number of stones can make a single-session treatment difficult. Therefore, it is important to carefully evaluate the patient's general condition, the number and diameter of stones, and the severity grade of cholangitis according to Tokyo Guidelines (TG) 18 before treatment. If the equipment in the facility including the skill of endoscopists is not sufficient to perform the procedure safely, transfer of the patient to a specialized center should be considered [142]

CQ3-(2)-4. Is endoscopic treatment recommended over conservative treatment for biliary pancreatitis?

Recommendation

  • Early endoscopic treatment is suggested for biliary pancreatitis associated with acute cholangitis.

(Recommendation: strong, 100% agreed, evidence level C).

Commentary

Multiple meta-analyses have compared early ERCP with conservative treatment for biliary pancreatitis [268272]. Since ERCP is necessary for the management of acute cholangitis, the inclusion of patients with or without acute cholangitis has a great impact on the results of the meta-analyses. In the analyses that excluded patients with biliary pancreatitis associated with acute cholangitis [269, 270], early ERCP for biliary pancreatitis did not show any difference in morbidity and mortality rates compared to conservative management, regardless of the severity of pancreatitis. According to the analysis by Tse in 2012 [271], early ERCP significantly reduced mortality rates (RR, 0.20; 95% CI 0.06–0.68) and both local (RR, 0.45; 95% CI 0.20–0.99) and the general (RR, 0.37; 95% CI 0.18–0.78) adverse event rates if only RCTs including patients with biliary pancreatitis associated with acute cholangitis were analyzed. However, early ERCP showed a tendency to increase the mortality rate (RR, 1.91; 95% CI 0.85–4.30) and the local (RR, 1.15; 95% CI 0.69–1.92) and general (RR, 1.02; 95% CI 0.44–2.36) adverse event rates when only RCTs that excluded patients with acute cholangitis were analyzed. Based on these results, it is not recommended to perform early ERCP routinely in all patients with biliary pancreatitis. Early endoscopic treatment is suggested for cases of biliary pancreatitis associated with definite/suspected acute cholangitis. The diagnosis of acute cholangitis should be based on cholestatic findings on blood examinations and imaging findings since inflammatory findings can be caused by pancreatitis only. When endoscopic treatment of biliary pancreatitis associated with acute cholangitis is difficult, PTBD should be considered to manage acute cholangitis.

CQ3-(2)-5. Is EPLBD more recommended than EST for large or multiple bile duct stones?

Recommendation

  • EPLBD is recommended for large or multiple bile duct stones.

(Recommendation: strong, 91% agreed, evidence level A).

Commentary

EPLBD, first reported by Ersoz et al. [273] in 2003, is a procedure to dilate the duodenal papilla using a large-diameter balloon of 12 mm or more in diameter with or without EST [274]. EPLBD is used to manage difficult bile duct stones, such as large or multiple stones because the biliary orifice is opened sufficiently after dilation using a large-diameter balloon. Several meta-analyses have evaluated the efficacy and safety of EPLBD in the management of bile duct stones [275280]. A recent meta-analysis, including 9 RCTs and 9 non-RCTs, compared EPLBD with EST to EST alone for large (≥ 10 mm) or multiple bile duct stones [279]. The results showed that EPLBD with EST was significantly superior in both the total stone removal rate and the rate of stone removal in the first ERCP session, with less frequent use of mechanical lithotripsy. With regard to safety, EPLBD with EST showed a lower rate of overall early adverse events than EST alone. The incidence of significant bleeding was lower in the EPLBD with EST group than in the EST group; however, no difference was observed in the incidence of pancreatitis, acute cholangitis, or perforation between the groups. According to the Japan Gastroenterological Endoscopy Society guidelines for EPLBD, EPLBD is contraindicated in cases of distal bile duct stricture or nondilated bile duct because of the higher risk of perforation [232]. A meta-analysis evaluated the significance of EST before EPLBD and reported that EPLBD with EST showed similar efficacy and safety as EPLBD without EST [280]. Some studies comparing the long-term results between EPLBD and EST for large/multiple bile duct stones showed no significant differences in the incidence of long-term adverse events between the procedures, although further evaluation of safety is required because these reports are retrospective studies with insufficient follow-up periods [281, 282].

CQ3-(2)-6. Is endoscopic treatment recommended for giant CBDS?

Recommendation

  • For giant stones, endoscopic treatment with ESWL or POCS is performed at specialized centers; however, there is little evidence to support recommending its use.

(Recommendation: none, 91% agreed, evidence level D).

Commentary

EPLBD is recommended for large stones (see CQ3-(2)-5), but giant stones > 3 cm are difficult to treat endoscopically, and ESWL has been used as an adjuvant treatment. It has been reported that a combination of ESWL with endoscopy achieves stone removal in 80–90% of the cases of giant bile duct stones [283]. Recently, with the advance of peroral cholangioscopy (POCS), endoscopic treatment of giant stones has been aggressively performed. In a meta-analysis of POCS for difficult-to-treat stones [284], the stone removal rate was 94.3%, of which 71.1% were successful in one session, and the complication rate was low (6.1%). Technically, lithotripsy under POCS is performed using laser or electrohydraulic lithotripsy (EHL); and the stone removal rate with the use of laser and that using EHL is reportedly 85–98% and 64–97%, respectively, while the removal rate using EHL is 64–97% [285].

In contrast, the stone removal rates of LCBDE and laparotomy in cases of unsuccessful endoscopic stone removal have been reported to be 95.2% and 95%, respectively [286].

The importance of POCS has been increasing with technological innovations and advances in equipment, and endoscopic treatment of giant stones, which was not previously indicated, is now being performed at specialized centers.

In addition to surgical and endoscopic treatment, stone removal by PTCS after PTBD is also useful [287].

CQ3-(2)-7. In the case of CBDS with altered anatomy after upper gastrointestinal surgery, what kind of treatment should be selected for stone removal?

Recommendation

  • Balloon endoscopy is proposed for CBDS removal by experienced surgeons in patients with post-surgically altered upper gastrointestinal anatomy.

  • (Recommendation: weak, 100% agreed, evidence level C).

Commentary

The treatment methods for CBDS in patients with altered anatomy after upper gastrointestinal surgery, such as Roux-en-Y (R-Y) or Billroth II (B-II), include endoscopic, percutaneous, and surgical stone removal. Each treatment has individual advantages and disadvantages [288]. However, no report has compared these three methods. Successful endoscopic approach to the papilla and treatment success in B-II reconstruction cases using a conventional endoscope are 72–97% and 49–92%, respectively [289293]; however, the results in R-Y cases are not satisfactory. The development of double-balloon and single-balloon endoscopes has made it easy to reach the duodenal papilla in cases of patients with a surgically altered anatomy [294296], and these scopes are now widely used in endoscopic biliopancreatic interventions in daily clinical practice. Satisfactory results of ERCP in R-Y cases using a balloon endoscope have been reported as 92.6–97% for successful approaches to the papilla, 58–95.6% for successful cannulation of the bile duct, with an adverse event rate of 7.3–10.3% [294, 297299]. However, this procedure remains challenging and entails a potential risk of severe adverse events. Therefore, balloon endoscopy-assisted ERCP should be performed by experienced endoscopists at specialized facilities [300, 301]. Recently, there have been several reports on the usefulness of interventional EUS for such patients, which is expected to be an alternative treatment method in cases of failed balloon endoscopy-assisted ERCP [302, 303].

BQ3-(2)-5. Is percutaneous transhepatic biliary drainage useful for acute cholangitis with CBDS when endoscopic transpapillary drainage is difficult?

Statement

  • Percutaneous transhepatic biliary drainage is useful in difficult cases for endoscopic transpapillary drainage, such as in patients with postoperative bowel reconstruction or unsuccessful transpapillary cannulation. EUS-BD has also emerged as a new treatment option.

This statement was made with reference to the following information and papers [304, 305].

BQ-3-(2)-6. What kind of patients with CBDS are good indications for EPBD?

Statement

  • Patients with bleeding diathesis are good indications for EPBD.

These statements were made with reference to the following information and papers [306314].

CQ3-(2)-8 Is endoscopic treatment recommended for CBDS in patients receiving antithrombotic therapy?

Statement:

  • Endoscopic treatment is recommended for CBDS in patients receiving antithrombotic therapy, as described in the relevant guidelines.

(Recommendation: weak, 82% agreed, evidence level C).

Commentary

According to the Japanese guidelines [315, 316], patients with CBDS and acute cholangitis who also have coagulopathy, and those receiving antithrombotic therapy should initially undergo ENBD or EBS, that is, drainage alone, to improve cholangitis along with coagulopathy, and then undergo CBDS removal via EST, which should be performed after the withdrawal of the antithrombotic agent, for safety [317]. Some patients may undergo ENBD or EBS alone depending on their condition. EST and EPLBD should be performed in accordance with the corresponding guidelines [231, 232]. In patients at high risk of thromboembolism, who develop acute cholangitis, if such patients are receiving aspirin alone, EST or EPLBD without drug withdrawal can be acceptable after consultations with specialists in antithrombotic therapy. Patients receiving thienopyridine derivatives other than aspirin have been reported to have a higher risk of accidental bleeding; therefore, these drugs should be substituted with aspirin or cilostazol [231, 232]. When only warfarin is used as an anticoagulant, EST or EPLBD can be performed with warfarin therapy if the international normalized ratio is within the therapeutic range. EST or EPLBD can be performed in patients with nonvalvular atrial fibrillation after temporarily switching from warfarin therapy to direct oral anticoagulant (DOAC) therapy [316]. DOAC monotherapy should be continued until the day before EST or EPLBD is performed and resumed on the 1st postoperative day.

EPBD is a good alternative to EST for the patient groups discussed here. The incidence of accidental procedure-related bleeding is significantly lower in patients undergoing EPBD than in those undergoing EST as reported in a meta-analysis [1].

CQ3-(2)-9 Is endoscopic stone removal recommended over permanent biliary stenting for CBDS in the elderly and in patients with serious underlying comorbidities?

Statement

  • Endoscopic stone removal is recommended over permanent biliary stenting for CBDS in the elderly and in patients with serious underlying comorbidities. Permanent biliary stenting should be considered only in patients with a poor prognosis.

  • (Recommendation: weak, 100% agreed, evidence level C).

Commentary

The mainstay of endoscopic treatment for CBDS is complete stone removal after the duodenal papillary intervention. However, the elderly and patients with serious underlying diseases may not be able to endure long procedure time for endoscopic treatment of stones and are at risk of developing procedural complications.

Three retrospective studies and one RCT compared endoscopic stone removal and permanent stent placement for CBDS in the elderly and in patients with serious underlying diseases [318320]. In all studies, no significant differences were observed in the incidence of short-term procedural complications between the two groups. However, the incidence of long-term biliary-related complications was significantly higher in the permanent biliary stenting group than in the endoscopic stone removal group, and the onset of long-term complications was earlier in patients undergoing permanent biliary stenting.

These findings suggest that endoscopic stone removal for CBDS is preferred over permanent biliary stenting, even in the elderly and patients with serious underlying diseases. Permanent biliary stenting should be considered only in patients with poor prognosis. After permanent stent placement, it is necessary to identify the signs of acute cholangitis, such as fever, jaundice, and abdominal pain, for the early detection and treatment of biliary stent-related complications.

CQ3-(2)-10. Is a balloon catheter more useful than a basket catheter in endoscopic stone removal for CBDS?

Recommendation

  • Balloon catheters are as useful as basket catheters in endoscopic stone removal for CBDS and both are recommended.

(Recommendation: strong, 100% agreed, evidence level B).

Commentary

Endoscopic extraction of CBDS is generally performed using a balloon or basket catheter following EST. The choice between the two devices depends largely on the preferences of the operator and the institution. Basket catheters are generally used first in Japan and Europe [321, 322], while balloons are overwhelmingly used in the United States because of concerns about basket impaction [323].

Ishiwatari et al. [324] compared the complete stone removal rate of a balloon and a basket in an RCT on 172 patients with CBDS with a diameter < 10 mm (bile duct diameter < 15 mm) and found that the rate was significantly higher in the balloon group than in the basket group (92.3 vs. 80.0%, p = 0.037). Ozawa et al. [325] also compared the successful complete stone removal rate within 10 min in a randomized noninferiority study of 184 patients (CBDS diameter < 11 mm)The success rates were comparable (83.9% in the balloon group and 81.3% in the basket group), while the incidence of adverse events was also similar (11.8% and 6.6%). The reasons for failure in the balloon group were that the balloon passed through the duct beside the stone or the operator lost sight of the stone during the procedure; moreover, small stones tend to lodge at the pocket-like lower-end corner of the bile duct terminal. On the other hand, in the basket group, when the stones were very small, they slipped between the wires and were difficult to grasp.

As the results of the two RCTs have led to different conclusions, additional studies are needed. The recently published guidelines of the European Society of Gastrointestinal Endoscopy have concluded that the efficacy and safety of the balloon and basket are equivalent [326].

CQ3-(2)-11. Is cholecystectomy recommended over follow-up after endoscopic choledocholithotomy?

Recommendation

  • For CBDS with gallstones, cholecystectomy is recommended after endoscopic choledocholithotomy.

(Recommendation: strong, 91% agreed, evidence level B).

  • For CBDS without gallstones, there is a lack of evidence to recommend additional cholecystectomy after endoscopic choledocholithotomy.

(Recommendation: none, 100% agreed, evidence level C).

Commentary

In a meta-analysis of five RCTs that compared cholecystectomy and follow-up in patients with gallstones who underwent endoscopic choledocholithotomy, there were significantly more deaths in the follow-up group, a higher incidence of pain due to biliary tract, a higher incidence of recurrent jaundice and cholangitis, and a higher incidence of repeat cholangiography, such as ERCP [243, 327330]. Furthermore, in the follow-up group, 35% of the patients underwent cholecystectomy during the follow-up period [331].

In a retrospective study of a large number of cases using the Korean National Health Insurance database, among the 16,910 patients with gallstones who were treated endoscopically for CBDS, the recurrence rate of CBDS was significantly lower among patients who underwent cholecystectomy, which was 8% (920 in 11,617 patients), compared to patients who did not undergo cholecystectomy, which was 15% (773 in 5293 patients) (p < 0.0001) [332]. These results indicate that there is a consensus that cholecystectomy is more effective than follow-up after endoscopic choledocholithotomy.

In contrast, a long-term retrospective study of patients with CBDS who were treated with endoscopic choledocholithotomy, including many cases without gallstones, showed no difference in the recurrence rate of CBDS between the follow-up and cholecystectomy groups at a median follow-up period of 5 years or longer (15 vs. 19%, p = 0.295) [333]. These results suggest that prophylactic cholecystectomy is not necessary after endoscopic choledocholithotomy in patients without gallstones, although further validation is necessary.

FRQ3-(2)-3. Is oral administration of a choleretic after removal of CBDS more useful than no treatment?

Statement

  • The efficacy of ursodeoxycholic acid (UDCA) after CBDS removal in preventing recurrence has not been proven.

Commentary

There are few reports on the outcomes of UDCA administration after the treatment of CBDS [334]. Yamamoto et al. reported in an RCT that the recurrence rate after the removal of CBDS was 6.6% in the UDCA group and 18.6% in the non-UDCA group, although the study included only a small number of patients [335]. In their multivariate analysis, only the UDCA group showed a significant difference, with a hazard ratio of 5.032 (95% CI 1.011–39.75, p = 0.048), indicating that the UDCA was effective against recurrent CBDS. Conversely, there have been reports of frequent recurrence of CBDS after the administration of UDCA [336, 337]. The acidic pH of bile is thought to be the cause of stone formation, as UDCA tends to precipitate more easily. In any case, there are no meta-analyses or large-scale randomized trials that provide clear evidence at present, and the choice of treatment should be determined on a case-by-case basis.

Hepatolithiasis (see Fig. 7a, b).

Fig. 7.

Fig. 7

a Flowchart for treatment of hepatolithiasis with previous choledochoenterostomy. b Flowchart for treatment of hepatolithiasis without previous choledochoenterostomy

BQ3-(3)-1. What are the procedures for treating hepatolithiasis?

Statements

  • Hepatectomy, choledochoenterostomy, choledochotomy, stone removal with or without T-tube drainage, and plasty of the duodenal papilla are surgical treatments for hepatolithiasis.

  • ESWL, percutaneous transhepatic cholangioscopic lithotripsy, EUS-guided hepaticogastrostomy, endoscopic retrograde cholangiography (ERC), balloon-assisted ERC with stone extraction, and POCS with stone extraction have also been performed as nonsurgical treatments.

These statements were made with reference to the following information and papers [11, 161].

BQ3-(3)-2. What are the indications for hepatectomy in cases of hepatolithiasis?

Statements

  • Hepatectomy is indicated in patients with concomitant intrahepatic cholangiocarcinoma and/or liver atrophy.

  • Hepatectomy is considered in patients with failed nonsurgical treatments.

These statements were made with reference to the following information and papers [1, 11, 101, 111, 338, 339].

CQ3-(3)-1. Is observation recommended for asymptomatic hepatolithiasis?

Statements

  • For asymptomatic hepatolithiasis without concomitant cholangiocarcinoma*, liver atrophy*, biliary stricture**, or biliary dilatation**, follow-up without surgery is suggested.

(*:Recommendation: weak, 100% agreed, evidence level C).

(**:Recommendation: weak, 82% agreed, evidence level D).

Commentary

Few studies have reported the long-term outcomes of asymptomatic hepatolithiasis. In asymptomatic hepatolithiasis, liver atrophy occurs less frequently than in symptomatic hepatolithiasis [340]. Furthermore, after hepatectomy for hepatolithiasis, cholangitis occurs more frequently in patients with remnant biliary strictures than in patients without biliary strictures [341]. Considering these results, follow-up is appropriate for asymptomatic hepatolithiasis without concomitant intrahepatic cholangiocarcinoma, liver atrophy, biliary strictures, or biliary dilatations. During follow-up, imaging studies and tests for tumor markers are required for the early detection of intrahepatic cholangiocarcinoma.

BQ3-(3)-3. Is ESWL useful for the treatment of hepatolithiasis?

Statement

  • The complete stone clearance rate of ESWL is not high. However, ESWL is useful when used in combination with endoscopic treatment.

This statement was made with reference to the following information and papers [1, 11, 342349].

BQ3-(3)-4. Is peroral endoscopic treatment useful compared with percutaneous transhepatic cholangioscopic lithotripsy in cases of hepatolithiasis?

Statement

  • The treatment outcomes of peroral endoscopic procedures, including ERC, balloon-assisted ERC, and peroral cholangioscopy on stone extraction, are similar to those of percutaneous transhepatic cholangioscopic lithotripsy.

This statement was made with reference to the following information and papers [11, 98, 113, 161, 285, 350352].

Prognosis and adverse events

BQ 4–1. What are the long-term complications after cholecystectomy for gallbladder stones?

Statement

  • Residual or new stones in the bile duct or cystic duct, intraperitoneal migration of gallstones, insufficiency of the papillary sphincter, biliary tract injury, incisional hernia, and surgically induced changes in bile acid metabolism have been reported.

This statement was made with reference to the following information and papers [353355].

BQ4-2. Does cholecystectomy impair digestive and absorptive function?

Statement

  • There is no clear evidence that cholecystectomy impairs digestive and absorptive function.

This statement was made with reference to the following information and papers [356362].

BQ4-3. Are residual stones a risk factor for acute cholangitis and liver abscess after removal of CBD or intrahepatic stones?

Statement

  • Although it is difficult to determine whether the stones are residual or recurrent, they might be risk factors for acute cholangitis and liver abscesses.

This statement was made with reference to the following information and papers [332, 363373].

BQ4-4. What are the long-term complications after treatment of CBDSs?

Statement

  • Long-term complications included recurrent bile duct stones, acute cholangitis, and acute cholecystitis.

This statement was made with reference to the following information and papers [273, 314, 332, 363, 364, 366380]

BQ4-5. What are the long-term complications after treatment of hepatolithiasis?

Statement

  • Stone recurrence was the most common complication, followed by acute cholangitis, liver abscess, and intrahepatic bile duct cancer.

This statement was made with reference to the following information and papers [93, 94, 98, 107, 381388].

Acknowledgements

This article was supported by a Grant-in-Aid from the JSGE. The authors thank Shigeto Ishii (Department of Gastroenterology, Graduate School of Medicine, Juntendo University), Tatsuya Ishii (Center for Gastroenterology, Teine Keijinkai Hospital), Akinori Suzuki (Department of Gastroenterology, Graduate School of Medicine, Juntendo University), Yusuke Takasaki (Department of Gastroenterology, Graduate School of Medicine, Juntendo University), Kazuhiro Takami (Division of Hepato-biliary and Pancreatic Surgery Tohoku Medical and Pharmaceutical University), Ko Tomishima (Department of Gastroenterology, Graduate School of Medicine, Juntendo University), Haruka Toyonaga (Center for Gastroenterology, Teine Keijinkai Hospital), Hiroshi Nasuno (Center for Gastroenterology, Teine Keijinkai Hospital), Toshio Fujisawa (Department of Gastroenterology, Graduate School of Medicine, Juntendo University), Yuki Honma (Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine), Ryusei Matsuyama (Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine), Kuniharu Yamamoto (Division of Hepato-biliary and Pancreatic Surgery Tohoku Medical and Pharmaceutical University) for great assistance with data collection, data analysis, and manuscript preparation.

Appendix 1

The members of the Guidelines Committee who created and evaluated the Japanese Society of Gastroenterology, ‘‘Evidence-based clinical practice guidelines for cholelithiasis’’ are listed below.

Creation Committee: Chair: Naotaka Fujita (Miyagi Medical Check-up Plaza). Vice-chair: Itaru Endo (Department of Gastroenterological Surgery, Yokohama City University), Ichiro Yasuda (Third Department of Internal Medicine, University of Toyama, Toyama). Members: Hiroyuki Isayama (Department of Gastroenterology, Graduate School of Medicine, Juntendo University), Takuji Iwashita (First Department of Internal Medicine, Gifu University Hospital) Toshiharu Ueki (Department of Gastroenterology, Fukuoka University Chikushi Hospital), Kenichiro Uemura (Department of Surgery, Graduate School of Biomedical & Health Sciences, Hiroshima University), Akiko Umezawa (Minimally Invasive Surgery Center, Yotsuya Medical Cube), Akio Katanuma (Center for Gastroenterology, Teine-Keijinkai Hospital), Yu Katayose (Division of Hepato-biliary-pancreatic Surgery, Tohoku Medical and Pharmaceutical University), Yutaka Suzuki (Department of General and Gastroenterological Surgery, Kyorin University School of Medicine).

Evaluation Committee: Chair: Michiaki Unno (Department of Surgery, Tohoku University Graduate School of Medicine). Vice-chair: Kazuo Inui (Department of Gastroenterology Yamashita Hospital). Members: Junichi Shoda (Division of Medical Sciences, Faculty of Medicine, University of Tsukuba), Toshio Tsuyuguchi (Department of Gastroenterology, Chiba Prefectural Sawara Hospital), Toshifumi Wakai (Division of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences).

The Japanese Society of Gastroenterology: President: Satoshi Mochida (Department of Gastroenterology and Hepatology, Faculty of Medicine, Saitama Medical University). Past President: Kazuhiko Koike (Kanto Central Hospital). Director Responsible: Yoshifumi Takeyama (Department of Surgery, Kindai University Faculty of Medicine), Takao Itoi (Department of Gastroenterology and Hepatology, Tokyo Medical University).

Author contributions

Writing—original draft: NF, IY, IE, HI, TI, TU, KU, AU, AK, YK, YS. Writing—review and editing: NF and IY. Supervision: JS, TT, TW, KI, MU, YT, TI, KK and SM. Approval of final manuscript: all authors.

Declarations

Conflict of interest

Any financial relationship with enterprises, businesses or academic institutions in the subject matter or materials discussed in the manuscript are listed as follows: (1) those from which the authors, the spouse, partner or immediate relatives of the authors have received individually any income, honoraria or any other type of renumeration; Asahi Kasei Pharma, Olympus Corporation, Daiichi Sankyo, Fuji Film, Taiho Pharmaceutical, Denka, and (2) those from which the authors have received scholarship/research grant; Taiho Pharmaceutical, Tsumura & Co., Bristol Myers Squibb, Ajimonoto, Hitachi, Boston Scientific Japan, Denka, Hospital Administration Niigata Prefecture, Brourbon, Yasuda Yogurt, Astellas Pharmaceutical, Abbvie, EA Pharma, Eisai, MSD, Ono Pharmaceutical, Covidien Japan, Taiho Pharmaceutical, Takeda Pharmaceutical, Chugai Pharmaceutical, Novaltis Japan, Bayer Japan, Asahi Kasei Pharma, Nippon Kayaku, Mochida Pharmaceutical, Eli Lilly Japan, Gadelius Medical, Boston Scientific Japan, JRA Facilities, and (3) those from which the academic institutions of the authors received support (commercial/academic cooperation); Eisai.

Footnotes

The original version of this article appeared in Japanese as ‘‘Tansekisho Shinryo Guidelines 2021,’’ from the Japanese Society of Gastroenterology published by Nankodo, Tokyo, in 2021. Please see the article on the standards, methods, and process of developing guidelines.

The members of the Guidelines Committee are listed in the Appendix.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Tazuma S, Unno M, Igarashi Y, et al. Evidence-based clinical practice guidelines for cholelithiasis 2016. J Gastroenterol. 2017;52:276–300. doi: 10.1007/s00535-016-1289-7. [DOI] [PubMed] [Google Scholar]
  • 2.Minds Manual Developing Committee. Minds Manual for Guideline Development 2017. Tokyo: Japan Council for Quality Health Care; 2017. (in Japanese)
  • 3.Qaseem A, Kansagara D, Lin JS, et al. The Development of Clinical Guidelines and Guidance Statements by the Clinical Guidelines Committee of the American College of Physicians: Update of Methods. Ann Intern Med. 2019;170:863–870. doi: 10.7326/M18-3290. [DOI] [PubMed] [Google Scholar]
  • 4.Yoshida M, Kinoshita Y, Watanabe M, et al. JSGE Clinical Practice Guidelines 2014: standards, methods, and process of developing the guidelines. J Gastroenterol. 2015;50:4–10. doi: 10.1007/s00535-014-1016-1. [DOI] [PubMed] [Google Scholar]
  • 5.Health Statistics Association of Japan. Estimated number of patients based on patient surveys. Index of Health. 1993;39:29–35 (in Japanese).
  • 6.Calle EE, Rodriguez C, Walker-Thurmond K, et al. Overweight, obesity, and mortality from cancer in a prospectively studied cohort of U.S. adults. N Engl J Med. 2003;348:1625–1638. doi: 10.1056/NEJMoa021423. [DOI] [PubMed] [Google Scholar]
  • 7.Kameda H, Kozuki T, Tanimura H, et al. Report of cholelithiasis investigation committee of the Japan Biliary Association. J Jpn Biliary Assoc. 1990;4:396–404 (in Japanese with English abstract).
  • 8.Tanimura H, Uchiyama K. Report on the results of the national survey on cholelithiasis 1996. J Jpn Biliary Assoc. 1997;11:133–140 (in Japanese with English abstract)
  • 9.The Japanese Biliary Society Cholelithiasis Survey Project National cholelithiasis survey report 1997. J Jpn Biliary Assoc. 1997;1998(12):276–293. [Google Scholar]
  • 10.Committee JBA. Report on the 2013 National Survey for biliary stone. J Jpn Biliary Assoc. 2014;28:612–617. [Google Scholar]
  • 11.Suzuki Y, Mori T, Yokoyama M, et al. Hepatolithiasis: analysis of Japanese nationwide surveys over a period of 40 years. J Hepatobiliary Pancreat Sci. 2014;21:617–622. doi: 10.1002/jhbp.116. [DOI] [PubMed] [Google Scholar]
  • 12.Hay DW, Carey MC. Pathophysiology and pathogenesis of cholesterol gallstone formation. Semin Liver Dis. 1990;10:159–170. doi: 10.1055/s-2008-1040470. [DOI] [PubMed] [Google Scholar]
  • 13.Shoda J. Classification and pathogenesis of gallstones. J Jpn Biliary Assoc. 2013;27:672–679 (in Japanese with English abstract)
  • 14.Ko CW, Sekijima JH, Lee SP. Biliary sludge. Ann Intern Med. 1999;130:301–311. doi: 10.7326/0003-4819-130-4-199902160-00016. [DOI] [PubMed] [Google Scholar]
  • 15.Jonkers IJ, Smelt AH, Ledeboer M, et al. Gall bladder dysmotility: a risk factor for gall stone formation in hypertriglyceridaemia and reversal on triglyceride lowering therapy by bezafibrate and fish oil. Gut. 2003;52:109–115. doi: 10.1136/gut.52.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Carey MC. Pathogenesis of gallstones. Am J Surg. 1993;165:410–419. doi: 10.1016/S0002-9610(05)80932-8. [DOI] [PubMed] [Google Scholar]
  • 17.Vitek L, Carey MC. New pathophysiological concepts underlying pathogenesis of pigment gallstones. Clin Res Hepatol Gastroenterol. 2012;36:122–129. doi: 10.1016/j.clinre.2011.08.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Ise H, Moriyasu A, Suzuki N, et al. Pathogenesis of black stones. J Hepatobiliary Pancreat Surg. 1997;4:412–416. doi: 10.1007/BF02488974. [DOI] [Google Scholar]
  • 19.Vitek L, Carey MC. Enterohepatic cycling of bilirubin as a cause of 'black' pigment gallstones in adult life. Eur J Clin Invest. 2003;33:799–810. doi: 10.1046/j.1365-2362.2003.01214.x. [DOI] [PubMed] [Google Scholar]
  • 20.Shaffer EA. Epidemiology and risk factors for gallstone disease: has the paradigm changed in the 21st century? Curr Gastroenterol Rep. 2005;7:132–140. doi: 10.1007/s11894-005-0051-8. [DOI] [PubMed] [Google Scholar]
  • 21.Stampfer MJ, Maclure KM, Colditz GA, et al. Risk of symptomatic gallstones in women with severe obesity. Am J Clin Nutr. 1992;55:652–658. doi: 10.1093/ajcn/55.3.652. [DOI] [PubMed] [Google Scholar]
  • 22.Halpern Z, Rubin M, Harach G, et al. Bile and plasma lipid composition in non-obese normolipidemic subjects with and without cholesterol gallstones. Liver. 1993;13:246–252. doi: 10.1111/j.1600-0676.1993.tb00639.x. [DOI] [PubMed] [Google Scholar]
  • 23.Kim HS, Cho SK, Kim CS, et al. Big data and analysis of risk factors for gallbladder disease in the young generation of Korea. PLoS ONE. 2019;14:e0211480. doi: 10.1371/journal.pone.0211480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Méndez-Sánchez N, Zamora-Valdés D, Chávez-Tapia NC, et al. Role of diet in cholesterol gallstone formation. Clin Chim Acta. 2007;376:1–8. doi: 10.1016/j.cca.2006.08.036. [DOI] [PubMed] [Google Scholar]
  • 25.Cuevas A, Miquel JF, Reyes MS, et al. Diet as a risk factor for cholesterol gallstone disease. J Am Coll Nutr. 2004;23:187–196. doi: 10.1080/07315724.2004.10719360. [DOI] [PubMed] [Google Scholar]
  • 26.Barbara L, Sama C, Labate AMM, et al. A population study on the prevalence of gallstone disease: the Sirmione Study. Hepatology. 1987;7:913–917. doi: 10.1002/hep.1840070520. [DOI] [PubMed] [Google Scholar]
  • 27.Grodstein F, Colditz GA, Hunter DJ, et al. A prospective study of symptomatic gallstones in women: relation with oral contraceptives and other risk factors. Obstet Gynecol. 1994;84:207–214. [PubMed] [Google Scholar]
  • 28.Everhart JE. Contributions of obesity and weight loss to gallstone disease. Ann Intern Med. 1993;119:1029–1035. doi: 10.7326/0003-4819-119-10-199311150-00010. [DOI] [PubMed] [Google Scholar]
  • 29.Ohya T, Tazuma S. Pathogenesis of Gallstone and Pancreatic Stone Formation. Endoscopia Digestiva. 2019;31:1594–1600 (in Japanese with English abstract).
  • 30.Tsai C-J, Leitzmann MF, Willett WC, et al. Macronutrients and insulin resistance in cholesterol gallstone disease. Off J Am Coll Gastroenterol ACG. 2008;103:2932–2939. doi: 10.1111/j.1572-0241.2008.02189.x. [DOI] [PubMed] [Google Scholar]
  • 31.Thomas LA, Veysey MJ, Bathgate T, et al. Mechanism for the transit-induced increase in colonic deoxycholic acid formation in cholesterol cholelithiasis. Gastroenterology. 2000;119:806–815. doi: 10.1053/gast.2000.16495. [DOI] [PubMed] [Google Scholar]
  • 32.Colecchia A, Mazzella G, Sandri L, et al. Ursodeoxycholic acid improves gastrointestinal motility defects in gallstone patients. World J Gastroenterol. 2006;12:5336. doi: 10.3748/wjg.v12.i33.5336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Gustafsson U, Benthin L, Granström L, et al. Changes in gallbladder bile composition and crystal detection time in morbidly obese subjects after bariatric surgery. Hepatology. 2005;41:1322–1328. doi: 10.1002/hep.20686. [DOI] [PubMed] [Google Scholar]
  • 34.Asai Y, Yamada T, Tsukita S, et al. Activation of the hypoxia inducible factor 1α subunit pathway in steatotic liver contributes to formation of cholesterol gallstones. Gastroenterology. 2017;152(1521–1535):e8. doi: 10.1053/j.gastro.2017.01.001. [DOI] [PubMed] [Google Scholar]
  • 35.Pomeranz IS, Shaffer EA. Abnormal gallbladder emptying in a subgroup of patients with gallstones. Gastroenterology. 1985;88:787–791. doi: 10.1016/0016-5085(85)90152-0. [DOI] [PubMed] [Google Scholar]
  • 36.Pauletzki J, Althaus R, Holl J, et al. Gallbladder emptying and gallstone formation: a prospective study on gallstone recurrence. Gastroenterology. 1996;111:765–771. doi: 10.1053/gast.1996.v111.pm8780583. [DOI] [PubMed] [Google Scholar]
  • 37.Portincasa P, Di Ciaula A, Wang HH, et al. Coordinate regulation of gallbladder motor function in the gut-liver axis. Hepatology. 2008;47:2112–2126. doi: 10.1002/hep.22204. [DOI] [PubMed] [Google Scholar]
  • 38.Inoue K, Fuchigami A, Higashide S, et al. Gallbladder sludge and stone formation in relation to contractile function after gastrectomy. A prospective study. Ann Surg. 1992;215:19. doi: 10.1097/00000658-199201000-00002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Shoda J, He B-F, Tanaka N, et al. Increase of deoxycholate in supersaturated bile of patients with cholesterol gallstone disease and its correlation with de novo syntheses of cholesterol and bile acids in liver, gallbladder emptying, and small intestinal transit. Hepatology. 1995;21:1291–1302. [PubMed] [Google Scholar]
  • 40.Tsai C-J, Leitzmann MF, Hu FB, et al. A prospective cohort study of nut consumption and the risk of gallstone disease in men. Am J Epidemiol. 2004;160:961–968. doi: 10.1093/aje/kwh302. [DOI] [PubMed] [Google Scholar]
  • 41.Leitzmann MF, Stampfer MJ, Willett WC, et al. Coffee intake is associated with lower risk of symptomatic gallstone disease in women. Gastroenterology. 2002;123:1823–1830. doi: 10.1053/gast.2002.37054. [DOI] [PubMed] [Google Scholar]
  • 42.Festi D, Colecchia A, Orsini M, et al. Gallbladder motility and gallstone formation in obese patients following very low calorie diets. Use it (fat) to lose it (well) Int J Obes. 1998;22:592–600. doi: 10.1038/sj.ijo.0800634. [DOI] [PubMed] [Google Scholar]
  • 43.Cha BH, Jang M-j, Lee SH. Alcohol consumption can reduce the risk of gallstone disease: a systematic review with a dose-response meta-analysis of case-control and cohort studies. Gut Liver. 2019;13:114. doi: 10.5009/gnl18278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Leitzmann MF, Rimm EB, Willett WC, et al. Recreational physical activity and the risk of cholecystectomy in women. N Engl J Med. 1999;341:777–784. doi: 10.1056/NEJM199909093411101. [DOI] [PubMed] [Google Scholar]
  • 45.Shoda J, Miyamoto J, Kano M, et al. Simultaneous determination of plasma mevalonate and 7 α-hydroxy-4-cholesten-3-one levels in hyperlipoproteinemia: Convenient indices for estimating hepatic defects of cholesterol and bile acid syntheses and biliary cholesterol supersaturation. Hepatology. 1997;25:18–26. doi: 10.1053/jhep.1997.v25.pm0008985259. [DOI] [PubMed] [Google Scholar]
  • 46.Tsai CJ, Leitzmann MF, Willett WC, et al. Statin use and the risk of cholecystectomy in women. Gastroenterology. 2009;136:1593–1600. doi: 10.1053/j.gastro.2009.01.042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Festi D, Frabboni R, Bazzoli F, et al. Gallbladder motility in cholesterol gallstone disease: effect of ursodeoxycholic acid administration and gallstone dissolution. Gastroenterology. 1990;99:1779–1785. doi: 10.1016/0016-5085(90)90487-L. [DOI] [PubMed] [Google Scholar]
  • 48.Veysey M, Malcolm P, Mallet A, et al. Effects of cisapride on gall bladder emptying, intestinal transit, and serum deoxycholate: a prospective, randomised, double blind, placebo controlled trial. Gut. 2001;49:828–834. doi: 10.1136/gut.49.6.828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Shoda J. Natural History of Gallstones. J Jpn Biliary Assoc. 2017;31:187–195 (in Japanese with English abstract)
  • 50.Festi D, Reggiani MLB, Attili AF, et al. Natural history of gallstone disease: expectant management or active treatment? Results from a population-based cohort study. J Gastroenterol Hepatol. 2010;25:719–724. doi: 10.1111/j.1440-1746.2009.06146.x. [DOI] [PubMed] [Google Scholar]
  • 51.Shabanzadeh DM, Sorensen LT, Jorgensen T. A Prediction Rule for Risk Stratification of Incidentally Discovered Gallstones: Results From a Large Cohort Study. Gastroenterology. 2016;150(156–167):e1. doi: 10.1053/j.gastro.2015.09.002. [DOI] [PubMed] [Google Scholar]
  • 52.Persson GE. Expectant management of patients with gallbladder stones diagnosed at planned investigation. A prospective 5- to 7-year follow-up study of 153 patients. Scand J Gastroenterol. 1996;31:191–199. doi: 10.3109/00365529609031985. [DOI] [PubMed] [Google Scholar]
  • 53.Dworken HJ. Recent experiences with spontaneously disappearing gallstones. Gastroenterology. 1960;38:76–86. doi: 10.1016/S0016-5085(60)80120-5. [DOI] [PubMed] [Google Scholar]
  • 54.Norman CH, Jr, Butera DG. Spontaneously disappearing gallstones. J Natl Med Assoc. 1979;71:61. [PMC free article] [PubMed] [Google Scholar]
  • 55.Friedman GD. Natural history of asymptomatic and symptomatic gallstones. Am J Surg. 1993;165:399–404. doi: 10.1016/S0002-9610(05)80930-4. [DOI] [PubMed] [Google Scholar]
  • 56.Thistle JL, Cleary PA, Lachin JM, et al. The natural history of cholelithiasis: the National Cooperative Gallstone Study. Ann Intern Med. 1984;101:171–175. doi: 10.7326/0003-4819-101-2-171. [DOI] [PubMed] [Google Scholar]
  • 57.Lamberts MP, Ozdemir C, Drenth JPH, et al. Cost-effectiveness of a new strategy to identify uncomplicated gallstone disease patients that will benefit from a cholecystectomy. Surg Endosc. 2017;31:2534–2540. doi: 10.1007/s00464-016-5256-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Brazzelli M, Cruickshank M, Kilonzo M, et al. Systematic review of the clinical and cost effectiveness of cholecystectomy versus observation/conservative management for uncomplicated symptomatic gallstones or cholecystitis. Surg Endosc. 2015;29:637–647. doi: 10.1007/s00464-014-3712-6. [DOI] [PubMed] [Google Scholar]
  • 59.Schmidt M, Sondenaa K, Vetrhus M, et al. A randomized controlled study of uncomplicated gallstone disease with a 14-year follow-up showed that operation was the preferred treatment. Dig Surg. 2011;28:270–276. doi: 10.1159/000329464. [DOI] [PubMed] [Google Scholar]
  • 60.Cariati A, Piromalli E, Cetta F. Gallbladder cancers: associated conditions, histological types, prognosis, and prevention. Eur J Gastroenterol Hepatol. 2014;26:562–569. doi: 10.1097/MEG.0000000000000074. [DOI] [PubMed] [Google Scholar]
  • 61.Diehl AK. Gallstone size and the risk of gallbladder cancer. JAMA. 1983;250:2323–2326. doi: 10.1001/jama.1983.03340170049027. [DOI] [PubMed] [Google Scholar]
  • 62.Lowenfels AB, Lindstrom CG, Conway MJ, et al. Gallstones and risk of gallbladder cancer. J Natl Cancer Inst. 1985;75:77–80. [PubMed] [Google Scholar]
  • 63.Nervi F, Duarte I, Gomez G, et al. Frequency of gallbladder cancer in Chile, a high-risk area. Int J Cancer. 1988;41:657–660. doi: 10.1002/ijc.2910410503. [DOI] [PubMed] [Google Scholar]
  • 64.WHO. Combined oral contraceptives and gallbladder cancer. The WHO Collaborative Study of Neoplasia and Steroid Contraceptives. Int J Epidemiol. 1989;18:309–14. [DOI] [PubMed]
  • 65.Kato K, Akai S, Tominaga S, et al. A case-control study of biliary tract cancer in Niigata Prefecture. Japan Jpn J Cancer Res. 1989;80:932–938. doi: 10.1111/j.1349-7006.1989.tb01629.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Kimura W, Shimada H, Kuroda A, et al. Carcinoma of the gallbladder and extrahepatic bile duct in autopsy cases of the aged, with special reference to its relationship to gallstones. Am J Gastroenterol. 1989;84:386–390. [PubMed] [Google Scholar]
  • 67.Zatonski WA, Lowenfels AB, Boyle P, et al. Epidemiologic aspects of gallbladder cancer: a case-control study of the SEARCH Program of the International Agency for Research on Cancer. J Natl Cancer Inst. 1997;89:1132–1138. doi: 10.1093/jnci/89.15.1132. [DOI] [PubMed] [Google Scholar]
  • 68.Okamoto M, Okamoto H, Kitahara F, et al. Ultrasonographic evidence of association of polyps and stones with gallbladder cancer. Am J Gastroenterol. 1999;94:446–450. doi: 10.1111/j.1572-0241.1999.875_d.x. [DOI] [PubMed] [Google Scholar]
  • 69.Khan ZR, Neugut AI, Ahsan H, et al. Risk factors for biliary tract cancers. Am J Gastroenterol. 1999;94:149–152. doi: 10.1111/j.1572-0241.1999.00786.x. [DOI] [PubMed] [Google Scholar]
  • 70.Scott TE, Carroll M, Cogliano FD, et al. A case-control assessment of risk factors for gallbladder carcinoma. Dig Dis Sci. 1999;44:1619–1625. doi: 10.1023/A:1026675329644. [DOI] [PubMed] [Google Scholar]
  • 71.Csendes A, Becerra M, Rojas J, et al. Number and size of stones in patients with asymptomatic and symptomatic gallstones and gallbladder carcinoma: a prospective study of 592 cases. J Gastrointest Surg. 2000;4:481–485. doi: 10.1016/S1091-255X(00)80090-6. [DOI] [PubMed] [Google Scholar]
  • 72.Serra I, Yamamoto M, Calvo A, et al. Association of chili pepper consumption, low socioeconomic status and longstanding gallstones with gallbladder cancer in a Chilean population. Int J Cancer. 2002;102:407–411. doi: 10.1002/ijc.10716. [DOI] [PubMed] [Google Scholar]
  • 73.Roa I, Ibacache G, Roa J, et al. Gallstones and gallbladder cancer-volume and weight of gallstones are associated with gallbladder cancer: a case-control study. J Surg Oncol. 2006;93:624–628. doi: 10.1002/jso.20528. [DOI] [PubMed] [Google Scholar]
  • 74.Ahrens W, Timmer A, Vyberg M, et al. Risk factors for extrahepatic biliary tract carcinoma in men: medical conditions and lifestyle: results from a European multicentre case-control study. Eur J Gastroenterol Hepatol. 2007;19:623–630. doi: 10.1097/01.meg.0000243876.79325.a1. [DOI] [PubMed] [Google Scholar]
  • 75.Grainge MJ, West J, Solaymani-Dodaran M, et al. The antecedents of biliary cancer: a primary care case-control study in the United Kingdom. Br J Cancer. 2009;100:178–180. doi: 10.1038/sj.bjc.6604765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Alvi AR, Siddiqui NA, Zafar H. Risk factors of gallbladder cancer in Karachi-a case-control study. World J Surg Oncol. 2011;9:164. doi: 10.1186/1477-7819-9-164. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Maringhini A, Moreau JA, Melton LJ, 3rd, et al. Gallstones, gallbladder cancer, and other gastrointestinal malignancies. An epidemiologic study in Rochester, Minnesota. Ann Intern Med. 1987;107:30–35. doi: 10.7326/0003-4819-107-1-30. [DOI] [PubMed] [Google Scholar]
  • 78.Chow WH, Johansen C, Gridley G, et al. Gallstones, cholecystectomy and risk of cancers of the liver, biliary tract and pancreas. Br J Cancer. 1999;79:640–644. doi: 10.1038/sj.bjc.6690101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Ishiguro S, Inoue M, Kurahashi N, et al. Risk factors of biliary tract cancer in a large-scale population-based cohort study in Japan (JPHC study); with special focus on cholelithiasis, body mass index, and their effect modification. Cancer Causes Control. 2008;19:33–41. doi: 10.1007/s10552-007-9067-8. [DOI] [PubMed] [Google Scholar]
  • 80.Randi G, Franceschi S, La Vecchia C. Gallbladder cancer worldwide: geographical distribution and risk factors. Int J Cancer. 2006;118:1591–1602. doi: 10.1002/ijc.21683. [DOI] [PubMed] [Google Scholar]
  • 81.Yagyu K, Lin Y, Obata Y, et al. Bowel movement frequency, medical history and the risk of gallbladder cancer death: a cohort study in Japan. Cancer Sci. 2004;95:674–678. doi: 10.1111/j.1349-7006.2004.tb03328.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Schnelldorfer T. Porcelain gallbladder: a benign process or concern for malignancy? J Gastrointest Surg. 2013;17:1161–1168. doi: 10.1007/s11605-013-2170-0. [DOI] [PubMed] [Google Scholar]
  • 83.Nomura Y, Inui K, Yoshino J, et al. Causes of cholelithiasis, epidemiology, gallbladder stones and gallbladder cancer. Naika. 2005;95:223–226. [Google Scholar]
  • 84.Otani K, Chijiiwa K, Ouchida J, et al. Indications for resection of cholelithiasis and gallbladder polyps. Surgery. 2009;71:29–33. [Google Scholar]
  • 85.Horiguchi Y, Sakamoto K, Harada M, et al. Treatment of cholelithiasis: The natural history and treatment strategy for asymptomatic gallbladder stones. Naika. 2005;95:251–254. [Google Scholar]
  • 86.Koga A, Ichimiya H, Yamaguchi K, et al. Hepatolithiasis associated with cholangiocarcinoma. Possible etiologic significance Cancer. 1985;55:2826–2829. doi: 10.1002/1097-0142(19850615)55:12<2826::aid-cncr2820551219>3.0.co;2-1. [DOI] [PubMed] [Google Scholar]
  • 87.Chen MF, Jan YY, Wang CS, et al. A reappraisal of cholangiocarcinoma in patient with hepatolithiasis. Cancer. 1993;71:2461–2465. doi: 10.1002/1097-0142(19930415)71:8&#x0003c;2461::AID-CNCR2820710806&#x0003e;3.0.CO;2-7. [DOI] [PubMed] [Google Scholar]
  • 88.Sheen-Chen SM, Chou FF, Eng HL. Intrahepatic cholangiocarcinoma in hepatolithiasis: a frequently overlooked disease. J Surg Oncol. 1991;47:131–135. doi: 10.1002/jso.2930470213. [DOI] [PubMed] [Google Scholar]
  • 89.Kawarada Y, Mita T. Cholangiocarcinoma associated with hepatolithiasis. Tan to Sui. 1994;15:435–446. [Google Scholar]
  • 90.Chijiiwa K, Yamashita H, Yoshida J, et al. Current management and long-term prognosis of hepatolithiasis. Arch Surg. 1995;130:194–197. doi: 10.1001/archsurg.1995.01430020084016. [DOI] [PubMed] [Google Scholar]
  • 91.Kubo S, Kinoshita H, Hirohashi K, et al. Hepatolithiasis associated with cholangiocarcinoma. World J Surg. 1995;19:637–641. doi: 10.1007/BF00294744. [DOI] [PubMed] [Google Scholar]
  • 92.Liu CL, Fan ST, Wong J. Primary biliary stones: diagnosis and management. World J Surg. 1998;22:1162–1166. doi: 10.1007/s002689900536. [DOI] [PubMed] [Google Scholar]
  • 93.Chen DW, Tung-Ping Poon R, Liu CL, et al. Immediate and long-term outcomes of hepatectomy for hepatolithiasis. Surgery. 2004;135:386–393. doi: 10.1016/j.surg.2003.09.007. [DOI] [PubMed] [Google Scholar]
  • 94.Cheung MT, Kwok PC. Liver resection for intrahepatic stones. Arch Surg. 2005;140:993–997. doi: 10.1001/archsurg.140.10.993. [DOI] [PubMed] [Google Scholar]
  • 95.Vetrone G, Ercolani G, Grazi GL, et al. Surgical therapy for hepatolithiasis: a Western experience. J Am Coll Surg. 2006;202:306–312. doi: 10.1016/j.jamcollsurg.2005.09.022. [DOI] [PubMed] [Google Scholar]
  • 96.Lee TY, Chen YL, Chang HC, et al. Outcomes of hepatectomy for hepatolithiasis. World J Surg. 2007;31:479–482. doi: 10.1007/s00268-006-0441-6. [DOI] [PubMed] [Google Scholar]
  • 97.Al-Sukhni W, Gallinger S, Pratzer A, et al. Recurrent pyogenic cholangitis with hepatolithiasis–the role of surgical therapy in North America. J Gastrointest Surg. 2008;12:496–503. doi: 10.1007/s11605-007-0398-2. [DOI] [PubMed] [Google Scholar]
  • 98.Cheon YK, Cho YD, Moon JH, et al. Evaluation of long-term results and recurrent factors after operative and nonoperative treatment for hepatolithiasis. Surgery. 2009;146:843–853. doi: 10.1016/j.surg.2009.04.009. [DOI] [PubMed] [Google Scholar]
  • 99.Uenishi T, Hamba H, Takemura S, et al. Outcomes of hepatic resection for hepatolithiasis. Am J Surg. 2009;198:199–202. doi: 10.1016/j.amjsurg.2008.08.020. [DOI] [PubMed] [Google Scholar]
  • 100.Tabrizian P, Jibara G, Shrager B, et al. Hepatic resection for primary hepatolithiasis: a single-center Western experience. J Am Coll Surg. 2012;215:622–626. doi: 10.1016/j.jamcollsurg.2012.07.005. [DOI] [PubMed] [Google Scholar]
  • 101.Suzuki Y, Mori T, Abe N, et al. Predictive factors for cholangiocarcinoma associated with hepatolithiasis determined on the basis of Japanese Multicenter study. Hepatol Res. 2012;42:166–170. doi: 10.1111/j.1872-034X.2011.00908.x. [DOI] [PubMed] [Google Scholar]
  • 102.Guglielmi A, Ruzzenente A, Valdegamberi A, et al. Hepatolithiasis-associated cholangiocarcinoma: results from a multi-institutional national database on a case series of 23 patients. Eur J Surg Oncol. 2014;40:567–575. doi: 10.1016/j.ejso.2013.12.006. [DOI] [PubMed] [Google Scholar]
  • 103.Zhu QD, Zhou MT, Zhou QQ, et al. Diagnosis and surgical treatment of intrahepatic hepatolithiasis combined with cholangiocarcinoma. World J Surg. 2014;38:2097–2104. doi: 10.1007/s00268-014-2476-4. [DOI] [PubMed] [Google Scholar]
  • 104.Furukawa M, Sasaki M, Ohtsubo M, et al. Natural history of primary hepatolithiasis. Tan to Sui. 1998;19:1021–1027. [Google Scholar]
  • 105.Jo JH, Chung MJ, Park JY, et al. High serum CA19-9 levels are associated with an increased risk of cholangiocarcinoma in patients with intrahepatic duct stones: a case-control study. Surg Endosc. 2013;27:4210–4216. doi: 10.1007/s00464-013-3025-1. [DOI] [PubMed] [Google Scholar]
  • 106.Liu ZY, Zhou YM, Shi LH, et al. Risk factors of intrahepatic cholangiocarcinoma in patients with hepatolithiasis: a case-control study. Hepatobiliary Pancreat Dis Int. 2011;10:626–631. doi: 10.1016/S1499-3872(11)60106-9. [DOI] [PubMed] [Google Scholar]
  • 107.Suzuki Y, Mori T, Yokoyama M, et al. Predictive factors for cholangiocarcinoma associated with hepatolithiasis determined on the basis of Japanese Multicenter study Journal of Japan Biliary Association. 2013;27:700–704 (in Japanese with English abstract) [DOI] [PubMed]
  • 108.Chijiiwa K, Ichimiya H, Kuroki S, et al. Late development of cholangiocarcinoma after the treatment of hepatolithiasis. Surg Gynecol Obstet. 1993;177:279–282. [PubMed] [Google Scholar]
  • 109.Jan YY, Chen MF, Wang CS, et al. Surgical treatment of hepatolithiasis: long-term results. Surgery. 1996;120:509–514. doi: 10.1016/S0039-6060(96)80071-7. [DOI] [PubMed] [Google Scholar]
  • 110.Huang MH, Chen CH, Yang JC, et al. Long-term outcome of percutaneous transhepatic cholangioscopic lithotomy for hepatolithiasis. Am J Gastroenterol. 2003;98:2655–2662. doi: 10.1111/j.1572-0241.2003.08770.x. [DOI] [PubMed] [Google Scholar]
  • 111.Li SQ, Liang LJ, Peng BG, et al. Outcomes of liver resection for intrahepatic stones: a comparative study of unilateral versus bilateral disease. Ann Surg. 2012;255:946–953. doi: 10.1097/SLA.0b013e31824dedc2. [DOI] [PubMed] [Google Scholar]
  • 112.Lin CC, Lin PY, Chen YL. Comparison of concomitant and subsequent cholangiocarcinomas associated with hepatolithiasis: clinical implications. World J Gastroenterol. 2013;19:375–380. doi: 10.3748/wjg.v19.i3.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Tsuyuguchi T, Miyakawa K, Sugiyama H, et al. Ten-year long-term results after non-surgical management of hepatolithiasis, including cases with choledochoenterostomy. J Hepatobiliary Pancreat Sci. 2014;21:795–800. doi: 10.1002/jhbp.134. [DOI] [PubMed] [Google Scholar]
  • 114.Kim HJ, Kim JS, Suh SJ, et al. Cholangiocarcinoma Risk as Long-term Outcome After Hepatic Resection in the Hepatolithiasis Patients. World J Surg. 2015;39:1537–1542. doi: 10.1007/s00268-015-2965-0. [DOI] [PubMed] [Google Scholar]
  • 115.Meng ZW, Han SH, Zhu JH, et al. Risk Factors for Cholangiocarcinoma After Initial Hepatectomy for Intrahepatic Stones. World J Surg. 2017;41:835–843. doi: 10.1007/s00268-016-3752-2. [DOI] [PubMed] [Google Scholar]
  • 116.Kim HJ, Kang TU, Swan H, et al. Incidence and Prognosis of Subsequent Cholangiocarcinoma in Patients with Hepatic Resection for Bile Duct Stones. Dig Dis Sci. 2018;63:3465–3473. doi: 10.1007/s10620-018-5262-6. [DOI] [PubMed] [Google Scholar]
  • 117.Gibney EJ. Asymptomatic gallstones. Br J Surg. 1990;77:368–372. doi: 10.1002/bjs.1800770405. [DOI] [PubMed] [Google Scholar]
  • 118.Portincasa P, Moschetta A, Petruzzelli M, et al. Gallstone disease: symptoms and diagnosis of gallbladder stones. Best Pract Res Clin Gastroenterol. 2006;20:1017–1029. doi: 10.1016/j.bpg.2006.05.005. [DOI] [PubMed] [Google Scholar]
  • 119.Tomida S, Abei M, Yamaguchi T, et al. Long-term ursodeoxycholic acid therapy is associated with reduced risk of biliary pain and acute cholecystitis in patients with gallbladder stones: a cohort analysis. Hepatology. 1999;30:6–13. doi: 10.1002/hep.510300108. [DOI] [PubMed] [Google Scholar]
  • 120.Tazuma S, Kanno K, Kubota K, et al. Report on the 2013 national cholelithiasis survey in Japan. J Hepatobiliary Pancreat Sci. 2015;22:392–395. doi: 10.1002/jhbp.206. [DOI] [PubMed] [Google Scholar]
  • 121.Peng WK, Sheikh Z, Paterson-Brown S, et al. Role of liver function tests in predicting common bile duct stones in acute calculous cholecystitis. Br J Surg. 2005;92:1241–1247. doi: 10.1002/bjs.4955. [DOI] [PubMed] [Google Scholar]
  • 122.Barakos JA, Ralls PW, Lapin SA, et al. Cholelithiasis: evaluation with CT. Radiology. 1987;162:415–418. doi: 10.1148/radiology.162.2.3797654. [DOI] [PubMed] [Google Scholar]
  • 123.Neitlich T, Neitlich J. The imaging evaluation of cholelithiasis in the obese patient-ultrasound vs CT cholecystography: our experience with the bariatric surgery population. Obes Surg. 2009;19:207–210. doi: 10.1007/s11695-008-9582-z. [DOI] [PubMed] [Google Scholar]
  • 124.Ito K, Fujita N, Noda Y, et al. [The significance of magnetic resonance cholangiopancreatography in acute cholecystitis]. Nihon Shokakibyo Gakkai Zasshi. 2000;97:1472–9 (in Japanese with English abstract) [PubMed]
  • 125.Dahan P, Andant C, Levy P, et al. Prospective evaluation of endoscopic ultrasonography and microscopic examination of duodenal bile in the diagnosis of cholecystolithiasis in 45 patients with normal conventional ultrasonography. Gut. 1996;38:277–281. doi: 10.1136/gut.38.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Yokoe M, Takada T, Strasberg SM, et al. New diagnostic criteria and severity assessment of acute cholecystitis in revised Tokyo Guidelines. J Hepatobiliary Pancreat Sci. 2012;19:578–585. doi: 10.1007/s00534-012-0548-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Naidu K, Beenen E, Gananadha S, et al. The yield of fever, inflammatory markers and ultrasound in the diagnosis of acute cholecystitis: a validation of the 2013 Tokyo guidelines. World J Surg. 2016;40:2892–2897. doi: 10.1007/s00268-016-3660-5. [DOI] [PubMed] [Google Scholar]
  • 128.Yokoe M, Takada T, Hwang TL, et al. Descriptive review of acute cholecystitis: Japan-Taiwan collaborative epidemiological study. J Hepatobiliary Pancreat Sci. 2017;24:319–328. doi: 10.1002/jhbp.450. [DOI] [PubMed] [Google Scholar]
  • 129.Gruber PJ, Silverman RA, Gottesfeld S, et al. Presence of fever and leukocytosis in acute cholecystitis. Ann Emerg Med. 1996;28:273–277. doi: 10.1016/S0196-0644(96)70025-2. [DOI] [PubMed] [Google Scholar]
  • 130.Strasberg SM. Clinical practice. Acute calculous cholecystitis. N Engl J Med. 2008;358:2804–2811. doi: 10.1056/NEJMcp0800929. [DOI] [PubMed] [Google Scholar]
  • 131.Yokoe M, Takada T, Strasberg SM, et al. TG13 diagnostic criteria and severity grading of acute cholecystitis (with videos) J Hepatobiliary Pancreat Sci. 2013;20:35–46. doi: 10.1007/s00534-012-0568-9. [DOI] [PubMed] [Google Scholar]
  • 132.Hammarstrom L, Ranstam J. Factors predictive of bile duct stones in patients with acute calculous cholecystitis. Dig Surg. 1998;15:323–327. doi: 10.1159/000018646. [DOI] [PubMed] [Google Scholar]
  • 133.Yarmish GM, Smith MP, Rosen MP, et al. ACR appropriateness criteria right upper quadrant pain. J Am Coll Radiol. 2014;11:316–322. doi: 10.1016/j.jacr.2013.11.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 134.Pinto A, Reginelli A, Cagini L, et al. Accuracy of ultrasonography in the diagnosis of acute calculous cholecystitis: review of the literature. Crit Ultrasound J. 2013;5(Suppl 1):S11. doi: 10.1186/2036-7902-5-S1-S11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.Ralls PW, Colletti PM, Lapin SA, et al. Real-time sonography in suspected acute cholecystitis. Prospective evaluation of primary and secondary signs. Radiology. 1985;155:767–771. doi: 10.1148/radiology.155.3.3890007. [DOI] [PubMed] [Google Scholar]
  • 136.Martinez A, Bona X, Velasco M, et al. Diagnostic accuracy of ultrasound in acute cholecystitis. Gastrointest Radiol. 1986;11:334–338. doi: 10.1007/BF02035103. [DOI] [PubMed] [Google Scholar]
  • 137.Cohan RH, Mahony BS, Bowie JD, et al. Striated intramural gallbladder lucencies on US studies: predictors of acute cholecystitis. Radiology. 1987;164:31–35. doi: 10.1148/radiology.164.1.3295991. [DOI] [PubMed] [Google Scholar]
  • 138.Ralls PW, Halls J, Lapin SA, et al. Prospective evaluation of the sonographic Murphy sign in suspected acute cholecystitis. J Clin Ultrasound. 1982;10:113–115. doi: 10.1002/jcu.1870100305. [DOI] [PubMed] [Google Scholar]
  • 139.Bree RL. Further observations on the usefulness of the sonographic Murphy sign in the evaluation of suspected acute cholecystitis. J Clin Ultrasound. 1995;23:169–172. doi: 10.1002/jcu.1870230304. [DOI] [PubMed] [Google Scholar]
  • 140.Harvey RT, Miller WT., Jr Acute biliary disease: initial CT and follow-up US versus initial US and follow-up CT. Radiology. 1999;213:831–836. doi: 10.1148/radiology.213.3.r99dc17831. [DOI] [PubMed] [Google Scholar]
  • 141.Mirvis SE, Vainright JR, Nelson AW, et al. The diagnosis of acute acalculous cholecystitis: a comparison of sonography, scintigraphy, and CT. AJR Am J Roentgenol. 1986;147:1171–1175. doi: 10.2214/ajr.147.6.1171. [DOI] [PubMed] [Google Scholar]
  • 142.Kiriyama S, Kozaka K, Takada T, et al. Tokyo Guidelines 2018: diagnostic criteria and severity grading of acute cholangitis (with videos) J Hepatobiliary Pancreat Sci. 2018;25:17–30. doi: 10.1002/jhbp.512. [DOI] [PubMed] [Google Scholar]
  • 143.Kiriyama S, Takada T, Strasberg SM, et al. New diagnostic criteria and severity assessment of acute cholangitis in revised Tokyo Guidelines. J Hepatobiliary Pancreat Sci. 2012;19:548–556. doi: 10.1007/s00534-012-0537-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 144.Abboud PA, Malet PF, Berlin JA, et al. Predictors of common bile duct stones prior to cholecystectomy: a meta-analysis. Gastrointest Endosc. 1996;44:450–455. doi: 10.1016/S0016-5107(96)70098-6. [DOI] [PubMed] [Google Scholar]
  • 145.Inui K, Fujita N. Diagnosis of choledocholithiasis. J Jpn Biliary Assoc. 2010;24:239–244 (in Japanese with English abstract)
  • 146.Tseng CW, Chen CC, Chen TS, et al. Can computed tomography with coronal reconstruction improve the diagnosis of choledocholithiasis? J Gastroenterol Hepatol. 2008;23:1586–1589. doi: 10.1111/j.1440-1746.2008.05547.x. [DOI] [PubMed] [Google Scholar]
  • 147.Mark DH, Flamm CR, Aronson N. Evidence-based assessment of diagnostic modalities for common bile duct stones. Gastrointest Endosc. 2002;56:S190–S194. doi: 10.1016/S0016-5107(02)70010-2. [DOI] [PubMed] [Google Scholar]
  • 148.Chen W, Mo JJ, Lin L, et al. Diagnostic value of magnetic resonance cholangiopancreatography in choledocholithiasis. World J Gastroenterol. 2015;21:3351–3360. doi: 10.3748/wjg.v21.i11.3351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 149.Jendresen MB, Thorboll JE, Adamsen S, et al. Preoperative routine magnetic resonance cholangiopancreatography before laparoscopic cholecystectomy: a prospective study. Eur J Surg. 2002;168:690–694. doi: 10.1080/11024150201680024. [DOI] [PubMed] [Google Scholar]
  • 150.Tse F, Liu L, Barkun AN, et al. EUS: a meta-analysis of test performance in suspected choledocholithiasis. Gastrointest Endosc. 2008;67:235–244. doi: 10.1016/j.gie.2007.09.047. [DOI] [PubMed] [Google Scholar]
  • 151.Gurusamy KS, Giljaca V, Takwoingi Y, et al. Endoscopic retrograde cholangiopancreatography versus intraoperative cholangiography for diagnosis of common bile duct stones. Cochrane Database Syst Rev. 2015;(2):CD011548. [DOI] [PMC free article] [PubMed]
  • 152.Endo T, Ito K, Fujita N, et al. Intraductal ultrasonography in the diagnosis of bile duct stones: when and whom? Dig Endosc. 2011;23:173–175. doi: 10.1111/j.1443-1661.2010.01071.x. [DOI] [PubMed] [Google Scholar]
  • 153.Kim DC, Moon JH, Choi HJ, et al. Usefulness of intraductal ultrasonography in icteric patients with highly suspected choledocholithiasis showing normal endoscopic retrograde cholangiopancreatography. Dig Dis Sci. 2014;59:1902–1908. doi: 10.1007/s10620-014-3127-1. [DOI] [PubMed] [Google Scholar]
  • 154.Meeralam Y, Al-Shammari K, Yaghoobi M. Diagnostic accuracy of EUS compared with MRCP in detecting choledocholithiasis: a meta-analysis of diagnostic test accuracy in head-to-head studies. Gastrointest Endosc. 2017;86:986–993. doi: 10.1016/j.gie.2017.06.009. [DOI] [PubMed] [Google Scholar]
  • 155.Liu CL, Lo CM, Chan JK, et al. Detection of choledocholithiasis by EUS in acute pancreatitis: a prospective evaluation in 100 consecutive patients. Gastrointest Endosc. 2001;54:325–330. doi: 10.1067/mge.2001.117513. [DOI] [PubMed] [Google Scholar]
  • 156.Liu CL, Fan ST, Lo CM, et al. Comparison of early endoscopic ultrasonography and endoscopic retrograde cholangiopancreatography in the management of acute biliary pancreatitis: a prospective randomized study. Clin Gastroenterol Hepatol. 2005;3:1238–1244. doi: 10.1016/S1542-3565(05)00619-1. [DOI] [PubMed] [Google Scholar]
  • 157.Petrov MS, Savides TJ. Systematic review of endoscopic ultrasonography versus endoscopic retrograde cholangiopancreatography for suspected choledocholithiasis. Br J Surg. 2009;96:967–974. doi: 10.1002/bjs.6667. [DOI] [PubMed] [Google Scholar]
  • 158.Tokumura H. Development of primary bile duct stones-function of the major papilla and biliary infection. Naika. 2005;95:217–222. [Google Scholar]
  • 159.Hasegawa H, Sakamoto E, Komatsu S, et al. Laparoscopic management of common bile duct stones. Journal of Japan Biliary Association. 2010;24:554–560 (in Japanese with English abstract).
  • 160.Ministry of Health, Labour, and Welfare. A guide to the treatment of intrahepatic stone disease. Research Group for Intractable Hepatobiliary Diseases, editor. Tokyo: Bunkodo; 2011 (in Japanese).
  • 161.Mori T, Suzuki Y, Tazuma S, et al. Hepatolithiasis; 8th nationwide cross-sectional survey. Report of the research group on intractable hepato-biliary diseases. 2019:75–80 (in Japanese).
  • 162.Tsuchiya S, Tsuyuguchi T, Sakai Y, et al. Lon-term follow-up of silent stones in the peripheral bile duct. Tan to Sui. 2007;28:505–508. [Google Scholar]
  • 163.Kudo M, Izumi N, Kubo S, et al. Report of the 20th Nationwide follow-up survey of primary liver cancer in Japan. Hepatol Res. 2020;50:15–46. doi: 10.1111/hepr.13438. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 164.Sasanuma H, Sata N, Endo K, et al. Profile of intrahepatic cholangiocarcinoma associated hepatolithiasis. J Jpn Biliary Assoc. 2014;28:741–746 (in Japanese with English abstract).
  • 165.Mayumi T, Okamoto K, Takada T, et al. Tokyo Guidelines 2018: management bundles for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018;25:96–100. doi: 10.1002/jhbp.519. [DOI] [PubMed] [Google Scholar]
  • 166.Catena F, Ansaloni L, Bianchi E, et al. The ACTIVE (Acute Cholecystitis Trial Invasive Versus Endoscopic) Study: multicenter randomized, double-blind, controlled trial of laparoscopic versus open surgery for acute cholecystitis. Hepatogastroenterology. 2013;60:1552–1556. [PubMed] [Google Scholar]
  • 167.Boo YJ, Kim WB, Kim J, et al. Systemic immune response after open versus laparoscopic cholecystectomy in acute cholecystitis: a prospective randomized study. Scand J Clin Lab Invest. 2007;67:207–214. doi: 10.1080/00365510601011585. [DOI] [PubMed] [Google Scholar]
  • 168.Johansson M, Thune A, Nelvin L, et al. Randomized clinical trial of open versus laparoscopic cholecystectomy in the treatment of acute cholecystitis. Br J Surg. 2005;92:44–49. doi: 10.1002/bjs.4836. [DOI] [PubMed] [Google Scholar]
  • 169.Gomi H, Solomkin JS, Schlossberg D, et al. Tokyo Guidelines 2018: antimicrobial therapy for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018;25:3–16. doi: 10.1002/jhbp.518. [DOI] [PubMed] [Google Scholar]
  • 170.Kim EY, Yoon YC, Choi HJ, et al. Is there a real role of postoperative antibiotic administration for mildmoderate acute cholecystitis? A prospective randomized controlled trial. J Hepatobiliary Pancreat Sci. 2017;24:550–558. doi: 10.1002/jhbp.495. [DOI] [PubMed] [Google Scholar]
  • 171.Charlson M, Szatrowski TP, Peterson J, et al. Validation of a combined comorbidity index. J Clin Epidemiol. 1994;47:1245–1251. doi: 10.1016/0895-4356(94)90129-5. [DOI] [PubMed] [Google Scholar]
  • 172.Sakamoto T, Fujiogi M, Matsui H, et al. Timing of cholecystectomy after percutaneous transhepatic gallbladder drainage for acute cholecystitis: a nationwide inpatient database study. HPB (Oxf) 2020;22:920–926. doi: 10.1016/j.hpb.2019.10.2438. [DOI] [PubMed] [Google Scholar]
  • 173.Siddiqui A, Kunda R, Tyberg A, et al. Three-way comparative study of endoscopic ultrasound-guided transmural gallbladder drainage using lumen-apposing metal stents versus endoscopic transpapillary drainage versus percutaneous cholecystostomy for gallbladder drainage in high-risk surgical patients with acute cholecystitis: clinical outcomes and success in an International, Multicenter Study. Surg Endosc. 2019;33:1260–1270. doi: 10.1007/s00464-018-6406-7. [DOI] [PubMed] [Google Scholar]
  • 174.Rothrock SG, Green SM, Gorton E. Atropine for the treatment of biliary tract pain: a double-blind, placebo-controlled trial. Ann Emerg Med. 1993;22:1324–1327. doi: 10.1016/S0196-0644(05)80118-0. [DOI] [PubMed] [Google Scholar]
  • 175.Miyoshi S. Effect of trihydroxy propiophenone on subjective symptoms (especially in bile duct diseases) Naika Hokan. 1967;14:187–191. [PubMed] [Google Scholar]
  • 176.Goldman G, Kahn PJ, Alon R, et al. Biliary colic treatment and acute cholecystitis prevention by prostaglandin inhibitor. Dig Dis Sci. 1989;34:809–811. doi: 10.1007/BF01540262. [DOI] [PubMed] [Google Scholar]
  • 177.Magrini M, Rivolta G, Movilia PG, et al. Successful treatment of biliary colic with intravenous ketoprofen or lysine acetylsalicylate. Curr Med Res Opin. 1985;9:454–460. doi: 10.1185/03007998509109619. [DOI] [PubMed] [Google Scholar]
  • 178.Al-Waili N, Saloom KY. The analgesic effect of intravenous tenoxicam in symptomatic treatment of biliary colic: a comparison with hyoscine N-butylbromide. Eur J Med Res. 1998;3:475–479. [PubMed] [Google Scholar]
  • 179.Akriviadis EA, Hatzigavriel M, Kapnias D, et al. Treatment of biliary colic with diclofenac: a randomized, double-blind, placebo-controlled study. Gastroenterology. 1997;113:225–231. doi: 10.1016/S0016-5085(97)70099-4. [DOI] [PubMed] [Google Scholar]
  • 180.Venneman NG, Besselink MG, Keulemans YC, et al. Ursodeoxycholic acid exerts no beneficial effect in patients with symptomatic gallstones awaiting cholecystectomy. Hepatology. 2006;43:1276–1283. doi: 10.1002/hep.21182. [DOI] [PubMed] [Google Scholar]
  • 181.May GR, Sutherland LR, Shaffer EA. Efficacy of bile acid therapy for gallstone dissolution: a meta-analysis of randomized trials. Aliment Pharmacol Ther. 1993;7:139–148. doi: 10.1111/j.1365-2036.1993.tb00082.x. [DOI] [PubMed] [Google Scholar]
  • 182.Yamaguchi A, Tazuma S, Chayama K. The modality of non-surgical treatments for gallstones: factors affecting gallstone recurrence after extracorporeal shock wave lithotripsy (ESWL) and post-therapeutic symptoms. J Jpn Biliary Assoc. 2004;18:108–113 (in Japanese with English abstract).
  • 183.Jain D, Bhandari BS, Agrawal N, et al. Endoscopic Ultrasound-Guided Gallbladder Drainage Using a Lumen-Apposing Metal Stent for Acute Cholecystitis: A Systematic Review. Clin Endosc. 2018;51:450–462. doi: 10.5946/ce.2018.024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 184.Ransohoff DF, Gracie WA. Treatment of gallstones. Ann Intern Med. 1993;119:606–619. doi: 10.7326/0003-4819-119-7_Part_1-199310010-00010. [DOI] [PubMed] [Google Scholar]
  • 185.Halldestam I, Enell EL, Kullman E, et al. Development of symptoms and complications in individuals with asymptomatic gallstones. Br J Surg. 2004;91:734–738. doi: 10.1002/bjs.4547. [DOI] [PubMed] [Google Scholar]
  • 186.Gurusamy KS, Davidson BR. Surgical treatment of gallstones. Gastroenterol Clin North Am. 2010;39:229–44, viii. [DOI] [PubMed]
  • 187.Shoda J, Kawamoto T. Gallbladder cancer and gallstone. J Jpn Biliary Assoc. 2012;26:205–211 (in Japanese with English abstract).
  • 188.Fendrick AM, Gleeson SP, Cabana MD, et al. Asymptomatic gallstones revisited. Is there a role for laparoscopic cholecystectomy? Arch Fam Med. 1993;2:959–968. doi: 10.1001/archfami.2.9.959. [DOI] [PubMed] [Google Scholar]
  • 189.Ibrahim M, Sarvepalli S, Morris-Stiff G, et al. Gallstones: watch and wait, or intervene? Cleve Clin J Med. 2018;85:323–331. doi: 10.3949/ccjm.85a.17035. [DOI] [PubMed] [Google Scholar]
  • 190.Watemberg S, Rahmani H, Avrahami R, et al. Agenesis of the gallbladder found at laparoscopy for cholecystectomy: an unpleasant surprise. Am J Gastroenterol. 1995;90:1020–1021. [PubMed] [Google Scholar]
  • 191.Reuther G, Kiefer B, Tuchmann A. Cholangiography before biliary surgery: single-shot MR cholangiography versus intravenous cholangiography. Radiology. 1996;198:561–566. doi: 10.1148/radiology.198.2.8596866. [DOI] [PubMed] [Google Scholar]
  • 192.Yamashita H, Chijiiwa K, Ogawa Y, et al. The internal biliary fistula–reappraisal of incidence, type, diagnosis and management of 33 consecutive cases. HPB Surg. 1997;10:143–147. doi: 10.1155/1997/95363. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 193.Kobari M, Ise H, Suzuki N. タイトルなし. The Biliary Tract & Pancreas. 1990;11:1317–1322 (Japanese).
  • 194.Tanaka N, Nobori M, Harihara Y, et al. Surgical treatment of 45 cases of contracted gallbladder. J Japanese Practical Surg Soc. 1990;52:319–325 (in Japanese with English abstract).
  • 195.Otani K, Chijiiwa K, Ohuchida J, et al. Surgical management of gallstones and gallbladder polyps with suspect of cancer. Surgery. 2009;71:29–33. [Google Scholar]
  • 196.Engel JM, Deitch EA, Sikkema W. Gallbladder wall thickness: sonographic accuracy and relation to disease. AJR Am J Roentgenol. 1980;134:907–909. doi: 10.2214/ajr.134.5.907. [DOI] [PubMed] [Google Scholar]
  • 197.Iwashita Y, Hibi T, Ohyama T, et al. Delphi consensus on bile duct injuries during laparoscopic cholecystectomy: an evolutionary cul-de-sac or the birth pangs of a new technical framework? J Hepatobiliary Pancreat Sci. 2017;24:591–602. doi: 10.1002/jhbp.503. [DOI] [PubMed] [Google Scholar]
  • 198.Okamoto K, Suzuki K, Takada T, et al. Tokyo Guidelines 2018: flowchart for the management of acute cholecystitis. J Hepatobiliary Pancreat Sci. 2018;25:55–72. doi: 10.1002/jhbp.516. [DOI] [PubMed] [Google Scholar]
  • 199.NIH Consensus Conference Gallstones and laparoscopic cholecystectomy. JAMA. 1993;269:1018–1024. doi: 10.1001/jama.1993.03500080066034. [DOI] [PubMed] [Google Scholar]
  • 200.Academic Committee of The Japanese Society for Endoscopic Surgery. Questionnaire Survey on Endoscopic Surgery—Report on the Results of the 14th Total Survey. J Jpn Soc Endosc Surg. 2018;23:727–890 (Japanese)
  • 201.Mentes BB, Akin M, Irkorucu O, et al. Gastrointestinal quality of life in patients with symptomatic or asymptomatic cholelithiasis before and after laparoscopic cholecystectomy. Surg Endosc. 2001;15:1267–1272. doi: 10.1007/s00464-001-9015-8. [DOI] [PubMed] [Google Scholar]
  • 202.Wakabayashi G, Iwashita Y, Hibi T, et al. Tokyo Guidelines 2018: surgical management of acute cholecystitis: safe steps in laparoscopic cholecystectomy for acute cholecystitis (with videos) J Hepatobiliary Pancreat Sci. 2018;25:73–86. doi: 10.1002/jhbp.517. [DOI] [PubMed] [Google Scholar]
  • 203.Endo I, Takada T, Hwang TL, et al. Optimal treatment strategy for acute cholecystitis based on predictive factors: Japan-Taiwan multicenter cohort study. J Hepatobiliary Pancreat Sci. 2017;24:346–361. doi: 10.1002/jhbp.456. [DOI] [PubMed] [Google Scholar]
  • 204.Kiviniemi H, Makela JT, Autio R, et al. Percutaneous cholecystostomy in acute cholecystitis in high-risk patients: an analysis of 69 patients. Int Surg. 1998;83:299–302. [PubMed] [Google Scholar]
  • 205.Sugiyama M, Tokuhara M, Atomi Y. Is percutaneous cholecystostomy the optimal treatment for acute cholecystitis in the very elderly? World J Surg. 1998;22:459–463. doi: 10.1007/s002689900416. [DOI] [PubMed] [Google Scholar]
  • 206.Akhan O, Akinci D, Ozmen MN. Percutaneous cholecystostomy. Eur J Radiol. 2002;43:229–236. doi: 10.1016/S0720-048X(02)00158-4. [DOI] [PubMed] [Google Scholar]
  • 207.Donald JJ, Cheslyn-Curtis S, Gillams AR, et al. Percutaneous cholecystolithotomy: is gall stone recurrence inevitable? Gut. 1994;35:692–695. doi: 10.1136/gut.35.5.692. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 208.Hultman CS, Herbst CA, McCall JM, et al. The efficacy of percutaneous cholecystostomy in critically ill patients. Am Surg. 1996;62:263–269. [PubMed] [Google Scholar]
  • 209.Melin MM, Sarr MG, Bender CE, et al. Percutaneous cholecystostomy: a valuable technique in high-risk patients with presumed acute cholecystitis. Br J Surg. 1995;82:1274–1277. doi: 10.1002/bjs.1800820939. [DOI] [PubMed] [Google Scholar]
  • 210.Davis CA, Landercasper J, Gundersen LH, et al. Effective use of percutaneous cholecystostomy in high-risk surgical patients: techniques, tube management, and results. Arch Surg. 1999;134:727–31 (discussion 731–2). [DOI] [PubMed]
  • 211.Jang JW, Lee SS, Song TJ, et al. Endoscopic ultrasound-guided transmural and percutaneous transhepatic gallbladder drainage are comparable for acute cholecystitis. Gastroenterology. 2012;142:805–811. doi: 10.1053/j.gastro.2011.12.051. [DOI] [PubMed] [Google Scholar]
  • 212.Itoi T, Coelho-Prabhu N, Baron TH. Endoscopic gallbladder drainage for management of acute cholecystitis. Gastrointest Endosc. 2010;71:1038–1045. doi: 10.1016/j.gie.2010.01.026. [DOI] [PubMed] [Google Scholar]
  • 213.Khan MA, Atiq O, Kubiliun N, et al. Efficacy and safety of endoscopic gallbladder drainage in acute cholecystitis: Is it better than percutaneous gallbladder drainage? Gastrointest Endosc. 2017;85(76–87):e3. doi: 10.1016/j.gie.2016.06.032. [DOI] [PubMed] [Google Scholar]
  • 214.Mohan BP, Khan SR, Trakroo S, et al. Endoscopic ultrasound-guided gallbladder drainage, transpapillary drainage, or percutaneous drainage in high risk acute cholecystitis patients: a systematic review and comparative meta-analysis. Endoscopy. 2020;52:96–106. doi: 10.1055/a-1020-3932. [DOI] [PubMed] [Google Scholar]
  • 215.Patel IJ, Davidson JC, Nikolic B, et al. Consensus guidelines for periprocedural management of coagulation status and hemostasis risk in percutaneous image-guided interventions. J Vasc Interv Radiol. 2012;23:727–736. doi: 10.1016/j.jvir.2012.02.012. [DOI] [PubMed] [Google Scholar]
  • 216.Hamada T, Yasunaga H, Nakai Y, et al. Severe bleeding after percutaneous transhepatic drainage of the biliary system: effect of antithrombotic agents–analysis of 34 606 cases from a Japanese nationwide administrative database. Radiology. 2015;274:605–613. doi: 10.1148/radiol.14140293. [DOI] [PubMed] [Google Scholar]
  • 217.Kalva NR, Vanar V, Forcione D, et al. Efficacy and Safety of Lumen Apposing Self-Expandable Metal Stents for EUS Guided Cholecystostomy: A Meta-Analysis and Systematic Review. Can J Gastroenterol Hepatol. 2018;2018:7070961. doi: 10.1155/2018/7070961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 218.Mohan BP, Asokkumar R, Shakhatreh M, et al. Adverse events with lumen-apposing metal stents in endoscopic gallbladder drainage: a systematic review and meta-analysis. Endosc Ultrasound. 2019;8:241–248. doi: 10.4103/eus.eus_63_18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 219.Cui Y, Liu Y, Li Z, et al. Appraisal of diagnosis and surgical approach for Mirizzi syndrome. ANZ J Surg. 2012;82:708–713. doi: 10.1111/j.1445-2197.2012.06149.x. [DOI] [PubMed] [Google Scholar]
  • 220.Kulkarni SS, Hotta M, Sher L, et al. Complicated gallstone disease: diagnosis and management of Mirizzi syndrome. Surg Endosc. 2017;31:2215–2222. doi: 10.1007/s00464-016-5219-9. [DOI] [PubMed] [Google Scholar]
  • 221.Gelbard R, Khor D, Inaba K, et al. Role of Laparoscopic Surgery in the Current Management of Mirizzi Syndrome. Am Surg. 2018;84:667–671. doi: 10.1177/000313481808400517. [DOI] [PubMed] [Google Scholar]
  • 222.Chen H, Siwo EA, Khu M, et al. Current trends in the management of Mirizzi Syndrome: A review of literature. Medicine (Baltimore) 2018;97:e9691. doi: 10.1097/MD.0000000000009691. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 223.Beltran MA. Mirizzi syndrome: history, current knowledge and proposal of a simplified classification. World J Gastroenterol. 2012;18:4639–4650. doi: 10.3748/wjg.v18.i34.4639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 224.Antoniou SA, Antoniou GA, Makridis C. Laparoscopic treatment of Mirizzi syndrome: a systematic review. Surg Endosc. 2010;24:33–39. doi: 10.1007/s00464-009-0520-5. [DOI] [PubMed] [Google Scholar]
  • 225.Shirah BH, Shirah HA, Albeladi KB. Mirizzi syndrome: necessity for safe approach in dealing with diagnostic and treatment challenges. Ann Hepatobiliary Pancreat Surg. 2017;21:122–130. doi: 10.14701/ahbps.2017.21.3.122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 226.Yuan H, Yuan T, Sun X, et al. A Minimally Invasive Strategy for Mirizzi Syndrome Type II: Combined Endoscopic With Laparoscopic Approach. Surg Laparosc Endosc Percutan Tech. 2016;26:248–252. doi: 10.1097/SLE.0000000000000260. [DOI] [PubMed] [Google Scholar]
  • 227.Mithani R, Schwesinger WH, Bingener J, et al. The Mirizzi syndrome: multidisciplinary management promotes optimal outcomes. J Gastrointest Surg. 2008;12:1022–1028. doi: 10.1007/s11605-007-0305-x. [DOI] [PubMed] [Google Scholar]
  • 228.Sepe PS, Berzin TM, Sanaka S, et al. Single-operator cholangioscopy for the extraction of cystic duct stones (with video) Gastrointest Endosc. 2012;75:206–210. doi: 10.1016/j.gie.2011.08.025. [DOI] [PubMed] [Google Scholar]
  • 229.Tsuyuguchi T, Sakai Y, Sugiyama H, et al. Long-term follow-up after peroral cholangioscopy-directed lithotripsy in patients with difficult bile duct stones, including Mirizzi syndrome: an analysis of risk factors predicting stone recurrence. Surg Endosc. 2011;25:2179–2185. doi: 10.1007/s00464-010-1520-1. [DOI] [PubMed] [Google Scholar]
  • 230.Bhandari S, Bathini R, Sharma A, et al. Usefulness of single-operator cholangioscopy-guided laser lithotripsy in patients with Mirizzi syndrome and cystic duct stones: experience at a tertiary care center. Gastrointest Endosc. 2016;84:56–61. doi: 10.1016/j.gie.2015.12.025. [DOI] [PubMed] [Google Scholar]
  • 231.Ryozawa S, Itoi T, Katanuma A, et al. Japan Gastroenterological Endoscopy Society guidelines for endoscopic sphincterotomy. Dig Endosc. 2018;30:149–173. doi: 10.1111/den.13001. [DOI] [PubMed] [Google Scholar]
  • 232.Itoi T, Ryozawa S, Katanuma A, et al. Japan Gastroenterological Endoscopy Society guidelines for endoscopic papillary large balloon dilation. Dig Endosc. 2018;30:293–309. doi: 10.1111/den.13029. [DOI] [PubMed] [Google Scholar]
  • 233.Yasuda I, Itoi T. Recent advances in endoscopic management of difficult bile duct stones. Dig Endosc. 2013;25:376–385. doi: 10.1111/den.12118. [DOI] [PubMed] [Google Scholar]
  • 234.Wandling MW, Hungness ES, Pavey ES, et al. Nationwide Assessment of Trends in Choledocholithiasis Management in the United States From 1998 to 2013. JAMA Surg. 2016;151:1125–1130. doi: 10.1001/jamasurg.2016.2059. [DOI] [PubMed] [Google Scholar]
  • 235.Ricci C, Pagano N, Taffurelli G, et al. Comparison of Efficacy and Safety of 4 Combinations of Laparoscopic and Intraoperative Techniques for Management of Gallstone Disease With Biliary Duct Calculi: A Systematic Review and Network Meta-analysis. JAMA Surg. 2018;153:e181167. doi: 10.1001/jamasurg.2018.1167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 236.Xu J, Yang C. Cholecystectomy outcomes after endoscopic sphincterotomy in patients with choledocholithiasis: a meta-analysis. BMC Gastroenterol. 2020;20:229. doi: 10.1186/s12876-020-01376-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 237.Bove A, Di Renzo RM, Palone G, et al. Single-stage procedure for the treatment of cholecysto-choledocolithiasis: a surgical procedures review. Ther Clin Risk Manag. 2018;14:305–312. doi: 10.2147/TCRM.S146461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 238.De Palma GD. Minimally invasive treatment of cholecysto-choledocal lithiasis: The point of view of the surgical endoscopist. World J Gastrointest Surg. 2013;5:161–166. doi: 10.4240/wjgs.v5.i6.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 239.Enochsson L, Lindberg B, Swahn F, et al. Intraoperative endoscopic retrograde cholangiopancreatography (ERCP) to remove common bile duct stones during routine laparoscopic cholecystectomy does not prolong hospitalization: a 2-year experience. Surg Endosc. 2004;18:367–371. doi: 10.1007/s00464-003-9021-0. [DOI] [PubMed] [Google Scholar]
  • 240.Liverani A, Muroni M, Santi F, et al. One-step laparoscopic and endoscopic treatment of gallbladder and common bile duct stones: our experience of the last 9 years in a retrospective study. Am Surg. 2013;79:1243–1247. doi: 10.1177/000313481307901213. [DOI] [PubMed] [Google Scholar]
  • 241.Lyu Y, Cheng Y, Li T, et al. Laparoscopic common bile duct exploration plus cholecystectomy versus endoscopic retrograde cholangiopancreatography plus laparoscopic cholecystectomy for cholecystocholedocholithiasis: a meta-analysis. Surg Endosc. 2019;33:3275–3286. doi: 10.1007/s00464-018-06613-w. [DOI] [PubMed] [Google Scholar]
  • 242.Schreurs WH, Vles WJ, Stuifbergen WH, et al. Endoscopic management of common bile duct stones leaving the gallbladder in situ. A cohort study with long-term follow-up. Dig Surg. 2004;21:60–4 (discussion 65). [DOI] [PubMed]
  • 243.Boerma D, Rauws EA, Keulemans YC, et al. Wait-and-see policy or laparoscopic cholecystectomy after endoscopic sphincterotomy for bile-duct stones: a randomised trial. Lancet. 2002;360:761–765. doi: 10.1016/S0140-6736(02)09896-3. [DOI] [PubMed] [Google Scholar]
  • 244.Dasari BV, Tan CJ, Gurusamy KS, et al. Surgical versus endoscopic treatment of bile duct stones. Cochrane Database Syst Rev. 2013;2013:CD003327. [DOI] [PubMed]
  • 245.Singh AN, Kilambi R. Single-stage laparoscopic common bile duct exploration and cholecystectomy versus two-stage endoscopic stone extraction followed by laparoscopic cholecystectomy for patients with gallbladder stones with common bile duct stones: systematic review and meta-analysis of randomized trials with trial sequential analysis. Surg Endosc. 2018;32:3763–3776. doi: 10.1007/s00464-018-6170-8. [DOI] [PubMed] [Google Scholar]
  • 246.Bansal VK, Misra MC, Rajan K, et al. Single-stage laparoscopic common bile duct exploration and cholecystectomy versus two-stage endoscopic stone extraction followed by laparoscopic cholecystectomy for patients with concomitant gallbladder stones and common bile duct stones: a randomized controlled trial. Surg Endosc. 2014;28:875–885. doi: 10.1007/s00464-013-3237-4. [DOI] [PubMed] [Google Scholar]
  • 247.Topal B, Vromman K, Aerts R, et al. Hospital cost categories of one-stage versus two-stage management of common bile duct stones. Surg Endosc. 2010;24:413–416. doi: 10.1007/s00464-009-0594-0. [DOI] [PubMed] [Google Scholar]
  • 248.Rogers SJ, Cello JP, Horn JK, et al. Prospective randomized trial of LC+LCBDE vs ERCP/S+LC for common bile duct stone disease. Arch Surg. 2010;145:28–33. doi: 10.1001/archsurg.2009.226. [DOI] [PubMed] [Google Scholar]
  • 249.Tokumura H, Matsumura N, Musha H, et al. Recurrence of Common bile duct stones after surgical stone removal with preservation of papillary function. Tan to Sui. 2010;31:305–308. [Google Scholar]
  • 250.Doi S, Yasuda I, Mabuchi M, et al. Long term outcome after EST and EPBD for bile duct stones with gallbladder stones. Tan to Sui. 2014;35:1365–1369 (in Japanese)
  • 251.Hasegawa H, Yamamoto H, Ymamoto R, et al. Results of the laparoscopic management of common bile duct stones –Significance of preservation of sphincter function. Tan to Sui. 2014;35:1339–1343. [Google Scholar]
  • 252.Yoshikawa J, Matsumoto J. Evaluation of endoscopic sphincter of Oddi manometry in patients with biliary diseases. J Jpn Biliary Assoc. 2003;17:396–401 (in Japanese with English abstract)
  • 253.Naito T, Hata T, Iseki M, et al. Manometric study of the bile duct. Tan to Sui. 2019;40:203–206. [Google Scholar]
  • 254.Aoki Y, Tanimura H, Kawashima H, et al. Cholescintigraphic observation of the sphincter of Oddi motor activity in patients with gallstone. Nihon Geka Hokan. 1989;58:289–298. [PubMed] [Google Scholar]
  • 255.Takehara Y. Assessment of sphincter of Oddi dysfunction with pharmaco-dynamic (functional) MRCP. Tan to Sui. 2008;29:813–822. [Google Scholar]
  • 256.Grubnik VV, Tkachenko AI, Ilyashenko VV, et al. Laparoscopic common bile duct exploration versus open surgery: comparative prospective randomized trial. Surg Endosc. 2012;26:2165–2171. doi: 10.1007/s00464-012-2194-7. [DOI] [PubMed] [Google Scholar]
  • 257.Wang X, Dai C, Jiang Z, et al. Endoscopic retrograde cholangiopancreatography versus laparoscopic exploration for common bile duct stones in post-cholecystectomy patients: a retrospective study. Oncotarget. 2017;8:82114–82122. doi: 10.18632/oncotarget.18839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 258.Johnson AG, Hosking SW. Appraisal of the management of bile duct stones. Br J Surg. 1987;74:555–560. doi: 10.1002/bjs.1800740703. [DOI] [PubMed] [Google Scholar]
  • 259.Joyce WP, Keane R, Burke GJ, et al. Identification of bile duct stones in patients undergoing laparoscopic cholecystectomy. Br J Surg. 1991;78:1174–1176. doi: 10.1002/bjs.1800781008. [DOI] [PubMed] [Google Scholar]
  • 260.Sarli L, Costi R, Gobbi S, et al. Asymptomatic bile duct stones: selection criteria for intravenous cholangiography and/or endoscopic retrograde cholangiography prior to laparoscopic cholecystectomy. Eur J Gastroenterol Hepatol. 2000;12:1175–1180. doi: 10.1097/00042737-200012110-00002. [DOI] [PubMed] [Google Scholar]
  • 261.Horwood J, Akbar F, Davis K, et al. Prospective evaluation of a selective approach to cholangiography for suspected common bile duct stones. Ann R Coll Surg Engl. 2010;92:206–210. doi: 10.1308/003588410X12628812458293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 262.Kim SB, Kim KH, Kim TN. Comparison of Outcomes and Complications of Endoscopic Common Bile Duct Stone Removal Between Asymptomatic and Symptomatic Patients. Dig Dis Sci. 2016;61:1172–1177. doi: 10.1007/s10620-015-3965-5. [DOI] [PubMed] [Google Scholar]
  • 263.Hakuta R, Hamada T, Nakai Y, et al. Natural history of asymptomatic bile duct stones and association of endoscopic treatment with clinical outcomes. J Gastroenterol. 2020;55:78–85. doi: 10.1007/s00535-019-01612-7. [DOI] [PubMed] [Google Scholar]
  • 264.Itoi T, Tsuyuguchi T, Takada T, et al. TG13 indications and techniques for biliary drainage in acute cholangitis (with videos) J Hepatobiliary Pancreat Sci. 2013;20:71–80. doi: 10.1007/s00534-012-0569-8. [DOI] [PubMed] [Google Scholar]
  • 265.Lee JK, Lee SH, Kang BK, et al. Is it necessary to insert a nasobiliary drainage tube routinely after endoscopic clearance of the common bile duct in patients with choledocholithiasis-induced cholangitis? A prospective, randomized trial. Gastrointest Endosc. 2010;71:105–110. doi: 10.1016/j.gie.2009.08.009. [DOI] [PubMed] [Google Scholar]
  • 266.Ueki T, Otani K, Fujimura N, et al. Comparison between emergency and elective endoscopic sphincterotomy in patients with acute cholangitis due to choledocholithiasis: is emergency endoscopic sphincterotomy safe? J Gastroenterol. 2009;44:1080–1088. doi: 10.1007/s00535-009-0100-4. [DOI] [PubMed] [Google Scholar]
  • 267.Eto K, Kawakami H, Haba S, et al. Single-stage endoscopic treatment for mild to moderate acute cholangitis associated with choledocholithiasis: a multicenter, non-randomized, open-label and exploratory clinical trial. J Hepatobiliary Pancreat Sci. 2015;22:825–830. doi: 10.1002/jhbp.296. [DOI] [PubMed] [Google Scholar]
  • 268.Ayub K, Imada R, Slavin J. Endoscopic retrograde cholangiopancreatography in gallstone-associated acute pancreatitis. Cochrane Database Syst Rev. 2004;(4):CD003630. 10.1002/14651858.CD003630.pub2. [DOI] [PubMed]
  • 269.Petrov MS, van Santvoort HC, Besselink MG, et al. Early endoscopic retrograde cholangiopancreatography versus conservative management in acute biliary pancreatitis without cholangitis: a meta-analysis of randomized trials. Ann Surg. 2008;247:250–257. doi: 10.1097/SLA.0b013e31815edddd. [DOI] [PubMed] [Google Scholar]
  • 270.Uy MC, Daez ML, Sy PP, et al. Early ERCP in acute gallstone pancreatitis without cholangitis: a meta-analysis. JOP. 2009;10:299–305. [PubMed] [Google Scholar]
  • 271.Tse F, Yuan Y. Early routine endoscopic retrograde cholangiopancreatography strategy versus early conservative management strategy in acute gallstone pancreatitis. Cochrane Database Syst Rev. 2012;(5):CD009779. [DOI] [PMC free article] [PubMed]
  • 272.Burstow MJ, Yunus RM, Hossain MB, et al. Meta-Analysis of Early Endoscopic Retrograde Cholangiopancreatography (ERCP) +/- Endoscopic Sphincterotomy (ES) Versus Conservative Management for Gallstone Pancreatitis (GSP) Surg Laparosc Endosc Percutan Tech. 2015;25:185–203. doi: 10.1097/SLE.0000000000000142. [DOI] [PubMed] [Google Scholar]
  • 273.Ersoz G, Tekesin O, Ozutemiz AO, et al. Biliary sphincterotomy plus dilation with a large balloon for bile duct stones that are difficult to extract. Gastrointest Endosc. 2003;57:156–159. doi: 10.1067/mge.2003.52. [DOI] [PubMed] [Google Scholar]
  • 274.Kim TH, Kim JH, Seo DW, et al. International consensus guidelines for endoscopic papillary large-balloon dilation. Gastrointest Endosc. 2016;83:37–47. doi: 10.1016/j.gie.2015.06.016. [DOI] [PubMed] [Google Scholar]
  • 275.Feng Y, Zhu H, Chen X, et al. Comparison of endoscopic papillary large balloon dilation and endoscopic sphincterotomy for retrieval of choledocholithiasis: a meta-analysis of randomized controlled trials. J Gastroenterol. 2012;47:655–663. doi: 10.1007/s00535-012-0528-9. [DOI] [PubMed] [Google Scholar]
  • 276.Liu Y, Su P, Lin Y, et al. Endoscopic sphincterotomy plus balloon dilation versus endoscopic sphincterotomy for choledocholithiasis: A meta-analysis. J Gastroenterol Hepatol. 2013;28:937–945. doi: 10.1111/jgh.12192. [DOI] [PubMed] [Google Scholar]
  • 277.Yang XM, Hu B. Endoscopic sphincterotomy plus large-balloon dilation vs endoscopic sphincterotomy for choledocholithiasis: a meta-analysis. World J Gastroenterol. 2013;19:9453–9460. doi: 10.3748/wjg.v19.i48.9453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 278.Jin PP, Cheng JF, Liu D, et al. Endoscopic papillary large balloon dilation vs endoscopic sphincterotomy for retrieval of common bile duct stones: a meta-analysis. World J Gastroenterol. 2014;20:5548–5556. doi: 10.3748/wjg.v20.i18.5548. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 279.Dong SQ, Singh TP, Zhao Q, et al. Sphincterotomy plus balloon dilation versus sphincterotomy alone for choledocholithiasis: a meta-analysis. Endoscopy. 2019;51:763–771. doi: 10.1055/a-0848-8271. [DOI] [PubMed] [Google Scholar]
  • 280.Liu P, Lin H, Chen Y, et al. Comparison of endoscopic papillary large balloon dilation with and without a prior endoscopic sphincterotomy for the treatment of patients with large and/or multiple common bile duct stones: a systematic review and meta-analysis. Ther Clin Risk Manag. 2019;15:91–101. doi: 10.2147/TCRM.S182615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 281.Kim KH, Rhu JH, Kim TN. Recurrence of bile duct stones after endoscopic papillary large balloon dilation combined with limited sphincterotomy: long-term follow-up study. Gut Liver. 2012;6:107–112. doi: 10.5009/gnl.2012.6.1.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 282.Maruta A, Iwashita T, Uemura S, et al. Comparison of late adverse events after endoscopic sphincterotomy versus endoscopic papillary large balloon dilation for common bile duct stones: A propensity score-based cohort analysis. Dig Endosc. 2018;30:493–500. doi: 10.1111/den.13031. [DOI] [PubMed] [Google Scholar]
  • 283.Miyoshi H, Inui K, Yamamoto S, et al. Extracorporeal Shock Wave Lithotripsy for Bile Duct Stones. Clin Gastroenterol. 2017;32:57–61 (in Japanese with English abstract)
  • 284.Jin Z, Wei Y, Tang X, et al. Single-operator peroral cholangioscope in treating difficult biliary stones: A systematic review and meta-analysis. Dig Endosc. 2019;31:256–269. doi: 10.1111/den.13307. [DOI] [PubMed] [Google Scholar]
  • 285.Yasuda I. Recent advances in endoscopic management of difficult bile duct stones. Nihon Shokakibyo Gakkai Zasshi. 2016;113:585–593. doi: 10.11405/nisshoshi.113.585. [DOI] [PubMed] [Google Scholar]
  • 286.Gad EH, Zakaria H, Kamel Y, et al. Surgical (Open and laparoscopic) management of large difficult CBD stones after different sessions of endoscopic failure: A retrospective cohort study. Ann Med Surg (Lond) 2019;43:52–63. doi: 10.1016/j.amsu.2019.05.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 287.Lee JH, Kim HW, Kang DH, et al. Usefulness of percutaneous transhepatic cholangioscopic lithotomy for removal of difficult common bile duct stones. Clin Endosc. 2013;46:65–70. doi: 10.5946/ce.2013.46.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 288.Jeong EJ, Kang DH, Kim DU, et al. Percutaneous transhepatic choledochoscopic lithotomy as a rescue therapy for removal of bile duct stones in Billroth II gastrectomy patients who are difficult to perform ERCP. Eur J Gastroenterol Hepatol. 2009;21:1358–1362. doi: 10.1097/MEG.0b013e328326caa1. [DOI] [PubMed] [Google Scholar]
  • 289.Thon HJ, Loffler A, Buess G, et al. Is ERCP a reasonable diagnostic method for excluding pancreatic and hepatobiliary disease in patients with a Billroth II resection? Endoscopy. 1983;15:93–95. doi: 10.1055/s-2007-1021476. [DOI] [PubMed] [Google Scholar]
  • 290.Forbes A, Cotton PB. ERCP and sphincterotomy after Billroth II gastrectomy. Gut. 1984;25:971–974. doi: 10.1136/gut.25.9.971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 291.Osnes M, Rosseland AR, Aabakken L. Endoscopic retrograde cholangiography and endoscopic papillotomy in patients with a previous Billroth-II resection. Gut. 1986;27:1193–1198. doi: 10.1136/gut.27.10.1193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 292.Nakahara K, Horaguchi J, Fujita N, et al. Therapeutic endoscopic retrograde cholangiopancreatography using an anterior oblique-viewing endoscope for bile duct stones in patients with prior Billroth II gastrectomy. J Gastroenterol. 2009;44:212–217. doi: 10.1007/s00535-008-2299-x. [DOI] [PubMed] [Google Scholar]
  • 293.Choi CW, Choi JS, Kang DH, et al. Endoscopic papillary large balloon dilation in Billroth II gastrectomy patients with bile duct stones. J Gastroenterol Hepatol. 2012;27:256–260. doi: 10.1111/j.1440-1746.2011.06863.x. [DOI] [PubMed] [Google Scholar]
  • 294.Shimatani M, Hatanaka H, Kogure H, et al. Diagnostic and Therapeutic Endoscopic Retrograde Cholangiography Using a Short-Type Double-Balloon Endoscope in Patients With Altered Gastrointestinal Anatomy: A Multicenter Prospective Study in Japan. Am J Gastroenterol. 2016;111:1750–1758. doi: 10.1038/ajg.2016.420. [DOI] [PubMed] [Google Scholar]
  • 295.Yane K, Katanuma A, Maguchi H, et al. Short-type single-balloon enteroscope-assisted ERCP in postsurgical altered anatomy: potential factors affecting procedural failure. Endoscopy. 2017;49:69–74. doi: 10.1055/s-0042-118301. [DOI] [PubMed] [Google Scholar]
  • 296.Itoi T, Ishii K, Sofuni A, et al. Long- and short-type double-balloon enteroscopy-assisted therapeutic ERCP for intact papilla in patients with a Roux-en-Y anastomosis. Surg Endosc. 2011;25:713–721. doi: 10.1007/s00464-010-1226-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 297.Ishii K, Itoi T, Tonozuka R, et al. Balloon enteroscopy-assisted ERCP in patients with Roux-en-Y gastrectomy and intact papillae (with videos) Gastrointest Endosc. 2016;83(377–86):e6. doi: 10.1016/j.gie.2015.06.020. [DOI] [PubMed] [Google Scholar]
  • 298.De Koning M, Moreels TG. Comparison of double-balloon and single-balloon enteroscope for therapeutic endoscopic retrograde cholangiography after Roux-en-Y small bowel surgery. BMC Gastroenterol. 2016;16:98. doi: 10.1186/s12876-016-0512-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 299.Yamauchi H, Kida M, Okuwaki K, et al. Therapeutic peroral direct cholangioscopy using a single balloon enteroscope in patients with Roux-en-Y anastomosis (with videos) Surg Endosc. 2018;32:498–506. doi: 10.1007/s00464-017-5742-3. [DOI] [PubMed] [Google Scholar]
  • 300.Itoi T, Ishii K, Itokawa F, et al. Large balloon papillary dilation for removal of bile duct stones in patients who have undergone a billroth ii gastrectomy. Dig Endosc. 2010;22(Suppl 1):S98–S102. doi: 10.1111/j.1443-1661.2010.00955.x. [DOI] [PubMed] [Google Scholar]
  • 301.Kim GH, Kang DH, Song GA, et al. Endoscopic removal of bile-duct stones by using a rotatable papillotome and a large-balloon dilator in patients with a Billroth II gastrectomy (with video) Gastrointest Endosc. 2008;67:1134–1138. doi: 10.1016/j.gie.2007.12.016. [DOI] [PubMed] [Google Scholar]
  • 302.Itoi T, Sofuni A, Tsuchiya T, et al. Endoscopic ultrasonography-guided transhepatic antegrade stone removal in patients with surgically altered anatomy: case series and technical review (with videos) J Hepatobiliary Pancreat Sci. 2014;21:E86–93. doi: 10.1002/jhbp.165. [DOI] [PubMed] [Google Scholar]
  • 303.Iwashita T, Nakai Y, Hara K, et al. Endoscopic ultrasound-guided antegrade treatment of bile duct stone in patients with surgically altered anatomy: a multicenter retrospective cohort study. J Hepatobiliary Pancreat Sci. 2016;23:227–233. doi: 10.1002/jhbp.329. [DOI] [PubMed] [Google Scholar]
  • 304.Miura F, Okamoto K, Takada T, et al. Tokyo Guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018;25:31–40. doi: 10.1002/jhbp.509. [DOI] [PubMed] [Google Scholar]
  • 305.Sharaiha RZ, Khan MA, Kamal F, et al. Efficacy and safety of EUS-guided biliary drainage in comparison with percutaneous biliary drainage when ERCP fails: a systematic review and meta-analysis. Gastrointest Endosc. 2017;85:904–914. doi: 10.1016/j.gie.2016.12.023. [DOI] [PubMed] [Google Scholar]
  • 306.Baron TH, Harewood GC. Endoscopic balloon dilation of the biliary sphincter compared to endoscopic biliary sphincterotomy for removal of common bile duct stones during ERCP: a metaanalysis of randomized, controlled trials. Am J Gastroenterol. 2004;99:1455–1460. doi: 10.1111/j.1572-0241.2004.30151.x. [DOI] [PubMed] [Google Scholar]
  • 307.Weinberg BM, Shindy W, Lo S. Endoscopic balloon sphincter dilation (sphincteroplasty) versus sphincterotomy for common bile duct stones. Cochrane Database Syst Rev. 2006;2006:CD004890. doi: 10.1002/14651858.CD004890.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 308.Liu Y, Su P, Lin S, et al. Endoscopic papillary balloon dilatation versus endoscopic sphincterotomy in the treatment for choledocholithiasis: a meta-analysis. J Gastroenterol Hepatol. 2012;27:464–471. doi: 10.1111/j.1440-1746.2011.06912.x. [DOI] [PubMed] [Google Scholar]
  • 309.Zhao HC, He L, Zhou DC, et al. Meta-analysis comparison of endoscopic papillary balloon dilatation and endoscopic sphincteropapillotomy. World J Gastroenterol. 2013;19:3883–3891. doi: 10.3748/wjg.v19.i24.3883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 310.Takahara N, Isayama H, Sasaki T, et al. Endoscopic papillary balloon dilation for bile duct stones in patients on hemodialysis. J Gastroenterol. 2012;47:918–923. doi: 10.1007/s00535-012-0551-x. [DOI] [PubMed] [Google Scholar]
  • 311.Kawabe T, Komatsu Y, Tada M, et al. Endoscopic papillary balloon dilation in cirrhotic patients: removal of common bile duct stones without sphincterotomy. Endoscopy. 1996;28:694–698. doi: 10.1055/s-2007-1005579. [DOI] [PubMed] [Google Scholar]
  • 312.Hung TH, Tseng CW, Chen YC, et al. Endoscopic papillary balloon dilation decreases the risk of bleeding in cirrhotic patients compared with endoscopic biliary sphincterotomy: A national population-based study. Medicine (Baltimore) 2019;98:e16529. doi: 10.1097/MD.0000000000016529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 313.Choi D, Lim HK, Kim MJ, et al. Liver abscess after percutaneous radiofrequency ablation for hepatocellular carcinomas: frequency and risk factors. AJR Am J Roentgenol. 2005;184:1860–1867. doi: 10.2214/ajr.184.6.01841860. [DOI] [PubMed] [Google Scholar]
  • 314.Yasuda I, Fujita N, Maguchi H, et al. Long-term outcomes after endoscopic sphincterotomy versus endoscopic papillary balloon dilation for bile duct stones. Gastrointest Endosc. 2010;72:1185–1191. doi: 10.1016/j.gie.2010.07.006. [DOI] [PubMed] [Google Scholar]
  • 315.Fujimoto K, Fujishiro M, Kato M, et al. Guidelines for gastroenterological endoscopy in patients undergoing antithrombotic treatment. Dig Endosc. 2014;26:1–14. doi: 10.1111/den.12183. [DOI] [PubMed] [Google Scholar]
  • 316.Kato M, Uedo N, Hokimoto S, et al. Guidelines for Gastroenterological Endoscopy in Patients Undergoing Antithrombotic Treatment: 2017 Appendix on Anticoagulants Including Direct Oral Anticoagulants. Dig Endosc. 2018;30:433–440. doi: 10.1111/den.13184. [DOI] [PubMed] [Google Scholar]
  • 317.Mukai S, Itoi T, Baron TH, et al. Indications and techniques of biliary drainage for acute cholangitis in updated Tokyo Guidelines 2018. J Hepatobiliary Pancreat Sci. 2017;24:537–549. doi: 10.1002/jhbp.496. [DOI] [PubMed] [Google Scholar]
  • 318.Slattery E, Kale V, Anwar W, et al. Role of long-term biliary stenting in choledocholithiasis. Dig Endosc. 2013;25:440–443. doi: 10.1111/j.1443-1661.2012.01399.x. [DOI] [PubMed] [Google Scholar]
  • 319.Chopra KB, Peters RA, O'Toole PA, et al. Randomised study of endoscopic biliary endoprosthesis versus duct clearance for bileduct stones in high-risk patients. Lancet. 1996;348:791–793. doi: 10.1016/S0140-6736(96)06316-7. [DOI] [PubMed] [Google Scholar]
  • 320.Akazawa Y, Ohtani M, Nosaka T, et al. Long-term prognosis after biliary stenting for common bile duct stones in high-risk elderly patients. J Dig Dis. 2018;19:626–634. doi: 10.1111/1751-2980.12656. [DOI] [PubMed] [Google Scholar]
  • 321.Seitz U, Bapaye A, Bohnacker S, et al. Advances in therapeutic endoscopic treatment of common bile duct stones. World J Surg. 1998;22:1133–1144. doi: 10.1007/s002689900532. [DOI] [PubMed] [Google Scholar]
  • 322.Itoi T, Wang HP. Endoscopic management of bile duct stones. Dig Endosc. 2010;22(Suppl 1):S69–75. doi: 10.1111/j.1443-1661.2010.00953.x. [DOI] [PubMed] [Google Scholar]
  • 323.ASoP Committee. Maple JT, Ikenberry SO, et al. The role of endoscopy in the management of choledocholithiasis. Gastrointest Endosc. 2011;74:731–744. doi: 10.1016/j.gie.2011.04.012. [DOI] [PubMed] [Google Scholar]
  • 324.Ishiwatari H, Kawakami H, Hisai H, et al. Balloon catheter versus basket catheter for endoscopic bile duct stone extraction: a multicenter randomized trial. Endoscopy. 2016;48:350–357. doi: 10.1055/s-0035-1569573. [DOI] [PubMed] [Google Scholar]
  • 325.Ozawa N, Yasuda I, Doi S, et al. Prospective randomized study of endoscopic biliary stone extraction using either a basket or a balloon catheter: the BasketBall study. J Gastroenterol. 2017;52:623–630. [DOI] [PubMed]
  • 326.Manes G, Paspatis G, Aabakken L, et al. Endoscopic management of common bile duct stones: European Society of Gastrointestinal Endoscopy (ESGE) guideline. Endoscopy. 2019;51:472–491. doi: 10.1055/a-0862-0346. [DOI] [PubMed] [Google Scholar]
  • 327.Hammarstrom LE, Holmin T, Stridbeck H, et al. Long-term follow-up of a prospective randomized study of endoscopic versus surgical treatment of bile duct calculi in patients with gallbladder in situ. Br J Surg. 1995;82:1516–1521. doi: 10.1002/bjs.1800821121. [DOI] [PubMed] [Google Scholar]
  • 328.Targarona EM, Ayuso RM, Bordas JM, et al. Randomised trial of endoscopic sphincterotomy with gallbladder left in situ versus open surgery for common bileduct calculi in high-risk patients. Lancet. 1996;347:926–929. doi: 10.1016/S0140-6736(96)91413-0. [DOI] [PubMed] [Google Scholar]
  • 329.Suc B, Escat J, Cherqui D, et al. Surgery vs endoscopy as primary treatment in symptomatic patients with suspected common bile duct stones: a multicenter randomized trial. French Associations for Surgical Research. Arch Surg. 1998;133:702–708. doi: 10.1001/archsurg.133.7.702. [DOI] [PubMed] [Google Scholar]
  • 330.Lau JY, Leow CK, Fung TM, et al. Cholecystectomy or gallbladder in situ after endoscopic sphincterotomy and bile duct stone removal in Chinese patients. Gastroenterology. 2006;130:96–103. doi: 10.1053/j.gastro.2005.10.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 331.McAlister VC, Davenport E, Renouf E. Cholecystectomy deferral in patients with endoscopic sphincterotomy. Cochrane Database Syst Rev. 2007;2007:CD006233. doi: 10.1002/14651858.CD006233.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 332.Park BK, Seo JH, Jeon HH, et al. A nationwide population-based study of common bile duct stone recurrence after endoscopic stone removal in Korea. J Gastroenterol. 2018;53:670–678. doi: 10.1007/s00535-017-1419-x. [DOI] [PubMed] [Google Scholar]
  • 333.Cui ML, Cho JH, Kim TN. Long-term follow-up study of gallbladder in situ after endoscopic common duct stone removal in Korean patients. Surg Endosc. 2013;27:1711–1716. doi: 10.1007/s00464-012-2662-0. [DOI] [PubMed] [Google Scholar]
  • 334.Suzuki Y, Mori T, Yokoyama M, et al. Effect of UDCA for bile duct stone recurrence and development of cholangiocarcinoma. KanTanSui. 2018;77:77–79. [Google Scholar]
  • 335.Yamamoto R, Tazuma S, Kanno K, et al. Ursodeoxycholic acid after bile duct stone removal and risk factors for recurrence: a randomized trial. J Hepatobiliary Pancreat Sci. 2016;23:132–136. doi: 10.1002/jhbp.316. [DOI] [PubMed] [Google Scholar]
  • 336.Akiyama S, Imamura T, Tamura T, et al. Recurrent common bile duct stones composed of ursodeoxycholic acid: a report of four cases. Intern Med. 2014;53:2489–2492. doi: 10.2169/internalmedicine.53.2886. [DOI] [PubMed] [Google Scholar]
  • 337.Nakagawara H, Yamao K, Nomura S, et al. A case of common bile duct stones composed of ursodeoxycholic acid associated with hereditary spherocytosis. J Jpn Biliary Assoc. 2017;31:279–283 (in Japanese with English abstract).
  • 338.Lin CC, Lin PY, Ko CJ, et al. Hepatic resection for bilateral hepatolithiasis: a 20-year experience. ANZ J Surg. 2013;83:978–984. doi: 10.1111/j.1445-2197.2012.06283.x. [DOI] [PubMed] [Google Scholar]
  • 339.Yang T, Lau WY, Lai EC, et al. Hepatectomy for bilateral primary hepatolithiasis: a cohort study. Ann Surg. 2010;251:84–90. doi: 10.1097/SLA.0b013e3181b2f374. [DOI] [PubMed] [Google Scholar]
  • 340.Kusano T, Isa T, Ohtsubo M, et al. Natural progression of untreated hepatolithiasis that shows no clinical signs at its initial presentation. J Clin Gastroenterol. 2001;33:114–117. doi: 10.1097/00004836-200108000-00004. [DOI] [PubMed] [Google Scholar]
  • 341.Kim KH, Sung CK, Park BG, et al. Clinical significance of intrahepatic biliary stricture in efficacy of hepatic resection for intrahepatic stones. J Hepatobiliary Pancreat Surg. 1998;5:303–308. doi: 10.1007/s005340050050. [DOI] [PubMed] [Google Scholar]
  • 342.Adamek HE, Schneider AR, Adamek MU, et al. Treatment of difficult intrahepatic stones by using extracorporeal and intracorporeal lithotripsy techniques: 10 years' experience in 55 patients. Scand J Gastroenterol. 1999;34:1157–1161. doi: 10.1080/003655299750024986. [DOI] [PubMed] [Google Scholar]
  • 343.Hochberger J, Tex S, Maiss J, et al. Management of difficult common bile duct stones. Gastrointest Endosc Clin N Am. 2003;13:623–634. doi: 10.1016/S1052-5157(03)00102-8. [DOI] [PubMed] [Google Scholar]
  • 344.Amplatz S, Piazzi L, Felder M, et al. Extracorporeal shock wave lithotripsy for clearance of refractory bile duct stones. Dig Liver Dis. 2007;39:267–272. doi: 10.1016/j.dld.2006.11.003. [DOI] [PubMed] [Google Scholar]
  • 345.Ellis RD, Jenkins AP, Thompson RP, et al. Clearance of refractory bile duct stones with extracorporeal shockwave lithotripsy. Gut. 2000;47:728–731. doi: 10.1136/gut.47.5.728. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 346.Muratori R, Brambati M, Rossi A, et al. Extracorporeal lithotripsy of intrahepatic stones with associated strictures of intrahepatic biliary ducts. Ital J Gastroenterol Hepatol. 1998;30:624–630. [PubMed] [Google Scholar]
  • 347.Kim MH, Lee SK, Min YI, et al. Extracorporeal shockwave lithotripsy of primary intrahepatic stones. Korean J Intern Med. 1992;7:25–30. doi: 10.3904/kjim.1992.7.1.25. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 348.Honjo M, Itoi T, Sofuni A, et al. Nonsurgical treatment for hepatolithiasis. Tan to Sui. 2013;34:1175–1182. [Google Scholar]
  • 349.Han JK, Choi BI, Park JH, et al. Percutaneous removal of retained intrahepatic stones with a pre-shaped angulated catheter: review of 96 patients. Br J Radiol. 1992;65:9–13. doi: 10.1259/0007-1285-65-769-9. [DOI] [PubMed] [Google Scholar]
  • 350.Miyoshi H, Inui K, Katano Y, et al. Percutaneous transhepatic management for postoperative anastomotic segment biliary stenosis, cholangitis and intrahepatic stones. Tan to Sui. 2018;39:395–401. [Google Scholar]
  • 351.Oh HC, Lee SK, Lee TY, et al. Analysis of percutaneous transhepatic cholangioscopy-related complications and the risk factors for those complications. Endoscopy. 2007;39:731–736. doi: 10.1055/s-2007-966577. [DOI] [PubMed] [Google Scholar]
  • 352.Furuta T, Kato M, Ito T, et al. 6th report of endoscopic complications: Results of theJapan Gastroenterological Endoscopy Sociery Survey from 2008 to 2012. Gastroenterological Endoscopy. 2016;58:1466–1491 (in Japanese with English abstract).
  • 353.Lamberts MP, Den Oudsten BL, Gerritsen JJ, et al. Prospective multicentre cohort study of patient-reported outcomes after cholecystectomy for uncomplicated symptomatic cholecystolithiasis. Br J Surg. 2015;102:1402–1409. doi: 10.1002/bjs.9887. [DOI] [PubMed] [Google Scholar]
  • 354.Wennmacker SZ, Dijkgraaf MGW, Westert GP, et al. Persistent abdominal pain after laparoscopic cholecystectomy is associated with increased healthcare consumption and sick leave. Surgery. 2018;163:661–666. doi: 10.1016/j.surg.2017.09.004. [DOI] [PubMed] [Google Scholar]
  • 355.Latenstein CSS, Wennmacker SZ, de Jong JJ, et al. Etiologies of long-term postcholecystectomy symptoms: a systematic review. Gastroenterol Res Pract. 2019;2019:4278373. doi: 10.1155/2019/4278373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 356.Sauter GH, Moussavian AC, Meyer G, et al. Bowel habits and bile acid malabsorption in the months after cholecystectomy. Am J Gastroenterol. 2002;97:1732–1735. doi: 10.1111/j.1572-0241.2002.05779.x. [DOI] [PubMed] [Google Scholar]
  • 357.Fort JM, Azpiroz F, Casellas F, et al. Bowel habit after cholecystectomy: physiological changes and clinical implications. Gastroenterology. 1996;111:617–622. doi: 10.1053/gast.1996.v111.pm8780565. [DOI] [PubMed] [Google Scholar]
  • 358.Arlow FL, Dekovich AA, Priest RJ, et al. Bile acid-mediated postcholecystectomy diarrhea. Arch Intern Med. 1987;147:1327–1329. doi: 10.1001/archinte.1987.00370070139021. [DOI] [PubMed] [Google Scholar]
  • 359.Fromm H, Tunuguntla AK, Malavolti M, et al. Absence of significant role of bile acids in diarrhea of a heterogeneous group of postcholecystectomy patients. Dig Dis Sci. 1987;32:33–44. doi: 10.1007/BF01296685. [DOI] [PubMed] [Google Scholar]
  • 360.Sciarretta G, Furno A, Mazzoni M, et al. Post-cholecystectomy diarrhea: evidence of bile acid malabsorption assessed by SeHCAT test. Am J Gastroenterol. 1992;87:1852–1854. [PubMed] [Google Scholar]
  • 361.Suhr O, Danielsson A, Nyhlin H, et al. Bile acid malabsorption demonstrated by SeHCAT in chronic diarrhoea, with special reference to the impact of cholecystectomy. Scand J Gastroenterol. 1988;23:1187–1194. doi: 10.3109/00365528809090189. [DOI] [PubMed] [Google Scholar]
  • 362.Porr PJ, Szantay J, Rusu M. Post-cholecystectomy syndrome and magnesium deficiency. J Am Coll Nutr. 2004;23:745S–S747. doi: 10.1080/07315724.2004.10719420. [DOI] [PubMed] [Google Scholar]
  • 363.Schreurs WH, Juttmann JR, Stuifbergen WN, et al. Management of common bile duct stones: selective endoscopic retrograde cholangiography and endoscopic sphincterotomy: short- and long-term results. Surg Endosc. 2002;16:1068–1072. doi: 10.1007/s00464-001-9104-8. [DOI] [PubMed] [Google Scholar]
  • 364.Sugiyama M, Atomi Y. Risk factors predictive of late complications after endoscopic sphincterotomy for bile duct stones: long-term (more than 10 years) follow-up study. Am J Gastroenterol. 2002;97:2763–2767. doi: 10.1111/j.1572-0241.2002.07019.x. [DOI] [PubMed] [Google Scholar]
  • 365.Ohashi A, Ueno N, Tamada K, et al. Assessment of residual bile duct stones with use of intraductal US during endoscopic balloon sphincteroplasty: comparison with balloon cholangiography. Gastrointest Endosc. 1999;49:328–333. doi: 10.1016/S0016-5107(99)70009-X. [DOI] [PubMed] [Google Scholar]
  • 366.Hammarstrom LE, Stridbeck H, Ihse I. Long-term follow-up after endoscopic treatment of bile duct calculi in cholecystectomized patients. World J Surg. 1996;20:272–276. doi: 10.1007/s002689900043. [DOI] [PubMed] [Google Scholar]
  • 367.Kageoka M, Watanabe F, Maruyama Y, et al. Long-term prognosis of patients after endoscopic sphincterotomy for choledocholithiasis. Dig Endosc. 2009;21:170–175. doi: 10.1111/j.1443-1661.2009.00880.x. [DOI] [PubMed] [Google Scholar]
  • 368.Tsujino T, Kawabe T, Isayama H, et al. Management of late biliary complications in patients with gallbladder stones in situ after endoscopic papillary balloon dilation. Eur J Gastroenterol Hepatol. 2009;21:376–380. doi: 10.1097/MEG.0b013e328317f4a0. [DOI] [PubMed] [Google Scholar]
  • 369.Fujimoto T, Tsuyuguchi T, Sakai Y, et al. Long-term outcome of endoscopic papillotomy for choledocholithiasis with cholecystolithiasis. Dig Endosc. 2010;22:95–100. doi: 10.1111/j.1443-1661.2010.00936.x. [DOI] [PubMed] [Google Scholar]
  • 370.Kogure H, Tsujino T, Isayama H, et al. Short- and long-term outcomes of endoscopic papillary large balloon dilation with or without sphincterotomy for removal of large bile duct stones. Scand J Gastroenterol. 2014;49:121–128. doi: 10.3109/00365521.2013.848470. [DOI] [PubMed] [Google Scholar]
  • 371.Chan HH, Lai KH, Lin CK, et al. Endoscopic papillary large balloon dilation alone without sphincterotomy for the treatment of large common bile duct stones. BMC Gastroenterol. 2011;11:69. doi: 10.1186/1471-230X-11-69. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 372.Kim KY, Han J, Kim HG, et al. Late Complications and Stone Recurrence Rates after Bile Duct Stone Removal by Endoscopic Sphincterotomy and Large Balloon Dilation are Similar to Those after Endoscopic Sphincterotomy Alone. Clin Endosc. 2013;46:637–642. doi: 10.5946/ce.2013.46.6.637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 373.Paspatis GA, Paraskeva K, Vardas E, et al. Long-term recurrence of bile duct stones after endoscopic papillary large balloon dilation with sphincterotomy: 4-year extended follow-up of a randomized trial. Surg Endosc. 2017;31:650–655. doi: 10.1007/s00464-016-5012-9. [DOI] [PubMed] [Google Scholar]
  • 374.Jeong S, Ki SH, Lee DH, et al. Endoscopic large-balloon sphincteroplasty without preceding sphincterotomy for the removal of large bile duct stones: a preliminary study. Gastrointest Endosc. 2009;70:915–922. doi: 10.1016/j.gie.2009.04.042. [DOI] [PubMed] [Google Scholar]
  • 375.Tanaka M, Takahata S, Konomi H, et al. Long-term consequence of endoscopic sphincterotomy for bile duct stones. Gastrointest Endosc. 1998;48:465–469. doi: 10.1016/S0016-5107(98)70086-0. [DOI] [PubMed] [Google Scholar]
  • 376.Tanaka M, Ogawa Y, Naritomi G, et al. Clinical significance of endoscopic sphincterotomy compared with surgical common bile duct exploration and surgical sphincterotomy. J Jpn Surg Soc. 1992;93:1119–22 (in Japanese with English abstract). [PubMed]
  • 377.Paganini AM, Guerrieri M, Sarnari J, et al. Thirteen years' experience with laparoscopic transcystic common bile duct exploration for stones. Effectiveness and long-term results. Surg Endosc. 2007;21:34–40. doi: 10.1007/s00464-005-0286-3. [DOI] [PubMed] [Google Scholar]
  • 378.Tokumura H, Matsumura N, Nomura R. Laparoscopic management of common bile duct stones. J Jpn Biliary Assoc. 2012;26:40–45 (in Japanese with English abstract).
  • 379.Uchiyama K, Onishi H, Tani M, et al. Long-term prognosis after treatment of patients with choledocholithiasis. Ann Surg. 2003;238:97–102. doi: 10.1097/01.sla.0000077923.38307.84. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 380.Natsui M, Saito Y, Abe S, et al. Long-term outcomes of endoscopic papillary balloon dilation and endoscopic sphincterotomy for bile duct stones. Dig Endosc. 2013;25:313–321. doi: 10.1111/j.1443-1661.2012.01393.x. [DOI] [PubMed] [Google Scholar]
  • 381.Ohya T, Tazuma S, Kanno K, et al. A nation-wide survey of hepatolithiasis. J Jpn Biliary Assoc. 2013;27:788–794 (in Japanese with English abstract)
  • 382.Yoon YS, Han HS, Shin SH, et al. Laparoscopic treatment for intrahepatic duct stones in the era of laparoscopy: laparoscopic intrahepatic duct exploration and laparoscopic hepatectomy. Ann Surg. 2009;249:286–291. doi: 10.1097/SLA.0b013e31818eea56. [DOI] [PubMed] [Google Scholar]
  • 383.Lai EC, Ngai TC, Yang GP, et al. Laparoscopic approach of surgical treatment for primary hepatolithiasis: a cohort study. Am J Surg. 2010;199:716–721. doi: 10.1016/j.amjsurg.2009.02.007. [DOI] [PubMed] [Google Scholar]
  • 384.Tu JF, Jiang FZ, Zhu HL, et al. Laparoscopic vs open left hepatectomy for hepatolithiasis. World J Gastroenterol. 2010;16:2818–2823. doi: 10.3748/wjg.v16.i22.2818. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 385.Ministry Of Health, Labour and Welfare. Research and Study on Refractory Liver and Biliary Diseases Tokyo: Bunkodo; 2011;32–59 (in Japanese).
  • 386.Li EL, Yuan RF, Liao WJ, et al. Intrahepatic bile duct exploration lithotomy is a useful adjunctive hepatectomy method for bilateral primary hepatolithiasis: an eight-year experience at a single centre. BMC Surg. 2019;19:16. doi: 10.1186/s12893-019-0480-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 387.Uchiyama K, Kawai M, Ueno M, et al. Reducing residual and recurrent stones by hepatectomy for hepatolithiasis. J Gastrointest Surg. 2007;11:626–630. doi: 10.1007/s11605-006-0024-8. [DOI] [PubMed] [Google Scholar]
  • 388.Otani K, Shimizu S, Chijiiwa K, et al. Comparison of treatments for hepatolithiasis: hepatic resection versus cholangioscopic lithotomy. J Am Coll Surg. 1999;189:177–182. doi: 10.1016/S1072-7515(99)00109-X. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Gastroenterology are provided here courtesy of Springer

RESOURCES