Abstract
BACKGROUND
The prophylactic use of antibiotics in endoscopic retrograde cholangiopancreatography (ERCP) is still controversial.
AIM
To assess whether antibiotic prophylaxis reduces the rates of complications in patients undergoing elective ERCP.
METHODS
This systematic review and meta-analysis were performed following the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines. A comprehensive search of multiple electronic databases was performed. Only randomized controlled trials were included. The outcomes analyzed included bacteremia, cholangitis, sepsis, pancreatitis, and mortality. The risk of bias was assessed by the Cochrane revised Risk-of-Bias tool for randomized controlled trials. The quality of evidence was assessed by the Grading of Recommendation Assessment, Development, and Evaluation. Meta-analysis was performed using the Review Manager 5.4 software.
RESULTS
Ten randomized controlled trials with a total of 1757 patients that compared the use of antibiotic and non-antibiotic prophylaxis in patients undergoing elective ERCP were included. There was no significant difference between groups regarding incidence of cholangitis after ERCP [risk difference (RD) = -0.02, 95% confidence interval (CI): -0.05, 0.02, P = 0.32], cholangitis in patients with suspected biliary obstruction (RD = 0.02, 95%CI: -0.08 to 0.13, P = 0.66), cholangitis on intravenous antibiotic prophylaxis (RD = -0.02, 95%CI: -0.05 to 0.01, P = 0.25), septicemia (RD = -0.02, 95%CI: -0.06 to 0.01, P = 0.25), pancreatitis (RD = -0.02, 95%CI: -0.06 to 0.01, P = 0.19), and all-cause mortality (RD = 0.00, 95%CI: -0.01 to 0.01, P = 0.71]. However, the antibiotic prophylaxis group presented a 7% risk reduction in the incidence of bacteremia (RD= -0.07, 95%CI: -0.14 to -0.01, P = 0.03).
CONCLUSION
The prophylactic use of antibiotics in patients undergoing elective ERCP reduces the risk of bacteremia but does not appear to have an impact on the rates of cholangitis, septicemia, pancreatitis, and mortality.
Keywords: Endoscopy, Antibiotics, Endoscopic retrograde cholangiopancreatography, Cholangitis, Infection
Core Tip: There is controversy about antibiotic prophylaxis in patients undergoing elective endoscopic retrograde cholangiopancreatography. This is a systematic review and meta-analysis based on randomized controlled trials that analyzed whether the use of antibiotic prophylaxis is beneficial in preventing complications after this procedure. Outcomes evaluated include the rate of cholangitis, bacteremia, sepsis, pancreatitis, and mortality. Based on this meta-analysis, antibiotic prophylaxis reduces the risk of bacteremia but does not impact the rate of cholangitis, septicemia, pancreatitis, and mortality.
INTRODUCTION
Endoscopic retrograde cholangiopancreatography (ERCP) is one of the most technically challenging procedures in digestive endoscopy, associated with high rates of adverse events (AEs), reported in up to 18.9% of cases[1-3]. The most common adverse events include bacteremia, cholangitis, and pancreatitis occurring in about 6.5% to 18.0%[4], 3.0%[5,6], and 5.5%[7] respectively.
Prophylactic antibiotics are used with the intent to prevent complications of ERCP. Their use is controversial and is currently being recommended in patients with incomplete biliary drainage, such as hilar tumors and primary sclerosing cholangitis[8] due to the potential risk of septic complications from the manipulation of obstructed bile ducts that could serve as a source of bacterial colonization, thus increasing the risk of bacteremia[4] and cholangitis.
The European Society for Gastrointestinal Endoscopy[9] and the American Society for Gastrointestinal Endoscopy[10] guidelines do not recommend routine antibiotics prophylaxis before elective ERCP in low-risk groups. Both guidelines recommend antibiotic prophylaxis in specific situations such as liver transplant[11], severe neutropenia, the impossibility of complete biliary drainage, use of cholangioscopy[12], and in patients with primary sclerosing cholangitis[13].
Although both guidelines regarding antibiotic prophylaxis for ERCP do not recommend its routine use, the data to support this recommendation is not robust. Therefore, we performed a systematic review and meta-analysis to evaluate whether the use of antibiotic prophylaxis has an impact on the rate of complications related to elective ERCP.
MATERIALS AND METHODS
Protocol and registration
The study protocol was registered in the International Prospective Register of Systematic Reviews under the file number CRD42022289127 and was approved by the Ethics Committee of Hospital das Clínicas, Faculty of Medicine at The University of São Paulo. This systematic review and meta-analysis were performed in conformity with the recommendations from the Cochrane Handbook of Systematic Reviews of Interventions and the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines[14].
Information source and literature search
Individualized searches of multiple electronic databases (MEDLINE, Embase, Cochrane, LILACS, clincaltrials.gov, and gray literature) were performed based upon a standardized protocol from their inception through February 2022. The search included the following Medical Subject Headings: “(Endoscopy OR Endoscopic) AND (Anti-Bacterial Agents OR Antibacterial Agents OR Antibacterial Agent OR Antibiotics OR Antibiotic) AND [prophylaxis OR preventive OR (prevention and control)].” A further literature search was conducted with the Reference Citation Analysis engine, an artificial intelligence technology-based open multidisciplinary citation analysis database (https://www.referencecitationanalysis.com). Following a search within the Reference Citation Analysis database no further studies were identified that fit our inclusion criteria.
Study selection
Two researchers independently conducted the eligibility screening. From the initial search results, duplicate articles were excluded, and the titles and abstracts of all potentially relevant studies were screened for eligibility. Any disagreements were settled by consensus or by consulting a third reviewer.
Only randomized controlled trials (RCTs) comparing antibiotic prophylaxis vs no use of prophylactic antibiotics in patients undergoing elective ERCP regardless of publication date or language were considered.
Patients with cholangitis or other types of active infection, history of antibiotic allergy, and immunosuppressed were excluded.
Data extraction and definitions
Items included in data extraction were first author, year of publication, study design, and outcomes of interest such as cholangitis, bacteremia, septicemia, pancreatitis, and mortality. We defined cholangitis as the presence of fever (> 38.5 °C), abdominal pain, leukocytosis, and elevated C-reactive protein. Blood cultures and bile samples were taken to evaluate for bacteremia. Bacteremia was defined as a positive culture with no evidence of systemic inflammatory response. Blood culture samples were taken before and after the ERCP procedure and in the presence of fever. In one of the studies a blood culture was obtained only if the patients presented signs of cholangitis. Septicemia was defined as a positive blood culture with systemic inflammatory response (fever, hypotension, tachycardia, leukocytosis > 10 g/dL, leukopenia < 3 g/L, and chills). The diagnosis of pancreatitis was based on clinical findings, increased serum amylase or lipase three-fold or more over the normal upper range. Antibiotic prophylaxis is defined as administering antibiotics to patients who underwent invasive procedures without evidence of infection at the time of the procedure. The goal of such prophylaxis was to reduce the risk of infection.
Risk of bias and quality of evidence
We assessed the risk of bias using the Cochrane Risk of Bias tool version 2[14].
The quality of evidence was assessed utilizing the objective criteria from Grading Recommendations Assessment, Development, and Evaluation for each of the prespecified results and outcomes using the GRADEpro-Guideline Development Tool software (McMaster University, 2015; Evidence Prime, Inc., Ontario, Canada)[15].
Statistical analysis
Continuous variables were analyzed using mean difference and standard deviation with a 95% confidence interval. For categorical variables, the risk difference (RD) was used, with a 95% confidence interval. The RD and mean difference were considered statistically significant at a value of P ≤ 0.05. If a study provided medians and interquartiles or ranges, they were attributed to means, and standard deviation was estimated as described by the McGrath et al[16] method.
The inconsistency index was evaluated using the Higgins I2 method[17], in which the presence of heterogeneity can be observed. The random effect was used for all analyses. The meta-analysis was performed using the RevMan software (Review Manager Software version 5.4-Cochrane Collaboration Copyright© 2020).
RESULTS
Study selection
The initial search strategy identified 5594 articles. Through the evaluation by title and abstract, 2999 articles were excluded, yielding 165 studies. Of these, 10 RCTs, including 1757 patients (843 in the control group and 914 in the intervention group) met the eligibility criteria and were included in this systematic review and meta-analysis (Figure 1). The characteristics and results of the included studies are summarized in Table 1.
Table 1.
Ref.
|
Year
|
Type of study
|
Intervention
|
Participants
|
Bacteremia
|
Cholangitis
|
Pancreatitis
|
Septicemia
|
Mortality
|
Brandes et al[23] | 1981 | RCT | Minocycline 300 mg orally | Total: 118 | N/A | Intervention: 0/39 | Intervention: 1/39 | N/A | N/A |
Antibiotics: 39 | Control: 1/79 | Control: 2/79 | |||||||
Control: 79 | |||||||||
Sauter et al[22] | 1990 | RCT | Cefotaxime 2 g IV, 15 min before ERCP | Total: 100 | Intervention: 1/50 | Intervention: 1/50 | Intervention: 0/50 | Intervention: 0/50 | Intervention: 0/50 |
Antibiotics: 50 | Control: 8/50 | Control: 2/50 | Control: 0/50 | Control: 0/50 | Control: 0/50 | ||||
Control: 50 | |||||||||
Niederau et al[21] | 1994 | RCT | Cefotaxime 2 g IV. 15 min before ERCP | Total: 100 | Intervention: 0/50 | Intervention: 0/50 | Intervention: 2/50 | Intervention: 0/50 | Intervention: 0/50 |
Antibiotics: 50 | Control: 4/50 | Control: 4/50 | Control: 3/50 | Control: 8/50 | Control: 0/50 | ||||
Control: 50 | |||||||||
Byl et al[20] | 1995 | RCT | Piperacillin, 4 g IV, 3/d | Total: 68 | Intervention: 0/30 | Intervention: 2/34 | N/A | Intervention: 0/30 | Intervention: 0/34 |
Antibiotics: 34 | Control: 7/32 | Control: 10/34 | Control: 5/32 | Control: 5/34 | |||||
Control: 34 | |||||||||
Finkelstein et al[27] | 1996 | RCT | Cefonicid 1 g IV, 1 h before ERCP | Total: 179 | Intervention: 3/88 | Intervention: 7/88 | N/A | Intervention: 0/88 | Intervention: 0/88 |
Antibiotics: 88 | Control: 2/91 | Control: 2/91 | Control: 0/91 | Control: 0/91 | |||||
Control: 91 | |||||||||
Lorenz et al[24] | 1996 | RCT | Cefuroxime 1.5 g IV, 30 min before ERCP | Total: 99 | Intervention: 3/49 | N/A | N/A | Intervention: 3/49 | Intervention: 0/49 |
Antibiotics: 49 | Control: 8/50 | Control: 5/50 | Control: 0/50 | ||||||
Control: 50 | |||||||||
van den Hazel et al[19] | 1996 | RCT | Piperacillin 4 g IV, 30 min before ERCP | Total: 551 | N/A | Intervention: 12/170 | N/A | Intervention: 2/170 | Intervention: 3/170 |
Antibiotics: 270 | Control: 17/281 | Control: 3/281 | Control: 2/281 | ||||||
Control: 281 | |||||||||
Räty et al[18] | 2001 | RCT | 2g of ceftazidime IV, 30 min before ERCP | Total: 315 | N/A | Intervention: 0/155 | Intervention: 4/155 | N/A | Intervention: 1/155 |
Antibiotics: 155 | Control: 7/160 | Control: 15/160 | Control: 0/160 | ||||||
Control: 160 | |||||||||
Spicak et al[26] | 2002 | RCT | Amoxicillin – clavulanic acid 2.4 g IV | Total 165 | Intervention: 18/73 | Intervention: 4/77 | Intervention: 6/77 | N/A | Intervention: 2/77 |
Antibiotics: 77 | Control: 24/84 | Control: 3/88 | Control: 10/88 | Control: 2/88 | |||||
Control: 88 | |||||||||
Llach et al[25] | 2006 | RCT | Clindamycin 600 mg and gentamicin 80 mg IM, 1 h before ERCP | Total: 62 | Intervention: 2/31 | Intervention: 1/31 | N/A | Intervention: 0/31 | Intervention: 0/31 |
Antibiotics: 31 | Control: 2/30 | Control: 1/31 | Control: 0/30 | Control: 0/30 | |||||
Control: 31 |
3/d: Three times a day; ERCP: Endoscopic retrograde cholangiopancreatography; IM: Intramuscular; IV: Intravenous; N/A: Not available; RCT: Randomized controlled trial.
Risk of bias and quality of evidence
All 10 studies[18-27] were RCTs. Three studies presented a low risk bias[19,20,22]. Three studies presented a moderate risk of bias[18,24,27]. Four studies presented a serious risk of bias[21,23,25,26]. Detailed information concerning the risk of bias for each outcome is described in Figure 2.
The overall quality of evidence was moderate for the outcomes of bacteremia, cholangitis, septicemia, pancreatitis, and cholangitis in patients with suspected biliary obstruction. The quality of evidence was high for the outcomes of cholangitis in patients on intravenous antibiotic prophylaxis and mortality. Detailed information on the quality of evidence (Grading Recommendations Assessment, Development, and Evaluation) is described in Figure 3.
Outcomes
Bacteremia: Data from seven studies[20-22,24-27] were evaluated in a total of 758 patients: 371 in the intervention group and 378 in the control group. The intervention group presented a bacteremia rate of less than 7% with a statistical difference compared to the control group (RD = -0.07, 95%CI: -0.14 to -0.01, P = 0.03) (Figure 4A).
Cholangitis: Analysis of nine studies[18-23,25-27], totaling 1658 patients (794 in the intervention group and 864 in the control group) showed no significant differences between the groups (RD = -0.02, 95%CI: -0.05 to 0.02, P = 0.32) (Figure 4B).
Septicemia: Septicemia was evaluated in seven studies[19-22,24,25,27], totaling 1152 patients (568 assigned to the intervention group and 584 to the control group) and showed no significant differences between the groups (RD = -0.02, 95%CI: -0.06 to 0.01, P = 0.18) (Figure 4C).
Pancreatitis: Pancreatitis was evaluated in five studies[18,21-23,26], totaling 798 patients (371 assigned to the intervention group and 427 to the control group) and showed no significant differences between the groups (RD = -0.02, 95%CI: -0.06 to 0.01, P = 0.19) (Figure 4D).
Cholangitis in patients with suspected biliary obstruction: Data from three studies[18,19,26] were evaluated in a total of 838 patients (302 assigned to the intervention group and 536 to the control group) and showed no significant difference between the groups (RD = 0.02, 95%CI: -0.08 to 0.13, P = 0.66) (Figure 5A).
Cholangitis in patients on intravenous antibiotic prophylaxis: Analysis of eight studies[18-22,24,26,27], totaling 1540 patients (755 assigned to the intervention group and 785 to the control group) showed no significant difference between the groups (RD = -0.02, 95%CI: -0.05 to 0.01, P = 0.25) (Figure 5B).
Mortality: Mortality rate was evaluated in nine studies[18-22,24-27], totaling 1638 patients (804 of the intervention group and 834 of the control group) and showed no significant difference between the groups (RD = 0.00, 95%CI: -0.01 to 0.01, P = 0.71) (Figure 4E).
DISCUSSION
We analyzed 10 RCTs to assess whether antibiotic prophylaxis positively impacts patients undergoing elective ERCP, thus preventing complications after the procedure. Including a total of 1757 patients, this meta-analysis showed no statistical difference in the rates of cholangitis, septicemia, pancreatitis, and mortality. However, our study showed a lower bacteremia rate in the antibiotic group.
Although our systematic review and meta-analysis revealed less risk of bacteremia in the group that underwent antibiotic prophylaxis, there are doubts about whether this finding has any clinical relevance. Antibiotics are highly prescribed drugs in clinical practice. It is estimated that about 50% of antibiotic use in hospitals (both outpatient and inpatient) is not appropriately prescribed[28]. A meta-analysis published in 2009, which evaluated ERCP-induced cholangitis as an outcome, showed that antibiotics do not prevent cholangitis[29]. However, another meta-analysis from 2010 showed that prophylactic antibiotics could reduce bacteremia rates and may prevent cholangitis in patients undergoing elective ERCP[30]. Nonetheless, due to conflicting findings in the literature, it is not possible to state that reducing bacteremia rates leads to less cholangitis. Another critical point is that the indiscriminate use of antibiotics has the potential to increase bacterial resistance and lead to the emergence of multiresistant germs[31]. Antimicrobial drug resistance is a global health problem that causes a high impact and inflicts an enormous economic burden worldwide. The World Health Organization reported that the ratio of morbidity and mortality rate of diseases due to the spreading of multidrug resistant strains will lead to a substantial economic loss of approximately 100 trillion US Dollars by 2050[32].
Post-ERCP cholangitis, although infrequent, is a significant concern due to its 3% mortality rate. It is mainly associated with incomplete drainage of the bile ducts, equipment contamination[8], or an immunosuppressed state[4]. Many studies[18-23,25-27] demonstrated that prophylactic antibiotics administered in patients undergoing elective ERCP do not reduce the risk of cholangitis. A prospective study that analyzed antibiotic prophylaxis in patients undergoing elective ERCP published[33] in 2014 with 138 patients who underwent this procedure showed that cholangitis was greater when incomplete biliary drainage was present. They concluded there was no benefit in using prophylactic antibiotics to reduce cholangitis and sepsis in patients with satisfactory biliary drainage. Another retrospective study published in 2008[11], with 11484 patients over 11 years to identify post-ERCP infections, was performed in patients with biliary obstruction and immunosuppression. This study showed that the higher risk of infection was in the group who underwent ERCP after liver transplantation.
Sepsis is a significant cause of morbidity and mortality worldwide[34]. Antibacterial therapy is the cornerstone treatment for infection[35], reducing the risk of septic complications and the length of stay. However, prophylactic use of antibiotic agents is not a consensus in terms of minimizing infection risk after some procedures. In ERCP, the main factor for developing clinically relevant sepsis appears to be biliary obstruction. The presumed mechanism by which obstruction leads to sepsis is increased biliary pressure leading to bile-venous reflux. The manner this manifests clinically depends on the content of the bile: whether it contains a contrast medium during ERCP or percutaneous transhepatic cholangiography[36]. The use of prophylactic antibiotics to prevent bacterial colonization in an unobstructed biliary system is not recommended because bacteria in the bile (bacterobilia) are clinically silent. On the other hand, using prophylactic antibiotics appears to be beneficial for patients with biliary obstruction and known or suspected bacterobilia. Antibiotics should be continued until the obstruction is relieved. In addition, antibiotic prophylaxis to prevent biliary colonization that can lead to systemic sepsis is warranted in particular circumstances of an immunocompromised patient or a patient with primary sclerosing cholangitis[37]. When analyzing specific trials of patients with suspected biliary obstruction[18,19,26], they also showed no significant effect in antibiotic prophylaxis to prevent cholangitis, especially when drainage was effective. The study published in 2007 by Thawee et al[38], including patients who underwent complete biliary drainage, showed that antibiotic prophylaxis did not reduce the rate of cholangitis.
Studies[18-22,24,26,27] that used the intravenous route of administration of prophylactic antibiotics found no significant differences in the incidence of cholangitis. The type of antibiotic also did not influence the prevention of infectious complications. It should be noted that many classes of antibiotics were used, so it is not possible to determine which of them may be indicated for antibiotic prophylaxis. Besides, it is important to study the best antibiotic regimen and dosage when indicated, which is still not clear in the current literature.
In the present study, there was no significant difference in the incidence of pancreatitis in patients undergoing ERCP. The most recent study[39] from 2015 demonstrated that antibiotic prophylaxis did not influence the rate of pancreatitis in patients with risk factors such as choledocholithiasis, primary sclerosing cholangitis, and incomplete biliary drainage.
Also, there was no significant difference between the intervention and control groups regarding mortality. In general, mortality rates in the analyzed studies were low. The deaths were related to bleeding from percutaneous transhepatic drainage, cholangitis, severe sepsis, and pancreatic cancer.
Despite this being the largest study on the subject and included only RCTs, our study was not exempt from limitations. Some of the included studies[21,23,25,26] presented a high risk of bias. Also, in some studies[27], some high-risk groups (patients with incomplete biliary drainage) were not excluded when analyzing the results of cholangitis and sepsis. The absence of a homogeneous antibiotic regimen protocol and standardized methods to assess bacterial resistance may also limit the interpretation of the results. Also, the studies included in this meta-analysis are not recent, but this could be explained because during our literature search we found randomized studies that did not reach the estimated sample size of patients and thus were not included for this reason. Others are still under development. However, for our systematic review and meta-analysis, we relied on current clinical guidelines with recommendations on the use of antibiotic prophylaxis as well as references from recent prospective clinical studies that also analyzed its use.
Overall, antibiotic prophylaxis for ERCP reduces the rate of bacteremia without affecting other complications. Bacteremia is defined as the presence of bacteria in the bloodstream[40]. Among hospitalized patients, the incidence of bacteremia is highest within a few days of admission and varies according to clinical and patient characteristics[41]. Bacteremia related to endoscopic procedures can result in local infections due to contamination of “sterile” bile ducts by an endoscopic accessory and contrast material[42]. Patients undergoing ERCP may develop infectious complications depending on their comorbidities, especially in those in whom immunity is compromised and in patients with incomplete biliary drainage. In these patients, the use of prophylactic antibiotics is recommended. Appropriate use of antibiotics will reduce hospitalization time, health care costs, and the risk of mortality. On the other hand, the indiscriminate and inappropriate use of antibiotics is of concern, and bacterial resistance has become an increasing challenge. Also, the profile of procedure-related pathogens has evolved in recent years and multidrug resistant organisms have been reported[42]. Therefore, appropriate and timely selection of empiric antimicrobial treatment has become difficult. The clinical relevance and bacterial resistance should be weighed before routinely using antibiotic prophylaxis for ERCP. Considering the findings of our meta-analysis and in agreement with previous studies[29,30], the recommendation to not use antibiotic prophylaxis is maintained.
CONCLUSION
Prophylactic antibiotics reduce the rate of bacteremia in patients undergoing elective ERCP. However, its use does not have an impact on other associated complications such as cholangitis, septicemia, pancreatitis, and mortality.
ARTICLE HIGHLIGHTS
Research background
The prophylactic use of antibiotics in endoscopic retrograde cholangiopancreatography (ERCP) is controversial. The most common adverse events include bacteremia, cholangitis, and pancreatitis. Although recent guidelines regarding antibiotic prophylaxis for ERCP do not recommend its routine use, the data to support this recommendation is not robust.
Research motivation
Antimicrobial drug resistance is a global health problem that causes a high impact and inflicts an enormous economic burden worldwide. The World Health Organization reported that the ratio of morbidity and the mortality rate of diseases due to the spreading of multidrug resistant strains will lead to a substantial economic loss by 2050. Due to the lack of data in the literature, we performed a systematic review and meta-analysis to evaluate whether antibiotic prophylaxis impacts the rate of complications related to elective ERCP.
Research objectives
This systematic review and meta-analysis aimed to assess whether antibiotic prophylaxis reduced the rates of complications such as bacteremia, cholangitis, sepsis, pancreatitis, and mortality in patients undergoing elective ERCP.
Research methods
This systematic review and meta-analysis was performed following the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines. A comprehensive search of multiple electronic databases was performed only including randomized controlled trials.
Research results
Ten randomized clinical trials with a total of 1757 patients that compared the use of antibiotic and non-antibiotic prophylaxis in patients undergoing elective ERCP were included. There was no significant difference between groups regarding the incidence of cholangitis [risk difference (RD) = -0.02, 95% confidence interval (CI): -0.05 to 0.02, P = 0.32], cholangitis in patients with suspected biliary obstruction (RD = 0.02, 95%CI: -0.08 to 0.13, P = 0.66), cholangitis on intravenous antibiotic prophylaxis (RD = -0.02, 95%CI: -0.05 to 0.01, P = 0.25), septicemia (RD = -0.02, 95%CI: -0.06 to 0.01, P = 0.25), pancreatitis (RD = -0.02, 95%CI: -0.06 to 0.01, P = 0.19), and all-cause mortality (RD = 0.00, 95%CI: -0.01 to 0.01, P = 0.71). However, the antibiotic prophylaxis group presented a 7% risk reduction in the incidence of bacteremia (RD= -0.07, 95%CI: -0.14 to -0.01, P = 0.03).
Research conclusions
Considering our findings, antibiotic prophylaxis in patients undergoing elective ERCP reduces the risk of bacteremia. Still, it does not appear to impact the rate of other adverse events.
Research perspectives
Antibiotics are highly prescribed drugs in clinical practice, but they can have adverse effects. Larger randomized controlled trials regarding the use of prophylactic antibiotics on ERCP in specific populations of patients are still warranted.
Footnotes
Conflict-of-interest statement: Diogo Turiani Hourneaux de Moura: BariaTek – Advisory Board Member (Consulting fees); Sergio A Sánchez-Luna: Recipient of the 2021 American Society for Gastrointestinal Endoscopy (ASGE) Endoscopic Training Award by the ASGE and Fujifilm; Eduardo Guimarães Hourneaux de Moura: Olympus – Consultant (Consulting fees), Boston Scientific – Consultant (Consulting fees); and other authors report no relevant conflicts of interest for this article.
PRISMA 2009 Checklist statement: All the authors in this manuscript have read the PRISMA 2009 Checklist, and the manuscript was prepared and revised according to the PRISMA 2009 Checklist.
Provenance and peer review: Invited article; Externally peer reviewed.
Peer-review model: Single blind
Peer-review started: May 27, 2022
First decision: June 9, 2022
Article in press: October 26, 2022
Specialty type: Gastroenterology and hepatology
Country/Territory of origin: Brazil
Peer-review report’s scientific quality classification
Grade A (Excellent): 0
Grade B (Very good): 0
Grade C (Good): C
Grade D (Fair): D
Grade E (Poor): 0
P-Reviewer: Chang A, Thailand; Ding J, China S-Editor: Gong ZM L-Editor: Filipodia P-Editor: Cai YX
Contributor Information
Maria Fernanda Shinin Merchan, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
Diogo Turiani Hourneaux de Moura, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
Guilherme Henrique Peixoto de Oliveira, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil. guilherme.hpoliveira@hc.fm.usp.br.
Igor Mendonça Proença, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
Epifanio Silvino do Monte Junior, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
Edson Ide, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
Caroline Moll, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
Sergio A Sánchez-Luna, Department of Internal Medicine, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35233, United States.
Wanderley Marques Bernardo, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
Eduardo Guimarães Hourneaux de Moura, Department of Gastroenterology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo 05403-010, Brazil.
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