Evidence-Based Medicine Open Access
Copyright ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 7, 2020; 26(37): 5718-5730
Published online Oct 7, 2020. doi: 10.3748/wjg.v26.i37.5718
Endoscopic retrograde cholangiopancreatography in the treatment of pancreaticopleural fistula in children
Jing Zhang, Shu Guo, Tian-Lu Mei, Jin Zhou, Guo-Li Wang, Fei-Hong Yu, Yong-Li Fang, Department of Gastroenterology, Beijing Children’s Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China
Liu-Cun Gao, Clinical Research Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China
Bao-Ping Xu, China National Clinical Research Center of Respiratory Diseases, Department of Respiratory, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s Health, Beijing 100045, China
ORCID number: Jing Zhang (0000-0002-2832-239X); Liu-Cun Gao (0000-0002-7264-0184); Shu Guo (0000-0002-4286-729X); Tian-Lu Mei (0000-0003-0689-241X); Jin Zhou (0000-0003-0770-5620); Guo-Li Wang (0000-0003-3093-3920); Fei-Hong Yu (0000-0001-8706-0337); Yong-Li Fang (0000-0002-8982-5759); Bao-Ping Xu (0000-0001-8938-7691).
Author contributions: Zhang J, Gao LC, Guo S, Mei TL, Zhou J, Wang GL, Yu FH, Fang YL, and Xu BP wrote and revised the manuscript.
Conflict-of-interest statement: There are no conflicts of interest arising from this work.
PRISMA 2009 Checklist statement: The authors have read the PRISMA 2009 Checklist, and the manuscript was prepared and revised according to the PRISMA 2009 Checklist.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Corresponding author: Jing Zhang, MD, Chief Physician, Department of Gastroenterology, Beijing Children’s Hospital, Capital Medical University, National Center for Children's Health, No. 56 Nanlishi Road, Xicheng District, Beijing 100045, China. zhjtg666@163.com
Received: May 31, 2020
Peer-review started: May 31, 2020
First decision: June 18, 2020
Revised: July 1, 2020
Accepted: September 15, 2020
Article in press: September 15, 2020
Published online: October 7, 2020
Processing time: 119 Days and 14.5 Hours

Abstract
BACKGROUND

Pancreaticopleural fistula (PPF) is a rare disease, especially in children. Conservative treatment and surgery are traditional therapies, but surgery is invasive. The emergence of endoscopic retrograde cholangiopancreatography (ERCP) has provided a new noninvasive treatment for PPF and may become the first choice for children with PPF.

AIM

To explore the treatment response to ERCP for PPF in children.

METHODS

Seven children with PPF were hospitalized in the Gastroenterology Department of Beijing Children’s Hospital from December 2007 to May 2019. Data on these seven patients’ clinical characteristics, diagnosis, treatments, and outcomes were analyzed, and their treatment responses following surgery and ERCP were compared. The correlation between the length of hospital stay and conservative treatment was analyzed. Peer-reviewed articles written in English and Chinese published from January 2009 to December 2019 were obtained from various open data sources and reviewed.

RESULTS

The seven patients comprised three boys and four girls with a mean age of 6.57 ± 3.26 years. The main symptoms were chest tightness and pain (n = 4), intermittent fever (n = 3), dyspnea (n = 3), and abdominal pain (n = 1), and all patients had bloody pleural effusion. All seven patients were diagnosed with PPF by magnetic resonance cholangiopancreatography, and all were initially treated conservatively for a mean of 34.67 ± 22.03 d with a poor response. Among five patients who underwent ERCP, one required surgery because of intubation failure; thus, the success rate of ERCP was 80%. Two patients were successfully treated with surgery (100%). The postoperative hospital stay of the two patients treated by surgery was 20 and 30 d, respectively (mean of 25 d), and that of the four patients treated by ERCP ranged from 12 to 30 d (mean of 19.25 ± 8.85 d). The recovery time after ERCP was short [time to oral feeding, 4-6 d (mean, 5.33 ± 1.15 d); duration of closed thoracic drainage, 2-22 d (mean, 13.3 d)]. Analysis of previous cases of PPF published worldwide during the past decade showed that the treatment success rate of ERCP is not lower than that of surgery. There was no significant difference in the postoperative hospital stay between surgery (16 ± 10.95 d) and ERCP (18.7 ± 6.88 d, P > 0.05). A positive linear correlation was found between the overall hospital stay and ERCP intervention time (R2 = 0.9992).

CONCLUSION

ERCP is recommended as the first-choice treatment for PPF in children. ERCP should be performed as early as possible if conditions permit.

Key Words: Pancreaticopleural fistula; Childhood; Endoscopic retrograde cholangiopancreatography; Magnetic resonance cholangiopancreatography; Diagnostic; Treatment

Core Tip: Data on the clinical characteristics, diagnosis, treatments, and outcomes of seven Chinese children with pancreaticopleural fistula (PPF) were analyzed and compared with those described in previous publications of children and adults with PPF worldwide. There was no significant difference in the postoperative hospital stays between surgical treatment (17.2 ± 11.9 d) and endoscopic retrograde cholangiopancreatography (ERCP) (20.75 ± 5.78 d). However, there was a positive linear correlation between the overall hospital stay and ERCP intervention time (R2 = 0.9992). Therefore, ERCP is recommended as the first-choice treatment of PPF in children. ERCP should be performed as early as possible if conditions permit.



INTRODUCTION

Pancreaticopleural fistula (PPF) is a rare complication of chronic pancreatitis in both adults and children. In adults, PPF is often secondary to chronic alcoholic pancreatitis, accounting for about 0.4%of patients with pancreatitis[1] and 4.5% of patients with pancreatic pseudocysts[2]. The cause and incidence of PPF in children are still unclear. PPF can be diagnosed by laboratory examination and imaging examination. The traditional treatments are conservative treatment and surgery[3]. ERCP was a breakthrough in the diagnosis and treatment of biliopancreatic diseases when it was developed in 1968, replacing some of the traditional methods of examination and treatment of biliopancreatic diseases with endoscopy[4]. In 1993, Saeed et al[5] performed pancreatic stent implantation to cure adult PPF for the first time. ERCP has since been performed increasingly more often in the diagnosis and treatment of PPF in adults. However, the experience of ERCP in the treatment of PPF in children is limited. In the present study, the clinical data of children with PPF diagnosed in Beijing Children’s Hospital from December 2007 to May 2019 were retrospectively analyzed, and the children’s therapeutic response to ERCP was explored by comparison with previous publications worldwide.

MATERIALS AND METHODS
Objective

To explore the treatment response to ERCP for PPF in children.

Setting, design, and sample size

From December 2007 to May 2019, the clinical data of seven children with PFF in our department were retrospectively analyzed. The patients comprised three boys and four girls ranging in age from 2 to 10 years (mean age, 6.57 ± 3.26 years). Their main symptoms were chest distress and pain (n = 3), intermittent fever (n = 3), dyspnea (n = 3), and abdominal pain and distention (n = 4). Five patients had massive pleural effusion, and two had moderate pleural effusion. Three patients had pleural effusion on the right side, one had effusion on the left, and three had effusion on both sides. One patient had a history of abdominal trauma, but no patients had a history of abdominal surgery.

Diagnostic criteria

All seven patients were confirmed to have PPF by laboratory and imaging examinations. The laboratory examinations mainly included pancreatic and pleural effusion biochemical examinations. The imaging examinations mainly included B-ultrasound, enhanced computed tomography, magnetic resonance cholangio-pancreatography, and ERCP.

Treatments

All seven children initially received conservative treatment, including fasting, a somatostatin prescription to inhibit pancreatic secretion, anti-infection medication, and nutritional support. After conservative treatment, the body temperature normalized and pleural effusion disappeared in one patient, while a poor response was seen in six patients. Therefore, two patients were treated by surgery and five underwent ERCP, however, one of the five patients who underwent ERCP required surgery because of ERCP intubation failure.

Literature review

Peer-reviewed English-language publications were retrieved from the PubMed database using the search term “[Pancreaticopleural Fistula] OR [PPF],” and Chinese publications were retrieved from the Wanfang and China National Knowledge Infrastructure databases using the search term “Pancreaticopleural Fistula.” The time limit for the literature search was January 2009 to December 2019.

Statistical analysis

SPSS 22.0 software (IBM Corp, Armonk, NY, United States) was used to analyze the correlation between the length of hospital stay and conservative treatment. Descriptive data are expressed as mean ± standard deviation. The effects of surgical treatment and ERCP were compared by a t-test, and P < 0.05 indicated a statistically significant difference.

RESULTS
Diagnostic results

All seven patients with pleural effusion had hemothorax. Four had a leukocyte count of > 500 × 106/L, and five had a pleural effusion protein concentration of > 30 g/L. The concentration of amylase in the pleural fluid was substantially increased in all patients (> 1000 U/L; reference, < 150 U/L); five patients had a pleural fluid amylase concentration of 1000 to 50000 U/L, and two had a pleural fluid amylase concentration of > 50000 U/L. Table 1 shows that five of the seven patients had a high serum amylase concentration (mean, 792.8 ± 409.97 U/L). The serum lipase concentration was increased in all seven children (mean, 1826.1 ± 1650.21 U/L), and one patient had a large amount of ascites with an amylase concentration of 13053 U/L. Table 2 shows that all seven patients had negative results of acid-fast staining and bacterial culture of the pleural effusion, and no tumor cells were found in the pathological examination. All seven patients were diagnosed with PPF by magnetic resonance cholangio-pancreatography. Pulmonary imaging showed a large amount of pleural effusion in all children; the effusion was present on the right side in three children, on the left side in one, and on both sides in three.

Table 1 Laboratory findings in patients with pancreaticopleural fistula.
PatientsAppearance of pleural effusionLeukocyte count of pleural fluid (× 106 L)Pleural effusion protein (g/L)Pleural amylase (U/L)Serum amylase (U/L)Blood lipase (U/L)Ascites amylase (U/L)
1Bloody30040.0662510263912.913053.0
2Bloody56034.0104774231051-
3Bloody3600403178409950-
4Bloody170017.450465284-654355.4-
5Bloody8004515841104470-
6Bloody120027.66500013681312.2
7Bloody646.725549738731.2-
Table 2 Clinical symptoms, treatments, and outcomes of seven children with pancreaticopleural fistula.
Patients1234567
Age (yr)810325810
GenderMaleFemaleMaleMaleFemaleFemaleFemale
SymptomFatigue, poor appetite, intermittent fever, abdominal distentionIntermittent chest tightness and upper abdominal painChronic pancreatitis, recurrent abdominal painWheezing, shortness of breath, repeated bloody pleural effusionAbdominal pain for half a year, fever and chest tightnessIntermittent chest tightness and dyspnea for more than 20 dChest pain with dyspnea
EtiologySuspected trauma and pseudocystDilatation and calculus of pancreatic ductCongenital pancreatic duct dysplasia and pseudocystPseudocyst and dilatation of pancreatic ductPseudocyst and dilatation of pancreatic ductDilatation and calculus of pancreatic ductPancreatic duct stone, pseudocyst, dilatation of pancreatic duct
Diagnosislaboratory examination, B ultrasound, MRCPlaboratory examination, MRCPlaboratory examination, enhanced CT, MRC, ERCPlaboratory examination, CT, B ultrasound, MRCPlaboratory examination, CT, B ultrasound, MRCPlaboratory examination, CT, MRCP, ERCPlaboratory examination, CT, B ultrasound, MRCP
Location of pleural effusionRightBilateralBilateralLeftRightBilateralRight
Amylase in pleural effusion (U/L)66251047731785046515846500025549
Conservative treatment time (d)10216024192010
ERCP treatmentYes (Surgical treatment after ERCP failure)No (Operation)YesYesNo (Operation)YesYes
Serum amylase concentration before operation (U/L)889.415336742993.0292283
Serum amylase concentration after operation (U/L)102267315105110
Time for amylase to return to normal (Days after operation)231094
Lipase concentration before operation/ERCP (U/L)5671051355.4115106731.2
Lipase concentration after operation/ERCP (U/L)51.762.4
Stop somatostatin pump maintenance time (days after operation)19534
Postoperative recovery time of eating (days after operation)3366415
Times of fever treated conservatively13534Normal temperature
Chest closed drainage time (days after operation)--16---
Postoperative hospital stay (d)203030121223
Total length of stay (d)305290363233
Treatments and outcomes

All seven patients with PPF were initially treated with conservative therapy for 10 to 60 d (mean, 34.67 ± 22.03 d). Six of them had a recurrent fever and continuous pleural effusion following the conservative treatment. Therefore, five patients underwent ERCP, and one of these patients was transferred to surgery after ERCP intubation failed. The remaining four children who underwent ERCP recovered well without a recurrent fever after the procedure. Their body temperature normalized within 2 to 4 d, and they began to eat within 4 to 6 d. Pump infusion of a somatostatin was continued for 4 to 20 d, and the amylase concentration recovered to normal in 4 to 23 d. The patients underwent 2 to 22 d of closed thoracic drainage; the one child who underwent drainage for 22 d required prolonged drainage because of obstruction of the ERCP tent by small stones. The hospitalization stay after ERCP ranged from 12 to 30 d among these four patients (mean, 18 ± 10.39 d) (Table 3).

Table 3 Comparison of therapeutic effect of endoscopic retrograde cholangiopancreatography vs conservative treatment.
PatientsConservative treatment time (d)Recovery time of indexes after ERCP (d)
Serum amylase concentration (U/L)
Hospital stay after different treatment (d)
Total length of stay (d)
Postoperative dischargeSomatostatin pump maintenanceRecovery time of eatingBlood amylase recovery2 d before operation2 d after operationOperationERCP
12102030
22213152
5219-
336030196233672923090
43241256102672491236
6320123494292831232
71,310234154315110-2333
Average (ERCP)34.67 ± 22.0318 ± 10.399 ± 8.725.33 ± 1.1514 ± 7.81344.5 ± 69.58233.5 ± 84.3925.5 ± 7.7818 ± 10.39-
Association between overall hospital stay and duration of conservative treatment

SPSS software was used to fit the overall hospital stay and duration of conservative treatment, and a positive linear correlation was obtained (R2 = 0.9992) (Figure 1).

Figure 1
Figure 1 The correlation between endoscopic retrograde cholangiopancreatography intervention time and total hospital stay. The linear equation is not a model prediction but only a correlation analysis.
Literature review

Articles describing clinical operations for PPF published worldwide during the past decade were reviewed and summarized (Table 4)[6-40]. In total, 37 case reports were found among 35 non-duplicated publications. The 37 patients comprised 25 adults and 12 children. Among seven patients who received conservative treatment, one died of a poor response. Thirteen patients received surgical treatment, and among the 17 patients who received ERCP treatment, three were converted to surgical treatment because of a poor response to ERCP. The duration of conservative treatment ranged from 7 to 60 d (mean, 30.76 ± 17.4 d). The postoperative hospital stay of patients who underwent surgical treatment ranged from 5 to 30 d (mean, 16 ± 10.95 d), and the postoperative hospital stay of patients who underwent ERCP ranged from 12 to 30 d (mean, 18.7 ± 6.88 d). There was no significant difference in the postoperative hospital stay between the two groups (P > 0.05).

Table 4 Worldwide cases of pancreaticopleural fistula published in the most recent 10 years.
Publication yearsGender/age (yr)DiagnosisTreatmentsConservative treatment time (d)Postoperative hospital stays (d)
OperationERCP
Adult
2009[6]F/52CT/MRCPConservative/ERCP147
2009[6]M/46MRCPConservative/ERCP2714
2010[7]F/44CTConservative/operation5
2012[8]M/64B ultrasound/ERCPConservative/ERCP
2012[9]F/52CTConservative/operation
2012[10]M/58CT/ERCPConservative/operation42
2013[11]F/47CTConservative
2013[12]M/59CT/ERCPConservative56
2013[13]F/58CT/MRIConservative/ERCP712
2016[14]F/65CT/MRCPConservative/operation21
2014[15]F/50CT/MRCPConservative/ERCP/operation
2014[16]M/49CT/MRCP/MRIConservative/operation
2015[17]M/43CT/ERCPConservative/operation3510
2015[18]M/43CT/MRCPConservative/ERCP/operation28
2016[19]M/58CTConservative/ERCP
2016[20]M/51CT/ERCP/MRIERCP21
2016[21]F/51CT/MRCPConservative/operation285
2016[22]F/63CT/MRCPConservative/operation30
2016[23]M/78CTConservative
2017[24]M/44MRCPConservative/ERCP
2017[25]M/52CT/MRCPConservative
2018[26]M/49CT/MRCP/ERCPConservative/ERCP
2019[27]M/52OperationConservative/ERCP21
2019[28]M/35CTConservative/ERCP1420
2019[29]M/65CT/MRCP/ERCPConservative/operation
Children
2009[30]M/4CT/MRCPConservative/ERCP6030
2013[31]F/5CTConservative50
2013[32]M/15CT/MRIConservative/ERCP28
2014[33]M/2.5B ultrasound/CTConservative/operation2611
2014[34]M/8CTConservative60
2014[34]M/2CTConservative
2016[35]M/2CToperation
2018[36]F/8CT/MRCPConservative/ERCP1719
2018[37]F/14CT/MRCPConservative/operation30
2019[38]M/3CT/MRCPConservative/ERCP18
2019[39]F/8CT/MRCPConservative/ERCP818
2019[40]M/14CTConservative/operation30
AVG30.76 ± 17.416 ± 10.9518.7 ± 6.88
P valueP > 0.05
DISCUSSION
Treatment status of PPF worldwide

PPF is a rare complication of chronic pancreatitis. The main symptoms of PPF are chest pain, tachypnea, and dyspnea, and the condition is difficult to diagnose. In 1976, Cameron et al[41] considered PPF to be caused by entry of pancreatic secretions into the body cavity rather than the duodenum. In the present study, PPF originated from a ruptured main pancreatic duct or leaking pseudocyst. If the front of the pancreatic duct is damaged, extrapancreatic secretions will leak into the abdominal cavity, resulting in pancreatic ascites; if the duct is damaged at the rear, extrapancreatic secretions will leak into the mediastinum through the posterior peritoneum via the aorta or esophageal hiatus; and if the secretion penetrates the pleura, it will cause fluid accumulation (with or without bleeding) in one or both thoracic cavities[41-44]. In adults, PPF is usually secondary to chronic alcoholic pancreatitis. However, the cause is unclear in children.

PPF can be treated by conservative therapy with medication, surgery, or endoscopic technology[9,44]. In previous research, 31% to 65% of adult patients with PPF fully responded to octreotide combined with total parenteral nutrition treatment and usually took 2 to 3 wk to recover[6,45]. However, because of the repeated occurrence of pleural effusion in children, a closed thoracic drainage tube should be placed. During conservative treatment, children may develop malnutrition, catheter infection, septicemia, and other complications that are difficult to treat[46]. Children who undergo failed conservative treatment need further surgical and endoscopic treatment. Surgery is one of the main treatment methods for PPF. The purpose of surgical treatment is to connect the pancreaticojejunal channel to drain fully the pancreatic juice. The most common surgical treatment is pancreatojejunostomy. Frey’s operation can be performed when a pancreatic head mass compresses the pancreatic duct and biliary tract; this procedure involves pancreatectomy and longitudinal pancreato-jejunostomy[47]. Placement of an ERCP stent is a new nonsurgical treatment for PPF. An ERCP stent can open the proximal end of the pancreatic duct, smoothly drain the pancreatic juice, allow the pancreatic juice to flow to the duodenum with low resistance, and close the fistula that is abnormally connecting the pancreatic duct and pleura[29].

In the present study, we summarized 37 cases of PPF treatment published in the past decade (25 adults and 12 children). The proportions of adults and children who received conservative treatment, surgical treatment, and ERCP treatment were 16.67% and 25%, 50% and 41.7%, and 42.7% and 33.3%, respectively. However, conservative treatment produced a limited response. One of seven patients who received conservative treatment died, and the success rate was only 16.67%. Surgery was historically the most frequently used treatment but was invasive. With the development of minimally invasive ERCP in recent years, ERCP is now being increasingly used in the treatment of patients with PPF, especially children.

Optimal PPF treatment method

PPF is a rare disease, and no systematic study has been performed to determine the best treatment; therefore, no consensus has been reached regarding the optimal therapy. Conservative treatment has a low success rate and is associated with many complications, and patients often need secondary surgery or endoscopic treatment. Both surgery and endoscopic treatment can effectively treat PPF. However, no systematic study has been performed to compare the efficacy of the two treatments. We herein performed a preliminary comparison of surgery and endoscopic treatment of PPF by summarizing the treatment results and prognosis of seven children treated in our hospital and both adults and children described in previous publications worldwide. The first case of PPF cured by surgery was reported in 1960[48]. The first adult with PPF cured by ERCP was reported by Saeed et al[5] in 1993. Current research data show that more adults and children with PPF choose ERCP treatment.

All seven patients with PPF in this study initially received conservative treatment, but the responses were poor. Among the five patients who received ERCP treatment, one was converted to surgery because of incubation failure; the treatment success rate was thus 80%. Two patients underwent surgery (one was lost to follow-up after transfer to another hospital), and both recovered. The mean postoperative hospital stay for the two patients who underwent surgery and the four patients who underwent ERCP was 25 d and 19.25 d, respectively. The preliminary conclusion was that the recovery time was shorter after ERCP than after surgical treatment. However, because of the small number of cases, the hospital stay of the two treatment methods could not be statistically analyzed. The present study also showed that patients with PPF who undergo ERCP require a very short time until they start to eat, discontinue somatostatin pump maintenance, return to a normal amylase concentration, and discontinue closed thoracic drainage.

Because children very rarely develop PPF, the present study summarized the clinical outcome data for both adults and children with PPF worldwide during the past decade for a comprehensive analysis. The mean postoperative hospital stay of patients treated with surgery and ERCP was 16 ± 10.95 d and 18.7 ± 6.88 d, respectively (P > 0.05). There was no significant difference in the postoperative hospital stay between the two treatment methods, and the curative effect of the two methods was equivalent. The success rate of ERCP treatment (80%) was slightly lower than that of surgical treatment (100%), which may have been due to the small number of patients. In some studies, the duration of using ERCP to cure PPF was 4 to 12 wk with different success rates. The success rates reported by Khan et al[49], Pai et al[50], and Varadarajulu et al[51] were 100%, 96.4%, and 50.0% (the low success rate was due to stent placement failure or failure to pass through the pancreatic duct rupture site), respectively, similar to the surgery success rate (94%) reported by King et al[7]. These findings indicate that the success rate of ERCP treatment is not lower than that of surgical treatment. Our data are consistent with the findings of most previous studies; statistical analysis was impossible because of the limited sample size. The results of the literature review of studies published in the past decade indicated that the average recovery time following ERCP was slightly longer than that following surgery. This result might have been related to either variations in techniques between surgery and ERCP or limited information from the publications reviewed. The literature describes multiple surgical procedures (including distal pancreatectomy with splenectomy, pancreatic duct anastomosis with an intestinal loop, pancreaticoduodenectomy, cystogastrostomy, and cystojejunostomy)[14], which are traumatizing and associated with many complications such as leakage, intra-abdominal infections, and fistula recurrence[7]. No further analysis was performed because of the limited number of cases reported. In addition, the results showed that the standard deviation of the ERCP group was smaller, suggesting that the ERCP group had less invasive treatment, a shorter postoperative recovery time, and a lower incidence of complications (infection, bleeding, destruction of pancreatic duct anatomy, repeated fluid accumulation, and pancreatitis). All four patients treated with ERCP reportedly had a good prognosis with no complications. The standard deviation of the postoperative recovery time in the surgery group was larger, indicating that the postoperative recovery time in the surgery group had greater variation and higher uncertainty. In summary, we believe that ERCP can reduce the hospitalization time and should be the preferred treatment for PPF in children.

Aswani et al[3] also reported that after ERCP, patients can quickly transition to the oral feeding stage and have a short recovery time, which reduces the hospital stay and mortality rate compared with a traditional operation. Therefore, existing research suggests that ERCP should be the first choice for patients with PPF who have a poor response to conservative treatment, and only after failure of conservative treatment and ERCP treatment should surgical treatment be considered. Because of the limited number of patients in the present study, further prospective studies are needed to compare the cost-effectiveness and long-term results of ERCP and surgery.

Best operation time for ERCP

Patients with PPF initially receive conservative treatment and will choose surgery or ERCP treatment if their condition does not fully respond. We recommend ERCP as the first-choice treatment. Pleural effusion readily recurs after conservative treatment, potentially resulting in malnutrition, catheter infection, septicemia, and other complications. A longer duration of conservative treatment is associated with a greater risk for the patient. The present study investigated the relationship between the duration of conservative treatment and the overall hospital stay. The fitting analysis of the conservative treatment time and the total length of stay of three patients who received ERCP showed a positive linear correlation and suggested that a shorter conservative treatment time is associated with earlier performance of ERCP and a shorter overall hospital stay. Although conservative treatment has a certain response rate for PPF, the rate is very low, and the treatment cycle is long. Some researchers have proposed that conservative treatment should only be used as the initial stage of PPF treatment to stabilize the condition and should not be used as the treatment plan for PPF[7,52]. For patients with PPF, the duration of conservative treatment should be reduced, and ERCP treatment should be carried out as early as possible.

CONCLUSION

In conclusion, the success rate of ERCP for patients with PPF was similar to that of surgical treatment, and the prognosis was not worse than that of surgical treatment. Compared with traditional surgery, ERCP does not require laparotomy, is a simple operation, induces less trauma and fewer complications, and promotes rapid fast recovery. Thus, it is very suitable for children and advanced-age patients who cannot tolerate surgery or have poor health conditions. Earlier performance of ERCP promotes faster recovery and a shorter total length of stay. Therefore, ERCP is recommended as the first-choice treatment for PPF in children. ERCP should be performed as early as possible if conditions permit during conservative treatment. Because PPF is a rare disease and it is difficult to obtain data on clinical cases, the present study included only seven patients, one of whom was lost to follow-up after discharge. Thus, we were unable to perform a scientific and systematic comparative analysis on the curative effect of surgery and ERCP. The conclusions of this study still need to be validated.

ARTICLE HIGHLIGHTS
Research background

Pancreaticopleural fistula (PPF) can be diagnosed by laboratory examination and imaging examination. The traditional treatments are conservative treatment and surgery. Endoscopic retrograde cholangiopancreatography (ERCP) has since been performed increasingly more often in the diagnosis and treatment of PPF in adults. However, the experience of ERCP in the treatment of PPF in children is limited.

Research motivation

In the present study, the clinical data of children with PPF diagnosed in Beijing Children’s Hospital were retrospectively analyzed, and the children’s therapeutic response to ERCP was explored by comparison with previous publications worldwide.

Research objectives

This study is aimed to explore the treatment response to ERCP for PPF in children.

Research methods

Data on the clinical characteristics, diagnosis, treatments, and outcomes of seven Chinese children with PPF were analyzed and compared with those described in previous publications of children and adults with PPF worldwide.

Research results

There was no significant difference in the postoperative hospital stays between surgical treatment and ERCP. However, there was a positive linear correlation between the overall hospital stay and ERCP intervention time.

Research conclusions

ERCP is recommended as the first-choice treatment of PPF in children. ERCP should be performed as early as possible if conditions permit.

Research perspectives

Because PPF is a rare disease and it is difficult to obtain data on clinical cases, the present study included only seven patients, one of whom was lost to follow-up after discharge. Thus, we were unable to perform a scientific and systematic comparative analysis on the curative effect of surgery and ERCP. The conclusions of this study still need to be validated.

ACKNOWLEDGEMENTS

We thank the families of these patients for their support in this study.

Footnotes

Manuscript source: Unsolicited manuscript

Specialty type: Gastroenterology and hepatology

Country/Territory of origin: China

Peer-review report’s scientific quality classification

Grade A (Excellent): A

Grade B (Very good): 0

Grade C (Good): C, C

Grade D (Fair): 0

Grade E (Poor): 0

P-Reviewer: Karagyozov PI, Makmun D S-Editor: Gong ZM L-Editor: A P-Editor: Wang LL

References
1.  Sut M, Gray R, Ramachandran M, Diamond T. Pancreaticopleural fistula: a rare complication of ERCP-induced pancreatitis. Ulster Med J. 2009;78:185-186.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Fulcher AS, Capps GW, Turner MA. Thoracopancreatic fistula: clinical and imaging findings. J Comput Assist Tomogr. 1999;23:181-187.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 46]  [Cited by in F6Publishing: 51]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
3.  Aswani Y, Hira P. Pancreaticopleural fistula: a review. JOP. 2015;16:90-94.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 14]  [Reference Citation Analysis (0)]
4.  McCune WS, Shorb PE, Moscovitz H. Endoscopic cannulation of the ampulla of vater: a preliminary report. Ann Surg. 1968;167:752-756.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 410]  [Cited by in F6Publishing: 348]  [Article Influence: 6.2]  [Reference Citation Analysis (0)]
5.  Saeed ZA, Ramirez FC, Hepps KS. Endoscopic stent placement for internal and external pancreatic fistulas. Gastroenterology. 1993;105:1213-1217.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 87]  [Cited by in F6Publishing: 90]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
6.  Ali T, Srinivasan N, Le V, Chimpiri AR, Tierney WM. Pancreaticopleural fistula. Pancreas. 2009;38:e26-e31.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 77]  [Cited by in F6Publishing: 80]  [Article Influence: 5.3]  [Reference Citation Analysis (0)]
7.  King JC, Reber HA, Shiraga S, Hines OJ. Pancreatic-pleural fistula is best managed by early operative intervention. Surgery. 2010;147:154-159.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 48]  [Cited by in F6Publishing: 49]  [Article Influence: 3.3]  [Reference Citation Analysis (0)]
8.  Kutz Leoz M, Irisarri Garde R, Vila Costas JJ, Martínez Echeverría A, Elizalde Apestegui I, Basterra Ederra M, Gómez Alonso M, Zozaya Urmeneta JM. [Pleural effusion secondary to pancreaticopleural fistula following acute pancreatitis]. Gastroenterol Hepatol. 2012;35:70-73.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
9.  Shah D, Desai AB, Salvi B. Pancreaticopleural fistula complicating chronic pancreatitis. BMJ Case Rep. 2012;2012.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 8]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
10.  Sonoda S, Taniguchi M, Sato T, Yamasaki M, Enjoji M, Mae S, Irie T, Ina H, Sumi Y, Inase N, Kobayashi T. Bilateral pleural fluid caused by a pancreaticopleural fistula requiring surgical treatment. Intern Med. 2012;51:2655-2661.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 8]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
11.  Huang TY, Tsai MJ. Education and imaging. Gastrointestinal: black pleural effusion induced by pancreaticopleural fistula. J Gastroenterol Hepatol. 2013;28:1798.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
12.  Okano A, Ohana M, Kusumi F, Nabeshima M. Education and imaging. Hepatobiliary and pancreatic: pancreaticopleural fistula. J Gastroenterol Hepatol. 2013;28:1692.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
13.  Houlihan MD, Bowyer BA, Barclay RL. Resolution of pancreatico-pleural fistula with endoscopic ultrasound-guided therapy. Respir Med Case Rep. 2013;9:30-33.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 3]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
14.  Tay CM, Chang SK. Diagnosis and management of pancreaticopleural fistula. Singapore Med J. 2013;54:190-194.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 37]  [Article Influence: 3.4]  [Reference Citation Analysis (0)]
15.  Choe IS, Kim YS, Lee TH, Kim SM, Song KH, Koo HS, Park JH, Pyo JS, Kim JY, Choi IS. Acute mediastinitis arising from pancreatic mediastinal fistula in recurrent pancreatitis. World J Gastroenterol. 2014;20:14997-15000.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 8]  [Cited by in F6Publishing: 9]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
16.  Thyagaraj VK, Rangappa P, Jacob I, Rao K. Recurrent pleural effusions: an unusual presentation of chronic pancreatitis. J Assoc Physicians India. 2014;62:627-630.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Soares JT, Ressurreição J, Marques I, Batista L, Pereira T, Mendes M. Pancreatopleural fistula contributing to a large volume recurrent pleural effusion. Rev Port Pneumol (2006). 2015;21:163-164.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 2]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
18.  Francisco E, Mendes M, Vale S, Ferreira J. Pancreaticopleural fistula: an unusual complication of pancreatitis. BMJ Case Rep. 2015;2015.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 9]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
19.  Hirosawa T, Shimizu T, Isegawa T, Tanabe M. Left pleural effusion caused by pancreaticopleural fistula with a pancreatic pseudocyst. BMJ Case Rep. 2016;2016.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 6]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
20.  Sánchez A, Ramírez de la Piscina P, Duca IM, Estrada S, Salvador M, Campos A, Ganchegui I, Urtasun L, Delgado E, García Campos F, Pérez Miranda M. [Right pleural effusion secondary to a pancreaticopleural fistula in a patient with asymptomatic chronic pancreatitis]. Gastroenterol Hepatol. 2016;39:529-531.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 2]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
21.  Chan EE, Shelat VG. Pancreaticopleural Fistula Causing Massive Right Hydrothorax and Respiratory Failure. Case Rep Surg. 2016;2016:8294056.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 7]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
22.  Abdalla S, Nikolopoulos I, Kerwat R. Pancreatic Pseudocyst Pleural Fistula in Gallstone Pancreatitis. Case Rep Emerg Med. 2016;2016:4269424.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 3]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
23.  Virgilio E, Mercantini P, Catta F, Grieco M, Cavallini M, Ferri M. Pancreaticopleural Fistula. Surg Infect (Larchmt). 2016;17:266-267.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 4]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
24.  Bustamante Bernal MA, Gonzalez Martinez JL, Ortiz A, Zuckerman MJ. Recurrent Pleural Effusion Secondary to a Pancreatic-Pleural Fistula Treated Endoscopically. Am J Case Rep. 2017;18:750-753.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 4]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
25.  Vijaykumar K, Dsouza KG, Lerner L. Pancreaticopleural Fistula: The Formidable Liaison. J Bronchology Interv Pulmonol. 2017;24:e60-e61.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
26.  Kord Valeshabad A, Acostamadiedo J, Xiao L, Mar W, Xie KL. Pancreaticopleural Fistula: A Review of Imaging Diagnosis and Early Endoscopic Intervention. Case Rep Gastrointest Med. 2018;2018:7589451.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 10]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
27.  Daza Fernández ML, Cuevas López L. Surgical management of pancreaticopleural fistula with video-assisted retroperitoneal pancreatic debridement: A case report. Int J Surg Case Rep. 2020;66:16-20.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
28.  Chawla G, Niwas R, Chauhan NK, Dutt N, Yadav T, Jain P. Pancreatic pleural effusion masquerading as right sided tubercular pleural effusion. Monaldi Arch Chest Dis. 2019;89.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
29.  Ramahi A, Aburayyan KM, Said Ahmed TS, Rohit V, Taleb M. Pancreaticopleural Fistula: A Rare Presentation and a Rare Complication. Cureus. 2019;11:e4984.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 4]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
30.  Li HM, Zhao SY, Zhou J, Zeng Q, Zeng JJ, Jiang ZF. [Recurrent massive bloody pleural effusion caused by pancreatic pleural fistula in a case]. Zhonghua Er Ke Za Zhi. 2009;47:621-623.  [PubMed]  [DOI]  [Cited in This Article: ]
31.  Ozbek S, Gumus M, Yuksekkaya HA, Batur A. An unexpected cause of pleural effusion in paediatric emergency medicine. BMJ Case Rep. 2013;2013.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 10]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
32.  Altasan T, Aljehani Y, Almalki A, Algamdi S, Talag A, Alkattan K. Pancreaticopleural fistula: an overlooked entity. Asian Cardiovasc Thorac Ann. 2014;22:98-101.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 12]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
33.  Zhang LL, Wu YL, Zhang HL, Zhang ZR, Xie XZ. [Polypnea-emaciation-hemorrhagic pleural effusion-pancreatic pleural fistula]. Zhonghua Yixue Zazhi. 2014;94:3681-3682.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Chen B, Mao J, Cheng JM, Xiong S, Xu X. [Two cases of pancreatic pleural fistula in children with massive pleural effusion as the first symptom]. Zhonghua Fangshexue Zazhi. 2014;48:606-607.  [PubMed]  [DOI]  [Cited in This Article: ]
35.  Daib A, Hellal Y, Boughdir M, Abdallah RB, Kaabar N. [Pancreatic-pleural fistula in children: a rare cause of great abundant pleurisy]. Pan Afr Med J. 2017;26:240.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 1]  [Article Influence: 0.1]  [Reference Citation Analysis (0)]
36.  Yu Y, Yu Z, Huang X. A rare case of pediatric pleural effusion: Pancreaticopleural fistula. Pediatr Pulmonol. 2019;54:5-6.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
37.  Zhuang LL, Gong HH. [A case of pancreatic pleural fistula and literature review]. Jiangsu Yiyao. 2018;44:973-976.  [PubMed]  [DOI]  [Cited in This Article: ]
38.  Lee D, Lee EJ, Kim JW, Moon JS, Kim YT, Ko JS. Endoscopic Management of Pancreaticopleural Fistula in a Child with Hereditary Pancreatitis. Pediatr Gastroenterol Hepatol Nutr. 2019;22:601-607.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
39.  Yu ZX, Yu YP, Huang XM. [Massive hemorrhagic pleural effusion caused by pancreaticopleural fistula in children: a case report and literature review]. Linchuang Erke Zazhi. 2019;37:427-431.  [PubMed]  [DOI]  [Cited in This Article: ]
40.  Liu XY, Li YL. [A case of pleural effusion caused by chronic pancreatic pleural fistula]. Linchuang Neike Zazhi. 2019;36:172-173.  [PubMed]  [DOI]  [Cited in This Article: ]
41.  Cameron JL, Kieffer RS, Anderson WJ, Zuidema GD. Internal pancreatic fistulas: pancreatic ascites and pleural effusions. Ann Surg. 1976;184:587-593.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 117]  [Cited by in F6Publishing: 119]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
42.  Lipsett PA, Cameron JL. Internal pancreatic fistula. Am J Surg. 1992;163:216-220.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 90]  [Cited by in F6Publishing: 91]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
43.  Lerner A, Branski D, Lebenthal E. Pancreatic diseases in children. Pediatr Clin North Am. 1996;43:125-156.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 58]  [Cited by in F6Publishing: 57]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
44.  Mihai C, Floria M, Vulpoi R, Nichita L, Cijevschi Prelipcean C, Drug V, Scripcariu V. Pancreatico-Pleural Fistula - from Diagnosis to Management. A Case Report. J Gastrointestin Liver Dis. 2018;27:465-469.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 5]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
45.  Oh YS, Edmundowicz SA, Jonnalagadda SS, Azar RR. Pancreaticopleural fistula: report of two cases and review of the literature. Dig Dis Sci. 2006;51:1-6.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 34]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
46.  Singh S, Yakubov M, Arya M. The unusual case of dyspnea: a pancreaticopleural fistula. Clin Case Rep. 2018;6:1020-1022.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 7]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
47.  Cazzo E, Apodaca-Rueda M, Gestic MA, Chaim FHM, Saito HPA, Utrini MP, Callejas-Neto F, Chaim EA. Management of pancreaticopleural fistulas secondary to chronic pancreatitis. Arq Bras Cir Dig. 2017;30:225-228.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 14]  [Cited by in F6Publishing: 17]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
48.  Anderson WJ, Skinner DB, Zuidema GD, Cameron JL. Chronic pancreatic pleural effusions. Surg Gynecol Obstet. 1973;137:827-830.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 1]  [Article Influence: 0.0]  [Reference Citation Analysis (0)]
49.  Khan AZ, Ching R, Morris-Stiff G, England R, Sherridan MB, Smith AM. Pleuropancreatic fistulae: specialist center management. J Gastrointest Surg. 2009;13:354-358.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 11]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
50.  Pai CG, Suvarna D, Bhat G. Endoscopic treatment as first-line therapy for pancreatic ascites and pleural effusion. J Gastroenterol Hepatol. 2009;24:1198-1202.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 49]  [Cited by in F6Publishing: 42]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
51.  Varadarajulu S, Noone TC, Tutuian R, Hawes RH, Cotton PB. Predictors of outcome in pancreatic duct disruption managed by endoscopic transpapillary stent placement. Gastrointest Endosc. 2005;61:568-575.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 188]  [Cited by in F6Publishing: 173]  [Article Influence: 9.1]  [Reference Citation Analysis (0)]
52.  Vanderbruggen W, Dhooghe V, Bracke B, Hartman V, Roeyen G, Ysebaert D, Van Schil P, Chapelle T. Pancreaticopleural fistula: a rare cause of pleural empyema. Acta Chir Belg. 2019;119:396-399.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]