Skip to main content

Clinical characteristics of acute pancreatitis in children: a single-center experience in Western China

Abstract

Background

The diagnosis of pediatric pancreatitis has been increasing over the last 20 years. We aimed to compare the clinical characteristics for pediatric acute pancreatitis (AP) with adult AP, and investigate the risk factor for acute recurrent pancreatitis (ARP) in children.

Method

From June 2013 to June 2019, a total of 130 pediatric patients with AP at the inpatient database were enrolled. Univariate analysis and multivariate Cox regression analysis were performed to identify the risk factors for ARP in children.

Result

Major etiologic factors in 130 patients were biliary (31.5%), idiopathic (28.5%). The etiology of pancreatitis in children was markedly different from that in adults (p < 0.001). Compared with the adult patients, the pediatric patients had significantly lower severity (p = 0.018) and occurrence rate of pancreatic necrosis (p = 0.041), SIRS (p = 0.021), acute peripancreatic fluid collection (p = 0.014). Univariate and Multivariate Cox regression analysis showed that female (p = 0.020; OR 3.821; 95% CI 1.231–11.861), hypertriglyceridemia (p = 0.045; OR 3.111; 95% CI 1.024–9.447), pancreatic necrosis (p = 0.023; OR 5.768; 95% CI 1.278–26.034) were the independent risk factors of ARP. Hypertriglyceridemia AP had the highest risk of recurrence compared to other etiology (p = 0.035).

Conclusion

Biliary and idiopathic disease were the major etiologies of AP in children. Children have simpler conditions than adults. Female, hypertriglyceridemia, and pancreatic necrosis were associated with the onset of ARP.

Peer Review reports

Background

Acute pancreatitis (AP) is an inflammatory reaction that causes the digestion, edema, bleeding, and necrosis of pancreatic tissue after activation of various trypsin enzymes in pancreatic tissue, caused by a variety of etiologies [1]. Clinically, it is characterized by acute epigastric pain, vomiting, and elevated pancreatic amylase. It has been reported that the incidence of AP in children has increased in the past 20 years [2, 3]. At present, AP is more common in children over five years old, with an incidence of 3/100 000, but its severity is similar in children of all ages [3, 4]. The overall case fatality rate is less than 5% [2, 5]. Compared with adults, there are significant differences in the incidence, etiology, clinical manifestation, and prognosis of AP in children [6]. Therefore, the purpose of this study was to analyze the demographic characteristics, etiology, clinical manifestations, and prognosis of AP, compare to adult AP, and to investigate the risk factors for acute recurrent pancreatitis (ARP) in children in southwest China.

Methods

Ethical approval

This study was approved by the Clinical trial Ethics Committee of the affiliated Hospital of Southwest Medical University (batch number: KY2019054). Informed consent was waived.

Study population

We collected data retrospectively on 130 children with first AP attack from June 2013 to June 2019 at the electronic inpatient database, while patients with relapse of AP or chronic pancreatitis were excluded. The diagnostic criteria for pediatric AP were in accordance with the guidelines of the International Pediatric Pancreatitis Study Group, the European Pancreatic Club, and the Hungarian Pancreatic Group [2, 7, 8]. Pediatric AP can be recognized in patients less than 18 years old, when two of the following three criteria are fulfilled: (1) abdominal pain compatible with AP, (2) serum amylase and/or lipase values ≥ 3 times the upper limits of normal, (3) imaging findings consistent with AP. The clinical classification of AP includes: mild acute pancreatitis (MAP), characterized by the absence of organ failure and local or systemic complications; moderately-severe acute pancreatitis (MSAP), characterized by transient organ failure (< 48 h), or accompanied by local or systemic complications; severe acute pancreatitis (SAP), characterized by persistent organ failure (> 48 h). The local complications include acute peripancreatic fluid collection (APFC), acute necrotic collection (ANC), and pancreatic pseudocyst (PPC). The systemic complications include organ failure, systemic inflammatory response syndrome (SIRS). The organ failure include acute respiratory distress syndrome (ARDS), shock, and acute renal failure (ARF). In addition, acute recurrent pancreatitis (ARP) is characterized by: Requires at least 2 distinct episodes of AP (each as defined above), along with: Complete resolution of pain (≥ 1-month pain-free interval between the diagnoses of AP) or complete normalization of serum pancreatic enzyme levels (amylase and lipase), before the subsequent episode of AP is diagnosed, along with complete resolution of pain symptoms, irrespective of a specific time interval between AP episodes [8]. We enrolled 130 adult patients with first AP attack from the medical record database as the control group using the random number table method. The criteria for adult AP were in accordance with the Atlanta International consensus 2012 [9]. We compared the clinical characteristics between children with AP (child group) and adults with AP (adult group). In order to analysis of the clinical characteristics of AP in children of different ages, patients were divided into two groups: younger and older children group (< 10 years and ≥ 10 years). Based on the follow-up results, we divided 130 children patients into recurrence groups and the non-recurrence group, and analyzed the risk factors associated with ARP in children.

Clinical data collection

Data were collected by researchers who were not informed of the detailed information of the study until collection was completed. The collected data were from computer-based case reports and were checked by another two researchers to ensure that there were no inconsistencies or errors. Basic information on these patients was collected, including age, sex, etiologies, clinical symptoms, laboratory indexes within 24 h of admission (blood amylase, lipase, triglyceride (TG), C-reactive protein (CRP)), imaging findings, complications, and treatment outcome. We retrieved the data of the second AP attack hospitalization in the database for 18 of the 130 children. They were labeled as ARP. We conducted telephone follow-up of 112 patients, an 8-years-old child with traumatic AP was diagnosed with RAP in another hospital due to abdominal pain after the first attack AP discharge 3 months, and the remaining 111 patients without abnormalities. The follow-up period was 1 to 72 months, with a mean time of 34.2 ± 20.8 months, and the median time of follow-up was 32.5 (IQR 16–50.3) months.

Statistical analysis

The data were analyzed using SPSS software version 25.0 (IBM Corporation, Armonk, NY, USA). Continuous variables were described by mean ± standard deviation or median (range) and classified variables by percentages. Comparison of non-normally distributed data and hierarchical data groups used the Mann–Whitney U test. The chi-squared test and Fisher’s exact probability test were employed to complete the univariate analysis. The chi-squared test for trend was used for unidirectional ordered classification, and Goodman–Kruskal gamma analysis was used for variables with bidirectional ordered classification. Univariate and multivariate Cox regression were used determine adjusted odds ratios. A Cox proportional hazards model was used to analyze etiology groups and time to ARP for the whole sample. The cumulative recurrence curve used Kaplan–Meier method through R software version 3.6.0 (https://www.r-project.org) and Log-rank test was used for comparison between groups. The software packages we used during the analysis include survival and survminer. p < 0.05 was considered statistically significant for analyses.

Results

Baseline characteristics

Major etiologic factors in 130 patients were biliary (31.5%)(including 29 cases of bile duct stones, 8 cases of congenital biliary dilatation, 4 cases of biliary tapeworm) and a significant proportion (28.5%) of cases no cause could be found, we label them as idiopathic. In addition, definite causes include trauma (16.2%), viral infection (10%), hyperlipidemia (9.3%)(TG > 11.30 mmol/L in 12 children), and drug-induced (4.6%)(including 5 children were taking dexamethasone and 1 child with leukemia was receiving chemotherapy with Cytarabine). There was a significant difference in the etiological constituent ratio between children and adults (p < 0.001): cases in children were mainly biliary and idiopathic, and those in adults were mainly biliary and hypertriglyceridemia. The severity of AP in the children was milder than that in the adult group (p = 0.018), and the rate of ANC, APFC, SIRS in the children was lower than that in the adult group (all p < 0.05).

Clinical characteristics based on age

AP was more likely to occur in older age groups of children. However, the severity of the disease was independent of the increase in age, and there was no significant difference in sex. There were significant differences in the etiology of different age groups, viral infectious pancreatitis was more likely to occur in younger children, and the older children were usually due to biliary and hypertriglyceridemia (p = 0.013). APFC was more likely to occur in older children (p = 0.024).

Treatment

All patients admitted were given standard medical treatment. Patients received treatment including fasting, early fluid resuscitation, analgesia, and nutritional support. 123 of 130 patients were cured and discharged, 7 patients were improved or discharged for further treatment. 8 of 130 children patients were treated with cholecystectomy, a child was treated with endoscopic retrograde cholangiopancreatography (ERCP). 14 of 130 children patients had pancreatic pseudocysts, 10 patients of which healed after medical treatment, 4 patients underwent pseudocyst drainage.

Risk factors for ARP

Of the 130 children with AP, 19 (14.6%) progressed to ARP during the study period. The mean interval from AP to ARP was 9.5 ± 6.9 months, and the mean age at the second AP attack was 12.1 ± 4.2 years. The recurrence rate increased with an increase in disease severity (p = 0.034). Female sex (p = 0.001), hypertriglyceridemia (p = 0.016), APFC (p = 0.044), and the presence of ANC during the first AP attack (p = 0.040) were significantly correlated with ARP (Table 1).

Table 1 Characteristics of patients in recurrence and non-recurrence groups

COX regression analysis for the above meaningful indicators. Univariate analysis and multivariate Cox regression analysis showed that female sex (p = 0.020; OR = 3.821; 95%CI 1.231–11.861), hypertriglyceridemia (p = 0.045; OR = 3.111; 95%CI 1.024–9.447), and pancreatic necrosis (p = 0.023; OR = 5.768; 95%CI 1.278–26.034) were the independent factors influencing ARP (Table 2).

Table 2 Univariate and Multivariate Cox regression analysis of factors associated with ARP in children

We were also interested in studying the etiology or risk factors associated with the first AP occurrence and their effect on progression to ARP over time for the whole sample. We compared patients with biliary, idiopathic, traumatic, hypertriglyceridemia, viral, and drug-induced AP. We found that hypertriglyceridemia AP had the highest risk of recurrence over time, while viral and drug-induced AP had the lowest risk of recurrence (p = 0.035). (Fig. 1).

Fig. 1
figure1

Risk of acute recurrent pancreatitis (ARP) by etiology

Discussion

In the past ten years, the epidemiology and etiology of pediatric pancreatitis has been greatly developed [10,11,12]. But AP is uncommon in children, and the limited number of examined children in the available, current literature, it seems necessary to plan a multi-center study in order to evaluate the incidence, etiology, natural history, and evaluation of the related risk factors [13]. In this study, the clinical characteristics of AP in children in southwest China were analyzed and summarized. As far as we know, this is the first report in English on the clinical features of AP in children from China.

The etiology of AP in children was significantly different from that in adults, as was found in this cohort. In previous studies, Poddar et al. [14] studied 320 children with AP from India and found that trauma (21%) and biliary tract disease (10%) were the most common causes of AP in children. Park et al. [15] found that the biliary tract (36.2%) and drugs (25.6%) were the leading causes of AP in 215 children in the United States. In another study of 115 children in the United States [16], idiopathic (31%) and drug associated (23%) were the main causes. We found that biliary (31.5%), idiopathic (28.5%) and traumatic (16.2%) were the main causes, which was consistent with most studies. In addition, metabolic problems such as hypertriglyceridemia in children were significantly rarer than in adults. Only 2–7% of children with AP have metabolic causative factors [10, 11]. In this study, 12 cases (9.2%) were caused by hypertriglyceridemia. In the control group of adults, high fat levels accounted for 26.2%, and the difference was significant. The most exciting finding in our study was that viral infectious pancreatitis was more common in young children and the rate was significantly different from that in adults. We consider that is was related to the incomplete development of the immune system in young children. The mechanism of AP related to virus infection is not clear at present, although some research has shown that the virus directly invades pancreatic cells [3]. Although drug-induced pancreatitis has increased significantly in recent years with the widespread use of drugs, it is still constitutes less than 10% of cases [17].

Our study showed that the severity of AP in children was similar in all age groups, which was consistent with a previous report [3], but the disease was less severe than in adults. Possible reasons are: (1) In terms of etiological composition, hyperlipidemia and alcoholic pancreatitis account for few cases in children, and some studies have shown that hyperlipidemia and alcohol can easily lead to SAP [18]; (2) In terms of complications, pancreatic necrosis was positively correlated with the severity and prognosis of the disease. Necrotizing pancreatitis was rare in children. According to the literature [19], necrotizing pancreatitis occurs in less than 1% of children with AP. Among the five large sample pediatric cases reported in the United States [20], only 3 of 1014 children with AP had pancreatic necrosis, which was significantly less severe than that of adults. Our research results also confirmed the above view.

For AP with specific causes, such as bile duct stones, anatomical abnormalities, bile duct dilatation, etc., it has been suggested that surgery should be performed as soon as possible after the condition is controlled and stable, to prevent recurrence [11, 21]. No child died in our research data. In other literature [22], the mortality rate of pediatric AP is less than 5%, which is significantly lower than that of adult AP, possibly because: (1) Alcoholic pancreatitis is rare in pediatric cases, and alcoholic pancreatitis is a known cause of high mortality, with a mortality rate as high as 30.6% [23]. (2) With age, adults may lose some critical protective mechanism, which children retain [6]. (3) Adult cases may be associated with severe underlying diseases, while AP in children is rarely associated with multiple problems with organ function. (4) The severity of the disease in children is significantly lower than that in adults, which has also been confirmed in this study.

Regarding ARP in children, some single-center studies have estimated that 10–35% of children with AP develop ARP [24, 25]. The main driving force behind the progression of acute pancreatitis to recurrent acute and chronic pancreatitis is genetic predisposition [26]. These studies showed that mutations of PRSS1, SPINK1, CFTR, and CTRC13 were firmly related to the progression of ARP. During the first attack of AP in children, age, male sex, pancreatic necrosis, and higher Body Mass Index (BMI) have been associated with the progression of ARP, anatomic abnormalities of the biliary tract, hyperlipidemia, and genetic factors should be evaluated in cases of recurrence [11, 16, 27]. We found that female sex, hypertriglyceridemia, and primary AP with pancreatic necrosis were significantly correlated with ARP, and the severity of primary AP was positively correlated with ARP. The relationship between ARP and sex is controversial and perhaps related to the predominance of hyperlipidemia and biliary tract disease in women [28, 29]. Differences in our findings from those of from previous studies may have resulted from differences in race, region, and environment. Hyperlipidemia is an apparent cause of AP and ARP in adults [30], but there has been no analysis of a large sample of ARP cases in children. It has been reported in the literature that hypertriglyceridemia occurring secondary to AP may be related to various genetic mutations [31]. From this point of view, our findings coincide with previous research results.

The disadvantage of this study was that it was a single-center study. Thus, the findings of this study cannot be generalized. For the 19 patients with ARP, the etiology of recurrence still needs to be examined by ERCP and genetic analysis, and there is a lack of corresponding genetic and clinical data in this study. In future, multi-center studies with a larger sample and more rational perspective are needed to analyze pediatric pancreatitis in order to facilitate better treatment.

Conclusion

Biliary disease and idiopathic cases were the leading causes of AP in children, and, when compared with adults, children tend to have milder disease and a better prognosis. The recurrence rate increased with an increase in disease severity. Female sex, hyperlipidemia, and a first AP attack involving pancreatic necrosis were associated with an increased risk of ARP. Genetic and anatomical factors need to be studied further in children with ARP.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Abbreviations

AP:

Acute pancreatitis

APFC:

Acute peripancreatic fluid collection

ARDS:

Acute respiratory distress syndrome

ARF:

Acute renal failure

ARP:

Acute recurrent pancreatitis

BMI:

Body Mass Index

CRP:

C-reactive protein

ERCP:

Endoscopic retrograde cholangiopancreatography

IQR:

Interquartile range

MAP:

Mild acute pancreatitis

MASP:

Moderately-severe acute pancreatitis

SAP:

Severe acute pancreatitis

SIRS:

Systemic inflammatory response syndrome

TG:

Triglyceride

References

  1. 1.

    Crockett SD, Wani S, Gardner TB, Falck-Ytter Y, Barkun AN, Crockett S, et al. American gastroenterological association institute guideline on initial management of acute pancreatitis. Gastroenterology. 2018;154(4):1096–101.

    Article  Google Scholar 

  2. 2.

    Abu-El-Haija M, Kumar S, Quiros JA, Balakrishnan K, Barth B, Bitton S, et al. Management of acute pancreatitis in the pediatric population: a clinical report from the North American society for pediatric gastroenterology, hepatology and nutrition pancreas committee. J Pediatr Gastroenterol Nutr. 2018;66(1):159–76.

    Article  Google Scholar 

  3. 3.

    Husain SZ, Srinath AI. What’s unique about acute pancreatitis in children: risk factors, diagnosis and management. Nat Rev Gastroenterol Hepatol. 2018;14(6):366–72.

    Article  Google Scholar 

  4. 4.

    Chang YJ, Chao HC, Kong MS, Hsia SH, Lai MW, Yan DC. Acute pancreatitis in children. Acta Paediatr. 2011;100(5):740–4.

    Article  Google Scholar 

  5. 5.

    Abu-El-Haija M, El-Dika S, Hinton A, Conwell DL. Acute pancreatitis admission trends: a national estimate through the kids’ inpatient database. J Pediatr. 2018;194:147–51.

    Article  Google Scholar 

  6. 6.

    Bai HX, Lowe ME, Husain SZ. What have we learned about acute pancreatitis in children? J Pediatr Gastroenterol Nutr. 2011;52(3):262–70.

    Article  Google Scholar 

  7. 7.

    Parniczky A, Abu-El-Haija M, Husain S, Lowe M, Oracz G, Sahin-Toth M, et al. EPC/HPSG evidence-based guidelines for the management of pediatric pancreatitis. Pancreatology. 2018;18(2):146–60.

    Article  Google Scholar 

  8. 8.

    Morinville VD, Husain SZ, Bai H, Barth B, Alhosh R, Durie PR, et al. Definitions of pediatric pancreatitis and survey of present clinical practices. J Pediatr Gastroenterol Nutr. 2012;55(3):261–5.

    Article  Google Scholar 

  9. 9.

    Gress TM, El-Omar EM. Revision of the Atlanta classification of acute pancreatitis: the editorial perspective. Gut. 2013;62(1):1.

    Article  Google Scholar 

  10. 10.

    Restrepo R, Hagerott HE, Kulkarni S, Yasrebi M, Lee EY. Acute pancreatitis in pediatric patients: demographics, etiology, and diagnostic imaging. AJR Am J Roentgenol. 2016;206(3):632–44.

    Article  Google Scholar 

  11. 11.

    Grzybowska-Chlebowczyk U, Jasielska M, Flak-Wancerz A, Wiecek S, Gruszczynska K, Chlebowczyk W, et al. Acute pancreatitis in children. Prz Gastroenterol. 2018;13(1):69–75.

    PubMed  Google Scholar 

  12. 12.

    Pant C, Deshpande A, Sferra TJ, Gilroy R, Olyaee M. Emergency department visits for acute pancreatitis in children: results from the Nationwide Emergency Department Sample 2006–2011. J Investig Med. 2015;63(4):646–8.

    Article  Google Scholar 

  13. 13.

    Majbar AA, Cusick E, Johnson P, Lynn RM, Hunt LP, Shield JP. Incidence and clinical associations of childhood acute pancreatitis. Pediatrics. 2016;138(3).

  14. 14.

    Poddar U, Yachha SK, Borkar V, Srivastava A, Kumar S. A report of 320 cases of childhood pancreatitis: increasing incidence, etiologic categorization, dynamics, severity assessment, and outcome. Pancreas. 2017;46(1):110–5.

    Article  Google Scholar 

  15. 15.

    Park A, Latif SU, Shah AU, Tian J, Werlin S, Hsiao A, et al. Changing referral trends of acute pancreatitis in children: A 12-year single-center analysis. J Pediatr Gastroenterol Nutr. 2009;49(3):316–22.

    Article  Google Scholar 

  16. 16.

    Sweeny KF, Lin TK, Nathan JD, Denson LA, Husain SZ, Hornung L, et al. Rapid progression of acute pancreatitis to acute recurrent pancreatitis in children. J Pediatr Gastroenterol Nutr. 2019;68(1):104–9.

    Article  Google Scholar 

  17. 17.

    Ksiadzyna D. Drug-induced acute pancreatitis related to medications commonly used in gastroenterology. Eur J Intern Med. 2011;22(1):20–5.

    CAS  Article  Google Scholar 

  18. 18.

    Zhu Y, Pan X, Zeng H, He W, Xia L, Liu P, et al. A study on the etiology, severity, and mortality of 3260 patients with acute pancreatitis according to the revised Atlanta classification in Jiangxi, china over an 8-year period. Pancreas. 2017;46(4):504–9.

    Article  Google Scholar 

  19. 19.

    Raizner A, Phatak UP, Baker K, Patel MG, Husain SZ, Pashankar DS. Acute necrotizing pancreatitis in children. J Pediatr. 2013;162(4):788–92.

    Article  Google Scholar 

  20. 20.

    Park AJ, Latif SU, Ahmad MU, Bultron G, Orabi AI, Bhandari V, et al. A comparison of presentation and management trends in acute pancreatitis between infants/toddlers and older children. J Pediatr Gastroenterol Nutr. 2010;51(2):167–70.

    CAS  Article  Google Scholar 

  21. 21.

    Alabdulkareem A, Almahmoud T, Al-Tahan H, Javad S, Al HM. Etiology and clinical characteristics of pediatric acute pancreatitis in Saudi Arabia: a 20-year experience from a single tertiary center. Int J Pediatr Adolesc Med. 2018;5(1):13–7.

    Article  Google Scholar 

  22. 22.

    Uc A, Husain SZ. Pancreatitis in children. Gastroenterology. 2019;156(7):1969–78.

    Article  Google Scholar 

  23. 23.

    Karjula H, Saarela A, Ohtonen P, Ala-Kokko T, Mäkelä J, Liisanantti JH. Long-term outcome and causes of death for working-age patients hospitalized due to acute pancreatitis with a median follow-up of 10 years. Ann Surg. 2019;269(5):932–6.

    Article  Google Scholar 

  24. 24.

    Kumar S, Ooi CY, Werlin S, Abu-El-Haija M, Barth B, Bellin MD, et al. Risk factors associated with pediatric acute recurrent and chronic pancreatitis. JAMA Pediatr. 2016;170(6):562–9.

    Article  Google Scholar 

  25. 25.

    Pant C, Sferra TJ, Lee BR, Cocjin JT, Olyaee M. Acute recurrent pancreatitis in children: a study from the pediatric health information system. J Pediatr Gastroenterol Nutr. 2016;62(3):450–2.

    Article  Google Scholar 

  26. 26.

    Poddar U, Yachha SK, Mathias A, Choudhuri G. Genetic predisposition and its impact on natural history of idiopathic acute and acute recurrent pancreatitis in children. Dig Liver Dis. 2015;47(8):709–14.

    Article  Google Scholar 

  27. 27.

    Abu-El-Haija M, Valencia CA, Hornung L, Youssef N, Thompson T, Barasa NW, et al. Genetic variants in acute, acute recurrent and chronic pancreatitis affect the progression of disease in children. Pancreatology. 2019;19(4):535.

    Article  Google Scholar 

  28. 28.

    Xu T, Liu J, Liu J, Zhu G, Han S. Relation between metabolic syndrome and body compositions among Chinese adolescents and adults from a large-scale population survey. BMC Public Health. 2017;17(1).

  29. 29.

    Sarrami M, Ridley W, Nightingale S, Wright T, Kumar R. Adolescent gallstones-need for early intervention in symptomatic idiopathic gallstones. Pediatr Surg Int. 2019;35(5):569–74.

    CAS  Article  Google Scholar 

  30. 30.

    Scherer J, Singh VP, Pitchumoni CS, Yadav D. Issues in hypertriglyceridemic pancreatitis: an update. J Clin Gastroenterol. 2014;48(3):195–203.

    CAS  Article  Google Scholar 

  31. 31.

    Jin JL, Sun D, Cao YX, Zhang HW, Guo YL, Wu NQ, et al. Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis. EBioMedicine. 2018;38:171–7.

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This study is independent research funded by the following grants: Medical science and technology plan projects of Zhejiang Province (No. 2017196257), Youth Foundation of Southwest Medical University (No. 0903–00031099), Doctoral research start-up funding project of Affiliated Hospital of Southwest Medical University (No. 16229).

Author information

Affiliations

Authors

Contributions

Study conception and design: XWT, YP, MHL. Drafting of manuscript: RZ and SLT. Acquisition of data and critical revision: HX, XJ, YFY. Revision of manuscript, and final approval of manuscript: LL and XWT. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Li Liu or Xiaowei Tang.

Ethics declarations

Ethics approval and consent to participate

This study was conducted according to the Declaration of Helsinki and approved by the Clinical trial Ethics Committee of the affiliated Hospital of Southwest Medical University (batch number: KY2019054). Informed consent by verbal was obtained from all participants approved by the ethics committee.

Consent for publication

Not Applicable.

Competing interests

The authors declare that they have no conflict of interest.

Additional information

Publisher's Note

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

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zhong, R., Tan, S., Peng, Y. et al. Clinical characteristics of acute pancreatitis in children: a single-center experience in Western China. BMC Gastroenterol 21, 116 (2021). https://doi.org/10.1186/s12876-021-01706-8

Download citation

Keywords

  • Acute pancreatitis
  • Acute recurrent pancreatitis
  • Child
  • Etiology