Cited by 7,187Pancreatitis Pathology and TreatmentGallbladder and Bile Duct DisordersPancreatic and Hepatic Oncology Research

The DOI matches its Crossref record; 75 of the 77 references it cites were found in a registry or an index.

Classification of acute pancreatitis—2012: revision of the Atlanta classification and definitions by international consensus

Open access

Banks, Peter A, Bollen, Thomas L, Dervenis, Christos, Gooszen, Hein G, Johnson, Colin D, Sarr, Michael G, Tsiotos, Gregory G, Vege, Santhi Swaroop·2013·Gut

DOI 10.1136/gutjnl-2012-302779

Open this paper in CoChat — free account Open PDF

Abstract

BACKGROUND AND OBJECTIVE: The Atlanta classification of acute pancreatitis enabled standardised reporting of research and aided communication between clinicians. Deficiencies identified and improved understanding of the disease make a revision necessary. METHODS: A web-based consultation was undertaken in 2007 to ensure wide participation of pancreatologists. After an initial meeting, the Working Group sent a draft document to 11 national and international pancreatic associations. This working draft was forwarded to all members. Revisions were made in response to comments, and the web-based consultation was repeated three times. The final consensus was reviewed, and only statements based on published evidence were retained. RESULTS: The revised classification of acute pancreatitis identified two phases of the disease: early and late. Severity is classified as mild, moderate or severe. Mild acute pancreatitis, the most common form, has no organ failure, local or systemic complications and usually resolves in the first week. Moderately severe acute pancreatitis is defined by the presence of transient organ failure, local complications or exacerbation of co-morbid disease. Severe acute pancreatitis is defined by persistent organ failure, that is, organ failure >48 h. Local complications are peripancreatic fluid collections, pancreatic and peripancreatic necrosis (sterile or infected), pseudocyst and walled-off necrosis (sterile or infected). We present a standardised template for reporting CT images. CONCLUSIONS: This international, web-based consensus provides clear definitions to classify acute pancreatitis using easily identified clinical and radiologic criteria. The wide consultation among pancreatologists to reach this consensus should encourage widespread adoption.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1136/gutjnl-2012-302779

Cites

75 of 75 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure: On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine (see contributors to the project in the appendix)
Vincent, J. L., Moreno, R., Takala, J., Willatts, S., De Mendonça, A., Bruining, H., Reinhart, C. K., Suter, P. M., & Thijs, L. G. (1996) · Intensive Care Medicine · doi:10.1007/bf01709751 · Cited by 11,674
AGREE II: advancing guideline development, reporting and evaluation in health care
Brouwers, M. C., Kho, M. E., Browman, G. P., Burgers, J. S., Cluzeau, F., Feder, G., Fervers, B., Graham, I. D., Grimshaw, J., Hanna, S. E., et al. (2010) · Canadian Medical Association Journal · doi:10.1503/cmaj.090449 · Cited by 3,790
A Clinically Based Classification System for Acute Pancreatitis
Bradley, E. L. (1993) · Archives of Surgery · doi:10.1001/archsurg.1993.01420170122019 · Cited by 2,748
Multiple Organ Dysfunction Score
Marshall, J. C., Cook, D. J., Christou, N. V., Bernard, G. R., Sprung, C. L., & Sibbald, W. J. (1995) · Critical Care Medicine · doi:10.1097/00003246-199510000-00007 · Cited by 2,539
American College of Gastroenterology guideline: management of acute pancreatitis
Tenner, S., Baillie, J., DeWitt, J., & Vege, S. S. (2013) · American Journal of Gastroenterology · doi:10.1038/ajg.2013.218 · Cited by 2,327
Self-citation
Practice guidelines in acute pancreatitis
Banks, P. A., Freeman, M. L., & the Practice Parameters Committee of the American College of Gastroenterology (2006) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2006.00856.x · Cited by 2,050
Self-citation
A Step-up Approach or Open Necrosectomy for Necrotizing Pancreatitis
van Santvoort, H. C., Besselink, M. G., Bakker, O. J., Hofker, H. S., Boermeester, M. A., Dejong, C. H. C., van Goor, H., Schaapherder, A. F., van Eijck, C. H. J., Bollen, T. L., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa0908821 · Cited by 1,713
Self-citation
Acute pancreatitis: value of CT in establishing prognosis.
Balthazar, E. J., Robinson, D. L., Megibow, A. J., & Ranson, J. H. C. (1990) · Radiology · doi:10.1148/radiology.174.2.2296641 · Cited by 1,682
Clinical practice guidelines : directions for a new program
Field, M. J., & Lohr, K. N. (1990) · Cited by 1,415
Probiotic prophylaxis in predicted severe acute pancreatitis: a randomised, double-blind, placebo-controlled trial
Besselink, M. G., van Santvoort, H. C., Buskens, E., Boermeester, M. A., van Goor, H., Timmerman, H. M., Nieuwenhuijs, V. B., Bollen, T. L., van Ramshorst, B., Witteman, B. J., et al. (2008) · The Lancet · doi:10.1016/s0140-6736(08)60207-x · Cited by 1,367
Self-citation

Show all 77 references

Research works printed but not linked: 2

Sakorafas GH, Tsiotos GG, Sarr MG. Extrapancreatic necrotizing pancreatitis with viable pancreas: a previously under- appreciated entity. J Am Coll Surg 1999;188:643-8. [CrossRef] [Medline]
Bradley EL III.. Atlanta redux. Pancreas 2003;26:105-6. [CrossRef] [Medline]

Sorted by citations

Items 801–900 of 1,002

Trends and recent developments in pharmacotherapy of acute pancreatitis
Hey‐Hadavi, J., Velisetty, P., & Mhatre, S. (2022) · Postgraduate Medicine · doi:10.1080/00325481.2022.2136390 · Cited by 39
Glucocorticoid Treatment in Acute Respiratory Distress Syndrome: An Overview on Mechanistic Insights and Clinical Benefit
Zhang, J., Ge, P., Liu, J., Luo, Y., Guo, H., Zhang, G., Xu, C., & Chen, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512138 · Cited by 40
A study of radiological scoring system evaluating extrapancreatic inflammation with conventional radiological and clinical scores in predicting outcomes in acute pancreatitis.
Sharma, V., Rana, S. S., Sharma, R. K., Kang, M., Gupta, R., & Bhasin, D. K. (2015) · PubMed Central · Cited by 39
Clinical evaluation of endoscopic ultrasonography-guided drainage using a novel flared-type biflanged metal stent for pancreatic fluid collection
Mukai, S., Itoi, T., Sofuni, A., Tsuchiya, T., Gotoda, T., & Moriyasu, F. (2015) · Endoscopic Ultrasound · doi:10.4103/2303-9027.156738 · Cited by 39
Frequency and prognosis of acute pancreatitis associated with acute hepatitis E: A systematic review
Haffar, S., Bazerbachi, F., Garg, S. K., Lake, J. R., & Freeman, M. L. (2015) · Pancreatology · doi:10.1016/j.pan.2015.05.460 · Cited by 39
Reduced lymphocyte count as an early marker for predicting infected pancreatic necrosis
Shen, X., Sun, J., Ke, L., Zou, L., Li, B., Tong, Z., Li, W., Li, N., & Li, J. (2015) · BMC Gastroenterology · doi:10.1186/s12876-015-0375-2 · Cited by 39
Clinical outcomes of combined necrotizing pancreatitis versus extrapancreatic necrosis alone
Wang, M., Wei, A., Guo, Q., Zhang, Z., Lü, H., Li, A., & Hu, W. (2015) · Pancreatology · doi:10.1016/j.pan.2015.10.010 · Cited by 39
Serum Concentrations of Angiopoietin-2 and Soluble fms-Like Tyrosine Kinase 1 (sFlt-1) Are Associated with Coagulopathy among Patients with Acute Pancreatitis
Dumnicka, P., Kuśnierz‐Cabala, B., Sporek, M., Mazur-Laskowska, M., Gil, K., Kuźniewski, M., Ceranowicz, P., Warzecha, Z., DEMBINSKI, A. B., Bonior, J., et al. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18040753 · Cited by 39
Molecular mechanisms of alcohol associated pancreatitis
Clemens, D. L., Wells, M. A., Schneider, K. J. M., & Singh, S. (2014) · World Journal of Gastrointestinal Pathophysiology · doi:10.4291/wjgp.v5.i3.147 · Cited by 39
Early prediction of persistent organ failure by serum apolipoprotein A-I and high-density lipoprotein cholesterol in patients with acute pancreatitis
Zhou, C., Zhang, C., Zhao, X., Chen, S.-H., Liang, H.-J., Hu, C.-L., & Chen, N. (2017) · Clinica Chimica Acta · doi:10.1016/j.cca.2017.11.028 · Cited by 39
Correlations of Inflammatory Factors with Intestinal Flora and Gastrointestinal Incommensurate Symptoms in Children with Asthma
Zhang, Y., Li, T., Yuan, H., Pan, W. D., & Dai, Q. (2018) · Medical Science Monitor · doi:10.12659/msm.910854 · Cited by 39
Usefulness of urinary trypsinogen-2 and trypsinogen activation peptide in acute pancreatitis: A multicenter study in Japan
Yasuda, H., Kataoka, K., Takeyama, Y., Takeda, K., Ito, T., Mayumi, T., Isaji, S., Mine, T., Kitagawa, M., Kiriyama, S., et al. (2019) · World Journal of Gastroenterology · doi:10.3748/wjg.v25.i1.107 · Cited by 39
Impact of visceral adiposity on severity of acute pancreatitis: a propensity score-matched analysis
Xie, J., Xu, L., Pan, Y., Liu, Y., Liu, Y., Pan, Y., & Xu, L. (2019) · BMC Gastroenterology · doi:10.1186/s12876-019-1015-z · Cited by 39
Precision medicine for acute pancreatitis: current status and future opportunities
Mukherjee, R., Nunes, Q. M., Huang, W., & Sutton, R. (2019) · Precision Clinical Medicine · doi:10.1093/pcmedi/pbz010 · Cited by 39
Adverse clinical outcomes associated with multidrug-resistant organisms in patients with infected pancreatic necrosis
Ning, C., Huang, G., Shen, D., Bonsu, A. A. F. K., Ji, L., Lin, C., Cao, X., & Li, J. (2019) · Pancreatology · doi:10.1016/j.pan.2019.09.008 · Cited by 39
CT imaging, classification, and complications of acute pancreatitis
Fung, C. I., Svystun, O., Fouladi, D. F., & Kawamoto, S. (2019) · Abdominal Radiology · doi:10.1007/s00261-019-02236-4 · Cited by 39
Inflammatory capacity of exosomes released in the early stages of acute pancreatitis predicts the severity of the disease
Carrascal, M., Areny‐Balagueró, A., de‐Madaria, E., Cárdenas‐Jaén, K., García‐Rayado, G., Rivera, R., Martín‐Mateos, R., Pascual, I., Gironella, M., Abián, J., et al. (2021) · The Journal of Pathology · doi:10.1002/path.5811 · Cited by 39
Therapeutic anticoagulation for splanchnic vein thrombosis in acute pancreatitis: A systematic review and meta-analysis
Sissingh, N. J., Groen, J. V., Koole, D., Klok, F. A., Boekestijn, B., Bollen, T. L., van Santvoort, H. C., Verdonk, R. C., Bonsing, B. A., van Eijck, C. H. J., et al. (2021) · Pancreatology · doi:10.1016/j.pan.2021.12.008 · Cited by 41
Self-citation
Changing management of gallstone-related disease in pregnancy – a retrospective cohort analysis
Hedström, J., Nilsson, J., Andersson, R. E., & Andersson, B. (2017) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365521.2017.1333627 · Cited by 39
Colonic interleukin‐22 protects intestinal mucosal barrier and microbiota abundance in severe acute pancreatitis
Jin, M., Zhang, H., Wu, M., Wang, Z., Chen, X., Guo, M., Zhou, R., Yang, H., & Qian, J. (2022) · The FASEB Journal · doi:10.1096/fj.202101371r · Cited by 38
Understanding Necroptosis in Pancreatic Diseases
He, R., Wang, Z., Dong, S., Chen, Z., & Zhou, W. (2022) · Biomolecules · doi:10.3390/biom12060828 · Cited by 38
Risk Factors and Outcome of Splanchnic venous thrombosis in Patients with necrotizing acute pancreatitis
Zhou, J., Ke, L., Tong, Z., Li, G., Li, W., Li, N., & Li, J. (2014) · Thrombosis Research · doi:10.1016/j.thromres.2014.10.021 · Cited by 38
Current concepts of the role of abdominal compartment syndrome in acute pancreatitis – An opportunity or merely an epiphenomenon
Trikudanathan, G., & Vege, S. S. (2014) · Pancreatology · doi:10.1016/j.pan.2014.06.002 · Cited by 38
Self-citation
Analysis of risk factors related to gastrointestinal fistula in patients with severe acute pancreatitis: a retrospective study of 344 cases in a single Chinese center
Hua, Z., Su, Y., Huang, X., Zhang, K., Yin, Z., Wang, X., & Liu, P. (2017) · BMC Gastroenterology · doi:10.1186/s12876-017-0587-8 · Cited by 38
Inflammatory mediators in the diagnosis and treatment of acute pancreatitis: pentraxin-3, procalcitonin and myeloperoxidase
Şimşek, O., Kocael, A., Kocael, A., Orhan, A., Cengız, M., Balcı, H., Ulualp, K. M., & Uzun, H. (2018) · Archives of Medical Science · doi:10.5114/aoms.2016.57886 · Cited by 38
Accelerating the Drug Delivery Pipeline for Acute and Chronic Pancreatitis
Abu‐El‐Haija, M. A., Gukovskaya, A. S., Andersen, D. K., Gardner, T. B., Hegyi, P. J., Pandol, S. J., Papachristou, G. I., Saluja, A. K., Singh, V. K., Uç, A., et al. (2018) · Pancreas · doi:10.1097/mpa.0000000000001175 · Cited by 38
Therapeutic EUS: New tools, new devices, new applications
Braden, B., Gupta, V., & Dietrich, C. F. (2019) · Endoscopic Ultrasound · doi:10.4103/eus.eus_39_19 · Cited by 38
Hypertriglyceridemia-Related Pancreatitis In Patients With Type 2 Diabetes: Links And Risks
Shemesh, E., & Zafrir, B. (2019) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s188856 · Cited by 38
Imaging guidelines for acute pancreatitis: when and when not to image
Rocha, A. P. C., Schawkat, K., & Mortelé, K. J. (2019) · Abdominal Radiology · doi:10.1007/s00261-019-02319-2 · Cited by 38
Current evidence on pancreatic involvement in SARS-CoV-2 infection
Thaweerat, W. (2020) · Pancreatology · doi:10.1016/j.pan.2020.05.015 · Cited by 38
Deceased serum bilirubin and albumin levels in the assessment of severity and mortality in patients with acute pancreatitis
Xu, X., Ai, F., & Huang, M. (2020) · International Journal of Medical Sciences · doi:10.7150/ijms.49606 · Cited by 38
Splanchnic Vein Thrombosis in Acute Pancreatitis and Its Consequences
Nawacki, Ł., Matykiewicz, J., Stochmal, E., & Głuszek, S. (2021) · Clinical and Applied Thrombosis/Hemostasis · doi:10.1177/10760296211010260 · Cited by 38
Automated Machine Learning for the Early Prediction of the Severity of Acute Pancreatitis in Hospitals
Yin, M., Zhang, R., Zhou, Z., Liu, L., Gao, J., Xu, W., Yu, C., Lin, J., Liu, X., Xu, C., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.886935 · Cited by 38
The role of pancreatic ducts in the pathogenesis of acute pancreatitis
Hegyi, P. J., & Rakonczay, Z. (2015) · Pancreatology · doi:10.1016/j.pan.2015.03.010 · Cited by 38
‘Step‐port’ laparoscopic cystgastrostomy for the management of organized solid predominant post‐acute fluid collections after severe acute pancreatitis
Gibson, S. C., Robertson, B. F., Dickson, E. J., McKay, C. J., & Carter, C. R. (2013) · HPB · doi:10.1111/hpb.12099 · Cited by 38
Laparoscopic approach in gastrointestinal emergencies
Rodríguez, R. M. J., Segura‐Sampedro, J. J., Cortés, M. F., López-Bernal, F., Martín-García, C., Díaz, V. P., Pareja-Ciuró, F., & Ruiz, F. J. P. (2016) · World Journal of Gastroenterology · doi:10.3748/wjg.v22.i9.2701 · Cited by 38
Increased Interleukin-23/17 Axis and C-reactive Protein Are Associated With Severity of Acute Pancreatitis in Patients
Jia, R., Tang, M., Qiu, L., Sun, R., Cheng, L., Ma, X., Yin, G., Hu, G., Wang, X., & Zhao, Y. F. (2014) · Pancreas · doi:10.1097/mpa.0000000000000284 · Cited by 38
Management of (Peri)Pancreatic Collections in Acute Pancreatitis
Bezmarević, M., van Dijk, S. M., Voermans, R. P., van Santvoort, H. C., Besselink, M. G., & Dutch Pancreatitis Study Group (2019) · Visceral Medicine · doi:10.1159/000499631 · Cited by 38
Prognostic value of the creatinine-albumin ratio in acute pancreatitis debridement
Zhao, Z., Yu, Y., Xie, R., Yang, K., Xu, D., Li, L., Lin, J., Zheng, L., Zhang, C., Xu, X., et al. (2020) · BMC Surgery · doi:10.1186/s12893-020-00991-6 · Cited by 37
Risk factors associated with intolerance to enteral nutrition in moderately severe acute pancreatitis: A retrospective study of 568 patients
Tian, F., Li, H., & Yang, Z. (2019) · Saudi Journal of Gastroenterology · doi:10.4103/sjg.sjg_550_18 · Cited by 37
Quantitative metabolic analysis of plasma extracellular vesicles for the diagnosis of severe acute pancreatitis
Lou, D., Shi, K., Li, H., Zhu, Q., Hu, L., Luo, J., Yang, R., & Liu, F. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01239-6 · Cited by 38
Machine learning for the prediction of post-ERCP pancreatitis risk: A proof-of-concept study
Archibugi, L., Ciarfaglia, G., Cárdenas‐Jaén, K., Poropat, G., Korpela, T., Maisonneuve, P., Aparicio, J. R., Casellas, J. A., Arcidiacono, P. G., Mariani, A., et al. (2022) · Digestive and Liver Disease · doi:10.1016/j.dld.2022.10.005 · Cited by 37
Bile acid metabolomics identifies chenodeoxycholic acid as a therapeutic agent for pancreatic necrosis
Zhu, Q., Yuan, C., Dong, X., Wang, Y., Li, B., Tu, B., Chen, W., Xu, X., Gong, W., Xiao, W., et al. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101304 · Cited by 37
Analysis of the clinical profile and treatment efficiency of hyperlipidemic acute pancreatitis
Zhou, W., Liu, Q., Wang, Z., Yao, L., Chen, J., & Yang, X. (2024) · Lipids in Health and Disease · doi:10.1186/s12944-024-02057-5 · Cited by 37
Pancreatic Morphology, Immunology, and the Pathogenesis of Acute Pancreatitis
Mihoc, T., Latcu, S. C., Secasan, C.-C., Dema, V., Cumpănaş, A. A., Șelaru, M., Pîrvu, C. A., Valceanu, A. P., Zara, F., Dumitru, C. Ș., et al. (2024) · Biomedicines · doi:10.3390/biomedicines12112627 · Cited by 37
Diagnostic value of magnetic resonance cholangiopancreatography to detect bile duct stones in acute biliary pancreatitis
Lee, S.-L., Kim, H.-K., Choi, H., Jeon, B. S., Kim, T., Choi, J.-M., Ku, Y. M., Kim, S. W., Kim, S., & Chae, H. (2017) · Pancreatology · doi:10.1016/j.pan.2017.12.004 · Cited by 37
Endoscopic sphincterotomy and cholecystectomy in acute biliary pancreatitis
da Costa, D. W., Schepers, N. J., Römkens, T., Boerma, D., Bruno, M. J., & Bakker, O. J. (2015) · The Surgeon · doi:10.1016/j.surge.2015.10.002 · Cited by 37
Differences in severity and outcomes between hypertriglyceridemia and alcohol-induced pancreatitis
Goyal, H., Smith, K. E. R., Bayer, C. E., Rutherford, C., & Shelnut, D. J. (2016) · North American Journal of Medical Sciences · doi:10.4103/1947-2714.177307 · Cited by 37
Performance of the revised Atlanta and determinant-based classifications for severity in acute pancreatitis
Bansal, S. S., Hodson, J. A., Sutcliffe, R. P., Marudanayagam, R., Muiesan, P., Mirza, D. F., Isaac, J., & Roberts, K. J. (2016) · British journal of surgery · doi:10.1002/bjs.10088 · Cited by 37
Mechanism of Increased Intestinal Permeability in Acute Pancreatitis
Sonika, U., Goswami, P., Thakur, B., Yadav, R., Das, P., Ahuja, V., & Saraya, A. (2016) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0000000000000612 · Cited by 37
Pancreatic Pseudocyst Dilemma: Cumulative Multicenter Experience in Management Using Endoscopy, Laparoscopy, and Open Surgery
Redwan, A. A., Hamad, M. A., & Omar, M. A. (2017) · Journal of Laparoendoscopic & Advanced Surgical Techniques · doi:10.1089/lap.2017.0006 · Cited by 37
Monocyte programmed death ligand-1 expression is an early marker for predicting infectious complications in acute pancreatitis
Pan, T., Zhou, T., Li, L., Liu, Z., Chen, Y., Mao, E., Li, M., Qu, H., & Liu, J. (2017) · Critical Care · doi:10.1186/s13054-017-1781-3 · Cited by 37
Epidemiology and Etiology of Acute Pancreatitis in Urban and Suburban Areas in Shanghai: A Retrospective Study
Fan, J., Ding, L., Lu, Y., Zheng, J., Zeng, Y., & Huang, C. (2018) · Gastroenterology Research and Practice · doi:10.1155/2018/1420590 · Cited by 37
Recurrent Acute Pancreatitis: Current Concepts in the Diagnosis and Management
Jagannath, S., & Garg, P. K. (2018) · Current Treatment Options in Gastroenterology · doi:10.1007/s11938-018-0196-9 · Cited by 37
Endoscopic and surgical drainage for pancreatic fluid collections are better than percutaneous drainage: Meta-analysis
Szakó, L., Mátrai, P., Hegyi, P., Pécsi, D., Gyöngyi, Z., Csupor, D., Bajor, J., Erőss, B. M., Mikó, A., Szakács, Z., et al. (2019) · Pancreatology · doi:10.1016/j.pan.2019.10.006 · Cited by 37
Nonaggressive Versus Aggressive Intravenous Fluid Therapy in Acute Pancreatitis With More Than 24 Hours From Disease Onset
Cuéllar-Monterrubio, J. E., Monreal‐Robles, R., González-Moreno, E. I., Borjas-Almaguer, O. D., Herrera-Elizondo, J. L., García‐Compeán, D., Maldonado-Garza, H. J., & González, J. A. (2020) · Pancreas · doi:10.1097/mpa.0000000000001528 · Cited by 37
Indwelling double-pigtail plastic stents for treating disconnected pancreatic duct syndrome-associated peripancreatic fluid collections: long-term safety and efficacy
Gkolfakis, P., Bourguignon, A., Arvanitakis, M., Baudewyns, A., Eisendrath, P., Bléro, D., Lemmers, A., Delhaye, M., & Deviere, J. M. E. (2020) · Endoscopy · doi:10.1055/a-1319-5093 · Cited by 37
Alternative uses of lumen apposing metal stents
Sharma, P., McCarty, T. R., Chhoda, A., Costantino, A., Loeser, C. S., Muniraj, T., Ryou, M. K., & Thompson, C. C. (2020) · World Journal of Gastroenterology · doi:10.3748/wjg.v26.i21.2715 · Cited by 37
Pancreatic Pseudocysts
Ge, P. S., Weizmann, M., & Watson, R. R. (2016) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2015.10.003 · Cited by 37
Comparison between minimally invasive and open surgical treatment in necrotizing pancreatitis
Wroński, M., Cebulski, W., Witkowski, B., Jankowski, M., Kluciński, A., Krasnodebski, I. W., & Słodkowski, M. (2016) · Journal of Surgical Research · doi:10.1016/j.jss.2016.10.022 · Cited by 37
Acute pancreatitis is characterized by generalized intestinal barrier dysfunction in early stage
Agarwal, S., Goswami, P., Poudel, S., Gunjan, D., Singh, N., Yadav, R., Kumar, U., Pandey, G., & Saraya, A. (2023) · Pancreatology · doi:10.1016/j.pan.2022.11.011 · Cited by 36
Abdominal Compartment Syndrome in Acute Pancreatitis: A Narrative Review
Zărnescu, N. O., Dumitrascu, I., Zarnescu, E. C., & Costea, R. (2022) · Diagnostics · doi:10.3390/diagnostics13010001 · Cited by 36
Justification of the Choice of the Model of Severe Acute Pancreatitis Suitable for Studying New Approaches to Its Treatment
Куделич, О. А., Кондратенко, Г. Г., Метелица, Т. Г., Колесникова, Т. С., & Ходосовская, Е. В. (2023) · Хирургия Восточная Европа · doi:10.34883/pi.2023.12.1.017 · Cited by 36
Efficacy and safety of endoscopic drainage versus percutaneous drainage for pancreatic fluid collection; a systematic review and meta-analysis
Khizar, H., Zhicheng, H., Le, C., Yanhua, W., & Jianfeng, Y. (2023) · Annals of Medicine · doi:10.1080/07853890.2023.2213898 · Cited by 36
Age-period-cohort analysis of pancreatitis epidemiological trends from 1990 to 2019 and forecasts for 2044: a systematic analysis from the Global Burden of Disease Study 2019
Jiang, W., Du, Y., Xiang, C., Li, X., & Zhou, W. (2023) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1118888 · Cited by 36
Clinical update on acute cholecystitis and biliary pancreatitis: between certainties and grey areas
Fugazzola, P., Podda, M., Tian, B. W., Cobianchi, L., Ansaloni, L., & Catena, F. (2024) · EClinicalMedicine · doi:10.1016/j.eclinm.2024.102880 · Cited by 36
Annexin A1 mRNA-loaded liposomes alleviate acute pancreatitis by suppressing STING pathway and promoting efferocytosis in macrophages
Fang, H., You, P., Lin, S., Wu, Y., Lin, J., Hou, Z., Liang, F., Chen, C., Wang, Z., Chen, L., et al. (2025) · Nature Nanotechnology · doi:10.1038/s41565-025-01979-0 · Cited by 36
Acute necrotizing pancreatitis: Surgical indications and technical procedures
Aranda-Narváez, J. M. (2014) · World Journal of Clinical Cases · doi:10.12998/wjcc.v2.i12.840 · Cited by 36
Association Between Severity and the Determinant-Based Classification, Atlanta 2012 and Atlanta 1992, in Acute Pancreatitis
Chen, Y., Ke, L., Tong, Z., Li, W., & Li, J. (2015) · Medicine · doi:10.1097/md.0000000000000638 · Cited by 36
Acute pancreatitis reclassified
Windsor, J. A., & Petrov, M. S. (2012) · Gut · doi:10.1136/gutjnl-2012-303725 · Cited by 36
Compliance with Evidence-Based Guidelines in Acute Pancreatitis: an Audit of Practices in University of Toronto Hospitals
Greenberg, J., Hsu, J. H., Bawazeer, M. A., Marshall, J. C., Friedrich, J. O., Nathens, A. B., Coburn, N. G., Huang, H., & McLeod, R. S. (2015) · Journal of Gastrointestinal Surgery · doi:10.1007/s11605-015-3023-9 · Cited by 36
A prognostic tool to predict severe acute pancreatitis in pediatrics
Szabó, F., Hornung, L. N., Murayi, J. O., Alhosh, R., Husain, S. Z., Liu, Q. Y., Palermo, J. J., Lin, T. K., Nathan, J. D., Podberesky, D. J., et al. (2016) · Pancreatology · doi:10.1016/j.pan.2016.03.002 · Cited by 36
Management of acute pancreatitis in Japan: Analysis of nationwide epidemiological survey
Hamada, S., Masamune, A., & Shimosegawa, T. (2016) · World Journal of Gastroenterology · doi:10.3748/wjg.v22.i28.6335 · Cited by 36
Decreased high density lipoprotein cholesterol is an independent predictor for persistent organ failure, pancreatic necrosis and mortality in acute pancreatitis
Zhang, Y., Guo, F., Li, S., Wang, F., Meng, Z., Zhao, J., Liu, Z., Wang, B., Fan, P., Wang, C., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-06618-w · Cited by 36
Missing in action—The meaning of cell death in tissue damage and inflammation
Munoz, L. E., Leppkes, M., Fuchs, T. A., Hoffmann, M. H., & i, M. H. (2017) · Immunological Reviews · doi:10.1111/imr.12569 · Cited by 36
Evolving treatment of necrotizing pancreatitis
Roch, A. M., Maatman, T. K., Carr, R. A., Easler, J. J., Schmidt, C. M., House, M. G., Nakeeb, A., Ceppa, E. P., & Zyromski, N. J. (2017) · The American Journal of Surgery · doi:10.1016/j.amjsurg.2017.11.020 · Cited by 36
Relationship between intra-abdominal hypertension, outcome and the revised Atlanta and determinant-based classifications in acute pancreatitis
Marcos-Neira, P., Zubia‐Olaskoaga, F., López‐Cuenca, S., Bordeje-Laguna, M. L., & on behalf of the Epidemiology of Acute Pancreatitis in Intensive Care Medicine study group (2017) · BJS Open · doi:10.1002/bjs5.29 · Cited by 36
Continuous glucose monitoring system can improve the quality of glucose control and glucose variability compared with point-of-care measurement in critically ill patients
Lu, M., Zuo, Y.-Y., Guo, J., Wen, X., & Kang, Y. M. (2018) · Medicine · doi:10.1097/md.0000000000012138 · Cited by 39
Vitamin D deficiency predicts severe acute pancreatitis
Huh, J. H., Kim, J. W., & Lee, K. J. (2018) · United European Gastroenterology Journal · doi:10.1177/2050640618811489 · Cited by 36
GC-MS based metabolomics strategy to distinguish three types of acute pancreatitis
Huang, J., He, D., Chen, L., Dong, C.-Y., Zhang, S.-H., Qin, Y., Yu, R., Ahmed, R., Kuang, J.-J., & Zhang, X. (2019) · Pancreatology · doi:10.1016/j.pan.2019.05.456 · Cited by 36
Bibliometric analysis of acute pancreatitis in Web of Science database based on CiteSpace software
Sun, W., Huang, P., Song, H., & Feng, D.-X. (2020) · Medicine · doi:10.1097/md.0000000000023208 · Cited by 36
Management of abdominal compartment syndrome in acute pancreatitis
Siebert, M. A., Fouler, A. L., Sitbon, N., Cohen, J., Abba, J., & Poupardin, É. (2021) · Journal of Visceral Surgery · doi:10.1016/j.jviscsurg.2021.01.001 · Cited by 36
The BISAP score, NLR, CRP, or BUN: Which marker best predicts the outcome of acute pancreatitis?
Dancu, G. M., Popescu, A., Șirli, R., Danila, M., Bende, F., Tarta, C., & Sporea, I. (2021) · Medicine · doi:10.1097/md.0000000000028121 · Cited by 36
Traumatic pancreatitis
Sharbidre, K., Galgano, S. J., & Morgan, D. E. (2019) · Abdominal Radiology · doi:10.1007/s00261-019-02241-7 · Cited by 36
Failure to follow evidence‐based best practice guidelines in the treatment of severe acute pancreatitis
Vlada, A. C., Schmit, B. M., Perry, A., Trevino, J. G., Behrns, K. E., & Hughes, S. J. (2013) · HPB · doi:10.1111/hpb.12140 · Cited by 36
A Combined Paging Alert and Web-Based Instrument Alters Clinician Behavior and Shortens Hospital Length of Stay in Acute Pancreatitis
Dimagno, M. J., Wamsteker, E., Rizk, R. S., Spaete, J. P., Gupta, S., Sahay, T., Costanzo, J., Inadomi, J. M., Napolitano, L. M., Hyzy, R. C., et al. (2014) · The American Journal of Gastroenterology · doi:10.1038/ajg.2013.282 · Cited by 36
Nonalcoholic fatty liver and the severity of acute pancreatitis
Mikolašević, I., Orlić, L., Poropat, G., Jakopčić, I., Štimac, D., Klanac, A., Carović, F., & Milić, S. (2016) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2016.10.019 · Cited by 36
Elevated Serum Fibroblast Growth Factor 21 in Humans with Acute Pancreatitis
Shenoy, V. K., Beaver, K. M., Fisher, F. M., Singhal, G., Dushay, J. R., Maratos–Flier, E., & Flier, S. N. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164351 · Cited by 36
The role of extra-pancreatic infections in the prediction of severity and local complications in acute pancreatitis
Pando, E., Alberti, P., Hidalgo, N. J., Vidal, L., Dopazo, C., Caralt, M., Blanco, L., Gómez‐Gavara, C., Bilbao, I., Balsells, J., et al. (2018) · Pancreatology · doi:10.1016/j.pan.2018.05.481 · Cited by 36
Obesity as a risk factor for severe acute pancreatitis patients
Kaťuchová, J., Bober, J., Harbul'ák, P., Hudák, A., Gajdzik, T., Kalanin, R., & Radoňak, J. (2014) · Wiener klinische Wochenschrift · doi:10.1007/s00508-014-0507-7 · Cited by 36
Establishment and validation of early prediction model for hypertriglyceridemic severe acute pancreatitis
Yi, S., Huiling, Z., Xunting, L., Yifang, D., Yu-fen, L., Shanshan, X., Lijuan, S., & Yunpeng, L. (2023) · Lipids in Health and Disease · doi:10.1186/s12944-023-01984-z · Cited by 35
Endoscopic Ultrasound-Guided Rendezvous Technique Versus Precut Sphincterotomy as Salvage Technique in Patients With Benign Biliary Disease and Difficult Biliary Cannulation
Choudhury, A. R., Samanta, J., Muktesh, G., Dhar, J., Kumar, A., Shah, J., Spadaccini, M., Gupta, P. C., Fugazza, A., Gupta, V. S., et al. (2024) · Annals of Internal Medicine · doi:10.7326/m24-0092 · Cited by 35
Hydrogen Sulfide: A Versatile Molecule and Therapeutic Target in Health and Diseases
Shahid, A., & Bhatia, M. (2024) · Biomolecules · doi:10.3390/biom14091145 · Cited by 35
Clinical Outcomes in a Multicenter Cohort Involving 919 Patients With Hypertriglyceridemia-Associated Acute Pancreatitis
Deng, H., Peng, K., Zhang, L., Lu, J., Mei, W., Shi, X., Peng, Y., Xu, K., Li, H., Wang, Z., et al. (2025) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000003319 · Cited by 35
Diagnosis and Management of Acute Pancreatitis
Mittal, N., Oza, V. M., Muniraj, T., & Kothari, T. H. (2025) · Diagnostics · doi:10.3390/diagnostics15030258 · Cited by 35
The Reduction of Peripheral Blood CD4+ T Cell Indicates Persistent Organ Failure in Acute Pancreatitis
Yang, Z., Zhang, Y., Dong, L., Yang, C., Gou, S., Yin, T., Wu, H., & Wang, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125529 · Cited by 35
Emergency abdominal MRI: current uses and trends
Yu, H., Gupta, A., Soto, J. A., & LeBedis, C. A. (2015) · British Journal of Radiology · doi:10.1259/bjr.20150804 · Cited by 35
Prevalence, Natural History, and Outcome of Acute Fluid Collection and Pseudocyst in Children With Acute Pancreatitis
Bolia, R. K., Srivastava, A., Yachha, S. K., Poddar, U., & Kumar, S. (2015) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000000800 · Cited by 35
Validation of the efficacy of the prognostic factor score in the Japanese severity criteria for severe acute pancreatitis: A large multicenter study
Ikeura, T., Horibe, M., Sanui, M., Sasaki, M., Kuwagata, Y., Nishi, K., Kariya, S., Sawano, H., Goto, T., Hamada, T., et al. (2016) · United European Gastroenterology Journal · doi:10.1177/2050640616670566 · Cited by 35
The expression and activation of the AIM2 inflammasome correlates with inflammation and disease severity in patients with acute pancreatitis
Algaba‐Chueca, F., de‐Madaria, E., Lozano‐Ruiz, B., Martínez‐Cardona, C., Quesada‐Vázquez, N., Bachiller, V., Tarín, F., Such, J. M., Francés, R., Zapater, P., et al. (2017) · Pancreatology · doi:10.1016/j.pan.2017.03.006 · Cited by 35

Authors: Banks, P. A., Bollen, T. L., Dervenis, C., Gooszen, H. G., Johnson, C. D., Sarr, M. G., Tsiotos, G. G., & Vege, S. S.
Affiliations: Brigham and Women's Hospital (US)
St. Antonius Ziekenhuis (NL)
Agia Olga Hospital (GR)
Radboud University Nijmegen (NL)
University Hospital Southampton NHS Foundation Trust (GB)
Mayo Clinic (US)
Metropolitan Hospital (GR)
Corresponding author: Sarr, Michael G
ORCID: Banks, Peter A
Gooszen, Hein G
Tsiotos, Gregory G
Vege, Santhi Swaroop
Venue: Gut
Publisher: BMJ
Published: 2012-10-25
Volume: 62
Issue: 1
Pages: 102-111
ISSN: 0017-5749 (ISSN-L)
1468-3288
DOI: 10.1136/gutjnl-2012-302779
OpenAlex: W2145758369
Cited by: 7,187
References: 77
Citations by year: 2026: 666 · 2025: 732 · 2024: 720 · 2023: 738 · 2022: 699 · 2021: 675 · 2020: 612 · 2019: 481 · 2018: 458 · 2017: 402 · 2016: 349 · 2015: 305 · 2014: 232 · 2013: 91 · 2012: 9
FWCI: 209.43
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Gut (publishedVersion)
PubMed (publishedVersion)
ePrints Soton (University of Southampton) (submittedVersion)
HighWire Press Open Archive (submittedVersion)
Radboud Repository (Radboud University) (submittedVersion)
ResearchSpace (University of Auckland) (submittedVersion)
CONICET Digital (CONICET) (submittedVersion, cc-by-nc-sa)
Funders: University of Pittsburgh
American Gastroenterological Association
Cancer Research UK (15957)
National Institute for Health and Care Research (NF-SI-0510-10126)
Ministry of Urban Development
Topics: Health Sciences › Medicine › Surgery › Pancreatitis Pathology and Treatment
Health Sciences › Medicine › Gastroenterology › Gallbladder and Bile Duct Disorders
Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
Keywords: acute pancreatitis, Atlanta classification, disease severity classification, organ failure, local complications, pancreatic necrosis, peripancreatic fluid collections, pseudocyst, walled-off necrosis, international consensus
MeSH terms: Acute Disease, Humans, Pancreatitis, Severity of Illness Index, Tomography, X-Ray Computed, Disease Progression

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Classification of acute pancreatitis—2012: revision of the Atlanta classification and definitions by international consensus

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks