Abstract
Purpose
High preoperative bilirubin levels and cholangitis are associated with poor peri-operative outcomes following pancreaticoduodenectomy (PD). However, the impact of deranged preoperative aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels on immediate postoperative outcomes is relatively unexplored. We hypothesized that deranged AST and ALT lead to worse postoperative outcomes after PD. The aim of this study was to assess the factors contributing to postoperative mortality (POM) following PD, and to study the impact of deranged aminotransferases.
Methods
This is a retrospective analysis of 562 patients. Risk factors for POM were computed using a multivariate logistic regression model.
Results
The rate of POM was 3.9%. On univariate analysis, the American Society of Anaesthesiologists grades, diabetes mellitus, cardiac comorbidity, preoperative biliary stenting, elevated serum bilirubin, AST, elevated serum creatinine, clinically relevant pancreatic fistula (CRPF), and grade B+C post-pancreatectomy hemorrhage (PPH) were associated with 30-day mortality. On multivariate analysis, preoperative elevated AST was independently predictive of 30-day POM (OR = 6.141, 95%CI 2.060–18.305, p = 0.001). Other factors independently predictive of POM were elevated serum creatinine, preoperative biliary stenting, CRPF and grade B and C PPH. The ratio of AST/ALT > 0.89 was associated with 8 times increased odds of POM.
Conclusion
Elevated preoperative AST emerged as a predictor of 30-day POM after PD, with an 8-times increased odds of death with an AST/ALT ratio > 0.89.
Similar content being viewed by others
Data Availability
Data in the manuscript is available.
References
Kimura W, Miyata H, Gotoh M et al (2014) A pancreaticoduodenectomy risk model derived from 8575 cases from a national single-race population (Japanese) using a Web-based data entry system: the 30-day and in-hospital mortality rates for pancreaticoduodenectomy. Annals Surg 259(4):773–780. https://doi.org/10.1097/SLA.0000000000000263
Parikh P, Shiloach M, Cohen ME et al (2010) Pancreatectomy risk calculator: an ACS-NSQIP resource. HPB 12(7):488–497. https://doi.org/10.1111/j.1477-2574.2010.00216.x
Vining CC, Kuchta K, Schuitevoerder D et al (2020) Risk factors for complications in patients undergoing pancreaticoduodenectomy: A NSQIP analysis with propensity score matching. J Surg Oncol 122(2):183–194. https://doi.org/10.1002/jso.25942
Pratt W, Joseph S, Callery MP, Vollmer CM (2008) POSSUM accurately predicts morbidity for pancreatic resection. Surgery 143(1):8–19. https://doi.org/10.1016/j.surg.2007.07.035
Are C, Afuh C, Ravipati L, Sasson A, Ullrich F, Smith L (2009) Preoperative nomogram to predict risk of perioperative mortality following pancreatic resections for malignancy. J Gastrointest Surg 13(12):2152–2162. https://doi.org/10.1007/s11605-009-1051-z
Hill JS, Zhou Z, Simons JP et al (2010) A simple risk score to predict in-hospital mortality after pancreatic resection for cancer. Ann Surg Oncol 17(7):1802–1807. https://doi.org/10.1245/s10434-010-0947-x
Aoki S, Miyata H, Konno H et al (2017) Risk factors of serious postoperative complications after pancreaticoduodenectomy and risk calculators for predicting postoperative complications: a nationwide study of 17,564 patients in Japan. J Hepatobiliary Pancreat Sci 24(5):243–251. https://doi.org/10.1002/jhbp.438
Beugniez C, Sauvanet A, Sulpice L et al (2021) Root-cause analysis of mortality following pancreatic resection (CARE Study): a multicenter cohort study. Ann Surg. Publish Ahead of Print. https://doi.org/10.1097/SLA.0000000000005118
Winter J, Cameron J, Campbell K et al (2006) 1423 pancreaticoduodenectomies for pancreatic cancer: a single-institution experience☆. J Gastrointest Surg 10(9):1199–1211. https://doi.org/10.1016/j.gassur.2006.08.018
Tol JAMG, Gouma DJ, Bassi C et al (2014) Definition of a standard lymphadenectomy in surgery for pancreatic ductal adenocarcinoma: a consensus statement by the International Study Group on Pancreatic Surgery (ISGPS). Surgery 156(3):591–600. https://doi.org/10.1016/j.surg.2014.06.016
Anderson DR, Morgano GP, Bennett C et al (2019) American Society of Hematology 2019 guidelines for management of venous thromboembolism: prevention of venous thromboembolism in surgical hospitalized patients. Blood Advances 3(23):3898–3944. https://doi.org/10.1182/bloodadvances.2019000975
Kapoor D, Perwaiz A, Singh A, Kumar AN, Chaudhary A (2021) Enhanced recovery after pancreatoduodenectomy—does age have a bearing? Langenbecks Arch Surg 406(4):1093–1101. https://doi.org/10.1007/s00423-021-02108-w
Lassen K, Coolsen MME, Slim K et al (2012) Guidelines for perioperative care for pancreaticoduodenectomy: Enhanced Recovery After Surgery (ERAS®) Society recommendations. Clin Nutri 31(6):817–830. https://doi.org/10.1016/j.clnu.2012.08.011
Clavien PA, Barkun J, de Oliveira ML et al (2009) The Clavien-Dindo classification of surgical complications: five-year experience. Annals Surg 250(2):187–196. https://doi.org/10.1097/SLA.0b013e3181b13ca2
Bassi C, Marchegiani G, Dervenis C et al (2017) The 2016 update of the International Study Group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 Years After. Surgery 161(3):584–591. https://doi.org/10.1016/j.surg.2016.11.014
Wente MN, Bassi C, Dervenis C et al (2007) Delayed gastric emptying (DGE) after pancreatic surgery: a suggested definition by the International Study Group of Pancreatic Surgery (ISGPS). Surgery 142(5):761–768. https://doi.org/10.1016/j.surg.2007.05.005
Wente MN, Veit JA, Bassi C et al (2007) Postpancreatectomy hemorrhage (PPH)–an International Study Group of Pancreatic Surgery (ISGPS) definition. Surgery 142(1):20–25. https://doi.org/10.1016/j.surg.2007.02.001
Berríos-Torres SI, Umscheid CA, Bratzler DW et al (2017) Centers for Disease Control and Prevention guideline for the prevention of surgical site infection, 2017. JAMA Surg 152(8):784. https://doi.org/10.1001/jamasurg.2017.0904
De Ritis F, Coltorti M, Giusti G (2006) An enzymic test for the diagnosis of viral hepatitis: the transaminase serum activities. Clinica Chimica Acta 369(2):148–152. https://doi.org/10.1016/j.cca.2006.05.001
Giffen PS, Pick CR, Price MA, Williams A, York MJ (2002) Alpha-glutathione S-transferase in the assessment of hepatotoxicity—its diagnostic utility in comparison with other recognized markers in the Wistar Han rat. Toxicol Pathol 30(3):365–372. https://doi.org/10.1080/01926230252929945
Ewid M, Sherif H, Allihimy AS et al (2020) AST/ALT ratio predicts the functional severity of chronic heart failure with reduced left ventricular ejection fraction. BMC Res Notes 13(1):178. https://doi.org/10.1186/s13104-020-05031-3
Simental-Mendía LE, Rodríguez-Morán M, Gómez-Díaz R, Wacher NH, Rodríguez-Hernández H, Guerrero-Romero F (2017) Insulin resistance is associated with elevated transaminases and low aspartate aminotransferase/alanine aminotransferase ratio in young adults with normal weight. Eur J Gastroenterol Hepatol 29(4):435–440. https://doi.org/10.1097/MEG.0000000000000811
Lin S, Tang L, Jiang R et al (2019) The relationship between aspartate aminotransferase to alanine aminotransferase ratio and metabolic syndrome in adolescents in northeast China. DMSO 12:2387–2394. https://doi.org/10.2147/DMSO.S217127
Nyblom H, Nordlinder H, Olsson R (2007) High aspartate to alanine aminotransferase ratio is an indicator of cirrhosis and poor outcome in patients with primary sclerosing cholangitis. Liver Int 27(5):694–699. https://doi.org/10.1111/j.1478-3231.2007.01471.x
Liu H, Ding C, Hu L et al (2021) The association between AST/ALT ratio and all-cause and cardiovascular mortality in patients with hypertension. Medicine 100(31):26693. https://doi.org/10.1097/MD.0000000000026693
Li S, Tan HY, Wang N et al (2015) The role of oxidative stress and antioxidants in liver diseases. IJMS 16(11):26087–26124. https://doi.org/10.3390/ijms161125942
Ramos D, Martins EG, Viana-Gomes D, Casimiro-Lopes G, Salerno VP (2013) Biomarkers of oxidative stress and tissue damage released by muscle and liver after a single bout of swimming exercise. Appl Physiol Nutr Metab 38(5):507–511. https://doi.org/10.1139/apnm-2012-0302
Li L, Zeng Q, Xue N et al (2020) A nomogram based on aspartate aminotransferase/alanine aminotransferase (AST/ALT) ratio to predict prognosis after surgery in gastric cancer patients. Cancer Control 27(1):107327482095445. https://doi.org/10.1177/1073274820954458
Lee H, Choi YH, Sung HH et al (2017) De Ritis ratio (AST/ALT) as a significant prognostic factor in patients with upper tract urothelial cancer treated with surgery. Clin Genitourin Cancer 15(3):e379–e385. https://doi.org/10.1016/j.clgc.2016.08.023
Winter JM, Cameron JL, Yeo CJ et al (2007) Biochemical markers predict morbidity and mortality after pancreaticoduodenectomy. J Am College Surg 204(5):1029–1036. https://doi.org/10.1016/j.jamcollsurg.2007.01.026
Su CH, Shyr YM, Lui WY, P’eng FK (1999) Factors affecting morbidity, mortality and survival after pancreaticoduodenectomy for carcinoma of the ampulla of Vater. Hepatogastroenterology 46(27):1973–1979
Chou FF, Sheen-Chen SM, Chen YS, Chen MC, Chen CL (1996) Postoperative morbidity and mortality of pancreaticoduodenectomy for periampullary cancer. Eur J Surg 162(6):477–481
Muscari F, Suc B, Kirzin S et al (2006) Risk factors for mortality and intra-abdominal complications after pancreatoduodenectomy: multivariate analysis in 300 patients. Surgery 139(5):591–598. https://doi.org/10.1016/j.surg.2005.08.012
Makary M, Winter J, Cameron J et al (2006) Pancreaticoduodenectomy in the very elderly. J Gastrointest Surg 10(3):347–356. https://doi.org/10.1016/j.gassur.2005.12.014
Bottger TC, Engelmann R, Junginger T (1999) Is age a risk factor for major pancreatic surgery? An analysis of 300 resections. Hepatogastroenterology 46(28):2589–2598
Adam U, Makowiec F, Riediger H, Schareck WD, Benz S, Hopt UT (2004) Risk factors for complications after pancreatic head resection. Am J Surg 187(2):201–208. https://doi.org/10.1016/j.amjsurg.2003.11.004
Povoski SP, Karpeh MS, Conlon KC, Blumgart LH, Brennan MF (1999) Association of preoperative biliary drainage with postoperative outcome following pancreaticoduodenectomy. Annals Surg 230(2):131. https://doi.org/10.1097/00000658-199908000-00001
van der Gaag NA, Rauws EAJ, van Eijck CHJ et al (2010) Preoperative biliary drainage for cancer of the head of the pancreas. N Engl J Med 362(2):129–137. https://doi.org/10.1056/NEJMoa0903230
Sewnath ME, Karsten TM, Prins MH, Rauws EJA, Obertop H, Gouma DJ (2002) A Meta-analysis on the efficacy of preoperative biliary drainage for tumors causing obstructive jaundice. Annals Surg 236(1):17–27. https://doi.org/10.1097/00000658-200207000-00005
Scheufele F, Schorn S, Demir IE et al (2017) Preoperative biliary stenting versus operation first in jaundiced patients due to malignant lesions in the pancreatic head: A meta-analysis of current literature. Surgery 161(4):939–950. https://doi.org/10.1016/j.surg.2016.11.001
Swanson RS, Pezzi CM, Mallin K, Loomis AM, Winchester DP (2014) The 90-day mortality after pancreatectomy for cancer is double the 30-day mortality: more than 20,000 resections from the national cancer data base. Ann Surg Oncol 21(13):4059–4067. https://doi.org/10.1245/s10434-014-4036-4
Author information
Authors and Affiliations
Contributions
Study design and conception—Deeksha Kapoor, Adarsh Chaudhary, Azhar Perwaiz, Arun Kumar N. Data acquisition—Deeksha Kapoor. Data analysis and interpretation—Deeksha Kapoor, Amanjeet Singh, Adarsh Chaudhary, Arun Kumar N. Drafting the article—Deeksha Kapoor, Azhar Perwaiz, Adarsh Chaudhary, Amanjeet Singh, Arun Kumar N. Critical review of intellectual content—Deeksha Kapoor, Azhar Perwaiz, Amanjeet Singh, Adarsh Chaudhary, Arun Kumar N.
Corresponding author
Ethics declarations
Ethics approval
We the authors, Deeksha Kapoor, Azhar Perwaiz, Amanjeet Singh, Arun Kumar N and Adarsh Chaudhary, have obeyed and complied with ethical standards. The study was reviewed by the Institutional Review Board and ethics committee approval was obtained (1247/2021). A part of the results was presented at the AHPBA 2021, on-demand presentation.
Conflict of interest
The authors declare no competing interests.
Disclaimer
This paper represents the original work of the authors and is a product of professional research.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Kapoor, D., Perwaiz, A., Singh, A. et al. Factors predicting 30-day mortality after pancreaticoduodenectomy—the impact of elevated aspartate aminotransferase. Langenbecks Arch Surg 408, 130 (2023). https://doi.org/10.1007/s00423-023-02865-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00423-023-02865-w