Factors predicting 30-day mortality after pancreaticoduodenectomy-the impact of elevated aspartate aminotransferase.


Journal

Langenbeck's archives of surgery
ISSN: 1435-2451
Titre abrégé: Langenbecks Arch Surg
Pays: Germany
ID NLM: 9808285

Informations de publication

Date de publication:
29 Mar 2023
Historique:
received: 27 02 2022
accepted: 19 03 2023
medline: 31 3 2023
entrez: 29 3 2023
pubmed: 30 3 2023
Statut: epublish

Résumé

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. This is a retrospective analysis of 562 patients. Risk factors for POM were computed using a multivariate logistic regression model. 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. 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.

Identifiants

pubmed: 36991246
doi: 10.1007/s00423-023-02865-w
pii: 10.1007/s00423-023-02865-w
doi:

Substances chimiques

Aspartate Aminotransferases EC 2.6.1.1
Creatinine AYI8EX34EU
Bilirubin RFM9X3LJ49
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

130

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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
doi: 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
doi: 10.1111/j.1477-2574.2010.00216.x pubmed: 20815858 pmcid: 3030758
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
doi: 10.1002/jso.25942 pubmed: 32445612
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
doi: 10.1016/j.surg.2007.07.035 pubmed: 18154928
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
doi: 10.1007/s11605-009-1051-z pubmed: 19806409
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
doi: 10.1245/s10434-010-0947-x pubmed: 20155401
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
doi: 10.1002/jhbp.438 pubmed: 28196308 pmcid: 5516144
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
doi: 10.1016/j.gassur.2006.08.018 pubmed: 17114007
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
doi: 10.1016/j.surg.2014.06.016 pubmed: 25061003
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
doi: 10.1182/bloodadvances.2019000975 pubmed: 31794602 pmcid: 6963238
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
doi: 10.1007/s00423-021-02108-w pubmed: 33774746
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
doi: 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
doi: 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
doi: 10.1016/j.surg.2016.11.014 pubmed: 28040257
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
doi: 10.1016/j.surg.2007.05.005 pubmed: 17981197
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
doi: 10.1016/j.surg.2007.02.001 pubmed: 17629996
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
doi: 10.1001/jamasurg.2017.0904 pubmed: 28467526
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
doi: 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
doi: 10.1080/01926230252929945 pubmed: 12051554
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
doi: 10.1186/s13104-020-05031-3 pubmed: 32209113 pmcid: 7092498
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
doi: 10.1097/MEG.0000000000000811 pubmed: 28009717
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
doi: 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
doi: 10.1111/j.1478-3231.2007.01471.x pubmed: 17498256
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
doi: 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
doi: 10.3390/ijms161125942 pubmed: 26540040 pmcid: 4661801
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
doi: 10.1139/apnm-2012-0302 pubmed: 23668757
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
doi: 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
doi: 10.1016/j.clgc.2016.08.023 pubmed: 27692696
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
doi: 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
pubmed: 10430380
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
pubmed: 8817225
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
doi: 10.1016/j.surg.2005.08.012 pubmed: 16701090
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
doi: 10.1016/j.gassur.2005.12.014 pubmed: 16504879
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
pubmed: 10522047
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
doi: 10.1016/j.amjsurg.2003.11.004 pubmed: 14769305
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
doi: 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
doi: 10.1056/NEJMoa0903230 pubmed: 20071702
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
doi: 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
doi: 10.1016/j.surg.2016.11.001 pubmed: 28043693
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
doi: 10.1245/s10434-014-4036-4 pubmed: 25190121

Auteurs

Deeksha Kapoor (D)

Division of GI Surgery, GI Oncology, Minimal Access and Bariatric Surgery, Institute of Digestive and Hepatobiliary Sciences, Medanta - the Medicity, Sector 38, Gurugram, Haryana, 122001, India.

Azhar Perwaiz (A)

Division of GI Surgery, GI Oncology, Minimal Access and Bariatric Surgery, Institute of Digestive and Hepatobiliary Sciences, Medanta - the Medicity, Sector 38, Gurugram, Haryana, 122001, India.

Amanjeet Singh (A)

Division of GI Surgery, GI Oncology, Minimal Access and Bariatric Surgery, Institute of Digestive and Hepatobiliary Sciences, Medanta - the Medicity, Sector 38, Gurugram, Haryana, 122001, India.

Arun N Kumar (AN)

Department of Data Science, Alke Research Private Limited, Bengaluru, Karnataka, India.

Adarsh Chaudhary (A)

Division of GI Surgery, GI Oncology, Minimal Access and Bariatric Surgery, Institute of Digestive and Hepatobiliary Sciences, Medanta - the Medicity, Sector 38, Gurugram, Haryana, 122001, India. adarsh_chaudhary@yahoo.com.

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