Transaminases on the First Day After Hepatectomy and Prediction of Outcomes in Malignant Disease

Authors

  • Lourdes Mollard Unidad de Cirugía Hepatobiliar Compleja y Trasplante Hepático. Hospital El Cruce. Florencio Varela, Provincia de Buenos Aires, Argentina. https://orcid.org/0000-0001-6504-7406
  • Rodrigo A Gasque Unidad de Cirugía Hepatobiliar Compleja y Trasplante Hepático. Hospital El Cruce. Florencio Varela, Provincia de Buenos Aires, Argentina.
  • Magalí Chahdi Beltrame Unidad de Cirugía Hepatobiliar Compleja y Trasplante Hepático. Hospital El Cruce. Florencio Varela, Provincia de Buenos Aires, Argentina. https://orcid.org/0000-0001-5138-0400
  • Marcelo E Lenz Unidad de Cirugía Hepatobiliar Compleja y Trasplante Hepático. Hospital El Cruce. Florencio Varela, Provincia de Buenos Aires, Argentina. https://orcid.org/0000-0001-9087-8703
  • Francisco J Mattera Unidad de Cirugía Hepatobiliar Compleja y Trasplante Hepático. Hospital El Cruce. Florencio Varela, Provincia de Buenos Aires, Argentina. https://orcid.org/0000-0002-1773-353X
  • Emilio G Quiñonez Unidad de Cirugía Hepatobiliar Compleja y Trasplante Hepático. Hospital El Cruce. Florencio Varela, Provincia de Buenos Aires, Argentina. https://orcid.org/0000-0003-4167-8814

DOI:

https://doi.org/10.52787/agl.v55i4.547

Keywords:

Hepatectomy, postoperative complications, mortality, aspartate aminotransferase, alanine aminotransferase

Abstract

Introduction. Advances in oncological liver surgery have improved the radicality of procedures and broadened the criteria for resectability. Transaminases can be indicators of postoperative hepatocellular injury.

Objectives. Evaluate the relationship between transaminase levels on the first postoperative day and morbidity and mortality in hepatectomies for malignant disease.

Materials and methods. A retrospective analysis was conducted on hepatectomies for malignant disease between March 2015 and February 2023. Demographic, intraoperative, and postoperative variables were evaluated. Optimal transaminase cutoff values and their relationship with complications and mortality were determined using ROC curves and sensitivity and specificity calculations.

Results. We performed 273 hepatectomies at our institution, 118 of which were for malignant pathology. We found a statistically significant relationship between elevated transaminase levels on the first postoperative day and the development of morbidity and mortality. The cutoff points for predicting mortality were 856 IU/L for glutamic-oxaloacetic transaminase and 1341 IU/L for glutamic-pyruvic transaminase (AUC: 0,714 and 0,579, respectively), and 530 IU/L and 257 IU/L for predicting the occurrence of complications (AUC: 0,700 and 0,663, respectively). Elevated glutamic-oxaloacetic transaminase values were associated with postoperative liver failure, with a cutoff point > 856 IU/L (AUC: 0,834).

Conclusion. Elevated transaminase values on the first postoperative day are associated with a higher occurrence of complications, the need for blood products and the use of vasoactive drugs. Elevated glutamic-oxaloacetic transaminase indicates a higher risk of postoperative liver failure and 90-day mortality. Transaminases are useful prognostic markers in hepatectomies for malignant pathology.

References

-1. Jarnagin WR, Gonen M, Fong Y, DeMatteo RP, Ben-Porat L, Little S, Corvera C, Weber S, Blumgart LH. Improvement in perioperative outcome after hepatic resection: analysis of 1,803 consecutive cases over the past decade. Ann Surg. 2002;236(4):397-407.

-2. Botea F, Ionescu M, Braşoveanu V, Hrehoreţ D, Alexandrescu S, Grigorie M, Stanciulea O, Nicolaescu D, Tomescu D, Droc G, Ungureanu D, Fota R, Croitoru A, Gheorghe L, Gheorghe C, Lupescu I, Grasu M, Boroş M, Dumitru R, Toma M, Herlea V, Popescu I. Liver Resections in a High-Volume Center: From Standard Procedures to Extreme Surgery and Ultrasound-guided Resections. Chirurgia (Bucur). 2017;112(3):259-277.

-3. Dokmak S, Ftériche FS, Borscheid R, Cauchy F, Farges O, Belghiti J. 2012 Liver resections in the 21st century: we are far from zero mortality. HPB (Oxford). 2013;15(11):908-15.

-4. Franken LC, Schreuder AM, Roos E, van Dieren S, Busch OR, Besselink MG, van Gulik TM. Morbidity and mortality after major liver resection in patients with perihilar cholangiocarcinoma: A systematic review and meta-analysis. Surgery. 2019;165(5):918-928.

-5. Azoulay D, Bhangui P, Pascal G, Salloum C, Andreani P, Ichai P, Saliba F, Lim C. The impact of expanded indications on short-term outcomes for resection of malignant tumours of the liver over a 30 year period. HPB (Oxford). 2017;19(7):638-648.

-6. Mahlmann JC, Wirth TC, Hartleben B, Schrem H, Mahlmann JF, Kaltenborn A, Klempnauer J, Kulik U. Chemotherapy and Hepatic Steatosis: Impact on Postoperative Morbidity and Survival after Liver Resection for Colorectal Liver Metastases. Visc Med. 2021;37(3):198-205.

-7. Bagante F, Ruzzenente A, Beal EW, Campagnaro T, Merath K, Conci S, Akgül O, Alexandrescu S, Marques HP, Lam V, Shen F, Poultsides GA, Soubrane O, Martel G, Iacono C, Guglielmi A, Pawlik TM. Complications after liver surgery: a benchmark analysis. HPB (Oxford). 2019;21(9):1139-1149.

-8. Rössler F, Sapisochin G, Song G, Lin YH, Simpson MA, Hasegawa K, Laurenzi A, Sánchez Cabús S, Nunez MI, Gatti A, Beltrame MC, Slankamenac K, Greig PD, Lee SG, Chen CL, Grant DR, Pomfret EA, Kokudo N, Cherqui D, Olthoff KM, Shaked A, García-Valdecasas JC, Lerut J, Troisi RI, De Santibanes M, Petrowsky H, Puhan MA, Clavien PA. Defining Benchmarks for Major Liver Surgery: A multicenter Analysis of 5202 Living Liver Donors. Ann Surg. 2016;264(3):492-500.

-9. Aloia TA, Fahy BN, Fischer CP, Jones SL, Duchini A, Galati J, Gaber AO, Ghobrial RM, Bass BL. Predicting poor outcome following hepatectomy: analysis of 2313 hepatectomies in the NSQIP database. HPB (Oxford). 2009;11(6):510-5.

-10. Vasavada B, Patel K. Postoperative Morbidity after Liver Resection - A Systemic Review, Meta-analysis and Metaregression of Factors Affecting Them. Surg Chron. 2022;27(2):143-149.

-11. Boleslawski E, Vibert E, Pruvot FR, Le Treut YP, Scatton O, Laurent C, Mabrut JY, Régimbeau JM, Adham M, Cosse C, Farges O. Relevance of postoperative peak transaminase after elective hepatectomy. Ann Surg. 2014;260(5):815-20; discussion 820-1.

-12. Bhogal RH, Nair A, Papis D, Hamady Z, Ahmad J, Lam FT, Khan S, Marangoni G. Postoperative day one serum alanine aminotransferase does not predict patient morbidity and mortality after elective liver resection in non-cirrhotic patients. Hepatobiliary Pancreat Dis Int. 2016;15(6):655-659.

-13. Grąt M, Hołówko W, Lewandowski Z, Kornasiewicz O, Barski K, Skalski M, Zieniewicz K, Krawczyk M. Early post-operative prediction of morbidity and mortality after a major liver resection for colorectal metastases. HPB (Oxford). 2013;15(5):352-8.

-14. de Klein GW, Brohet RM, Liem MSL, Klaase JM. Post-operative Day 1 Serum Transaminase Levels in Relation to Morbidity After Liver Resection. World J Surg. 2022;46(2):433-440.

-15. Olthof PB, Huiskens J, Schulte NR, Wicherts DA, Besselink MG, Busch OR, Heger M, van Gulik TM. Postoperative peak transaminases correlate with morbidity and mortality after liver resection. HPB (Oxford). 2016;18(11):915-921.

-16. D'Amico G, Garcia-Tsao G, Pagliaro L. Natural history and prognostic indicators of survival in cirrhosis: a systematic review of 118 studies. J Hepatol. 2006;44(1):217-31.

-17. Lee JS, Choi HW, Kim JS, Lee TY, Yoon YC. Update on Resection Strategies for Hepatocellular Carcinoma: A Narrative Review. Cancers (Basel). 2024;16(23):4093.

-18. Delis SG, Bakoyiannis A, Biliatis I, Athanassiou K, Tassopoulos N, Dervenis C. Model for end-stage liver disease (MELD) score, as a prognostic factor for post-operative morbidity and mortality in cirrhotic patients, undergoing hepatectomy for hepatocellular carcinoma. HPB (Oxford). 2009;1(4):351-7.

-19. Elshaarawy O, Aman A, Zakaria HM, Zakareya T, Gomaa A, Elshimi E, Abdelsameea E. Outcomes of curative liver resection for hepatocellular carcinoma in patients with cirrhosis. World J Gastrointest Oncol. 2021;13(5):424-439.

-20. Torzilli G, Viganò L, Cimino M, Imai K, Vibert E, Donadon M, Mansour D, Castaing D, Adam R. Is Enhanced One-Stage Hepatectomy a Safe and Feasible Alternative to the Two-Stage Hepatectomy in the Setting of Multiple Bilobar Colorectal Liver Metastases? A Comparative Analysis between Two Pioneering Centers. Dig Surg. 2018;35(4):323-332.

-21. Torzilli G, Serenari M, Viganò L, Cimino M, Benini C, Massani M, Ettorre GM, Cescon M, Ferrero A, Cillo U, Aldrighetti L, Jovine E. Outcomes of enhanced one-stage ultrasound-guided hepatectomy for bilobar colorectal liver metastases compared to those of ALPPS: a multicenter case-match analysis. HPB (Oxford). 2019;21(10):1411-1418.

-22. Ironside N, Bell R, Bartlett A, McCall J, Powell J, Pandanaboyana S. Systematic review of perioperative and survival outcomes of liver resections with and without preoperative portal vein embolization for colorectal metastases. HPB (Oxford). 2017;19(7):559-566.

-23. Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40(5):373-83.

-24. Pang YY. The Brisbane 2000 terminology of liver anatomy and resections. HPB. 2000;2:333-39. HPB (Oxford). 2002;4(2):99; author reply 99-100.

-25. Dindo D, Demartines N, Clavien PA. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240(2):205-213.

-26. Rahbari NN, Garden OJ, Padbury R, Brooke-Smith M, Crawford M, Adam R, Koch M, Makuuchi M, Dematteo RP, Christophi C, Banting S, Usatoff V, Nagino M, Maddern G, Hugh TJ, Vauthey JN, Greig P, Rees M, Yokoyama Y, Fan ST, Nimura Y, Figueras J, Capussotti L, Büchler MW, Weitz J. Posthepatectomy liver failure: a definition and grading by the International Study Group of Liver Surgery (ISGLS). Surgery. 2011;149(5):713-24.

-27. Sultana A, Brooke-Smith M, Ullah S, Figueras J, Rees M, Vauthey JN, Conrad C, Hugh TJ, Garden OJ, Fan ST, Crawford M, Makuuchi M, Yokoyama Y, Büchler M, Padbury R. Prospective evaluation of the International Study Group for Liver Surgery definition of post hepatectomy liver failure after liver resection: an international multicentre study. HPB (Oxford). 2018;20(5):462-469.

-28. Mullen JT, Ribero D, Reddy SK, Donadon M, Zorzi D, Gautam S, Abdalla EK, Curley SA, Capussotti L, Clary BM, Vauthey JN. Hepatic insufficiency and mortality in 1,059 noncirrhotic patients undergoing major hepatectomy. J Am Coll Surg. 2007;204(5):854-62; discussion 862-4.

-29. Balzan S, Belghiti J, Farges O, Ogata S, Sauvanet A, Delefosse D, Durand F. The "50-50 criteria" on postoperative day 5: an accurate predictor of liver failure and death after hepatectomy. Ann Surg. 2005;242(6):824-8, discussion 828-9.

-30. Mayo SC, Shore AD, Nathan H, Edil BH, Hirose K, Anders RA, Wolfgang CL, Schulick RD, Choti MA, Pawlik TM. Refining the definition of perioperative mortality following hepatectomy using death within 90 days as the standard criterion. HPB (Oxford). 2011;13(7):473-82.

-31. Egger ME, Ohlendorf JM, Scoggins CR, McMasters KM, Martin RC 2nd. Assessment of the reporting of quality and outcome measures in hepatic resections: a call for 90-day reporting in all hepatectomy series. HPB (Oxford). 2015;17(9):839-45.

-32. Schiergens TS, Dörsch M, Mittermeier L, Brand K, Küchenhoff H, Lee SM, Feng H, Jauch KW, Werner J, Thasler WE. Thirty-day mortality leads to underestimation of postoperative death after liver resection: A novel method to define the acute postoperative period. Surgery. 2015;158(6):1530-7.

-33. Azoulay D, Pascal G, Salloum C, Adam R, Castaing D, Tranecol N. Vascular reconstruction combined with liver resection for malignant tumours. Br J Surg. 2013;100(13):1764-75.

-34. Giovannini I, Chiarla C, Giuliante F, Vellone M, Ardito F, Sarno G, Nuzzo G. Analysis of the components of hypertransaminasemia after liver resection. Clin Chem Lab Med. 2007;45(3):357-60.

-35. Gurusamy KS, Sheth H, Kumar Y, Sharma D, Davidson BR. Methods of vascular occlusion for elective liver resections. Cochrane Database Syst Rev. 2009;Jan 21;(1):CD007632.

-36. Belghiti J, Noun R, Malafosse R, Jagot P, Sauvanet A, Pierangeli F, Marty J, Farges O. Continuous versus intermittent portal triad clamping for liver resection: a controlled study. Ann Surg. 1999;229(3):369-75.

-37. van den Broek MA, Shiri-Sverdlov R, Schreurs JJ, Bloemen JG, Bieghs V, Rensen SS, Dejong CH, Olde Damink SW. Liver manipulation during liver surgery in humans is associated with hepatocellular damage and hepatic inflammation. Liver Int. 2013;33(4):633-41.

-38. van de Poll MC, Derikx JP, Buurman WA, Peters WH, Roelofs HM, Wigmore SJ, Dejong CH. Liver manipulation causes hepatocyte injury and precedes systemic inflammation in patients undergoing liver resection. World J Surg. 2007;31(10):2033-8.

-39. Fung J, Poon RT, Yu WC, Chan SC, Chan AC, Chok KS, Cheung TT, Seto WK, Lo CM, Lai CL, Yuen MF. Use of liver stiffness measurement for liver resection surgery: correlation with indocyanine green clearance testing and post-operative outcome. PLoS One. 2013;8(8):e72306.

-40. Vassanasiri W, Rungsakulkij N, Suragul W, Tangtawee P, Muangkaew P, Mingphruedhi S, Aeesoa S. Early postoperative serum aspartate aminotransferase for prediction of post-hepatectomy liver failure. Perioper Med (Lond). 2022;11(1):51.

-41. Boissel JP, Collet JP, Moleur P, Haugh M. Surrogate endpoints: a basis for a rational approach. Eur J Clin Pharmacol. 1992;43(3):235-44.

Published

2025-12-23

How to Cite

Mollard, L., Gasque, R. A., Chahdi Beltrame, M., Lenz, M. E., Mattera, F. J., & Quiñonez, E. G. (2025). Transaminases on the First Day After Hepatectomy and Prediction of Outcomes in Malignant Disease. Acta Gastroenterológica Latinoamericana, 55(4), 358–370. https://doi.org/10.52787/agl.v55i4.547

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