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Annaly khirurgicheskoy gepatologii = Annals of HPB Surgery

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Infectious complications after elective surgeries on the liver and pancreas

https://doi.org/10.16931/1995-5464.2023-4-71-80

Abstract

Aim. To analyze the complications of liver and pancreas surgeries, including infectious complications, and to describe the evolution of microbial flora in the hepatopancreatobiliary surgery unit.

Materials and methods. The study involved 650 patients who underwent pancreatoduodenectomy and 1253 patients after liver resection. Types of preoperative biliary drainage were evaluated in terms of their influence on the treatment results. The incidence and nature of postoperative bile leakage were studied. The study included an analysis of microbial flora in the hepatopancreatobiliary surgery unit for 10 years.

Results. The rate of significant complications, including infectious complications, appeared to be unaffected by a type of bile ducts drainage with potential infection at a standard course after pancreatoduodenectomy. A pancreatic fistula is considered to be a major factor in the development of abdominal infectious complications and the main cause of unfavorable outcomes. A bile leakage was most often revealed after liver resection in 95 observations (7.5%), and significantly more often after extensive liver resections. Gram-negative flora prevailed in bile from external drains of bile ducts and wound exudates in two thirds of cases. Gram-positive microorganisms were detected in one third of patients, fungi – in less than 5% of cases. The drainage fluids mostly obtained polyresistant gram-negative microorganisms. The majority of strains revealed resistance to cephalosporins, fluoroquinolones, penicillins, and an increasing resistance to carbapenems in dynamics.

Conclusion. Bacterobilia after bile duct drainage significantly determines a microbial landscape of a hepatopancreatobiliary surgery unit. Pancreatodigestive anastomotic leakage is recognized as an important predictor of infectious complications in the area of intervention after pancreatoduodenectomy. Cases of this kind require the antimicrobial therapy with respect to the initial flora of the biliary tract. A bile leakage is considered to be a main contributor to infectious complications after liver resection. Extensive liver resection can lead to a sepsis-like state in the early postoperative period, predisposing to infectious complications.

About the Authors

V. E. Zagainov
Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation; State Budgetary Healthcare Institution “Nizhny Novgorod Regional Clinical Oncological Dispensary”
Russian Federation

Vladimir E. Zagainov – Doct. of Sci. (Med.), Director of the Institute of Surgery and Oncology; Head of the Department of Faculty Surgery and Transplantology

10/1, pl. Minin and Pozharsky, Nizhny Novgorod, 603005, Russian Federation

11/1, Delovaya str., Nizhny Novgorod, 603163, Russian Federation



O. V. Ruina
Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation; State Budgetary Healthcare Institution “Nizhny Novgorod Regional Clinical Oncological Dispensary”
Russian Federation

Olga V. Ruina – Cand. of Sci. (Med.), Associate Professor, Department of General and Clinical Pharmacology; Clinical Pharmacologist

10/1, pl. Minin and Pozharsky, Nizhny Novgorod, 603005, Russian Federation

11/1, Delovaya str., Nizhny Novgorod, 603163, Russian Federation



N. V. Zarechnova
Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation; State Budgetary Healthcare Institution “Nizhny Novgorod Regional Clinical Oncological Dispensary”
Russian Federation

Natalya V. Zarechnova – Cand. of Sci. (Med.), Head of the Center for Anesthesiology and Resuscitation – Anesthesiologist and Resuscitator; Assistant of the Department of Anesthesiology,
Resuscitation and Transfusiology

10/1, pl. Minin and Pozharsky, Nizhny Novgorod, 603005, Russian Federation

11/1, Delovaya str., Nizhny Novgorod, 603163, Russian Federation



D. M. Kuchin
Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation
Russian Federation

Denis M. Kuchin – Cand. of Sci. (Med.), Associate Professor, Department of General Surgery

10/1, pl. Minin and Pozharsky, Nizhny Novgorod, 603005, Russian Federation



N. M. Kiselev
Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation; State Budgetary Healthcare Institution “Nizhny Novgorod Regional Clinical Oncological Dispensary”
Russian Federation

Nikolai M. Kiselev – Cand. of Sci. (Med.), Associate Professor of the Department of Faculty Surgery and Transplantology; Head

10/1, pl. Minin and Pozharsky, Nizhny Novgorod, 603005, Russian Federation

11/1, Delovaya str., Nizhny Novgorod, 603163, Russian Federation



N. U. Naraliev
Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation; State Budgetary Healthcare Institution “Nizhny Novgorod Regional Clinical Oncological Dispensary”
Russian Federation

Nasipbek U. Naraliev – Assistant of the Department of Faculty Surgery and Transplantology; Oncologist

10/1, pl. Minin and Pozharsky, Nizhny Novgorod, 603005, Russian Federation

11/1, Delovaya str., Nizhny Novgorod, 603163, Russian Federation



Sh. Kh. Mukhanzaev
Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation; Privolzhsky District Medical Center, FMBA of Russia
Russian Federation

Shamsudin Кh. Mukhanzaev – Assistant of the Department of Faculty Surgery and Transplantology; Oncologist

10/1, pl. Minin and Pozharsky, Nizhny Novgorod, 603005, Russian Federation

20а, Nizhny Novgorod, Marshal Voronov str., 603074, Russian Federation



References

1. Kokudo T., Uldry E., Demartines N., Halkic N. Risk factors for incisional and organ space surgical site infections after liver resection are different. World J. Surg. 2015; 39 (5): 1185–1192. https://doi.org/10.1007/s00268-014-2922-3

2. Morikawa T., Ishida M., Iseki M., Aoki S., Hata T., Kawaguchi K., Ohtsuka H., Mizuma M., Hayashi H., Nakagawa K., Kamei T., Unno M. Liver resections in patients with prior bilioenteric anastomosis are predisposed to develop organ/space surgical site infections and biliary leakage: results from a propensity score matching analysis. Surg. Today. 2021; 51 (4): 526–536. https://doi.org/10.1007/s00595-020-02105-4

3. Nakagawa K., Tanaka K., Nojiri K., Sawada Y., Kumamoto T., Ueda M., Minami Y., Mochizuki Y., Morioka D., Kubota T., Kamiya N., Yoshida K., Yonemoto N., Endo I. Predictive factors for bile leakage after hepatectomy for hepatic tumors: a retrospective multicenter study with 631 cases at Yokohama Clinical Oncology Group (YCOG). J. Hepatobiliary Pancreat. Sci. 2017; 24 (1): 33–41. https://doi.org/10.1002/jhbp.411

4. Yang X., Qiu Y., Wang W., Feng X., Shen S., Li B., Wen T., Yang J., Xu M., Chen Z., Yan L. Risk factors and a simple model for predicting bile leakage after radical hepatectomy in patients with hepatic alveolar echinococcosis. Medicine (Baltimore). 2017; 96 (46): e8774. https://doi.org/10.1097/MD.0000000000008774

5. Mentor K., Ratnayake B., Akter N., Alessandri G., Sen G., French J.J., Manas D.M., Hammond J.S., Pandanaboyana S. Meta-analysis and meta-regression of risk factors for surgical site infections in hepatic and pancreatic resection. World J. Surg. 2020; 44 (12): 4221–4230. https://doi.org/10.1007/s00268-020-05741-6

6. Takahashi Y., Takesue Y., Fujiwara M., Tatsumi S., Ichiki K., Fujimoto J., Kimura T. Risk factors for surgical site infection after major hepatobiliary and pancreatic surgery. J. Infect. Chemother. 2018; 24 (9): 739–743. https://doi.org/10.1016/j.jiac.2018.05.007

7. Wei T., Zhang X.F., Bagante F., Ratti F., Marques H.P., Silva S., Soubrane O., Lam V., Poultsides G.A., Popescu I., Grigorie R., Alexandrescu S., Martel G., Workneh A., Guglielmi A., Hugh T., Aldrighetti L., Endo I., Pawlik T.M. Postoperative infectious complications worsen long-term survival after curative-intent resection for hepatocellular carcinoma. Ann. Surg. Oncol. 2022; 29 (1): 315–324. https://doi.org/10.1245/s10434-021-10565-2

8. Müssle B., Hempel S., Kahlert C., Distler M., Weitz J., Welsch T. Prognostic impact of bacterobilia on morbidity and postoperative management after pancreatoduodenectomy: a systematic review and meta-analysis. World J. Surg. 2018; 42 (9): 2951–2962. https://doi.org/10.1007/s00268-018-4546-5

9. Mentor K., Ratnayake B., Akter N., Alessandri G., Sen G., French J.J., Manas D.M., Hammond J.S., Pandanaboyana S. Meta-analysis and meta-regression of risk factors for surgical site infections in hepatic and pancreatic resection. World J. Surg. 2020; 44 (12): 4221–4230. https://doi.org/10.1007/s00268-020-05741-6

10. Takahashi Y., Takesue Y., Fujiwara M., Tatsumi S., Ichiki K., Fujimoto J., Kimura T. Risk factors for surgical site infection after major hepatobiliary and pancreatic surgery. J. Infect. Chemother. 2018; 24 (9): 739–743. https://doi.org/10.1016/j.jiac.2018.05.007

11. Matsumura M., Saiura A., Inoue Y., Ishizawa T., Mise Y., Takahashi Y. High rate of organ/space surgical site infection after hepatectomy with preexisting bilioenteric anastomosis. World J. Surg. 2016; 40 (4): 937–945. https://doi.org/10.1007/s00268-015-3340-x

12. Sugawara G., Yokoyama Y., Ebata T., Igami T., Yamaguchi J., Mizuno T., Onoe S., Watanabe N., Nagino M. Postoperative infectious complications caused by multidrug-resistant pathogens in patients undergoing major hepatectomy with extrahepatic bile duct resection. Surgery. 2020; 167 (6): 950–956. https://doi.org/10.1016/j.surg.2020.02.015

13. The Sanford Guide to Antimicrobial Therapy. 44th edition. 2014. 243 p.

14. Sugawara G., Yokoyama Y., Ebata T., Igami T., Yamaguchi J., Mizuno T., Yagi T., Nagino M. Preoperative biliary colonization/ infection caused by multidrug-resistant (MDR) pathogens in patients undergoing major hepatectomy with extrahepatic bile duct resection. Surgery. 2018; 163 (5): 1106–1113. https://doi.org/10.1016/j.surg.2017.12.031

15. Firsova V.G., Parshikov V.V., Chebotar’ I.V., Lazareva A.V., Pogorelov A.G. Microbiological diagnosis and choice of antibacterialis therapy of biliary tract infection. Annaly khirurgicheskoy gepatologii = Annals of HPB Surgery. 2015; 20 (1): 124–131. https://doi.org/10.16931/1995-5464.20151124-131 (In Russian)

16. Li W., Li L., Hui L. Cell plasticity in liver regeneration. Trends Cell. Biol. 2020; 30 (4): 329–338. https://doi.org/10.1016/j.tcb.2020.01.007

17. Yagi S., Hirata M., Miyachi Y., Uemoto S. Liver regeneration after hepatectomy and partial liver transplantation. Int. J. Mol. Sci. 2020; 21 (21): 8414. https://doi.org/10.3390/ijms21218414

18. Sato Y., Koyama S., Tsukada K., Hatakeyama K. Acute portal hypertension reflecting shear stress as a trigger of liver regeneration following partial hepatectomy. Surg. Today. 1997; 27 (6): 518–526. https://doi.org/10.1007/BF02385805

19. Nishii K., Brodin E., Renshaw T., Weesner R., Moran E., Soker S., Sparks J.L. Shear stress upregulates regenerationrelated immediate early genes in liver progenitors in 3D ECM-like microenvironments. J. Cell. Physiol. 2018; 233 (5): 4272–4281. https://doi.org/10.1002/jcp.26246

20. Ozaki M. Cellular and molecular mechanisms of liver regeneration: proliferation, growth, death and protection of hepatocytes. Semin. Cell. Dev. Biol. 2020; 100: 62–73. https://doi.org/10.1016/j.semcdb.2019.10.007

21. Gao B., Jeong W.I., Tian Z. Liver: an organ with predominant innate immunity. Hepatology. 2008; 47 (2): 729–736. https://doi.org/10.1002/hep.22034

22. Schmidt-Arras D., Rose-John S. IL-6 pathway in the liver: from physiopathology to therapy. J. Hepatol. 2016; 64 (6): 1403–1415. https://doi.org/10.1016/j.jhep.2016.02.004

23. Abu Rmilah A., Zhou W., Nelson E., Lin L., Amiot B., Nyberg S.L. Understanding the marvels behind liver regeneration. Wiley Interdiscip. Rev. Dev. Biol. 2019; 8 (3): e340. https://doi.org/10.1002/wdev.340

24. Fang H., Liu A., Chen X., Cheng W., Dirsch O., Dahmen U. The severity of LPS induced inflammatory injury is negatively associated with the functional liver mass after LPS injection in rat model. J. Inflamm. (Lond). 2018; 15: 21. https://doi.org/10.1186/s12950-018-0197-4

25. Simmons J.D., Lee Y.L., Mulekar S., Kuck J.L., Brevard S.B., Gonzalez R.P., Gillespie M.N., Richards W.O. Elevated levels of plasma mitochondrial DNA DAMPs are linked to clinical outcome in severely injured human subjects. Ann. Surg. 2013; 258 (4): 591–596; discussion 596–598. https://doi.org/10.1097/SLA.0b013e3182a4ea46

26. Rampes S., Ma D. Hepatic ischemia-reperfusion injury in liver transplant setting: mechanisms and protective strategies. J. Biomed. Res. 2019; 33 (4): 221–234. https://doi.org/10.7555/JBR.32.20180087

27. Borjas T., Jacob A., Yen H., Patel V., Coppa G.F., Aziz M., Wang P. Inhibition of the interaction of TREM-1 and eCIRP attenuates inflammation and improves survival in hepatic ischemia/reperfusion. Shock. 2022; 57 (2): 246–255. https://doi.org/10.1097/SHK.0000000000001894

28. Land W.G. The Role of damage-associated molecular patterns (DAMPs) in human diseases: Part II: DAMPs as diagnostics, prognostics and therapeutics in clinical medicine. Sultan Qaboos Univ. Med. J. 2015; 15 (2): e157 70. PMID: 26052447

29. Singer M., Deutschman C.S., Seymour C.W., Shankar-Hari M., Annane D., Bauer M., Bellomo R., Bernard G.R., Chiche J.D., Coopersmith C.M., Hotchkiss R.S., Levy M.M., Marshall J.C., Martin G.S., Opal S.M., Rubenfeld G.D., van der Poll T., Vincent J.L., Angus D.C. The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA. 2016; 315 (8): 801–810. https://doi.org/10.1001/jama.2016.0287


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For citations:


Zagainov V.E., Ruina O.V., Zarechnova N.V., Kuchin D.M., Kiselev N.M., Naraliev N.U., Mukhanzaev Sh.Kh. Infectious complications after elective surgeries on the liver and pancreas. Annaly khirurgicheskoy gepatologii = Annals of HPB Surgery. 2023;28(4):71-80. (In Russ.) https://doi.org/10.16931/1995-5464.2023-4-71-80

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ISSN 1995-5464 (Print)
ISSN 2408-9524 (Online)