Skip to main content

Antibiotic prophylaxis with piperacillin–tazobactam reduces organ/space surgical site infection after pancreaticoduodenectomy: a retrospective and propensity score-matched analysis

Abstract

Background

The occurrence of surgical site infection (SSI) after pancreaticoduodenectomy (PD) is still relatively high. The aim of this retrospective study is to evaluate the efficacy of piperacillin-tazobactam as perioperative prophylactic antibiotic on organ/space SSI for patients underwent PD.

Methods

Four hundred seven consecutive patients who underwent PD between January 2018 and December 2022 were enrolled and analyzed retrospectively. The univariate and multivariate analysis were used to identify independent risk factors of organ/space SSI. Postoperative complications were compared between the two groups according to the use of prophylactic antibiotics by a ratio of 1:1 propensity score-matched (PSM) analysis.

Results

Based on perioperative prophylactic antibiotic use, all 407 patients were divided into the ceftriaxone group (n = 192, 47.2%) and piperacillin–tazobactam group (n = 215, 52.8%). The rate of organ/space SSI was 31.2% with the choice of perioperative antibiotics (OR = 2.837, 95%CI = 1.802–4.465, P < 0.01) as one of independent risk factors. After PSM, there were similar baseline characteristics among the groups. Meanwhile, the piperacillin–tazobactam group had a significant lower rate of organ/space SSI compared to the ceftriaxone group both before and after PSM(P < 0.05).

Conclusions

The adoption of piperacillin–tazobactam as perioperative prophylaxis for patients underwent PD reduced organ/space SSI significantly.

Peer Review reports

Introduction

Pancreaticoduodenectomy (PD) is a conventional surgical procedure performed for both benign or malignant disease localized in the pancreatic head or periampullary region with relative high risk of morbidity and mortality [1]. Organ/space surgical site infection (SSI) after PD, which is one of the most frequent postoperative complications as we reported previously [2], sometimes triggers life-threatening complications, such as postoperative fistula (POPF), post-pancreatectomy hemorrhage (PPH), and sepsis [3, 4]. Current guidelines of hepatopancreatobiliary surgery recommend second-generation cephalosporins (cefoxitin or cefotetan) or third-generation cephalosporins (ceftriaxone) as perioperative prophylaxis [5]. As antibiotic resistance increases, the perioperative prophylactic antibiotics provide limited coverage of resistant pathogens, particularly in PD [5, 6]. Yet, the effect of taking broader-spectrum agents as perioperative prophylactic antibiotic regimen for preventing SSI after PD has been investigated in several studies with opposite results [7,8,9,10].

Given the high rate of postoperative organ/space SSI and the controversy over perioperative antimicrobial prophylaxis regimens for PD, in current study we evaluate the efficacy of piperacillin-tazobactam as perioperative prophylactic antibiotic for patients underwent PD.

Methods

Patients

The medical data of consecutive patients who underwent PD between January 2018 and December 2022 in the Drum Tower Hospital of Nanjing University Medical School were collected retrospectively. The inclusion criteria were as follows: (a)underwent conventional PD or pylorus-preserving PD (PPPD); (b) no evidence of local unresectable or other active cancers at diagnosis, and (c) > 18 years of age. The exclusion criteria were as follows: (a)underwent simultaneous hepatic or colon resection; (b)clinical data were incomplete, and (c)history of neoadjuvant chemotherapy. The study was approved by the Health Research Ethics Board of Drum Tower Hospital of Nanjing University Medical School (2021–271-01).

Surgical procedures and perioperative management

All PDs were performed by two experienced teams. Standard perioperative managements instead of the choice of prophylactic antibiotics were applied for all patients. The PD procedure and indications of preoperative biliary drainage (PBD) were as previously described [11].

All patients delivered intravenous antibiotics within a 30 min window prior to skin incision [5]. The choice of antibiotic was at the discretion of the operating surgeon. For patients without signs of organ/space SSI [12] during early postoperative period, regardless of whether the ascites culture was positive or negative, intravenous ceftriaxone was administered routinely for 3 days (the operation day and postoperative day 1 and 2) in the ceftriaxone group and piperacillin–tazobactam (4.5 g/500 mg) was given and continued at 13.5 g/1500 mg daily after surgery until postoperative day (POD) 5 intravenous in the piperacillin–tazobactam group. For patients with signs of organ/space SSI, the antibiotics were altered based on bacteriologic profiles and antibiogram of the pathogens in ascites.

Drain fluid test consist of amylase concentration, bacterial smear, and culture were conducted on POD 1,3, 5 and every 2 to 3 days thereafter until drains were removed, regardless of whether the patients underwent CR-POPF and/or SSI. The drainage tubes were removed on POD 7 after the abdominal enhanced computed tomography (CT) conducted on POD 7 showed no evidences of CR-POPF or fluid collection were found.

Clinical data collection and definition of complication

Demographic data (age, gender, high blood pressure, diabetic mellitus, BMI, preoperative jaundice, preoperative biliary drainage), preoperative laboratory data (alanine aminotransferase, total bilirubin, direct bilirubin, albumin), intraoperative variables (diameter of main pancreatic duct, vessel resection, operating time, volume of blood loss and transfusion), pathological diagnosis were all collected. Postoperative complications were classified according to the Clavien–Dindo classification, with major complications being defined as grade ≥ III [13]. The assessment of SSI which includes incisional and organ/space SSI was based on the Centers for Disease Control and Prevention (CDC) guidelines [12]. Clinically relevant postoperative pancreatic fistula (CR-POPF), and post-pancreatectomy hemorrhage (PPH) were diagnosed according to the International Study Group of Pancreatic Surgery (ISGPS) [14, 15]. Bacteremia, pneumonia and urinary tract infection were all included and diagnosed as previous described [16, 17].

Statistical analysis

Clinical data was analyzed using SPSS 26.0 software for Windows (SPSS Inc.) was used for clinical data analyses. χ2 test or Fisher’s exact test was performed for categorical variables, which expressed as absolute number and percentage. Normally distributed continuous variables were analyzed by independent t-test, which expresses by mean and standard deviation (SD). Mann–Whitney U test was applied and showed as median (interquartile range, IQR) for non-normally distributed clinical data. Univariate and multivariate logistic regression analysis of organ/space SSI were completed with the entire cohort of 407 patients. All variables with P < 0.1 in univariate analysis entered the multivariate logistic regression model to find out the independent risk factors for organ/space SSI. Odds ratio (OR) and 95% confidence intervals (95%CI) were obtained. For all analyses, P < 0.05 was considered as statistics significantly.

To compare the difference of ceftriaxone group and piperacillin–tazobactam group, a 1:1 nearest-neighbor propensity score-matching (PSM) analysis was performed which modifying total bilirubin, direct bilirubin, pancreas consistency, vessel resection, diameter of MPD, operating time, blood loss volume and blood transfusion volume. Caliper matching on propensity score was estimated, and pairs were matched to within a range of 0.2 standard deviation of the logistic model of the propensity score.

Results

Patient characteristics

The study enrolled 407 patients during the 5-year study period. They were classified into two groups as piperacillin–tazobactam group (n = 215, 52.8%) and ceftriaxone group (n = 192, 47.2%) according to the use of perioperative antibiotics. The clinical and baseline characteristics were shown in Table 1. The study included 263(64.6%) men and 144(35.4%) women with the mean age of the entire cohort was 61.7 ± 11.5 years. A total of 146(35.9%) were diagnosed with preoperative jaundice and 100(24.6%) received PBD. 152(37.3%) patients occurred infectious complications which consisted with SSI, bacteremia pneumonia and urinary tract infection. Organ/space SSI was the most common complication after surgery, accounting for 31.2%. 101(24.8%) patients developed CR-POPF and 69(16.9%) patients underwent postoperative major complication (Calvien-Dindo grade ≥ III).

Table 1 Clinical characteristic of all patients

Comparison of postoperative complications

Regardless of whether PBD was performed or not, the incidence of infectious complications (P = 0.017 and P < 0.001), organ/space SSI (P = 0.018 and P < 0.001) and organ/space SSI combined with CR-POPF (P = 0.023 and P = 0.016) were significantly lower in the piperacillin-tazobactam group. As to the severity of complications, the occurrence of CR-POPF (P < 0.001), PPH (P < 0.001), infectious complications (P < 0.001), organ/space SSI (P < 0.001), isolated CR-POPF (P = 0.016) and organ/space SSI combined with CR-POPF (P < 0.001) was significantly higher in patients with major complication (Clavien-Dindo grade ≥ III) (Tables 2 and 3).

Table 2 Comparison of postoperative complications according to the preoperative biliary drainage and perioperative antibiotics regimes
Table 3 Comparison of postoperative complications according to the severity of postoperative complications

Microbiological analysis

The profile of bacteria in intraoperative bile and postoperative drain fluid was listed in Table 4. K. pneumoniae is the most common microorganism in intraoperative bile culture (n = 20, 15.3%). Other common bacteria were E. coli (n = 11, 8.4%) and E. faecalis (n = 8, 6.1%). The most common bacterial species isolated from postoperative drain fluid were K. pneumoniae (n = 56, 13.8%), followed by E. faecalis (n = 49, 12.0%), E. coli (n = 28, 6.9%), E. faecium (n = 28, 6.9%), fungus (n = 28, 6.9%), and E. cloacae (n = 23, 5.7%). Based on the relative high prevalence of the pathogens detected in intraoperative bile and postoperative ascites drainage, the resistance profile of the selected antibiotics/antimycotics was shown in Supplemental Tables S1 and S2. Bacterial resistance was generally elevated in postoperative abdominal drainage fluid compared with intraoperative bile bacterial resistance. Targeting bacteria in postoperative peritoneal drainage, subgrouped according to the perioperative antibiotic regimen, bacterial resistance in the piperacillin-tazobactam group was essentially similar to that in the ceftriaxone group.

Table 4 Microorganisms cultured from intraoperative bile and drainage fluid after pancreaticoduodenectomy

Risk factors for organ/space SSI

In univariate analysis, gender (OR = 1.676, 95%CI = 1.060–2.647, P = 0.027), PBD (OR = 1.891, 95%CI = 1.183–3.024, P = 0.008), the choice of perioperative antibiotic (ceftriaxone vs. piperacillin–tazobactam) (OR = 2.681, 95%CI = 1.737–4.137 P < 0.001) and the diameter of main pancreatic duct (MPD) (OR = 0.872 95%CI = 0.777–0.979, P = 0.021) were associated with the development of organ/space SSI significantly. In multivariate analysis, gender (OR = 1.956, 95%CI = 1.204–3.177 P = 0.007), PBD (OR = 1.730, 95%CI = 1.041–2.875, P = 0.034), the choice of perioperative antibiotic (ceftriaxone vs. piperacillin–tazobactam) (OR = 2.837, 95%CI = 1.802–4.465, P < 0.001) and the diameter of MPD (OR = 0.879, 95%CI = 0.776–0.995 P = 0.041) were also the independent risk factors of organ/space SSI (Table 5).

Table 5 Risk factors of organ/space SSI: Univariate and multivariate logistic regression analysis

Propensity score-matched analysis

As shown in Table 6, patients treated with piperacillin–tazobactam had lower level of total bilirubin (TB) and direct bilirubin (DB). At the same time, patients in the ceftriaxone group had higher level of operating time, blood loss volume and blood transfusion volume compared with the piperacillin–tazobactam group. Furthermore, the rate of vessel resection and consistency of pancreas showed statistical difference.

Table 6 Baseline characteristics in the unmatched and matched group according to the perioperative antibiotics

In order to adjust the differences of baseline variables in each group, a 1:1 nearest-neighbor propensity score matching (PSM) analysis was conducted. After PSM, a balanced cohort included the piperacillin–tazobactam group as observational group (110 patients) and the ceftriaxone group as the control group (110 patients). All baseline characteristics were comparable after PSM.

Postoperative complications according to PSM

After PSM, organ/space SSI occurred in 43(39.1%) patients in the ceftriaxone group and 21(19.1%) patients in the piperacillin–tazobactam group (P = 0.001; Table 7). Both before and after PSM, the major complication occurred more frequently in the ceftriaxone group significantly. Furthermore, the rates of CR-POPF, BL, PPH, incisional SSI, bacteremia, pneumonia, and urinary tract infection were comparable between the two groups (Table 7).

Table 7 Postoperative mortality and morbidity according to the perioperative antibiotics

Discussion

In this study, the occurrence of postoperative major complication (Clavien–Dindo grade ≥ III), infectious complication, and organ/space SSI were 16.9%, 37.3%, and 31.2%, respectively, and consistent with previous studies [10, 17, 18]. We also identified that the choice of perioperative prophylactic antibiotic was one of the independent risk factors for organ/space SSI. Meanwhile, K. pneumonia, E. coli and E. faecalis were the most frequently isolated pathogens in both intraoperative bile and postoperative drain fluids. In addition, we conducted an additional analysis by propensity score-matching (PSM) to lessen the bias of baseline variables between two groups. Both before and after PSM, the occurrence of major complication, infectious complications and organ/space SSI were significantly higher in the ceftriaxone group. Meanwhile, the additional therapeutic antibiotics administration rates after PD according to clinical symptoms of organ/space SSI in piperacillin-tazobactam and ceftriaxone group were 25.5% and 59.9%, respectively.

Despite the dramatic improvements in surgical techniques of PD, postoperative morbidity has persistently remained high. Given that organ/space SSI is the most frequent cause of postoperative complications, which may trigger subsequent events such as CR-POPF, sepsis, readmission or even death, this retrospective study’s findings are notable. As we reported previously and showed in this study, PBD was substantially correlated with postoperative infectious complications especially organ/space SSI [2, 11, 19]. This invasive operation destroys the function of Oddi’s sphincter, increase the contamination of surgical field with bile which may contain microbes resistant to ceftriaxone after the resection of common bile duct [20, 21].

The microbiology of ascites after PD, which carries a significant risk of digestive anastomotic leakage and abdominal infection, is still challenging. Several reports had indicated that Enterococcus, Enterobacter and Klebsiella species were the predominant organisms isolated from SSI after PD [21,22,23]. Our previous research identified K. pneumoniae, E. faecalis and S. haemolyticus were the most frequently isolated bacteria in bile culture [24]. Moreover, the most common bacterial species isolated from the drainage fluid in current study were K. pneumoniae, followed by E. faecalis, E. coli and E. faecium, which were almost consistent with the existing studies leading us to speculate that intraoperative bile contamination might correlate and promote the organ/space SSI [18, 25]. This speculation is supported indirectly by the fact that a number of studies had demonstrated that specific antibiotic based on bile culture was effective on reducing the incidence of organ/space SSI [26,27,28]. We identified K. pneumoniae had negative impacts on organ/space SSI, major complications, CR-POPF based on past research [11]. The study focused on the anastomoses of the digestive tract had implicated collagenase-producing pathogens, such as Enterococcus, in the formation of anastomotic leakage which may result in subsequent organ/space SSI [29,30,31]. The administration of piperacillin-tazobactam may cover more pathogens especially Enterococcus which contaminate the surgical field during the operation than ceftriaxone, thus reducing the incidence of organ/space SSI. The reduced rates of major complication and infectious complications are likely to be related to the percutaneous drainage placement, reoperation and postoperative mortality.

The regimes recommended by guidelines for perioperative prophylactic antibiotic are variable. Additionally, there is a lack of compliance with guidelines. For the purpose of decreasing the occurrence of organ/space SSI, piperacillin-tazobactam was utilized as prophylactic antibiotic. Patients underwent pancreatic resection especially pancreaticoduodenectomy, however, still lack a clear indication of perioperative prophylactic antibiotic. The Japanese investigation conducted by Kimura et al. revealed significant variation in the pancreaticoduodenectomy perioperative prophylactic scheme, including the application of ampicillin, various cephalosporin classes, cefoperazone-sulbactam, and carbapenems [32]. At the same time, the study identified substantial variation in the time requisite for surgical prophylaxis, in the range of 1 to 14 postoperative days. As the increasing antibiotic resistance of the organisms colonizing on the bile duct, institutional data and policy were revised according to earlier researches. According to a recent meta-analysis conducted by Droogh et al. that included 8 studies, prolonged prophylactic antibiotic usage for patients who underwent PBD before surgery significantly reduced the incidence of abdominal infections [33]. In addition, the article suggests that the antibiotic resistance of patients undergoing perioperative or long-term prevention was comparable. Pastena et al. reported adopting antibiotic prophylaxis on the basis of piperacillin-tazobactam was associated with reducing postoperative SSI [10]. The randomized controlled study conducted by D’Angelica et al. found that the use of piperacillin-tazobactam as perioperative prophylactic antibiotic for PD was effective in reducing several postoperative complications including organ/space SSI [1]. The data gathered as a result of current study supported the hypothesis that organ/space SSI can be reduced by the application of the proper antibiotic prophylaxis, such as piperacillin-tazobactam.

To the best of our knowledge, the present study is the first retrospective cohort utilizing PSM for identifying the impact of piperacillin-tazobactam about the postoperative complications especially organ/space SSI. After PSM, the introduction of piperacillin-tazobactam decreases the development several postoperative complications, especially organ/space SSI. Furthermore, according to the results of current study, postoperative drainage bacterial resistance showed an elevated trend compared to intraoperative bile. Meanwhile, abdominal isolates resistance in patients who introduced piperacillin-tazobactam as perioperative prophylactic antibiotic was basically similar compared to ceftriaxone, which consistent with Droogh et al. [33]. The retrospective cohort study conducted by Tarvainen et al. revealed that the resistance of second-generation cephalosporin in intraoperative bile was common in patients who underwent PBD. They pointed out that the take broad-spectrum antibiotics as perioperative prophylaxis may be beneficial for these high-risk patients [34]. These indicate that the emergence of multi-drug resistant microorganisms, broader spectrum antibiotics such as piperacillin-tazobactam can be adapted as prophylactic antibiotic especially after PD, especially for those who underwent PBD.

The present study has several limitations. First, it was a single center retrospective study accompanied by unavoidable biases, such as year of surgery and the surgeon's choice of antibiotics, even though the patients in the time period of current study were under a relatively fixed perioperative treatment regimen at our center. Further multicenter and randomize controlled trails are indispensable to validate the impact of piperacillin-tazobactam on organ/space SSI. Second, even though we utilized propensity score to reduce the effect of confounding variables on the results of the study, there were still some confounders that remained unobserved. At the same time, the introducing of propensity scores raised the issue of potentially dropping cases (i.e., dropping participants who cannot be matched), which lead to imperfect matching (i.e., missing cases and reduced sample size). Therefore, further randomized controlled studies are needed to confirm the results of this study. Third, the present study design cannot determine whether the reduction in organ/space SSI was related to the duration of antibiotic administration. A further prospective trial investigating the duration of antibiotic administration on postoperative complications is currently underway.

In conclusion, the outcomes of our study showed that the regime of perioperative antibiotics was an independent risk factor of organ/space SSI after PD. At the same time, the patients take piperacillin-tazobactam as prophylactic antibiotic experience a lower rate of organ/space SSI even after PSM.

Availability of data and materials

The datasets generated and/or analyzed during the present study are not publicly available due to patient privacy concerns, but are available from the corresponding author upon reasonable request.

References

  1. D’Angelica MI, Ellis RJ, Liu JB, Brajcich BC, Gönen M, et al. Piperacillin-tazobactam compared with cefoxitin as antimicrobial prophylaxis for pancreatoduodenectomy: a randomized clinical trial. JAMA. 2023;329(18):1579–88. https://0-doi-org.brum.beds.ac.uk/10.1001/jama.2023.5728.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Fu X, Yang Y, Mao L, Qiu Y. Risk factors and microbial spectrum for infectious complications after pancreaticoduodenectomy. Gland Surg. 2021;10(12):3222–32. https://0-doi-org.brum.beds.ac.uk/10.21037/gs-21-590.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Kone LB, Torres C, Banulescu M, Maker VK, Maker AV. Perioperative broad-spectrum antibiotics are associated with decreased surgical site infections compared to 1st-3rd generation Cephalosporins after Open Pancreaticoduodenectomy in patients with jaundice or a biliary stent. Ann Surg. 2022;275(6):1175–83. https://0-doi-org.brum.beds.ac.uk/10.1097/SLA.0000000000004216.

    Article  PubMed  Google Scholar 

  4. Beane JD, Borrebach JD, Zureikat AH, Kilbane EM, Thompson VM, Pitt HA. Optimal pancreatic surgery: are we making progress in North America. Ann Surg. 2021;274(4):e355-5363. https://0-doi-org.brum.beds.ac.uk/10.1097/SLA.0000000000003628.

    Article  PubMed  Google Scholar 

  5. Bratzler DW, Dellinger EP, Olsen KM, Perl TM, Auwaerter PG, Bolon MK, et al. Clinical practice guidelines for antimicrobial prophylaxis in surgery. Surg Infect (Larchmt). 2013;14(1):73–156. https://0-doi-org.brum.beds.ac.uk/10.1089/sur.2013.9999.

    Article  PubMed  Google Scholar 

  6. Lübbert C, Wendt K, Feisthammel J, Moter A, Lippmann N, Busch T, et al. Epidemiology and resistance patterns of bacterial and fungal colonization of biliary plastic stents: a prospective cohort study. PLoS ONE. 2016;11(5): e0155479. https://0-doi-org.brum.beds.ac.uk/10.1371/journal.pone.0155479.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Macedo F, Mowzoon M, Parikh J, Sathyanarayana SA, Jacobs MJ. Disparities in the management and prophylaxis of surgical site infection and pancreatic fistula after pancreatoduodenectomy. J Hepatobiliary Pancreat Sci. 2017;24(5):268–80. https://0-doi-org.brum.beds.ac.uk/10.1002/jhbp.443.

    Article  PubMed  Google Scholar 

  8. Gavazzi F, Ridolfi C, Capretti G, Angiolini MR, Morelli P, Casari E, et al. Role of preoperative biliary stents, bile contamination and antibiotic prophylaxis in surgical site infections after pancreaticoduodenectomy. BMC Gastroenterol. 2016;16:43. https://0-doi-org.brum.beds.ac.uk/10.1186/s12876-016-0460-1.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Donald GW, Sunjaya D, Lu X, Chen F, Clerkin B, Eibl G, et al. Perioperative antibiotics for surgical site infection in pancreaticoduodenectomy: does the SCIP-approved regimen provide adequate coverage. Surgery. 2013;154(2):190–6. https://0-doi-org.brum.beds.ac.uk/10.1016/j.surg.2013.04.001.

    Article  PubMed  Google Scholar 

  10. De Pastena M, Paiella S, Azzini AM, Zaffagnini A, Scarlini L, Montagnini G, et al. Antibiotic prophylaxis with piperacillin-tazobactam reduces post-operative infectious complication after pancreatic surgery: an Interventional, non-randomized study. Surg Infect (Larchmt). 2021;22(5):536–42. https://0-doi-org.brum.beds.ac.uk/10.1089/sur.2020.260.

    Article  PubMed  Google Scholar 

  11. Yang Y, Fu X, Cai Z, Qiu Y, Mao L. The occurrence of Klebsiella pneumoniae in drainage fluid after pancreaticoduodenectomy: risk factors and clinical impacts. Front Microbiol. 2021;12: 763296. https://0-doi-org.brum.beds.ac.uk/10.3389/fmicb.2021.763296.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Horan TC, Andrus M, Dudeck MA. CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting. Am J Infect Control. 2008;36(5):309–32. https://0-doi-org.brum.beds.ac.uk/10.1016/j.ajic.2008.03.002.

    Article  PubMed  Google Scholar 

  13. 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):205–13. https://doi.org/10.1097/01.sla.0000133083.54934.ae.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Besselink MG, van Rijssen LB, Bassi C, Dervenis C, Montorsi M, Adham M, et al. Definition and classification of chyle leak after pancreatic operation: a consensus statement by the International Study Group on pancreatic surgery. Surgery. 2017;161(2):365–72. https://0-doi-org.brum.beds.ac.uk/10.1016/j.surg.2016.06.058.

    Article  PubMed  Google Scholar 

  15. Wente MN, Veit JA, Bassi C, Dervenis C, Fingerhut A, Gouma DJ, et al. Postpancreatectomy hemorrhage (PPH): an International Study Group of pancreatic surgery (ISGPS) definition. Surgery. 2007;142(1):20–5. https://0-doi-org.brum.beds.ac.uk/10.1016/j.surg.2007.02.001.

    Article  PubMed  Google Scholar 

  16. Guidelines for the management of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia. Am J Respir Crit Care Med. 2005;171(4):388–416. https://0-doi-org.brum.beds.ac.uk/10.1164/rccm.200405-644ST.

  17. Degrandi O, Buscail E, Martellotto S, Gronnier C, Collet D, Adam JP, et al. Perioperative antibiotherapy should replace prophylactic antibiotics in patients undergoing pancreaticoduodenectomy preceded by preoperative biliary drainage. J Surg Oncol. 2019;120(4):639–45. https://0-doi-org.brum.beds.ac.uk/10.1002/jso.25622.

    Article  CAS  PubMed  Google Scholar 

  18. Tanaka K, Nakamura T, Imai S, Kushiya H, Miyasaka D, Nakanishi Y, et al. The use of broad-spectrum antibiotics reduces the incidence of surgical site infection after pancreatoduodenectomy. Surg Today. 2018;48(9):825–34. https://0-doi-org.brum.beds.ac.uk/10.1007/s00595-018-1658-3.

    Article  CAS  PubMed  Google Scholar 

  19. Zhu L, Li T, Yang Y, Tang N, Fu X, Qiu Y. Development and validation of a nomogram for predicting post-operative abdominal infection in patients undergoing pancreaticoduodenectomy. Clin Chim Acta. 2022;534:57–64. https://0-doi-org.brum.beds.ac.uk/10.1016/j.cca.2022.07.003.

    Article  CAS  PubMed  Google Scholar 

  20. Limongelli P, Pai M, Bansi D, Thiallinagram A, Tait P, Jackson J, et al. Correlation between preoperative biliary drainage, bile duct contamination, and postoperative outcomes for pancreatic surgery. Surgery. 2007;142(3):313–8. https://0-doi-org.brum.beds.ac.uk/10.1016/j.surg.2007.04.022.

    Article  PubMed  Google Scholar 

  21. Fong ZV, McMillan MT, Marchegiani G, Sahora K, Malleo G, De Pastena M, et al. Discordance between perioperative antibiotic prophylaxis and wound infection cultures in patients undergoing pancreaticoduodenectomy. JAMA Surg. 2016;151(5):432–9. https://0-doi-org.brum.beds.ac.uk/10.1001/jamasurg.2015.4510.

    Article  PubMed  Google Scholar 

  22. Mohammed S, Evans C, VanBuren G, Hodges SE, Silberfein E, Artinyan A, et al. Treatment of bacteriobilia decreases wound infection rates after pancreaticoduodenectomy. HPB (Oxford). 2014;16(6):592–8. https://0-doi-org.brum.beds.ac.uk/10.1111/hpb.12170.

    Article  PubMed  Google Scholar 

  23. Sugiura T, Mizuno T, Okamura Y, Ito T, Yamamoto Y, Kawamura I, et al. Impact of bacterial contamination of the abdominal cavity during pancreaticoduodenectomy on surgical-site infection. Br J Surg. 2015;102(12):1561–6. https://0-doi-org.brum.beds.ac.uk/10.1002/bjs.9899.

    Article  CAS  PubMed  Google Scholar 

  24. Zhu L, Yang Y, Cheng H, Cai Z, Tang N, Mao L, et al. The role of preoperative biliary drainage on postoperative outcome after pancreaticoduodenectomy in patients with obstructive jaundice. Gland Surg. 2023;12(5):593–608. https://0-doi-org.brum.beds.ac.uk/10.21037/gs-22-648.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Chinikar R, Patricio D, Gosse J, Ickx B, Delhaye M, Closset J, et al. Perioperative antimicrobial prophylaxis in patients undergoing pancreatoduodenectomy: retrospective analysis of bacteriological profile and susceptibility. Acta Chir Belg. 2023;123(4):337–44. https://0-doi-org.brum.beds.ac.uk/10.1080/00015458.2021.2006887.

    Article  PubMed  Google Scholar 

  26. Sudo T, Murakami Y, Uemura K, Hayashidani Y, Hashimoto Y, Ohge H, et al. Specific antibiotic prophylaxis based on bile cultures is required to prevent postoperative infectious complications in pancreatoduodenectomy patients who have undergone preoperative biliary drainage. World J Surg. 2007;31(11):2230–5. https://0-doi-org.brum.beds.ac.uk/10.1007/s00268-007-9210-4.

    Article  PubMed  Google Scholar 

  27. Augenstein VA, Reuter NP, Bower MR, McMasters KM, Scoggins CR, Martin RC. Bile cultures: a guide to infectious complications after pancreaticoduodenectomy. J Surg Oncol. 2010;102(5):478–81. https://0-doi-org.brum.beds.ac.uk/10.1002/jso.21612.

    Article  PubMed  Google Scholar 

  28. Sudo T, Murakami Y, Uemura K, Hashimoto Y, Kondo N, Nakagawa N, et al. Perioperative antibiotics covering bile contamination prevent abdominal infectious complications after pancreatoduodenectomy in patients with preoperative biliary drainage. World J Surg. 2014;38(11):2952–9. https://0-doi-org.brum.beds.ac.uk/10.1007/s00268-014-2688-7.

    Article  PubMed  Google Scholar 

  29. Belmouhand M, Krohn PS, Svendsen LB, Henriksen A, Hansen CP, Achiam MP. The occurrence of Enterococcus faecium and faecalis is significantly associated with anastomotic leakage after pancreaticoduodenectomy. Scand J Surg. 2018;107(2):107–13. https://0-doi-org.brum.beds.ac.uk/10.1177/1457496917731188.

    Article  CAS  PubMed  Google Scholar 

  30. Shogan BD, Belogortseva N, Luong PM, Zaborin A, Lax S, Bethel C, et al. Collagen degradation and MMP9 activation by enterococcus faecalis contribute to intestinal anastomotic leak. Sci Transl Med. 2015;7(286):286ra68. https://0-doi-org.brum.beds.ac.uk/10.1126/scitranslmed.3010658.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Wiegerinck M, Hyoju SK, Mao J, Zaborin A, Adriaansens C, Salzman E, et al. Novel de novo synthesized phosphate carrier compound ABA-PEG20k-Pi20 suppresses collagenase production in Enterococcus faecalis and prevents colonic anastomotic leak in an experimental model. Br J Surg. 2018;105(10):1368–76. https://0-doi-org.brum.beds.ac.uk/10.1002/bjs.10859.

    Article  CAS  PubMed  Google Scholar 

  32. Takahashi Y, Takesue Y, Fujiwara M, Tatsumi S, Ichiki K, Fujimoto J, et al. Risk factors for surgical site infection after major hepatobiliary and pancreatic surgery. J Infect Chemother. 2018;24(9):739–43. https://0-doi-org.brum.beds.ac.uk/10.1016/j.jiac.2018.05.007.

    Article  PubMed  Google Scholar 

  33. Droogh D, Groen JV, de Boer M, van Prehn J, Putter H, Bonsing BA, et al. Prolonged antibiotic prophylaxis after pancreatoduodenectomy: systematic review and meta-analysis. Br J Surg. 2023;110(11):1458–66. https://0-doi-org.brum.beds.ac.uk/10.1093/bjs/znad213.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Tarvainen T, Bonsdorff A, Kolho E, Sirén J, Kokkola A, Sallinen V. Association of cephalosporin resistance in intraoperative biliary cultures with surgical site infections in patients undergoing pancreaticoduodenectomy. A retrospective cohort study. HPB (Oxford). 2023. https://0-doi-org.brum.beds.ac.uk/10.1016/j.hpb.2023.10.011.

Download references

Acknowledgements

We would like to offer our special thanks to members of the multidisciplinary biliopancreatic cancer team of the Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School for their guidance.

Funding

Not applicable.

Author information

Authors and Affiliations

Authors

Contributions

Yifei Yang did the investigation and wrote original draft. Jianjie Sheng did formal analysis and validation. Zhenghua Cai, Linxi Zhu, Chenglin Lu, Liang Mao collected data. Xu Fu participated in conceptualization, methodology and project administration. Yudong Qiu did supervision and project administration. All authors reviewed the manuscript.

Corresponding authors

Correspondence to Yudong Qiu or Xu Fu.

Ethics declarations

Ethics approval and consent to participate

The study was approved by the Health Research Ethics Board of Drum Tower Hospital of Nanjing University Medical School (2021–271-01). Informed consent was obtained from all subjects and/or their legal guardian(s).

Consent for publication

Written informed consent for publication was obtained from all participants.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Supplemental Table S1.

The profile of antibiotics resistance in microorganisms cultured from intraoperative bile. Supplemental Table S2. The profile of antibiotics resistance in microorganisms cultured from postoperative drainage fluid.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yang, Y., Sheng, J., Cai, Z. et al. Antibiotic prophylaxis with piperacillin–tazobactam reduces organ/space surgical site infection after pancreaticoduodenectomy: a retrospective and propensity score-matched analysis. BMC Cancer 24, 251 (2024). https://0-doi-org.brum.beds.ac.uk/10.1186/s12885-024-11955-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s12885-024-11955-x

Keywords