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The goal of this multicenter randomized controlled trial is to evaluate the additional value of pre-emptive antibiotic treatment on clinically relevant organ/space surgical site infections (OSIs) in patients undergoing pancreatoduodenectomy with a high risk for contaminated bile. The main objectives it aims to answer are:
Participants will be randomized with a 1:1 allocation before surgery into the intervention or control group:
Rationale: The additional value of pre-emptive antibiotic treatment after pancreatoduodenectomy is undetermined as previous research reported conflicting results regarding infectious complications. Prolonged antibiotic prophylaxis (formally pre-emptive antibiotic treatment) after pancreatoduodenectomy might reduce the rate of surgical site infections in patients with a high risk for contaminated bile (predominantly patients with preoperative biliary drainage or an ampullary malignancy). Current national and international guidelines lack clear recommendations regarding pre-emptive antibiotic treatment leading to substantially varying antibiotic prophylactic regimes between institutes.
Objective: This trial evaluates the additional value of pre-emptive antibiotic treatment on clinically relevant organ/space surgical site infections (OSIs) in patients undergoing pancreatoduodenectomy with a high risk for contaminated bile.
Study design: This multicenter, randomized controlled, superiority trial compares perioperative versus pre-emptive antibiotic treatment during five postoperative days after pancreatoduodenectomy in patients with a high risk for contaminated bile.
Study population: Adult patients undergoing pancreatoduodenectomy with a high risk for contaminated bile (patients with preoperative biliary drainage or an ampullary malignancy). Patients with a contraindication for the study antibiotics or a preoperative indication for antibiotics (e.g. cholangitis of preoperative abscesses) are excluded.
Intervention: Participants will be randomized to either perioperative prophylaxis (cefazolin, metronidazole and a single dose of 5-7mg/kg gentamicin, control arm) or additional cefuroxime and metronidazole for five postoperative days (experimental arm).
Main study endpoints: The primary endpoint are organ/space infections (OSIs) within 90 days after surgery requiring a therapeutic intervention. Secondary endpoints are OSIs, isolated OSIs, wound infections, postoperative pancreatic fistula, bile or enteric anastomotic leakage, post pancreatectomy hemorrhage, delayed gastric emptying, bacteremia, Clostridium difficile infection, major morbidity (Clavien-Dindo ≥III), reintervention, ICU admission, length of hospital stay, readmission, and in-hospital and 90-day mortality. Besides, switch of postoperative antibiotics, antibiotic sensitivity patterns and concordance between perioperative bile and postoperative surgical site cultures are analyzed.
Sample size: The sample size is calculated for superiority to achieve an OSI difference of 15% (40% vs 25%). With a 80% power (1-β) and a two-sided significance level (α) of 5.0%, a sample of 304 evaluable patients is required for superiority. Assuming a 3% non-resection rate due to metastatic disease and a 3% loss-of-follow-up rate, an expected number of 322 included patients are needed to reach the sample size of 304 evaluable patients to demonstrate superiority for the intervention.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Perioperative plus prolonged antibiotic prophylaxis | Experimental | Prolonged prophylaxis: a single dose of 5-7mg/kg gentamicin followed by 2gr IV cefazolin and 500mg IV metronidazole every 4 hours of surgery (perioperative prophylaxis) followed by five days of 1500mg IV cefuroxime and 500mg IV metronidazole thrice daily |
|
| Only perioperative prophylaxis | No Intervention | Perioperative prophylaxis: a single dose of 5-7mg/kg gentamicin followed by 2gr IV cefazolin and 500mg IV metronidazole every 4 hours of surgery. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cefuroxime | Drug | 1500mg IV cefuroxime thrice daily during five days. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Rate of clinically relevant organ/space surgical site infection (OSI) between patients with perioperative versus prolonged antibiotic prophylaxis | A clinically relevant OSI is defined by the following criteria:
| 90 days after surgery |
| Measure | Description | Time Frame |
|---|---|---|
| The rate of organ/Space Infection (OSI) between patients with perioperative versus prolonged antibiotic prophylaxis | An OSI is defined by the CDC definition: o The infection appears to be related to the operative procedure and infection involves any part of the anatomy (e.g., organs or spaces) other than the incision opened or manipulated during the operative procedure, and at least one of the following is present:
|
| Measure | Description | Time Frame |
|---|---|---|
| The percentage of patients with a deviation from antibiotic study protocol | Study protocol:
| 5 days |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Daphne HM Droogh, MD | Contact | 071 5261334 | d.h.m.droogh@lumc.nl |
| Name | Affiliation | Role |
|---|---|---|
| J. Sven D. Mieog, MD PhD | Leiden University Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Leiden University Medical Center | Recruiting | Leiden | South Holland | 2333 ZA | Netherlands |
Available upon request to the principal investigator
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Patients will be randomized with a 1:1 allocation before surgery into the intervention or control group:
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| Metronidazole | Drug | 500mg IV metronidazole thrice daily during five days. |
|
|
| 90 days |
| The rate of isolated OSI between patients with perioperative versus prolonged antibiotic prophylaxis | Isolated OSI is defined as an OSI without concurrent anastomotic leakage (pancreatojejunostomy, hepaticojejunostomy or gastrojejunostomy). The concept of an isolated OSI is used to separately classify abdominal infections without concurrent anastomotic leakage. | 90 days |
| The rate of superficial incisional SSI between patients with perioperative versus prolonged antibiotic prophylaxis | A superficial surgical site infection after surgery which involves superficial or deep soft tissue (skin, muscle or fascia, but no intra-abdominal tissue), and at least one of the following criteria is present:
| 90 days |
| The rate of clinically relevant postoperative pancreatic fistula between patients with perioperative versus prolonged antibiotic prophylaxis | Grade B or C postoperative pancreatic fistula (POPF) defined by the International Study Group of Pancreatic Surgery definition: Grade A: Amylase >3 times upper limit of the institutional normal serum amylase value Grade B: Grade A + persistant drainage >3 weeks, clinically relevant change in management of POPF, percutaneous or endoscopic drainage, angiographic procedures for bleeding, or signs of infection without organ failure. Grade C: Grade A or B requiring reoperation, resulting in organ failure or death. | 90 days |
| The rate of bile leakage between patients with perioperative versus prolonged antibiotic prophylaxis | Grade A, B or C defined by the ISGLS definition: Grade A: Bile leakage requiring no or little change in patients' clinical management. Grade B: Bile leakage requiring a change in patients clinical management (eg, additional diagnostic or interventional procedures) but manageable without relaparotomy, or a Grade A bile leakage lasting for >1 week. Grade C: Bile leakage requiring relaparotomy | 90 days |
| The rate of post pancreatectomy hemorrhage between patients with perioperative versus prolonged antibiotic prophylaxis | Grade A, B or C defined by the ISGPS definition: Grade A: Early (<24h after surgery), intra- or extraluminal, clinically mild. Grade B: Early (<24h after surgery), intra- or extraluminal and clinically severe OR later (>24h after surgery), intra- or extraluminal and clincally mild. Grade C: Late (>24h after surgery), intra- or extraluminal and clinically severe. | 90 days |
| The rate of delayed gastric emptying between patients with perioperative versus prolonged antibiotic prophylaxis | Grade A, B or C defined by the ISGPS definition: Grade A: Until day 4-7 or replacement of feeding tube > 3 days after surgery Grade B: Until day 8-14 or replacement of feeding tube > 7 days after surgery Grade C: >day 14 or replacement of feeding tube > 14 after surgery | 90 days |
| The rate of postoperative bacteremia between patients with perioperative versus prolonged antibiotic prophylaxis | Defined as a positive blood culture obtained during a septic period (defined as two or more SIRS criteria) | 90 days |
| The rate of Clostridium difficile infection between patients with perioperative versus prolonged antibiotic prophylaxis | Defined by a positive fecal culture for Clostridium difficile | 90 days |
| Rate of major complications between patients with perioperative versus prolonged antibiotic prophylaxis | Major complications is defined by a Clavien-Dindo score of ≥III. Clavien-Dindo classification of Surgical Complications: Grade I: Any deviation from the normal postoperative course without the need for pharmacological treatment or surgical, endoscopic and radiological interventions. Grade II: Requiring pharmacological treatment with drugs other than such allowed for grade I complications. Grade IIIa: Requiring surgical, endoscopic or radiological intervention not under general anesthesia Grade IIIb: Requiring surgical, endoscopic or radiological intervention under general anesthesia Grade IVa: Life-threatening complication (including CNS complications)* requiring IC/ICU-management with single organ dysfunction (including dialysis). Grade IVb: Life-threatening complication (including CNS complications)* requiring IC/ICU-management with multi organ dysfunction. Grade V: Death of a patient | 90 days |
| The number of reinterventions in patients with perioperative versus prolonged antibiotic prophylaxis | Reinterventions could be either radiological, surgical or endoscopic reinterventions | 90 days |
| The number of ICU admission in patients with perioperative versus prolonged antibiotic prophylaxis | ICU admission | 90 days |
| Length of hospital stay in patients with perioperative versus prolonged antibiotic prophylaxis | In days | 90 days |
| The number of readmissions between patients with perioperative versus prolonged antibiotic prophylaxis | Readmission into the hospital | 90 days |
| Mortality | In-hospital and 90-days mortality | 90 days |
| Antibiotic sensitivity patterns of microorganisms cultured from bile cultures and postoperative cultures from infectious sites between patients with perioperative versus prolonged antibiotic prophylaxis |
Rate of Antibiotic sensitivity patterns in bile cultures and cultures from surgical sites |
| 90 days |
| The percentage of concordance of microorganisms in bile and cultures from infectious sites postoperatively | Defined as the similarity of microorganisms between perioperative bile cultures and postoperative cultures from infectious sites. | 90 days |
| Jeroen Bosch Ziekenhuis | Not yet recruiting | 's-Hertogenbosch | Netherlands |
|
| Amsterdam University Medical Center | Recruiting | Amsterdam | Netherlands |
|
| Amphia Ziekenhuis | Recruiting | Breda | Netherlands |
|
| Catharina Ziekenhuis | Recruiting | Eindhoven | Netherlands |
|
| Medisch Spectrum Twente | Recruiting | Enschede | Netherlands |
|
| Groningen University Medical Center | Recruiting | Groningen | Netherlands |
|
| Maastricht University Medical Center | Recruiting | Maastricht | Netherlands |
|
| Radboud University Medical Center | Recruiting | Nijmegen | Netherlands |
|
| Erasmus MC Cancer Institute | Recruiting | Rotterdam | Netherlands |
|
| Regional Academic Cancer Center Utrecht | Recruiting | Utrecht | Netherlands |
|
| ID | Term |
|---|---|
| D010190 | Pancreatic Neoplasms |
| D013530 | Surgical Wound Infection |
| ID | Term |
|---|---|
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D004701 | Endocrine Gland Neoplasms |
| D004066 | Digestive System Diseases |
| D010182 | Pancreatic Diseases |
| D004700 | Endocrine System Diseases |
| D014946 | Wound Infection |
| D007239 | Infections |
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D002444 | Cefuroxime |
| D008795 | Metronidazole |
| ID | Term |
|---|---|
| D002511 | Cephalosporins |
| D047090 | beta-Lactams |
| D007769 | Lactams |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D013843 | Thiazines |
| D013457 | Sulfur Compounds |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
| D009593 | Nitroimidazoles |
| D009574 | Nitro Compounds |
| D007093 | Imidazoles |
| D001393 | Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
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