Optimized Perioperative Antibiotic Prophylaxis in Radical Cystectomy

Surgical Site Infection Clinical Trial

— PAPRAC  

Official title:

Optimized Perioperative Antibiotic Prophylaxis in Radical Cystectomy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03305627
• Other study ID #: 2017-01480
• Status: Completed
• Phase: N/A
• Start date: April 9, 2018
• Est. completion date: February 28, 2024

Study information

• Verified date: May 2024
• Source: Insel Gruppe AG, University Hospital Bern
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cystectomy with urinary diversion (ileal conduit, orthotopic ileal bladder substitute, continent catheterizable pouch) is the best treatment option for patients with muscle-invasive bladder cancer. This intervention is one of the most challenging in urology and has a high rate of postoperative complications including around 30% of postoperative infections.

Perioperative antibiotic prophylaxis (PAP) is widely accepted as a crucial preventive measure to reduce the incidence of surgical site infections (SSI). The rationale for PAP is the reduction of the local bacterial load at the site and time of intervention, and therefore a short duration of PAP of 24 to maximal 48 hours is recommended for all clean to clean-contaminated procedures..

Evidence supporting the optimal duration of PAP for radical cystectomy with urinary diversion is lacking. Based on data extrapolated from abdominal surgery, current guidelines recommend short-term PAP (≤24h) for all clean-contaminated procedures including radical cystectomy.

However, a recent evaluation revealed a significant inter-hospital variability of PAP and showed that extended use (>48h) was common in patients undergoing radical cystectomy. Importantly, this study also demonstrated that longer duration of PAP incurred higher costs and was associated with an increased rate of C. difficile colitis. A small, prospective, non-randomized study showed equal efficacy of short-term PAP in preventing postoperative infections in patients undergoing radical cystectomy with ileum conduit compared to extended PAP. Nonetheless, larger randomized clinical trials supporting these findings are lacking.

The unwarranted extended use of antibiotics is a major concern as exposure to antibiotics is a driving force for the development of (multi-) resistant bacteria and will lead to an increasing number of difficult-to-treat infections. This has been recognized on both national and international levels and is addressed within antimicrobial stewardship frameworks.

This study will compare current practice (>48h PAP, "extended PAP") with the guideline recommended approach (24h PAP, "short term PAP") in a single-centre, prospective, randomised clinical non-inferiority trial. The primary outcome is the rate of SSI within 90 days post surgery. The aim of the study is to generate currently lacking evidence allowing for an optimised PAP strategy in a challenging surgical setting.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 196
• Est. completion date: February 28, 2024
• Est. primary completion date: February 28, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Written informed consent

• Age >18 years

• Planned radical cystectomy at the Department of Urology, Bern University Hospital

Exclusion Criteria:

• Contraindications to the classes of drugs under study, e.g. known hypersensitivity or allergy to class of drugs including alternatives described in the protocol or the investigational product,

• Women who are pregnant or breast feeding (exclusion for surgery),

• Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant,

• Previous enrolment into the current study,

• Enrolment of the investigator, his/her family members, employees and other dependent persons,

Related Conditions & MeSH terms

• Antibiotic Resistant Infection
• Antibiotic Side Effect
• Antibiotic-associated Diarrhea
• Communicable Diseases
• Diarrhea
• Infections
• Perioperative/Postoperative Complications
• Postoperative Complications
• Radical Cystectomy
• Surgical Site Infection
• Surgical Wound Infection
• Urologic Cancer
• Urologic Neoplasms

Intervention

Other:
• Short PAP
Perioperative antibiotic prophylaxis for 24h
• Extended PAP
Perioperative antibiotic prophylaxis for >48h

Locations

Country	Name	City	State
Switzerland	Department of Infectious Diseases, University Hospital Bern	Bern
Switzerland	Department of Urology, University Hopspital Bern	Bern

Sponsors (1)

Lead Sponsor	Collaborator
Insel Gruppe AG, University Hospital Bern

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of Surgical Site infections (SSI)	Rate of surgical site infections occurring within 90 days post surgery will be calculated for each patient.	90 days
Primary	Time to event of SSI	Time to event of SSI (event free survival analysis)	90 days
Primary	Rate of Urinary tract infections (UTI)	Rate of urinary tract infections occurring within 90 days post surgery will be calculated for each patient.	90 days
Primary	Time to event of UTI	Time to event of UTI (event free survival analysis)	90 days
Secondary	Rate and type of Antibiotic associated adverse events (AEs)	Rates and types of antibiotic associated AEs occurring within 30 days post surgery (direct AEs such as hypersensitivity reaction, hepatotoxicity, renal toxicity etc and indirect AEs such as line associated infections, C.difficile diarrhoea) will be assessed for each patient.	30 days
Secondary	Frequency of multi-drug-resistant bacteria in urinary samples	The frequency of multi-drug-resistant bacteria in urine samples obtained at predefined time points during the first 30 days post surgery will be calculated for each patient	30 days
Secondary	Changes in fecal flora	Changes in the composition of the fecal flora will be assessed in fecal samples collected at pre-specified time points	30 days
Secondary	Antibiotic associated costs	Directly antibiotic associated costs incurred during 30days post surgery will be assessed	30 days