CHAMGAP
VERIFIEDPassed the Codex final verification and publication gate. Evidence-verification cutoff: 2026-08-26. AI was used for research and drafting; the existence of all 1 cited sources was verified at the original page, followed by blind grading, adversarial audit, and build validation. Methodology v0.8.
Verdict No. 2934 · Search date 2026-08-26 · Methodology v0.8

Twenty-four-hour perioperative antibiotic prophylaxis after open cystectomy and urinary diversion,
does it really help with Noninferior 90-day surgical-site infection versus prophylaxis continued until catheter removal?

30-Second Summary
C
Evidence Grade C · 56 · Safety caution
Twenty-four-hour prophylaxis preserved infection outcomes while reducing median exposure by 7 days
Ninety-day all-cause mortality was 6/95 (6.3%) versus 5/98 (5.1%), P=.96, and all infections resolved with appropriate treatment. Antibiotic choice requires attention to allergy, renal function, and local resistance.
What the
research shows
Grade C. Among 193 analyzed PAPRAC participants, 90-day SSI occurred in 8/95 (8.4%) versus 12/98 (12.2%), risk difference -3.8 points (90% CI -11.1 to 3.4), within the prespecified 10-point margin. Median exposure fell from 8 days to 1 day, a 7-day or 87.5% reduction.
What the
ads claim
The practical benefit is 7 fewer antibiotic days, with less selection pressure and cost. The trial did not directly test individual resistance emergence or costs.
*

Useful facts when choosing a product

  • Only open cystectomy with urinary diversion was studied.
  • The short arm stopped prophylaxis after 24 hours.
  • The extended arm continued until catheters and stents were removed.
Gap Measurement · Verdict 2934 · C 56
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

PAPRAC randomized 196 and used a prespecified per-protocol primary analysis of 193 after three canceled surgeries. SSI was adjudicated using CDC criteria by infectious-disease and non-treating clinicians. The risk difference was -3.8 points, within the 10-point margin. Median prophylaxis was 1 day versus 8 days. No external grant or company in-kind support was reported; Insel Gruppe AG, University Hospital Bern sponsored and conducted the study.

02

Why this is classified as C (56)

The margin was met while exposure fell by 7 days, but noninferiority, small size, and completer analysis limit the verdict to C with 56 points.

Counterpoint. Antibiotic-stewardship value is not direct proof of less resistance in each patient.

Rejudgment record. Cross-check applied — The prespecified 10-point margin and 7-day exposure reduction were balanced against noninferiority, small size, and completer-analysis limitations

Scoring profile behind this grade
EndpointHHard endpoint - actual events such as death
ReplicationR1Single confirmatory trial
IndependenceI2Decisive evidence is publicly or non-profit funded
Effect sizeE+Meets the clinically important threshold

The scoring table and the verdict agree (C).

Sub-claim grades by effect

This ingredient is marketed for several effects. A single overall grade blends strong and weak claims together, so each effect is graded separately here. The overall grade reflects the strongest disconfirming or core claim.

Effect (sub-claim)GradeBasis
Noninferior 90-day surgical-site infectionCThe prespecified 10-point margin was met.
Reduced antibiotic exposureCMedian exposure fell from 8 days to 1 day.

Cross-check — AI research and Codex final gate

AI was used for research and drafting. Blind grading, adversarial audit, and the methodology boundary rules were then reapplied before Codex performed the final evidence, grade, copy, and build checks. If a grade cannot be narrowed, both evidence positions and their reasons are published.
03

Evidence Table

StudyDesignSampleFundingEndpointResultWeight
PAPRACSingle-center open-label noninferiority randomized trial193No external grant or company in-kind support reported; sponsored and conducted by Insel Gruppe AG, University Hospital BernCDC-defined surgical-site infection within 90 days8.4% vs 12.2%, risk difference -3.8 points (90% CI -11.1 to 3.4), margin 10 points; duration 1 vs 8 daysPivotal noninferiority evidence
§

Receipt — 1 References

All 1 cited sources were verified for existence at the original page (as of 2026-08-26).

Thurnheer MC, et al. JAMA Netw Open. 2024;7:e2439382. PMID: 39422911.
checked
Research and draft: AI used · Cross-check: blind grading and adversarial audit
Final verification and publication gate: Codex · Verification cutoff: 2026-08-26 · Corrections: none

Cite this verdict

Benefit of Twenty-Four-Hour Antibiotic Prophylaxis for Noninferior Surgical-Site Infection After Cystectomy Evidence Grade C card
[Chamgap] Benefit of Twenty-Four-Hour Antibiotic Prophylaxis for Noninferior Surgical-Site Infection After Cystectomy — Evidence Grade C·56. 1 cited sources checked. Source: https://chamgap.com/en/verdicts/mens/24-hour-antibiotic-prophylaxis-cystectomy-ssi/ · CC BY 4.0

CC BY 4.0 — free to use with attribution; do not distort grades, numbers, or verdict meaning.

!

What this document does and does not do

Chamgap is an information source. It reports what research has and has not confirmed; it does not tell readers what to take or buy. That decision belongs to readers and, when needed, medical or legal professionals. This verdict reflects literature available up to the search date and may change as new research appears. Nothing here is medical advice.