Evidence map›Paper›PMID 41085801›Full record

Trial reportAnnals of surgical oncology2026

Antibiotics and Surgical Site Infection in Expander-Based Breast Reconstruction Trial (ASSERT).

Surinder Kaur, Brian Gastman, Kristen P Broderick, Adeyiza O Momoh, Brett T Phillips, Graham Schwarz, Summer E Hanson, Geoffrey E Hespe, Carisa M Cooney, Katie Sommers and 3 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Annals of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Surinder KaurThe Plastic Surgery Foundation, Arlington Heights, IL, USA.
Brian GastmanCleveland Clinic, Cleveland, OH, USA.
Kristen P BroderickJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Adeyiza O MomohUniversity of Michigan Medical Center, Ann Arbor, MI, USA.
Brett T PhillipsDuke University Medical Center, Durham, NC, USA.
Graham SchwarzCleveland Clinic, Cleveland, OH, USA.
Summer E HansonThe University of Chicago Medical Center, Chicago, IL, USA.
Geoffrey E HespeUniversity of Michigan Medical Center, Ann Arbor, MI, USA.
Carisa M CooneyJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Katie SommersThe Plastic Surgery Foundation, Arlington Heights, IL, USA.
Cheng-Shiun LeuColumbia University Mailman School of Public Health, New York, NY, USA.
Christine H RohdeColumbia University Irving Medical Center, New York, NY, USA. chr2111@cumc.columbia.edu.ORCID http://orcid.org/0000-0001-9005-7753
ASSERT Group

Funding

Plastic Surgery Foundation SSI Study Grant
6 · The paper itself

Abstract

backgroundThe use of prophylactic antibiotics following postmastectomy tissue expander breast reconstruction (TE-BR) varies widely. The Centers for Disease Control and Prevention (CDC) recommends a single preoperative antibiotic dose for clean and clean-contaminated procedures. This multi-institutional, prospective, randomized controlled trial (RCT) examined whether the CDC-recommended single preoperative dose (SPD) of antibiotics is not inferior to an additional week of postoperative (WPO) prophylactic antibiotics in preventing surgical site infection (SSI) in immediate TE-BR following mastectomy.

methodsWomen aged ≥ 18 years undergoing immediate TE-BR were randomized to SPD or WPO groups. The primary outcome was SSI by CDC guidelines within 30 days of surgery. The study used a noninferiority trial design to examine whether the test product (single preoperative dose (SPD)) was not worse than the comparator (1 week of postoperative (WPO) prophylactic antibiotics) by more than a set noninferiority margin of 6%.

resultsIn total, five participating centers screened 499 women; 235 were enrolled. A total of 102 patients were randomized to the SPD arm and 112 to the WPO arm, with 21 patients withdrawn. The SSI rate in the SPD arm was 17% as compared with 11% in WPO arm, which is within the noninferiority margin set for this study but not significantly noninferior (p = 0.496). The rate of unplanned TE removal for infection, hospitalization rate, and return to OR rate within 30 days of surgery were comparable between the two groups.

conclusionsThis multi-institutional RCT did not definitively demonstrate that a single preoperative dose of antibiotics is not inferior to a 7-day postoperative antibiotic regimen in preventing SSI in immediate TE-BR; there was also no evidence to support that the 7-day regimen was significantly better. As this represents one of the largest multi-institutional study of its kind, these results have practice-management considerations.

Indexed as

Anti-Bacterial AgentsAntibiotic ProphylaxisBreast NeoplasmsMammaplastyMastectomySurgical Wound InfectionTissue ExpansionTissue Expansion DevicesAdultAgedFemaleFollow-Up StudiesHumansMiddle AgedPrognosisProspective StudiesAnti-Bacterial Agents

Identifiers

PMID41085801
PMCPMC12982282

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.