# Infection-targeted innovations in anastomotic leak management: endoscopic advances, antimicrobial biomaterials, and precision strategies

**Authors:** Yansong Xu

PMC · DOI: 10.1080/07853890.2026.2619218 · Annals of Medicine · 2026-01-23

## TL;DR

This paper reviews new infection-focused strategies for managing anastomotic leaks after gastrointestinal surgery, including endoscopic treatments and smart biomaterials.

## Contribution

The paper highlights novel infection-targeted innovations and their potential to shift AL management from reactive to proactive prevention.

## Key findings

- Endoscopic Vacuum Therapy shows high fistula closure rates and reduced sepsis risk.
- Antibiotic-eluting hydrogels and AI-driven models show promise but need clinical validation.
- Future AL management may integrate endoscopic and biomaterial-based approaches.

## Abstract

Anastomotic leakage (AL) is a devastating complication of gastrointestinal surgery and a critical source of hospital-acquired infections. This review synthesizes recent advances in AL management, with a focus on infection-targeted strategies. A narrative review of the literature was conducted, encompassing established clinical therapies and emerging preclinical innovations. For mature endoscopic modalities, such as Endoscopic Vacuum Therapy (EVT), clinical cohort data and meta-analyses support high fistula closure rates (74–94.4%) and a significant reduction in sepsis risk. In parallel, novel preclinical strategies—including antibiotic-eluting hydrogels, reversible endoscopic bypass procedures, and artificial intelligence-driven prediction models—demonstrate transformative potential in early-stage studies but require robust clinical validation. The future management of AL is evolving towards an integrated model, combining evidence-based endoscopic interventions with intelligent biomaterial-based approaches. Translating preclinical innovations into practice will necessitate overcoming challenges related to cost, standardization, and long-term safety, ultimately enabling a paradigm shift from reactive repair to proactive, precision prevention.

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}
- **Diseases:** leakage (MESH:D003763), infectious complications (MESH:D003141), multiple organ failure (MESH:D009102), sepsis (MESH:D018805), intra-abdominal infection (MESH:D059413), adhesion (MESH:D000267), Infection (MESH:D007239), AL (MESH:D057868), fistula (MESH:D005402), HOCL (MESH:D016534), rectal strictures (MESH:D003251), Perforations (MESH:D057112), incisional infections (MESH:D000069290), duodenal fistula (MESH:D004382), blood loss (MESH:D016063), septic shock (MESH:D012772), abscess (MESH:D000038), leak (MESH:D019559), UGI (MESH:D005767), enterocutaneous fistula (MESH:D007412), abdominal pain (MESH:D015746), Esophageal leaks (MESH:D004941), trauma (MESH:D014947), rectal cancer (MESH:D012004)
- **Chemicals:** EVT (-), hyaluronic acid (MESH:D006820), ICG (MESH:D007208), tobramycin (MESH:D014031), gamma-polyglutamic acid (MESH:C511775)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833900/full.md

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Source: https://tomesphere.com/paper/PMC12833900