Application of Closed Incision Negative Pressure Wound Therapy in Ventral Hernia Repair Surgery Using a Polypropylene Mesh: A Randomized Clinical Trial
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, randomizované kontrolované studie
Grantová podpora
01/RVO-FNOs/2021
Ministry of Health of the Czech Republic
SP2024/021
Ministry of Education of of the Czech Republic
CZ.10.03.01/00/22_003/0000048
European Union Operational Programme Just Transition
PubMed
39336589
PubMed Central
PMC11434378
DOI
10.3390/medicina60091548
PII: medicina60091548
Knihovny.cz E-zdroje
- Klíčová slova
- aseptic wounds, negative pressure therapy, polypropylene mesh, randomized trial, ventral hernia repair, wound infection,
- MeSH
- chirurgické síťky * MeSH
- dospělí MeSH
- incidence MeSH
- infekce chirurgické rány * prevence a kontrola epidemiologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- operace kýly * metody škodlivé účinky MeSH
- polypropyleny * MeSH
- senioři MeSH
- terapie ran pomocí řízeného podtlaku * metody MeSH
- ventrální hernie * chirurgie MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- polypropyleny * MeSH
Background and Objectives: Surgical site infections (SSIs) are a significant complication following ventral hernia repair, potentially leading to prolonged hospital stays and increased morbidity. This study aimed to evaluate whether closed incision negative pressure wound therapy (ciNPWT) reduces the incidence of SSI after ventral hernia repair with polypropylene mesh compared to standard wound care. Materials and Methods: A randomized study was conducted with 100 patients undergoing ventral hernia repair using a polypropylene mesh. Participants were divided into two groups: a control group (n=50), which received standard sterile gauze dressing with an iodine-based disinfectant, and an intervention group (n=50), treated with the ciNPWT system (Vivano® by HARTMANN) for 5 days postoperatively. The primary outcome was the incidence of SSI within one year after surgery. Secondary outcomes included the influence of factors such as age, sex, smoking status, and hernia size on SSI occurrence. The study was approved by the Ethics Committee at the University Hospital Ostrava, adhering to the ethical standards of the Helsinki Declaration. Results: The incidence of SSI was lower in the ciNPWT group compared to the standard care group (4% vs. 12%), though this difference did not reach statistical significance. No significant effect of sex or smoking status on SSI was observed. The control group had a shorter mean length of hospital stay. Larger hernias in the non-ciNPWT group were more prone to SSIs, as expected. Conclusions: Although limited by a small sample size, the findings suggest that ciNPWT may be associated with a reduced rate of SSI following ventral hernia repair. Further studies with larger populations are needed to confirm these results.
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