Evidence map›Paper›PMID 40965704›Full record

Observational studyHernia : the journal of hernias and abdominal wall surgery2025

Prevention of incisional hernia with biosynthetic mesh at the site of temporary ileostomy closure (PRINCESS Study): Preliminary Results.

Roberto Peltrini, Carla Rognoni, Giovanni Bellanova, Marco Caricato, Massimo Carlini, Stefania Cimbanassi, Francesco Corcione, Federico Cozzani, Diego Cuccurullo, Giuseppe Faillace and 25 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Hernia : the journal of hernias and abdominal wall surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

35 authors.

Roberto PeltriniDepartment of Public Health, University of Naples Federico II, Via Pansini 5, Naples, 80131, Italy. roberto.peltrini@gmail.com.ORCID 0000-0003-0445-2269
Carla RognoniCentre for Research on Health and Social Care Management (CERGAS), School of Management, SDA Bocconi, Bocconi University, Via Sarfatti 10, Milan, 20136, Italy.
Giovanni BellanovaUOC Chirurgia Generale, "D. Camberlingo" Hospital, Francavilla Fontana, Italy.
Marco CaricatoUOC Chirurgia Colorettale, Fondazione Policlinico Universitario Campus Bio-Medico Di Roma, Via Alvaro del Portillo, Rome, 21 - 00128, Italy.
Massimo CarliniDepartment of General Surgery, General Surgery Unit, S. Eugenio Hospital, Rome, Italy.
Stefania CimbanassiGeneral Surgery and Trauma Team, GOM Niguarda, Piazza Ospedale Maggiore 3, Milan, 20162, Italy.
Francesco CorcioneClinica Mediterranea, Via Orazio, 2, Naples, 80122, Italy.
Federico CozzaniGeneral Surgery Unit, University Hospital Parma, Parma, Italy.
Diego CuccurulloDepartment of Surgery, Monaldi Hospital, Azienda Ospedaliera dei Colli, Naples, Italy.
Giuseppe FaillaceDepartment of General Surgery, ASST Nord Milano, Sesto San Giovanni Hospital, Milano, Italy.
Silvia NeriUnit of General Surgery, Sassuolo Hospital, Azienda USL of Modena, Sassuolo, Modena, Italy.
Alberto PatritiDepartment of Surgery, S. Salvatore Hospital, AST Marche 1, Pesaro e Fano, PU, Italy.
Mauro SantarelliDipartimento di Chirurgia Generale e Specialistica, Chirurgia Generale, d'Urgenza e PS, Azienda Ospedaliera Universitaria Città Della Salute e Della Scienza di Torino, Turin, Italy.
Vincenzo TrapaniDepartment of General, Emergency Surgery and New Technologies, Baggiovara General Hospital Azienda Ospedaliero Universitaria di Modena, Via Pietro Giardini 1355, Modena, 41126, Italy.
Gabriella Teresa CapolupoUOC Chirurgia Colorettale, Fondazione Policlinico Universitario Campus Bio-Medico Di Roma, Via Alvaro del Portillo, Rome, 21 - 00128, Italy.
Gabriele CarboneDepartment of Surgery, Monaldi Hospital, Azienda Ospedaliera dei Colli, Naples, Italy.
Desiree CianfloccaDipartimento di Chirurgia Generale e Specialistica, Chirurgia Generale, d'Urgenza e PS, Azienda Ospedaliera Universitaria Città Della Salute e Della Scienza di Torino, Turin, Italy.
Stefano CioffiGeneral Surgery and Trauma Team, GOM Niguarda, Piazza Ospedale Maggiore 3, Milan, 20162, Italy.
Maria Michela Di NuzzoClinica Mediterranea, Via Orazio, 2, Naples, 80122, Italy.
Davide FerraraDepartment of General Surgery, ASST Nord Milano, Edoardo Bassini Hospital, Milano, Italy.
Paola Antonella GrecoDepartment of Surgery, S. Salvatore Hospital, AST Marche 1, Pesaro e Fano, PU, Italy.
Biancamaria IaconeDepartment of Public Health, University of Naples Federico II, Via Pansini 5, Naples, 80131, Italy.
Francesca PecchiniDepartment of General, Emergency Surgery and New Technologies, Baggiovara General Hospital Azienda Ospedaliero Universitaria di Modena, Via Pietro Giardini 1355, Modena, 41126, Italy.
Matteo RossiniGeneral Surgery Unit, University Hospital Parma, Parma, Italy.
Michele SaccoUOC Chirurgia Generale, "D. Camberlingo" Hospital, Francavilla Fontana, Italy.
Stefano SalaUnit of General Surgery, Sassuolo Hospital, Azienda USL of Modena, Sassuolo, Modena, Italy.
Domenico SpoletiniDepartment of General Surgery, General Surgery Unit, S. Eugenio Hospital, Rome, Italy.
Salvatore TramontanoDepartment of Medicine, Surgery and Dentistry, University of Salerno, Salerno, Italy.
Rosanna TarriconeCentre for Research on Health and Social Care Management (CERGAS), School of Management, SDA Bocconi, Bocconi University, Via Sarfatti 10, Milan, 20136, Italy.
Giampiero CampanelliGruppo Ospedaliero San Donato, University of Insubria, Milan, Italy.
Giuseppe CavallaroDepartment of Surgery, Sapienza University, Rome, Italy.
Micaela PiccoliDepartment of General, Emergency Surgery and New Technologies, Baggiovara General Hospital Azienda Ospedaliero Universitaria di Modena, Via Pietro Giardini 1355, Modena, 41126, Italy.
Giorgio SolianiDepartment of Surgery, S. Anna University Hospital and University of Ferrara, Ferrara, Italy.
Cesare StabiliniDepartment of Surgical Sciences, University of Genoa, Genoa, Italy.
Umberto BracaleDepartment of Medicine, Surgery and Dentistry, University of Salerno, Salerno, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIncisional hernia after ileostomy closure is a complication that adversely affects patient outcomes, quality of life (QoL), healthcare resources, and related costs. Prophylactic mesh reinforcement, both biological and synthetic, has been shown to be safe and effective in preventing stoma site incisional hernia (SSIH). This study aimed to evaluate the use of a slowly absorbable biosynthetic mesh at the site of temporary ileostomy closure to prevent SSIH.

methodsThis prospective, single-arm observational study was conducted across 14 Italian hospitals. Patients undergoing ileostomy reversal with retromuscular placement of a poly-4-hydroxybutyrate (Phasix™) mesh were enrolled. Endpoints included the incidence of radiologically and clinically detected SSIH at 1-year, postoperative morbidity, wound complications, and QoL assessed using the EuroQoL 5D-5 L and Carolinas Comfort Scale (CCS) questionnaires.

resultsA total of 115 patients completed at least 1 year of follow-up and were included in the analysis. Seromas was the most frequent complication (8.6%). Superficial and deep SSIs occurred in 6% and 1.7% of patients, respectively. Three complications required intervention (2.6%), including one mesh removal. The 1-year SSIH rate was 1.7%, with a median follow-up of 477 d (range: 263-880). Considering the 55 patients (47.8%) who completed 2-year follow-up, the cumulative SSIH rate was 4.3%. EuroQoL 5D-5 L and CCS scores demonstrated progressive improvement in QoL and symptom reduction over time (p < 0.0001).

conclusionThese preliminary findings suggest that prophylactic placement of a slowly absorbable biosynthetic mesh (Phasix™) is safe and effective for SSIH prevention following ileostomy closure, without negatively impacting the patient's QoL. The use of biosynthetic meshes may be considered a valid alternative to biological or synthetic meshes in this setting.

Indexed as

IleostomyIncisional HerniaSurgical MeshAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPostoperative ComplicationsProspective StudiesQuality of LifeBiosynthetic meshIleostomy closureProphylactic meshQuality of lifeStoma site incisional herniaSurgical site complications

Identifiers

PMID40965704
PMCPMC12446398

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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.