Evidence map›Paper›PMID 42553308›Full record

ArticleFrontiers in medicine2026

Robotic-assisted bronchoscopy combined with digital tomosynthesis for pulmonary nodules characterization: a single center experience.

Flavio Marco Mirabelli, Emma Repaci, Gian Piero Bandelli, Thomas Galasso, Martina Ferioli, Marco Ferrari, Filippo Natali, Tommaso Abbate, Teresa Calari, Stefania Damiani and 8 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 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

18 authors.

Flavio Marco MirabelliRespiratory Medicine and Thoracic Endoscopy Unit, Ospedale Regina Apostolorum, Albano Laziale, Rome, Italy.
Emma RepaciDepartment of Internal Medicine, Ospedale Policlinico Casilino, Rome, Italy.
Gian Piero BandelliInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Thomas GalassoInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Martina FerioliInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Marco FerrariInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Filippo NataliInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Tommaso AbbateInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Teresa CalariInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Stefania DamianiPathological Anatomy and Histology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Francesca GiunchiPathological Anatomy and Histology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Mattia RiefoloPathological Anatomy and Histology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Lorenzo ScrofaniInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Annalisa AltimariSolid Tumor Molecular Pathology Laboratory, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Elisa GruppioniSolid Tumor Molecular Pathology Laboratory, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Daniela Di LucaCardio-thoracic and Vascular Anesthesia and Intensive Care Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Federica PasqualiClinical Engineering Division, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Piero CandoliInterventional Pulmonology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Diagnostic work-up of peripheral pulmonary lesions (PPLs) remains a challenge in interventional pulmonology. Conventional bronchoscopy and trans-thoracic needle aspiration (TTNA) often entail limitations in accuracy or safety. Robotic-assisted bronchoscopy with shape-sensing technology (ssRAB) combined with artificial intelligence (AI)-aided augmented fluoroscopy (LungVision system) represents an innovative approach to enhance lesion localization and diagnostic yield for small or otherwise hard-to-reach lesions while maintaining the safety profile of the procedure. Materials and methods: This retrospective observational study included all procedures performed under general anesthesia using the ssRAB (Ion™ robotic platform) in combination with C-arm based computed tomography (LungVision System) at the Interventional Pulmonology Unit of IRCCS Azienda Ospedaliero-Universitaria, Policlinico Sant'Orsola, Bologna (Italy), between December 2024 and September 2025. Overall, 82 patients with 94 sampled pulmonary lesions were included; in 12 patients, two distinct nodules were sampled during the same bronchoscopic procedure. Lesions features, procedural characteristics, diagnostic yield and complications were collected and statistically analyzed. Diagnostic yield was defined according to the 2024 Delphi consensus and STARD 2015 guidelines. Results: This study included 82 patients and 94 sampled pulmonary nodules. The median size of the lesion was 14 mm (IQR 11-18 mm). Target lesions were identified by radial endobronchial ultrasound (r-EBUS) in 80% of cases. A definitive cyto-histologic diagnosis was achieved in 74.5% of cases. Lesions ≥10 mm yielded a 79.2% diagnostic rate, versus 59.1% for smaller nodules. Diagnostic success was independently predicted by upper lobe location (OR 3.28; Discussion and conclusions: The integration of robotic-assisted bronchoscopy with the LungVision system exhibited high diagnostic efficacy and a strong safety profile when sampling peripheral lung lesions. The synergy of real-time AI aided augmented fluoroscopy and robotic technologies facilitates precise lesion targeting, even within anatomically complex areas. However, follow-up data were not available for non-diagnostic cases; therefore, false-negative rates, sensitivity, and diagnostic accuracy could not be assessed. Given the significant cost associated with this procedure, future prospective studies are warranted to further validate these results and refine patient selection criteria to optimize its clinical application.

Indexed as

AI–tomographyartificial intelligenceaugmented fluoroscopydiagnostic yieldinterventional pulmonologyLungVisionperipheral pulmonary lesionsrobotic-assisted bronchoscopy

Identifiers

PMID42553308
PMCPMC13433741

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