Luca Pantano

Dr. Luca Pantano


Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 September 2025 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
Guido MarchiGuido Marchi
Guido Marchi
SCSara Cinquini
Sara Cinquini
Francesco TannuraFrancesco Tannura
Francesco Tannura
GGGiacomo Guglielmi
Giacomo Guglielmi
RGRiccardo Gelli
Riccardo Gelli
Laura CarrozziLaura Carrozzi
Laura Carrozzi
Hemorrhagic complications during pleural interventions—such as thoracentesis and chest tube insertion—remain a significant clinical concern, primarily due to inadvertent injury of the intercostal artery (ICA). The highly variable ICA anatomy is frequently not visualized on conventional imaging, limiting the reliability of landmark-based techniques. Color Doppler thoracic ultrasound (CDUS) has emerged as a non-invasive, real-time modality capable of identifying ICAs and their anatomical variants prior to pleural access. This narrative review synthesizes current evidence on CDUS-guided ICA screening, focusing on its technical principles, diagnostic performance, and clinical applicability. While feasibility and utility are supported by multiple observational studies, robust evidence demonstrating a reduction in bleeding complications is still lacking. Barriers to widespread implementation include heterogeneous scanning protocols, operator dependency, and the absence of standardized training. We discuss the anatomical rationale for pre-procedural vascular mapping and highlight emerging protocols aimed at standardizing ICA visualization. Although not yet incorporated into major clinical guidelines, CDUS represents a promising tool to enhance procedural safety. Emerging AI applications may further improve vessel detection by reducing operator dependency and enhancing reproducibility. High-quality prospective studies are essential to validate potential clinical benefits, optimize implementation strategies, and support integration into routine pleural practice.

24 October 2026 in Methods and Protocols
Verified
Journal Article
Open access
PDF file
RPRoberta Pancani
Roberta Pancani
LMLetizia Marconi
Letizia Marconi
Francesco TannuraFrancesco Tannura
Francesco Tannura
CCCostanza Cerrini
Costanza Cerrini
LPLuca Pantano
Luca Pantano
Chiara RomeiChiara Romei
Chiara Romei
Background: Coronavirus Disease 19 (COVID-19)-associated pneumonia is characterized by a broad spectrum of severity. Endothelial injury is a prominent component of the disease, but the relative contribution of vessels of different sizes to this condition has not been extensively investigated. Quantitative computed tomography (CT) represents a potential tool to evaluate pulmonary vascular involvement. Objectives: To investigate the relative contribution of vessels of different sizes in COVID-19-associated pneumonia of different severity using the Computer-Aided Lung Informatics for Pathology Evaluation and Rating (CALIPER) software. Methods: We conducted a single-center retrospective study, including patients admitted to the Pisa University Hospital between March and April 2020 with COVID-19-associated pneumonia. We excluded patients with severe motion artifacts, inadequate CALIPER segmentation, or inconclusive etiologic confirmation. All CT scans were analyzed using CALIPER, which automatically segmented lung parenchyma and vascular-related structures (VRSs). VRS volumes were stratified by vessel cross-sectional area (20 mm2). Results: We analyzed 258 patients. We observed that an increase in the percentages of VRSs with cross-sectional areas up to 20 mm2 was associated with the need for lower intensity of care and with better gas exchange. The opposite trend was observed for the percentages of >20 mm2. Conclusions: Our data provide novel information on the involvement of blood vessels of different sizes in the gas exchange impairment of COVID-19 patients. CALIPER represents a promising application for the study of vascular structures of the lung.