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Background: Endovascular treatment (EVT) of intracranial aneurysms (IAs) has improved significantly with the integration of virtual simulation software (VSS) in surgical planning and device selection. Despite promising outcomes, discrepancies remain between physician and VSS recommendations. This review synthesizes evidence on (1) comparisons between VSS-chosen and physician-chosen dimensions; (2) VSS-chosen and postoperative measured dimensions; and (3) the success rate of VSS-guided device deployment.
Methods: A systematic search adhering to PRISMA guidelines was conducted in Medline, Embase, Web of Science, and Cochrane databases up to January 2024. Eligible studies included case series, cohort studies, and randomized trials assessing VSS for stent selection in IAs treatment. Mean difference (MD) and single-arm meta-analysis with 95% confidence intervals (CIs) under a random-effects model were performed for continuous and binary outcomes. Subanalyses were conducted for Sim&Size and PreSize software.
Results: Ten studies comprising 658 IAs were included. Pipeline Embolization Device was most commonly used. Findings demonstrated (1) high accuracy of VSS when comparing simulated and postoperative lengths (MD -1.7 mm; 95% CI -4.37 to 0.98 mm); (2) physician-chosen lengths overestimated compared to VSS (MD -2.11 mm; -3.43 to -0.79 mm); (3) no significant difference in physician- versus VSS-chosen diameters (MD -0.04 mm; -0.13 to 0.06 mm); and (4) high VSS-guided deployment success (96%; 93-99%) with low complications (4%). Subanalyses showed 95% and 92% deployment success rates for Sim&Size and PreSize, respectively.
Conclusion: VSS effectively estimates device length and achieves high deployment success, with low complication rates, supporting its utility in EVT planning.
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http://dx.doi.org/10.1177/15910199251323006 | DOI Listing |
Am J Surg
August 2025
Emory University School of Medicine, USA; Grady Health System, USA. Electronic address:
Introduction: We sought to develop, implement and evaluate an urban prehospital whole blood (PH-WB) program.
Methods: Using retrospective heat map data, Quick Response Vehicles (QRVs) carrying PH-WB were strategically placed throughout the city and dispatched using dynamic deployment. Patient inclusion criteria were age ≥15 years, traumatic mechanism, and SBP ≤90 mmHg.
JACC Case Rep
September 2025
Division of Cardiology, Department of Medicine, University of Florida Health, Jacksonville, Florida, USA. Electronic address:
We present a case of successful transfemoral transcatheter aortic valve replacement for a rare quadricuspid aortic valve with pure aortic regurgitation. Procedural challenges included identifying the annular plane, determining the appropriate deployment view, annular sizing, the absence of annular calcium, and the lack of a dedicated transcatheter device for pure aortic regurgitation.
View Article and Find Full Text PDFFront Med (Lausanne)
August 2025
Care Access Research LLC, Boston, MA, United States.
Introduction: Recruitment and retention remain critical challenges in clinical trials, particularly in neurodegenerative diseases, which require large participant populations, rigorous screening, and prolonged follow-up periods. Care Access is a global research site management organization that operates clinical trial sites employing various operational models. This study evaluates the operational performance of Care Access site models-including traditional sites, hub-and-spoke, and decentralized community-integrated research (DCIR) sites-within a Phase 3 neurodegenerative disease trial, focusing on their relative efficiency in recruitment, randomization, and retention.
View Article and Find Full Text PDFBackground: In the presence of a potent P2Yinhibitor such as prasugrel, the additional clinical antithrombotic benefit of aspirin is unclear. The feasibility of prasugrel monotherapy without aspirin after percutaneous coronary intervention (PCI) has been demonstrated in chronic coronary syndrome, but is yet to be assessed in patients with non-ST elevation acute coronary syndrome (NSTE-ACS) and low anatomical complexity.
Methods And Results: ASET-Japan is a single-arm study investigating the safety of prasugrel 12-month monotherapy with a locally approved dose (loading 20 mg; maintenance 3.
J Vasc Interv Radiol
September 2025
Rush University Medical Center, Chicago, IL, USA.
Purpose: To characterize the histologic and inflammatory changes that resulted from peripheral embolization using Onyx (EVOH) in an animal model. This study also assessed the radiopacity of the Onyx after a 1-minute mixing time.
Methods: Embolization using EVOH alone or in combination with coils/plugs was performed on large vessel, small vessel, and very small vessel (3-5 mm, 1-3 mm, and <1 mm in diameter, respectively) targets in the peripheral vasculature of Yucatan miniature pigs.