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Percutaneous coronary intervention (PCI) on heavily calcified lesions has been associated with more complications.1 Intravascular lithotripsy (IVL) was recently approved for treating de novo calcified coronary lesions based on excellent safety and efficacy on several studies, but there are limited "real world" outcomes. We conducted a comprehensive search of the MAUDE database between February 12, 2021, and February 28, 2023 using the manufacturer and brand name tabs with the keywords "Shockwave Medical" and "Shockwave," respectively. Given that a single IVL catheter can fail or cause multiple adverse events through different mechanisms, we considered all possible outcomes. The MAUDE database is freely accessible and de-identified, obviating the need for institutional review board approval.
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http://dx.doi.org/10.25270/jic/23.00111 | DOI Listing |
Respir Med
September 2025
Department of Medicine, Pulmonary and Critical Care Medicine, Albany Medical Center, Albany, NY.
Study Objectives: Mandibular repositioning appliances (MRAs) are widely used for obstructive sleep apnea (OSA) and snoring, but their safety profile remains underexplored. This study analyzes adverse events associated with MRAs using the FDA Manufacturer and User Facility Device Experience (MAUDE) database.
Methods: A retrospective review of the MAUDE database identified adverse events related to MRAs under the product code "LRK" from January 1, 2015, to February 8, 2025.
Spine (Phila Pa 1976)
September 2025
Department of Neurosurgery, Donald and Barbara Zucker Hofstra School of Medicine at Northwell, Manhasset, NY, USA.
Study Design: Cross-sectional study.
Objective: This study aimed to analyze the failure patterns of expandable corpectomy cages.
Summary Of Background Data: Expandable corpectomy cages offer significant advantages for anterior column reconstruction but introduce unique mechanical complexities.
Minerva Urol Nephrol
August 2025
Department of Urology, Sapienza University, Rome, Italy.
Background: Real life data on adverse events of penile prosthesis are lacking. Aim of this study is to summarize medical device reports (MDRs) related to penile prosthesis implants within the Manufacturer and User Facility Device Experience (MAUDE) database held by The Food and Drug Administration (FDA).
Methods: We examined all MDRs from MAUDE database reported in the last ten years related to each FDA-approved penile implant.
Ophthalmol Ther
August 2025
National Clinical Research Center for Ocular Diseases, Eye Hospital, Wenzhou Medical University, Wenzhou, 325027, China.
Introduction: To evaluate and characterize adverse events (AEs) associated with EVO and EVO+ implantable collamer lens (ICL) using real-world post-marketing surveillance data from the Food and Drug Administration (FDA)'s MAUDE database.
Methods: A retrospective analysis was conducted on AE reports related to EVO and EVO+ ICLs, including both spherical and toric models, submitted between 2015 and 2023. After excluding duplicate entries and incomplete records, reports were stratified by lens model and optical type into four groups: spherical EVO, toric EVO, spherical EVO+, and toric EVO+.
BMC Prim Care
August 2025
Centre de recherche du CHU de Québec-Université Laval, Axe Santé des populations et pratiques optimales en santé, Québec, QC, Canada.
Background: General practitioners (GPs) extensively used synchronous teleconsultation (STC) during the COVID-19 pandemic. Although this utilization decreased after the state of sanitary emergency was lifted, it remains higher than pre-pandemic levels.
Methods: The aim is to summarize the scientific evidence on the factors influencing GPs’ decision to conduct STC instead of face-to-face consultation.