Hypothesis / aims of study
Fluoroscopy has significantly improved lead placement and decreased surgical time for implantable sacral neuromodulation. Despite the Food and Drug Administration public health advisory encouraging physicians to limit the use of fluoroscopy, there is a paucity of data regarding radiation and safety of fluoroscopy during sacral neuromodulation procedures. The aim of our study is to characterize fluoroscopy time and dose used during sacral neuromodulation surgery.
Study design, materials and methods
Electronic medical record was queried for sacral neuromodulation procedures (Stage 1 and full implant) between July 1, 2016 and July 1, 2021 at three academic institutions. Demographic data including age, sex, weight, body mass index (BMI), tobacco use and perioperative data including procedural indications, procedure, surgeon, surgeon specialty, operative setting, presence of trainees, operative time, fluoroscopy time, and dosimetry were collected. The data was entered into a centralized REDCap database. Statistical analyses were performed using STATA/BE 17.0.
Interpretation of results
Our data displays significant variation in both the radiation time and dose utilized among different specialties and among urogynecologists with different background training during sacral neuromodulation procedures. We also saw that the presence of trainees as well as bilateral lead placement significantly increased fluoroscopy time. Given the significant variation, there is room for improvement with radiation safety training and best practices guidelines to limit the usage of radiation during these frequently performed procedures. There are also future studies to be performed to analyze exactly where providers should stand during sacral neuromodulation procedures to best limit the radiation exposure.