Stetz, Eric Michael2011-12-142011-12-142011-11https://hdl.handle.net/11299/119039University of Minnesota M.S. thesis. November 2009. Major: Integrative biology and physiology. Advisors: Stephen A. Katz, Ph. D.,Kenneth P. Roberts, Ph. D., Anthony J. Weinhaus, Ph. D. 1 computer file (PDF); x, 47 pages, appendices A-C.Urinary incontinence and overactive bladder are medical conditions where the patient either has frequent urges to urinate (urinary urgency-frequency), the inability to urinate despite the feelings of a full bladder (urinary urge incontinence) or the inability to completely empty the bladder (urinary retention). These conditions affect around 72 million people in North America and around 348 million people world wide. The patient population breakdown is around 72% female and 28% male.1 Many options are available for treating urinary incontinence. These include incontinence pads to absorb unintentional voiding episodes, physical therapy, pharmacologic drug therapy, surgical interventions such as urethral slings and sacral nerve stimulation (SNS). Most patients proceed from pads and physical therapy to drugs and finally nerve stimulation. InterStim is the only FDA approved neurostimulation system currently on the market for treating urinary urge incontinence, urinary urgencyfrequency and non-obstructive urinary retention.2 The therapy consists of an implantable neurostimulator (INS) and an associated lead which delivers the electrical stimulation from the INS to the target sacral nerve. One aspect for successful application of SNS therapy is using a foramen needle to locate the S3 sacral foramen and place the lead electrodes adjacent to the S3 sacral nerve. The activities documented in this thesis centered on the collection of sacral anatomy data as a design input for the evaluation of a lead implant template for use in locating the S3 foramen. The project hypothesis is “Will the use of a lead implant template help to improve the efficacy for locating the S3 foramen when implanting a Sacral Nerve Stimulation lead for treating urinary incontinence?". The project was split into two primary studies. The first half of the project centered on an anatomical study of the morphological variation in dry bone sacrum and cadavers. The anatomical study was intended to quantify the amount of variation that needs to be accommodated by the implant template. The second half of the project centered on the efficacy evaluation of the prototype template.en-USIntegrative biology and physiologyThesis or Dissertation