Introduction
A limiting factor in the passage of a ureteral access sheath (UAS) is the small diameter of the ureter. Electromotive Drug Administration (EMDA) has the ability to drive a drug deep into the wall of the bladder urothelium. Accordingly, we used EMDA to test ureteral distensibility with three smooth muscle relaxants.
Materials
In 18 female Yorkshire pigs, baseline distensibility of both ureters was determined by passing 35 cm long, Cook Medical® urethral dilators (10 Fr to 24 Fr) in 2 Fr increments at a maximal force of 3.5 Newtons as determined by the UCI UAS force sensor. The size of the UAS passed and the highest ureteral location reached (i.e. proximal, middle, or distal ureter) was recorded. Flexible ureteroscopy was performed and a post-ureteroscopic lesion scale (PULS) grade was recorded. Next, a proprietary EMDA catheter was passed into both ureters. On the experimental side, the EMDA catheter was activated while three different medications diluted in 100 ml sterile water were infused at 5 ml/min for 20 minutes: alfuzosin 10 mg, isoproterenol 1 mg, and aminophylline 500 mg (six pigs per drug). In the contralateral control ureter, the EMDA catheter was not activated while saline was infused at 5 ml/min for 20 minutes. Ureteral distensibility was determined at 3.5N; flexible ureteroscopy was performed and a PULS grade was recorded. Pigs were euthanized, and ureters were excised and snap-frozen for histopathological analysis.
Results
,Intraureteral EMDA administration of alfuzosin and isoproterenol resulted in insertion of a larger dilator in 2/6 and 1/6 experimental ureters, respectively. When compared to their respective contralateral control ureter (i.e., R program, and Wilcoxon signed rank test) neither reached statistical significance (p = 0.17, p = 0.68, respectively). No ureter in the aminophylline group accommodated a larger dilator. Among the ureters without augmentation in UAS size, there was increased progress of the same size UAS in 100%, 60% and 66% of the alfuzosin, isoproterenol and aminophylline infused ureters, respectively. PULS grades were all low grade (i.e., < 2).

Conclusion
Among three EMDA tested drugs, only alfuzosin trended to improve ureteral distensibility, albeit without attaining statistical significance.
Funding
None
Lead Authors
Ralph V. Clayman, MD
Department of Urology, University of California, Irvine, CA, USA
Co-Authors
Zachary E. Tano, MD
Department of Urology, University of California, Irvine, CA, USA
Seyed Amiryaghoub M. Lavasani, Junior Research Assistant
Department of Urology, University of California, Irvine, CA, USA
Yi Xi Wu, PHD
Department of Urology, University of California, Irvine, CA, USA
Babak Naimi, PHD
Quantitative Biodiversity Dynamics – Utrecht University
Seyedamirvala Saadat, Junior Research Assistant
Department of Urology, University of California, Irvine, CA, USA
Ahmad Abdel-Aziz, MD
Department of Urology, University of California, Irvine, CA, USA
Sohrab Naushad Ali, MD
Department of Urology, University of California, Irvine, CA, USA
Pengbo Jiang, MD
Department of Urology, University of California, Irvine, CA, USA
Roshan M. Patel, MD
Department of Urology, University of California, Irvine, CA, USA
Jaime Landman, MD
Department of Urology, University of California, Irvine, CA, USA
Ralph V. Clayman, MD
Department of Urology, University of California, Irvine, CA, USA
Bruce Gao, MD
Department of Urology, University of California, Irvine, CA, USA
Intraoperative Acute Ureteral Dilation using Electromotive Drug Administration (EMDA) in an In-Vivo Animal Study
Category
Abstract
Description
MP27: 11Session Name:Moderated Poster Session 27: Stones: Instrumentation and New Technology 1