PE43: Tablet based image guided robotic surgery – first in man

PE43: Tablet based image guided robotic surgery – first in man

U N M O D E R A T E D P O S T E R P R E S E N T A T I O N S / E U R O P E A N U R O L O G Y S U P P L E M E N T S 13 (2014) 1—60 quired 2 to 10 pads ...

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U N M O D E R A T E D P O S T E R P R E S E N T A T I O N S / E U R O P E A N U R O L O G Y S U P P L E M E N T S 13 (2014) 1—60

quired 2 to 10 pads inclusive per day (PPD) – were eligible for 1:1 randomization ratio to either 5 mg SS daily or placebo. Randomized patients kept the SPH for another 12 weeks and answered daily inquiries, such as the number of PPD used over the prior 24 hours. The primary endpoint was the time interval from randomization to continence – defined as 0 pads use or a security pad completely dry for 3 consecutive days. Average PPD change from baseline to each visit was a secondary endpoint and the number of patients who reached 0–1 PPD use on any day of study was also analyzed as a post-hoc analysis. Results: Of the 1125 screened patients, 1086 had SPH data and 837 (77.1%) wore one or less PPD by 15 weeks after RALP. 640 patients met randomization criteria and 622 patients had complete post-baseline SPH data. There was no significant difference in the continence time interval – primary endpoint (p=0.17). Mean change from baseline to end of treatment in average daily pad use was −2.9 and −3.2, for placebo and SS, respectively (p=0.033). By study end, 202/309 (65.4%) in placebo and 233/313 (74.4%) in SS reported 0–1 PPD use (p=0.0137). Dry mouth was the onlycommon adverse event: 0.6% and 6.1% of placebo and SS, respectively. Conclusions: Solifenacin succinate did not significantly affect time to continence following RALP, but was significantly associated with reaching the 0–1 PPD milestone by the end of the study. Among 1086 screened subjects with SPH data 77% reach the 0–1 PPD milestone 15 weeks after RALP (Level 1–B evidence). PE43 Tablet based image guided robotic surgery – first in man A. Gavazzi 1 , A. Belba 1 , S. Tazzioli 1 , B. Willis 2 , A. Grogan 2 , D. Wallace 2 , S. Chew 3 , P. Amoroso 3 , I. Gill 4 , P. Dasgupta 5 . 1 Centro Oncologico Fiorentino, Dept. of Urology, Florence, Italy; 2 Translucent Medical, Dept. of Urology, San Francisco, United States of America; 3 The London Clinic, Dept. of Urology, London, United Kingdom; 4 USC, Dept. of Urology, Los Angeles, United States of America; 5 Guy’s Hospital, Dept. of Urology, London, United Kingdom Introduction & Objectives: Preoperative MR and CT images contain large amounts of anatomical data, but this powerful information is under-utilised during actual interventional procedures. The aim of this study is to report the feasibility of using a tablet/iPad based 3D imaging device for the first 2 cases of robotic assisted radical prostatectomy (RARP). Material & Methods: The Translucent Medical system is comprised of a tablet computer with a touch screen display, a tracking system housed in a portable cart, a magnetic field generator and position sensors. Proprietary software uses the tracking data from the sensors to present 3D patient images in alignment with the patient’s anatomy. As the tablet computer display is moved, the system software updates image data over 20 times per second to show the patient’s internal anatomy in motion on the tablet display. After extensive laboratory and cadaveric testing it was used in two RARP patients with informed consent. The tumours were colour coded for accurate visualisation. Results: The average operative time was 120 minutes. Both patients had negative margins – the first had two Gleason 6 cancers, one suspected T3 at the apex, the second patient had a Gleason 7 anterior tumour at the bladder neck. Both achieved continence, at 3 months and 2 weeks respectively and are undergoing penile rehabilitation. Conclusions: This new tablet-like device is small, portable and easy to use. The 3D images align to the position of the patient on the operating table as well as during the movement of the prostate and its neighbouring structures during RARP. The device is undergoing further clinical testing based on IDEAL principles within the framework of a health technology assessment.

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PE44 Setting up a new robot assisted radical cystectomy service G. Athanasiadis 1 , R. Soares 1 , M. Swinn 2 , M. Perry 3 , C. Jones 1 , K. Patil 1 . 1 Royal Surrey County Hospital, Dept. of Urology, Guildford, United Kingdom; 2 East Surrey Hospital, Dept. of Urology, Redhill, United Kingdom; 3 St George’s Hospital, Dept. of Urology, London, United Kingdom Introduction & Objectives: Radical cystectomy is the treatment of choice for muscle invasive bladder cancer in fit patients. However, it is associated with significant morbidity and mortality of 48% and 4.2% respectively at 90 days. Median length of stay in UK is 13 days. A carefully designed service combining minimally invasive surgery with an Enhanced Recovery Programme may reduce length of stay, complications and mortality. We describe our experience in setting up and implementing such a service. Material & Methods: A new regional robot assisted radical cystectomy service started in April 2013. Between April 2013 and June 2014, 23 patients (19 men and 4 women), of average age 72 years old (range: 56–81) and median ASA grade 2 (range: 1–3), underwent robot assisted radical cystectomy with extended pelvic lymph node dissection. 21 of the patients had ileal conduit and 2 orthotopic neobladder formation. As part of our Enhanced Recovery Programme, patient education, pre-operative carbohydrate drinks, spinal analgesia, goal-directed fluid therapy, early feeding (with nutritional supplementation) and intensive early mobilisation were applied and opioid analgesics and nasogastric tube insertion were avoided. Results: Median surgical time was 6.5 h (range: 5 h 30 min–8 h 53 min), median blood loss was 223 ml (range: 30–500 ml) and median length of stay was 8 days (range: 5–29 days). One death was recorded (Clavien 5), one patient underwent laparotomy (Clavien 3b), one patient required readmission for transfusion and drainage of pelvic haematoma (Clavien 3a) and one more patient was transfused (Clavien 2). There were no other significant complications. Conclusions: A well designed Enhanced Recovery Programme in combination with minimally invasive surgery can dramatically improve complications and length of stay compared to the national standards, even from its beginning. Long term results are awaited. PE45 Simultaneous robotic partial nephrectomy and laparoscopic hemicolectomy: Report of a case A. Gavazzi 1 , A. Belba 1 , C. Urena 2 , P. Trevisan 2 . 1 Centro Oncologico Fiorentino, Dept. of Urology, Florence, Italy; 2 Centro Oncologico Fiorentino, Dept. of General Surgery, Florence, Italy Introduction & Objectives: Primary cancer may occur synchronously in different organs. Synchronous renal cell carcinoma in patients with colorectal carcinoma is reported in various percentages ranging from 0.03 to 4.85%. When surgical treatment is indicated, usually two separate operations are planned for resection. To our knowledge this is the first report about a synchronous Robotic left partial nephrectomy with contralateral laparoscopic hemicolectomy. Material & Methods: A 65-year-old male was studied with an US of the abdomen due to strong urinary symptoms. The US showed a left renal mass of 4 cm. The abdominal CT confirmed the tumor of the left kidney and showed a syncronous tumor of the right colon ascendens with lymphadenopathy. The patient subsequently underwent synchronous Robotic resection of the renal tumor and laparoscopic resection of the colon. Results: Total operation time and blood loss were 210 minutes and 100 milliliter. The operation time needed for laparoscopic tumor nephrectomy was 110 minutes, and blood loss was 50 milliliter. For the hemicolectomy, operative time and blood loss were 100 minutes and 50 milliliter, respectively. The procedure was uncomplicated. On postoperative day 2 the wound drain was removed, and on day 4 the patient had flatus and the first bowel motion. The patient was dis-