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1.
BJU Int ; 120(3): 422-427, 2017 09.
Article in English | MEDLINE | ID: mdl-28371167

ABSTRACT

OBJECTIVES: To identify the long-term sexual health outcomes and relationships in men born with classic bladder exstrophy (CBE). MATERIALS AND METHODS: A prospectively maintained institutional database comprising 1248 patients with exstrophy-epispadias was used. Men aged ≥18 years with CBE were included in the study. A 42-question survey was designed using a combination of demographic information and previously validated questionnaires. RESULTS: A total of 215 men met the inclusion criteria, of whom 113 (53%) completed the questionnaire. The mean age of the respondents was 32 years. Ninety-six (85%) of the respondents had been sexually active in their lifetime, and 66 of these (58%) were moderately to very satisfied with their sex life. The average Sexual Health Inventory for Men score was 19.8. All aspects of assessment using the Penile Perception Score questionnaire were on average between 'very dissatisfied' and 'satisfied'. Thirty-two respondents (28%) had attempted to conceive with their partner. Twenty-three (20%) were successful in conceiving, while 31 (27%) reported a confirmed fertility problem. A total of 31 respondents (27%) reported undergoing a semen analysis or post-ejaculatory urine analysis. Of these, only four respondents reported azoospermia. CONCLUSION: Patients with CBE have many of the same sexual and relationship successes and concerns as the general population. This is invaluable information to give to both the parents of boys with CBE, and to the boys themselves as they transition to adulthood.


Subject(s)
Bladder Exstrophy/epidemiology , Reproductive Health/statistics & numerical data , Sexual Behavior/statistics & numerical data , Adult , Bladder Exstrophy/physiopathology , Bladder Exstrophy/psychology , Epispadias/epidemiology , Fertility/physiology , Humans , Male , Prospective Studies , Semen Analysis , Surveys and Questionnaires , Young Adult
2.
J Surg Res ; 203(2): 313-8, 2016 06 15.
Article in English | MEDLINE | ID: mdl-27363638

ABSTRACT

BACKGROUND: Technetium-99m dimercaptosuccinic acid (DMSA) scans are often used in the evaluation of pediatric patients with febrile urinary tract infections (UTIs). Given the prevalence of febrile UTIs, we sought to quantify the cost, radiation exposure, and clinical utility of DMSA scans when compared with dedicated pediatric renal ultrasounds (RUSs). MATERIALS AND METHODS: An institutional review board approved retrospective study of children under the age of 18 years evaluated at our institution for febrile UTIs between the years 2004-2013 was conducted. The patients had to meet all of the following inclusion criteria: a diagnosis of vesicoureteral reflux, a fever >38°C, a positive urine culture, and evaluation with a DMSA scan and RUS. A chart review was used to construct a cost analysis of technical and professional fees, radiographic results, and radiation dose equivalents. RESULTS: Overall, 104 children met the inclusion criteria. A total of 122 RUS and 135 DMSA scans were performed. The technical costs of a DMSA scan incurred a 35% cost premium as compared to an RUS. The average effective radiation dose of a single DMSA scan was 2.84 mSv. New radiographic findings were only identified on 7% of those patients who underwent greater than 1 DMSA scan. CONCLUSIONS: The utility of the unique information acquired from a DMSA scan as compared to a RUS in the evaluation of febrile UTI must be evaluated on an individual case-by-case basis given the increased direct costs and radiation exposure to the patient.


Subject(s)
Cost-Benefit Analysis/statistics & numerical data , Health Care Costs/statistics & numerical data , Radiation Exposure/statistics & numerical data , Urinary Tract Infections/diagnostic imaging , Urinary Tract Infections/economics , Adolescent , Child , Child, Preschool , Female , Fever/etiology , Follow-Up Studies , Humans , Infant , Infant, Newborn , Male , Maryland , Radionuclide Imaging/economics , Radiopharmaceuticals/economics , Retrospective Studies , Technetium Tc 99m Dimercaptosuccinic Acid/economics , Ultrasonography/economics , Urinary Tract Infections/complications
3.
Can J Urol ; 23(2): 8240-2, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27085831

ABSTRACT

Tandem cuff artificial urinary sphincter (AUS) is a well-accepted treatment modality for refractory urinary incontinence following prostatectomy. We present a unique case of a 60-year-old male who experienced spontaneous urethral perforation between tandem AUS cuffs following a strong valsalva maneuver. The patient was treated with immediate AUS explant and transcorporal single cuff placement several months later.


Subject(s)
Urethra/surgery , Urethral Diseases/etiology , Urinary Incontinence, Stress/surgery , Urinary Sphincter, Artificial/adverse effects , Humans , Male , Middle Aged , Prosthesis Failure , Reoperation , Rupture, Spontaneous , Urethra/diagnostic imaging , Urethral Diseases/diagnosis , Urethral Diseases/surgery , Urinary Incontinence, Stress/diagnosis , Urography
4.
Am J Med Qual ; 31(5): 408-14, 2016 09.
Article in English | MEDLINE | ID: mdl-25888549

ABSTRACT

The objective was to evaluate the effect of TeamSTEPPS on operating room efficiency and patient safety. TeamSTEPPS consisted of briefings attended by all health care personnel assigned to the specific operating room to discuss issues unique to each case scheduled for that day. The operative times, on-time start rates, and turnover times of all cases performed by the urology service during the initial year with TeamSTEPPS were compared to the prior year. Patient safety issues identified during postoperative briefings were analyzed. The mean case time was 12.7 minutes less with TeamSTEPPS (P < .001). The on-time first-start rate improved by 21% with TeamSTEPPS (P < .001). The mean room turnover time did not change. Patient safety issues declined from an initial rate of 16% to 6% at midyear and remained stable (P < 0.001). TeamSTEPPS was associated with improved operating room efficiency and diminished patient safety issues in the operating room.


Subject(s)
Efficiency, Organizational , Operating Rooms/standards , Patient Safety , Quality Improvement/organization & administration , Checklist , Efficiency, Organizational/standards , Humans , Operating Rooms/methods , Operating Rooms/organization & administration , Operative Time , Patient Safety/standards , Quality of Health Care/organization & administration , Quality of Health Care/standards , Surgical Procedures, Operative/methods , Surgical Procedures, Operative/standards
5.
J Endourol ; 29(9): 1019-24, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25897552

ABSTRACT

BACKGROUND AND PURPOSE: Liposomal bupivacaine is a delayed-release preparation providing up to 72 hours of local analgesia. It costs much more than standard bupivacaine, however. A prospective, randomized, patient-blinded, controlled trial was performed to assess the efficacy of liposomal bupivacaine versus 0.25% bupivacaine when injected into surgical incisions during laparoscopic and robot-assisted urologic surgery. METHODS: A total of 206 adults were randomized to receive liposomal bupivacaine or 0.25% bupivacaine. All surgical incisions were injected with liposomal bupivacaine or 0.25% bupivacaine with systematic dosing. The primary outcome was total opioid consumption during the postoperative hospital stay. All opioid doses were converted to morphine equivalents. Secondary end points included pain scores using visual analog pain scales, duration of hospital stay, and the time to first opioid use. A subgroup analysis was performed for renal surgery patients. RESULTS: There was no significant difference in median total opioid use during the hospital stay between those who received liposomal bupivacaine (15 [interquartile range (IQR) 6.7-27] mg) and 0.25% bupivacaine (17.3 [IQR 8.3-30.5] mg) (P=0.39). Furthermore, pain scores, length of hospital stay, and time to first opioid use did not differ between groups. Subgroup analysis of laparoscopic renal surgery revealed no difference between liposomal bupivacaine and 0.25% bupivacaine. CONCLUSIONS: For laparoscopic and robot-assisted urologic surgery, there is no significant difference between liposomal bupivacaine and 0.25% bupivacaine for local analgesia at the incision sites.


Subject(s)
Analgesics, Opioid/administration & dosage , Anesthetics, Local/administration & dosage , Bupivacaine/administration & dosage , Laparoscopy/methods , Liposomes/chemistry , Urologic Surgical Procedures/methods , Aged , Female , Humans , Length of Stay , Male , Middle Aged , Pain Management , Pain Measurement , Pain, Postoperative/drug therapy , Prospective Studies , Robotic Surgical Procedures , Surgery, Computer-Assisted
6.
World J Urol ; 33(1): 119-24, 2015 Jan.
Article in English | MEDLINE | ID: mdl-24562314

ABSTRACT

PURPOSE: To determine predictors of fluoroscopy time during uncomplicated, unilateral ureteroscopy for urolithiasis performed by urology residents during the first 2 years of residency. METHODS: The patient charts and computed tomography scans of consecutive, unilateral, uncomplicated ureteroscopy cases for urolithiasis were retrospectively reviewed. The cases were performed by beginning urology residents over the course of their first 2 years of urology residency training. RESULTS: A total of 200 ureteroscopy cases were reviewed. The mean stone diameter was 7.1 (±3.2) mm. Forty-three percent of cases were performed for renal stones and 58 % for ureteral stones. The mean operative time was 80.2 (±36.9) min. The mean fluoroscopy time was 69.1 (±38.2) s. No significant differences existed between cases performed by each of the two residents, and no statistical differences in case difficulty were observed throughout the study period. Linear regression analysis revealed the strongest association with lower fluoroscopy time to be increasing resident experience (p < 0.001). By the end of the 2-year review, fluoroscopy time decreased by 79 % from 135 to 29 s per case. Other significant factors associated with increasing fluoroscopy time were placement of a postoperative stent under fluoroscopic guidance (p < 0.001), utilization of a flexible ureteroscope as opposed to a semirigid ureteroscope (p < 0.001), and balloon dilation of the ureteral orifice (p < 0.001). CONCLUSIONS: Fluoroscopy time during uncomplicated, unilateral ureteroscopy for urolithiasis decreases with increasing urology resident operative experience. Other technical options during ureteroscopy were also found to influence fluoroscopy time.


Subject(s)
Fluoroscopy , Internship and Residency , Operative Time , Ureteroscopy , Urolithiasis/surgery , Urology/education , Adult , Aged , Clinical Competence , Female , Humans , Linear Models , Male , Middle Aged , Radiation Exposure , Retrospective Studies , Tomography, X-Ray Computed , Urolithiasis/diagnostic imaging
7.
Urology ; 84(3): 520-5, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24909957

ABSTRACT

OBJECTIVE: To determine the impact of Safety, Minimization and Awareness Radiation Training (SMART) on fluoroscopy time during unilateral uncomplicated ureteroscopy for urolithiasis performed by urology residents. MATERIALS AND METHODS: All consecutive ureteroscopy cases for urolithiasis meeting inclusion criteria and performed by first-year urology residents over a 2-year period were reviewed. Fluoroscopy times during SMART and without SMART were compared. RESULTS: A total of 202 ureteroscopy cases were reviewed. The mean patient age was 48.7 years. The mean stone diameter was 7.6 ± 3.3 mm. The mean operating time was 79.8 ± 34.3 minutes. The mean cumulative fluoroscopy time was 85.6 ± 36.9 seconds per case. A Spearman rank correlation identified 8 variables significantly correlated with fluoroscopy time, with the most significant correlation between shorter fluoroscopy time and SMART exposure (rho = 0.532; P <.001). Multivariate regression analysis (r = 0.701) revealed that fluoroscopy time was significantly shorter with SMART (P <.001). Post hoc comparisons revealed the fluoroscopy time of the cases performed during SMART (mean, 45 seconds) to be significantly shorter than the fluoroscopy time of cases performed by the same residents before SMART (mean, 102 seconds; P = .005), and the fluoroscopy time of cases performed by residents the previous year with similar ureteroscopic experience but without SMART (mean, 78 seconds; P <.001). CONCLUSION: SMART reduces fluoroscopy time during unilateral uncomplicated ureteroscopy for urolithiasis performed by urology residents by 56%.


Subject(s)
Fluoroscopy/methods , Ureteral Calculi/therapy , Ureteroscopy/methods , Urology/education , Adult , Female , Humans , Internship and Residency , Male , Middle Aged , Patient Safety , Reproducibility of Results , Tomography, X-Ray Computed , Ureteral Calculi/diagnostic imaging , Urolithiasis
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