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2020 CUA Abstracts






                                                              UP-2.6. Table 3. Estimated mean difference and 95%
          36 men were initially enrolled in study
              (i.e. signed consent)                           upper limit in ICIQ-SF from baseline by day
                             6 subjects excluded or withdrew prior to start of testing (day 0)  Day  Estimate  Upper
                              • 1 was excluded by investigator due a pre-existing condition,
                               which could lead to increased infection risk  Interim  -2.471        -0.796
                              • 1 pursued alternative treatment
                              • 2 felt study would be too time consuming/complicated
                              • 2 did not provide reason for withdrawal   End        -4             -1.827
             30 men started testing of
               device at day 0
                             15 subjects withdrew during testing (between day 0 and day 30)
                              • 1 was excluded by the investigator due to subject starting new
                               immunosuppressive medication   UP-2.6. Table 4. Estimated mean percent change and 95%
                              • 1 chose an alternative treatment
                              • 4 withdrew due to urine leakage (i.e. size of required device not   upper limit in pad weight from baseline by day
                               available)
                              • 4 found that study/device was incompatible with lifestyle  Day  Estimate  Upper
                              • 5 withdrew due to pain or difficulty with insertion
            15 men completed study to                          Interim             -54.21           -38.32
                day 30
                 &
            all subjects completed day 56                      End                 -71.76           -54.3
              close out interview
                                                             Apps were rated on the the quality of information, functionality, engage-
        UP-2.6. Fig. 1. Study participants.
                                                             ment, and esthetics, as well as overall impact and impression on a Likert
                                                             scale of 0–5.
        Methods: This multisite study enrolled 36 men with SUI. Each patient
        subsequently underwent personalized device sizing and teaching. The   Results: There were 37 apps reviewed, listed under the categories
        primary endpoints of the study were a change from baseline to interim/end   “Medical,” “Health and Fitness,” and “Education.” Most apps were avail-
        of study on the following: 1) International Consultation on Incontinence   able free (82%). The developer credentials were unknown for 70% of
        Questionnaire-Short Form (ICIQ-SF); 2) pad weight to assess urine loss;   apps, and 64% of apps were affiliated with a commercial organization.
        and 3) adverse events. The trial was 30 days, with data collected at the   The average global quality star rating was 3.1. The top-rated section was
        start, interim, and end of study.                    functionality at 4.3, while the worst-rated was engagement at 3.2. Only
        Results: A total of 15 participants completed the study (Fig. 1). Repeat   9% of apps had been trialed and verified by evidence in scientific lit-
        subjects or those with missing data were removed from the statistical   erature.
        analysis completed post-hoc by UBC. The use of the device resulted in   Conclusions: There are several publicly available apps related to lower
        the reduction of mean scores of ICIQ-SF from baseline (16.5) to day 30   urinary tract health marketed towards various demographics. Most apps
        (12.2) (Table 1). Mean pad weight also decreased from baseline (471.4 g)   have not been trialed and are not based on scientific evidence. Many
        to day 30 (149.1 g) (Table 2). The t-distribution is assumed for calculating   apps are not of high quality and fail to engage the user. Future apps
        confidence intervals. One-sided 95% confidence intervals were used and   should improve on these aspects and exploit the capabilities of current
        gave an upper bound of the estimates (Tables 3, 4). The adverse events   mobile devices.
        (AE) were primarily mild and non-serious (Fig. 5).   References
                          ®
        Conclusions: The Contino  device resulted in a reduction in urine loss and   1.   Pereira-Azevedo N, Carrasquinho E, Cardoso de Oliveira E, et al.
        improved patient perception with urinary incontinence. It is well-tolerated   mHealth in urology: A review of experts’ involvement in app devel-
        with minimal AE. The Contino  device may serve as an alternative, non-  opment. PLoS One 2015;10:e0125547. https://doi.org/10.1371/jour-
                             ®
        invasive option for men with SUI.                        nal.pone.0125547
                                                             2.   Stoyanov SR, Hides L, Kavanagh DJ, et al. Mobile app rating scale:
                                                                 A new tool for assessing the quality of health mobile apps. JMIR
        UP-2.7                                                   Mhealth Uhealth 2015;3:e27. https://doi.org/10.2196/mhealth.3422
        Measuring the quality of mobile apps for lower urinary tract
        health                                               UP-2.8
        Louisa Ho , Lynn Stothers 1
               1
        1 Department of Urologic Sciences, University of British Columbia,   Do larger cuff sizes with artificial urinary sphincter placement
        Vancouver, BC, Canada                                increase the risk of leakage postoperatively?
                                                                                            1
                                                                             1
        Introduction: Overactive bladder (OAB) is a common symptom complex   Thomas J. De los Reyes , Sidney B. Radomski
                                                             1
        that causes significant detriment to quality of life in patients. A mainstay   Division of Urology, Toronto Western Hospital, University Health
        of first-line treatment is behavioral modifications, focusing on lifestyle   Network, Toronto, ON, Canada
        changes. Urological mobile health (mHealth) applications are gaining   Introduction: The artificial urinary sphincter (AUS) remains the gold stan-
        popularity among clinicians and patients as an adjunct to these interven-  dard for post-radical prostatectomy (RP) stress incontinence. Appropriate
            1
        tions.  However, few of these apps have been scientifically evaluated. The   AUS cuff size is an intraoperative decision impacted by measured urethral
        purpose of the study was review and measure the quality of mHealth apps   circumference, history of radiation, and surgeon experience. Cuff sizes
        targeted to the management of OAB and lower urinary tract symptoms.  that are too tight are at risk of erosion, whereas persistent leakage is a
        Methods: A systematic search of the Apple iTunes store was performed.   concern if the cuff is too loose. The aim of this study is to determine
        We included all apps related to lower urinary tract health for health   whether AUS cuff sizes of ≥5.0 cm have an impact on urinary inconti-
        professionals and patients. Expert raters trialed each of the apps and inde-  nence after AUS implantation.
        pendently rated their quality using a Mobile App Rating Scale (MARS). 2   Methods: A retrospective review of AUS implants at our institution from
                                                             1991 to present was performed. All patients who had an AUS cuff size
         UP-2.6. Table 2. Pad weight data summaries by day
         Day                  n       Mean      SD       Min      Median    Max        Q1       Q3       IQR
         Baseline            26       471.4    310.9      33       403.4    1007      186      778.5     592.5
         Interim             11       291.2    261.5      2.7      231.7     721      76.5      472      395.5
         End                 11       149.1    159.7      1.3      120       433      7.8       261      253.2
        S60                                     CUAJ • June 2020 • Volume 14, Issue 6(Suppl2)
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