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1.
Neurourol Urodyn ; 42(8): 1722-1732, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37555436

ABSTRACT

PURPOSE: To assess noninferiority of the safety and effectiveness of the Altis® Single Incision Sling (SIS) with standard midurethral transobturator and/or retropubic slings through 36 months in a prospective, longitudinal, nonrandomized US Food and Drug Administration (FDA) 522 cohort study. MATERIALS AND METHODS: Adult females with confirmed predominant stress urinary incontinence (UI) through cough stress test (CST) or urodynamics and failed two noninvasive incontinence therapies. Effectiveness endpoints included objective dryness, negative CST, adverse events, and revision/resurgery through 36 months. The primary effectiveness endpoint was reduction from baseline in 24-h pad weight of ≥50% at 6 months, as requested by the FDA, and is included as a study point in this paper. Primary safety endpoint was rate of related serious adverse events (SAE) through 36 months. Noninferiority margins of 15% and 10% were prespecified for the effectiveness and safety endpoints. Due to the observational nature of the cohort study, a propensity methodology was conducted to assess the effect of potential confounding variables on the primary endpoints between groups. RESULTS: Three hundred fifty-five women underwent the sling procedure (n = 184 Altis; n = 171 Comparator). One hundred fourty (76%) Altis subjects and 101 (59%) Comparator subjects completed follow-up through 36 months. At 36 months, for the effectiveness endpoint, the difference in proportions of -0.005 for Altis versus Comparator (95% confidence interval [CI]: -0.102 to 0.092) was statistically significant (p = 0.002), supporting the hypothesis that Altis is noninferior to Comparator. Furthermore, both groups demonstrated high objective efficacy; in the Altis arm n = 99 (81.8%) subjects were a success, and in the Comparator arm, n = 79 (82.3%) subjects were a success. Additionally, regarding the CST, Altis was found to be noninferior to the Comparator at every study visit, and the rate of negative CST remained above 80% for both groups (p < 0.001). At 36 months, Altis (n = 2; 1.1%) and Comparator (n = 4; 2.3%) subjects experienced a device and/or procedure-related SAE. The difference in proportions of 0.013 for Altis versus Comparator (95% CI: -0.023 to 0.048) was statistically significant (p < 0.001), demonstrating that Altis is noninferior to Comparator with respect to the primary safety endpoint throughout the study. There were 62 (36.3%) retropubic midurethral slings (RMUS), 96 (56.1%) transobturator midurethral slings (TMUS), and 13 (7.6%) SIS slings in the Comparator group. For the 36 month effectiveness endpoint, assessing the noninferiority of Altis versus RMUS and Altis versus TMUS, 99 (81.8%) Altis and 37 (90.2%) RMUS were a success, trending toward statistical significance, however, it cannot be determined to be noninferior (p = 0.092). Ninty-nine (81.8%) Altis and 33 (71.7%) TMUS were a success; this was statistically significant (p < 0.001), demonstrating Altis was noninferior to TMUS. Rates of negative CST were 122 (87.1%) Altis, 40 (93.0%) RMUS (p < 0.001), and 44 (91.7%) TMUS (p < 0.001). CST demonstrated that Altis was noninferior to RMUS and Altis was noninferior to TMUS at 36 months. CONCLUSION: Altis single-incision sling was noninferior to standard midurethral sling for treatment of stress UI, throughout the study and at 36 months. Furthermore, adverse event rates were low.


Subject(s)
Suburethral Slings , Surgical Wound , Urinary Incontinence, Stress , Urinary Incontinence , United States , Adult , Female , Humans , Urinary Incontinence, Stress/surgery , Urinary Incontinence, Stress/etiology , Cohort Studies , Prospective Studies , Urinary Incontinence/etiology , Suburethral Slings/adverse effects , Surgical Wound/etiology
2.
Soc Sci Med ; 55(5): 791-802, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12190271

ABSTRACT

The identification of spatial clusters of alcohol mortality can be a key tool in identifying locations that are suffering from alcohol-related problems or are at risk of experiencing those types of problems. This study compares two methods for identifying statistically significant spatial clusters of county-level alcohol mortality rates in New York. One method utilizes a local indicator of spatial association to determine which groups of neighboring counties have rates that are significantly related to each other. The other method is a spatial scan technique that calculates a maximum likelihood ratio of cases relative to the underlying population to identify the group of counties that rejects the null hypothesis of "no clustering". The results show that because each technique bases its cluster detection on its own criteria, different counties are selected by each method. However, the overlap of the selections indicates that the two analytic methods illustrate different elements of the same clusters. Consequently, these spatial analytic techniques are seen as complimentary and are best used in tandem rather than individually. These findings suggest that multiple methods are a preferred approach to identifying clusters of alcohol-related mortality at the county level.


Subject(s)
Alcoholism/mortality , Small-Area Analysis , Space-Time Clustering , Age Distribution , Geography , Humans , Incidence , New York/epidemiology , Pattern Recognition, Automated
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