Predicting outcomes after intradetrusor onabotulinumtoxina for non-neurogenic urgency incontinence in women.

dc.contributor.author

Hendrickson, Whitney K

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Xie, Gongbo

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Rahn, David D

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Amundsen, Cindy L

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Hokanson, James A

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Bradley, Megan

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Smith, Ariana L

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Sung, Vivian W

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Visco, Anthony G

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Luo, Sheng

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Jelovsek, J Eric

dc.date.accessioned

2022-01-01T14:34:01Z

dc.date.available

2022-01-01T14:34:01Z

dc.date.issued

2021-12-02

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2022-01-01T14:34:00Z

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Aims

Develop models to predict outcomes after intradetrusor injection of 100 or 200 units of onabotulinumtoxinA in women with non-neurogenic urgency urinary incontinence (UUI).

Methods

Models were developed using 307 women from two randomized trials assessing efficacy of onabotulinumtoxinA for non-neurogenic UUI. Cox, linear and logistic regression models were fit using: (1) time to recurrence over 12 months, (2) change from baseline daily UUI episodes (UUIE) at 6 months, and (3) need for self-catheterization over 6 months. Model discrimination of Cox and logistic regression models was calculated using c-index. Mean absolute error determined accuracy of the linear model. Calibration was demonstrated using calibration curves. All models were internally validated using bootstrapping.

Results

Median time to recurrence was 6 (interquartile range [IQR]: 2-12) months. Increasing age, 200 units of onabotulinumtoxinA, higher body mass index (BMI) and baseline UUIE were associated with decreased time to recurrence. The c-index was 0.63 (95% confidence interval [CI]: 0.59, 0.67). Median change in daily UUIE from baseline at 6 months was -3.5 (IQR: -5.0, -2.3). Increasing age, lower baseline UUIE, 200 units of onabotulinumtoxinA, higher BMI and IIQ-SF were associated with less improvement in UUIE. The mean absolute error predicting change in UUIE was accurate to 1.6 (95% CI: 1.5, 1.7) UUI episodes. The overall rate of self-catheterization was 17.6% (95% CI: 13.6%-22.4%). Lower BMI, 200 units of onabotulinumtoxinA, increased baseline postvoid residual and maximum capacity were associated with higher risk of self-catheterization. The c-index was 0.66 (95% CI: 0.61, 0.76). The three calculators are available at http://riskcalc.duke.edu.

Conclusions

After external validation, these models will assist clinicians in providing more accurate estimates of expected treatment outcomes after onabotulinumtoxinA for non-neurogenic UUI in women.
dc.identifier.issn

0733-2467

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1520-6777

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https://hdl.handle.net/10161/24154

dc.language

eng

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Wiley

dc.relation.ispartof

Neurourology and urodynamics

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10.1002/nau.24845

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ABC

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BoNT-A

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ROSETTA

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UUI

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botox

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prediction model

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urgency urinary incontinence

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Predicting outcomes after intradetrusor onabotulinumtoxina for non-neurogenic urgency incontinence in women.

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Journal article

duke.contributor.orcid

Luo, Sheng|0000-0003-4214-5809

duke.contributor.orcid

Jelovsek, J Eric|0000-0002-7196-817X

pubs.organisational-group

School of Medicine

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Duke Clinical Research Institute

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Biostatistics & Bioinformatics

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Duke

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Institutes and Centers

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Basic Science Departments

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Obstetrics and Gynecology, Urogynecology

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Obstetrics and Gynecology

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Clinical Science Departments

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Surgery, Urology

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Surgery

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