Outcomes of Intradetrusor OnabotulinumtoxinA Injection in Adults with Congenital Spinal Dysraphism in Tertiary Transitional Urology Clinic.


Journal

Urology practice
ISSN: 2352-0779
Titre abrégé: Urol Pract
Pays: United States
ID NLM: 101635343

Informations de publication

Date de publication:
Mar 2019
Historique:
entrez: 26 3 2019
pubmed: 25 3 2019
medline: 25 3 2019
Statut: ppublish

Résumé

Published data regarding intradetrusor injection of onabotulinumtoxinA in adults with congenital spinal dysraphism are scarce. In this study, we retrospectively investigated the outcomes of intradetrusor injection of onabotulinumtoxinA in this setting. Billing codes were used to identify 149 patients who underwent onabotulinumtoxinA injection between 2012-2016 at our tertiary transitional urology clinic. Charts were then reviewed to identify patients with congenital spinal dysraphism. A total of 18 patients with the mean age of 20.76 (±3.03) years at the time of 1st onabotulinumtoxinA injection were identified. All patients had urinary incontinence. Urinary incontinence improved by injection of 200 or 300 U of onabotulinumtoxinA in 81.2% of patients and 63.6% of them became dry (p= 0.023). Mean glomerular filtration rate before and 13.3 (±9) months after treatment was 100.2 (±17.2) and 120.1 (±16.6) mL/min/1.73 m2 respectively (p= 0.41). Baseline hydronephrosis improved in 3 of 4 patients. Repeat urodynamic study after injection was done in 11 patients who did not clinically improve or who had loss of bladder compliance at baseline (29.3 Vs. 67.2 ml/cmH2O). Mean maximum cystometric capacity before and after injection was 310.1 and 380.2 mL (p= 0.045). Mean bladder compliance before and after treatment was 29.2 and 28.7 ml/cmH2O respectively (p= 0.48) in this high risk group. Intradetrusor onabotulinumtoxinA injection may improve refractory urinary incontinence in selected adults with spinal dysraphism. However, despite improvement in maximum cystometric capacity, bladder compliance does not improve following therapy in patients who had loss of compliance at baseline.

Identifiants

pubmed: 30906822
doi: 10.1016/j.urpr.2018.06.002
pmc: PMC6428434
mid: NIHMS988871
doi:

Types de publication

Journal Article

Langues

eng

Pagination

112-116

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK118209
Pays : United States

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Auteurs

Aaron Kaviani (A)

Department of Urology, Houston Methodist Hospital, Houston, TX.

Rashmi Pande (R)

Department of Urology, Houston Methodist Hospital, Houston, TX.

Timothy B Boone (TB)

Department of Urology, Houston Methodist Hospital, Houston, TX.

Rose Khavari (R)

Department of Urology, Houston Methodist Hospital, Houston, TX.

Classifications MeSH