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Title: | Non-invasive evaluation of botulinum-A toxin treatment efficacy in children with refractory overactive bladder |
Authors: | Uçar, Murat Akgül, Ahsen Karagözlü Yücel, Cem Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi Anabilim Dalı. Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi Anabilim Dalı/Çocuk Ürolojisi Bilim Dalı. 0000-0001-7686-2561 Parlak, Ayşe Kılıç, Nizamettin Balkan, Emin AAH-6766-2021 AAI-3656-2021 AAI-2145-2021 57202853581 7005266570 7004109012 |
Keywords: | Urology & nephrology Botulinum toxin A. Children Overactive bladder Urgency Urinary incontinence Idiopathic detrusor overactivity Urinary-incontinence Intravesical oxybutynin Therapy |
Issue Date: | 28-Jun-2018 |
Publisher: | Springer |
Citation: | Uçar, M. vd. (2018). ''Non-invasive evaluation of botulinum-A toxin treatment efficacy in children with refractory overactive bladder''. International Urology and Nephrology, 50(8), 1367-1373. |
Abstract: | We aimed to evaluate the efficacy and safety of intravesical onabotulinum toxin A (onaBoNTA) injections for the treatment of children diagnosed with refractory overactive bladder (OAB) by using non-invasive methods. A total of 31 pediatric patients with a mean age of 10.2 years received intravesical onaBoNTA injection at the dose of 10 U/kg (max: 200 U). Twenty-one patients who failed to respond to the first injection, received second injection 6 months after the first one. The patients were retrospectively evaluated after the 1st and the 2nd injections by means of standardized questionnaire forms and voiding diary records. In the 6-month follow-up, 10 patients (32.2%) were determined to have full response after the first injection. The number of patients with partial response and no response were found to be 15 (48.4%) and 6 (19.4%), respectively. The mean value of Dysfunctional Voiding and Incontinence Symptom Score (DVISS) of the patients with full response was 8.5 before the injection, which decreased to 1 at 6-month follow-up and to 0.5 at 12-month follow-up (p < 0.001). Twenty-one patients without full response after the first injection received a second injection 6 months after the first one. Full response was achieved in 9 (42.9%) of the 21 patients who had a second injection, but only partial response was achieved in 9 (42.9%). Three (14.3%) of the remaining patients did not respond to the second injection either. 1-year follow-up evaluations revealed that the rates of the full response, partial response, and no response were 61.3, 29, and 9.7%, respectively. Based on our results, onaBoNTA therapy is an effective and reliable second-line off-label therapy in the management of patients with non-neurogenic OAB that is refractory to medical therapy. Asking the patients/guardians to fill out a standardized questionnaire form before and after the therapy enables easy and non-invasive assessment of the response to the therapy. |
URI: | https://doi.org/10.1007/s11255-018-1926-6 https://link.springer.com/article/10.1007/s11255-018-1926-6 http://hdl.handle.net/11452/34154 |
ISSN: | 0301-1623 1573-2584 |
Appears in Collections: | Scopus Web of Science |
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