Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/34154
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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