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http://hdl.handle.net/11452/34154
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DC Field | Value | Language |
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dc.contributor.author | Uçar, Murat | - |
dc.contributor.author | Akgül, Ahsen Karagözlü | - |
dc.contributor.author | Yücel, Cem | - |
dc.date.accessioned | 2023-09-29T08:24:56Z | - |
dc.date.available | 2023-09-29T08:24:56Z | - |
dc.date.issued | 2018-06-28 | - |
dc.identifier.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. | en_US |
dc.identifier.issn | 0301-1623 | - |
dc.identifier.issn | 1573-2584 | - |
dc.identifier.uri | https://doi.org/10.1007/s11255-018-1926-6 | - |
dc.identifier.uri | https://link.springer.com/article/10.1007/s11255-018-1926-6 | - |
dc.identifier.uri | http://hdl.handle.net/11452/34154 | - |
dc.description.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. | en_US |
dc.description.sponsorship | Sağlık Bilimleri Üniversitesi Tepecik Eğitim ve Araştırma Hastanesi - 2018/4-13 | tr_TR |
dc.language.iso | en | en_US |
dc.publisher | Springer | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Urology & nephrology | en_US |
dc.subject | Botulinum toxin A. | en_US |
dc.subject | Children | en_US |
dc.subject | Overactive bladder | en_US |
dc.subject | Urgency | en_US |
dc.subject | Urinary incontinence | en_US |
dc.subject | Idiopathic detrusor overactivity | en_US |
dc.subject | Urinary-incontinence | en_US |
dc.subject | Intravesical oxybutynin | en_US |
dc.subject | Therapy | en_US |
dc.subject.mesh | Administration, intravesical | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Botulinum toxins, type A. | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Dose-response relationship, drug | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Follow-up studies | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Neuromuscular agents | en_US |
dc.subject.mesh | Retrospective studies | en_US |
dc.subject.mesh | Time factors | en_US |
dc.subject.mesh | Treatment outcome | en_US |
dc.subject.mesh | Urinary bladder, overactive | en_US |
dc.subject.mesh | Urination | en_US |
dc.title | Non-invasive evaluation of botulinum-A toxin treatment efficacy in children with refractory overactive bladder | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000440607100001 | tr_TR |
dc.identifier.scopus | 2-s2.0-85049600125 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi Anabilim Dalı/Çocuk Ürolojisi Bilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0001-7686-2561 | tr_TR |
dc.identifier.startpage | 1367 | tr_TR |
dc.identifier.endpage | 1373 | tr_TR |
dc.identifier.volume | 50 | tr_TR |
dc.identifier.issue | 8 | tr_TR |
dc.relation.journal | International Urology and Nephrology | en_US |
dc.contributor.buuauthor | Parlak, Ayşe | - |
dc.contributor.buuauthor | Kılıç, Nizamettin | - |
dc.contributor.buuauthor | Balkan, Emin | - |
dc.contributor.researcherid | AAH-6766-2021 | tr_TR |
dc.contributor.researcherid | AAI-3656-2021 | tr_TR |
dc.contributor.researcherid | AAI-2145-2021 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.identifier.pubmed | 29968144 | tr_TR |
dc.subject.wos | Urology & nephrology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q3 | en_US |
dc.contributor.scopusid | 57202853581 | tr_TR |
dc.contributor.scopusid | 7005266570 | tr_TR |
dc.contributor.scopusid | 7004109012 | tr_TR |
dc.subject.scopus | Type A Botulinum Toxins; Incobotulinumtoxina; Intravesical Drug Administration | en_US |
dc.subject.emtree | Botulinum toxin A. | en_US |
dc.subject.emtree | Cephalosporin | en_US |
dc.subject.emtree | Oxybutynin | en_US |
dc.subject.emtree | Tolterodine | en_US |
dc.subject.emtree | Botulinum toxin A | en_US |
dc.subject.emtree | Muscle relaxant agent | en_US |
dc.subject.emtree | Adolescent | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Child | en_US |
dc.subject.emtree | Clinical article | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Drug efficacy | en_US |
dc.subject.emtree | Drug safety | en_US |
dc.subject.emtree | Drug treatment failure | en_US |
dc.subject.emtree | Dysfunctional voiding and incontinence symptom score | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Non invasive procedure | en_US |
dc.subject.emtree | Off label drug use | en_US |
dc.subject.emtree | Overactive bladder | en_US |
dc.subject.emtree | Questionnaire | en_US |
dc.subject.emtree | Retrospective study | en_US |
dc.subject.emtree | School child | en_US |
dc.subject.emtree | Scoring system | en_US |
dc.subject.emtree | Treatment response | en_US |
dc.subject.emtree | Dose response | en_US |
dc.subject.emtree | Intravesical drug administration | en_US |
dc.subject.emtree | Micturition | en_US |
dc.subject.emtree | Overactive bladder | en_US |
dc.subject.emtree | Pathophysiology | en_US |
dc.subject.emtree | Physiology | en_US |
dc.subject.emtree | Time factor | en_US |
dc.subject.emtree | Treatment outcome | en_US |
Appears in Collections: | Scopus Web of Science |
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