| Literature DB >> 27032562 |
Nathan Hoag1, Vincent Tse2, Audrey Wang3, Eric Chung4, Johan Gani1.
Abstract
The efficacy of intravesical onabotulinumtoxinA (BTXA) in the treatment of overactive bladder (OAB) has been well documented. The use of BTXA injection in orthotopic neobladders is yet to be studied. We present 4 cases of patients injected with intravesical BTXA for overactive orthotopic ileal neobladder. We recorded patient demographics, presenting and follow-up symptoms, urodynamic profiles, and Patient Global Impression of Improvement (PGI-I) scores. The 4 patients reported varying degrees of subjective improvements in the symptoms, including urgency, urge incontinence, and pad usage. Mean follow-up duration was 8.3 months (range, 5-14 months). Average PGI-I score was 3 ("a little better") (range, 2-4). To our knowledge, the current study is the first case series examining BTXA injection for orthotopic neobladder overactivity. BTXA injection yielded varying degrees of objective and subjective improvements, without significant complications. Intravesical BTXA injection is feasible and may be considered as a potential treatment alternative for OAB in orthotopic neobladders, although further study is warranted.Entities:
Keywords: Administration, Intravesical; OnabotulinumtoxinA; Urinary Bladder, Overactive; Urinary Diversion; Urinary Reservoirs, Continent
Year: 2016 PMID: 27032562 PMCID: PMC4819152 DOI: 10.5213/inj.1630380.190
Source DB: PubMed Journal: Int Neurourol J ISSN: 2093-4777 Impact factor: 2.835
Patient demographics, clinical parameters, procedure information, and outcomes
| Case | Age/sex | Preinjection | OnabotulinumtoxinA | Postinjection | Notes |
|---|---|---|---|---|---|
| 1 | 53/M | 24-Hour pad weight 400 g | 150 Units in 20-mL NS | Abolition of NO on UDS | Underwent artificial urinary sphincter for SUI |
| NO on UDS at 25 mL with urge leakage at 173 mL | Cystometric capacity 400 mL “Decreased pad use” | Improvement in pain | |||
| Cystometric capacity 218 mL | PGI-I score 3 | ||||
| 2 | 60/M | 1–2 Pads/day | 200 Units in 20-mL NS | 0 Pad/day | |
| NO on UDS at 200 mL | Functional capacity 350 mL | ||||
| Cystometric capacity 250 mL | PGI-I score 2 | ||||
| 3 | 65/M | 7 Pads/day | 100 Units in 20-mL NS | 3 pads/day | Electro-fulguration required at 2 injection sites |
| Nocturia × 6 | Nocturia x 4 | ||||
| NO on UDS up to 79 cm H2O | PGI-I score 4 | ||||
| 4 | 58/M | NO on UDS up to 23 cm H2O | 100 Units in 10-mL NS | “Improved nocturia” | SUI with valsalva leak point pressure of 100 cm |
| Cystometric capacity 300 mL | Unchanged urge incontinence | H2O | |||
| Poor compliance | PGI-I score 3 |
NO, neobladder overactivity; NS, normal saline; UDS, urodynamic studies; SUI, stress urinary incontinence; PGI-I, Patient Global Impression of Improvement.
Fig. 1.“Case 1” preinjection urodynamic study demonstrating phasic neobladder overactivity and maximum cystometric capacity of 218 mL.
Fig. 2.“Case 1” postinjection urodynamic study demonstrating abolition of phasic neobladder overactivity and maximum cystometric capacity of 400 mL.
Fig. 3.Intraoperative endoscopic view demonstrating onabotulinumtoxinA injection into the neobladder mucosa.
| Check the one number that best describes how your urinary tract condition is now compared with how it was before you received onabotulinumtoxinA treatment. | |
|---|---|
| 1 | Very much better |
| 2 | Much better |
| 3 | A little better |
| 4 | No change |
| 5 | A little worse |
| 6 | Much worse |
| 7 | Very much worse |