Intravesical Injection of Botulinum Toxin Type A in Patients with Refractory Overactive Bladder—Results between Young and Elderly Populations, and Factors Associated with Unfavorable Outcomes
Abstract
1. Introduction
2. Results
3. Discussion
4. Conclusions
5. Materials and Methods
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Haylen, B.T.; de Ridder, D.; Freeman, R.M.; Swift, S.E.; Berghmans, B.; Lee, J.; Monga, A.; Petri, E.; Rizk, D.E.; Sand, P.K.; et al. An International Urogynecological Association (IUGA)/International Continence Society (ICS) joint report on the terminology for female pelvic floor dysfunction. Int. Urogynecol. J. 2010, 21, 5–26. [Google Scholar] [CrossRef] [PubMed]
- Abrams, P.; Cardozo, L.; Fall, M.; Griffiths, D.; Rosier, P.; Ulmsten, U.; van Kerrebroeck, P.; Victor, A.; Wein, A. The standardisation of terminology of lower urinary tract function: Report from the Standardisation Sub-committee of the International Continence Society. Neurourol. Urodyn. 2002, 21, 167–178. [Google Scholar] [CrossRef] [PubMed]
- Irwin, D.E.; Milsom, I.; Hunskaar, S.; Reilly, K.; Kopp, Z.; Herschorn, S.; Coyne, K.; Kelleher, C.; Hampel, C.; Artibani, W.; et al. Population-based survey of urinary incontinence, overactive bladder, and other lower urinary tract symptoms in five countries: Results of the EPIC study. Eur. Urol. 2006, 50, 1306–1314; discussion 1305–1314. [Google Scholar] [CrossRef] [PubMed]
- Milsom, I.; Abrams, P.; Cardozo, L.; Roberts, R.G.; Thüroff, J.; Wein, A.J. How widespread are the symptoms of an overactive bladder and how are they managed? A population-based prevalence study. BJU Int. 2001, 87, 760–766. [Google Scholar] [CrossRef] [PubMed]
- Teloken, C.; Caraver, F.; Weber, F.A.; Teloken, P.E.; Moraes, J.F.; Sogari, P.R.; Graziottin, T.M. Overactive bladder: Prevalence and implications in Brazil. Eur. Urol. 2006, 49, 1087–1092. [Google Scholar] [CrossRef] [PubMed]
- Gomes, C.M.; Averbeck, M.A.; Koyama, M.; Soler, R. Impact of OAB symptoms on work, quality of life and treatment-seeking behavior in Brazil. Curr. Med. Res. Opin. 2020, 36, 1403–1415. [Google Scholar] [CrossRef]
- Patrick, D.L.; Khalaf, K.M.; Dmochowski, R.; Kowalski, J.W.; Globe, D.R. Psychometric performance of the incontinence quality-of-life questionnaire among patients with overactive bladder and urinary incontinence. Clin. Ther. 2013, 35, 836–845. [Google Scholar] [CrossRef] [PubMed]
- Bartoli, S.; Aguzzi, G.; Tarricone, R. Impact on quality of life of urinary incontinence and overactive bladder: A systematic literature review. Urology 2010, 75, 491–500. [Google Scholar] [CrossRef] [PubMed]
- Amarenco, G.; Arnould, B.; Carita, P.; Haab, F.; Labat, J.J.; Richard, F. European psychometric validation of the CONTILIFE: A Quality of Life questionnaire for urinary incontinence. Eur. Urol. 2003, 43, 391–404. [Google Scholar] [CrossRef]
- Kosilov, K.; Loparev, S.; Kuzina, I.; Kosilova, L.; Prokofyeva, A. Socioeconomic status and health-related quality of life among adults and older with overactive bladder. Int. J. Qual. Health Care J. Int. Soc. Qual. Health Care 2019, 31, 289–297. [Google Scholar] [CrossRef]
- El-Gharib, A.K.; Manzour, A.F.; El-Mallah, R.; El Said, S.M.S. Impact of urinary incontinence on physical performance and quality of life (QOL) amongst a group of elderly in Cairo. Int. J. Clin. Pract. 2021, 75, e14947. [Google Scholar] [CrossRef] [PubMed]
- Dugan, E.; Cohen, S.J.; Bland, D.R.; Preisser, J.S.; Davis, C.C.; Suggs, P.K.; McGann, P. The association of depressive symptoms and urinary incontinence among older adults. J. Am. Geriatr. Soc. 2000, 48, 413–416. [Google Scholar] [CrossRef] [PubMed]
- Abrams, P.; Andersson, K.E. Muscarinic receptor antagonists for overactive bladder. BJU Int. 2007, 100, 987–1006. [Google Scholar] [CrossRef] [PubMed]
- Chapple, C.R.; Nazir, J.; Hakimi, Z.; Bowditch, S.; Fatoye, F.; Guelfucci, F.; Khemiri, A.; Siddiqui, E.; Wagg, A. Persistence and Adherence with Mirabegron versus Antimuscarinic Agents in Patients with Overactive Bladder: A Retrospective Observational Study in UK Clinical Practice. Eur. Urol. 2017, 72, 389–399. [Google Scholar] [CrossRef]
- Hampel, C.; Betz, D.; Burger, M.; Nowak, C.; Vogel, M. Solifenacin in the Elderly: Results of an Observational Study Measuring Efficacy, Tolerability and Cognitive Effects. Urol. Int. 2017, 98, 350–357. [Google Scholar] [CrossRef] [PubMed]
- Wagg, A.; Arumi, D.; Herschorn, S.; Angulo Cuesta, J.; Haab, F.; Ntanios, F.; Carlsson, M.; Oelke, M. A pooled analysis of the efficacy of fesoterodine for the treatment of overactive bladder, and the relationship between safety, co-morbidity and polypharmacy in patients aged 65 years or older. Age Ageing 2017, 46, 620–626. [Google Scholar] [CrossRef]
- Wagg, A.; Khullar, V.; Michel, M.C.; Oelke, M.; Darekar, A.; Bitoun, C.E. Long-term safety, tolerability and efficacy of flexible-dose fesoterodine in elderly patients with overactive bladder: Open-label extension of the SOFIA trial. Neurourol. Urodyn. 2014, 33, 106–114. [Google Scholar] [CrossRef]
- Cai, X.; Campbell, N.; Khan, B.; Callahan, C.; Boustani, M. Long-term anticholinergic use and the aging brain. Alzheimers Dement. J. Alzheimers Assoc. 2013, 9, 377–385. [Google Scholar] [CrossRef]
- Gray, S.L.; Anderson, M.L.; Dublin, S.; Hanlon, J.T.; Hubbard, R.; Walker, R.; Yu, O.; Crane, P.K.; Larson, E.B. Cumulative use of strong anticholinergics and incident dementia: A prospective cohort study. JAMA Intern. Med. 2015, 175, 401–407. [Google Scholar] [CrossRef]
- Nitti, V.W.; Rosenberg, S.; Mitcheson, D.H.; He, W.; Fakhoury, A.; Martin, N.E. Urodynamics and safety of the β3-adrenoceptor agonist mirabegron in males with lower urinary tract symptoms and bladder outlet obstruction. J. Urol. 2013, 190, 1320–1327. [Google Scholar] [CrossRef]
- Herschorn, S.; Staskin, D.; Schermer, C.R.; Kristy, R.M.; Wagg, A. Safety and Tolerability Results from the PILLAR Study: A Phase IV, Double-Blind, Randomized, Placebo-Controlled Study of Mirabegron in Patients ≥ 65 years with Overactive Bladder-Wet. Drugs Aging 2020, 37, 665–676. [Google Scholar] [CrossRef] [PubMed]
- Wagg, A.; Staskin, D.; Engel, E.; Herschorn, S.; Kristy, R.M.; Schermer, C.R. Efficacy, safety, and tolerability of mirabegron in patients aged ≥65yr with overactive bladder wet: A phase IV, double-blind, randomised, placebo-controlled study (PILLAR). Eur. Urol. 2020, 77, 211–220. [Google Scholar] [CrossRef] [PubMed]
- Staskin, D.; Frankel, J.; Varano, S.; Shortino, D.; Jankowich, R.; Mudd, P.N., Jr. International Phase III, Randomized, Double-Blind, Placebo and Active Controlled Study to Evaluate the Safety and Efficacy of Vibegron in Patients with Symptoms of Overactive Bladder: EMPOWUR. J. Urol. 2020, 204, 316–324. [Google Scholar] [CrossRef] [PubMed]
- Staskin, D.; Frankel, J.; Varano, S.; Shortino, D.; Jankowich, R.; Mudd, P.N., Jr. Once-Daily Vibegron 75 mg for Overactive Bladder: Long-Term Safety and Efficacy from a Double-Blind Extension Study of the International Phase 3 Trial (EMPOWUR). J. Urol. 2021, 205, 1421–1429. [Google Scholar] [CrossRef]
- Varano, S.; Staskin, D.; Frankel, J.; Shortino, D.; Jankowich, R.; Mudd, P.N., Jr. Efficacy and Safety of Once-Daily Vibegron for Treatment of Overactive Bladder in Patients Aged ≥65 and ≥75 Years: Subpopulation Analysis from the EMPOWUR Randomized, International, Phase III Study. Drugs Aging 2021, 38, 137–146. [Google Scholar] [CrossRef]
- Nitti, V.W.; Dmochowski, R.; Herschorn, S.; Sand, P.; Thompson, C.; Nardo, C.; Yan, X.; Haag-Molkenteller, C. OnabotulinumtoxinA for the treatment of patients with overactive bladder and urinary incontinence: Results of a phase 3, randomized, placebo controlled trial. J. Urol. 2013, 189, 2186–2193. [Google Scholar] [CrossRef]
- Chapple, C.; Sievert, K.D.; MacDiarmid, S.; Khullar, V.; Radziszewski, P.; Nardo, C.; Thompson, C.; Zhou, J.; Haag-Molkenteller, C. OnabotulinumtoxinA 100 U significantly improves all idiopathic overactive bladder symptoms and quality of life in patients with overactive bladder and urinary incontinence: A randomised, double-blind, placebo-controlled trial. Eur. Urol. 2013, 64, 249–256. [Google Scholar] [CrossRef] [PubMed]
- Liao, C.H.; Chen, S.F.; Kuo, H.C. Different number of intravesical onabotulinumtoxinA injections for patients with refractory detrusor overactivity do not affect treatment outcome: A prospective randomized comparative study. Neurourol. Urodyn. 2016, 35, 717–723. [Google Scholar] [CrossRef] [PubMed]
- Liao, C.H.; Kuo, H.C. Increased risk of large post-void residual urine and decreased long-term success rate after intravesical onabotulinumtoxinA injection for refractory idiopathic detrusor overactivity. J. Urol. 2013, 189, 1804–1810. [Google Scholar] [CrossRef]
- Kuo, H.C.; Liao, C.H.; Chung, S.D. Adverse events of intravesical botulinum toxin a injections for idiopathic detrusor overactivity: Risk factors and influence on treatment outcome. Eur. Urol. 2010, 58, 919–926. [Google Scholar] [CrossRef]
- Mateu Arrom, L.; Mayordomo Ferrer, O.; Sabiote Rubio, L.; Gutierrez Ruiz, C.; Martínez Barea, V.; Palou Redorta, J.; Errando Smet, C. Treatment Response and Complications after Intradetrusor OnabotulinumtoxinA Injection in Male Patients with Idiopathic Overactive Bladder Syndrome. J. Urol. 2020, 203, 392–397. [Google Scholar] [CrossRef] [PubMed]
- Habashy, D.; Losco, G.; Tse, V.; Collins, R.; Chan, L. Botulinum toxin (OnabotulinumtoxinA) in the male non-neurogenic overactive bladder: Clinical and quality of life outcomes. BJU Int. 2015, 116 (Suppl. S3), 61–65. [Google Scholar] [CrossRef] [PubMed]
- Kim, S.H.; Habashy, D.; Pathan, S.; Tse, V.; Collins, R.; Chan, L. Eight-Year Experience With Botulinum Toxin Type-A Injections for the Treatment of Nonneurogenic Overactive Bladder: Are Repeated Injections Worthwhile? Int. Neurourol. J. 2016, 20, 40–46. [Google Scholar] [CrossRef][Green Version]
- White, W.M.; Pickens, R.B.; Doggweiler, R.; Klein, F.A. Short-term efficacy of botulinum toxin a for refractory overactive bladder in the elderly population. J. Urol. 2008, 180, 2522–2526. [Google Scholar] [CrossRef] [PubMed]
- Yokoyama, O.; Honda, M.; Yamanishi, T.; Sekiguchi, Y.; Fujii, K.; Nakayama, T.; Mogi, T. OnabotulinumtoxinA (botulinum toxin type A) for the treatment of Japanese patients with overactive bladder and urinary incontinence: Results of single-dose treatment from a phase III, randomized, double-blind, placebo-controlled trial (interim analysis). Int. J. Urol. Off. J. Jpn. Urol. Assoc. 2020, 27, 227–234. [Google Scholar] [CrossRef] [PubMed]
- Ouchi, Y.; Rakugi, H.; Arai, H.; Akishita, M.; Ito, H.; Toba, K.; Kai, I. Redefining the elderly as aged 75 years and older: Proposal from the Joint Committee of Japan Gerontological Society and the Japan Geriatrics Society. Geriatr. Gerontol. Int. 2017, 17, 1045–1047. [Google Scholar] [CrossRef]
- Manns, K.; Khan, A.; Carlson, K.V.; Wagg, A.; Baverstock, R.J.; Trafford Crump, R. The use of onabotulinumtoxinA to treat idiopathic overactive bladder in elderly patients is in need of study. Neurourol. Urodyn. 2022, 41, 42–47. [Google Scholar] [CrossRef]
- Kao, Y.L.; Ou, Y.C.; Kuo, H.C. Bladder Dysfunction in Older Adults: The Botulinum Toxin Option. Drugs Aging 2022, 39, 401–416. [Google Scholar] [CrossRef]
- Chen, L.C.; Kuo, H.C. Pathophysiology of refractory overactive bladder. Low. Urin. Tract Symptoms 2019, 11, 177–181. [Google Scholar] [CrossRef]
- Mansfield, K.J.; Liu, L.; Mitchelson, F.J.; Moore, K.H.; Millard, R.J.; Burcher, E. Muscarinic receptor subtypes in human bladder detrusor and mucosa, studied by radioligand binding and quantitative competitive RT-PCR: Changes in ageing. Br. J. Pharmacol. 2005, 144, 1089–1099. [Google Scholar] [CrossRef]
- Azadzoi, K.M.; Shinde, V.M.; Tarcan, T.; Kozlowski, R.; Siroky, M.B. Increased leukotriene and prostaglandin release, and overactivity in the chronically ischemic bladder. J. Urol. 2003, 169, 1885–1891. [Google Scholar] [CrossRef] [PubMed]
- Lowe, E.M.; Anand, P.; Terenghi, G.; Williams-Chestnut, R.E.; Sinicropi, D.V.; Osborne, J.L. Increased nerve growth factor levels in the urinary bladder of women with idiopathic sensory urgency and interstitial cystitis. Br. J. Urol. 1997, 79, 572–577. [Google Scholar] [CrossRef] [PubMed]
- Avelino, A.; Cruz, C.; Nagy, I.; Cruz, F. Vanilloid receptor 1 expression in the rat urinary tract. Neuroscience 2002, 109, 787–798. [Google Scholar] [CrossRef] [PubMed]
- Baron, R.; Hans, G.; Dickenson, A.H. Peripheral input and its importance for central sensitization. Ann. Neurol. 2013, 74, 630–636. [Google Scholar] [CrossRef] [PubMed]
- Birder, L.A.; Kullmann, A.F.; Chapple, C.R. The aging bladder insights from animal models. Asian J. Urol. 2018, 5, 135–140. [Google Scholar] [CrossRef]
- Suskind, A.M. The Aging Overactive Bladder: A Review of Aging-Related Changes from the Brain to the Bladder. Curr. Bladder Dysfunct. Rep. 2017, 12, 42–47. [Google Scholar] [CrossRef]
- de Rijk, M.M.; Wolf-Johnston, A.; Kullmann, A.F.; Taiclet, S.; Kanai, A.J.; Shiva, S.; Birder, L.A. Aging-Associated Changes in Oxidative Stress Negatively Impacts the Urinary Bladder Urothelium. Int. Neurourol. J. 2022, 26, 111–118. [Google Scholar] [CrossRef]
- Fusco, F.; Creta, M.; De Nunzio, C.; Iacovelli, V.; Mangiapia, F.; Li Marzi, V.; Finazzi Agrò, E. Progressive bladder remodeling due to bladder outlet obstruction: A systematic review of morphological and molecular evidences in humans. BMC Urol. 2018, 18, 15. [Google Scholar] [CrossRef]
- Lin, Y.H.; Chiang, B.J.; Liao, C.H. Mechanism of Action of Botulinum Toxin A in Treatment of Functional Urological Disorders. Toxins 2020, 12, 129. [Google Scholar] [CrossRef]
- Chen, J.L.; Kuo, H.C. Clinical application of intravesical botulinum toxin type A for overactive bladder and interstitial cystitis. Investig. Clin. Urol. 2020, 61, S33–S42. [Google Scholar] [CrossRef]
- Anger, J.T.; Weinberg, A.; Suttorp, M.J.; Litwin, M.S.; Shekelle, P.G. Outcomes of intravesical botulinum toxin for idiopathic overactive bladder symptoms: A systematic review of the literature. J. Urol. 2010, 183, 2258–2264. [Google Scholar] [CrossRef] [PubMed]
- Miotla, P.; Cartwright, R.; Skorupska, K.; Bogusiewicz, M.; Markut-Miotla, E.; Futyma, K.; Rechberger, T. Urinary retention in female OAB after intravesical Botox injection: Who is really at risk? Int. Urogynecol. J. 2017, 28, 845–850. [Google Scholar] [CrossRef] [PubMed]
- Wang, C.C.; Jiang, Y.H.; Kuo, H.C. The Pharmacological Mechanism of Diabetes Mellitus-Associated Overactive Bladder and Its Treatment with Botulinum Toxin A. Toxins 2020, 12, 186. [Google Scholar] [CrossRef] [PubMed]
- Wang, C.C.; Liao, C.H.; Kuo, H.C. Diabetes mellitus does not affect the efficacy and safety of intravesical onabotulinumtoxinA injection in patients with refractory detrusor overactivity. Neurourol. Urodyn. 2014, 33, 1235–1239. [Google Scholar] [CrossRef]
- Kuo, H.C. Clinical Application of Botulinum Neurotoxin in Lower-Urinary-Tract Diseases and Dysfunctions: Where Are We Now and What More Can We Do? Toxins 2022, 14, 498. [Google Scholar] [CrossRef]
- Truzzi, J.C.; Lapitan, M.C.; Truzzi, N.C.; Iacovelli, V.; Averbeck, M.A. Botulinum toxin for treating overactive bladder in men: A systematic review. Neurourol. Urodyn. 2022, 41, 710–723. [Google Scholar] [CrossRef]
- Lee, P.J.; Kuo, H.C. High incidence of lower urinary tract dysfunction in women with recurrent urinary tract infections. Low. Urin. Tract Symptoms 2020, 12, 33–40. [Google Scholar] [CrossRef]
- Seki, N.; Masuda, K.; Kinukawa, N.; Senoh, K.; Naito, S. Risk factors for febrile urinary tract infection in children with myelodysplasia treated by clean intermittent catheterization. Int. J. Urol. Off. J. Jpn. Urol. Assoc. 2004, 11, 973–977. [Google Scholar] [CrossRef]
- Vasudeva, P.; Madersbacher, H. Factors implicated in pathogenesis of urinary tract infections in neurogenic bladders: Some revered, few forgotten, others ignored. Neurourol. Urodyn. 2014, 33, 95–100. [Google Scholar] [CrossRef]
- McKibben, M.J.; Seed, P.; Ross, S.S.; Borawski, K.M. Urinary Tract Infection and Neurogenic Bladder. Urol. Clin. N. Am. 2015, 42, 527–536. [Google Scholar] [CrossRef]
- Drake, M.J.; Doumouchtsis, S.K.; Hashim, H.; Gammie, A. Fundamentals of urodynamic practice, based on International Continence Society good urodynamic practices recommendations. Neurourol. Urodyn. 2018, 37, S50–S60. [Google Scholar] [CrossRef] [PubMed]
- Nitti, V.W. Pressure flow urodynamic studies: The gold standard for diagnosing bladder outlet obstruction. Rev. Urol. 2005, 7 (Suppl. 6), S14–S21. [Google Scholar] [PubMed]
- Hsiao, S.M.; Lin, H.H.; Kuo, H.C. Videourodynamic Studies of Women with Voiding Dysfunction. Sci. Rep. 2017, 7, 6845. [Google Scholar] [CrossRef]
- Lee, E.S.; Lee, S.W.; Lee, K.W.; Kim, J.M.; Kim, Y.H.; Kim, M.E. Effect of transurethral resection with hydrodistention for the treatment of ulcerative interstitial cystitis. Korean J. Urol. 2013, 54, 682–688. [Google Scholar] [CrossRef] [PubMed]
Young Group (<75) Years | Elderly Group (≥75 Years) | ||
---|---|---|---|
Mean ± SD or No. (%) | Mean ± SD or No. (%) | p-Value | |
Number of patients | 127 | 65 | |
Age (years) | 58.8 ± 11.9 | 82.0 ± 4.6 | |
Gender (male) | 44 (34.6) | 51 (75.5) | <0.001 |
Baseline multichannel urodynamic parameters | |||
FSF (mL) | 110.4 ± 64.4 | 96.3 ± 66.4 | 0.051 |
FS (mL) | 171.5 ± 102.1 | 135.6 ± 87.3 | 0.010 |
US (mL) | 201.7 ± 117.1 | 152.4 ± 100.8 | 0.003 |
CBC (mL) | 272.6 ± 161.1 | 184.7 ± 109.7 | <0.001 |
Compliance (mL/cmH2O) | 66.4 ± 76.8 | 57.2 ± 65.3 | 0.437 |
PdetQmax (cmH2O) | 23.7 ± 16.6 | 31.5 ± 20.6 | 0.003 |
Qmax (mL/s) | 12.7 ± 7.8 | 7.8 ± 4.5 | <0.001 |
VV (mL) | 230.3 ± 142.4 | 155.7 ± 103.4 | <0.001 |
PVR (mL) | 42.2 ± 100.8 | 29.3 ± 50.6 | 0.109 |
Comorbidities | |||
Hypertension | 66 (52.0) | 46 (70.8) | 0.012 |
DM | 24 (18.9) | 25 (38.5) | 0.003 |
CVA | 16 (12.6) | 13 (20.0) | 0.175 |
Dementia | 5 (3.9) | 10 (15.4) | 0.005 |
CAD | 5 (3.9) | 13 (20.0) | <0.001 |
CHF | 3 (2.4) | 2 (3.1) | 1.000 |
CKD | 2 (1.6) | 5 (7.7) | 0.045 |
Young Group (<75 Years) (n = 127) | Elderly Group (≥75 Years) (n = 65) | p-Value | |
---|---|---|---|
Mean ± SD or No. (%) | Mean ± SD or No. (%) | ||
Subjective success (No.) | |||
At 3 months | 124 (97.6%) | 63 (96.9%) | 1.000 |
At 6 months | 98 (77.2%) | 55 (84.6%) | 0.225 |
At 12 months | 31 (24.4%) | 31 (32.3%) | 0.244 |
Subjective dryness (No.) | 85 (66.9%) | 39 (60.0%) | 0.342 |
Uroflowmetry | |||
Qmax (mL/s) | |||
Baseline | 17.0 ± 13.3 | 11.3 ± 7.4 | 0.001 |
3 months | 15.5 ± 10.7 | 11.0 ± 7.3 | 0.004 |
VV (mL) | |||
Baseline | 211.8 ± 149.6 | 138.6 ± 84.7 | 0.002 |
3 months | 220.4 ± 139.6 | 156.9 ± 106.1 | 0.007 |
PVR (mL) | |||
Baseline | 48.7 ± 85.0 | 38.5 ± 48.7 | 0.876 |
3 months | 144.4 ± 114.9 * | 149.3 ± 117.3 * | 0.757 |
CBC (mL) | |||
Baseline | 260.6 ± 164.8 | 177.1 ± 99.1 | 0.001 |
3 months | 332.5 ± 158.1 * | 265.8 ± 126.0 * | 0.010 |
VE (%) | |||
Baseline | 81.8 ± 21.6 | 79.8 ± 21.0 | 0.292 |
3 months | 65.2 ± 71.8 * | 57.4 ± 27.3 * | 0.106 |
Unfavorable outcomes | |||
Large PVR (> 200 mL) (No.) | 29 (22.8%) | 18 (27.7%) | 0.459 |
Urinary retention (No.) | 11 (8.7%) | 8 (12.3%) | 0.423 |
UTI (No.) | 18 (14.2%) | 6 (9.2%) | 0.327 |
Unfavorable Outcomes | UTI | Large PVR | Urinary Retention | ||||||
---|---|---|---|---|---|---|---|---|---|
No | Yes | p-Value | ≤200 mL | >200 mL | p-Value | No | Yes | p Value | |
Number of patients | 59 | 6 | 47 | 18 | 57 | 8 | |||
Age (years) | 81.9 ± 4.6 | 82.8 ± 5.5 | 0.650 | 81.4 ± 4.5 | 83.4 ± 4.8 | 0.106 | 81.7 ± 4.6 | 84.1 ± 4.5 | 0.176 |
Gender (male) | 48 (81.4) | 3 (50.0) | 0.108 | 36 (76.6) | 15 (83.3) | 0.740 | 44 (77.2) | 7 (87.5) | 0.675 |
Baseline multichannel urodynamic parameters | |||||||||
FSF (mL) | 98.1 ± 68.9 | 78.8 ± 29.5 | 0.903 | 94.6 ± 66.6 | 100.8 ± 67.6 | 0.747 | 95.7 ± 67.8 | 100.4 ± 59.6 | 0.660 |
FS (mL) | 137.1 ± 89.7 | 120.8 ± 62.1 | 0.903 | 133.7 ± 86.2 | 140.3 ± 92.6 | 0.889 | 135.1 ± 86.5 | 138.6 ± 98.9 | 0.944 |
US (mL) | 154.5 ± 103.9 | 131.8 ± 66.8 | 0.834 | 150.0 ± 97.4 | 158.7 ± 112.1 | 1.000 | 152.4 ± 100.5 | 152.8 ± 110.2 | 0.992 |
CBC (mL) | 189.8 ± 111.1 | 135.0 ± 88.2 | 0.223 | 179.7 ± 96.7 | 197.7 ± 140.6 | 0.953 | 188.3 ± 109.7 | 159.3 ± 113.5 | 0.442 |
Compliance (mL/cmH2O) | 61.0 ± 67.3 | 19.7 ± 12.5 | 0.014 | 53.9 ± 63.1 | 65.7 ± 71.8 | 0.639 | 59.0 ± 68.2 | 43.9 ± 39.5 | 0.472 |
PdetQmax (cmH2O) | 29.0 ± 17.4 | 56.2 ± 33.2 | 0.013 | 28.3 ± 18.6 | 40.1 ± 23.4 | 0.029 | 28.2 ± 17.3 | 55.5 ± 27.1 | 0.001 |
Qmax (mL/s) | 7.9 ± 4.4 | 6.5 ± 5.7 | 0.485 | 7.8 ± 4.5 | 7.6 ± 4.6 | 0.860 | 7.9 ± 4.5 | 6.6 ± 4.5 | 0.496 |
VV (mL) | 162.5 ± 102.4 | 85.0 ± 92.7 | 0.048 | 154.7 ± 93.6 | 157.2 ± 128.5 | 0.671 | 159.6 ± 99.8 | 125.5 ± 130.0 | 0.235 |
PVR (mL) | 27.2 ± 47.9 | 50.0 ± 75.4 | 0.214 | 25.0 ± 47.0 | 40.6 ± 59.1 | 0.332 | 28.7 ± 48.2 | 33.8 ± 69.5 | 0.550 |
Comorbidities | |||||||||
Hypertension | 42 (71.2%) | 4 (66.7%) | 1.000 | 33 (70.2) | 13 (72.2) | 0.873 | 39 (68.4) | 7 (87.5) | 0.420 |
DM | 24 (40.7%) | 1 (16.7%) | 0.393 | 15 (31.9) | 10 (55.6) | 0.080 | 19 (33.3) | 6 (75.0) | 0.047 |
CVA | 11 (18.6%) | 2 (33.3%) | 0.591 | 7 (14.9) | 6 (33.3) | 0.162 | 9 (15.8) | 4 (50.0) | 0.044 |
Dementia | 7 (11.9%) | 3 (50.0%) | 0.042 | 7 (14.9) | 3 (16.7) | 1.000 | 7 (12.3) | 3 (37.5) | 0.098 |
CAD | 11 (18.6%) | 2 (33.3%) | 0.591 | 9 (19.1) | 4 (22.2) | 0.743 | 12 (21.1) | 1 (12.5) | 1.000 |
CHF | 2 (3.4%) | 0 (0.0%) | 1.000 | 2 (4.3) | 0 (0.0) | 1.000 | 2 (3.5) | 0 (0.0) | 1.000 |
CKD | 4 (6.8%) | 1 (16.7%) | 0.394 | 4 (8.5) | 1 (5.6) | 1.000 | 4 (7.0) | 1 (12.5) | 0.493 |
Postoperative UTI (n = 6) | Large PVR > 200 mL (n = 18) | Urinary Retention (n = 8) | |||||||
---|---|---|---|---|---|---|---|---|---|
OR (95% CI) | Adjusted OR (95% CI) | p-Value ** | OR (95% CI) | Adjusted OR (95% CI) | p-Value ** | OR (95% CI) | Adjusted OR (95% CI) | p-Value ** | |
Age | 1.044 (0.873–1.249) | 1.344 (0.892–2.026) | 0.157 | 1.101 (0.975–1.242) | 1.099 (0.960–1.257) | 0.170 | 1.120 (0.953–1.315) | 1.245 (0.942–1.646) | 0.124 |
Gender (male) | 0.229 (0.041–1.292) | 0.000 (0.000–0.400) | 0.029 | 1.528 (0.372–6.268) | 0.803 (0.167–3.866) | 0.785 | 2.068 (0.233–18.382) | 0.309 (0.018–5.255) | 0.416 |
Compliance | 0.951 (0.904–1.000) | 0.903 (0.820–0.995) | 0.040 | 1.003 (0.995–1.010) | 0.994 (0.976–1.013) | ||||
PdetQmax | 1.048 (1.009–1.089) * | 1.214 (1.007–1.464) | 0.042 | 1.028 (0.999–1.057) | 1.027 (0.997–1.058) | 0.075 | 1.058 (1.013–1.104) * | 1.077 (1.012–1.145) | 0.019 |
DM | 0.292 (0.032–2.656) | 2.667 (0.876–8.122) | 6.000 (1.104–32.595) * | 29.042 (1.114–756.870) | 0.043 | ||||
CVA | 2.182 (0.354–13.458) | 2.857 (0.805–10.143) | 5.333 (1.123–25.331) * | 4.683 (0.587–37.359) | 0.145 | ||||
Dementia | 7.429 (1.247–44.239) * | 0.026 (0.000–3.144) | 0.136 | 1.143 (0.261–5.005) | 4.286 (0.835–21.991) |
Subsequent Injection Cycle(s) | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 |
---|---|---|---|---|---|---|---|---|
Young patients (n) | 84 | 22 | 10 | 4 | 2 | 2 | 2 | 1 |
Elderly patients (n) | 51 | 10 | 3 | 1 | 0 | 0 | 0 | 0 |
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Ou, Y.-C.; Kao, Y.-L.; Ho, Y.-H.; Wu, K.-Y.; Kuo, H.-C. Intravesical Injection of Botulinum Toxin Type A in Patients with Refractory Overactive Bladder—Results between Young and Elderly Populations, and Factors Associated with Unfavorable Outcomes. Toxins 2023, 15, 95. https://doi.org/10.3390/toxins15020095
Ou Y-C, Kao Y-L, Ho Y-H, Wu K-Y, Kuo H-C. Intravesical Injection of Botulinum Toxin Type A in Patients with Refractory Overactive Bladder—Results between Young and Elderly Populations, and Factors Associated with Unfavorable Outcomes. Toxins. 2023; 15(2):95. https://doi.org/10.3390/toxins15020095
Chicago/Turabian StyleOu, Yin-Chien, Yao-Lin Kao, Yi-Hui Ho, Kuan-Yu Wu, and Hann-Chorng Kuo. 2023. "Intravesical Injection of Botulinum Toxin Type A in Patients with Refractory Overactive Bladder—Results between Young and Elderly Populations, and Factors Associated with Unfavorable Outcomes" Toxins 15, no. 2: 95. https://doi.org/10.3390/toxins15020095
APA StyleOu, Y.-C., Kao, Y.-L., Ho, Y.-H., Wu, K.-Y., & Kuo, H.-C. (2023). Intravesical Injection of Botulinum Toxin Type A in Patients with Refractory Overactive Bladder—Results between Young and Elderly Populations, and Factors Associated with Unfavorable Outcomes. Toxins, 15(2), 95. https://doi.org/10.3390/toxins15020095