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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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] [Green Version]
- 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