1.New Frontiers in the Treatment of Overactive Bladder.
Dae Kyung KIM ; Michael B CHANCELLOR
Journal of the Korean Continence Society 2003;7(1):1-8
No abstract available.
Urinary Bladder, Overactive*
;
Duloxetine Hydrochloride
2.Urologic Applications of Botulium Toxin.
Ji Youl LEE ; Michael B CHANCELLOR
Journal of the Korean Continence Society 2002;6(1):22-32
There has been tremendous excitement with the use of Botulinum toxin for the treatment of various urethral and bladder dysfunction over the past several years. Botulinum Toxin is the most lethal naturally occurring toxin known to mankind. Why, then, would an urologist want to use this agent to poison the bladder or urethral sphincter? In this review article we will review the mechanisms underlying the effects of botulinum toxin treatment, We will discuss the current usage of this agent within the urologic community and will provide perspectives on future targets of botulinum toxin.
Botulinum Toxins
;
Urethra
;
Urinary Bladder
3.Advances in the Management of Neurogenic Voiding Dysfunction.
Journal of the Korean Continence Society 1997;1(1):11-11
No abstract available.
4.High Prevalence of Dysplastic Development of Sacral Vertebral Arches in Pediatric Enuresis
Hideo OZAWA ; Takakuki SHIBANO ; Isao TANAKA ; Toshitaka TANIGUCHI ; Michael B. CHANCELLOR ; Naoki YOSHIMURA
International Neurourology Journal 2023;27(2):124-128
Purpose:
This is the first report to compare 3-dimensional computed tomography (3D-CT) images between pediatric patients with enuresis and children without lower urinary tract symptoms who underwent pelvic CT for other reasons.
Methods:
Forty-seven children (33 boys and 14 girls) with primary enuresis underwent 3D-CT of sacrococcygeal bones. The control group consisted of 138 children (78 boys and 60 girls) who underwent pelvic CT for other reasons. First, we determined the presence or absence of unfused sacral arches at the L4-S3 levels in both cohorts. Subsequently, we compared the fusion of sacral arches in age- and sex-matched children from these 2 groups.
Results:
Dysplastic sacral arches, characterized by lack of fusion at 1 or more levels of the S1–3 arches, were observed in nearly all patients in the enuresis group. In the control group (n=138), 54 of 79 children over 10 years old (68%) exhibited fused sacral arches at 3 S1–3 levels. All 11 control children under 4 years old displayed at least 2 unfused sacral arches at the S1–3 levels. In a comparative study of age- and sex-matched patients with enuresis and control children aged 5 to 13 years (n=32 for each group, with 21 boys and 11 girls; mean age, 8.0±2.2 years [range, 5–13 years]), only 1 patient (3%) in the enuresis group exhibited fusion of all S1–3 arches. In contrast, 20 of 32 control group participants (63%) had 3 fused sacral arches (P<0.0001).
Conclusions
Sacral vertebral arches typically fuse by the age of 10 years. However, in this study, children with enuresis exhibited a significantly elevated prevalence of unfused sacral arches, suggesting that dysplastic development of sacral vertebral arches may play a pathological role in enuresis.
5.Neural Mechanisms Underlying Lower Urinary Tract Dysfunction.
Naoki YOSHIMURA ; Teruyuki OGAWA ; Minoru MIYAZATO ; Takeya KITTA ; Akira FURUTA ; Michael B CHANCELLOR ; Pradeep TYAGI
Korean Journal of Urology 2014;55(2):81-90
This article summarizes anatomical, neurophysiological, and pharmacological studies in humans and animals to provide insights into the neural circuitry and neurotransmitter mechanisms controlling the lower urinary tract and alterations in these mechanisms in lower urinary tract dysfunction. The functions of the lower urinary tract, to store and periodically release urine, are dependent on the activity of smooth and striated muscles in the bladder, urethra, and external urethral sphincter. During urine storage, the outlet is closed and the bladder smooth muscle is quiescent. When bladder volume reaches the micturition threshold, activation of a micturition center in the dorsolateral pons (the pontine micturition center) induces a bladder contraction and a reciprocal relaxation of the urethra, leading to bladder emptying. During voiding, sacral parasympathetic (pelvic) nerves provide an excitatory input (cholinergic and purinergic) to the bladder and inhibitory input (nitrergic) to the urethra. These peripheral systems are integrated by excitatory and inhibitory regulation at the levels of the spinal cord and the brain. Therefore, injury or diseases of the nervous system, as well as disorders of the peripheral organs, can produce lower urinary tract dysfunction, leading to lower urinary tract symptoms, including both storage and voiding symptoms, and pelvic pain. Neuroplasticity underlying pathological changes in lower urinary tract function is discussed.
Animals
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Brain
;
Humans
;
Lower Urinary Tract Symptoms
;
Muscle, Smooth
;
Muscle, Striated
;
Nerve Growth Factor
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Nervous System
;
Neuronal Plasticity
;
Neurotransmitter Agents
;
Pelvic Pain
;
Pons
;
Relaxation
;
Spinal Cord
;
Urethra
;
Urinary Bladder
;
Urinary Bladder, Overactive
;
Urinary Tract*
;
Urination
6.Underactive Bladder; Review of Progress and Impact From the International CURE-UAB Initiative
Michael B. CHANCELLOR ; Sarah N. BARTOLONE ; Laura E. LAMB ; Elijah WARD ; Bernadette M.M. ZWAANS ; Ananias DIOKNO
International Neurourology Journal 2020;24(1):3-11
There is a significant need for research and understanding of underactive bladder (UAB). The International Congress of Urologic Research and Education on Aging UnderActive Bladder (CURE-UAB) was organized by Doctors Michael Chancellor and Ananias Diokno in order to address these concerns. CURE-UAB was supported, in part, by the US National Institute of Aging and National Institute of Diabetes Digestive and Kidney. Since 2014, there have been 5 successful CURE-UAB congresses. They have brought together diverse stakeholders in the UAB field to identify areas of major scientific challenge and initiated a call to action among the medical community. In this review, we will highlight current and novel treatments under development for UAB and the progress and impact from the CURE-UAB initiative.