TY - JOUR
T1 - Urinary disturbance in olivopontocerebellar atrophy (OPCA) - Changes during the progression of the disease
AU - Kaiho, Yasuhiro
AU - Namima, Takashige
AU - Uchi, Keiichiro
AU - Nakagawa, Haruo
AU - Aizawa, Masataka
AU - Nishimura, Yosuke
AU - Orikasa, Seiichi
PY - 1999/3
Y1 - 1999/3
N2 - (Purpose) Among spinocerebellar degeneration, syndromes categorized as multiple system atrophy (MSA) are commonly associated with neurogenic bladder, and urinary disturbances change with the disease progression. Accordingly, the changes in the urodynamic findings during the progression of the disease have been studied in the case of Olivopontocerebellar atrophy (OPCA) and OPCA type of MSA. (Methods) Urodynamic study (UDS) was performed more than twice in eight patients (5 males, 3 females, age 48~76, mean 55.0). The interval range between the first examination and follow up examination was 9~93 months (mean 42.4). UDS included cystogram, intravenous pyelography, residual urine volume, cystometry, urethral pressure profilometry, and external sphincter electromyography. (Results) The bladder was deformed in almost all patients with the progression of the disease, but the upper urinary tract was properly preserved. Residual urine volume tended to increase, and residual urine rate worsened significantly. The stable detrusor activity seemed to become overactive accompanied by detrusor hyperreflexia, and finally seemed to be acontractile. The normal sphincter activity seemed to become overactive accompanied by detrusor-sphincter dyssynergia, and finally complete relaxation could't be observed. (Conclusion) These results suggest that urinary disturbance deteriorates together with other neuropathies as the disease progresses in OPCA. These patients should be continuously observed along with proper urinary management depending on the disease progression.
AB - (Purpose) Among spinocerebellar degeneration, syndromes categorized as multiple system atrophy (MSA) are commonly associated with neurogenic bladder, and urinary disturbances change with the disease progression. Accordingly, the changes in the urodynamic findings during the progression of the disease have been studied in the case of Olivopontocerebellar atrophy (OPCA) and OPCA type of MSA. (Methods) Urodynamic study (UDS) was performed more than twice in eight patients (5 males, 3 females, age 48~76, mean 55.0). The interval range between the first examination and follow up examination was 9~93 months (mean 42.4). UDS included cystogram, intravenous pyelography, residual urine volume, cystometry, urethral pressure profilometry, and external sphincter electromyography. (Results) The bladder was deformed in almost all patients with the progression of the disease, but the upper urinary tract was properly preserved. Residual urine volume tended to increase, and residual urine rate worsened significantly. The stable detrusor activity seemed to become overactive accompanied by detrusor hyperreflexia, and finally seemed to be acontractile. The normal sphincter activity seemed to become overactive accompanied by detrusor-sphincter dyssynergia, and finally complete relaxation could't be observed. (Conclusion) These results suggest that urinary disturbance deteriorates together with other neuropathies as the disease progresses in OPCA. These patients should be continuously observed along with proper urinary management depending on the disease progression.
KW - Olivopontocerebellar atrophy (OPCA)
KW - Urinary disturbance
KW - Urodynamic study (UDS)
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U2 - 10.5980/jpnjurol1989.90.454
DO - 10.5980/jpnjurol1989.90.454
M3 - Article
C2 - 10349304
AN - SCOPUS:0032940553
SN - 0021-5287
VL - 90
SP - 454
EP - 461
JO - Japanese Journal of Urology
JF - Japanese Journal of Urology
IS - 3
ER -