2019, Number 4
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Rev Mex Urol 2019; 79 (4)
Effect of percutaneous tibial nerve stimulation on pelvic floor muscles in patients with overactive bladder
Pérez-Martínez C, Palacios-Galicia JL, Vargas-Díaz IB, Cruz-Gómez Y, García-Sánchez D
Language: Spanish
References: 32
Page: 1-11
PDF size: 315.27 Kb.
ABSTRACT
Introduction and objective: Overactive bladder syndrome is associated with
motor disorders, such as hypertonic pelvic floor. The aim of the present study
was to demonstrate the characteristics of pelvic floor muscle surface electromyography
(SEMG) in patients with overactive bladder treated with percutaneous
tibial nerve stimulation (PTNS).
Materials and methods: A prospective, observational, controlled study was
conducted. Seventeen patients with treatment-refractory overactive bladder
volunteered to undergo pelvic floor muscle semg before, during, and 72 hours
after treatment with PTNS. The study volunteers were divided into 2 groups:
14 in the ptns group and 3 in the placebo group. The inclusion criteria were
overactive bladder progression of at least 6 months, urinary frequency of 8 or
more daily episodes, and no medication use. The exclusion criteria were positive
urine or semen cultures, lithiasis, biopsy and/or pelvic organ surgery, pelvic
cancer, and central nervous system lesions. The variables were analyzed using
the anova and the Tukey post-hoc test, with a 95% ci. The SPSS version 10.1.
software was employed.
Results: Mean patient age was 34.23±12.90 years and mean progression time
was 19.58±12.08 months, with no statistically significant difference between
groups. There were significant differences in the PTNS group in the mean average
semg (AVG SEMG) in relation to preptns vs intraptns (0.125 µV) and preptns
vs the 72-hour postPTNS (0.171 µV) (p‹0.05), whereas the differences in
the mean Avg SEMGS of 0.013 µV and 0.006 µV in the placebo group were not
statistically significant (p›0.05).
Conclusion: The immediate change in the pelvic floor muscles that lasts up to
72 hours after PTNS is a possible mechanism of action of the neuroplasticity
resulting from tibial nerve neuromodulation.
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