and efferent pathways between the brain, brain stem,
and pelvic organs and eventually modulate the
voiding reflex and facilitate storage (Wall and
Heesakkers, 2017).
Neuromodulation utilizes electrical stimulation
to target specific nerves that control bladder function
(Burton, Sajja and Latthe, 2012). In various studies,
PTNS was done by using Urgent®PC (Uroplasty,
Minnetonka, MN, USA). In this study, electrical
stimulation was done by using a modified device
with the same parameters with Urgent®PC as a
stimulator due to unavailability of Urgent®PC. We
modified an electrical stimulation device (Everyway
EV-807P NMES) as a substitute for Urgent®PC.
The modifications were made for the needle
electrode and power source. For the needle
electrode, a modification was made by changing the
pad electrode with a crocodile clip. As for the power
source, modification was made by changing the
power source from batteries to direct electricity
through an adapter. The voltage of the adapter was
set at 9V as described in a study (Burton, Sajja and
Latthe, 2012). The setting for pulse width and
frequency were set in 200 microseconds, 20 Hz as
the standard settings of the device (Peters et al.,
2012).
In this study, the protocol of treatment was done
following standard protocol as mention in many
studies (Burton, Sajja and Latthe, 2012; Peters et al.,
2012; Gaziev et al., 2013; Wall and Heesakkers,
2017). Each treatment was done for 30 minutes, and
the electrical stimulations were applied once a week
for 12 weeks. The placement of the needle electrode
at the posterior edge of the tibia and superior to
medial malleolus and grounding electrode at the
medial surface of the calcaneus.
In some systematic reviews the range of
successful treatment was 37-82% (Burton, Sajja and
Latthe, 2012), 54.5-79.5% (Gaziev et al., 2013),
37.3-81.8% (Wibisono and Rahardjo, 2015). The
success rate was varied depending on the criteria
determined by each author as mentioned in a
systematic review (Burton, Sajja and Latthe, 2012).
The criteria
were 50% reduction in symptoms (frequency or
urgency incontinence episodes); 25% reduction in
daytime and/or night time frequency; < 8 voids/24
hr, 0–1 urgency episode in 24 hr, no urgency
incontinence; < 8 voids, < 2 nocturia episodes and
0–1 g on pad test. In this case series, the success
treatment criteria was defined as patients who had at
least a 25% reduction in daytime and/or nighttime
frequency as in a study by Govier et al., 2001. From
the study, 71% of patients were classified as
successfully treated after 12 weeks. In this case
series, four patients (66.6%) from six patients were
classified as successfully treated.
From the studies reported in a meta-analysis
(Wibisono and Rahardjo, 2015), PTNS had no
serious adverse event. The rare complications found
in PTNS treatment were ankle bruising, discomfort/
pain at the needle site, bleeding at the needle site,
tingling in leg, generalized swelling, worsening
incontinence, headache, hematuria, inability to
tolerate stimulation, intermittent foot/toe pain and
foot cramp. In this case series, there were no major
complications had been reported.
4 CONCLUSIONS
PTNS with a modified electrical stimulator may
reduce urinary frequency and maybe a safe option to
treat patients with symptoms from OAB. Need
further research to know the definitive result.
REFERENCES
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