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09:27 - 09:30

S22-5

(PP)

FIVE YEARS FOLLOW-UP OF INTRAVESICAL ELECTROMOTIVE BOTULINUM TOXIN

TYPE A ADMINISTRATION FOR MANAGEMENT OF NEUROPATHIC DETRUSOR

OVERACTIVITY IN CHILDREN

Abdol-Mohammad KAJBAFZADEH, Lida SHARIFI-RAD and Seyedeh-Sanam LADI-SEYEDIAN1

Tehran University of Medical Science, Pediatric Center of Excellence, Section of Tissue Engineering and Stem Cell

Therapy, Tehran, IRAN (ISLAMIC REPUBLIC OF)

PURPOSE

To investigated the long-term efficacy and success rate of intravesical electromotive botulinum toxin type A (BTX-A)

administration in myelomeningocele (MMC) patients who had urinary incontinence due to neuropathic detrusor

overactivity (NDO).

MATERIAL AND METHODS

Twenty four MMC patients (mean age: 8.8 years, range: 3-18) were included in the study and followed up for 5 years.

Using an electrode bladder catheter, 10 IU/kg of BTX-A was inserted into the bladder for electromotive drug

administration (EMDA) without anesthesia and as outpatient basis. The EMDA equipment was connected to the electrode

of indwelling catheter and 2 dispersive electrodes, a pulsed current generator delivered 10 mA for 20 minutes. The

preliminary assessments were voiding diary, urodynamic study (UDS), kidney, bladder ultrasound and

cystourethrography then annually.

RESULTS

Prior to the treatment, all patients had refractory NDO and urinary incontinence. During the follow up, 6/24 (25%) ,

7/24(29.1%) and 3/24(12.5%) of patients needed to repeat EMDA after 1, 2 and 3 years, respectively, while remaining

8 (33.3%) patients were completely dry between CICs at 5 years follow-up. Mean maximum detrusor pressure

significantly decreased and mean maximum bladder capacity increased at follow-up (P<0.05). Reflux was resolved in

80% of patients.

CONCLUSIONS

The results of present study have shown that EMDA/BTX-A is a feasible, safe, reproducible, cost benefit and pain free

method as an outpatient's basis with long-term effects and no need for anesthesia and cystoscopy. This novel delivery

system resulted in considerable improvement in the UDS parameters, urinary incontinence, and VUR in patients with

refractory NDO.