Efficacy of Intravesical Oxybutynin in Children With Neurogenic Bladder Dysfunction: A Randomized, Prospective Controlled Multi-center Trial
Malformation of the lumbosacral region (spina bifida) affects the innervation of the bladder in children. The usual evolution leads to a neurological bladder with small capacity, poor compliancy and overactivity, exposing to incontinence and obstruction to the evacuation of urine. It is responsible for renal failure requiring dialysis and transplantation. Current therapeutics aim to evacuate urine and reduce intravesical pressure. It gradually combines 1) intermittent catheterization, 2) anticholinergics, 3) botulinum toxin (Botox®) injection into the detrusor (bladder muscle) by cystoscopy and 4) surgery (vesicostomy, Bricker, enterocystoplasty). Oxybutynin relaxes the detrusor, improves continence and reduces intravesical pressure. It is usually administered per os, but there are contraindications (glaucoma, myasthenia), side effects (constipation, dry mouth). It can be difficult to swallow for children, and drug resistance may develop. It can lead to ineffective treatment requiring therapeutic escalation. The next step, intradetrusor Botox® injection, is invasive (cystoscopy), has a limited duration of action (6 months) and must be performed under general anesthesia in children. Surgical treatments are effective but irreversible and responsible for morbidity and mortality. A randomized study was performed demonstrating the efficacy of intravesical oxybutynin compared to oral administration in adult patients. This study found a significant increase in bladder capacity and a significant decrease in side effects in the intravesical oxybutynin group. Due to the relative difficulties of intravesical oxybutynin delivery (preparation, cost) and the more invasive nature, it is not used as an alternative to oral oxybutynin. Our hypothesis is that this treatment may have a legitimate place in the treatment of neurogenic bladder in patients with failure of anticholinergic treatment before a therapeutic escalation requiring an invasive procedure (Botox®, enterocystoplasty) especially in children for whom repeated general anesthesia for Botox® injection may interfere with brain development. In this way, we aim to extend the time to therapeutic escalation in the pediatric population. The main objective of the trial is to compare the efficacy on maximal bladder capacity of intravesical oxybutynin instillation versus placebo in the treatment of children with overactive neurogenic bladder (spina bifida), performing intermittent catheterization, for whom oral anticholinergic treatment is ineffective or poorly tolerated.
Urodynamic and anamnestic profiles as a standardized instrument for treatment initiation and dose titration with VESOXX® - Real World study in patients with neurogenic detrusor overactivity - UPSIDE
Open label, Randomized, Multicentric Study to Evaluate Safety, Tolerability and Performance of mediNiK in Comparison to Standard of Care in Removal of Kidney Stones - MediNiK-02
Intravesikale Oxybutynin-Behandlung der neurogenen Detrusorüberaktivität
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作者: Schmitz, F ; Schindler, O ; Ho, H ; Kalke, Y-B ; Frech-Dörfler, M ; Queissert, F ; Reitz, A ; Leidl, Q ; Schultz-Lampel, D ; Tornic, J ; Kirschner-Herrmanns, R ; Rehme, C ; Hirsch, A ; Angermund, A ; Rahnama'i, S ; Elishar, R ; Gedamke, M
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作者: Pizarro-Cerdá, Javier ; Kühbacher, Andreas ; Cossart, Pascale
Prefilled syringes have been used primarily in self-medication for years. To facilitate this use, the Klosterfrau Healthcare Group and its subsidiary Farco-Pharma have joined forces with the Sanner Group to develop a new polypropylene (PP)-based syringe system.
To date, the syringes and the connecting piece to the catheter were removed from sterile packaging. This resulted in handling difficulties, particularly for patients with motor impairments. The adapter was not to be touched and was firmly attached to the syringe. The syringe and adapter were then connected to the catheter access. In doing so, contamination had to be avoided under all circumstances.
Focus on ease of use and sustainability
To improve the process of administration and adherence, Klosterfrau and Farco-Pharma now rely on a new solution developed jointly with Sanner. The new concept, which was launched this year, attaches the syringe directly to the catheter. This not only makes the application easier and more hygienic. It also saves on the plastic connector and is therefore more sustainable when it comes to using scarce resources.
Sanner has been manufacturing PP syringes for Klosterfrau for many years. The in-house product design department developed two proposals and created prototypes using 3D printing. After several application tests, Klosterfrau chose the concept with the advantage of a round cone that takes over the function of the adapter.
Implementation in the shortest possible time
What is unusual here is that Sanner does not set the injection point at the thickest spot, i.e. not on the round cone, but at a more suitable location, which ensures an absolutely secure sealing fit on the catheter access. “This is supported by compliance with the tightest tolerances in manufacturing,” says Beatrix Höber, account manager at Sanner. “Thanks to our decades of experience in injection moulding, we were able to implement the entire project within a very short time.” Less than nine months passed from the development of the concepts to the qualification of the 16-cavity mould. “Fast and targeted development is characteristic of Sanner,” says Höber. “With the construction of the new plant at our headquarters in Bensheim, we will have even better possibilities for the rapid implementation of new devices as of fall 2024.”