A new urethral catheterisation device (UCD) to manage difficult urethral catheterisation

S Bugeja, K Mistry, I H W Yim, A Tamimi, N Roberts, A R Mundy, S Bugeja, K Mistry, I H W Yim, A Tamimi, N Roberts, A R Mundy

Abstract

The cost of urethral catheterisation injury (UCI) is significant, but the true incidence of patient care error is difficult to establish in the absence of specific hospital codes recording difficult urethral catheterisation (DUC) and UCI. For many years urologists are familiar passing a non-traumatic hydrophilic guidewire blindly into the bladder to aid urethral catheter insertion in difficult circumstances. However, so far, no purpose-built regulated medical device was available on the market and clinicians had to improvise. Urethrotech filled that gap and developed the Urethral Catheterisation Device (UCD®), which integrates a standard hydrophilic Nitinol guidewire into a 3-way 16F Silicone urethral catheter design to enable safe second-line urethral catheterisation when first-line catheterisation with a standard urethral catheter is unsuccessful. The safety and efficacy of UCD® catheterisation were evaluated in consecutive cohorts of men undergoing cardiac surgery and compared to the incidence of DUC and UCI with standard Foley catheterisation. A simple new Male Catheterisation Algorithm is proposed that can deliver a safe male urethral catheterisation treatment protocol for all clinical settings of healthcare services, which is easy to implement and integrate into standard catheterisation training programs to manage DUC and avoid UCI, empowering a frontline workforce to deliver better patient care.

Keywords: Difficult urethral catheterisation; Male catheterisation algorithm; Urethral catheterisation device; Urethral catheterisation injury; Urethrotech.

Conflict of interest statement

Conflict of interest

The authors declare that they have no conflict of interest.

Research involving human participants

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Figures

Fig. 1
Fig. 1
Urethrotech Urethral Catheterisation Device (UCD®)
Fig. 2
Fig. 2
New Male Catheterisation Algorithm to manage difficult urethral catheterisation
Fig. 3
Fig. 3
Urethral catheterisation adverse events. Group A: standard Foley catheterisation; group B: UCD® catheterisation

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Source: PubMed

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