Study design, materials and methods
A group of 50 patients after anti-incontinence surgery using polypropylene tape took part in the study: 25 patients with the implant localised exactly under the midurethra centrally and 25 patients with the implant under the urethra but slightly distally to its middle.
The patients from both of these groups were similar in terms of age, BMI, type of procedure (retropubical tape) and time of the follow-up (3-month follow-up) performed postoperatively. The assessment consisted of medical history, urogynecological examination and introital ultrasonography. Translated questionnaires (UDI-6, Sandvik, IIQ-7, VAS- patient’s subjective assessment: 0= poor, 100= excellent) were also completed. The visualisation of the tape was performed at rest in mediosaggital plane using introital two – dimensional ultrasonography [3]. There were two parameters measured, which specified the tape position [Figure 1]. On the mediosaggital plane we measured the distance between the external orifice and the lower edge of the tape (T) and the total urethral length (U). Then the value of the Tape Index was determined as a quotient (T/U) showing in a calculable way the position of the tape. In relation to the Tape Index, the study group was divided into two subgroups – the patients with the tape localised under the midurethra centrally (Tape Index 0,25 – 0,36) and with the tape localised under the midurethra distal part (Tape Index <= 0,24). The correlation between the tape localisation (mid- and distal part of the urethra) and the VAS of the patient’s subjective assessment (<85 and => 85) was analysed using a Chi square test.
Interpretation of results
In our population the preliminary results showed no differences between the compared groups.