Abstract
Objectives
The aim of this study was to demonstrate the feasibility of a modified sling mid-urethral suspension + subcutaneous tunnel-double point fixation technique for the treatment of male urinary incontinence and to preliminarily evaluate the short-term clinical efficacy of this technique.
Patients and methods
The clinical data of patients treated with the modified sling mid-urethral suspension + subcutaneous tunnel-double point fixation technique using a Pelvimesh pelvic floor repair patch as a sling were collected. The primary evaluation criteria were surgery-related indicators and daily urinal pad usage before and after treatment, and the secondary evaluation criteria were the corresponding incontinence scores and the results of surgery-related questionnaires.
Results
After 1–12 months of follow-up, seven patients were clinically cured. Follow-up 1 month after surgery showed that one patient (14.3%) used one pad daily, and six patients (85.7%) did not need pads. The incontinence quality of life questionnaire (I-QOL) scores at 3 days and 1 month postoperatively were 89.4 ± 2.5 and 88.1 ± 6.7, respectively, which were significantly higher than the preoperative scores (31.5 ± 18.9) (P < 0.05). The scores of the International Continence Control Association Incontinence Questionnaire Short Form (ICI-Q-SF) at 3 days and 1 month postoperatively were 3.2 ± 0.9 and 4.2 ± 1.7, respectively, which were significantly lower than the preoperative scores of 19.4 ± 5.0 (P < 0.05). In addition, the results of the surgery-related questionnaires were positive. No serious complications occurred in any of the patients.
Conclusion
The modified sling mid-urethral suspension + subcutaneous tunnel-double point fixation technique for the treatment of male urinary incontinence patients is safe, effective, minimally invasive, and has few complications. However, further validation in large sample, randomized, comparative, and longer-term follow-up studies is still needed.
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Data availability statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.
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Acknowledgements
This study was sponsored by the Top-level Clinical Discipline Project of Shanghai Pudong (No.PWYgf 2021-06); Key Medical Specialties of Shanghai Health and Health System (ZK2019A09).
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YC and XS designed the study with the help of ZC and and JY. YC and ZC performed the surgical operation. TL and JH analyzed the data, and JY also contributed to the data. The manuscript was written by YC and JY. All authors reviewed and approved the final version of the manuscript.
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The study involved human participants (not applicable to animal studies) and was approved by the Ethics Committee of Shanghai Pudong New Area Gongli Hospital (Medical ethics approval number: GLYYls2023-010), and all patients signed an informed consent form. The procedures followed in this study followed the Declaration of Helsinki of the World Medical Association, as amended in 2013 and the study was registered with Chinese Clinical Trial Registry (ChiCTR2300072254).
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Appendices
Appendices
Specific evaluation scores used to assess the surgical treatment.
Appendix 1
Daily urine pad usage questionnaire.
Please tick a number between 0 (no urine pads) and 10 or above (use 10 or more pads):
Note: the higher the value, the higher was the number of pads used daily (day/tablet).
Appendix 2
The Patient Satisfaction Quality Scores (PSQ).
Please tick a number between 1 (completely dissatisfied) and 10 (completely/ considerably satisfied):
Note: 1–2 is completely dissatisfied; 3–4 is moderately dissatisfied; 5–6 is halfway satisfied; 7–8 is moderately satisfied; 9–10 is completely/considerably satisfied. Higher scores indicate higher satisfaction.
Appendix 3
The surgical expectation conformity scores (TSEC-S).
Please tick a number between 1 (not meet expectations at all) and 10 (completely /considerably met expectations):
Note: 1–2 is not meet expectations at all; 3–4 is not meet expectations moderately; 5–6 is met expectations halfway; 7–8 is met expectations moderately; 9–10 is completely/considerably met expectations. Higher scores indicate higher completely/considerably met expectations.
Appendix 4
Preoperative anticipation score questionnaire.
Appendix 5
Surgical efficacy satisfaction score questionnaire.
Appendix 6
Recommendation score questionnaire.
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Chen, Y., Song, X., Lv, T. et al. A modified sling mid-urethral suspension + subcutaneous tunnel-double point fixation technique for male stress urinary incontinence: a pilot study. Int Urol Nephrol 56, 901–912 (2024). https://doi.org/10.1007/s11255-023-03822-8
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DOI: https://doi.org/10.1007/s11255-023-03822-8