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Published on: May 9, 2018
Sexual and Urinary Outcomes After iTind for Benign Prostatic Hyperplasia: A Systematic Review and Meta-analysis
Fernando Loyola-Nieto1, Giulia Almiron da R Soares2, Marcelo Mass Lindenbaum3
1Men's Health Section, Glickman Urological Institute, Cleveland Clinic Foundation, Cleveland, OH; Universidad Panamericana School of Medicine, Mexico City, Mexico.
The iTind device offers significant improvements in urinary symptoms for men with benign prostatic hyperplasia (BPH) over 12 months. Sexual function, including ejaculation and erectile function, remained largely unchanged, with low reintervention rates.
Area of Science:
- Urology
- Medical Devices
- Men's Health
Background:
- Lower urinary tract symptoms (LUTS) secondary to benign prostatic hyperplasia (BPH) significantly impact men's quality of life.
- Current treatments for BPH carry risks of sexual dysfunction, necessitating alternative therapeutic options.
Purpose of the Study:
- To evaluate the efficacy and safety of the temporary implantable nitinol device (iTind) for LUTS/BPH.
- To characterize urinary and sexual outcomes following iTind therapy through a systematic review and meta-analysis.
Main Methods:
- A systematic review and single-arm meta-analysis of prospective studies.
- Searched PubMed, Embase, and Cochrane Central for studies on iTind treatment for LUTS/BPH.
- Assessed changes in International Prostate Symptom Score (IPSS), IPSS quality-of-life (IPSS-QoL), maximum urinary flow rate (Qmax), post-void residual volume (PVR), and Sexual Health Inventory for Men (SHIM/IIEF-5) scores.
Main Results:
- Five prospective studies (431 patients) were included, with 12-month follow-up.
- Significant improvements observed in IPSS (-10.44 points) and IPSS-QoL (-2.08 points).
- Qmax increased (+5.38 mL/s), PVR decreased (-12.21 mL), and sexual function (SHIM/IIEF-5) showed no significant change. Ejaculatory function was preserved, with no de novo retrograde ejaculation. 12-month reintervention rates were low (0-4.7%).
Conclusions:
- iTind therapy provides consistent and clinically meaningful improvements in urinary outcomes up to 12 months.
- The device preserves ejaculatory function and does not significantly alter erectile function.
- Further comparative trials using validated sexual function instruments are recommended.
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