| dc.creator | Sebastianelli A., Spatafora P., Morselli S., Vignozzi L., Serni S., McVary K.T., Kaplan S., Gravas S., Chapple C., Gacci M. | en |
| dc.date.accessioned | 2023-01-31T09:54:54Z | |
| dc.date.available | 2023-01-31T09:54:54Z | |
| dc.date.issued | 2020 | |
| dc.identifier | 10.1007/s11934-020-01009-7 | |
| dc.identifier.issn | 15272737 | |
| dc.identifier.uri | http://hdl.handle.net/11615/78876 | |
| dc.description.abstract | Purpose of Review: Aim of our systematic review is to evaluate and summarize the efficacy and safety of tadalafil alone or in combination with tamsulosin for the management of lower urinary tract symptoms (LUTS)/benign prostatic hyperplasia (BPH) and erectile dysfunction (ED). Recent Findings: Daily tadalafil, in particular 5 mg, according to retrieved studies, appears to be both safe and effective in treating LUTS/BPH and ED, compared with placebo or tamsulosin. The combination of daily tadalafil 5 mg and tamsulosin 0.4 mg allows a better improvement of LUTS compared with both the monotherapies, even if with an increased, but acceptable and tolerated, adverse events rate. After discontinuation of tamsulosin or tadalafil in patients previously treated with their combination, the improvement of LUTS retains significance compared with baseline. Summary: Tadalafil 5 mg should be considered a primary treatment option for patients with LUTS/BPH and ED. Evidence highlight an excellent tolerability, safety, and effectiveness profile, both alone or in combination with tamsulosin 0.4 mg. A better efficacy on LUTS relief has been observed for combination therapy, preserving also sexual function. The further switch to monotherapy allows to preserve LUTS relief, but tadalafil only is able to retain ED improvement. Our results support the evidence for a more and more tailored and modular LUTS treatment. © 2020, The Author(s). | en |
| dc.language.iso | en | en |
| dc.source | Current Urology Reports | en |
| dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85094197256&doi=10.1007%2fs11934-020-01009-7&partnerID=40&md5=c21d4f378ad650b579ae4193fb55ba94 | |
| dc.subject | placebo | en |
| dc.subject | tadalafil | en |
| dc.subject | tamsulosin | en |
| dc.subject | tadalafil | en |
| dc.subject | tamsulosin | en |
| dc.subject | urinary tract agent | en |
| dc.subject | backache | en |
| dc.subject | bladder outlet obstruction index | en |
| dc.subject | Clinical Global Impression scale | en |
| dc.subject | combination drug therapy | en |
| dc.subject | dizziness | en |
| dc.subject | drug dose comparison | en |
| dc.subject | drug dose escalation | en |
| dc.subject | drug efficacy | en |
| dc.subject | drug safety | en |
| dc.subject | drug tolerability | en |
| dc.subject | drug withdrawal | en |
| dc.subject | dyspepsia | en |
| dc.subject | erectile dysfunction | en |
| dc.subject | headache | en |
| dc.subject | heartburn | en |
| dc.subject | human | en |
| dc.subject | hyperemia | en |
| dc.subject | hypotension | en |
| dc.subject | International Index of Erectile Function | en |
| dc.subject | International Prostate Symptom Score | en |
| dc.subject | lower urinary tract symptom | en |
| dc.subject | monotherapy | en |
| dc.subject | myalgia | en |
| dc.subject | nose obstruction | en |
| dc.subject | ocular hyperemia | en |
| dc.subject | postvoid residual urine volume | en |
| dc.subject | prostate hypertrophy | en |
| dc.subject | quality of life | en |
| dc.subject | Review | en |
| dc.subject | rhinopharyngitis | en |
| dc.subject | sexual satisfaction | en |
| dc.subject | side effect | en |
| dc.subject | systematic review | en |
| dc.subject | urine flow rate | en |
| dc.subject | complication | en |
| dc.subject | erectile dysfunction | en |
| dc.subject | lower urinary tract symptom | en |
| dc.subject | male | en |
| dc.subject | multimodality cancer therapy | en |
| dc.subject | randomized controlled trial (topic) | en |
| dc.subject | treatment outcome | en |
| dc.subject | Combined Modality Therapy | en |
| dc.subject | Erectile Dysfunction | en |
| dc.subject | Humans | en |
| dc.subject | Lower Urinary Tract Symptoms | en |
| dc.subject | Male | en |
| dc.subject | Prostatic Hyperplasia | en |
| dc.subject | Randomized Controlled Trials as Topic | en |
| dc.subject | Tadalafil | en |
| dc.subject | Tamsulosin | en |
| dc.subject | Treatment Outcome | en |
| dc.subject | Urological Agents | en |
| dc.subject | Springer | en |
| dc.title | Tadalafil Alone or in Combination with Tamsulosin for the Management for LUTS/BPH and ED | en |
| dc.type | other | en |