Finasterida: Diez Años De Uso Clínico. Revisión Sistemática De La Literatura

Cruz, J.F. Jiménez; Gutiérrez, L. Quecedo; Señarís, J. Del Llano

doi:10.1016/s0210-4806(03)72906-4

Cited by 13 publications

(1 citation statement)

References 35 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Fifteen systematic reviews or meta-analyses of 5α-RI clinical trial reports each concluded that 5α-RI-associated sexual adverse events are infrequent, mild, and reversible. None of these prior meta-analyses assessed the adequacy of evaluation of adverse events in primary clinical trial reports (Boyle, Gould & Roehrborn, 1996; Chin, 2013; Edwards & Moore, 2002; Gacci et al, 2014; Gupta & Charrette, 2014; Jimenez Cruz, Quecedo Gutierrez & Del Llano Senaris, 2003; Mella et al, 2010; Oelke et al, 2015; Park & Choi, 2014; Tacklind et al, 2010; Trost, 2013; Varothai & Bergfeld, 2014; Wu et al, 2014; Yin et al, 2015; Yuan et al, 2015). A meta-analysis of clinical trials in men with prostatic hyperplasia found that the risk of ED was significantly increased with combined 5α-RI plus α 2 adrenergic receptor blocker compared to α 2 adrenergic receptor blocker alone (Favilla et al, 2016).…”

Section: Introductionmentioning

confidence: 99%

Persistent erectile dysfunction in men exposed to the 5α-reductase inhibitors, finasteride, or dutasteride

Kiguradze

Temps

Yarnold³

et al. 2017

PeerJ

View full text Add to dashboard Cite

ImportanceCase reports describe persistent erectile dysfunction (PED) associated with exposure to 5α-reductase inhibitors (5α-RIs). Clinical trial reports and the manufacturers’ full prescribing information (FPI) for finasteride and dutasteride state that risk of sexual adverse effects is not increased by longer duration of 5α-RI exposure and that sexual adverse effects of 5α-RIs resolve in men who discontinue exposure.ObjectiveOur chief objective was to assess whether longer duration of 5α-RI exposure increases risk of PED, independent of age and other known risk factors. Men with shorter 5α-RI exposure served as a comparison control group for those with longer exposure.DesignWe used a single-group study design and classification tree analysis (CTA) to model PED (lasting ≥90 days after stopping 5α-RI). Covariates included subject attributes, diseases, and drug exposures associated with sexual dysfunction.SettingOur data source was the electronic medical record data repository for Northwestern Medicine.SubjectsThe analysis cohorts comprised all men exposed to finasteride or dutasteride or combination products containing one of these drugs, and the subgroup of men 16–42 years old and exposed to finasteride ≤1.25 mg/day.Main outcome and measuresOur main outcome measure was diagnosis of PED beginning after first 5α-RI exposure, continuing for at least 90 days after stopping 5α-RI, and with contemporaneous treatment with a phosphodiesterase-5 inhibitor (PDE5I). Other outcome measures were erectile dysfunction (ED) and low libido. PED was determined by manual review of medical narratives for all subjects with ED. Risk of an adverse effect was expressed as number needed to harm (NNH).ResultsAmong men with 5α-RI exposure, 167 of 11,909 (1.4%) developed PED (persistence median 1,348 days after stopping 5α-RI, interquartile range (IQR) 631.5–2320.5 days); the multivariable model predicting PED had four variables: prostate disease, duration of 5α-RI exposure, age, and nonsteroidal anti-inflammatory drug (NSAID) use. Of 530 men with new ED, 167 (31.5%) had new PED. Men without prostate disease who combined NSAID use with >208.5 days of 5α-RI exposure had 4.8-fold higher risk of PED than men with shorter exposure (NNH 59.8, all p < 0.002). Among men 16–42 years old and exposed to finasteride ≤1.25 mg/day, 34 of 4,284 (0.8%) developed PED (persistence median 1,534 days, IQR 651–2,351 days); the multivariable model predicting PED had one variable: duration of 5α-RI exposure. Of 103 young men with new ED, 34 (33%) had new PED. Young men with >205 days of finasteride exposure had 4.9-fold higher risk of PED (NNH 108.2, p < 0.004) than men with shorter exposure.Conclusion and relevanceRisk of PED was higher in men with longer exposure to 5α-RIs. Among young men, longer exposure to finasteride posed a greater risk of PED than all other assessed risk factors.

show abstract