Cargando…

Efficacy and Safety of the Hexanic Extract of Serenoa repens vs. Watchful Waiting in Men with Moderate to Severe LUTS-BPH: Results of a Paired Matched Clinical Study

We investigated changes in symptoms and quality of life (QoL) in men with moderate-to-severe lower urinary tract symptoms associated with benign prostatic hyperplasia (LUTS/BPH) receiving the hexanic extract of Serenoa repens (HESr) and compared results with a matched group on watchful waiting (WW)....

Descripción completa

Detalles Bibliográficos
Autores principales: Alcaraz, Antonio, Gacci, Mauro, Ficarra, Vincenzo, Medina-Polo, José, Salonia, Andrea, Fernández-Gómez, Jesús M., Ciudin, Alexandru, Castro-Díaz, David, Rodríguez-Antolín, Alfredo, Carballido-Rodríguez, Joaquín, Cózar-Olmo, José M., Búcar-Terrades, Santiago, Pérez-León, Noemí, Brenes-Bermúdez, Francisco J., Molero-García, José M., Ledesma, Antonio Fernández-Pro, Herdman, Michael, Manasanch, José, Angulo, Javier C., Group, on behalf of the QUALIPROST Study
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878824/
https://www.ncbi.nlm.nih.gov/pubmed/35207238
http://dx.doi.org/10.3390/jcm11040967
Descripción
Sumario:We investigated changes in symptoms and quality of life (QoL) in men with moderate-to-severe lower urinary tract symptoms associated with benign prostatic hyperplasia (LUTS/BPH) receiving the hexanic extract of Serenoa repens (HESr) and compared results with a matched group on watchful waiting (WW). Data was from a real-world, open-label, prospective, multicenter study. This sub-group analysis included patients with moderate-to-severe symptoms receiving either the HESr 320 mg/daily for six months (HESr) or who remained untreated for LUTS/BPH (WW). Changes in urinary symptoms and QoL were measured by IPSS and BII questionnaires. Two statistical approaches (iterative matching and propensity score pairing) were used to maximize between-group comparability at baseline. Tolerability was assessed in the HESr group. After iterative matching, data for analysis was available for 783 patients (102 WW, 681 HESr). IPSS scores improved by a mean (SD) of 3.8 (4.4) points in the HESr group and by 2.2 (4.5) points in the WW group (p = 0.002). Changes in BII score were 1.8 (2.4) points and 1.0 (2.2) points, respectively (p < 0.001). Three patients (0.9%) treated with the HESr reported mild adverse effects. Moderate-severe LUTS/BPH patients treated for six months with the HESr showed greater improvements in symptoms and QoL than matched patients on WW, with a very low rate of adverse effects.