Please use this identifier to cite or link to this item: http://hdl.handle.net/10668/9773
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dc.contributor.authorAlcaraz, Antonio
dc.contributor.authorCarballido-Rodríguez, Joaquín
dc.contributor.authorUnda-Urzaiz, Miguel
dc.contributor.authorMedina-López, Rafael
dc.contributor.authorRuiz-Cerdá, José L
dc.contributor.authorRodríguez-Rubio, Federico
dc.contributor.authorGarcía-Rojo, Darío
dc.contributor.authorBrenes-Bermúdez, Francisco J
dc.contributor.authorCózar-Olmo, José M
dc.contributor.authorBaena-González, Víctor
dc.contributor.authorManasanch, José
dc.date.accessioned2023-01-25T08:30:44Z-
dc.date.available2023-01-25T08:30:44Z-
dc.date.issued2016-01-25
dc.identifier.urihttp://hdl.handle.net/10668/9773-
dc.description.abstractTo evaluate change in quality of life (QoL) and symptoms in patients with lower urinary tract symptoms/benign prostatic hyperplasia (LUTS/BPH) in conditions of current clinical practice. Prospective, longitudinal, multicenter open-label study was carried out in urology outpatient clinics. Patients were ≥40 years of age with an International Prostate Symptom Score (IPSS) score ≥ 8. QoL and symptoms were measured at baseline and 6 months using the Benign Prostatic Hyperplasia Impact Index (BII) and the IPSS. 1713 patients were included for analysis. Mean (SD) IPSS and BII scores at baseline were 16.8 (5.4) and 6.8 (2.6), respectively. 8.9 % (n = 153) of study participants did not receive treatment (watchful waiting, WW), 70.3 % (n = 1204) were prescribed monotherapy (alpha-adrenergic blockers [AB]; phytotherapy [PT, of which 95.2 % was the hexanic extract of Serenoa repens, HESr]; or 5-alpha-reductase inhibitors [5ARI]), and 20.8 % (n = 356) received combined treatment (AB + 5ARI; AB + HESr; others). At 6 months, improvements in QoL were similar across the different medical treatment (MT) groups, both for monotherapy (AB: mean improvement [SD] of 2.4 points [2.4]; PT: 1.9 [2.4]; 5ARI: 2.5 [2.3]) and combined therapy (AB + 5ARI: 3.1 [2.9]; AB + PT: 3.1 [2.5]). There were no clinically significant differences between MT groups and all showed significant improvement over WW (p Improvements in QoL and symptoms were equivalent across the medical treatments most widely used in real-life practice to manage patients with moderate or severe LUTS. HESr showed an equivalent efficacy to AB and 5ARI with fewer side effects.
dc.language.isoen
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBII
dc.subjectBPH
dc.subjectIPSS
dc.subjectLUTS
dc.subjectQuality of life
dc.subjectReal-life practice
dc.subject.mesh5-alpha Reductase Inhibitors
dc.subject.meshAdrenergic alpha-Antagonists
dc.subject.meshAged
dc.subject.meshDrug Therapy, Combination
dc.subject.meshDutasteride
dc.subject.meshFinasteride
dc.subject.meshHumans
dc.subject.meshLongitudinal Studies
dc.subject.meshLower Urinary Tract Symptoms
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPhytotherapy
dc.subject.meshPlant Extracts
dc.subject.meshProspective Studies
dc.subject.meshProstatic Hyperplasia
dc.subject.meshProstatism
dc.subject.meshQuality of Life
dc.subject.meshSerenoa
dc.subject.meshSeverity of Illness Index
dc.subject.meshSulfonamides
dc.subject.meshTamsulosin
dc.subject.meshWatchful Waiting
dc.titleQuality of life in patients with lower urinary tract symptoms associated with BPH: change over time in real-life practice according to treatment--the QUALIPROST study.
dc.typeresearch article
dc.identifier.pmid26810324
dc.rights.accessRightsopen access
dc.identifier.doi10.1007/s11255-015-1206-7
dc.identifier.essn1573-2584
dc.identifier.pmcPMC4839045
dc.identifier.unpaywallURLhttps://link.springer.com/content/pdf/10.1007%2Fs11255-015-1206-7.pdf
dc.issue.number5
dc.journal.titleInternational urology and nephrology
dc.journal.titleabbreviationInt Urol Nephrol
dc.organizationHospital Universitario de Puerto Real
dc.organizationHospital Universitario Regional de Málaga
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number645-56
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeObservational Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.volume.number48
dc.type.hasVersionVoR
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839045/pdf
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