Adherence to Initial PDE-5 Inhibitor Treatment: Randomized Open-Label Study Comparing Tadalafil Once a Day, Tadalafil on Demand, and Sildenafil on Demand in Patients with Erectile Dysfunction

被引:29
作者
Buvat, Jacques [1 ]
Buettner, Hartwig [2 ]
Hatzimouratidis, Konstantinos [3 ]
Vendeira, Pedro A. S. [4 ]
Moncada, Ignacio [5 ]
Boehmer, Michael
Henneges, Carsten [6 ]
Boess, Frank G. [2 ]
机构
[1] Ctr ETPARP, Lille, France
[2] Lilly Deutschland GmbH, Dept Med, D-61352 Bad Homburg, Germany
[3] Aristotle Univ Thessaloniki, Dept Urol 2, GR-54006 Thessaloniki, Greece
[4] Saude Atlantica, Clin Dragao, Oporto, Portugal
[5] Hosp La Zarzuela, Dept Urol, Madrid, Spain
[6] Lilly Deutschland GmbH, Global Stat Sci, D-61352 Bad Homburg, Germany
关键词
PDE-5; Inhibitor; Treatment Adherence; Erectile Dysfunction; Tadalafil; Sildenafil; Psychosocial Outcomes; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; INTERNATIONAL INDEX; MEN NAIVE; EFFICACY; CROSSOVER; SAFETY; MULTICENTER; CITRATE; PREFERENCE;
D O I
10.1111/jsm.12130
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction Phosphodiesterase type 5 (PDE-5) inhibitor treatment for erectile dysfunction (ED) is frequently discontinued; adherence may vary depending on the initial regimen. Aim To evaluate the effects of initiating treatment with tadalafil once a day (OaD), tadalafil on demand (pro re nata [PRN]), or sildenafil PRN on treatment adherence. Methods In this multicenter, open-label study, men (18 years) with ED, naive to PDE-5 inhibitors, were randomized (1:1:1) to tadalafil 5mg OaD, tadalafil 10mg PRN, or sildenafil 50mg PRN. An 8-week randomized treatment (RT) period (dose adjustment possible) was succeeded by 16 weeks of pragmatic treatment (switches between PDE-5 inhibitors allowed). Main Outcome Measures Treatment adherence was measured as time to discontinuation of RT (any cause), estimated by Kaplan-Meier product-limit method. Treatment-group differences were estimated as hazard ratio (HR; Cox proportional hazards). Results Seven hundred seventy patients (mean age 53 years) were randomized to tadalafil OaD (N=257), tadalafil PRN (N=252), and sildenafil PRN (N=261). Kaplan-Meier estimates for patients discontinuing RT were 52.2, 42.0, and 66.7%, respectively. Median time to discontinuation of RT was significantly longer for tadalafil OaD and PRN (130 and >168 days) compared with sildenafil (67 days) (HR [97.5% confidence interval]: 0.66 [0.51, 0.85] and 0.49 [0.37, 0.65]; P<0.001). Reasons for discontinuation with significant differences between groups (P<0.05) included lack of efficacy (duration of erection) (sildenafil 9.2% vs. tadalafil OaD 4.3%, PRN 2.8%), time constraints due to short window of action (sildenafil 4.2% vs. tadalafil OaD 0%, PRN 0.4%), and feel medication controls my sexual life (sildenafil 2.7% vs. tadalafil OaD 0%). No between-group differences were found in International Index of Erectile Function-Erectile Function domain change from baseline to end of RT (least squares mean: 9.4-10.0, P=0.359) or discontinuations due to adverse events (1.2-1.6%). The most common adverse event (4%) was headache. Conclusions ED patients assigned to tadalafil OaD or PRN adhered significantly longer to initial treatment than patients assigned to sildenafil PRN. Improvement of erectile function and safety profiles were similar in all three treatment groups.
引用
收藏
页码:1592 / 1602
页数:11
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