Phosphodiesterase Type-5 Inhibitor Prescription Patterns in the United States Among Men With Erectile Dysfunction: An Update

被引:6
|
作者
Mulhall, John P. [1 ]
Chopra, Ishveen [2 ]
Patel, Dipen [3 ]
Hassan, Tarek A. [4 ]
Tang, Wing Yu [5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Urol Serv, 353 E 68th St, New York, NY 10021 USA
[2] Pharmerit Int, Hlth Econ & Outcomes Res, Bethesda, MD USA
[3] Pharmerit Int, HEOR & Market Access, Bethesda, MD USA
[4] Pfizer Upjohn, Med Affairs, New York, NY USA
[5] Pfizer Inc, Patient & Hlth Impact, New York, NY USA
来源
JOURNAL OF SEXUAL MEDICINE | 2020年 / 17卷 / 05期
关键词
Erectile Dysfunction; Phosphodiesterase Type-5 Inhibitors; PDE5I; Sildenafil; Real-World Evidence; Treatment Patterns; PREFERENCE; PATIENT;
D O I
10.1016/j.jsxm.2020.01.027
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
Background: While phosphodiesterase type-5 inhibitors (PDE5Is) are highly effective for the treatment of erectile dysfunction (ED) and well tolerated, updated data on prescription patterns have been limited in real-world settings. Aim: To describe men in the United States who are prescribed PDE5Is for ED treatment and to evaluate patterns of initiation, switching, and treatment overlap. Methods: This retrospective claims study used MarketScan Commercial and Medicare Supplement Databases from January 1, 2010, to December 31, 2015, to identify initial PDE5I claims (index date) for sildenafil, tadalafil, and/or vardenafil. Adults aged >= 18 years with ED were identified between July 1, 2010, and December 31, 2014, allowing for a 6-month preindex and 12-month follow-up period from the index date. Outcomes: Outcomes included patient demographics and treatment-related patterns after treatment initiation. Results: A total of 106,206 identified patients met all inclusion criteria. Of these, 51,694, 40,193, and 14,319 had initial claims for sildenafil, tadalafil, and vardenafil, respectively. Mean age was 50.35 years, and comorbidities included dyslipidemia (44.17%), hypertension (43.09%), diabetes (15.32%), and depression (10.61%). More patients (48.67%) initiated on sildenafil than tadalafil (37.85%) or vardenafil (13.48%). Rate of switching was lower in the 60 days after the end of day supply of the initial prescription in the sildenafil cohort (2.71%) compared with the tadalafil (2.81%) and vardenafil (3.88%) cohorts (P < .001 for sildenafil vs tadalafil or vardenafil). Treatment overlap was lower in the sildenafil cohort (0.35%) than in the tadalafil (0.75%) and vardenafil (0.62%) groups (P < .001 for sildenafil vs tadalafil or vardenafil). Clinical Implications: These findings provide insight into updated patterns of PDE5I prescriptions in the United States and may aid in clinical decision-making. Strengths & Limitations: Strengths include the large sample size, long data coverage period, and the real-world nature of the study. Limitations include the retrospective study design, use of data collected with a primary focus of claims, and lack of further details regarding reasons that drive switching. Actual rates of ED and impact on prescription patterns may be underestimated because the claims database only captured patients electing to visit a health-care provider. Conclusion: Among men with ED in the United States, rates of switching and treatment overlap were low for all PDE5Is but were found to be the lowest for sildenafil compared with tadalafil and vardenafil. Copyright (C) 2020, International Society for Sexual Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:941 / 948
页数:8
相关论文
共 50 条
  • [21] ASSESSMENT OF HEADACHE IN MEN TAKING PHOSPHODIESTERASE-5 INHIBITOR (TADALAFIL) FOR ERECTILE DYSFUNCTION
    Okuyucu, E. Esra
    Guven, Oguz
    Ucar, Edip
    Duman, Taskin
    ACTA MEDICA MEDITERRANEA, 2014, 30 (05): : 1007 - 1011
  • [22] CESSATION OF PHOSPHODIESTERASE 5 INHIBITOR USE IN MEN WITH ERECTILE DYSFUNCTION FOLLOWING TESTOSTERONE THERAPY
    Lin, J. S.
    Pastuszak, A. W.
    Ohlander, S. J.
    Hakky, T. S.
    Lamb, D. J.
    Lipshultz, L., I
    JOURNAL OF SEXUAL MEDICINE, 2017, 14 (02): : E10 - E10
  • [23] Phosphodiesterase Type 5 Inhibitor and Erectile Dysfunction in Lower Urinary Tract Symptoms
    Zhao, Chen
    Park, Jong Kwan
    LUTS-LOWER URINARY TRACT SYMPTOMS, 2012, 4 : 75 - 80
  • [24] MEDICATION UTILIZATION IN PATIENTS RECEIVING PHOSPHODIESTERASE TYPE 5 INHIBITOR FOR ERECTILE DYSFUNCTION
    Mulhall, J. P.
    Chopra, I
    Patel, D.
    Tang, W. Y.
    Hassan, T. A.
    JOURNAL OF SEXUAL MEDICINE, 2018, 15 (07): : S370 - S370
  • [25] Phosphodiesterase type 5 inhibitors for erectile dysfunction
    Carson, CC
    Lue, TF
    BJU INTERNATIONAL, 2005, 96 (03) : 257 - 280
  • [26] Phosphodiesterase Type 5 Inhibitors and Erectile Dysfunction
    Whittaker, Catherine
    SA PHARMACEUTICAL JOURNAL, 2009, 76 (05) : 24 - 26
  • [27] Phosphodiesterase type 5 inhibitors and erectile dysfunction
    Whittaker, C.
    SOUTH AFRICAN FAMILY PRACTICE, 2010, 52 (03) : 207 - 210
  • [28] Vardenafil -: Treatment of erectile dysfunction -: Phosphodiesterase 5 inhibitor
    Sorbera, LA
    Martin, L
    Rabasseda, X
    Castañer, J
    DRUGS OF THE FUTURE, 2001, 26 (02) : 141 - 144
  • [29] Improvement in duration of erection following phosphodiesterase type 5 inhibitor therapy with vardenafil in men with erectile dysfunction: the ENDURANCE study
    Rosenberg, M. T.
    Adams, P. L.
    McBride, T. A.
    Roberts, J. N.
    McCallum, S. W.
    INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2009, 63 (01) : 27 - 34
  • [30] Factors associated with ejaculatory and orgasmic dysfunction in men with erectile dysfunction: analysis of clinical trials involving the phosphodiesterase type 5 inhibitor tadalafil
    Paduch, Darius A.
    Bolyakov, Alexander
    Beardsworth, Anthony
    Watts, Steven D.
    BJU INTERNATIONAL, 2012, 109 (07) : 1060 - 1067