Tags

Type your tag names separated by a space and hit enter

Assessing satisfaction in men with premature ejaculation after dapoxetine treatment in real-world practice.
Int J Clin Pract. 2015 Nov; 69(11):1326-33.IJ

Abstract

INTRODUCTION

There are limited data on the treatment satisfaction with dapoxetine in patients with premature ejaculation (PE).

AIMS

We aimed to evaluate the treatment satisfaction, effectiveness and safety of dapoxetine for PE patients.

METHODS

Subjects received dapoxetine (30 mg or 60 mg) alone or in combination with a phosphodiesterase type 5 inhibitor, if concurrent with erectile dysfunction for more than 4 weeks in clinical practice. Main outcome measures include Clinical Global Impression of Change (CGIC) and Clinical Global Impression of Satisfaction (CGIS).

RESULTS

From March 2014 to January 2015, a total of 286 PE patients received dapoxetine treatment in this study, with 137 (47.9%) patients diagnosed with lifelong PE and 149 (52.1%) patients diagnosed with acquired PE. At the final follow-up visit, the mean intravaginal ejaculatory latency time (an increase of 3.4 min) and mean score of Premature Ejaculation Diagnostic Tool (a decrease of -5.0) improved significantly from baseline, and the satisfaction rate and response rate to dapoxetine treatment were 45.0% and 74.6%, respectively. Satisfaction with dapoxetine treatment was highly correlated with treatment response, and might be improved by scheduled follow-up visits and escalation to a higher dose. Subjects with diabetes mellitus (DM) reported a lower treatment response than those without DM. Treatment-emergent adverse event (TEAEs) occurred in 47.7% of patients, but no serious TEAEs were reported.

CONCLUSION

Our real-world data highlight the effectiveness of dapoxetine and the importance of follow-up visits for the treatment of PE. Half of PE patients were not satisfied with dapoxetine treatment, which reflects an unmet need of present approach or an unrealistic expectation from PE patients.

Authors+Show Affiliations

Division of Basic Medical Research, Department of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan. School of Medicine, National Yang-Ming University, Taipei, Taiwan.Human Clinical Trial and Subject Protection Center, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan. Graduate School of Human Sexuality, Shu-Te University, Kaohsiung, Taiwan.

Pub Type(s)

Clinical Trial, Phase IV
Journal Article

Language

eng

PubMed ID

26194604

Citation

Jiann, B-P, and Y-J Huang. "Assessing Satisfaction in Men With Premature Ejaculation After Dapoxetine Treatment in Real-world Practice." International Journal of Clinical Practice, vol. 69, no. 11, 2015, pp. 1326-33.
Jiann BP, Huang YJ. Assessing satisfaction in men with premature ejaculation after dapoxetine treatment in real-world practice. Int J Clin Pract. 2015;69(11):1326-33.
Jiann, B. P., & Huang, Y. J. (2015). Assessing satisfaction in men with premature ejaculation after dapoxetine treatment in real-world practice. International Journal of Clinical Practice, 69(11), 1326-33. https://doi.org/10.1111/ijcp.12700
Jiann BP, Huang YJ. Assessing Satisfaction in Men With Premature Ejaculation After Dapoxetine Treatment in Real-world Practice. Int J Clin Pract. 2015;69(11):1326-33. PubMed PMID: 26194604.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Assessing satisfaction in men with premature ejaculation after dapoxetine treatment in real-world practice. AU - Jiann,B-P, AU - Huang,Y-J, Y1 - 2015/07/21/ PY - 2015/03/30/received PY - 2015/06/12/accepted PY - 2015/7/22/entrez PY - 2015/7/22/pubmed PY - 2016/12/15/medline SP - 1326 EP - 33 JF - International journal of clinical practice JO - Int J Clin Pract VL - 69 IS - 11 N2 - INTRODUCTION: There are limited data on the treatment satisfaction with dapoxetine in patients with premature ejaculation (PE). AIMS: We aimed to evaluate the treatment satisfaction, effectiveness and safety of dapoxetine for PE patients. METHODS: Subjects received dapoxetine (30 mg or 60 mg) alone or in combination with a phosphodiesterase type 5 inhibitor, if concurrent with erectile dysfunction for more than 4 weeks in clinical practice. Main outcome measures include Clinical Global Impression of Change (CGIC) and Clinical Global Impression of Satisfaction (CGIS). RESULTS: From March 2014 to January 2015, a total of 286 PE patients received dapoxetine treatment in this study, with 137 (47.9%) patients diagnosed with lifelong PE and 149 (52.1%) patients diagnosed with acquired PE. At the final follow-up visit, the mean intravaginal ejaculatory latency time (an increase of 3.4 min) and mean score of Premature Ejaculation Diagnostic Tool (a decrease of -5.0) improved significantly from baseline, and the satisfaction rate and response rate to dapoxetine treatment were 45.0% and 74.6%, respectively. Satisfaction with dapoxetine treatment was highly correlated with treatment response, and might be improved by scheduled follow-up visits and escalation to a higher dose. Subjects with diabetes mellitus (DM) reported a lower treatment response than those without DM. Treatment-emergent adverse event (TEAEs) occurred in 47.7% of patients, but no serious TEAEs were reported. CONCLUSION: Our real-world data highlight the effectiveness of dapoxetine and the importance of follow-up visits for the treatment of PE. Half of PE patients were not satisfied with dapoxetine treatment, which reflects an unmet need of present approach or an unrealistic expectation from PE patients. SN - 1742-1241 UR - https://www.unboundmedicine.com/medline/citation/26194604/Assessing_satisfaction_in_men_with_premature_ejaculation_after_dapoxetine_treatment_in_real_world_practice_ DB - PRIME DP - Unbound Medicine ER -