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枸橼酸西地那非对使用性体验问卷评估的男性性体验的影响:一项多中心、双盲、安慰剂对照并开放标签扩展的试验。

Effect of sildenafil citrate on the male sexual experience assessed with the Sexual Experience Questionnaire: a multicenter, double-blind, placebo-controlled trial with open-label extension.

作者信息

Jones LeRoy A, Klimberg Ira W, McMurray James G, Padula Rebecca, Tseng Li-Jung, Stecher Vera J

机构信息

Urology San Antonio Research, PA, San Antonio, TX 78229, USA.

出版信息

J Sex Med. 2008 Aug;5(8):1955-64. doi: 10.1111/j.1743-6109.2008.00879.x. Epub 2008 Jun 28.

Abstract

INTRODUCTION

The Sexual Experience Questionnaire (SEX-Q) enables quick and easy assessment of functional, emotional, and satisfaction-related aspects of the sexual experience in men with erectile dysfunction (ED).

AIM

To assess correlations between improvement on the SEX-Q and outcomes on other validated questionnaires. METHODS. Men with ED (score < or =25 on the Erectile Function domain of the International Index of Erectile Function [IIEF]) who had used less than or equal to six doses of any phosphodiesterase 5 inhibitor (none within 6 months) were randomized to 10 weeks of double-blind, placebo-controlled (DBPC) flexible-dose sildenafil citrate (50 or 100 mg, as needed), followed by 6 weeks of open-label (OL) sildenafil.

MAIN OUTCOME MEASURES

SEX-Q, IIEF, Quality of Erection Questionnaire (QEQ), Self-Esteem and Relationship (SEAR) Questionnaire, Erection Hardness Score (EHS), successful intercourse attempts (SIAs), Erectile Dysfunction Inventory of Treatment Satisfaction (EDITS), and global efficacy questions (GEQs).

RESULTS

Compared with the placebo group (N = 105), the sildenafil group (N = 104) at DBPC end of treatment (EOT) had significantly more improvement (P < 0.05) on all SEX-Q, IIEF (except the Sexual Desire domain), QEQ, and SEAR outcomes, more frequent SIAs and EHS 3 (hard enough for penetration but not completely hard) or EHS 4 (completely hard) erections (odds ratio [OR], 2.52 and 3.46, respectively), EHS 4 erections four times as often (OR, 6.41), more men satisfied with treatment (EDITS; OR, 2.6), approximately twice as many men with improved erections (GEQ1; OR, 5.8) and ability to have sexual intercourse (GEQ2; OR, 5.4), and GEQ3 scores that indicated better sex (P < 0.0001). SEX-Q score improvements correlated positively with all other outcomes. At OL EOT, most outcomes were >60% (and approximately half were > or =80%) of the maximum positive result.

CONCLUSIONS

SEX-Q change scores correlate with several other functional, emotional, and satisfaction-related outcomes in men treated with sildenafil for ED, allowing a simple and focused evaluation of the sexual experience.

摘要

引言

性体验问卷(SEX-Q)能够快速简便地评估勃起功能障碍(ED)男性的性功能、情感及与满意度相关的性体验方面。

目的

评估SEX-Q的改善情况与其他经过验证的问卷结果之间的相关性。方法:国际勃起功能指数(IIEF)勃起功能领域得分小于或等于25分且使用任何磷酸二酯酶5抑制剂剂量小于或等于6剂(6个月内未使用过)的ED男性被随机分为接受10周双盲、安慰剂对照(DBPC)的按需灵活剂量枸橼酸西地那非(50或100毫克)治疗,随后进行6周开放标签(OL)西地那非治疗。

主要观察指标

SEX-Q、IIEF、勃起质量问卷(QEQ)、自尊与关系(SEAR)问卷、勃起硬度评分(EHS)、成功性交尝试次数(SIA)、治疗满意度勃起功能障碍量表(EDITS)以及总体疗效问题(GEQ)。

结果

与安慰剂组(N = 105)相比,西地那非组(N = 104)在DBPC治疗结束时(EOT),在所有SEX-Q、IIEF(性欲领域除外)、QEQ和SEAR结果方面有显著更多改善(P < 0.05),SIA更频繁,EHS 3(硬度足以插入但未完全坚硬)或EHS 4(完全坚硬)勃起更频繁(优势比[OR]分别为2.52和3.46),EHS 4勃起频率为四倍(OR,6.41),更多男性对治疗满意(EDITS;OR,2.6),勃起改善的男性数量约为两倍(GEQ1;OR,5.8)以及有性交能力的男性数量约为两倍(GEQ2;OR,5.4),且GEQ3得分表明性生活更好(P < 0.0001)。SEX-Q得分改善与所有其他结果呈正相关。在OL EOT时,大多数结果为最大阳性结果的>60%(约一半为>或=80%)。

结论

对于接受西地那非治疗ED的男性,SEX-Q变化得分与其他几个性功能、情感及与满意度相关的结果相关,可对性体验进行简单且有针对性的评估。

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