Cutoff Score of the Sexual Interest and Desire Inventory-Female for Diagnosis of Hypoactive Sexual Desire Disorder

被引:22
|
作者
Clayton, Anita H. [1 ]
Segraves, Robert T. [2 ]
Bakish, David [3 ]
Goldmeier, David [4 ]
Tignol, Jean [5 ]
van Lunsen, Rik H. W. [6 ]
Nappi, Rossella E. [7 ]
Wunderlich, Glen [8 ]
Kimura, Toshio [9 ]
Lewis-D'Agostino, Diane J. [9 ]
Pyke, Robert [9 ]
机构
[1] Univ Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA 22903 USA
[2] Case Western Reserve Univ, Sch Med, Cleveland, OH USA
[3] Ottawa Psychopharmacol Clin, Ottawa, ON, Canada
[4] St Marys Hosp, Jane Wadsworth Sexual Funct Clin, London, England
[5] Victor Segalen Univ, Sch Med, Bordeaux, France
[6] Univ Amsterdam, Acad Med Ctr, Dept Sexol & Psychosomat Ob Gyn, Div Obstet & Gynaecol, NL-1012 WX Amsterdam, Netherlands
[7] Univ Pavia, Res Ctr Reprod Med, IRCCS Maugeri Fdn, I-27100 Pavia, Italy
[8] Boehringer Ingelheim Canada Ltd, Burlington, ON, Canada
[9] Boehringer Ingelheim Pharmaceut Inc, Ridgefield, CT USA
关键词
INDEX FSFI; WOMEN; VALIDATION; INSTRUMENT;
D O I
10.1089/jwh.2010.1995
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: To determine the most appropriate cutoff value for the Sexual Interest and Desire Inventory-Female (SIDI-F) score to discriminate between women with hypoactive sexual desire disorder (HSDD) and those with no female sexual dysfunction (FSD). The SIDI-F is a clinician-rated instrument consisting of 13 items designed to assess HSDD severity in women. The total score ranges from 0 to 51, with higher scores indicating better sexual function. Methods: Data from patients enrolled in a North American nontreatment study and a European nontreatment study were analyzed. Both studies were 4-week, prospective, multicenter trials designed to assess the reliability and validity of the SIDI-F. Only patients with HSDD or no FSD were included in this analysis. Receiver operating characteristics (ROC) analysis was used to determine the ability of the SIDI-F to differentiate between patients with HSDD and those with no FSD at baseline. Results: A total of 428 women were included in this analysis: 174 from North America (HSDD 113, no FSD 61) and 254 from Europe (HSDD 130, no FSD 124). In the North American study, a SIDI-F cutoff score of 33 minimized the difference between sensitivity (94.7%) and specificity (93.4%). In the European study, SIDI-F cutoff scores of both 33 and 34 minimized the difference between sensitivity (95.2%) and specificity (94.4%). Conclusions: In appropriately screened women, a SIDI-F score of <= 33 indicates the presence of HSDD.
引用
收藏
页码:2191 / 2195
页数:5
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