Tu Frank F, Fitzgerald Colleen M, Kuiken Todd, Farrell Todd, Norman Harden Robert
Department of Obstetrics and Gynecology Feinberg School of Medicine and Evanston Northwestern Healthcare, Evanston, IL 60201, USA.
Clin J Pain. 2008 Jan;24(1):45-50. doi: 10.1097/AJP.0b013e318156db13.
Pelvic muscle pain syndromes are poorly understood and lack reliable diagnostic criteria. Furthermore, animal models suggest that somatic pain can influence the development of pelvic visceral pain dysfunction. To develop psychophysical measures to facilitate diagnosis of pelvic floor myofascial pain syndromes, this pilot was designed to preliminarily test the feasibility, reliability, and validity of pressure-pain thresholds (PPTs) to identify and quantify pelvic floor pain sensitivity.
We conducted a cross-sectional study of pelvic floor PPTs using 19 healthy women. Using a prototype vaginal pressure algometer, we measured PPTs and calculated intraclass correlations for short-term and intermediate-term reliability. Validity was assessed by correlating numerical rating scores for pain (0 to 100) at standard pressure levels applied to the right iliococcygeus muscle.
The mean PPT of all pelvic floor sites was 1.52 kg/cm (SD=0.62), whereas thresholds of nonmuscle vaginal sites (anterior and posterior wall) were 1.65 kg/cm (SD=0.64). Pain numerical rating scores were positively correlated with stimulus intensity at the right iliococcygeus (Pearson r=0.61). Intraclass correlation demonstrated good short-term reliability at this same site for the first versus second, and second versus third measurements (0.75, 0.64); 1-week repeat reliability was also good for the right pubococcygeus, iliococcygeus, and obturator (0.69, 0.84, and 0.61, respectively), and both nonmuscle vaginal sites.
These data suggest that PPTs may prove to be valid and reliable measures of pelvic floor somatic pain sensitivity in healthy women. Broader studies including a pelvic pain cohort should be conducted to corroborate these results and determine the technique's external validity and clinical relevance.
盆腔肌肉疼痛综合征的病因尚不明确,且缺乏可靠的诊断标准。此外,动物模型表明,躯体疼痛会影响盆腔内脏疼痛功能障碍的发展。为了开发心理物理学测量方法以促进盆底肌筋膜疼痛综合征的诊断,本试验旨在初步测试压力痛阈(PPT)识别和量化盆底疼痛敏感性的可行性、可靠性和有效性。
我们对19名健康女性进行了盆底PPT的横断面研究。使用原型阴道压力痛觉计,我们测量了PPT,并计算了短期和中期可靠性的组内相关性。通过将应用于右髂尾肌的标准压力水平下的疼痛数字评分(0至100)进行相关性分析来评估有效性。
所有盆底部位的平均PPT为1.52kg/cm(标准差=0.62),而非肌肉阴道部位(前壁和后壁)的阈值为1.65kg/cm(标准差=0.64)。右髂尾肌的疼痛数字评分与刺激强度呈正相关(Pearson r=0.61)。组内相关性表明,在同一部位,第一次与第二次测量以及第二次与第三次测量的短期可靠性良好(分别为0.75、0.64);1周重复测量的可靠性在右耻骨尾骨肌、髂尾肌和闭孔肌(分别为0.69、0.84和0.61)以及两个非肌肉阴道部位也良好。
这些数据表明,PPT可能是健康女性盆底躯体疼痛敏感性的有效且可靠的测量指标。应开展包括盆腔疼痛队列在内的更广泛研究,以证实这些结果,并确定该技术的外部有效性和临床相关性。