Transperineal ultrasound versus digital palpation: Identifying key parameters for objective pelvic floor muscle contraction assessment.

IF 3.1 2区 医学 Q1 OBSTETRICS & GYNECOLOGY
Yun Lin, Honghong Pan, Yupeng Chen, Chenshan Dong, Yijia Luo
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引用次数: 0

Abstract

Introduction: The assessment of pelvic floor muscle function is crucial for managing pelvic floor dysfunctions, yet digital palpation is subjective and lacks reproducibility. This study aimed to correlate pelvic floor muscle contractility assessed by digital palpation with transperineal ultrasound measurements and evaluate the reliability of the Modified Oxford Scale and key ultrasound-derived parameters. By comparing these methods, the study sought to establish transperineal ultrasound as a reliable, objective, and non-invasive tool for assessing pelvic floor muscle contractility.

Material and methods: A cross-sectional study was conducted at Shengli Provincial Hospital from November 2019 to July 2024. 442 of 512 screened women were included. Digital palpation was performed by two independent clinicians, and ultrasound measurements were conducted by two separate raters. Ultrasound raters were blinded to palpation (Modified Oxford Scale) findings. Transperineal ultrasound quantified multiple pelvic floor parameters, including proximal urethral axis angle change (maximal contraction-rest) and levator hiatus area. Inter-rater reliability was assessed using intraclass correlation coefficients for ultrasound measures and Cohen's kappa for MOS ratings. Correlations between ultrasound and palpation scores were analyzed using Spearman's rank. Cut-off values for key ultrasound parameters corresponding to palpation grades were determined via receiver operating characteristic curve analysis.

Results: Significant correlations (p < 0.001) were found between ultrasound parameters and MOS scores, with the strongest correlations observed for proximal urethral axis angle change (maximal contraction-rest) (rs = 0.727) and proportional change in levator hiatus area (rs = 0.717). Ultrasound assessments showed high inter-rater reliability (intraclass correlation coefficient = 0.92 for proximal urethral axis angle change), while palpation demonstrated moderate agreement (Cohen's kappa = 0.55). Cut-off values for key parameters were derived, such as proximal urethral axis angle change <9.5° for absent contraction and >16.5° for strong contraction.

Conclusions: Transperineal ultrasound demonstrated high reliability and provided an objective, non-invasive method for assessing pelvic floor muscle contractility. While digital palpation assessed functional strength, ultrasound visualized structural displacement during contraction. The two methods addressed complementary aspects of pelvic floor function, and their combined use enhanced clinical assessment.

经会阴超声与数字触诊:确定客观盆底肌肉收缩评估的关键参数。
导读:骨盆底肌肉功能的评估是治疗盆底功能障碍的关键,但指诊是主观的,缺乏可重复性。本研究旨在将手指触诊评估的盆底肌肉收缩力与经会阴超声测量结果相关联,并评估改良牛津量表和超声衍生关键参数的可靠性。通过比较这些方法,本研究试图建立经会阴超声作为评估盆底肌肉收缩性的可靠、客观和非侵入性工具。材料与方法:横断面研究于2019年11月至2024年7月在胜利省立医院进行。512名接受筛查的妇女中有442人被纳入研究。数字触诊由两名独立的临床医生进行,超声测量由两名独立的评分者进行。超声评分者对触诊结果(改良牛津量表)不知情。经会阴超声量化盆底多项参数,包括尿道近端轴角变化(最大收缩-休止)和提上睑肌裂孔面积。采用超声测量的类内相关系数和MOS评分的Cohen’s kappa来评估等级间的信度。超声与触诊评分之间的相关性采用Spearman秩进行分析。通过受试者工作特征曲线分析确定与触诊分级对应的关键超声参数的截止值。结果:提肌裂孔面积呈显著相关(p = 0.727),比例变化(rs = 0.717)。超声评估显示高等级间的可靠性(尿道近端轴角度变化的等级内相关系数= 0.92),而触诊显示中等程度的一致性(Cohen’s kappa = 0.55)。得出关键参数的截止值,如尿道近端轴角改变16.5°为强收缩。结论:经会阴超声具有较高的可靠性,为评估盆底肌肉收缩性提供了客观、无创的方法。当数字触诊评估功能强度时,超声显示收缩期间的结构位移。这两种方法解决了盆底功能的互补方面,它们的联合使用增强了临床评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
180
审稿时长
3-6 weeks
期刊介绍: Published monthly, Acta Obstetricia et Gynecologica Scandinavica is an international journal dedicated to providing the very latest information on the results of both clinical, basic and translational research work related to all aspects of women’s health from around the globe. The journal regularly publishes commentaries, reviews, and original articles on a wide variety of topics including: gynecology, pregnancy, birth, female urology, gynecologic oncology, fertility and reproductive biology.
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