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经产妇中应用肛提肌缺陷评分的三维经阴道超声评估:一项复制研究。

Three-dimensional endovaginal ultrasound assessment using the levator ani deficiency score in primiparas: A replication study.

机构信息

Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Department of Women's Health, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Acta Obstet Gynecol Scand. 2023 Sep;102(9):1236-1242. doi: 10.1111/aogs.14633. Epub 2023 Jul 20.

Abstract

INTRODUCTION

It is essential to assess the levator ani properly as part of clinical care in patients presenting with pelvic floor dysfunction. The levator ani deficiency scoring system is a previously published method to assess levator ani defects with three-dimensional endovaginal ultrasound. The primary aim of this study was to determine the intra- and interrater reliability of the levator ani deficiency score in a cohort of non-instrumentally delivered primiparas.

MATERIAL AND METHODS

Primiparas (n = 141) were examined at least 1 year after vaginal birth. Three-dimensional endovaginal ultrasound volumes were acquired by a single examiner using two different automated ultrasound probes. The volumes were analyzed by two separate raters who were blinded to each other's assessments. Descriptive statistics were calculated for levator ani deficiency score and categorized into three levels (mild, moderate, severe). Kendall's tau-b was calculated for intra- and interrater comparisons.

RESULTS

Intrarater comparisons of levator ani deficiency score and levator ani deficiency category were high (Kendall's tau-b ≥0.80 for Rater 1; >0.79 for Rater 2). Interrater comparisons of levator ani deficiency score and levator ani deficiency category were also high (Kendall's tau-b >0.9 for assessment 1 and >0.78 for assessment 2). Varying by rater, probe and assessment, 75.9%-80.1% of the study population had no/mild deficiency, 6.4%-9.2% had moderate deficiency, and 4.3%-6.4% had severe levator ani deficiency.

CONCLUSIONS

The levator ani deficiency scoring system is a feasible method to assess defects of the levator ani muscle and can be reproduced with high intra- and interrater correlations. Using the scoring system in clinical practice may facilitate concordant assessment between different examiners. However, the system should be used to support clinical findings and symptomatology and not as a screening tool, as the score is lacking the category of no levator ani deficiency.

摘要

简介

在出现盆底功能障碍的患者的临床护理中,对肛提肌进行适当评估至关重要。肛提肌缺陷评分系统是一种先前发表的方法,用于通过三维经阴道超声评估肛提肌缺陷。本研究的主要目的是确定未经器械分娩的初产妇队列中肛提肌缺陷评分的内部和内部评分者之间的可靠性。

材料和方法

初产妇(n=141)在阴道分娩后至少 1 年进行检查。一位检查者使用两种不同的自动超声探头采集三维经阴道超声容积。两个独立的评估者对容积进行分析,彼此不知道对方的评估结果。计算肛提肌缺陷评分和分类为三个水平(轻度、中度、重度)的描述性统计数据。计算了 Kendall's tau-b 以进行内部和内部评分者比较。

结果

肛提肌缺陷评分和肛提肌缺陷类别的内部评分者比较高(评分者 1 的 Kendall's tau-b≥0.80;评分者 2 的 Kendall's tau-b>0.79)。肛提肌缺陷评分和肛提肌缺陷类别的内部评分者比较也很高(评估 1 的 Kendall's tau-b>0.9,评估 2 的 Kendall's tau-b>0.78)。根据评分者、探头和评估的不同,75.9%-80.1%的研究人群无/轻度缺陷,6.4%-9.2%中度缺陷,4.3%-6.4%严重肛提肌缺陷。

结论

肛提肌缺陷评分系统是一种评估肛提肌缺陷的可行方法,具有较高的内部和内部评分者相关性。在临床实践中使用评分系统可以促进不同检查者之间的一致评估。但是,该系统应用于支持临床发现和症状,而不作为筛查工具,因为该评分系统缺乏无肛提肌缺陷的类别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d5e/10407012/28a5f08cd7f5/AOGS-102-1236-g004.jpg

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