影像方式检测后盆底障碍的妇女与排便障碍综合征。

Isabelle Ma van Gruting, Aleksandra Stankiewicz, Ranee Thakar, Giulio A Santoro, Joanna IntHout, Abdul H Sultan
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引用次数: 0

摘要

背景:排便障碍综合征(ODS)是指排便困难,需要用力排便,有排便不完全的感觉,或需要手动辅助排便。这是由于在排便过程中由于直肠膨出、肠膨出、肠套叠、斜视或盆底下降而导致的粪便流的物理阻塞。排液直肠造影(EP)是诊断后盆底疾病最常用的影像学技术。由于广泛的经验,它已被视为参考标准,尽管它已被证明没有完美的准确性。此外,EP是侵入性的,令人尴尬的,并且使用电离辐射。解决这些问题的替代成像技术已经开发出来,并对其准确性进行了评估。由于结果不同,导致缺乏共识,需要对文献进行系统回顾和荟萃分析。目的:在没有参考标准的情况下,通过潜在分类分析,确定EP、动态磁共振成像(MRI)和盆底超声检测ODS女性后盆底疾病的诊断试验准确性,并评估MRI或超声是否可以替代EP。次要目的是研究与直肠造影剂使用、排出期、患者体位和截止值相关的诊断测试准确性差异,这些差异可能会影响测试结果。检索方法:我们于2019年12月18日在Cochrane图书馆、MEDLINE、Embase、SCI、CINAHL和CPCI中进行了电子检索。参考书目,谷歌学者。我们还检索了WHO ICTRP和clinicaltrials.gov找到符合条件的文章。两位综述作者进行了标题和摘要筛选和全文评估,解决了与第三位综述作者的分歧。选择标准:诊断测试准确性和队列研究如果评估EP、MRI或盆底超声或两者检测ODS女性后盆底疾病的准确性,则符合入选条件。我们排除了病例对照研究。如果研究部分符合纳入标准,我们会联系作者以获取更多信息。数据收集和分析:两位综述作者进行了数据提取,包括研究特征、“偏倚风险”评估、异质性来源和测试准确性结果。我们排除了尽管所有努力都无法检索到测试准确性数据的研究。我们使用贝叶斯层次潜类分析进行meta分析。对于有资格作为EP替代试验的指标试验,敏感性和特异性应相似或高于历史参考标准(EP),对于分诊试验,特异性或敏感性应相似或更高。我们进行异质性分析,评估不同测试条件对测试准确性的影响。我们通过排除高偏倚风险、关注适用性或2010年之前发表的研究来进行敏感性分析。我们根据GRADE评估总体证据质量(QoE)。主要结果:39项研究共纳入2483名受试者。我们对每个目标条件下所有指标测试的敏感性和特异性进行了汇总估计。敏感性分析结果与主分析结果一致。EP诊断直肠膨出的敏感性为98%(可信区间(CrI)94% ~ 99%),肠膨出的敏感性为91%(CrI 83% ~ 97%),肠套叠的敏感性为89%(CrI 79% ~ 96%),盆底下降的敏感性为98%(CrI 93% ~ 100%);小肠膨出的特异性为96%(CrI 93% ~ 99%),肠套叠的特异性为92%(CrI 86% ~ 97%),斜视的特异性为97%(CrI 94% ~ 99%),均具有较高的QoE。中低QoE对斜视的敏感性为80%(CrI 63%-94%),对直肠前突的特异性为78%(CrI 63%-90%),盆底下降的特异性为83%(CrI 59%-96%)。MRI诊断直肠膨出的特异性为90% (CrI 79% ~ 97%),肠膨出的特异性为99% (CrI 96% ~ 100%),肠套叠的特异性为97% (CrI 88% ~ 100%),符合高质量oe的分诊检查标准。MRI不符合替代EP的标准。异质性分析显示,有排空期的MRI对直肠膨出(94%,CrI 87%-98%)和小肠膨出(87%,CrI 74%-95%对62%,CrI 51%-88%)的敏感性高于无排空期的MRI (94%, CrI 87%-98%),无排空期的MRI敏感性明显低于EP。经会阴超声(tpu)诊断直肠膨出的特异性为89% (CrI 81% ~ 96%),小肠膨出的特异性为98% (CrI 95% ~ 100%),肠套叠的特异性为96% (CrI 91% ~ 99%);对斜视的敏感度为92% (CrI为72%-98%),符合高质量评价(QoE)的分诊试验标准。TPUS不符合替代EP的标准。 异质性分析显示,直肠造影剂行tpu对直肠膨出(92%,CrI 69%-99%对81%,CrI 58%-95%)、肠膨出(90%,CrI 71%-99%对67%,CrI 51%-90%)和肠套叠(90%,CrI 69%-98%对61%,CrI 51%-86%)的敏感性不显著高于未行直肠造影剂的敏感性,且低于EP。阴道内超声(EVUS)诊断直肠膨出的特异性为76% (CrI 54% ~ 93%),小肠膨出的特异性为97% (CrI 80% ~ 99%),肠套叠的特异性为93% (CrI 72% ~ 99%);对斜视的敏感度为84% (CrI为59%-96%),符合极低至中等质量评价(QoE)的分诊试验标准。EVUS不符合取代EP的标准。动态肛门超声(DAE)诊断直肠膨出的特异性为88% (CrI 62%-99%),肠膨出的特异性为97% (CrI 75%-100%),肠套叠的特异性为93% (CrI 65%-99%),符合极低至中等QoE的分诊检查标准。DAE不符合替代EP的标准。超声造影(EDF)对肠套叠的敏感性为89% (CrI 65%-98%),特异性为92% (CrI 72%-99%),符合替代EP的标准,但QoE很低。EDF诊断直肠膨出的特异性为89% (CrI 60%-99%),诊断肠膨出的特异性为97% (CrI 87%-100%);对斜视的敏感性为87% (CrI为72%-96%),符合低至极低QoE的分诊试验标准。作者的结论是:在有ODS症状的女性人群中,没有一种影像学技术符合替代EP的标准。MRI和tpu符合分诊检查的标准,阳性检查可诊断为直肠膨出、肠膨出和肠套叠,阴性检查可排除斜视的诊断。疏散期增加了MRI的敏感性。直肠造影剂未增加tpu的敏感性。EVUS、DAE和EDF的QoE过低,无法得出结论。需要更多精心设计的研究来确定它们在ODS诊断途径中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Imaging modalities for the detection of posterior pelvic floor disorders in women with obstructed defaecation syndrome.

Imaging modalities for the detection of posterior pelvic floor disorders in women with obstructed defaecation syndrome.

Imaging modalities for the detection of posterior pelvic floor disorders in women with obstructed defaecation syndrome.

Background: Obstructed defaecation syndrome (ODS) is difficulty in evacuating stools, requiring straining efforts at defaecation, having the sensation of incomplete evacuation, or the need to manually assist defaecation. This is due to a physical blockage of the faecal stream during defaecation attempts, caused by rectocele, enterocele, intussusception, anismus or pelvic floor descent. Evacuation proctography (EP) is the most common imaging technique for diagnosis of posterior pelvic floor disorders. It has been regarded as the reference standard because of extensive experience, although it has been proven not to have perfect accuracy. Moreover, EP is invasive, embarrassing and uses ionising radiation. Alternative imaging techniques addressing these issues have been developed and assessed for their accuracy. Because of varying results, leading to a lack of consensus, a systematic review and meta-analysis of the literature are required.

Objectives: To determine the diagnostic test accuracy of EP, dynamic magnetic resonance imaging (MRI) and pelvic floor ultrasound for the detection of posterior pelvic floor disorders in women with ODS, using latent class analysis in the absence of a reference standard, and to assess whether MRI or ultrasound could replace EP. The secondary objective was to investigate differences in diagnostic test accuracy in relation to the use of rectal contrast, evacuation phase, patient position and cut-off values, which could influence test outcome.

Search methods: We ran an electronic search on 18 December 2019 in the Cochrane Library, MEDLINE, Embase, SCI, CINAHL and CPCI. Reference list, Google scholar. We also searched WHO ICTRP and clinicaltrials.gov for eligible articles. Two review authors conducted title and abstract screening and full-text assessment, resolving disagreements with a third review author.

Selection criteria: Diagnostic test accuracy and cohort studies were eligible for inclusion if they evaluated the test accuracy of EP, and MRI or pelvic floor ultrasound, or both, for the detection of posterior pelvic floor disorders in women with ODS. We excluded case-control studies. If studies partially met the inclusion criteria, we contacted the authors for additional information.

Data collection and analysis: Two review authors performed data extraction, including study characteristics, 'Risk-of-bias' assessment, sources of heterogeneity and test accuracy results. We excluded studies if test accuracy data could not be retrieved despite all efforts. We performed meta-analysis using Bayesian hierarchical latent class analysis. For the index test to qualify as a replacement test for EP, both sensitivity and specificity should be similar or higher than the historic reference standard (EP), and for a triage test either specificity or sensitivity should be similar or higher. We conducted heterogeneity analysis assessing the effect of different test conditions on test accuracy. We ran sensitivity analyses by excluding studies with high risk of bias, with concerns about applicability, or those published before 2010. We assessed the overall quality of evidence (QoE) according to GRADE.

Main results: Thirty-nine studies covering 2483 participants were included into the meta-analyses. We produced pooled estimates of sensitivity and specificity for all index tests for each target condition. Findings of the sensitivity analyses were consistent with the main analysis. Sensitivity of EP for diagnosis of rectocele was 98% (credible interval (CrI)94%-99%), enterocele 91%(CrI 83%-97%), intussusception 89%(CrI 79%-96%) and pelvic floor descent 98%(CrI 93%-100%); specificity for enterocele was 96%(CrI 93%-99%), intussusception 92%(CrI 86%-97%) and anismus 97%(CrI 94%-99%), all with high QoE. Moderate to low QoE showed a sensitivity for anismus of 80%(CrI 63%-94%), and specificity for rectocele of 78%(CrI 63%-90%) and pelvic floor descent 83%(CrI 59%-96%). Specificity of MRI for diagnosis of rectocele was 90% (CrI 79%-97%), enterocele 99% (CrI 96%-100%) and intussusception 97% (CrI 88%-100%), meeting the criteria for a triage test with high QoE. MRI did not meet the criteria to replace EP. Heterogeneity analysis showed that sensitivity of MRI performed with evacuation phase was higher than without for rectocele (94%, CrI 87%-98%) versus 65%, CrI 52% to 89%, and enterocele (87%, CrI 74%-95% versus 62%, CrI 51%-88%), and sensitivity of MRI without evacuation phase was significantly lower than EP. Specificity of transperineal ultrasound (TPUS) for diagnosis of rectocele was 89% (CrI 81%-96%), enterocele 98% (CrI 95%-100%) and intussusception 96% (CrI 91%-99%); sensitivity for anismus was 92% (CrI 72%-98%), meeting the criteria for a triage test with high QoE. TPUS did not meet the criteria to replace EP. Heterogeneity analysis showed that sensitivity of TPUS performed with rectal contrast was not significantly higher than without for rectocele(92%, CrI 69%-99% versus 81%, CrI 58%-95%), enterocele (90%, CrI 71%-99% versus 67%, CrI 51%-90%) and intussusception (90%, CrI 69%-98% versus 61%, CrI 51%-86%), and was lower than EP. Specificity of endovaginal ultrasound (EVUS) for diagnosis of rectocele was 76% (CrI 54%-93%), enterocele 97% (CrI 80%-99%) and intussusception 93% (CrI 72%-99%); sensitivity for anismus was 84% (CrI 59%-96%), meeting the criteria for a triage test with very low to moderate QoE. EVUS did not meet the criteria to replace EP. Specificity of dynamic anal endosonography (DAE) for diagnosis of rectocele was 88% (CrI 62%-99%), enterocele 97% (CrI 75%-100%) and intussusception 93% (CrI 65%-99%), meeting the criteria for a triage test with very low to moderate QoE. DAE did not meet the criteria to replace EP. Echodefaecography (EDF) had a sensitivity of 89% (CrI 65%-98%) and specificity of 92% (CrI 72%-99%) for intussusception, meeting the criteria to replace EP but with very low QoE. Specificity of EDF for diagnosis of rectocele was 89% (CrI 60%-99%) and for enterocele 97% (CrI 87%-100%); sensitivity for anismus was 87% (CrI 72%-96%), meeting the criteria for a triage test with low to very low QoE.

Authors' conclusions: In a population of women with symptoms of ODS, none of the imaging techniques met the criteria to replace EP. MRI and TPUS met the criteria of a triage test, as a positive test confirms diagnosis of rectocele, enterocele and intussusception, and a negative test rules out diagnosis of anismus. An evacuation phase increased sensitivity of MRI. Rectal contrast did not increase sensitivity of TPUS. QoE of EVUS, DAE and EDF was too low to draw conclusions. More well-designed studies are required to define their role in the diagnostic pathway of ODS.

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