Gourcerol G, Granier S, Bridoux V, Menard J F, Ducrotté P, Leroi A M
INSERM U1073, Service de Physiologie Digestive, CHU Rouen, INSERM CIC 0204 Rouen, Rouen, France.
INSERM U1073, Service de Chirurgie Digestive, CHU Rouen, Rouen, France.
Neurogastroenterol Motil. 2016 Mar;28(3):399-409. doi: 10.1111/nmo.12740. Epub 2015 Dec 15.
Anal manometry is the standard technique for evaluating anal sphincter function. However, the functional lumen imaging probe (EndoFLIP(®) ) can be used to measure sphincter distensibility during volume-controlled distensions. Our aims were (i) to assess anal distensibility in patients with fecal incontinence (FI) and in healthy subjects using the EndoFLIP(®) and (ii) to compare the results with anal pressures measured by 3D high-resolution manometry (3D-HRM) to determine whether the EndoFLIP(®) was more sensitive and specific for diagnosing FI than 3D-HRM.
EndoFLIP(®) and 3D-HRM assessments of 34 female FI patients and 40 healthy female subjects were performed. Anal distensibility was measured as the median cross-sectional area at the narrowest point divided by the corresponding intra-bag pressure at rest and during peak voluntary contraction and was expressed in mm(2) /mmHg.
A 40-mL anal distensibility index was selected for further comparisons as it provided the best discrimination between the FI patients and the healthy subjects. The index was significantly higher in the FI patients than in the healthy subjects at rest (p = 1.10(-4) ) and during voluntary contraction (p = 1.10(-4) ). The index at rest and during voluntary contraction appeared to be more appropriate than anal pressures for discriminating between FI patients and healthy subjects.
CONCLUSIONS & INFERENCES: The present study confirmed that FI is associated with an abnormally high distensibility index at rest and during voluntary contraction. The ability of the distensibility index to discriminate between FI patients and healthy subjects was significantly better than anal pressure.
肛管测压是评估肛门括约肌功能的标准技术。然而,功能性管腔成像探头(EndoFLIP®)可用于在容量控制扩张期间测量括约肌的扩张性。我们的目的是:(i)使用EndoFLIP®评估大便失禁(FI)患者和健康受试者的肛管扩张性;(ii)将结果与三维高分辨率测压法(3D-HRM)测量的肛管压力进行比较,以确定EndoFLIP®在诊断FI方面是否比3D-HRM更敏感、更具特异性。
对34名女性FI患者和40名健康女性受试者进行了EndoFLIP®和3D-HRM评估。肛管扩张性通过最窄点的中位横截面积除以静息时和最大自主收缩时相应的囊内压力来测量,单位为mm²/mmHg。
选择40 mL的肛管扩张性指数进行进一步比较,因为它能最好地区分FI患者和健康受试者。该指数在FI患者静息时(p = 1.10⁻⁴)和自主收缩时(p = 1.10⁻⁴)显著高于健康受试者。静息时和自主收缩时的该指数在区分FI患者和健康受试者方面似乎比肛管压力更合适。
本研究证实,FI与静息时和自主收缩时异常高的扩张性指数相关。扩张性指数区分FI患者和健康受试者的能力明显优于肛管压力。