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宫腔凝胶超声造影评估。

Gel infusion sonography in the evaluation of the uterine cavity.

机构信息

Department of Obstetrics and Gynecology, University Hospitals, KU Leuven, Leuven, Belgium.

出版信息

Ultrasound Obstet Gynecol. 2009 Dec;34(6):711-4. doi: 10.1002/uog.7463.

Abstract

OBJECTIVES

To compare gel infusion sonohysterography (GIS) with saline contrast sonohysterography (SCSH) with regard to technical feasibility and procedure-related pain experienced by patients.

METHODS

This prospective observational cohort study included 551 consecutive patients with abnormal bleeding: SCSH was attempted in the first 402 women and GIS was attempted in the following 149. All procedures were performed by the same examiner, in the same clinical setting, using a 2-mm diameter catheter. After contrast sonohysterography, most patients underwent office hysteroscopy (n = 502) and endometrial sampling (n = 323). The women were asked to rate the pain experienced during each procedure using a 100-mm visual analog scale (VAS). Patients' characteristics, ultrasound findings, histological diagnosis, technical failures and procedure-related pain were compared between the two procedures.

RESULTS

The mean +/- SD VAS score for contrast sonography, subsequent hysteroscopy and endometrial biopsy were 22.9 +/- 21.7, 38.8 +/- 26.6 and 50.0 +/- 26.3, respectively, in the SCSH subgroup vs. 16.5 +/- 21.5, 27.6 +/- 28 and 33.6 +/- 30.3, respectively, in the GIS subgroup (P = 0.0051, P = 0.0005 and P = 0.0003, respectively). The technical failure rate was 5% in the SCSH subgroup vs. 2% in the GIS subgroup (P = 0.1522).

CONCLUSIONS

GIS and SCSH showed similar technical feasibility. The procedure-related pain reported by patients during contrast sonohysterography, as well as during subsequent hysteroscopy and endometrial sampling, was less in the GIS group.

摘要

目的

比较凝胶灌注超声造影(GIS)与生理盐水宫腔对比超声造影(SCSH)在技术可行性和患者术中相关疼痛方面的差异。

方法

本前瞻性观察性队列研究纳入了 551 例异常子宫出血患者:前 402 例患者行 SCSH,后 149 例患者行 GIS。所有检查均由同一位检查者,在相同的临床环境下,使用 2mm 直径的导管进行。对比超声造影后,大多数患者行门诊宫腔镜检查(n=502)和子宫内膜活检(n=323)。患者被要求使用 100mm 视觉模拟评分(VAS)评估每种检查的疼痛程度。比较两种检查的患者特征、超声发现、组织学诊断、技术失败和术中相关疼痛。

结果

SCSH 组的造影超声、随后的宫腔镜检查和子宫内膜活检的平均 VAS 评分分别为 22.9±21.7、38.8±26.6 和 50.0±26.3,GIS 组分别为 16.5±21.5、27.6±28 和 33.6±30.3(P=0.0051,P=0.0005 和 P=0.0003)。SCSH 组的技术失败率为 5%,GIS 组为 2%(P=0.1522)。

结论

GIS 和 SCSH 具有相似的技术可行性。与 SCSH 组相比,GIS 组患者在进行对比超声造影、随后的宫腔镜检查和子宫内膜活检时,报告的术中相关疼痛较轻。

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