Is hysterosalpingography a good tool to confirm the patency of tubes?
Fa‐Kung Lee, Wen-Ling Lee, Peng‐Hui Wang
- Year
- 2016
- Citations
- 11
Abstract
Hysterosalpingography (HSG) plays a crucial role in determining the anatomic causes of female subfertility and/or infertility, especially for uterine structure and tubal status abnormalities.1 These structural abnormalities include septum or tumor of the intrauterine cavity, adhesion or filling defect of the intrauterine cavity, and hydrosalpinx, tubal adhesion, or tubal occlusion, which may be detected by HSG examination. However, reliability of HSG is always questionable, especially for the diagnosis of tubal occlusion. Spasms of the lower genital tracts might be one of the single most factors contributing to pseudo-obstruction of tubes during HSG examination. In fact, HSG is still considered to be a relatively uncomfortable and an even painful procedure, which might be bothersome to women during examination.2,3 However, tubal occlusion, when the diagnosis is made, may result in different therapeutic choices for the affected couples. In theory, it is impossible to use less invasive and more economically assisted reproductive techniques, such as an intrauterine insemination,4 to facilitate these infertile couples with tubal occlusion. By contrast, a true tubal occlusion should be treated with recanalization either through an advanced technological method such as robotic surgery or microscopic surgery,5 and directly by in vitro fertilization and/or embryo transplantation,6 which is not required for tubal spasm. Therefore, an accurate determination of the potential causes of female infertility is required to facilitate effective treatment and avoid pitfalls related to inappropriate or delayed therapy. Subsequent confirmation of tubal problems is especially critical when assisted reproductive techniques are planned. Laparoscopy might be the optimum and thus the "gold standard" procedure for this purpose.7 Therefore, it is not surprising that Kahyaoglu and colleagues8 used diagnostic laparoscopy as a reference to evaluate the reliability and accuracy of HSG in infertile women in their study published in this issue of the Journal of the Chinese Medical Association. The study by Kahyaoglu and colleagues8 examined 89 infertile women who had received HSG and diagnostic laparoscopy procedures simultaneously, and found that women with diagnostic laparoscopy-confirmed tubal patency might have shorter time-period intervals between the first HSG and distal tubal filling than those with tubal occlusion (8.4 seconds vs. 12.0 seconds, p=0.057). Based on the absence of statistical significance, the authors concluded that it remained uncertain as to the value necessary to detect the clinically reliable objective time-period interval for finalizing the HSG procedure and proceeding with diagnostic laparoscopy.8 This study is interesting and worthy of further discussion. It is necessary to exclude the potential pitfalls during the HSG examination, including tubal spasm, mucus plugging, infection, prior surgery, and granulomatous salpingitis.9 Adequate pain control, delayed radiography, the use of a spasmolytic agent, three-dimensional hysterosalpingo-contrast-sonography (3-D sono-HSG) or hysterosalpingosonography (sono-HSG), and repeated HSG examination might be performed to help differentiate tubal spasm from true tubal occlusion in infertile women with suspicious structure abnormalities.9–12 In addition, the use of sono-HSG should be reconsidered in place of conventional HSG as the tool of choice to diagnose structural abnormalities in infertile women, based on the following advantages of sono-HSG over HSG: obviating ionizing radiation, the risk of iodine allergy, and sono-HSG's greater sensitivity and specificity in detecting abnormalities of the uterine cavity and permitting concomitant visualization of the ovaries and myometrium.11 A recent systematic review with meta-analysis showed that 3-D sono-HSG has pooled estimated sensitivity of 98% [95% confidence interval (CI): 91–100), pooled estimated specificity of 90% (95% CI: 83–95), positive
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