Department of Obstetrics & Gynecology (623), Radboud University Medical Center, P.O. Box 9101, 6500, HB, Nijmegen, the Netherlands.
Department of Obstetrics & Gynaecology, Reinier de Graaf Gasthuis, P.O. Box 5011, 2600, GA, Delft, the Netherlands.
Int Urogynecol J. 2023 Jul;34(7):1645-1651. doi: 10.1007/s00192-022-05442-9. Epub 2023 Jan 20.
The present study describes an extended follow-up study after 12 years and focusses on subjective outcomes of women who underwent surgery for recurrent pelvic organ prolapse in the randomized index study.
One hundred and ninety-four (194) women had been randomized in the original study and in the present study, 45 (47%) in the vaginal mesh repair versus 43 (43%) women with conventional vaginal native tissue repair completed the long-term questionnaires. The mesh used was a first-generation non-absorbable mesh kit. All types of conventional vaginal native tissue repairs were allowed, and additional vaginal native tissue repairs were allowed in the mesh group. The questionnaires as applied at baseline were used. The Patient Global Impression of Improvement questionnaire (PGI-I) was the primary outcome.
At 12 years, 30 (71%) women in the mesh group versus 23 (59%) women in the native tissue repair group reported to be PGI-I (very) much improved (p=0.24). There were no differences found in any of the questionnaire domains. There was, however, a higher number of women who had had additional operations for recurrent pelvic organ prolapse, stress urinary incontinence, and/or exposure in the mesh group: 18 women (40%) in the mesh group versus 8 women (19%) in the native tissue repair group (p=0.03).
There was no difference in subjective outcome between the groups, but there was a statistically significant higher number of women who had needed further operations. This study confirms that vaginal mesh should not be used in all women with recurrent pelvic organ prolapse.
本研究在 12 年后进行了扩展随访,重点关注接受复发性盆腔器官脱垂手术的女性的主观结果,这些女性在原始索引研究中接受了随机分组。
194 名女性在原始研究中接受了随机分组,在本研究中,45 名(47%)接受阴道网片修复的女性和 43 名(43%)接受常规阴道固有组织修复的女性完成了长期问卷调查。使用的网片是第一代不可吸收网片套件。允许进行所有类型的常规阴道固有组织修复,并且允许在网片组中进行额外的阴道固有组织修复。应用于基线的问卷包括在内。患者整体改善印象问卷(PGI-I)是主要结局。
在 12 年时,网片组中有 30 名(71%)女性报告 PGI-I(非常)明显改善,而固有组织修复组中有 23 名(59%)女性报告改善(p=0.24)。在任何问卷领域都没有发现差异。然而,网片组中有更多的女性需要进行额外的手术治疗复发性盆腔器官脱垂、压力性尿失禁和/或暴露:网片组中有 18 名(40%)女性,固有组织修复组中有 8 名(19%)女性(p=0.03)。
两组之间的主观结局没有差异,但需要进一步手术的女性数量统计学上显著更高。这项研究证实,阴道网片不应在所有复发性盆腔器官脱垂的女性中使用。