4.4 Article

Long-term outcomes of pelvic organ prolapse repair using a mesh-capturing device when comparing single- versus multicenter use

期刊

ARCHIVES OF GYNECOLOGY AND OBSTETRICS
卷 303, 期 1, 页码 135-142

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00404-020-05764-3

关键词

Pelvic organ prolapse; Transvaginal mesh; Surgical volume; Safety; Effectiveness

资金

  1. Karolinska Institute
  2. Johnson Johnson
  3. Astellas
  4. Boston Scientific
  5. Finnish Medical Foundation
  6. Swedish Research Council

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The study found that for pelvic organ prolapse repair using a mesh-capturing device, the outcomes were better in a single-center approach compared to a multicenter trial. Recurrence rates and complications were higher in the multicenter study, indicating the benefits of centralizing the use of standardized procedures for this type of surgery.
Purpose The aim of this study was to compare long-term effects of high-volume surgery at a single-center to multicenter use when using a mesh-capturing device for pelvic organ prolapse (POP) repair. Methods Five years after surgery 101 (88%) at the single center were compared with 164 (81.2%) in the multicenter trial. Outcome measurements included clinical examination, prolapse-specific symptom questionnaires [Pelvic Floor Distress Inventory 20 (PFDI-20), Pelvic Floor Impact Questionnaire-short form (PFIQ-7), Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12)] and pain estimation by VAS (0-10). Results Optimal apical segment outcome was 95% in the single- compared to 83.3% in the multicenter study (p < 0.001). POP recurrence in the anterior and posterior walls (POP-Q, Ba and Bp >= 0) was more common at the multicenter as compared to the single center [(19.8% vs 5.4%) and (26% vs 2.7%), (p < 0.001)]. Reoperations for POP and mesh-related complications were more frequent in the multicenter study [31/202 (15.3%) vs 7/116 (6.1%),p < 0.001]. Total PFDI-20, PFIQ-7 and PISQ-12 scores were comparable between the cohorts. There were no significant differences in overall pain scores in-between the cohorts during follow-up. At the single center, 1/81 patients (1.2%) had VAS 7/10, i.e. severe pain, as compared to 3/131 (2.3%) in the multicenter study (p = 0.277). Conclusions Despite the high objective and subjective long-term effectiveness of the procedure in both regular use, and at a high-volume center, centralizing the use of a standardized capturing-device guided transvaginal mesh for POP repair reduced secondary interventions by more than half.

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