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Comparative Study
. 2018 Jan;29(1):99-107.
doi: 10.1007/s00192-017-3372-x. Epub 2017 Jun 9.

Primary treatment of pelvic organ prolapse: pessary use versus prolapse surgery

Affiliations
Comparative Study

Primary treatment of pelvic organ prolapse: pessary use versus prolapse surgery

Anne-Lotte W M Coolen et al. Int Urogynecol J. 2018 Jan.

Abstract

Introduction and hypothesis: The objective of this study was to compare the functional outcomes after pessary treatment and after prolapse surgery as primary treatments for pelvic organ prolapse (POP).

Methods: This was a prospective cohort study performed in a Dutch teaching hospital in women with symptomatic POP of stage II or higher requiring treatment. Patients were treated according to their preference with a pessary or prolapse surgery. The primary endpoint was disease-specific quality of life at 12 months follow-up according to the prolapse domain of the Urogenital Distress Inventory (UDI) questionnaire. Secondary outcomes included adverse events and additional interventions. To show a difference of ten points in the primary outcome, we needed to randomize 80 women (power 80%, α 0.05, taking 10% attrition into account).

Results: We included 113 women (74 in the pessary group, 39 in the surgery group). After 12 months, the median prolapse domain score was 0 (10th to 90th percentile 0-33) in the pessary group and 0 (10th to 90th percentile 0-0) in the surgery group (p < 0.01). Differences in other domain scores were not statistically significant. In the pessary group, 28% (21/74) of the women had a surgical intervention versus 3% (1/39) reoperations in the surgery group (p = 0.01).

Conclusions: In women with POP of stage II or higher undergoing surgery, prolapse symptoms were less severe than in those who were treated with a pessary, but 72% of women who were treated with a pessary did not opt for surgery.

Trial registration number: Dutch trial register NTR2856.

Keywords: Pelvic organ prolapse; Pessary; Prolapse surgery.

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Conflict of interest statement

Conflicts of interest

None.

Ethical approval

The study was approved by the ethics committee of the Máxima Medical Centre.

Trial registration number: Dutch trial register NTR2856.

Figures

Fig. 1
Fig. 1
Patient flow chart

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