Postoperative maintenance levonorgestrel-releasing intrauterine system and endometrioma recurrence: a randomized controlled study - 27/09/17

, Teh-Fu Hsu, MD b, c, Ben-Shian Huang, MD a, c, d, Hsiao-Wen Tsai, MD c, d, f, Yen-Hou Chang, MD a, c, Peng-Hui Wang, MD, PhD a, c, d, gAbstract |
Background |
According to 3 randomized trials, the levonorgestrel-releasing intrauterine system significantly reduced recurrent endometriosis-related pelvic pain at postoperative year 1. Only a few studies have evaluated the long-term effectiveness of the device for preventing endometrioma recurrence, and the effects of a levonorgestrel-releasing intrauterine system as a maintenance therapy remain unclear.
Objective |
The objective of the study was to evaluate whether a maintenance levonorgestrel-releasing intrauterine system is effective for preventing postoperative endometrioma recurrence.
Study Design |
From May 2011 through March 2012, a randomized controlled trial including 80 patients with endometriomas undergoing laparoscopic cystectomy followed by six cycles of gonadotropin-releasing hormone agonist treatment was conducted. After surgery, the patients were randomized to groups that did or did not receive a levonorgestrel-releasing intrauterine system (intervention group, n = 40, vs control group, n = 40). The primary outcome was endometrioma recurrence 30 months after surgery. The secondary outcomes included dysmenorrhea, CA125 levels, noncyclic pelvic pain, and side effects.
Results |
Endometrioma recurrence at 30 months did not significantly differ between the 2 groups (the intervention group, 10 of 40, 25% vs the control group 15 of 40, 37.5%; hazard ratio, 0.60, 95% confidence interval, 0.27–1.33, P = .209). The intervention group exhibited a lower dysmenorrhea recurrence rate, with an estimated hazard ratio of 0.32 (95% confidence interval, 0.12–0.83, P = .019). Over a 30 month follow-up, the intervention group exhibited a greater reduction in dysmenorrhea as assessed with a visual analog scale score (mean ± SD, 60.8 ± 25.5 vs 38.7 ± 25.9, P < .001, 95% confidence interval, 10.7–33.5), noncyclic pelvic pain visual analog scale score (39.1 ± 10.9 vs 30.1 ± 14.7, P = .014, 95% confidence interval, 1.9–16.1), and CA125 (median [interquartile range], –32.1 [–59.1 to 14.9], vs –15.6 [–33.0 to 5.0], P = .001) compared with the control group. The number-needed-to-treat benefit for dysmenorrhea recurrence at 30 months was 5. The number of recurrent cases requiring further surgical or hormone treatment in the intervention group (1 of 40, 2.5%, 95% confidence interval, –2.3% to 7.3%) was significantly lower than that in the control group (8 of 40, 20%, 95% confidence interval, 7.6–32.4%; P = .031).
Conclusion |
Long-term maintenance therapy using a levonorgestrel-releasing intrauterine system is not effective for preventing endometrioma recurrence.
Le texte complet de cet article est disponible en PDF.Key words : endometrioma, levonorgestrel-releasing intrauterine system, maintenance therapy, postoperative, recurrence
Plan
| This work was supported in part by the Ministry of Science and Technology (NSC 100-2314-B-075-008, NSC 101-2314-B-075-028-MY3, MOST 104-2314-B-075-022, and MOST 104-2314-B-075-058, to Y.-J.C.), Taipei Veterans General Hospital (VGH-104C-042 and VGH-104-EA-0012, to Y.-J.C.), Yen-Tjing-Ling Medical Foundation (CI-104-15, to Y.-J.C.), and the Szu-Yuan Research Foundation of Internal Medicine. |
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| The authors report no conflict of interest. |
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| Cite this article as: Chen Y-J, Hsu T-F, Huang B-S, et al. Postoperative maintenance levonorgestrel-releasing intrauterine system and endometrioma recurrence: a randomized controlled study. Am J Obstet Gynecol 2017;216:582.e1-9. |
Vol 216 - N° 6
P. 582.e1-582.e9 - juin 2017 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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