Endrikat Jan, Shapiro Heather, Lukkari-Lax Eeva, Kunz Michael, Schmidt Werner, Fortier Michel
Bayer Inc., Toronto ON; Universitätskliniken des Saarlandes, Frauenklinik, Germany.
University of Toronto, Mount Sinai Hospital, Toronto ON.
J Obstet Gynaecol Can. 2009 Apr;31(4):340-347. doi: 10.1016/S1701-2163(16)34151-2.
To evaluate the efficacy of a levonorgestrel-releasing intrauterine system (LNG-IUS) compared with a combined oral contraceptive containing 1 mg norethindrone acetate and 20 mg ethinyl estradiol (OC1/20) in reducing menstrual blood loss (MBL) in women with idiopathic menorrhagia.
A prospective, randomized, open-label study was conducted in nine centres in Canada. Healthy women over 30 years of age suffering from idiopathic menorrhagia were treated either with LNG-IUS (n = 20) or with OC1/20 (n = 19) over 12 months. The primary endpoint was the change in MBL from baseline to 12 months. Secondary endpoints included treatment success (defined as a MBL score < 100 after 12 months), hemoglobin levels, and the menorrhagia severity score.
In both treatment groups, MBL decreased significantly from baseline to 12 months (P < 0.001). For the primary endpoint, the MBL score decreased significantly more in the LNG-IUS group (median from 228 to 13, mean percent change-83%) compared to the OC1/20 group (median from 290 to 72; mean percent change-68%) (P = 0.002) after 12 months. In the LNG-IUS group, 80% of subjects had treatment success compared with 36.8 % in the OC1/20 group (P < 0.009). Both treatments increased hemoglobin concentrations significantly between baseline and 12 months. The menorrhagia severity score was consistently lower in the LNG-IUS group at all study time points and was significantly lower (P = 0.045) at six months. Both treatments were well tolerated.
Both the LNG-IUS and the combined oral contraceptive effectively decreased menstrual blood loss in women with idiopathic menorrhagia. The overall clinical benefit was more pronounced with LNG-IUS than with OC1/20.
评估左炔诺孕酮宫内节育系统(LNG-IUS)与含1mg醋酸炔诺酮和20mg炔雌醇的复方口服避孕药(OC1/20)相比,在减少特发性月经过多女性月经量方面的疗效。
在加拿大的九个中心进行了一项前瞻性、随机、开放标签研究。30岁以上患有特发性月经过多的健康女性接受LNG-IUS(n = 20)或OC1/20(n = 19)治疗12个月。主要终点是从基线到12个月月经量的变化。次要终点包括治疗成功(定义为12个月后月经量评分<100)、血红蛋白水平和月经过多严重程度评分。
在两个治疗组中,从基线到12个月月经量均显著减少(P < 0.001)。对于主要终点,12个月后,LNG-IUS组的月经量评分显著低于OC1/20组(中位数从228降至13,平均变化百分比 - 83%)(中位数从290降至72;平均变化百分比 - 68%)(P = 0.002)。在LNG-IUS组中,80%的受试者治疗成功,而OC1/20组为36.8%(P < 0.009)。两种治疗在基线和12个月之间均显著提高了血红蛋白浓度。在所有研究时间点,LNG-IUS组的月经过多严重程度评分始终较低,在6个月时显著更低(P = 0.045)。两种治疗耐受性均良好。
LNG-IUS和复方口服避孕药均有效减少特发性月经过多女性的月经量。LNG-IUS的总体临床益处比OC1/20更显著。