Shrader Sarah P, Dickerson Lori M
Department of Clinical Pharmacy and Outcome Sciences, South Carolina College of Pharmacy, Medical University of South Carolina, 295 Calhoun Street, Charleston, SC 29425, USA.
Pharmacotherapy. 2008 Aug;28(8):1033-40. doi: 10.1592/phco.28.8.1033.
Five new oral contraceptives, classified as extended- or continuous-cycle oral contraceptives, have been approved by the United States Food and Drug Administration. These agents have various combinations of estrogen and progestin, and different effects on the length of women's menstrual cycles. Usually they shorten the duration of menses, decrease the frequency of menses to 4 times/year, or completely eliminate menses. These new oral contraceptives are given in the following regimens: 24 days followed by placebo for 4 days (24/4), 84 days followed by placebo for 7 days (84/7), or continuously (without placebo). These agents contain ethinyl estradiol 20 microg-drospirenone 3 mg (24/4); ethinyl estradiol 20 microg-norethindrone 1 mg (24/4); ethinyl estradiol 30 microg-levonorgestrel 150 microg (84/7); ethinyl estradiol 30 microg-levonorgestrel 150 microg (84/7) with very low-dose ethinyl estradiol (10 microg/day) for 7 days; and ethinyl estradiol 20 microg-levonorgestrel 90 microg continuously. Clinical trials have demonstrated that extended- and continuous-cycle oral contraceptives are as effective in preventing pregnancy as traditional oral contraceptives. These new agents also have similar adverse effects; however, the only significantly different adverse effect compared with traditional oral contraceptives in clinical trials was change in bleeding pattern. These oral contraceptives are associated with more breakthrough bleeding and spotting than the traditional pills. Long-term effects on efficacy and safety are not known, as these new products generally have been used for only 1-2 years. Extended- and continuous-cycle oral contraceptives are a new option for women desiring decreased menses or for whom decreased menses may alleviate symptoms of coexisting medical conditions.
美国食品药品监督管理局已批准了五种新型口服避孕药,它们被归类为延长周期或连续周期口服避孕药。这些药物含有不同组合的雌激素和孕激素,对女性月经周期的长度有不同影响。通常它们会缩短经期时长,将月经频率降低至每年4次,或完全停经。这些新型口服避孕药的给药方案如下:服用24天药物后接着服用4天安慰剂(24/4方案);服用84天药物后接着服用7天安慰剂(84/7方案);或持续服药(无安慰剂)。这些药物包括:炔雌醇20微克 - 屈螺酮3毫克(24/4方案);炔雌醇20微克 - 炔诺酮1毫克(24/4方案);炔雌醇30微克 - 左炔诺孕酮150微克(84/7方案);炔雌醇30微克 - 左炔诺孕酮150微克(84/7方案),并在最后7天加用极低剂量的炔雌醇(10微克/天);以及炔雌醇20微克 - 左炔诺孕酮90微克持续服药方案。临床试验表明,延长周期和连续周期口服避孕药在预防妊娠方面与传统口服避孕药同样有效。这些新型药物也有类似的不良反应;然而,在临床试验中,与传统口服避孕药相比,唯一显著不同的不良反应是出血模式的改变。与传统避孕药相比,这些口服避孕药更容易出现突破性出血和点滴出血。由于这些新产品普遍仅使用了1 - 2年,其对疗效和安全性的长期影响尚不清楚。延长周期和连续周期口服避孕药为希望减少月经或月经减少可缓解并存疾病症状的女性提供了新的选择。