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延长口服避孕药方案期间突破性出血发生情况及处理的前瞻性分析

Prospective analysis of occurrence and management of breakthrough bleeding during an extended oral contraceptive regimen.

作者信息

Sulak Patricia J, Kuehl Thomas J, Coffee Andrea, Willis Sherilyn

机构信息

Department of Obstetrics and Gynecology, Scott & White Memorial Hospital, Texas A & M University System Health Science Center College of Medicine, Temple, TX 76508, USA.

出版信息

Am J Obstet Gynecol. 2006 Oct;195(4):935-41. doi: 10.1016/j.ajog.2006.02.048. Epub 2006 May 2.

DOI:10.1016/j.ajog.2006.02.048
PMID:16647684
Abstract

OBJECTIVE

The purpose of this study was to assess the bleeding patterns of an extended oral contraceptive (OC) regimen and management of breakthrough bleeding/breakthrough spotting (BTB/BTS).

STUDY DESIGN

This was a single-center prospective analysis of self-rated menstrual flow during a 21/7-day versus a 168-day extended regimen of on OC containing 3 mg of drosperinone and 30 mcg of ethinyl estradiol (DRSP/EE) with institution of a randomized protocol to manage BTB/BTS.

RESULTS

Of the 111 patients initiating the extended OC regimen, 102 (92%) completed the 168-day regimen. Subjects having a heavier daily flow rating during the 21/7-day pre-extension cycle had greater daily flow ratings (P < .001) and tended to have earlier occurrence of BTB during the extended regimen (P = .07) than subjects with lighter daily flow ratings. If BTB/BTS of at least 7 consecutive days occurred, patients were randomized to taking a 3-day hormone free interval (HFI) versus continuing active pills. Instituting a 3-day HFI was significantly more effective in resolving BTB/BTS than continuing active pills (P < .0001). Patients with heavier daily flow ratings during the 21/7-day cycle were not more likely to be randomized for BTB/BTS than those with lighter flow ratings (P = .53).

CONCLUSION

A 168-day extended regimen of DRSP/EE had an acceptable bleeding profile with a high continuation rate. Bleeding during the extended cycle was effectively managed with institution of a 3-day HFI.

摘要

目的

本研究旨在评估延长口服避孕药(OC)方案的出血模式以及突破性出血/突破性点滴出血(BTB/BTS)的管理。

研究设计

这是一项单中心前瞻性分析,对含3毫克屈螺酮和30微克炔雌醇(DRSP/EE)的OC在21/7天与168天延长方案期间的自评月经流量进行分析,并采用随机方案管理BTB/BTS。

结果

在开始延长OC方案的111例患者中,102例(92%)完成了168天方案。在21/7天延长前周期中每日经量评分较高的受试者,与每日经量评分较低的受试者相比,在延长方案期间每日经量评分更高(P <.001),且BTB出现时间往往更早(P =.07)。如果连续至少7天出现BTB/BTS,患者被随机分为接受3天无激素间隔期(HFI)或继续服用活性药丸。采用3天HFI在解决BTB/BTS方面比继续服用活性药丸显著更有效(P <.0001)。在21/7天周期中每日经量评分较高的患者与经量评分较低的患者相比,因BTB/BTS被随机分组的可能性并无差异(P =.53)。

结论

DRSP/EE的168天延长方案具有可接受的出血特征且持续率高。通过采用3天HFI有效管理了延长周期中的出血情况。

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