Hines Genesis, Wang Carrie, Walker Treasure, Jereen Amyeo, Quinones Joanne N, Waxman Andrea
Obstetrics and Gynecology, Lehigh Valley Health Network, Allentown, USA.
Obstetrics and Gynecology/University of South Florida Morsani College of Medicine, Lehigh Valley Health Network, Allentown, USA.
Cureus. 2023 Mar 14;15(3):e36117. doi: 10.7759/cureus.36117. eCollection 2023 Mar.
The etonogestrel implant is generally considered an effective, three-year, long-acting reversible contraceptive device. Previous research, such as the landmark CHOICE study, has reported a one-year continuation rate of 72% to 84%, however, in a real-world setting these rates may be significantly lower.
To study etonogestrel implant continuation rates and factors associated with early discontinuation in a specific clinical setting.
Single-center, retrospective cohort study of patients who received the etonogestrel implant between January 1, 2015, and December 31, 2017, at several practices at an academic community hospital network. Records were reviewed up to three years after implant insertion to determine continuation rates (one to three years), early discontinuation rates (≤12 months), and reasons for early discontinuation. A sample size calculation was performed to guide a subanalysis of side effects.
A total of 774 patients underwent etonogestrel insertion during the study period. The one-year continuation rate was lower than that of the CHOICE study (62% vs. 83%, P <0.001). A subanalysis (n=216) revealed that a majority (82%, n=177) of patients reported side effects. Side effects were more common in patients with early discontinuation compared with patients who continued use longer than one year (93% vs. 71%, P <0.001). The most common side effect, abnormal uterine bleeding, was not significantly associated with early discontinuation. A significant association (P=0.02) was found between early discontinuation and neurologic/psychiatric complaints.
The one-year continuation rate of the etonogestrel implant in our population is significantly lower than the value reported by CHOICE. Implant side effects are common and significantly affect rates of discontinuation. Our data suggest there is an opportunity for education and counseling for individuals opting for this method of long-acting contraception.
依托孕烯植入剂通常被认为是一种有效的、为期三年的长效可逆避孕装置。以往的研究,如具有里程碑意义的CHOICE研究,报告的一年续用率为72%至84%,然而,在实际应用中,这些比率可能会显著降低。
研究依托孕烯植入剂在特定临床环境中的续用率以及与早期停用相关的因素。
对2015年1月1日至2017年12月31日期间在一所学术社区医院网络的多家医疗机构接受依托孕烯植入剂的患者进行单中心回顾性队列研究。在植入后长达三年的时间里对记录进行审查,以确定续用率(一至三年)、早期停用率(≤12个月)以及早期停用的原因。进行样本量计算以指导对副作用的亚分析。
在研究期间,共有774名患者接受了依托孕烯植入。一年续用率低于CHOICE研究(62%对83%,P<0.001)。一项亚分析(n = 216)显示,大多数(82%,n = 177)患者报告有副作用。与继续使用超过一年的患者相比,早期停用的患者副作用更常见(93%对71%,P<0.001)。最常见的副作用,异常子宫出血,与早期停用没有显著关联。早期停用与神经/精神方面的主诉之间存在显著关联(P = 0.02)。
我们人群中依托孕烯植入剂的一年续用率显著低于CHOICE报告的值。植入剂的副作用很常见,并显著影响停用率。我们的数据表明,对于选择这种长效避孕方法的个体,有进行教育和咨询的机会。