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Clinical Study

User satisfaction with an intrauterine system containing 52 mg levonorgestrel: a Portuguese study

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Pages 113-118 | Received 17 Oct 2022, Accepted 25 Jan 2023, Published online: 20 Feb 2023
 

Abstract

Objective

To characterise patient satisfaction 6 and 12 months after insertion of a 52 mg levonorgestrel‐releasing intrauterine system (LNG-IUS) in Portuguese women.

Study design

A non-interventional and prospective study was conducted in Portuguese women of reproductive age who had Levosert® inserted. Two questionnaires (administered 6 and 12 months after 52 mg LNG-IUS insertion) were used to collect information on the patients’ menstrual pattern, discontinuation rate, and satisfaction rate with Levosert®.

Results

A total of 102 women were enrolled, of which only 94 (92.2%) completed the study. Seven participants discontinued the use of the 52 mg LNG-IUS. At 6 and 12 months, 90.7% and 90.4% of participants, respectively, were either satisfied or very satisfied with the 52 mg LNG-IUS. At 6 and 12 months, 73.2% and 72.3% of participants, respectively, indicated that they were very likely to recommend the 52 mg LNG-IUS to a friend or family member. Most women (92.2%) continued to use the 52 mg LNG-IUS for the first year. The percentage of women who were ‘much more satisfied’ with Levosert® than with their previous contraceptive methods was 55.9% and 57.8% at 6 and 12 months, respectively, per questionnaire assessment. Satisfaction was associated with age (p = 0.004), amenorrhoea (p < 0.003) and absence of dysmenorrhoea (p = 0.003), but not with parity (p = 0.922).

Conclusions

These data suggest that the continuation and satisfaction rates with Levosert® were very high, and that this system is well accepted among Portuguese women. Patient satisfaction was driven by a favourable bleeding pattern and absence of dysmenorrhoea.

Short Condensation

Satisfaction with the 52 mg levonorgestrel‐releasing intrauterine system was high among Portuguese women. Patient satisfaction was mainly driven by a favourable bleeding pattern and absence of dysmenorrhoea.

摘要

目的:了解葡萄牙妇女在植入52毫克左炔诺孕酮宫内缓释系统(LNG-IUS)6个月和12个月后的患者满意度。

研究设计:对植入了LevosertR的葡萄牙妇女进行了一项前瞻性、非干预性的研究。两份调查问卷(在植入52毫克LNG-IUS后6个月和12个月进行)用于收集患者的月经模式、停药率和对LevosertR的满意率等信息。

结果:共有102名女性参与了研究, 其中只有94人(92.2%)完成了研究。七名参与者停止使用52 mg LNG-IUS。在6个月和12个月时, 分别有90.7%和90.4%的参与者对52 mg LNG-IUS感到满意或非常满意。在6个月和12个月时, 分别有73.2%和72.3%的参与者表示, 他们很可能向朋友或家人推荐52 mg LNG-IUS。大多数女性(92.2%)在第一年继续使用52 mg LNG-IUS。根据问卷评估, 在 6 个月和 12 个月时, 对LevosertR比对以前的避孕方法“更满意”的女性比例分别为 55.9% 和 57.8%。满意度与年龄(p=0.004)、闭经(p<0.003)和无痛经(p=0.003)有关, 但与产次无关(p=0.922)。

结论:这些数据表明, LevosertR的持续使用率和满意率非常高, 这一系统在葡萄牙妇女中得到了广泛接受。良好的出血模式和无痛经令患者感到满意。

简短概括

葡萄牙妇女对52毫克左炔诺孕酮宫内缓释系统的满意度很高。患者的满意度主要来自于良好的出血模式和无痛经。

Disclosure statement

No potential conflict of interest was reported by the author(s).

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