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苯扎氯铵杀精乳膏对40岁及以上有避孕需求女性的有效性、安全性及可接受性:一项前瞻性多中心研究

Efficacy, safety and acceptability of a benzalkonium chloride spermicide cream in women aged 40 years and over needing contraception: A prospective multicentre study.

作者信息

Serfaty David, Prilepskaya Vera, Graesslin Olivier, Benifla Jean-Louis, Aubin François, Verriere François, Mas Yana, Escola Julie, Coatantiec Erwana, Carrois Frédéric

机构信息

9 rue de Villersexel, Paris 75007, France.

ул. Академика Опарина, д.4, 117997 Moscow, Russia.

出版信息

J Gynecol Obstet Hum Reprod. 2023 Sep;52(7):102616. doi: 10.1016/j.jogoh.2023.102616. Epub 2023 Jun 1.

Abstract

OBJECTIVE

This multicenter prospective study (BZK40+) aims to determine the efficacy and tolerance of a benzalkonium chloride-containing spermicide as contraceptive among women aged 40 and over.

PROCEDURE

Fertile women enrolled in this open single-arm study were instructed to systematically use the benzalkonium chloride spermicide before each intercourse. At the end of a 6-month mandatory period, participants were given the option of continuing the study for a further 6 months. The primary endpoint for contraceptive efficacy was the Pearl Index (PI) up to 12 months of typical use.

MAIN FINDINGS

A total of 151 women (mean age: 45.9 years) were enrolled, 144 (95.4%) completed the initial 6-month period and 63 (41.7%) completed the optional 6-month period. The median number of intercourses ranged from 3 to 5 per month. The spermicide was applied before 96.3% of the 5,895 sexual intercourses. The PI up to 12 months of typical use was 0 pregnancies (95% confidence interval: 0-2.88). The cumulative treatment exposure was 1249.7 women-months.

CONCLUSION

This first study in women aged 40 years and over shows that benzalkonium chloride spermicide (Pharmatex®) is effective, well tolerated and well accepted in this population. Although very interesting, these results with a PI equal to zero are surprising and not in accordance with the low efficacy of spermicides in the overall population according to the WHO. So, our results should be interpreted with caution and confirmed by future research. Clinical trial registration number (EudraCT): 2016-004,188-38.

摘要

目的

这项多中心前瞻性研究(BZK40+)旨在确定含苯扎氯铵的杀精剂对40岁及以上女性作为避孕药具的有效性和耐受性。

程序

参与这项开放单臂研究的育龄妇女被指导在每次性交前系统地使用苯扎氯铵杀精剂。在6个月的强制期结束时,参与者可以选择继续研究另外6个月。避孕效果的主要终点是典型使用12个月的 Pearl 指数(PI)。

主要发现

共招募了151名女性(平均年龄:45.9岁),144名(95.4%)完成了最初的6个月,63名(41.7%)完成了可选的6个月。每月性交次数中位数为3至5次。在5895次性交中,96.3%在性交前使用了杀精剂。典型使用12个月的PI为0妊娠(95%置信区间:0-2.88)。累积治疗暴露为1249.7妇女-月。

结论

这项针对40岁及以上女性的首次研究表明,苯扎氯铵杀精剂(Pharmatex®)在该人群中有效、耐受性良好且接受度高。尽管这些结果非常有趣,但PI等于零的结果令人惊讶,且与世界卫生组织公布的杀精剂在总体人群中的低有效性不符。因此,我们的结果应谨慎解读,并有待未来研究证实。临床试验注册号(EudraCT):2016-004,188-38。

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