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一项在尼泊尔 18-49 岁女性中评估 Sayana Press 可接受性的前瞻性队列研究。

A prospective cohort study to assess the acceptability of Sayana Press among 18-49-year-old women in Nepal.

机构信息

Ipas Nepal, Kathmandu, Nepal.

Family Welfare Division, Ministry of Health and Population, Kathmandu, Nepal.

出版信息

Contraception. 2021 Dec;104(6):623-627. doi: 10.1016/j.contraception.2021.07.009. Epub 2021 Jul 16.

DOI:10.1016/j.contraception.2021.07.009
PMID:34280441
Abstract

OBJECTIVE

We compared acceptability and continuation of Sayana Press, a subcutaneous formulation of depot-medroxyprogesteone acetate (DMPA) in a Uniject injection system, to intramuscular (IM) DMPA, among both current users of DMPA-IM and new users in Nepal.

STUDY DESIGN

We recruited women seeking injectable contraception at 14 public health facilities in Nepal selected for geographic diversity. We enrolled women who self-selected either Sayana Press or DMPA-IM and used structured interviews to obtain baseline demographics and assess satisfaction and continuation rates at 1, 3, and 6 months.

RESULTS

Seven hundred ninety-four women (71%) selected and received Sayana Press, while 318 women (28.6%) selected and received DMPA-IM. One hundred and seventy-eight (48%) women continuing Sayana Press injection reported that they experienced "no possible side effects" compared to 29 (22%) among DMPA-IM selectors during the previous 6 months. The continuation rate of Sayana Press at 6 months was higher than DMPA-IM (Sayana Press 46.5% vs DMPA-IM 34.4%; p < 0.001). Selection of Sayana Press method (OR. 1.74; 95% confidence interval 1.32-2.3) and approval from husband (OR. 1.59; 95% confidence interval 1.21-2.09) were associated with injection continuation.

CONCLUSION

Sayana Press is acceptable to women in Nepal with the preference for Sayana Press over DMPA-IM (higher proportion chose the method when counseled and given the option, better continuation).

IMPLICATIONS

The potential for self-injection with Sayana Press® may have implications for continuation and opportunity for future research and strategies to roll out this innovative technology must be explored.

摘要

目的

我们比较了皮下注射醋酸甲羟孕酮储库(DMPA)的苏娜依®(一种 Uniject 注射系统)在尼泊尔的当前 DMPA-IM 用户和新用户中的可接受性和持续性,与肌内(IM)DMPA 进行比较。

研究设计

我们在尼泊尔的 14 个公共卫生机构招募了正在寻求注射避孕的女性,这些机构的选择考虑了地理位置的多样性。我们招募了自我选择苏娜依®或 DMPA-IM 的女性,并使用结构化访谈获得基线人口统计学数据,并在 1、3 和 6 个月时评估满意度和持续率。

结果

794 名女性(71%)选择并接受了苏娜依®,而 318 名女性(28.6%)选择并接受了 DMPA-IM。178 名(48%)继续使用苏娜依®注射的女性报告说,与前 6 个月内选择 DMPA-IM 的 29 名女性(22%)相比,她们“没有可能的副作用”。6 个月时苏娜依®的持续率高于 DMPA-IM(苏娜依®46.5% vs DMPA-IM 34.4%;p<0.001)。选择苏娜依®方法(OR. 1.74;95%置信区间 1.32-2.3)和获得丈夫的同意(OR. 1.59;95%置信区间 1.21-2.09)与注射的持续有关。

结论

苏娜依®在尼泊尔的女性中是可以接受的,与 DMPA-IM 相比,女性更喜欢苏娜依®(当被咨询和给予选择时,更多的人选择该方法,持续率更高)。

意义

苏娜依®的自我注射潜力可能对持续率产生影响,需要进一步研究和探索推出这一创新技术的机会。

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