Using updated clinical recommendations to support contraceptive decision-making: U.S. Medical Eligibility Criteria for Contraceptive Use, 2024.

Kathryn M Curtis, Antoinette T Nguyen, Naomi K Tepper, Maura K Whiteman
{"title":"Using updated clinical recommendations to support contraceptive decision-making: U.S. Medical Eligibility Criteria for Contraceptive Use, 2024.","authors":"Kathryn M Curtis, Antoinette T Nguyen, Naomi K Tepper, Maura K Whiteman","doi":"10.1016/j.contraception.2025.111015","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>In August 2024, the U.S. Centers for Disease Control and Prevention updated U.S. Medical Eligibility Criteria for Contraceptive Use (U.S. MEC), which provides recommendations for safe use of contraception for women with certain characteristics and medical conditions. This paper provides a summary of the evidence and context for new and updated U.S. MEC recommendations.</p><p><strong>Study design: </strong>The 2024 U.S. MEC was updated through a rigorous, multi-year process of determining priorities that would have high impact on clinical care, conducting systematic reviews of the evidence, and considering perspectives of health care providers and patients on how the evidence could best support updated recommendations.</p><p><strong>Results: </strong>New U.S. MEC recommendations were added for chronic kidney disease, specifically for three subconditions: current nephrotic syndrome, hemodialysis, and peritoneal dialysis. Revisions were made to several existing recommendations, such as those for sickle cell disease, anticoagulant therapy use, various thrombogenic conditions, cirrhosis, liver tumors, solid organ transplantation, and intrauterine device placement in the postpartum period. Updated recommendations include those that reflect decreased safety concerns for some medical conditions (e.g., progestin-only contraception and some liver diseases) and increased safety concerns for others (e.g., combined hormonal contraception and depot medroxyprogesterone acetate for women with sickle cell disease). Recommendations for new contraceptive methods were added.</p><p><strong>Conclusions: </strong>Evidence-based clinical guidelines can be used by health care providers to support patient-centered contraceptive counseling and services and remove unnecessary barriers to accessing and using contraception. Provider tools including a mobile app are available to help with implementation of the updated recommendations.</p><p><strong>Implications: </strong>Keeping U.S. MEC up-to-date is critical for supporting contraceptive decision-making and improving access to contraception and reproductive health care. This includes new research to address current evidence gaps, rigorous methodology for continuous evidence identification and synthesis, state-of-the-art methods for guideline development, and a broad range of dissemination and implementation strategies.</p>","PeriodicalId":93955,"journal":{"name":"Contraception","volume":" ","pages":"111015"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Contraception","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.contraception.2025.111015","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: In August 2024, the U.S. Centers for Disease Control and Prevention updated U.S. Medical Eligibility Criteria for Contraceptive Use (U.S. MEC), which provides recommendations for safe use of contraception for women with certain characteristics and medical conditions. This paper provides a summary of the evidence and context for new and updated U.S. MEC recommendations.

Study design: The 2024 U.S. MEC was updated through a rigorous, multi-year process of determining priorities that would have high impact on clinical care, conducting systematic reviews of the evidence, and considering perspectives of health care providers and patients on how the evidence could best support updated recommendations.

Results: New U.S. MEC recommendations were added for chronic kidney disease, specifically for three subconditions: current nephrotic syndrome, hemodialysis, and peritoneal dialysis. Revisions were made to several existing recommendations, such as those for sickle cell disease, anticoagulant therapy use, various thrombogenic conditions, cirrhosis, liver tumors, solid organ transplantation, and intrauterine device placement in the postpartum period. Updated recommendations include those that reflect decreased safety concerns for some medical conditions (e.g., progestin-only contraception and some liver diseases) and increased safety concerns for others (e.g., combined hormonal contraception and depot medroxyprogesterone acetate for women with sickle cell disease). Recommendations for new contraceptive methods were added.

Conclusions: Evidence-based clinical guidelines can be used by health care providers to support patient-centered contraceptive counseling and services and remove unnecessary barriers to accessing and using contraception. Provider tools including a mobile app are available to help with implementation of the updated recommendations.

Implications: Keeping U.S. MEC up-to-date is critical for supporting contraceptive decision-making and improving access to contraception and reproductive health care. This includes new research to address current evidence gaps, rigorous methodology for continuous evidence identification and synthesis, state-of-the-art methods for guideline development, and a broad range of dissemination and implementation strategies.

使用最新的临床建议来支持避孕决策:美国医疗避孕使用资格标准,2024。
目标:2024年8月,美国疾病控制和预防中心更新了美国避孕药具使用医疗资格标准(U.S. MEC),该标准为具有某些特征和医疗条件的女性安全使用避孕药具提供了建议。本文提供了新的和更新的美国MEC建议的证据和背景的总结。研究设计:2024年美国MEC的更新是通过一个严格的、多年的过程来确定对临床护理有重大影响的优先事项,对证据进行系统审查,并考虑医疗保健提供者和患者的观点,以确定证据如何最好地支持更新的建议。结果:新的美国MEC推荐用于慢性肾脏疾病,特别是三种亚条件:当前肾病综合征、血液透析和腹膜透析。修订了一些现有的建议,如镰状细胞病、抗凝治疗使用、各种血栓形成条件、肝硬化、肝脏肿瘤、实体器官移植和产后放置宫内节育器。更新的建议包括那些反映某些医疗条件(例如,仅使用孕激素避孕和某些肝脏疾病)的安全性问题减少的建议,以及对其他医疗条件(例如,镰状细胞病妇女的联合激素避孕和醋酸甲羟孕酮)安全性问题增加的建议。增加了新的避孕方法的建议。结论:循证临床指南可被卫生保健提供者用于支持以患者为中心的避孕咨询和服务,并消除获取和使用避孕措施的不必要障碍。包括移动应用程序在内的提供商工具可用于帮助实施更新后的建议。意义:保持美国MEC最新是支持避孕决策和改善获得避孕和生殖保健至关重要。这包括解决当前证据差距的新研究、持续证据识别和合成的严格方法、制定指南的最先进方法以及广泛的传播和实施战略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信