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Crisis Pregnancy Centers: An Inherently Unjust Limitation to Reproductive Rights. 危机怀孕中心:对生殖权利的内在不公正限制。
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.28
Rebecca Feinberg, Danielle Pacia
Abortion, though afforded certain legal protections, can be challenging to access in many areas of the United States, a problem exacerbated by the presence of Crisis Pregnancy Centers (CPCs). CPCs present themselves as clinics that provide a full spectrum of free pregnancy consultation services, but in fact are pro-life, anti-abortion organizations.1 From the outside, CPCs appear to be neutral health and welfare establishments, leading women *to believe they will receive unbiased guidance based on their best interests. In reality, CPCs recruit unsuspecting women into their facilities to deter them from accessing abortions, promoting only two options: parenthood or adoption.2 Women are lured into CPCs with the promise of free services which range from medical care to clothing and other items. At its most basic level, these deceptive practices violate the autonomy of women seeking reproductive care, perpetuating unjust limitation of access to quality medical care.
堕胎虽然有一定的法律保护,但在美国的许多地区,堕胎仍然是一项挑战,而危机怀孕中心(cpc)的存在加剧了这一问题。cpc自称是提供全方位免费妊娠咨询服务的诊所,但实际上是反堕胎、反堕胎的组织从表面上看,中心似乎是中立的健康和福利机构,这让女性*相信她们会得到基于自身最大利益的公正指导。实际上,cpc招募不知情的妇女到他们的设施阻止她们堕胎,只宣传两种选择:父母或收养妇女被承诺提供免费服务(从医疗到服装和其他物品)吸引到cpc。在最基本的层面上,这些欺骗性做法侵犯了寻求生殖保健的妇女的自主权,使获得高质量医疗保健的机会永远受到不公正的限制。
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引用次数: 0
Reforming Medicaid Coverage Toward Reproductive Justice. 改革医疗补助计划以实现生殖公正。
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.27
Madeline T Morcelle

As the United States' largest public health insurance program, Medicaid has since 1965 played a crucial role in the struggle for equitable health care access. It has the potential to be a powerful instrument of reproductive justice, yet discriminatory policies that deny coverage for vital sexual, reproductive, or other health services, or exclude entire populations of people with low incomes from coverage altogether, constrain peoples' health and reproductive futures. Resulting discrimination in Medicaid law and policy thwart the program's ability to promote intergenerational health equity and reproductive justice for underserved communities.This Article provides an account of why reproductive justice is a necessary framework for examining, reimagining, and reforming Medicaid coverage law and policy. Part I gives a brief history and overview of reproductive justice, which serves as "an open source code that people have used to pursue fresh critical thinking regarding power and powerlessness." Part II argues that we should utilize that open source code in Medicaid coverage reform. Using some of the reproductive justice movement's critiques as a starting point, it explores how reproductive oppression has shaped Medicaid coverage law, policy, and mainstream reproductive and health care reform movements' proposals, and to what effect. It argues that examining Medicaid law, policy, and proposed reforms through this lens and in collaboration with the reproductive justice movement can enable health advocates and policymakers to more fully understand, disrupt, and dismantle reproductive injustices that drive health inequities. Ultimately, it can empower reformers to build a more equitable public health insurance safety net that brings us closer to reproductive justice for all.

作为美国最大的公共医疗保险计划,自1965年以来,医疗补助计划在争取公平医疗服务方面发挥了至关重要的作用。它有可能成为生殖正义的有力工具,然而,拒绝为至关重要的性健康、生殖健康或其他健康服务提供保险,或将整个低收入人群完全排除在保险之外的歧视性政策,限制了人们的健康和生殖未来。因此,医疗补助法律和政策中的歧视阻碍了该计划促进代际健康公平和服务不足社区生殖正义的能力。本文解释了为什么生殖正义是检查、重新构想和改革医疗补助覆盖法律和政策的必要框架。第一部分简要介绍了生殖正义的历史和概述,它是“人们用来追求关于权力和无能为力的新鲜批判性思维的开放源代码”。第二部分认为,我们应该在医疗补助覆盖改革中利用开源代码。以一些生殖正义运动的批评为出发点,探讨生殖压迫如何影响医疗补助覆盖法律、政策以及主流生殖和医疗改革运动的建议,以及产生了什么影响。它认为,通过这一视角,并与生殖正义运动合作,审视医疗补助法律、政策和拟议的改革,可以使健康倡导者和政策制定者更充分地理解、破坏和消除导致健康不平等的生殖不公正。最终,它可以使改革者有能力建立一个更公平的公共医疗保险安全网,使我们更接近人人享有生殖公正。
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引用次数: 0
Reason-Based Abortion Bans, Disability Rights, and the Future of Prenatal Genetic Testing. 基于理性的堕胎禁令、残疾人权利和产前基因检测的未来。
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.21
Nina Roesner, Leila Jamal, David Wasserman, Benjamin E Berkman

Recent advances in prenatal genetic testing have made testing for congenital disorders more accessible, with emerging technologies promising further expansion of available testing options. In particular, non-invasive prenatal testing ("NIPT") has allowed women to identify more fetal disorders earlier in pregnancy than was possible only a decade ago. In addition to allowing women to prepare for the birth of a child with a disability, prenatal diagnoses give women the ability to terminate a pregnancy to avoid raising a child with a disability, a choice driven by myriad factors.

产前基因检测的最新进展使先天性疾病的检测更容易获得,新兴技术有望进一步扩大现有的检测选择。特别是,与十年前相比,非侵入性产前检查(“NIPT”)使妇女能够在怀孕早期识别更多的胎儿疾病。除了让妇女为残疾孩子的出生做准备外,产前诊断还使妇女有能力终止妊娠,以避免抚养残疾孩子,这是一种由无数因素驱动的选择。
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引用次数: 1
Do Pluripotent Stem Cells Offer a New Path to Reproduction? 多能干细胞为生殖提供了一条新途径吗?
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.23
Audrey R Chapman

The ability of pluripotent stem to develop into any of the cell types in the human body has meant that it was only a matter of time before scientists would try to transform them into human gametes. Up to now though it has not been possible to do so. Nevertheless a 2016 book written by Henry Greely speculated that in twenty to forty years most people in developed countries will cease reproduction through sex, using sex exclusively for pleasure, and instead will rely on reproduction through pluripotent stem cell-derived gametes. This paper will offer a different perspective. After describing the process through which human pluripotent stem cells might eventually be coaxed into gametes, it will show why the use of pluripotent stem cell-derived gametes for reproductive purposes would present significant safety, ethical, and regulatory challenges.

多能干细胞能够发育成人体中的任何一种细胞类型,这意味着科学家试图将其转化为人类配子只是时间问题。到目前为止,虽然还不可能这样做。尽管如此,亨利·格里利(Henry Greely)在2016年写的一本书中推测,在20到40年内,发达国家的大多数人将不再通过性来繁殖,而是通过多能干细胞衍生的配子来繁殖。本文将提供一个不同的视角。在描述了人类多能干细胞最终可能被诱导成配子的过程之后,它将说明为什么将多能干细胞衍生的配子用于生殖目的会带来重大的安全、伦理和监管挑战。
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引用次数: 1
Pregnant Women and Opioid Use Disorder: Examining the Legal Landscape for Controlling Women's Reproductive Health. 孕妇和阿片类药物使用障碍:检查控制妇女生殖健康的法律环境。
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.26
Lynn M Madden, Jenn Oliva, Anthony Eller, Elizabeth DiDomizio, Mat Roosa, Lisa Blanchard, Natalie Kil, Frederick L Altice, Kimberly Johnson

Women with opioid use disorder ("OUD") are more likely than other women to experience sexual assault, unintentional pregnancy, transactional sex and coercion regarding reproductive health care choices than women without OUD. Laws described as family friendly may be punitive rather than helpful to women and rarely apply to men. Laws regarding reproductive health and OUD are unevenly enforced and therefore biased against poor, minority women. As part of a larger study oriented toward strengthening systems of care related to the intersection of HIV and OUD, we conducted an analysis of state laws related to pregnant and postpartum women with OUD. Data on disparities in child removals and pregnant women's use of evidence-based treatment for OUD by income and race were captured for the five states with the most restrictive laws in both categories. Laws that were purportedly designed to improve reproductive health outcomes for women with OUD and/or their children often have the opposite of the expressed intended outcome. There is a relationship between restrictive reproductive choice and coercive OUD treatment policy for women. Restrictive state regulations for pregnant women with OUD persist despite negative outcomes for maternal and child health. Altering coercive and/or criminalizing regulation and redefining 'family friendly' may improve outcomes for individuals and families.

与没有阿片类药物使用障碍的妇女相比,患有阿片类药物使用障碍的妇女比其他妇女更容易遭受性侵犯、意外怀孕、交易性行为和生殖保健选择方面的强迫。被描述为家庭友好的法律可能对女性是惩罚性的,而不是有益的,而且很少适用于男性。有关生殖健康和OUD的法律执行不均衡,因此对贫穷的少数民族妇女有偏见。作为一项旨在加强与HIV和OUD交叉相关的护理系统的大型研究的一部分,我们对与孕妇和产后OUD妇女相关的州法律进行了分析。根据收入和种族,收集了在这两个类别中法律最严格的五个州的儿童移除和孕妇使用循证治疗OUD方面的差异数据。据称旨在改善OUD妇女和/或其子女生殖健康结果的法律往往与所表达的预期结果相反。限制性生育选择与强制性妇女OUD治疗政策之间存在一定的关系。尽管对孕产妇和儿童健康产生负面影响,但国家对患有OUD的孕妇的限制性规定仍然存在。改变强制性和/或刑事化监管,重新定义“家庭友好”,可能会改善个人和家庭的结果。
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引用次数: 1
Remote Reproductive Rights. 远程生殖权利。
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.29
Rachel Rebouché
Abstract In July 2020, a federal district court lifted the U.S. Food & Drug Administration’s (“FDA”) restriction requiring patients to pick up the first drug of a medication abortion—mifepristone—at a healthcare facility. Soon after, an ongoing experiment with remote care for abortion expanded, as telemedicine did in other areas, and virtual clinics began offering no-touch abortions. Growth of virtual care stalled in January 2021 when the Supreme Court stayed a district court’s order pending the appeals process. But in April 2022, persuaded by the evidence of remote abortion’s safety and efficacy, the FDA suspended enforcement of the in-person rule for the course of the pandemic. On December 16, 2021, the FDA lifted the requirement that patients pick up mifepristone at a healthcare facility, clearing the way for supervised mail delivery and pharmacy dispensation. The expansion of virtual clinics, however, is not without significant limitations. First, questions remain about how to implement the new FDA regulation, specifically regarding certified pharmacies, and several FDA restrictions on mifepristone remain in place. Second, about half the country prohibits telehealth for abortion by either banning all abortion or by requiring the physical presence of a healthcare professional. Third, participation in telemedicine depends on various forms of privilege. Patients must have a stable internet connection or smartphone as well as an uncomplicated pregnancy, which, in part because of U.S. health disparities, is more likely for wealthier and white people. Even with the expansion of remote care, the need for clinical spaces will not disappear; in fact, it will come under increasing pressure. This Article maps the emergence of virtual abortion care and analyzes the potential trajectory of medication abortion access, given that the Supreme Court has overturned constitutional protections for abortion. It considers the limits of telehealth for abortion—who telehealth can reach and who it cannot. Those living in states that permit abortion will have new options for ending early pregnancies. Those residing in states hostile to abortion will have to seek cross-border care, carry pregnancies to term, or find other avenues to end pregnancies. But the portability of abortion pills, when mailed by prescribers or dispensed by certified pharmacies, will test how closely states officials (or anyone else) can police or impede access to medication abortion.
2020年7月,一家联邦地区法院取消了美国食品和药物管理局(FDA)的限制,该限制要求患者在医疗机构购买流产药物的第一种药物——米非司酮。不久之后,就像远程医疗在其他领域所做的那样,一项正在进行的堕胎远程护理实验扩大了,虚拟诊所开始提供无接触堕胎服务。2021年1月,最高法院暂缓了地区法院的命令,等待上诉程序,虚拟医疗的增长陷入停滞。但在2022年4月,在远程堕胎安全性和有效性的证据说服下,FDA暂停了在大流行期间实施面对面规则的执行。2021年12月16日,FDA取消了患者在医疗机构领取米非司酮的要求,为监督邮件递送和药房分配扫清了道路。然而,虚拟诊所的扩张并非没有明显的限制。首先,关于如何实施FDA新规定的问题仍然存在,特别是关于经过认证的药店,FDA对米非司酮的一些限制仍然存在。其次,大约一半的国家禁止远程堕胎,要么禁止所有堕胎,要么要求医疗保健专业人员亲自到场。第三,参与远程医疗取决于各种形式的特权。患者必须有稳定的互联网连接或智能手机,并且怀孕过程简单,这在一定程度上是因为美国的健康差距,更有可能出现在富裕和白人身上。即使随着远程医疗的扩大,对临床空间的需求也不会消失;事实上,它将面临越来越大的压力。鉴于最高法院推翻了宪法对堕胎的保护,本文描绘了虚拟堕胎护理的出现,并分析了药物堕胎获得的潜在轨迹。它考虑了远程医疗对堕胎的限制——远程医疗可以接触到谁,不能接触到谁。那些生活在允许堕胎州的人将有新的选择来终止早孕。那些居住在反对堕胎的州的人将不得不寻求跨境护理,将怀孕进行到足月,或寻找其他途径终止怀孕。但是,堕胎药的可携带性,无论是由处方医生邮寄还是由认证药房配发,都将考验州政府官员(或其他任何人)能在多大程度上监督或阻止药物流产。
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引用次数: 0
AMJ volume 48 issue 2-3 Cover and Back matter AMJ第48卷第2-3期封面和封底
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.31
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引用次数: 0
Access to Medication Abortion: Now More Important Than Ever. 获得药物流产:现在比以往任何时候都更重要。
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.24
Rebecca Fliegel
In 2017, 39% of all abortions in the United States were medication abortions, a safe and effective option for those seeking abortions through up to ten weeks of pregnancy.2 The United States Food and Drug Administration (FDA) approved medication abortion, composed of a combination of mifepristone and misoprostol, in 2000, making the method available for the first time.3 The FDA’s choice to approve medication abortion gave abortion activists hope that abortion would bemore readily accessible.4 One of the many barriers to abortion is the social outing one must undertake when visiting a doctor’s office to obtain the procedure—visits often accompanied by protestors outside those offices shouting at the patient. Medication abortion allows for patients to essentially perform their abortions privately, in their own homes, without suffering that social condemnation.5 However, starting in 2004, numerous states began restricting access to medication abortion.6 Many states require that medication abortion only be prescribed and administered7 by a physician who is in the same room as the patient, which essentially prevents physician assistants or advanced practice nurses from prescribing the medication, and any clinician from prescribing and administering the medication via telemedicine.8 These restrictions became problematic during the COVID-19 pandemic when doctors’ offices were either closed or dangerous places to visit for people with certain health conditions.9
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引用次数: 1
AMJ volume 48 issue 2-3 Cover and Front matter AMJ第48卷第2-3期封面和封面问题
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-07-01 DOI: 10.1017/amj.2022.30
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引用次数: 0
Ignoring the Experts: Implications of the FDA's Aduhelm Approval. 忽视专家:FDA Aduhelm批准的影响。
IF 0.6 4区 社会学 Q3 LAW Pub Date : 2022-03-01 DOI: 10.1017/amj.2022.15
Alexandra Maulden

In early June 2021, the U.S. Food and Drug Administration ("FDA") granted Accelerated Approval to Aducanumab ("Aduhelm") for treating Alzheimer's disease. The decision was immediately engulfed in controversy because the agency ignored the Scientific Drugs Advisory Committee's unanimous recommendation not to approve the drug. The FDA granted the approval based on Aduhelm's ability to lower beta-amyloid levels. However, the agency had not previously indicated this as a surrogate clinical end for the trial, and its own scientific analysis failed to show that amyloid changes correlate with cognitive or functional changes for Alzheimer's patients. This decision sets dangerous precedent and has the potential to transform the approval process for new drugs including, but not limited to, those meant to treat Alzheimer's.

2021年6月初,美国食品和药物管理局(FDA)加速批准Aducanumab (Aduhelm)用于治疗阿尔茨海默病。这一决定立即引发了争议,因为该机构无视科学药物咨询委员会(Scientific drug Advisory Committee)的一致建议,不批准该药物。FDA基于Aduhelm降低β -淀粉样蛋白水平的能力批准了该药物。然而,该机构此前并未将其作为试验的替代临床目的,其自己的科学分析也未能显示淀粉样蛋白变化与阿尔茨海默病患者的认知或功能变化相关。这一决定开创了危险的先例,有可能改变新药的审批程序,包括但不限于治疗阿尔茨海默病的药物。
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引用次数: 1
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American Journal of Law & Medicine
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