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Sexual and Reproductive Health Matters最新文献

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Ethical concerns facing abortion researchers in restrictive settings: the need for guidelines. 堕胎研究人员在限制性环境下面临的伦理问题:需要指导方针。
IF 3.3 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 DOI: 10.1080/26410397.2023.2193315
Grace W Kimemia, Caroline W Kabiru, Boniface Ayanbekongshie Ushie
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引用次数: 0
The impact of COVID-19 mitigation measures on sexual and reproductive health in low- and middle-income countries: a rapid review. 新冠肺炎缓解措施对中低收入国家性健康和生殖健康的影响:快速审查。
IF 3.3 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 DOI: 10.1080/26410397.2023.2203001
Elizabeth Ochola, Maheshwari Andhavarapu, Poppy Sun, Abdu Mohiddin, Okwaro Ferdinand, Marleen Temmerman

Pandemic mitigation measures can have a negative impact on access and provision of essential healthcare services including sexual and reproductive health (SRH) services. This rapid review looked at the literature on the impact of COVID-19 mitigation measures on SRH and gender-based violence (GBV) on women in low- and middle-income countries (LMIC) using WHO rapid review guidance. We looked at relevant literature published in the English language from January 2020 to October 2021 from LMICs using WHO rapid review methods. A total of 114 articles were obtained from PubMed, Google Scholar and grey literature of which 20 met the eligible criteria. Our review found that there was an overall reduction in; (a) uptake of services as shown by lower antenatal, postnatal and family planning clinic attendance, (b) service delivery as shown by reduced health facility deliveries, and post abortion care services and (c) reproductive health outcomes as shown by an increase in incidence of GBV especially intimate partner violence. COVID-19 mitigation measures negatively impact SRH of women in LMICs. Findings from this review could inform policy makers in the health sector to recognise the potential adverse effects of COVID-19 responses on SRH in the country, and therefore implement mitigation measures.

流行病缓解措施可能会对获得和提供包括性健康和生殖健康服务在内的基本医疗服务产生负面影响。这项快速审查利用世界卫生组织快速审查指南,查阅了关于新冠肺炎缓解措施对低收入和中等收入国家妇女性健康和基于性别的暴力(GBV)的影响的文献。我们使用世界卫生组织快速审查方法,查看了2020年1月至2021年10月LMIC以英语发表的相关文献。共从PubMed、Google Scholar和灰色文献中获得114篇文章,其中20篇符合合格标准。我们的审查发现;(a) 产前、产后和计划生育诊所就诊率较低所显示的服务接受情况,(b)卫生设施分娩和堕胎后护理服务减少所显示的提供服务情况,以及(c)基于性别的暴力,特别是亲密伴侣暴力发生率增加所显示的生殖健康结果。新冠肺炎缓解措施对LMIC中妇女的SRH产生负面影响。这项审查的结果可以让卫生部门的政策制定者认识到新冠肺炎应对措施对该国SRH的潜在不利影响,并因此实施缓解措施。
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引用次数: 0
Internet use, exposure to digital family planning messages, and sexual agency among partnered women in Northern Nigeria: implications for digital family planning intervention. 尼日利亚北部伴侣妇女的互联网使用、接触数字计划生育信息和性代理:对数字计划生育干预的影响。
IF 6 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 Epub Date: 2023-10-23 DOI: 10.1080/26410397.2023.2261681
David Aduragbemi Okunlola, Oluwatobi Abel Alawode, Abayomi Folorunso Awoleye, Benjamin Bukky Ilesanmi

Digital health interventions are gaining ground in conflict-affected countries, but studies on their reproductive health benefits for women are scanty. Focusing on conflict-affected northern Nigeria, this study examined the relationships between Internet use, exposure to digital family planning messages via text messages or social media, and sexual agency - measured as the ability to refuse sex and ask a male partner to use a condom - among partnered women including the rural-urban differentials. Partnered women's data (n= 18,205) from the 2018 Nigeria Demographic and Health Survey were analysed using descriptive and multinomial logistic regression analyses. 44.6% of women are able to refuse sex, and 31.4% to ask a male partner to use a condom. Internet use was positively associated with women's ability to refuse sex in the northern region and urban areas, and across the region to ask a male partner to use a condom. It was also positively associated with women's uncertainty about asking a male partner to use a condom. Exposure to digital family planning messages was positively associated with women's ability to ask a male partner to use a condom across the region, in both urban and rural areas. However, exposure to digital family planning messages was negatively associated with women's uncertainty in urban areas about their ability to refuse sex. Implications of these findings for digital family planning interventions are discussed.

在受冲突影响的国家,数字健康干预措施正在取得进展,但对其对妇女生殖健康益处的研究很少。这项研究以受冲突影响的尼日利亚北部为重点,调查了伴侣女性之间的互联网使用、通过短信或社交媒体接触数字计划生育信息以及性代理(以拒绝性行为和要求男性伴侣使用避孕套的能力衡量)之间的关系,包括城乡差异。使用描述性和多项逻辑回归分析对2018年尼日利亚人口与健康调查中的伴侣女性数据(n=18205)进行了分析。44.6%的女性能够拒绝性行为,31.4%的女性要求男性伴侣使用避孕套。在北部地区和城市地区,以及在整个地区,使用互联网与女性拒绝性行为的能力呈正相关,她们要求男性伴侣使用避孕套。这也与女性在要求男性伴侣使用避孕套方面的不确定性呈正相关。在整个地区的城市和农村地区,接触数字计划生育信息与女性要求男性伴侣使用避孕套的能力呈正相关。然而,接触数字计划生育信息与城市地区女性拒绝性行为能力的不确定性呈负相关。讨论了这些发现对数字计划生育干预措施的影响。
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引用次数: 0
Autonomy in labour and delivery in a Latin American urban centre: a qualitative phenomenological analysis. 拉丁美洲城市中心的分娩自主权:定性现象学分析。
IF 6 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 Epub Date: 2024-03-25 DOI: 10.1080/26410397.2024.2310889
Maribel Mella-Guzmán, Lorena Binfa, Fiona Weeks

The medicalisation of childbirth has diminished the role of labouring people. We conducted an exploratory phenomenological qualitative study, using purposive sampling, and then conducted 17 semi-structured interviews between December 2016 and October 2017 with people who had recently given birth in a public hospital in the Northern Metropolitan area of Santiago, Chile. The sufficiency of the study group was determined according to saturation criteria. Triangulated content analysis was applied to explore the clinical relationship and processes of autonomy and decision-making. The predominant clinical relationship observed was paternalism. The participation of labouring people in decision-making is scarce, with no evidence of ethically valid processes of informed consent.

分娩医疗化削弱了产妇的作用。我们进行了一项探索性的现象学定性研究,采用目的性抽样,然后在 2016 年 12 月至 2017 年 10 月期间,对智利圣地亚哥北部都市区一家公立医院的产妇进行了 17 次半结构式访谈。根据饱和度标准确定了研究群体的充分性。采用三角内容分析法探讨了临床关系以及自主和决策过程。观察到的主要临床关系是家长制。劳工参与决策的情况很少,没有证据表明知情同意程序在道德上是有效的。
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引用次数: 0
Preferences for onward health data use in the electronic age among maternity patients and providers in South Africa: a qualitative study. 南非产妇患者和提供者在电子时代对后续健康数据使用的偏好:一项定性研究。
IF 3.3 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 Epub Date: 2023-11-20 DOI: 10.1080/26410397.2023.2274667
Amnesty LeFevre, Olivia Welte, Kearabetswe Moopelo, Nicki Tiffin, Gaolatlhe Mothoagae, Nobukhosi Ncube, Nasiphi Gwiji, Manape Shogole, Amy L Slogrove, Nomakhawuta Moshani, Andrew Boulle, Jane Goudge, Frances Griffiths, Lee Fairlie, Ushma Mehta, Kerry Scott, Nirvana Pillay

Despite the expanding digitisation of individual health data, informed consent for the collection and use of health data is seldom explicitly sought in public sector clinics in South Africa. This study aims to identify perceptions of informed consent practices for health data capture, access, and use in Gauteng and the Western Cape provinces of South Africa. Data collection from September to December 2021 included in-depth interviews with healthcare providers (n = 12) and women (n = 62) attending maternity services. Study findings suggest that most patients were not aware that their data were being used for purposes beyond the individualised provision of medical care. Understanding the concept of anonymised use of electronic health data was at times challenging for patients who understood their data in the limited context of paper-based folders and booklets. When asked about preferences for electronic data, patients overwhelmingly were in favour of digitisation. They viewed electronic access to their health data as facilitating rapid and continuous access to health information. Patients were additionally asked about preferences, including delivery of health information, onward health data use, and recontacting. Understanding of these use cases varied and was often challenging to convey to participants who understood their health data in the context of information inputted into their paper folders. Future systems need to be established to collect informed consent for onward health data use. In light of perceived ties to the care received, these systems need to ensure that patient preferences do not impede the content nor quality of care received.

尽管个人健康数据的数字化不断扩大,但南非公共部门诊所很少明确征求收集和使用健康数据的知情同意。本研究旨在确定对南非豪登省和西开普省卫生数据获取、获取和使用的知情同意做法的看法。2021年9月至12月的数据收集包括对医疗保健提供者(n = 12)和参加产科服务的妇女(n = 62)的深入访谈。研究结果表明,大多数患者并不知道他们的数据被用于提供个性化医疗服务以外的目的。理解匿名使用电子健康数据的概念有时对在纸质文件夹和小册子的有限背景下理解其数据的患者具有挑战性。当被问及对电子数据的偏好时,患者压倒性地支持数字化。他们认为以电子方式获取其卫生数据有助于快速和持续地获取卫生信息。此外,还询问了患者的偏好,包括提供健康信息、继续使用健康数据和再次联系。对这些用例的理解各不相同,而且往往很难向参与者传达,因为他们了解自己的健康数据是在输入到纸质文件夹中的信息背景下进行的。未来需要建立系统来收集知情同意,以便进一步使用卫生数据。考虑到与所接受护理的关系,这些系统需要确保患者的偏好不会影响所接受护理的内容和质量。
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引用次数: 0
"It's not safe for me and what would it achieve?" Acceptability of patient-referral partner notification for sexually transmitted infections to young people, a mixed methods study from Zimbabwe. “这对我来说不安全,它会实现什么?”津巴布韦的一项混合方法研究表明,年轻人对性传播感染的患者转诊伴侣通知的可接受性。
IF 3.3 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 DOI: 10.1080/26410397.2023.2220188
Joni Lariat, Chido Dziva Chikwari, Ethel Dauya, Valentine T Baumu, Victor Kaisi, Laura Kafata, Esnath Meza, Victoria Simms, Constance Mackworth-Young, Helena Rochford, Anna Machiha, Tsitsi Bandason, Suzanna C Francis, Rashida A Ferrand, Sarah Bernays
<p><p>Partner notification (PN) is considered integral to the management of sexually transmitted infections (STI). Patient-referral is a common PN strategy and relies on index cases notifying and encouraging their partners to access treatment; however, it has shown limited efficacy. We conducted a mixed methods study to understand young people's experiences of PN, particularly the risks and challenges encountered during patient-referral. All young people (16-24 years) attending a community-based sexual and reproductive health service in Zimbabwe who were diagnosed with an STI were counselled and offered PN slips, which enabled their partners to access free treatment at the service. PN slip uptake and partner treatment were recorded. Among 1807 young people (85.0% female) offered PN slips, 745 (41.2%) took up ≥1 PN slip and 103 partners (5.7%) returned for treatment. Most participants described feeling ill-equipped to counsel and persuade their partners to seek treatment. Between June and August 2021, youth researchers conducted in-depth interviews with 41 purposively selected young people diagnosed with an STI to explore their experiences of PN. PN posed considerable social risks, threatening their emotional and physical safety. Except for a minority in long-term, publicly acknowledged relationships, participants did not expect PN would achieve successful outcomes. Public health discourse, which constructs PN as "the right thing to do", influenced participants to adopt narratives that concealed the difficulties of PN and their unmet needs. Urgent interrogation is needed of whether PN is a suitable or constructive strategy to continue pursuing with young people. To improve the outcomes of preventing reinfection and onward transmission of STIs, we must consider developing alternative strategies that better align with young people's lived experiences.<b>Plain language summary</b> Partner notification is a public health strategy used to trace the sexual partners of people who have received a sexually transmitted infection (STI) diagnosis. It aims to interrupt the chains of STI transmission and prevent reinfection by treating both the person diagnosed and their sexual partners. The least effective but most common partner notification strategy used in many resource-limited settings is called "patient referral". This involves a sexual healthcare provider encouraging the person diagnosed to give a "partner notification slip" to their potentially exposed sexual partner/s and persuading them to access treatment. This research sought to better understand young people's experiences of partner notification, particularly the risks and challenges they faced during patient-referral.All young people (16-24 years) attending a community-based sexual and reproductive health service in Zimbabwe who were diagnosed with an STI were counselled and offered PN slips, which enabled their partners to access free treatment at the service. Young people trained as researchers
伴侣通知(PN)被认为是性传播感染(STI)管理的组成部分。患者转诊是一种常见的PN策略,依赖于指数病例通知和鼓励其伴侣接受治疗;然而,它的疗效有限。我们进行了一项混合方法研究,以了解年轻人的PN经历,特别是在患者转诊过程中遇到的风险和挑战。在津巴布韦,所有参加社区性健康和生殖健康服务的被诊断为性传播疾病的年轻人(16-24岁)都接受了咨询,并获得了PN单,这使他们的伴侣能够在该服务中获得免费治疗。记录PN滑动摄取和伴侣治疗。在1807名提供PN单的年轻人(85.0%的女性)中,745人(41.2%)接受了≥1个PN单,103名伴侣(5.7%)返回治疗。大多数参与者描述说,他们觉得自己没有能力为伴侣提供咨询和说服他们寻求治疗。2021年6月至8月,青年研究人员对41名被诊断为STI的年轻人进行了深入采访,以探索他们的PN经历。PN带来了相当大的社会风险,威胁到他们的情感和身体安全。除了少数处于长期、公开承认的关系中的人外,参与者并不期望PN会取得成功。公共卫生话语将PN构建为“正确的做法”,影响参与者采用掩盖PN困难及其未满足需求的叙事。需要紧急询问PN是否是继续与年轻人合作的合适或建设性策略。为了提高预防性传播感染再次感染和继续传播的效果,我们必须考虑制定更符合年轻人生活经历的替代策略。简明语言摘要伴侣通知是一种公共卫生策略,用于追踪被诊断为性传播感染(STI)的人的性伴侣。它旨在通过治疗确诊者及其性伴侣来阻断STI传播链,防止再次感染。在许多资源有限的环境中,最不有效但最常见的伴侣通知策略被称为“患者转诊”。这包括性保健提供者鼓励被诊断者向其潜在的性伴侣提供“伴侣通知单”,并说服他们接受治疗。这项研究试图更好地了解年轻人的伴侣通知经历,特别是他们在患者转诊过程中面临的风险和挑战。在津巴布韦,所有参加社区性健康和生殖健康服务的被诊断为性传播疾病的年轻人(16-24岁)都接受了咨询,并获得了PN单,这使他们的伴侣能够在该服务中获得免费治疗。接受研究人员培训的年轻人采访了41名被诊断为STI的年轻人,以探索他们的伴侣通知经历。只有一小部分(5.7%)的偷工减料者的伴侣参加了治疗服务。大多数参与者认为他们没有准备、技能或资源说服伴侣寻求治疗。许多人描述了在伴侣通知期间和之后的负面经历,包括关系破裂、名誉受损和身体暴力。这些发现表明,我们应该重新考虑伴侣通知是否适合或有效地用于年轻人。我们应该探索不给年轻人的社会、情感和身体安全与福祉带来风险的替代方法。
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引用次数: 0
Adapting to a global pandemic: a qualitative assessment of programmatic responses to COVID-19 in the multi-country Women's Integrated Sexual Health (WISH) programme. 适应全球大流行:对多国妇女综合性健康(WISH)计划中应对新冠肺炎的方案进行定性评估。
IF 6 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 Epub Date: 2023-10-13 DOI: 10.1080/26410397.2023.2260174
Katy Footman, Pippa Page, Victoria Boydell, Megan McLaren, Sandra Mudhune

The COVID-19 pandemic caused significant disruption to sexual and reproductive health and rights (SRHR) globally but there is little published evidence on the COVID-19 response of SRHR programmes, or lessons learned through their adaptations. To document the COVID-19 response of a global SRHR programme (the Women's Integrated Sexual Health programme), in-depth interviews were conducted between April and July 2021 with 22 key informants from implementing partners in Sierra Leone, Ethiopia and central or regional offices, the UK Foreign, Commonwealth and Development Office and the third-party monitoring partner. Framework analysis methods were used. Several rapid COVID-19 adaptations were identified: the development of crisis management and communication teams; increased partnership and engagement with government; reduced contact and risk in service delivery; reformulated community mobilisation; flexible performance management and remote methods of quality assurance; and sharing of learnings alongside the development of new guidance and tools. Throughout the pandemic, the programme was able to continue high-quality service delivery, though equity goals proved more difficult to reach. Challenges included the continually changing environment, competing pressures on governments, burdensome reporting, and staff burnout. The pandemic response was facilitated by prior experience of health emergencies, strong government relationships, a supportive workforce and some pre-existing approaches, tools, and systems. This study has identified important lessons that can inform programming in future crises, including the need for immediate recognition of SRHR as essential, sustained support for staff, use of multiple mechanisms to reach marginalised groups, adequate funding for equity goals, and a better balance between the burden of reporting and accountability needs.

新冠肺炎大流行对全球性健康和生殖健康与权利(SRHR)造成了重大破坏,但几乎没有公开的证据表明性健康和生育健康与权利方案对新冠肺炎的反应,或通过其改编吸取的经验教训。为了记录全球性健康和生殖健康方案(妇女综合性健康方案)对新冠肺炎的反应,在2021年4月至7月期间,对来自塞拉利昂、埃塞俄比亚和中央或区域办事处的执行伙伴、英国外交、联邦和发展办公室以及第三方监测伙伴的22名关键线人进行了深入采访。采用了框架分析方法。确定了新冠肺炎的几种快速适应:危机管理和沟通团队的发展;加强与政府的伙伴关系和参与;减少服务提供中的接触和风险;重新制定的社区动员;灵活的绩效管理和远程质量保证方法;在制定新的指导方针和工具的同时分享经验教训。在整个疫情期间,该计划能够继续提供高质量的服务,尽管公平目标更难实现。挑战包括不断变化的环境、政府面临的竞争压力、繁重的报告和员工倦怠。先前的卫生紧急情况经验、强有力的政府关系、支持性的劳动力以及一些预先存在的方法、工具和系统为应对疫情提供了便利。这项研究确定了可以为未来危机中的方案制定提供信息的重要经验教训,包括需要立即承认SRHR是必不可少的,对工作人员的持续支持,使用多种机制来接触边缘化群体,为公平目标提供充足的资金,以及在报告负担和问责需求之间更好地平衡。
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引用次数: 0
The effectiveness of combined approaches towards improving utilisation of adolescent sexual and reproductive health services in Kenya: a quasi-experimental evaluation. 肯尼亚提高青少年性健康和生殖健康服务利用率的综合方法的有效性:一项准实验性评估。
IF 6 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 Epub Date: 2023-10-04 DOI: 10.1080/26410397.2023.2257073
Lilian Mutea, Justinah Maluni, Mark Kabue, Vincent Were, Susan Ontiri, Kristien Michielsen, Peter Gichangi

Adolescent sexual and reproductive health (ASRH) services are key to improving the health of adolescents. This study aimed to establish the effectiveness of an intervention that combined activities in health facilities and communities in Kenya to increase utilisation of ASRH services. A quasi-experimental evaluation design was used to assess the effectiveness of the intervention. Using a stratified cluster sampling approach, two cross-sectional household surveys targeting girls aged 15-19 were conducted at baseline (September 2019) and endline (December 2020) in intervention and comparison. We combined the difference-in-difference approach to analyse the net change in outcomes between intervention and comparison arms of the study at baseline and endline and coarsened exact matching for variables that were significantly different to address the imbalance. There were a total of 1011 participants in the intervention arm and 880 in the comparison arm. Descriptive results showed a net increase of 12.7% in intervention sites in the knowledge of misconceptions about sex, pregnancy, and contraception, compared to 10.4% in the control site. In the multivariate regression analysis, two outcomes remained significant: decreases in adolescents' discomfort when seeking ASRH services because of either fear of parents (aPR = 0.58, 95% CI = 0.42-0.79, P = 0.001) or a lack of support from their partner (aPR = 0.25, 95% CI = 0.08-0.82, P = 0.023). The intervention combining a facility and community approach was not effective in increasing the use of ASRH information and services. Possible reasons for this are explored.

青少年性健康和生殖健康服务是改善青少年健康的关键。这项研究旨在确定将肯尼亚卫生设施和社区的活动相结合的干预措施的有效性,以提高ASRH服务的利用率。采用准实验评估设计来评估干预的有效性。采用分层整群抽样方法,在基线(2019年9月)和终点(2020年12月)进行了两项针对15-19岁女孩的横断面家庭调查,以进行干预和比较。我们将差异中的差异方法结合起来,分析研究干预组和对照组在基线和终点的结果净变化,并对显著不同的变量进行粗略的精确匹配,以解决不平衡问题。干预组共有1011名参与者,对照组共有880名参与者。描述性结果显示,干预地点对性、怀孕和避孕的误解知识净增加12.7%,而对照地点为10.4%。在多元回归分析中,有两个结果仍然显著:青少年在寻求ASRH服务时因害怕父母而感到不适的情况减少(aPR = 0.58,95%CI = 0.42-0.79,P = 0.001)或缺乏伴侣的支持(aPR = 0.25,95%CI = 0.08-0.82,P = 0.023)。设施和社区相结合的干预措施在增加ASRH信息和服务的使用方面并不有效。对此可能的原因进行了探讨。
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引用次数: 0
Setting research priorities for prevention and response to child marriage in communities in the Arab region: findings from a multi-stage Delphi study involving practitioners across the region. 确定阿拉伯地区社区预防和应对童婚的研究重点:来自该地区从业人员的多阶段德尔菲研究的结果。
IF 6 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-12-01 Epub Date: 2023-11-27 DOI: 10.1080/26410397.2023.2275840
Janna Metzler, Aisha Hutchinson, Katrina Kiss

Globally, more than 12 million girls under the age of 18 are forced to marry every year. Progress on ending child marriage in the Arab region is slowing, and risks being reversed, due to an increase in conflict-affected populations and widespread economic crisis. The aim of this paper is to consider the research priorities across the region to inform effective and accelerated child marriage prevention and response programming within the Arab region. Seventy-three specialists supporting child marriage prevention and response programming in the Arab region engaged with up to three phases of an online Delphi consultation process on research gaps and the research environment between July 2019 and December 2021. Proposals of research gaps were elicited, reviewed, and rated by participants to confirm a shared learning agenda. Participants identified 50 different research gaps across 7 main areas, reaching a high level of consensus support for 23 of 50 statements. Clear consensus was reached in relation to an increased need to produce and use evidence to support programme development, and further research on specific drivers and consequences of child marriage. The least consensus was found in relation to how research can inform prevention and response efforts within the law and legal system. The results provide the foundation of a child marriage research agenda for the Arab region which takes into account regional distinctiveness and builds on the global momentum for child marriage research. Mechanisms are in place to do this through the Regional Action Forum, and other networks across the region.

在全球范围内,每年有超过1200万18岁以下的女孩被迫结婚。由于受冲突影响人口的增加和广泛的经济危机,阿拉伯地区在消除童婚方面的进展正在放缓,并有逆转的风险。本文的目的是考虑整个区域的研究重点,以便为阿拉伯区域内有效和加速的童婚预防和应对规划提供信息。在2019年7月至2021年12月期间,73名支持阿拉伯地区童婚预防和应对规划的专家就研究差距和研究环境进行了多达三个阶段的在线德尔菲咨询。研究差距的建议由参与者引出,审查和评分,以确定共享的学习议程。参与者在7个主要领域确定了50个不同的研究差距,对50个陈述中的23个达成了高度一致的支持。会议在以下方面达成了明确的共识:更需要编制和使用证据来支持方案制定,并进一步研究童婚的具体驱动因素和后果。在研究如何在法律和法律制度范围内为预防和应对工作提供信息方面达成的共识最少。这些结果为阿拉伯区域的童婚研究议程提供了基础,该议程考虑到区域特殊性,并以全球童婚研究的势头为基础。通过区域行动论坛和整个区域的其他网络,已经建立了这样做的机制。
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引用次数: 0
Donors: curious connections in donor conception 捐赠者:捐赠者概念中的奇怪联系
IF 6 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2023-09-01 DOI: 10.1080/26410397.2023.2245617
Jung Chen
This is an important book in the field of studying reproduction and health, and a timely response to the social changes following the policy shift that abolished the anonymity of gamete donors. Many scholars have been looking at relevant issues, mostly in relation to donor-recipient people, yet less attention has been paid to donors and their families. Petra Nordqvist and Leah Gilman examine gamete donors’ experiences from a relational perspective. Donors: Curious Connections in Donor Conception aims to explore the effects of changes in the legal, social, cultural, and technological context at this specific historical moment on people who have been or are considering becoming gamete (sperm or ovum) donors and how they make sense of the connections with the donorconceived children and the families. The shift from donor anonymity to traceability in the UK, which began in 2005, signifies a great transition from secrecy to openness in terms of the identity of people who donate sperm and ova. This regulatory change is the response to donorconceived people’s campaign for openness and the right for them to contact donors after they reach the age of 18 (p. 16). It has resulted in a new protocol for clinical practice in reproductive medicine and reflects wider sociocultural changes. By depicting donors’ lived experiences, Donors explains “the broader shift in donor conception practices and cultures” as the consent donor policy enacted and, at the same time, the emerging use of the Internet and social media to perform informal donation (p. 211). Thus, Donors examins both people who participate in donations in clinics, and those who donate informally, who are already acquainted with recipient parents. By looking at various donations, Donors captures how people perceive donation differently through investigating donors’ experiences as well as their relationships and their personal lives. With the expansion of reproductive gamete donation in the UK and worldwide, increasing research interests have been addressed around recipients, including recipient parents and donor-conceived children. However, there is a shortage of scholarly literature on the donor families and their relationships, especially research conducted via qualitative approaches, which can give a more in-depth understanding of how donation decisions shape donors’ lives and those with whom they share connections. Methodologically, Petra Nordqvist and Leah Gilman explore gamete donors’ experiences from a relational perspective and employ the personal life approach in sociology, to explore how social policies impact on people’s perceptions of connectedness. Donors sees gamete donation as a reflection of practices and relatedness negotiations, as well as a response to shifting social and political agendas. In the Introduction, the authors begin with the story of a sperm donor, Zak, to bring out the pressing questions: What does it mean to be a donor? (p. 1) How does that affect the donor, and their f
这是研究生殖与健康领域的一本重要书籍,也是对废除配子捐献者匿名的政策转变后的社会变化的及时回应。许多学者一直在研究相关问题,主要是与捐赠者和接受者有关的问题,但对捐赠者及其家人的关注较少。Petra Nordqvist和Leah Gilman从关系的角度研究配子捐献者的经历。捐赠者:捐赠者概念中的好奇联系旨在探索在这一特定历史时刻,法律、社会、文化和技术背景的变化对已经或正在考虑成为配子(精子或卵子)捐赠者的人的影响,以及他们如何理解与捐赠者所生子女和家庭的联系。从2005年开始,英国从捐赠者匿名向可追踪的转变,标志着捐赠精子和卵子的人的身份从保密向公开的巨大转变。这种监管变化是对捐赠者倡导的开放运动的回应,以及他们在年满18岁后联系捐赠者的权利(第16页)。它产生了一个新的生殖医学临床实践方案,并反映了更广泛的社会文化变化。通过描述捐赠者的生活经历,捐赠者解释了随着同意捐赠者政策的颁布,以及互联网和社交媒体进行非正式捐赠的新兴用途,“捐赠者概念实践和文化的更广泛转变”(第211页)。因此,捐赠者既要检查在诊所参与捐赠的人,也要检查那些已经认识受赠父母的非正式捐赠者。通过观察各种捐赠,捐赠者通过调查捐赠者的经历、他们的关系和个人生活,了解人们对捐赠的不同看法。随着生殖配子捐赠在英国和世界范围内的扩大,越来越多的研究兴趣围绕接受者展开,包括接受者的父母和捐赠者怀上的孩子。然而,缺乏关于捐赠者家庭及其关系的学术文献,尤其是通过定性方法进行的研究,这些研究可以更深入地了解捐赠决策如何影响捐赠者的生活以及他们与哪些人有共同关系。在方法论上,Petra Nordqvist和Leah Gilman从关系的角度探讨配子捐献者的经历,并运用社会学中的个人生活方法,探讨社会政策如何影响人们对连通性的感知。捐赠者将配子捐赠视为实践和相关谈判的反映,也是对不断变化的社会和政治议程的回应。在引言中,作者从精子捐献者Zak的故事开始,提出了紧迫的问题:作为捐献者意味着什么?(第1页)这对捐赠者、他们的家人以及他们生活中的其他相关关系有何影响?(第2页)第一章首先描述了英国“身份释放政策”产生的法律变化的历史背景。这项研究是捐赠者所基于的,应用了定性社会学方法,对精子和卵子捐赠者、23名捐赠者亲属、,以及2017年至2021年帮助捐赠过程的医疗专业人员和顾问(第11页,第233页)。第2章通过默认地关注从采访中选出的10个故事,详细阐述了不同捐赠在匿名或公开生活经历方面的意义,而不是通常在诊所内定义并贴上捐赠者标签的静态类别。捐赠者建议用更动态的“途径”概念取代捐赠的类型:身份释放途径,即BOOKSHELF
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引用次数: 0
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Sexual and Reproductive Health Matters
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