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The first International Association of Diabetes and Pregnancy Study Groups summit on the diagnosis of gestational diabetes in early pregnancy: TOBOGM Summit Report. 首届国际糖尿病与妊娠研究小组协会妊娠早期妊娠糖尿病诊断峰会:TOBOGM 峰会报告。
IF 1.7 4区 医学 Q2 Medicine Pub Date : 2024-04-18 DOI: 10.1111/ajo.13823
Arianne Sweeting, Freya MacMillan, David Simmons

The first International Association of Diabetes and Pregnancy Study Groups Summit on the diagnosis of gestational diabetes in early pregnancy (Treatment of Booking Gestational Diabetes Mellitus (TOBOGM) Summit) was held on the 17 November 2022 in Sydney, Australia. It sought to use the TOBOGM trial findings to scope the issues involved with early screening, to inform future discussions over possible approaches for diagnosing gestational diabetes mellitus (GDM) in early pregnancy. Most delegates supported testing for early GDM using a one-step 75 g oral glucose tolerance test approach with Canadian Diabetes Association criteria preferred, but highlighted the importance of considering resources, cost, consumer perspectives and equity in translating TOBOGM results into a clinical approach to screening for, and diagnosing, early GDM.

首届国际糖尿病与妊娠研究小组协会妊娠早期糖尿病诊断峰会(Treatment of Booking Gestational Diabetes Mellitus (TOBOGM) Summit)于2022年11月17日在澳大利亚悉尼举行。会议旨在利用 TOBOGM 试验的结果来探讨早期筛查所涉及的问题,为今后讨论诊断孕早期妊娠糖尿病(GDM)的可行方法提供参考。大多数与会代表支持采用一步法 75 克口服葡萄糖耐量试验检测早期 GDM,并首选加拿大糖尿病协会的标准,但强调在将 TOBOGM 试验结果转化为筛查和诊断早期 GDM 的临床方法时,必须考虑资源、成本、消费者观点和公平性等因素。
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引用次数: 0
Reply to perinatal outcomes after regional analgesia during labour 对分娩区域镇痛后围产期结果的答复
IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-04-17 DOI: 10.1111/ajo.13811
Kara Thompson, Nisha Khot
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引用次数: 0
Editor-in-chief's introduction to ANZJOG 64(2) ANZJOG 64(2)主编简介
IF 1.7 4区 医学 Q2 Medicine Pub Date : 2024-04-10 DOI: 10.1111/ajo.13818
Scott W. WHITE

Welcome to the April 2024 issue of ANZJOG. Thank you to the many contributors to ANZJOG who have submitted manuscripts and contributed to the peer review process as this maintains the journal as a source of robust clinical science for clinicians and researchers in Australia and New Zealand and further afield.

This issue begins with two stimulating articles about severe maternal morbidity. Most of us are fortunate to live and work in locations with historically low rates of maternal mortality, although there remain lessons to be learned and improvements to be made from the rare but tragic maternal deaths that still occur. Although there are robust and well-resourced processes for review of maternal mortality, the recognition, review and reporting of severe maternal morbidity are much less systematic, resulting in missed opportunities for the detection and improvement of system-level weaknesses which underlie preventable severe adverse maternal outcomes. The review by Frost et al. provides an excellent overview of the current situation of maternal morbidity review in Australia. The authors conclude by outlining a number of key steps towards implementing a systematic maternal morbidity review jurisdictionally and nationally.1 In their editorial, MacDonald et al. go further, calling upon us, clinicians and researchers, to make the case for progress in this area and to drive it.2 Major change will require policy and resource attention from government, but we can take valuable action prior to that: to demonstrate why this is important, our willingness to work towards improvements in maternal and related health outcomes and to spur policymakers into action.

This issue also includes reports of two randomised controlled trials. Fahy et al. present their trial of placental cord drainage at caesarean section.3 This practice has been shown to reduce the duration of the third stage of labour at vaginal birth although without a clinically significant reduction in blood loss. The authors compared placental cord drainage to delayed cord clamping at planned caesarean section, finding no significant differences between the two groups, and concluded that this study supports the routine use of delayed cord clamping.

The second trial compared sonographer-performed ultrasound-guided embryo transfer versus standard embryo transfer, including rates of intrauterine air bubble visualisation, clinical pregnancy and live birth as outcomes.4 Of these, only air bubble visualisation was significantly different between the groups, with sonographer-performed ultrasound proving beneficial. Given the resource implications of sonographer assistance and the lack of impact on clinical outcomes, this study does not provide compelling evidence to change standard practice in routine cases.

Two groups present systematic reviews of gynaecological interes

8 这一发现非常重要,因为它让我们了解到非高加索妇女死产率(尤其是晚期死产率)上升的机理,以及可以采取哪些策略来更好地识别高风险胎儿,从而有针对性地加强监测或采取其他预防措施。9 尽管这些证据表明,对这些家庭的护理还有待改进,但令人欣慰的是,所发现的主题与现有的丧亲护理临床指南密切相关。由此看来,通过进一步的教育和现有资源的实施,丧亲护理的改善是有可能实现的。
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引用次数: 0
A study protocol for live and deceased donor uterus transplantation as a treatment for women with uterine factor infertility 活体和死亡供体子宫移植治疗子宫因素性不孕妇女的研究方案。
IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-03-28 DOI: 10.1111/ajo.13810
Jana Pittman, Mats Brännström, Neill Keily, Brigitte Gerstl, Elena Cavazzoni, Henry Pleass, Mianna Lotz, Natasha Rogers, Germaine Wong, Wayne Hsueh, Ashraf Hanafy, Jason A. Abbott, Rebecca Deans

Aim

Uterus transplantation (UTx) is an emerging treatment option for women with uterine factor infertility (UFI) or the absence of a functional uterus. This is the study protocol for the first human UTx clinical trial in Australia.

Materials and Methods

This protocol outlines the approved training program used to plan, diagnose, screen, and treat patients who may be eligible for UTx using living and deceased donors. This multi-site clinical research study includes three tertiary hospital sites within New South Wales (NSW), Australia – Prince of Wales, Royal Hospital for Women and Westmead Hospitals. Our UTx protocol is based on that used by our collaborative partner, the inaugural UTx team in Gothenburg, Sweden. The Swedish UTx team provides ongoing preceptorship for the Australian UTx team. Ethics approval for six UTx procedures using living or deceased donors (Western Sydney Local Health District Human Research Ethics Committee: 2019/ETH138038) was granted in 2020.

Results

Results from surgeries and live births will be published. Data will be prospectively entered into the registry of the International Society of Uterus Transplantation (ISUTx), a sub-section of The Transplantation Society (TTS). Trial Id: ACTRN12622000917730.

Discussion

A multidisciplinary research team has been formed between three tertiary hospitals in Sydney – The Royal Hospital for Women, Prince of Wales and Westmead Hospitals; and with the Swedish UTx, University of Gothenburg. The Swedish team pioneered animal and human UTx studies since 1998, including publishing the first live birth after UTx. (1) This Australian trial commenced in January 2023.

Conclusion

Uterus transplantation gives women with UFI the opportunity to be gestational and genetic mothers. It is a complex procedure for both the donor and recipient, with medical and surgical risks. An extensive multidisciplinary approach is required to optimise patient safety and graft outcomes. This protocol outlines our Australian UTx team strategy for screening, recruitment, surgical approach, and clinical management of UTx recipients and donors.

目的:子宫移植(UTx)是治疗子宫因素性不孕(UFI)或无功能性子宫妇女的一种新兴治疗方法。这是澳大利亚首例人类子宫移植临床试验的研究方案:本方案概述了已获批准的培训计划,用于计划、诊断、筛选和治疗可能符合使用活体和死亡供体进行UTx的患者。这项多站点临床研究包括澳大利亚新南威尔士州(NSW)的三家三级医院--威尔士王子医院、皇家妇女医院和韦斯特米德医院。我们的UTx方案是基于我们的合作伙伴--瑞典哥德堡的首家UTx团队所使用的方案。瑞典UTx团队为澳大利亚UTx团队提供持续的指导。使用活体或死亡供体进行的六项UTx程序获得了伦理批准(西悉尼地方卫生区人类研究伦理委员会,2019/ETH138038):结果:将公布手术和活产的结果。数据将前瞻性地录入国际子宫移植学会(ISUTx)的登记册,该学会是移植学会(TTS)的一个分会:ACTRN12622000917730.Discussion:悉尼三家三级医院--皇家妇女医院、威尔士亲王医院和韦斯特米德医院,以及瑞典哥德堡大学UTx共同组成了一个多学科研究小组。自 1998 年以来,瑞典团队率先开展了动物和人类UTx 研究,包括发表了第一例UTx 后的活产婴儿。(1)这项澳大利亚试验于2023年1月开始:结论:子宫移植为患有子宫内膜异位症的妇女提供了成为妊娠母亲和遗传母亲的机会。对于供体和受体来说,这是一项复杂的手术,存在医疗和手术风险。需要采用广泛的多学科方法来优化患者安全和移植结果。本方案概述了澳大利亚UTx团队对UTx受体和供体进行筛选、招募、手术方法和临床管理的策略。
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引用次数: 0
Severe maternal morbidity – we need more action to prevent harm 严重的孕产妇发病率--我们需要采取更多行动来预防伤害。
IF 1.7 4区 医学 Q2 Medicine Pub Date : 2024-03-28 DOI: 10.1111/ajo.13813
Evelyn Jane MacDonald, Beverley Lawton, Francesca Storey, Kendall Stevenson, John David Tait, Peter Stone

Reviewing severe maternal morbidity (SMM) is considered a marker of the quality of maternity care, as in high income countries (HIC) maternal mortality is thankfully now rare.1 SMM disrupts maternal (and wider family) wellbeing, causing considerable personal and public cost. SMM preventability review has the potential to reduce this and the associated harm. To do this, we must identify its occurrence, review these cases, and analyse findings to develop appropriate system improvements.

As Joanne Frost and her colleagues in this current Australian and New Zealand Journal of Obstetrics and Gynaecology state, there is currently no national consensus or agreement in Australia on terms to use, definitions to follow and therefore no ability to compare inter-state data on the rates and causes of SMM. There is also no defined process to assess preventability in Australia and without this at the outset it is difficult to see how change would be effected. While in Aotearoa (New Zealand), our Health Research Council has previously funded research to enable national SMM preventability reviews, across both countries there appears to be no will by our respective governments to provide ongoing funding to enable routine SMM preventability reviews to take place.2 No funding is currently available at regional, state, or national levels, and there is no apparent plan for these reviews to become ‘business as usual’. This is regrettable, as opportunities are being missed to improve poor maternal and baby outcomes.

There is no global agreement on how to define and implement SMM or maternal near-miss (MNM) reviews. There is not even agreement on what to call it. Professor Marion Knight stated four years ago in an editorial for another equally high-quality journal, – ‘As we publish yet more studies (re)defining severe maternal morbidity, should we be questioning whether it is time to draw a line on this research waste and instead initiate a truly international consensus process?’3

And ‘ay, there is the rub’.4 How do we initiate a ‘truly international consensus process’? A systematic review of global practices in monitoring of MNM/SMM showed inconsistencies in monitoring with low /middle income countries (LIC/MIC) using predominantly the World Health Organization (WHO) definition of MNM and tools, and high-income countries (HIC) using the SMM definition tools such as the Geller tool for reviewing preventability. The authors concluded that global standardising was ‘not feasible at this time’.5 Even a good news recent systemic review and meta-analysis of the WHO MNM criteria uptake in LIC showed that despite good uptake in these countries enabling some intercountry comparisons, there was still the need in individual countries for contextual adaptations.6

Surely the conversation needs to change. A se

20、21 由于脐带间质瘤与婴儿不良预后之间存在明显联系,一些司法管辖区开始将可预防性审查扩展到整个围产期--从妊娠、分娩到新生儿预后。与非SMM病例相比,SMM病例的死胎率、早产率、低出生体重率和新生儿重症监护室(NICU)入院率都更高。22-25 让Frost等人的论文和本社论成为一项紧急行动呼吁--一项专门针对澳大拉西亚的行动呼吁。我们--临床医生、研究人员和政策制定者--都知道,对SMM进行多学科、非惩罚性的可预防性审查是可能的,也是我们所需要的,而且可以提出改变政策、实施临床指南、改善临床教育和卫生系统的建议。选择一个定义,与一个多学科团队建立一个流程,使用一个经过验证的工具,然后开始审核 SMM 病例。关于如何建立 SMM 可预防性审查,文献中介绍了几种工具和指南。27-29 当然,我们不会捕捉到所有病例,但我们必须从某个地方开始。我们在奥特亚罗亚开展的 SMM 研究病例已去除种族标识,以最大限度地减少病例审查中的无意识偏见--这是首个在此过程中解决种族主义问题的全国性 SMM 研究。29 重要的是,研究结果以土著非赤字为重点,强调了改善护理、减少 SMM 和减少不公平结果的系统改进机会。将这些方法纳入 SMM 审查(如去标识种族),是解决不平等问题的必要步骤。根据我们在奥特亚罗瓦(当时有 20 个卫生区)进行 SMM 可预防性审查的经验,将全国各地的产科、麻醉科、重症监护室和其他临床医生聚集在一起产生了多种积极的连锁反应:增进了同事间的尊重;建立了专业关系;临床医生将从参与审查中获得的经验和建议带回自己的部门和专业团体进行传播。考虑研究资助机会,探索 SMM 可预防性审查的各个方面,并/或进一步扩展到围产期的连续性。加入围产期和生殖正义联盟(www.perinataljustice.org)等国际联盟,游说各方提供文化安全、顺应需求的孕产妇护理途径,以消除可预防的伤害和死亡。当然,作为研究人员和临床医生,我们必须在各个层面、利用各种机会游说我们各自的政策资助者,使这项旨在改善孕产妇预后的质量措施得到应有的认可和资助。
{"title":"Severe maternal morbidity – we need more action to prevent harm","authors":"Evelyn Jane MacDonald,&nbsp;Beverley Lawton,&nbsp;Francesca Storey,&nbsp;Kendall Stevenson,&nbsp;John David Tait,&nbsp;Peter Stone","doi":"10.1111/ajo.13813","DOIUrl":"10.1111/ajo.13813","url":null,"abstract":"<p>Reviewing severe maternal morbidity (SMM) is considered a marker of the quality of maternity care, as in high income countries (HIC) maternal mortality is thankfully now rare.<span><sup>1</sup></span> SMM disrupts maternal (and wider family) wellbeing, causing considerable personal and public cost. SMM preventability review has the potential to reduce this and the associated harm. To do this, we must identify its occurrence, review these cases, and analyse findings to develop appropriate system improvements.</p><p>As Joanne Frost and her colleagues in this current <i>Australian and New Zealand Journal of Obstetrics and Gynaecology</i> state, there is currently no national consensus or agreement in Australia on terms to use, definitions to follow and therefore no ability to compare inter-state data on the rates and causes of SMM. There is also no defined process to assess preventability in Australia and without this at the outset it is difficult to see how change would be effected. While in Aotearoa (New Zealand), our Health Research Council has previously funded research to enable national SMM preventability reviews, across both countries there appears to be no will by our respective governments to provide ongoing funding to enable routine SMM preventability reviews to take place.<span><sup>2</sup></span> No funding is currently available at regional, state, or national levels, and there is no apparent plan for these reviews to become ‘business as usual’. This is regrettable, as opportunities are being missed to improve poor maternal and baby outcomes.</p><p>There is no global agreement on how to define and implement SMM or maternal near-miss (MNM) reviews. There is not even agreement on what to call it. Professor Marion Knight stated four years ago in an editorial for another equally high-quality journal, – ‘As we publish yet more studies (re)defining severe maternal morbidity, should we be questioning whether it is time to draw a line on this research waste and instead initiate a truly international consensus process?’<span><sup>3</sup></span></p><p>And ‘ay, there is the rub’.<span><sup>4</sup></span> How do we initiate a ‘truly international consensus process’? A systematic review of global practices in monitoring of MNM/SMM showed inconsistencies in monitoring with low /middle income countries (LIC/MIC) using predominantly the World Health Organization (WHO) definition of MNM and tools, and high-income countries (HIC) using the SMM definition tools such as the Geller tool for reviewing preventability. The authors concluded that global standardising was ‘not feasible at this time’.<span><sup>5</sup></span> Even a good news recent systemic review and meta-analysis of the WHO MNM criteria uptake in LIC showed that despite good uptake in these countries enabling some intercountry comparisons, there was still the need in individual countries for contextual adaptations.<span><sup>6</sup></span></p><p>Surely the conversation needs to change. A se","PeriodicalId":55429,"journal":{"name":"Australian & New Zealand Journal of Obstetrics & Gynaecology","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ajo.13813","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140319895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Health needs, treatment decisions and experience of traditional complementary and integrative medicine use by women with diminished ovarian reserve: A cross-sectional survey 卵巢储备功能减退妇女的健康需求、治疗决定以及使用传统补充和综合疗法的经验:一项横断面调查。
IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-03-21 DOI: 10.1111/ajo.13805
Alison Maunder, Susan Arentz, Mike Armour, Michael F Costello, Carolyn Ee

Background

Women with diminished ovarian reserve (DOR) have fewer eggs than would be expected at their age. It is estimated that 10% of women seeking fertility treatment are diagnosed with DOR. However, the success rate of medically assisted reproduction (MAR) is significantly lower in women with DOR, thus many seek additional approaches.

Aim

To explore the health needs of women with DOR, treatment options and experience of treatment including traditional complementary integrative medicine (TCIM).

Methods

Anyone with a diagnosis of DOR, living in Australia or New Zealand, aged over 18 were invited to complete an online survey distributed via fertility support networks and social media platforms from April to December 2021.

Results

Data from 67 respondents were included. The main aspects of health that were impacted by DOR were fertility (91.0%) and mental health (52.2%). The main treatment recommended was MAR with most women either currently using MAR (38.8%) or having previously used MAR (37.3%). TCIM was widely used with 88.1% of women utilising supplements, 74.6% consulting with TCIM practitioners, and 65.7% adopting self-care practices. The main reasons for using TCIM were to improve fertility or support pregnancy, and to support general health and well-being.

Conclusions

Women with DOR have additional health needs apart from infertility, most notably mental health support. The main form of treatment utilised is MAR, despite DOR being challenging for fertility clinicians. TCIM was widely used, and respondents perceived benefits related to improving fertility, supporting pregnancy, or improving well-being through use of acupuncture, meditation, naturopathy, massage, yoga.

背景:卵巢储备功能减退(DOR)妇女的卵子数量比其年龄预期的要少。据估计,在寻求生育治疗的妇女中,有 10% 被诊断出患有 DOR。目的:探讨患有 DOR 的妇女的健康需求、治疗选择和治疗经验,包括传统补充综合医学(TCIM):方法:2021 年 4 月至 12 月期间,通过生育支持网络和社交媒体平台,邀请任何被诊断出患有 DOR、居住在澳大利亚或新西兰、年龄超过 18 岁的女性完成在线调查:67 名受访者的数据被纳入调查。受 DOR 影响的主要健康方面是生育能力(91.0%)和心理健康(52.2%)。建议的主要治疗方法是 MAR,大多数妇女目前正在使用 MAR(38.8%)或曾经使用过 MAR(37.3%)。TCIM 被广泛使用,88.1% 的妇女使用补充剂,74.6% 的妇女向 TCIM 从业人员咨询,65.7% 的妇女采用自我保健方法。使用TCIM的主要原因是为了提高生育能力或帮助怀孕,以及促进一般健康和幸福:结论:患有 DOR 的妇女除不孕症外,还有其他健康需求,其中最主要的是心理健康支持。尽管 DOR 对不孕不育临床医生来说具有挑战性,但使用的主要治疗形式是 MAR。TCIM 被广泛使用,受访者认为其益处与改善生育能力、支持怀孕或通过使用针灸、冥想、自然疗法、按摩和瑜伽改善身心健康有关。
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引用次数: 0
Improving accuracy of outcome prediction for infants born extremely preterm using a digital tool: Translating ‘NIC-PREDICT’ into clinical practice, the first steps 利用数字工具提高极早产儿预后预测的准确性:将 "NIC-PREDICT "转化为临床实践的第一步
IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-03-01 DOI: 10.1111/ajo.13808
Rosemarie A. Boland, Jeanie L.Y. Cheong, Michael J. Stewart, Stefan C. Kane, Lex W. Doyle

Background

Many clinicians overestimate mortality and disability rates in infants born extremely preterm. We developed a digital tool (‘NIC-PREDICT’) that predicts infant mortality and survival with and without major disability in infants born 23–27 weeks' gestation.

Aims

To determine if clinicians could use NIC-PREDICT accurately, and if their perceptions of infant outcomes improved after its release in 2021.

Materials and Methods

Midwives, nurses, obstetricians, neonatologists and paediatricians working in tertiary and non-tertiary hospitals in Victoria were asked to use NIC-PREDICT to estimate three mutually exclusive outcomes: (i) mortality; (ii) survival free of major disability; and (iii) survival with major disability for six different scenarios where a liveborn infant was offered survival-focused care after birth. The proportions who completed the survey (responded to all six scenarios) and the proportions able to provide 100% accurate results for all scenarios were determined. Estimates of the three outcomes were compared with true rates.

Results

A total of 85 clinicians responded: 70 (82%) completed the survey, with an overall accuracy of 76%. Overall, predictions of mortality were accurate (mean difference from true value 0.7% (95% confidence interval (CI) −0.7, 2.1) P = 0.33), as were predictions of survival without major disability (mean difference − 0.7 (95% CI –3.0, 1.7) P = 0.58). However, survival with major disability was overestimated by 4.9% ((95% CI 1.7, 8.0) P = 0.003).

Conclusions

Most perinatal clinicians who responded used NIC-PREDICT correctly to estimate expected outcomes in infants born extremely preterm who are offered intensive care. Undue pessimism about survival with major disability remains an ongoing concern.

许多临床医生高估了极早产儿的死亡率和残疾率。我们开发了一种数字工具("NIC-PREDICT"),可预测妊娠 23-27 周出生婴儿的死亡率和存活率,以及有无严重残疾。
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引用次数: 0
Colposcopy performance in the new primary HPV screening in Australia: How to determine colposcopy competency? 澳大利亚新的 HPV 初筛中阴道镜检查的表现:如何确定阴道镜检查能力?
IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-03-01 DOI: 10.1111/ajo.13807
Jeffrey H.J. Tan, Deborah Neesham, Rebecca A. Szabo, Natalia Khomko, Desiree Yap, C. David H. Wrede

Aims

To assess colposcopic performance and determine indicators for competency within the new Australian primary human papillomavirus (HPV) cervical screening program.

Materials and methods

A retrospective observational study of 4542 women seen at The Royal Women's Hospital Colposcopy Clinic in Melbourne, from 1 December 2017 to 31 July 2020 after a higher-risk cervical screening test (CST) result.

Results

Histological CIN2+ was detected in 25.1% up to two years from first colposcopy visit (FCV). The majority (86.7%) of CIN2+ was detected early within the first six months of presentation. Biopsy rate overall was 96.1% with abnormal colposcopic impression. Of four colposcopists with a lower biopsy rate, only one was able to achieve this early detection rate. Biopsy was also taken in over 30% of cases with negative reflex cytology and normal colposcopy, with CIN2+ detected in 5.0% among positive HPV16/18 and 3.8% with non-16/18 HPV. Positive predictive value of high-grade colposcopic impression at FCV averaged 66.4% (range: 54.9–81.6% among our colposcopists) and is poorly correlated with early detection rate of CIN2+. Overall accuracy of colposcopy is 84.5% (range: 78.7–90.3%), buoyed by high true negative colposcopic predictions secondary to high rates of negative reflex cytology referral with the new screening algorithm and is also unlikely to be a useful colposcopy indicator.

Conclusions

Early detection rate of CIN2+ within the first six months of presentation is a useful measure of colposcopy competency and we would encourage our National Cancer Screening Register to explore this with the participating colposcopists.

目的:评估阴道镜的性能,并确定澳大利亚新的初级人类乳头瘤病毒(HPV)宫颈筛查计划的能力指标:对2017年12月1日至2020年7月31日期间在墨尔本皇家妇女医院阴道镜诊所就诊的4542名妇女进行回顾性观察研究:在首次阴道镜检查(FCV)后的两年内,25.1%的患者被检测出组织学CIN2+。大部分(86.7%)CIN2+是在就诊后六个月内早期发现的。阴道镜印象异常的活检率为 96.1%。在活检率较低的四位阴道镜医生中,只有一位能达到这一早期发现率。在反射细胞学阴性和阴道镜检查正常的病例中,超过 30% 的病例也进行了活检,在 HPV16/18 阳性病例中,有 5.0% 检测出 CIN2+,在 HPV16/18 非阳性病例中,有 3.8% 检测出 CIN2+。FCV 阴道镜检查高级别阴道印象的阳性预测值平均为 66.4%(阴道镜医师的预测值范围为 54.9%-81.6%),与 CIN2+ 的早期检出率关系不大。阴道镜检查的总体准确率为 84.5%(范围:78.7%-90.3%),这得益于新筛查算法的高反射性细胞学阴性转诊率所带来的高阴道镜真阴性预测,而且也不太可能成为阴道镜检查的有用指标:我们鼓励全国癌症筛查注册机构与参与筛查的阴道镜医师共同探讨这一问题。
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引用次数: 0
‘I was able to make a better decision about my health.’ Wāhine experiences of colposcopy at a marae-based health clinic: A qualitative study 我能够对自己的健康做出更好的决定。妇女在马拉维医疗诊所接受阴道镜检查的经历:定性研究。
IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-02-29 DOI: 10.1111/ajo.13803
Judy Ormandy, Simon Phillips, Maringikura Campbell, Bernie Haenga-Melvin, Luana Phillips-Govind, Sara Filoche

Background

Equitable access to colposcopy services is required if we are to realise the benefit of the introduction of human papilloma virus (HPV) screening in Aotearoa New Zealand. We piloted a community colposcopy clinic, co-located at an urban marae health clinic.

Aim

To describe the experiences of wāhine (women) attending the marae-based colposcopy clinic.

Methods

An in-depth reflexive thematic analysis from 34 people's accounts was undertaken.

Results

Five themes were identified from the experiences of wāhine attending the clinic. Three themes related to how having a local clinic supported access: everyone was welcoming and friendly, the environment was familiar and non-clinical and the clinic was accessible. The fourth theme related to how this contributed to agency. A fifth theme relates to wāhine views about informing the ongoing provision of colposcopy services. The experiences reflected the principles and values practised at the marae health clinic. Wāhine described feeling cared for as soon as they entered the clinic. As the clinic was local, and for some based at their marae, it was a known space where they knew the experience would be safe. Whānau were welcome with spaces for children to play. Being local meant there were fewer logistics to manage, all of which supported access.

Discussion

Prioritising wāhine through the provision of culturally safe and accessible colposcopy is feasible. It has the potential to contribute to the elimination of cervical cancer in Aotearoa, New Zealand.

背景:如果我们要在新西兰奥特亚罗瓦实现人类乳头瘤病毒(HPV)筛查的益处,就需要公平地获得阴道镜检查服务。我们在一个城市的Marae健康诊所试办了社区阴道镜检查诊所。目的:描述在Marae阴道镜检查诊所就诊的妇女的经历:方法:对 34 人的叙述进行深入的反思性主题分析:结果:从就诊妇女的经历中确定了五个主题。其中三个主题与当地诊所如何支持就诊有关:每个人都热情友好,环境熟悉且非临床,诊所方便就诊。第四个主题与这如何促进代理有关。第五个主题涉及妇女对持续提供阴道镜检查服务的看法。这些经历反映了Marae健康诊所所奉行的原则和价值观。妇女们描述了她们一进入诊所就感受到的关怀。由于诊所就在当地,而且对一些人来说,诊所就在他们的部落里,这是一个众所周知的空间,他们知道在这里就医是安全的。这里有供儿童玩耍的空间,也欢迎土著人前来就诊。本地化意味着需要管理的后勤工作更少,所有这些都有助于儿童的参与:讨论:通过提供文化上安全和方便的阴道镜检查来优先考虑妇女是可行的。它有可能为消除新西兰奥特亚罗瓦地区的宫颈癌做出贡献。
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引用次数: 0
Efficacy and feasibility of the RADA16 self-assembling peptide, PuraStat® for haemostasis in laparoscopic gynaecological surgery: A pilot study RADA16 自组装肽 PuraStat® 用于腹腔镜妇科手术止血的有效性和可行性:试点研究。
IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-02-29 DOI: 10.1111/ajo.13798
Philip Hall

Bleeding after laparoscopic gynaecological surgery remains a potential complication. We assessed RADA16 (PuraStat®), a topical self-assembling peptide haemostatic agent, in a pilot study of 46 women undergoing laparoscopic gynaecological surgery. The primary outcome was intraoperative haemostatic efficacy for resection site bleeding. Haemostasis was achieved in all intraoperative bleeding situations (40/40 participants: 100%) with no clinically significant surgical bed bleeding or complications. Mean volume and time required to achieve haemostasis were 6 mL and 14 sec, respectively. This study suggests that PuraStat® is a safe, effective haemostatic agent in laparoscopic gynaecological surgery. Randomised controlled trials are warranted to confirm these findings.

腹腔镜妇科手术后出血仍是一种潜在的并发症。我们在一项试点研究中评估了 RADA16(PuraStat®),这是一种局部自组装多肽止血剂,有 46 名妇女接受了腹腔镜妇科手术。主要结果是切除部位出血的术中止血效果。在所有术中出血情况下(40/40 名参与者:100%)都能止血,没有出现临床上明显的手术床出血或并发症。止血的平均用量和所需时间分别为 6 毫升和 14 秒。这项研究表明,在腹腔镜妇科手术中,PuraStat® 是一种安全、有效的止血剂。有必要进行随机对照试验来证实这些研究结果。
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引用次数: 0
期刊
Australian & New Zealand Journal of Obstetrics & Gynaecology
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