second trimester

中期妊娠
  • 文章类型: Journal Article
    妊娠期糖尿病(GDM)是一种高血糖状态,通常通过口服葡萄糖耐量试验(OGTT)来诊断,这是令人不快的,耗时,重现性低,结果很慢。已提出用于改善GDM诊断的机器学习(ML)预测模型通常基于花费数小时才能产生结果的仪器方法。近红外(NIR)光谱是一种简单的,快,以及从未评估过GDM预测的低成本分析技术。本研究旨在开发基于近红外光谱的GDMML预测模型,并根据其预测能力和分析持续时间评估其作为早期检测或替代筛查工具的潜力。通过NIR光谱分析妊娠的前三个月(GDM诊断前)和第二个三个月(GDM诊断时)的血清样品。考虑了四个光谱范围,并对每种进行了80种数学预处理。使用单块和多块ML技术建立了基于NIR数据的模型。每个模型都经过双重交叉验证。第一和第二三个月的最佳模型在接收器工作特性曲线下的面积分别为0.5768±0.0635和0.8836±0.0259。这是第一项报告基于近红外光谱的GDM预测方法的研究。开发的方法允许仅在32分钟内从10µL血清中预测GDM。它们很简单,快,并在临床实践中具有巨大的应用潜力,特别是作为GDM诊断的OGTT的替代筛查工具。
    Gestational diabetes mellitus (GDM) is a hyperglycemic state that is typically diagnosed by an oral glucose tolerance test (OGTT), which is unpleasant, time-consuming, has low reproducibility, and results are tardy. The machine learning (ML) predictive models that have been proposed to improve GDM diagnosis are usually based on instrumental methods that take hours to produce a result. Near-infrared (NIR) spectroscopy is a simple, fast, and low-cost analytical technique that has never been assessed for the prediction of GDM. This study aims to develop ML predictive models for GDM based on NIR spectroscopy, and to evaluate their potential as early detection or alternative screening tools according to their predictive power and duration of analysis. Serum samples from the first trimester (before GDM diagnosis) and the second trimester (at the time of GDM diagnosis) of pregnancy were analyzed by NIR spectroscopy. Four spectral ranges were considered, and 80 mathematical pretreatments were tested for each. NIR data-based models were built with single- and multi-block ML techniques. Every model was subjected to double cross-validation. The best models for first and second trimester achieved areas under the receiver operating characteristic curve of 0.5768 ± 0.0635 and 0.8836 ± 0.0259, respectively. This is the first study reporting NIR-spectroscopy-based methods for the prediction of GDM. The developed methods allow for prediction of GDM from 10 µL of serum in only 32 min. They are simple, fast, and have a great potential for application in clinical practice, especially as alternative screening tools to the OGTT for GDM diagnosis.
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  • 文章类型: Journal Article
    背景这项研究探讨了妊娠中期孕妇牙周健康与特定血液生物标志物之间的复杂关系。它特别关注白细胞介素-6(IL-6)的水平,乳酸脱氢酶(LDH),与健康对照组相比,患有慢性牙周炎的患者的C反应蛋白(CRP)。方法采用详细的方法,根据是否存在慢性牙周炎,将60名孕妇分为两组。在60名孕妇中,30人患有慢性牙周炎,而其他30人作为对照组,从学院的常规患者人群中选择。该研究利用血液样本分析和先进的统计工具进行数据分析,确保准确可靠的结果。IL-6、LDH、与健康对照组相比,检查了患有慢性牙周炎的患者的CRP。结果发现IL-6、LDH、两组CRP水平比较。患有慢性牙周炎的女性表现出明显更高水平的这些生物标志物。统计分析加强了这些差异的有效性,强调其意义。结论该研究强调了高水平的IL-6,LDH,和CRP和孕妇慢性牙周炎的存在。这些生物标志物作为早期检测和监测牙周健康的潜在指标出现。
    Background The research delves into the intricate relationship between periodontal health and specific blood biomarkers in pregnant women during their second trimester. It specifically focuses on the levels of interleukin-6 (IL-6), lactate dehydrogenase (LDH), and C-reactive protein (CRP) in those suffering from chronic periodontitis compared to healthy controls. Methodology A detailed approach was taken involving 60 pregnant women categorized into two groups based on the presence or absence of chronic periodontitis. Out of 60 pregnant women, 30 had chronic periodontitis, while the other 30 served as controls selected from the regular patient population of the college. The study utilized blood sample analysis and advanced statistical tools for data analysis, ensuring precise and reliable results. Levels of IL-6, LDH, and CRP in those suffering from chronic periodontitis compared to healthy controls were checked. Results The findings revealed a notable variance in IL-6, LDH, and CRP levels between the two groups. Women with chronic periodontitis exhibited significantly higher levels of these biomarkers. The statistical analysis reinforced the validity of these differences, highlighting their significance. Conclusions The study underscored a clear link between higher levels of IL-6, LDH, and CRP and the presence of chronic periodontitis in pregnant women. These biomarkers emerge as potential indicators for early detection and monitoring of periodontal health in this demographic.
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  • 文章类型: Journal Article
    目的:比较经阴道(TV)和经腹(TA)超声评估孕中期胎儿畸形时的宫颈长度(CL)。
    方法:这是一项前瞻性研究,包括在意大利两个胎儿医学中心的低风险超声诊所就诊的连续孕妇。纳入标准为妊娠19+0至22+0周的女性,到产前超声诊所进行常规的孕中期筛查胎儿畸形。主要结果是将在电视上获得的CL测量值与TA超声进行比较;次要结果是报告用两种不同方法测量的CL的观察者之间和观察者之间的变异性。所有女性都接受了由两名经验丰富的认证操作员对子宫颈进行的电视和TA评估,对彼此视而不见。使用类内相关系数(ICC)和Bland-Altman分析来分析数据。
    结果:两百五十名妇女被纳入分析。所有妇女都有前子宫。超声检查时的平均胎龄为20.7±0.7周;19周时进行了1.2%(3/250)的扫描,20周时49.2%(123/250),妊娠21周时为44.8%(112/250),妊娠22周时为4.8%(12/250)。在所有纳入的病例中,都可以在TA超声下识别CL的主要标志。在TA测量的CL之间有很好的可靠性(观察者1的ICC0.95,95%CI0.93-0.97和0.92%,观察者2的95%CI0.89-0.94)和电视超声0.97,观察者1的95%CI0.96-0.98和观察者2的0.96,95%CI0.95-0.97)。对于CL的TA和TV评估,两位观察员之间也具有良好的可靠性。观察者1的平均TACL为41.4±5.5,观察者2的平均TACL为40.5±4.8,两次测量之间没有显着差异(平均差0.92mm,95%CI-9.7至11.2)。同样,两位观察者在电视超声下测得的CL之间没有差异(平均差-0.83mm,95%CI-5.97至4.30)。最后,与TV相比,TA测量的平均CL没有差异,要么考虑女性的总人口(平均差:-0.43,955CI-8.65至7.79),或根据奇偶校验状态和操作员对分析进行分层时。
    结论:在经验丰富的操作员中,在常规异常扫描胎儿异常时,TV和TA超声对CL的评估没有差异.
    OBJECTIVE: To compare transvaginal (TV) and trans-abdominal (TA) ultrasound assessment of cervical length (CL) at the time of the second-trimester scan for fetal anomalies.
    METHODS: This was a prospective study including consecutive pregnant women attending the low-risk ultrasound clinic of two fetal medicine centres in Italy. The inclusion criteria were women between 19 + 0 and 22 + 0 weeks of gestation, attending the prenatal ultrasound clinic for the routine second trimester screening for fetal anomalies. The primary outcome was to compare the CL measurement obtained at TV compared to TA ultrasound; the secondary outcome was to report the inter and intra-observer variability of CL measured with the two different approaches. All women underwent TV and TA assessment of the cervix performed by two experienced certified operators, blinded to each other. Intra-class correlation coefficients (ICC) and Bland-Altman analyses were used to analyse the data.
    RESULTS: Two hundred and fifty women were included in the analysis. All women had anteverted uterus. The mean gestational age at ultrasound was 20.7 ± 0.7 weeks; 1.2 % (3/250) scans were performed at 19 weeks, 49.2 % (123/250) at 20 weeks, 44.8 % (112/250) at 21 weeks and 4.8 % (12/250) at 22 weeks of gestations. Identification of the major landmarks of CL at TA ultrasound was achieved in all the included cases. There was good reliability between CL measured at TA (ICC 0.95, 95 % CI 0.93-0.97 for observer 1 and 0.92 %, 95 % CI 0.89-0.94 for observer 2) and TV ultrasound 0.97, 95 % CI 0.96-0.98 for observer 1 and 0.96, 95 % CI 0.95-0.97 for observer 2). There was also good reliability between the two observers for both the TA and TV assessment of the CL. Mean TA CL was 41.4 ± 5.5 for observer 1 and 40.5 ± 4.8 for observer 2 with no significant differences between the two measurements (mean difference 0.92 mm, 95 % CI -9.7 to 11.2). Likewise, there was no difference between the CL measured at TV ultrasound between the two observers (mean difference -0.83 mm, 95 % CI -5.97 to 4.30). Finally, there was no difference in the mean CL measured at TA compared to TV, either considering the overall population of women (mean difference: -0.43, 955 CI -8.65 to 7.79), or when stratifying the analysis according to the parity status and the operator.
    CONCLUSIONS: Among experienced operators, there was no difference between TV and TA ultrasound assessment of the CL at the time of the routine anomaly scan for fetal anomaly.
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  • 文章类型: Randomized Controlled Trial
    评估堕胎后护理任务共享的研究主要集中在妊娠早期的妇女,许多研究缺乏定性成分。我们旨在与医生相比,评估使用助产士提供的米索前列醇治疗不完全妊娠中期流产的患者可接受性,并对乌干达患者的生活治疗经验有了更深入的了解。
    我们的混合方法研究结合了来自随机对照等效试验的1140个结构化访谈数据,以及在乌干达14个公共卫生机构接受米索前列醇治疗的中期妊娠不完全流产妇女的深度访谈(n=28)。可接受性,我们的主要结果,在14天的随访中使用结构化问卷作为复合变量进行测量:1)治疗经验(如预期/好于预期/差于预期),和2)满意度-如果患者会向朋友推荐治疗或再次选择方法。我们使用广义混合效应模型来获得助产士和医生组之间可接受的流产后护理的风险差异。我们对定性数据采用归纳内容分析。
    从2018年8月14日至2021年11月16日,我们评估了7190名妇女的资格,并随机分配了1191名妇女(593名助产士和598名医生)。我们成功随访了1140名妇女和1071名(94%),发现治疗可接受。两组之间调整后的风险差异为1.2%(95%CI,-1.2至3.6%),并且在我们预定义的-5至+5%的等效范围内。治疗成功,治疗后感到平静和安全提高了可接受性,而副作用和令人担忧的出血模式的经验降低了满意度。
    与医生相比,由助产士提供护理时,米索前列醇治疗无并发症的妊娠中期不完全流产的妇女同样且高度可接受。在缺乏足够的医生人员配备水平或助产士可以提供米索前列醇的环境中,与助产士共享孕中期医疗PAC的任务增加了患者获得堕胎后护理服务的机会。
    ClinicalTrials.govNCT03622073。
    大约9.6%的堕胎相关死亡发生在撒哈拉以南非洲。如果避免意外怀孕,这些死亡是可以预防的,妇女可以在国家法律的期望范围内获得安全堕胎,并公平提供堕胎后护理(PAC)服务。先前的研究表明,在怀孕的头三个月有流产并发症的妇女可以由助产士或医生用米索前列醇治疗。助产士和医生之间的任务共享是安全的,有效,并且可以接受。然而,妊娠中期任务分担的证据存在差距。检查中孕期任务分担的实用性,我们的目的是评估患者接受由助产士提供的米索前列醇治疗不完全妊娠中期流产的可接受性,并对患者的生活治疗经验有了更深入的了解。因此,我们的研究结合了定量和定性方法。与医生相比,由助产士提供的米索前列醇治疗妊娠中期不完全流产的妇女可接受性同样可接受。治疗成功,治疗后感到平静和安全,增加了可接受性,而副作用和令人担忧的出血模式的经验降低了满意度。为妇女提供咨询可以解决其中一些问题,因为它提供了保证并减少了焦虑。在缺乏足够的医生人员配备水平或助产士可以提供米索前列醇的环境中,与助产士共享孕中期医疗PAC的任务增加了患者对PAC服务的访问。
    Studies evaluating task sharing in postabortion care have mainly focused on women in first trimester and many lack a qualitative component. We aimed to evaluate patient acceptability of treatment of incomplete second trimester abortion using misoprostol provided by midwives compared with physicians and also gained a deeper understanding of the patients\' lived treatment experiences in Uganda.
    Our mixed methods study combined 1140 structured interview data from a randomized controlled equivalence trial and in-depth interviews (n = 28) among women managed with misoprostol for second trimester incomplete abortion at 14 public health facilities in Uganda. Acceptability, our main outcome, was measured at the 14-day follow-up visit using a structured questionnaire as a composite variable of: 1) treatment experience (as expected/ better than expected/ worse than expected), and 2) satisfaction - if patient would recommend the treatment to a friend or choose the method again. We used generalized mixed effects models to obtain the risk difference in acceptable post abortion care between midwife and physician groups. We used inductive content analysis for qualitative data.
    From 14th August 2018 to 16th November 2021, we assessed 7190 women for eligibility and randomized 1191 (593 to midwife and 598 to physician). We successfully followed up 1140 women and 1071 (94%) found the treatment acceptable. The adjusted risk difference was 1.2% (95% CI, - 1.2 to 3.6%) between the two groups, and within our predefined equivalence range of - 5 to + 5%. Treatment success and feeling calm and safe after treatment enhanced acceptability while experience of side effects and worrying bleeding patterns reduced satisfaction.
    Misoprostol treatment of uncomplicated second trimester incomplete abortion was equally and highly acceptable to women when care was provided by midwives compared with physicians. In settings that lack adequate staffing levels of physicians or where midwives are available to provide misoprostol, task sharing second trimester medical PAC with midwives increases patient\'s access to postabortion care services.
    ClinicalTrials.gov NCT03622073.
    Approximately 9.6% of abortion-related deaths occur in Sub-Saharan Africa. These deaths can be prevented if unintended pregnancies are avoided, women can access safe abortions within the expectations of the country’s laws, and post abortion care (PAC) services are provided equitably. Previous research shows that women with abortion complications in the first trimester of pregnancy can be treated with misoprostol by either midwives or physicians. This sharing of tasks between the midwives and physicians is safe, effective, and acceptable. However, there is a gap in evidence on task sharing in the second trimester. To check practicability of task sharing in second trimester, we aimed to evaluate patient acceptability of treatment of incomplete second trimester abortion using misoprostol provided by midwives compared with physicians and also gained a deeper understanding of the patients’ lived treatment experiences. Our study therefore combined quantitative and qualitative approaches. Women’s acceptability of misoprostol treatment for incomplete second trimester abortion was found to be equally acceptable when provided by midwives compared with physicians. Treatment success, feeling calm and safe after treatment increased acceptability, while experience of side effects and worrying bleeding patterns reduced satisfaction. Counselling of women may address some of these problems since it provides reassurance and reduces anxiety. In settings that lack adequate staffing levels of physicians or where midwives are available to provide misoprostol, task sharing second trimester medical PAC with midwives increases patient’s access to PAC services.
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  • 文章类型: Randomized Controlled Trial
    据报道,终止妊娠中期妊娠的产妇发病率和死亡率比终止妊娠中期妊娠高3-5倍。医疗方法已经过全面评估,被认为是安全堕胎护理的基础。Howevere,关于在瘢痕子宫中诱导中期妊娠流产的理想方法,全球尚无共识。这项研究的目的是以更少的母体并发症的快速方式实现阴道排出。共有158名妇女,既往剖腹产经历过中期妊娠终止的病史,随机分为组(1)阴道米索前列醇组(n=79)或组(2)联合宫颈内foley\'s导管加静脉催产素输注组(n=79)。主要终点是胎儿完全排出。同时,次要结局是产妇并发症的发生率,就保留的受孕产物(ERPOC)的手术疏散需求而言,严重出血,子宫破裂,输血,宫颈裂伤,腹泻,呕吐和发烧。此试验的注册号https://clinicaltrials.gov/ct2/show/NCT04501809。这项研究表明,宫颈内foley导管和催产素的联合使用是一种有效的,和阴道米索前列醇的安全替代品,用于终止先前剖腹产的妇女的中期妊娠。影响声明为什么进行这项研究?这项研究的目的是通过机械和药理相结合的方法在疤痕子宫中快速分娩以终止中期妊娠,而不会导致明显的发病率。医生应平衡以快速方式实现阴道拔除的益处与子宫破裂或任何其他母体并发症的风险。这项研究表明,机械和药理学相结合的方法终止妊娠的中期妊娠与阴道米索前列醇具有相当的疗效和安全性,这对于资源匮乏的国家来说是更负担得起的,因为在疤痕子宫中终止妊娠仍然增加了孕产妇发病率。这项研究对临床实践有什么意义?与阴道米索前列醇相比,联合使用宫颈内Foley导管与静脉内催产素输注是一种更安全的选择,其产妇并发症较少。
    Second trimester pregnancy termination has been reported to be associated with 3-5 times higher maternal morbidity and mortality risks more than first trimester termination. Medical methods had been thoroughly assessed and it is considered the anchor of the safe abortion care. Howevere, there is no global agreement regarding the ideal method for induction of the second trimester abortion in a scarred uterus. The aim of this study was to achieve vaginal expulsion in an expeditious manner with less maternal complications. A total of 158 women having, a history of previous caesarean section undergoing second trimester pregnancy termination, were randomly allocated into group (1) vaginal misoprostol group (n = 79) or group (2) combined intracervical foley\'s catheter plus intravenous oxytocin infusion group (n = 79). The primary endpoint was complete fetal expulsion. Meanwhile, secondary outcomes were the rates of maternal complications, in terms of the need for surgical evacuation of retained product of conception (ERPOC), severe haemorrhage, uterine rupture, blood transfusion, cervical laceration, diarrhoea, vomiting and fever. The registration number of this trial https://clinicaltrials.gov/ct2/show/NCT04501809. This study showed that the combined use of intracervical foley\'s catheter and oxytocin is an effective, and safe alternative to vaginal misoprostol for termination of the second trimester pregnancy in women having a previous caesarean delivery.Impact statementWhy was this study conducted? The purpose of this study is to achieve an expeditious delivery for second trimester pregnancy termination in a scarred uterus by combined mechanical and pharmacological methods without significant morbidity. Physicians should balance the benefit of achieving vaginal exlpusion in an expeditious manner versus the risk of uterine rupture or any other maternal complications.What does this add to what is known? This study showed that a combined mechanical and pharmacolohical approach for second trimester termination of pregnancy has comparable efficacy and safety to vaginal misoprostol which is more affordable to the low resources countries where termination of pregnancy in a scarred uterus still has an increased maternal morbidity.What is the implication of this study on clinical practice? The combined use of intracervical foley\'s catheter with intravenous oxytocin infusion is a safer option than vaginal misoprostol with less serious maternal complications.
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  • 文章类型: Clinical Trial
    背景:抗甲状腺过氧化物酶抗体(TPOAb)阳性有助于抑制甲状腺素合成。肠道微生物群可以与代谢或免疫疾病相互作用。然而,在TPOAb阳性/阴性亚临床甲状腺功能减退症(TPOAb+/TPOAb-SCH)的女性患者中,从妊娠中期(T2)到妊娠中期(T3)的肠道菌群动态尚未见报道.因此,我们旨在评估肠道菌群是否可以成为管理TPOAb+SCH的潜在治疗靶点.
    方法:在这项单中心前瞻性队列研究中,我们通过对T2(20-23+6周)和T3(28-33+6周)收集的粪便样本中的16SrRNA进行测序,观察了肠道微生物群动态.TPOAb+/TPOAb-SCH根据他们在怀孕期间是否使用左甲状腺素(LT4)(LT4+/LT4-)进行分层。使用QIIME2进行微生物组生物信息学分析。线性判别分析效应大小(LEfSe)用于生物标志物的定量分析。用PICRUSt2进行功能分析。
    结果:在TPOAb-(n=68)和TPOAb+(n=64)SCH组中观察到从T2到T3的不同肠道微生物群动态。TPOAb+LT4-组的特征在于富集的细菌扩增子序列变体(ASV)的Prevotella在T2和细菌,湖水螺旋藻,落叶松科,Blautia,和T3中的Agathobacter和耗尽的γ变形杆菌的ASV,肠杆菌,T2和放线菌的肠杆菌科,科氏杆菌,放线菌,Coriobacteriales,双歧杆菌,双歧杆菌科,双歧杆菌,多雷亚形族,T3中长双歧杆菌。TPOAb+LT4+组的特征是布劳特氏菌的富集细菌ASV,唾液链球菌,和T3中长双歧杆菌和耗尽的拟杆菌ASV,细菌,拟杆菌,T2中的Prevotella和T3中的Agathobacter。此外,我们确定了53种主要涉及糖的代谢功能,脂质,和氨基酸代谢。
    结论:我们的结果表明,从T2到T3,肠道菌群组成的低动力学和其代谢功能的高动力学与TPOAbSCH有关。我们得出结论,肠道菌群可能是治疗妊娠期TPOAbSCH的新靶点。
    背景:本研究于2021年6月10日在中国临床试验注册中心(注册号ChiCTR2100047175)进行了回顾性注册。
    BACKGROUND: Anti-thyroid peroxidase antibody (TPOAb) positivity can contribute to inhibit thyroxine synthesis. Gut microbiota can interact with metabolic or immune diseases. However, dynamics of gut microbiota from the second (T2) to the third trimester (T3) in women with TPOAb-positive/negative subclinical hypothyroidism (TPOAb+/TPOAb- SCH) have not been reported. Therefore, we aimed to evaluate whether gut microbiota can be potential therapeutic targets for managing TPOAb+ SCH.
    METHODS: In this single-center prospective cohort study, we observed gut microbiota dynamics by sequencing 16S rRNA from fecal samples collected in T2 (20-23+ 6 weeks) and T3 (28-33+ 6 weeks). TPOAb+/TPOAb- SCH were stratified depending on whether or not they used levothyroxine (LT4) during the pregnancy (LT4+/LT4-). Microbiome bioinformatics analyses were performed using QIIME2. The linear discriminant analysis effect size (LEfSe) was used for the quantitative analysis of biomarkers. Functional profiling was performed with PICRUSt2.
    RESULTS: Distinct gut microbiota dynamics from T2 to T3 were noted in the TPOAb- (n = 68) and TPOAb+ (n = 64) SCH groups. The TPOAb+ LT4- group was characterized by enriched bacterial amplicon sequence variants (ASVs) of Prevotella in T2 and Bacteria, Lachnospirales, Lachnospiraceae, Blautia, and Agathobacter in T3 and by depleted ASVs of Gammaproteobacteria, Enterobacterales, and Enterobacteriaceae in T2 and Actinobacteriota, Coriobacteriia, Actinobacteria, Coriobacteriales, Bifidobacteriales, Bifidobacteriaceae, Bifidobacterium, Dorea formicigenerans, and Bifidobacterium longum in T3. The TPOAb+ LT4+ group was characterized by enriched bacterial ASVs of Blautia, Streptococcus salivarius, and Bifidobacterium longum in T3 and by depleted ASVs of Bacteroidota, Bacteroidia, Bacteroidales, and Prevotella in T2 and Agathobacter in T3. Moreover, we identified 53 kinds of metabolic functions that were mainly involved in sugar, lipid, and amino acid metabolism.
    CONCLUSIONS: Our results indicated that low dynamics of gut microbiota composition and high dynamics of its metabolic function from T2 to T3 were associated with TPOAb+ SCH. We concluded that gut microbiota could be new targets for treatment of TPOAb+ SCH during pregnancy.
    BACKGROUND: This study was retrospectively registered at the Chinese Clinical Trial Registry (registration number ChiCTR2100047175 ) on June 10, 2021.
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  • 文章类型: Journal Article
    孕妇发生亚临床甲状腺功能减退症(SCH)的风险很高,抗甲状腺过氧化物酶抗体(TPOAb)阳性可进一步抑制甲状腺素的合成。新的证据表明,肠道菌群可以调节代谢和免疫稳态。TPOAb阳性孕妇妊娠中期的肠道菌群特征尚未见报道。这项单中心前瞻性观察队列研究使用16SrRNA基因测序研究了75名TPOAb阳性SCH女性和90名TPOAb阴性SCH女性在妊娠中期的粪便样本中的肠道微生物组成和代谢功能。妇女不接受左甲状腺素(LT4)治疗,低剂量LT4(≤50ug/d),或高剂量LT4(>50ug/d)。分类分析表明,厚壁菌和拟杆菌是主要的门,其次是放线菌和变形菌。粪杆菌,拟杆菌,普雷沃氏菌9号,双歧杆菌,下颗粒,落叶螺旋体,Megamonas是主要的属。未接受LT4的TPOAb阳性SCH女性的肠道菌群的特征在于富含下颗粒属的细菌扩增子序列变体(ASV)/操作分类单位(OTU)。接受低剂量或高剂量LT4的TPOAb阳性SCH女性的肠道菌群的特征是细菌ASV/OTU耗尽了Ruminococussp。_或拟南芥,分别。肠道菌群共有19种代谢功能,主要涉及脂质和氨基酸代谢,区分TPOAb阳性和TPOAb阴性的SCH女性。我们的研究表明,在妊娠中期,接受不同剂量LT4治疗的TPOAb阳性和TPOAb阴性的SCH女性的肠道菌群组成和代谢功能存在差异。这些发现提供了对肠道菌群作为治疗妊娠期TPOAb阳性SCH女性的新靶标的见解。
    Pregnant women are at high risk of developing subclinical hypothyroidism (SCH), and anti-thyroid peroxidase antibody (TPOAb) positivity can further inhibit thyroxine synthesis. Emerging evidence indicates that intestinal flora can modulate metabolic and immune homeostasis. The characteristics of intestinal flora of TPOAb-positive women with SCH in their second trimester of pregnancy have not been reported. This single-center prospective observational cohort study investigated gut microbial composition and metabolic function using sequencing of the 16S rRNA gene in fecal samples from 75 TPOAb-positive women with SCH and 90 TPOAb-negative women with SCH during their second trimester of pregnancy. Women were treated with no levothyroxine (LT4), low-dose LT4 (≤50ug/d), or high-dose LT4 (>50ug/d). Taxonomic analysis showed Firmicutes and Bacteroidetes were the dominant phyla, followed by Actinobacteria and Proteobacteria. Faecalibacterium, Bacteroides, Prevotella 9, Bifidobacterium, Subdoligranulum, Lachnospira, and Megamonas were the predominant genera. The intestinal flora of TPOAb-positive women with SCH who received no LT4 was characterized by bacterial amplicon sequence variants (ASVs)/operational taxonomic units (OTUs) enriched in the genus Subdoligranulum. The intestinal flora of TPOAb-positive women with SCH who received low-dose or high-dose LT4 were characterized by bacterial ASVs/OTUs depleted of the species Ruminococcus sp._or Bacteroides massiliensis, respectively. A total of 19 metabolic functions of intestinal flora, mainly involving lipid and amino acid metabolism, discriminated TPOAb-positive and TPOAb-negative women with SCH. Our study suggests that there are differences in the composition and metabolic function of intestinal flora of TPOAb-positive and TPOAb-negative women with SCH treated with different doses of LT4 in the second trimester of pregnancy. The findings provide insight into intestinal flora as novel targets for the treatment of TPOAb-positive women with SCH during pregnancy.
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  • 文章类型: Journal Article
    目的:比较阴道使用米索前列醇与静脉(IV)催产素在孕中期宫内死亡(IUFD)中终止妊娠的成功率。
    方法:这是一项针对106例妊娠中期IUFD女性的开放标签随机对照研究。患者被随机分为两组:给予阴道米索前列醇的女性(每6小时至48小时400mcg)与给予IV催产素的女性(从50个单位开始,最多300个单位)。当一线治疗(如上所述)失败时,治疗方法相互替代。当二线治疗失败时,患者接受了扩张和疏散。
    结果:米索前列醇与催产素的一线治疗成功率分别为88.7%和73.7%,分别(p=0.047)。在一线治疗失败的人中,二线治疗的成功率为85.7%,而米索前列醇与催产素相比为83.3%(p=0.891).最初接受米索前列醇与催产素治疗后,一线治疗成功的女性的平均诱导分娩时间为28.72和20.55小时,分别(p<0.001)。在二线治疗期间,米索前列醇与催产素组之间的平均间期无显著差异(p=0.128).没有观察到严重的不良事件。
    结论:阴道米索前列醇作为一线治疗时,其终止率高于催产素,无不良事件。当用作二线治疗时,两种方法的成功率相同。
    OBJECTIVE: To compare the success rate of vaginal misoprostol versus intravenous (IV) oxytocin in termination of pregnancy in the second trimester intrauterine fetal death (IUFD).
    METHODS: This was an open-label randomized controlled study for 106 women with second trimester IUFD. Patients were randomly divided into two groups: women given vaginal misoprostol (400 mcg every 6 h up to 48 h) versus those given IV oxytocin (starting with 50 units up to a maximum of 300 units). When the first-line treatment (as mentioned above) failed, treatment methods were replaced with each other. When the second-line treatment failed, the patients underwent dilation and evacuation.
    RESULTS: The first-line treatment yielded the successful rate of 88.7% versus 73.7% for misoprostol versus oxytocin, respectively (p = 0.047). Among those with first-line treatment failure, the second-line treatment yielded success rate of 85.7% versus 83.3% for misoprostol versus oxytocin (p = 0.891). The mean duration of induction to delivery in women with successful response to first-line treatment was 28.72 and 20.55 h after initially receiving misoprostol versus oxytocin, respectively (p < 0.001). While during second-line treatment, this mean interval was not significantly different among those with misoprostol versus oxytocin (p = 0.128). No severe adverse events were observed.
    CONCLUSIONS: Vaginal misoprostol was associated with higher termination rate than oxytocin without adverse events when used as the first-line treatment. Both methods yielded the same success rate when used as the second-line treatment.
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  • 文章类型: Journal Article
    Intrauterine growth restriction is associated with an increased risk of cardiovascular changes neonatally. However, the underlying pathways are poorly understood, and it is not clear whether the dysfunction is already present in the fetus.
    This study aimed to investigate fetal cardiac dimensions assessed from images at the second trimester anatomy scan from fetuses classified postnatally as small for gestational age and intrauterine growth restricted and compare them with appropriate for gestational age fetuses.
    This was a substudy from The Copenhagen Baby Heart Study, a prospective, multicenter cohort study including fetuses from the second trimester of pregnancy in Copenhagen from April 2016 to October 2018. The mothers were recruited at the second trimester anatomy scan that included extended cardiovascular image documentation followed by consecutively measured heart biometry by 2 investigators blinded for the pregnancy outcome. The fetuses were classified postnatally as small for gestational age and intrauterine growth restricted according to the International Society of Ultrasound in Obstetrics and Gynecology 2020 guidelines using birthweight and with a retrospective assessment of Doppler flow. The mean differences in the cardiovascular biometry were adjusted for gestational age at the time of the second trimester scan and the abdominal circumference. The z-scores were calculated, and the comparisons were Bonferroni corrected (significance level of P<.005). Receiver operating characteristic curves were computed after performing backward regression on several maternal characteristics and biomarkers.
    We included 8278 fetuses, with 625 (7.6%) of them being small for gestational age and 289 (3.5%) being intrauterine growth restricted. Both small for gestational age and intrauterine growth restricted fetuses had smaller heart biometry, including the diameter at the location of the aortic valve (P<.005), the ascending aorta in the 3-vessel view (P<.005), and at the location of the pulmonary valve (P<.005). The intrauterine growth restricted group had significantly smaller hearts with respect to length and width (P<.005) and smaller right and left ventricles (P<.005). After adjusting for the abdominal circumference, the differences in the aortic valve and the pulmonary valve remained significant in the intrauterine growth restricted group. Achievement of an optimal receiver operating characteristic curve included the following parameters: head circumference, abdominal circumference, femur length, gestational age, pregnancy associated plasma protein-A multiples of median, nullipara, spontaneous conception, smoking, body mass index <18.5, heart width, and pulmonary valve with an area under the curve of 0.91 (0.88-0.93) for intrauterine growth restricted cases.
    Intrauterine growth restricted fetuses had smaller prenatal cardiovascular biometry, even when adjusting for abdominal circumference. Our findings support that growth restriction is already associated with altered cardiac growth at an early stage of pregnancy. The heart biometry alone did perform well as a screening test, but combined with other factors, it increased the sensitivity and specificity for intrauterine growth restriction.
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  • 文章类型: Journal Article
    目的:这项研究的目的是比较标准超声(US)估计胎儿体重(EFW)和MRI体积衍生方法对中期胎儿的影响。
    方法:25个配对的US和MRI扫描计算了EFW(胎龄[GA]范围=20-26周)。评估了每种方法的观察者内部和观察者之间的变异性(2个操作员/模式)。对5例早产(平均GA29+3周)的胎儿进行了小的亚分析,并与实际出生体重进行了比较。
    结果:在中期妊娠胎儿中,两个MRI容积EFW公式与US相比测量不足-10.9%和-14.5%(p<0.001),但具有出色的观察者内和观察者之间的一致性(组内相关系数=0.998和0.993)。在早产胎儿中,MRI体积得出的EFW(MRI-EFW)与实际预期出生体重(在扫描GA时)之间的平均相对差异(MRD)为-13.7%(-159.0g,95%CI:-341.7至23.7g)和-17.1%(-204.6g,95%CI:-380.4至-28.8g),对于2个MRI公式。美国的MRD较小,为5.3%(69.8克,95%CI:-34.3至173.9)。
    结论:MRI-EFW结果在妊娠中期应谨慎解释。尽管观察者与MRI容量非常一致,在孕中期需要完善EFW配方,对于小胎儿和GA和早产胎儿,以补偿较低的胎儿密度。
    OBJECTIVE: The aim of this study was to compare the standard ultrasound (US) estimated fetal weight (EFW) and MRI volume-derived methods for the midtrimester fetus.
    METHODS: Twenty-five paired US and MRI scans had the EFW calculated (gestational age [GA] range = 20-26 weeks). The intra- and interobserver variability of each method was assessed (2 operators/modality). A small sub-analysis was performed on 5 fetuses who were delivered preterm (mean GA 29 +3 weeks) and compared to the actual birthweight.
    RESULTS: Two MRI volumetry EFW formulae under-measured compared to US by -10.9% and -14.5% in the midpregnancy fetus (p < 0.001) but had excellent intra- and interobserver agreement (intraclass correlation coefficient = 0.998 and 0.993). In the preterm fetus, the mean relative difference (MRD) between the MRI volume-derived EFW (MRI-EFW) and actual expected birthweight (at the scan GA) was -13.7% (-159.0 g, 95% CI: -341.7 to 23.7 g) and -17.1% (-204.6 g, 95% CI: -380.4 to -28.8 g), for the 2 MRI formulae. The MRD was smaller for US at 5.3% (69.8 g, 95% CI: -34.3 to 173.9).
    CONCLUSIONS: MRI-EFW results should be interpreted with caution in midpregnancy. Despite excellent observer agreement with MRI volumetry, refinement of the EFW formula is needed in the second trimester, for the small and for the GA and preterm fetus to compensate for lower fetal densities.
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