fetofetal transfusion

胎儿输血
  • 文章类型: Journal Article
    由于胎盘血管吻合的存在,单绒毛膜双胞胎有并发症的风险,包括双胎输血综合征,双胎贫血-红细胞增多症序列,选择性胎儿生长受限,和双反向动脉灌注序列。虽然超声是筛查这些并发症发展的主要方式,MRI在评估单绒毛膜双胎妊娠其他并发症的发展中起着重要作用。比如神经损伤。在这篇文章中,作者回顾了与单绒毛膜双胞胎并发症相关的超声成像结果,管理选项,以及MRI在这些怀孕中的作用。
    Monochorionic twins are at risk for complications due to the presence of placental vascular anastomoses, including twin-twin transfusion syndrome, twin anemia-polycythemia sequence, selective fetal growth restriction, and twin reversed arterial perfusion sequence. While ultrasound is the primary modality to screen for the development of these complications, MRI plays an important role in assessing monochorionic twin pregnancies for the development of other complications, such as neurologic injury. In this article, the authors review the ultrasound imaging findings associated with monochorionic twin complications, management options, and the role for MRI in these pregnancies.
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  • 文章类型: Journal Article
    将机器学习应用于医学领域的主要障碍是训练图像的数据分布与诊所中遇到的数据之间的差异。这种现象可以通过不一致的采集技术和跨患者频谱的大变化来解释。结果是训练过的模型在临床上的翻译很差,这限制了它们在医疗实践中的实施。特定于患者的经过训练的网络可以提供潜在的解决方案。尽管由于与即时标签相关的费用,针对患者的方法通常不可行,使用生成对抗网络可以实现这种方法。本研究提出了一种基于生成对抗网络的针对患者的方法。在提出的培训管道中,用户使用极其有限的数据训练患者特定的分割网络,该网络补充了由生成对抗模型生成的人工样本。在胎儿镜激光凝固过程中捕获的内窥镜视频数据中证明了这种方法,一种通过切除胎盘血管治疗双胎对双胎输血综合征的方法。与标准的深度学习分割方法相比,与使用标准方法的100张图像相比,仅使用20张注释图像,管道就能够实现0.60的联合得分相交。此外,在不使用管道的情况下,用20个带注释的图像进行训练,获得了0.30的联合分数的交点,因此,对应于合并管道时性能的100%提高。使用GAN的管道用于生成补充真实数据的人工数据,这允许对分割网络进行患者特定的训练。我们表明,使用GAN生成的人工图像显着提高了血管分割的性能,并且训练患者特定的模型可以成为将自动血管分割带入临床的可行解决方案。
    A major obstacle in applying machine learning for medical fields is the disparity between the data distribution of the training images and the data encountered in clinics. This phenomenon can be explained by inconsistent acquisition techniques and large variations across the patient spectrum. The result is poor translation of the trained models to the clinic, which limits their implementation in medical practice. Patient-specific trained networks could provide a potential solution. Although patient-specific approaches are usually infeasible because of the expenses associated with on-the-fly labeling, the use of generative adversarial networks enables this approach. This study proposes a patient-specific approach based on generative adversarial networks. In the presented training pipeline, the user trains a patient-specific segmentation network with extremely limited data which is supplemented with artificial samples generated by generative adversarial models. This approach is demonstrated in endoscopic video data captured during fetoscopic laser coagulation, a procedure used for treating twin-to-twin transfusion syndrome by ablating the placental blood vessels. Compared to a standard deep learning segmentation approach, the pipeline was able to achieve an intersection over union score of 0.60 using only 20 annotated images compared to 100 images using a standard approach. Furthermore, training with 20 annotated images without the use of the pipeline achieves an intersection over union score of 0.30, which, therefore, corresponds to a 100% increase in performance when incorporating the pipeline. A pipeline using GANs was used to generate artificial data which supplements the real data, this allows patient-specific training of a segmentation network. We show that artificial images generated using GANs significantly improve performance in vessel segmentation and that training patient-specific models can be a viable solution to bring automated vessel segmentation to the clinic.
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  • 文章类型: Journal Article
    目的:以母体“镜像”综合征为背景,评估胎儿干预后的母体和围产期结局。
    方法:一项多中心回顾性研究,在1995年至2022年期间,所有胎儿积水并发母体“镜子”综合征,并接受任何形式的胎儿治疗。回顾所有病例的病历和超声图像。“镜像”综合征被定义为胎儿水肿和/或胎盘肥大与产妇明显水肿的发展有关,有或没有先兆子痫。胎儿积液定义为在≥2个体腔中存在异常的液体聚集。
    结果:21例妊娠符合纳入标准。胎儿水肿和/或胎盘肿大的原因包括胎儿肺部病变(n=9),双胎输血综合征(n=6),严重的胎儿贫血(n=4),和其他人(n=2)。“镜像”时的平均胎龄为27.0±3.8周。14例(66.6%)在胎儿治疗干预后发现母亲“镜子”综合征。8例(38.1%)患者的“镜像”症状在分娩前得到缓解或明显改善,从胎儿干预到产妇恢复的平均间隔为13.1天(范围4-35)。由于“镜子”综合症恶化,需要分娩三名妇女。在接受治疗的21例怀孕(27例胎儿)中,有15例(55.5%)活体分娩,新生儿死亡7例(25.9%),宫内死亡5例(18.5%)。
    结论:成功治疗和解决胎儿积水后,产妇“镜子”综合征可以在分娩前改善或有时完全消退。此外,认识到“镜像”综合征可能只有在胎儿介入后才会出现,因此在胎儿积水的情况下需要对患者进行更高的母体监测。
    OBJECTIVE: To evaluate maternal and perinatal outcomes following fetal intervention in the context of maternal \"mirror\" syndrome.
    METHODS: A multicenter retrospective study of all cases of fetal hydrops complicated by maternal \"mirror\" syndrome and treated by any form of fetal therapy between 1995 and 2022. Medical records and ultrasound images of all cases were reviewed. \"Mirror\" syndrome was defined as fetal hydrops and/or placentomegaly associated with the maternal development of pronounced edema, with or without pre-eclampsia. Fetal hydrops was defined as the presence of abnormal fluid collections in ≥2 body cavities.
    RESULTS: Twenty-one pregnancies met the inclusion criteria. Causes of fetal hydrops and/or placentomegaly included fetal lung lesions (n = 9), twin-twin transfusion syndrome (n = 6), severe fetal anemia (n = 4), and others (n = 2). Mean gestational age at \"mirror\" presentation was 27.0 ± 3.8 weeks. Maternal \"mirror\" syndrome was identified following fetal therapeutic intervention in 14 cases (66.6%). \"Mirror\" symptoms resolved or significantly improved before delivery in 8 (38.1%) cases with a mean interval from fetal intervention to maternal recovery of 13.1 days (range 4-35). Three women needed to be delivered because of worsening \"mirror\" syndrome. Of the 21 pregnancies treated (27 fetuses), there were 15 (55.5%) livebirths, 7 (25.9%) neonatal deaths and 5 (18.5%) intra-uterine deaths.
    CONCLUSIONS: Following successful treatment and resolution of fetal hydrops, maternal \"mirror\" syndrome can improve or sometimes completely resolve before delivery. Furthermore, the recognition that \"mirror\" syndrome may arise only after fetal intervention necessitates hightened patient maternal surveillance in cases of fetal hydrops.
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  • 文章类型: Journal Article
    目的:描述产前诊断为双胎贫血-红细胞增多症(TAPS)的一系列单绒毛膜(MC)妊娠的胎儿脑磁共振成像(MRI)发现,因此,为了描述与这种情况相关的潜在颅内并发症,他们的频率和潜在的治疗选择。
    方法:这是一项回顾性研究,涉及2006年至2023年在单一机构中并发TAPS并接受胎儿MRI的MC双胎妊娠。进行MRI控制,产后超声(US)或MRI可用。
    结果:我们机构评估了1250例MC妊娠。50例怀孕(4%)被诊断为TAPS,29例接受了胎儿脑MRI检查。13/29例妊娠(44.8%)至少在双胞胎中表现出MRI的脑部发现。在14/57双胞胎(24.6%)中检测到神经放射学发现。我们发现了四个主要类别的发现:出血性病变,T2加权白质高强度(WMH),脑水肿肿胀和静脉充血。贫血者有19项发现,红细胞增多症双胞胎有3项发现,两组之间的比率具有统计学意义(p值=0.01)。宫内MRI随访显示出血性病变的后遗症。脑肿胀完全消退,治疗后显示静脉突出和T2-WMHs。产后影像学证实了产前特征。
    结论:我们的工作表明,TAPS相关的MRI异常包括水肿/出血性病变,这些病变主要发生在贫血而不是红细胞增多的双胞胎中。胎儿镜激光手术可能具有潜在的减充血作用。因此,产前MRI可能有助于TAPS妊娠的咨询和管理,特别是治疗计划和疗效监测。
    OBJECTIVE: To describe fetal brain Magnetic Resonance Imaging (MRI) findings in a large series of monochorionic (MC) pregnancies complicated by Twin Anemia-Polycythemia Sequence (TAPS) prenatally diagnosed, so to characterize the potential intracranial complications associated with this condition, their frequency and potential treatment options.
    METHODS: This is a retrospective study of MC twin pregnancies complicated by TAPS and undergone fetal MRI in a single institution from 2006 to 2023. MRI control was performed and post-natal ultrasound (US) or MRI were available.
    RESULTS: 1250 MC pregnancies were evaluated in our institution. 50 pregnancies (4%) were diagnosed with TAPS, 29 underwent a fetal brain MRI. 13/29 pregnancies (44.8%) demonstrated brain findings at MRI in at least a twin. Neuroradiological findings were detected in 14/57 twins (24.6%). We detected four main categories of findings: hemorrhagic lesions, T2-weighted white-matter hyperintensities (WMH), brain edema-swelling and venous congestion. Nineteen findings were present in the anemic and three in the polycythemic twins, with a statistically significant ratio between the two groups (p-value = 0.01). Intrauterine MRI follow-up demonstrated the sequalae of hemorrhagic lesions. A complete regression of brain swelling, veins prominence and T2-WMHs was demonstrated after treatment. Postnatal imaging confirmed prenatal features.
    CONCLUSIONS: Our work demonstrates that TAPS-related MRI anomalies consisted in edematous/hemorrhagic lesions that occur mostly in anemic rather than in polycythemic twins. Fetoscopic laser surgery could have a potential decongestant role. Therefore, prenatal MRI may help in counselling and management in TAPS pregnancies, especially for the planning of therapy and the monitoring of its efficacy.
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  • 文章类型: Systematic Review
    目的:本系统综述探讨了单绒毛膜(MC)双胞胎合并双胎输血综合征(TTTS)或选择性胎儿生长受限(sFGR)的心脏适应,并评估了先天性心脏缺陷(CHDs)的风险。
    方法:遵守PRISMA指南,回顾了63项研究(49项关于心脏适应,13关于CHD,两者都有一个)。进行了心脏适应模式的叙事合成。此外,一项荟萃分析比较了TTTS和sFGR中CHD与单纯性MC双胞胎的产前患病率.
    结果:在TTTS收件人中,心脏功能可能因舒张功能受损,收缩压,以及全球功能,而在捐赠者中,心脏功能通常被保留。在sFGR中,大双胞胎可能显示肥厚型心肌病,小双胞胎可能表现出收缩功能受损。TTTS和sFGR的同时发生会放大心脏影响,但经常被低估。CHD患病率的荟萃分析显示,与无并发症的MC双胞胎相比,TTTS的相对风险比为3.5(95%CI:2.5-4.9),sFGR的相对风险比为2.2(95CI:1.3-3.5)。
    结论:这项研究强调了TTTS中记录良好的心脏适应,与sFGR中有限的理解形成对比。在这两种情况下均观察到CHD风险升高。在复杂的MC双胎妊娠中,有必要加强心血管监测。未来的研究应该探索sFGR的心脏适应及其长期后果。
    OBJECTIVE: This systematic review explores cardiac adaptation in monochorionic (MC) twins with twin-twin transfusion syndrome (TTTS) or selective fetal growth restriction (sFGR) and assesses the risk of congenital heart defects (CHDs).
    METHODS: Adhering to PRISMA guidelines, 63 studies were reviewed (49 on cardiac adaptation, 13 on CHD, one on both). A narrative synthesis of cardiac adaptation patterns was performed. Additionally, a meta-analysis compared the livebirth prevalence of CHD in TTTS and sFGR against uncomplicated MC twins.
    RESULTS: In TTTS recipients, cardiac function may be impaired for diastolic, systolic, as well as global functions, while in donors, cardiac function is generally preserved. In sFGR, large twins may show hypertrophic cardiomyopathy, and small twins may show impaired systolic function. Co-occurrence of TTTS and sFGR magnifies cardiac impact but is often underreported. Meta-analysis for CHD prevalence revealed a relative risk ratio of 3.5 (95% CI: 2.5-4.9) for TTTS and 2.2 (95%CI: 1.3-3.5) for sFGR compared with uncomplicated MC twins.
    CONCLUSIONS: This study highlights the well-documented cardiac adaptation in TTTS, contrasting with limited understanding in sFGR. Elevated CHD risks were observed in both conditions. Enhanced cardiovascular surveillance is warranted in complicated MC twin pregnancies. Future research should explore cardiac adaptation in sFGR and its long-term consequences.
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  • 文章类型: Journal Article
    目的:单绒毛膜妊娠并发双胎性贫血红细胞增多症(TAPS)的产前管理仍未达到最佳定义。我们的目的是评估胎儿镜选择性激光光凝术对胎儿和新生儿存活的安全性和有效性。
    方法:报告了一个病例系列,患者转诊至德克萨斯州儿童胎儿中心,以评估和处理2014年至2023年疑似自发性TAPS,但没有合并双胎对双胎综合征。所有评估均由我们的团队进行,并为II-IV期TAPS患者提供预期管理,宫内输血,或激光治疗。本研究排除了激光后TAPS的病例。从电子病历中获得妊娠和新生儿结局。
    结果:在10年的时间内,向我们的TAPS管理中心介绍了18例患者。13例患者患有II-IV期TAPS(13/18,72%),并选择进行激光光凝。所有的程序都完成了,12/13进行了“solomization”。在所有病例之后,注意到两个胎儿的大脑中动脉多普勒正常。激光治疗后26例存活胎儿有1例胎儿宫内死亡,由于选择性生长限制而变得复杂。大多数患者(12/13)通过剖宫产分娩,平均胎龄为29±3周。随后,有1名前供者新生儿死亡的婴儿有产前水肿.总的来说,产后30天生存率为24/26个胎儿(92.3%)。
    结论:在自发TAPS的设置中,激光治疗是可行的,并且似乎是一种有效的方法,具有良好的围产期结局.
    OBJECTIVE: Antenatal management of monochorionic pregnancies complicated by twin anemia polycythemia sequence (TAPS) remains sub-optimally defined. Our objective was to evaluate the safety and efficacy of fetoscopic selective laser photocoagulation with respect to fetal and neonatal survival.
    METHODS: A case series is reported with patients referred to the Texas Children\'s Fetal Center for evaluation and management of suspected spontaneous TAPS without concomitant twin-to-twin syndrome from 2014 to 2023. All evaluations were performed by our team and patients with stage II-IV TAPS were offered expectant management, intrauterine transfusion, or laser therapy. Cases of post-laser TAPS were excluded from this study. Pregnancy and neonatal outcomes were obtained from electronic medical records.
    RESULTS: During a 10-year time period, 18 patients presented to our center for the management of TAPS. Thirteen patients had stage II-IV TAPS (13/18, 72%) and elected to proceed with laser photocoagulation. All procedures were completed, and \"solomonization\" was performed for 12/13. Normalization of middle cerebral artery Dopplers in both fetuses was noted after all cases. There was one intrauterine fetal death of the 26 viable fetuses after laser treatment, which was complicated by selective growth restriction. Most patients (12/13) were delivered by Cesarean section at a mean gestational age of 29 ± 3 weeks. Subsequently, there was one ex-donor neonatal death in an infant who had prenatal hydrops. Overall, 30-day postnatal survival was 24/26 fetuses (92.3%).
    CONCLUSIONS: In the setting of spontaneous TAPS, laser therapy is feasible and appears to be an effective approach with overall favorable perinatal outcomes.
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  • 文章类型: Journal Article
    目的:胎儿镜下激光凝固胎盘吻合术通常用于治疗双胎对双胎输血综合征(TTTS)。用于TTTS的胎儿镜激光凝固术的常见并发症是早产胎膜初步破裂(PPROM)显着加重了新生儿结局。然而,使用带弯曲鞘的1mm柔性胎儿镜可减少羊膜医源性损伤,改善激光治疗后新生儿结局.这项研究的目的是比较使用这种带弯曲鞘的柔性胎儿镜与新生儿的结局。使用标准的镜头技术。
    方法:在两个德国胎儿外科中心使用2mm的标准晶状体胎儿镜(前胎盘鞘6.63mm2或11.27mm2)和1mm或1.2mm的柔性胎儿镜(鞘2.65mm2或3.34mm2)后,对结果进行了回顾性分析。在2006-2019年期间执行。
    结果:分析了247例TTTS患者的新生儿结局,包括双胎和单胎存活率。超薄技术组(n=154)中至少一个胎儿的存活率为97.2%,而标准晶状体胎儿镜组(p=0.008)中的存活率为88.3%(n=93)。两组胎儿的生存率没有差异(81.0vs.75.3%)。使用超薄胎儿镜,手术至分娩间隔显着增加(89.1±35.0d与71.4±35.4d,p=0.001)导致分娩时平均胎龄增加11天(231.9±28.1天vs.221.1±32.7d,p=0.012)。
    结论:使用1mm或1.2mm的柔性胎儿镜(护套2.65mm2或3.34mm2)进行TTTS后,胎儿的存活率可以显着增加。
    OBJECTIVE: Fetoscopic laser coagulation of placental anastomoses is usually performed for a treatment of twin-to-twin transfusion syndrome (TTTS). A common complication of fetoscopic laser coagulation for TTTS is preterm preliminary rupture of fetal membranes (PPROM) aggravating the neonatal outcome significantly. However, use of an flexible 1 mm fetoscope with an curved sheath could reduce iatrogenic damage of the amniotic membrane and improve neonatal outcomes after laser treatment. The aim of this study was to compare neonatal outcomes using this flexible fetoscope with curved sheath vs. use of a standard lens technique.
    METHODS: Outcomes were retrospective analyzed after use of a standard lens fetoscope of 2 mm (sheath 6.63 mm2 or 11.27 mm2 for anterior placenta) and a flexible fetoscope of 1 mm or 1.2 mm (sheath 2.65 mm2 or 3.34 mm2) in two German centers of fetal surgery, performed during 2006-2019.
    RESULTS: Neonatal outcome of 247 TTTS patients were analyzed including the rates of double and single fetal survival. The survival of at least one fetus was 97.2 % in the group with the ultrathin technique (n=154) compared to 88.3 % (n=93) in the group with the standard lens fetoscope (p=0.008). Survival of both fetuses was not different between groups (81.0 vs. 75.3 %). The procedure to delivery interval was significantly increased using the ultrathin fetoscope (89.1±35.0 d vs. 71.4±35.4 d, p=0.001) resulting in an increased gestational age at delivery by 11 days on average (231.9±28.1 d vs. 221.1±32.7 d, p=0.012).
    CONCLUSIONS: Fetal survival can be significantly increased following TTTS using flexible fetoscope of 1 mm or 1.2 mm (sheath 2.65 mm2 or 3.34 mm2).
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  • 文章类型: Journal Article
    胎儿经历了主要的手术压力以及继发于双胎输血(TTTS)以及用于治疗TTTS的胎儿镜手术的液体移位。虽然人们了解TTTS的病理生理学,胎儿从胎儿镜手术中经历的急性代谢变化没有。我们试图评估继发于TTTS手术的受体代谢组学特征的变化。在12/2022-2/2023进行的4例TTTS手术病例的开始和结束时收集羊水。立即处理样品并通过基于NMR的代谢组学设施方案进行评估。在单变量分析中,12种代谢物(葡萄糖,乳酸,和10种关键氨基酸)在手术开始和结束之间显示出统计学上的显着变化。其中,11种代谢物在结束时减少,而只有乳酸增加。监督的OPLS-DA模型显示丙酮酸和乳酸作为两种代谢物对病例之间的差异影响最大。并且40%的代谢组学变化可以直接归因于样本采集的时间(即,如果术前或术后)。这些结果表明,在TTTS的胎儿镜手术期间,受体双胞胎的代谢发生了显着变化。这些葡萄糖下降的发现,乳酸增加,和减少的羊膜酸将表明增加的分解代谢在手术过程中。这项研究提出了有关手术期间最佳母体和胎儿营养的问题,以及是否可以优化营养状况以进一步提高胎儿镜手术期间的双胎生存率。
    Fetuses undergo major surgical stress as well as fluid shifts secondary to both twin-twin transfusion (TTTS) as well as the fetoscopic surgery for treatment of TTTS. While the pathophysiology of TTTS is understood, the acute metabolic changes that fetuses experience from fetoscopic surgery are not. We sought to evaluate the changes in recipient metabolomic profile secondary to TTTS surgery. Amniotic fluid was collected at the beginning and end of four TTTS surgical cases performed from 12/2022-2/2023. Samples were immediately processed and evaluated via NMR-based Metabolomics Facility protocol. In univariate analysis, 12 metabolites (glucose, lactate, and 10 key amino acids) showed statistically significant changes between the beginning and end of the surgery. Among these, 11 metabolites decreased at the end, while only lactate increased. Supervised oPLS-DA modeling revealed pyruvate and lactate as the two metabolites most impact on the variance between cases, and that 40% of metabolomic changes could be attributed directly to the timing that the sample was taken (i.e., if pre- or postoperatively). These results indicate significant metabolic changes in the recipient twin during fetoscopic surgery for TTTS. These findings of decreased glucose, increased lactate, and decreased amnio acids would indicate increased catabolism during surgery. This study raises questions regarding optimal maternal and fetal nutrition during surgery and if nutritional status could be optimized to further improve twin survival during fetoscopic surgery.
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  • 文章类型: Journal Article
    背景:双反向动脉灌注(TRAP)序列是单绒毛膜多胎妊娠的罕见并发症,其中泵双胎为无活力的同胎(acardius)提供血液动力学支持。胎儿磁共振成像(MRI)用于检测泵双胎异常,尤其是脑缺血,在胎儿介入之前中断脐血流到心包。
    目的:总结一系列TRAP序列妊娠的影像学表现。
    方法:对所有接受胎儿MRI(2004-2021年)的TRAP序列妊娠进行单中心回顾性分析。胎儿核磁共振,超声,并收集超声心动图数据。
    结果:纳入了88例经MRI检查的TRAP序列妊娠(平均胎龄,19.8±2.8周)。在进行MRI检查时,在两次怀孕中发现了双胎泵的死亡。通过核磁共振,12%(10/86)的活泵双胞胎有异常,包括3%(3/86)的脑异常和9%(8/86)的颅外异常。通过超声心动图,7%(6/86)的泵双生有结构性心脏异常。通过MRI确定了三种无心畸形形态亚型:无脑(55%,48/88),anceps(39%,34/88),和无定形(7%,6/88)。平均超声心痛与泵双比A/P比,为每对双胞胎计算为无心躯干(和头部,如果存在)加上泵双胎估计胎儿体重的肢体体积)在三种心包亚型之间有所不同(P=.03)。平均A/P比与泵双心胸比率和联合心输出量中度相关(Pearson\sr=0.45和0.48,分别两者P<.001)。
    结论:TRAP序列妊娠的胎儿MRI在相当数量的泵双胎中发现异常。三种心痛亚型的A/P比不同,与泵双心胸比率和联合心输出量中度相关。
    Twin reversed arterial perfusion (TRAP) sequence is a rare complication of monochorionic multiple gestation pregnancies, in which the pump twin provides hemodynamic support to a nonviable co-twin (acardius). Fetal magnetic resonance imaging (MRI) is used to detect pump twin abnormalities, particularly brain ischemia, prior to fetal intervention to interrupt umbilical blood flow to the acardius.
    To summarize the imaging findings of TRAP sequence pregnancies in a large series.
    A single-center retrospective review was performed of all TRAP sequence pregnancies referred for fetal MRI (2004-2021). Fetal MRI, ultrasound, and echocardiography data were collected.
    Eighty-eight TRAP sequence pregnancies with MRI were included (mean gestational age, 19.8±2.8 weeks). Demise of the pump twin was noted in two pregnancies at the time of MRI. By MRI, 12% (10/86) of live pump twins had abnormalities, including 3% (3/86) with brain abnormalities and 9% (8/86) with extra-cranial abnormalities. By echocardiography, 7% (6/86) of pump twins had structural cardiac abnormalities. Three acardius morphological subtypes were identified by MRI: acephalus (55%, 48/88), anceps (39%, 34/88), and amorphous (7%, 6/88). The mean ultrasound acardius to pump twin ratio A/P ratio, calculated for each twin pair as the ratio of the acardius trunk (and head, if present) plus limb volume to the pump twin estimated fetal weight) differed among the three acardius subtypes (P=.03). The mean A/P ratio moderately correlated with pump twin cardiothoracic ratio and combined cardiac output (Pearson\'s r=0.45 and 0.48, respectively, both P<.001).
    Fetal MRI of TRAP sequence pregnancies found anomalies in a substantial number of pump twins. The three acardius subtypes differed in A/P ratio, which moderately correlated with the pump twin cardiothoracic ratio and combined cardiac output.
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  • 文章类型: Case Reports
    双胞胎反向动脉灌注(TRAP)序列是单绒毛膜双胞胎的罕见并发症,供体双胞胎通过异常的血管吻合对无心双胞胎进行灌注。由此产生的矛盾的逆行血流供应无心双胞胎是缺氧的,导致人类遇到的一些最严重的畸形。尽管对无心双胞胎的最早描述可以追溯到至少16世纪,支持TRAP序列发育的病理生理过程仍在阐明中。关于TRAP序列发病机理的理论包括胚胎固有的缺陷和胎盘脉管系统的原发性异常。尸检研究继续为TRAP序列的潜在发病机制提供线索,以及可以在无心双胞胎中观察到的表现谱的特征。在这里,我们提出了临床,尸检,以及在一个独特的TRAP序列病例中的分子发现。新发现包括原始的泄殖腔样结构和涉及6q11.1和15q25.1的染色体畸变。
    Twin reversed arterial perfusion (TRAP) sequence is a rare complication of monochorionic twinning whereby a donor twin perfuses an acardiac twin via aberrant vascular anastomoses. The resulting paradoxical retrograde blood flow supplying the acardiac twin is oxygen-poor, leading to some of the most severe malformations encountered in humans. Though the first descriptions of acardiac twins date back to at least the 16th century, the pathophysiologic processes which underpin the development of TRAP sequence are still being elucidated. Theories on the pathogenesis of TRAP sequence include deficiencies intrinsic to the embryo and primary abnormalities of the placental vasculature. Autopsy studies continue to provide clues to the underlying pathogenesis of TRAP sequence, and the characterization of the spectrum of manifestations that can be observed in acardiac twins. Herein, we present the clinical, autopsy, and molecular findings in a unique case of TRAP sequence. Novel findings include a primitive cloaca-like structure and chromosomal aberrations involving 6q11.1 and 15q25.1.
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