Cardiac Structural and Functional Assessment of Monochorionic Twin Pregnancies Complicated by Type II and Type III Selective Fetal Growth Restriction.

IF 1.6 3区 医学 Q3 OBSTETRICS & GYNECOLOGY
Jessian L Munoz, Betul Yilmaz Furtun, Cara Buskmiller, Magdalena Sanz Cortes, Roopali V Donepudi, Michael A Belfort, Ahmed A Nassr
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引用次数: 0

Abstract

Introduction: Selective fetal growth restriction (sFGR) complicates 10-15% of monochorionic twin gestations. Prior studies reported neonatal cardiac hypertrophy present in 25% of twins impacted by sFGR, most commonly the larger twin (80%). Our primary objective was to characterize fetal cardiac structural and functional echocardiogram findings in sFGR twins.

Methods: A retrospective cohort analysis was performed of monochorionic twin pregnancies complicated by type II or type III sFGR managed and delivered at a single tertiary center from 2015 to 2023. Patients diagnosed with twin to twin transfusion syndrome, twin anemia-polycythemia sequence, or undergoing laser treatment for any indication were excluded. All twin pairs underwent fetal echocardiogram by board-certified pediatric cardiologists at our center. In cases of abnormal fetal echocardiograms, a pediatric echocardiogram was performed after birth. Clinically relevant data were obtained from electronic medical records. Right and left myocardial performance index (MPI) were calculated incorporating ejection, isovolumetric contraction, and isovolumetric relaxation times as well as combined cardiac output, cardiac hypertrophy, and tricuspid regurgitation.

Results: During the study period, 35 pregnancies complicated by type II or type III sFGR were managed by our team. Two patients were excluded as they did not undergo fetal echocardiograms as planned. The remaining 33 twin pairs underwent echocardiogram analysis at 20 weeks ± 6 days on average. Compared to the sFGR fetuses, appropriate for gestational age (AGA) fetuses were more likely to have tricuspid regurgitation (TR, 37 vs. 9%, p = 0.02), right ventricular hypertrophy (RVH, 42 vs. 9%, p = 0.003), left ventricular hypertrophy (31 vs. 3%, p = 0.006), elevated right MPI (0.36 [0.26, 0.49] vs. 0.29 [0.24, 0.35], p = 0.03), and elevated left MPI (0.32 [0.29, 0.47] vs. 0.29 [0.25, 0.35], p = 0.02). No difference was noted in combined cardiac output (534 [483, 596] vs. 522 [447, 596], p = 0.41). At birth, 55% (6/11) of AGA fetuses with abnormal fetal echocardiograms had RVH and TR compared to 25% (1/4) of sFGR fetuses.

Conclusion: In this cohort of expectantly managed monochorionic twins complicated by type II and type III sFGR, larger twins were noted to have several findings consistent with hemodynamic changes which could reflect cardiac overload in the prenatal period. In addition, these may persist during neonatal life. Further assessment of neonatal and pediatric outcomes is needed to determine the long-term implications of these sonographic findings.

单绒毛膜双胎合并II型和III型选择性胎儿生长受限的心脏结构和功能评估。
选择性胎儿生长受限(sFGR)并发症10-15%的单绒毛膜双胎妊娠。先前的研究报道,25%的sFGR影响的双胞胎存在新生儿心脏肥厚,最常见的是较大的双胞胎(80%)。我们的主要目的是描述sFGR双胞胎胎儿心脏结构和功能超声心动图的发现。方法:回顾性队列分析2015-2023年单绒毛膜双胎合并II型或III型sFGR在单一三级中心管理和分娩的病例。所有的双胞胎都由认证的儿科心脏病专家进行了胎儿超声心动图检查。在胎儿超声心动图异常的情况下,在出生后进行儿科超声心动图检查。计算左、右心肌性能指数(MPI),包括射血、等容收缩和等容舒张时间,以及合并心输出量、心肌肥厚和三尖瓣反流。结果:在研究期间,本组共处理了35例合并II型或III型sFGR的妊娠。2例患者因未按计划进行胎儿超声心动图检查而被排除。其余33对双胞胎在平均20周±6天接受超声心动图分析。与sFGR胎儿相比,适合胎龄(AGA)的胎儿更容易出现三尖瓣反流(TR, 37 vs 9%, p=0.02)、右心室肥厚(RVH, 42 vs 9%, p=0.003)、左心室肥厚(31 vs 3%, p=0.006)、右MPI升高(0.36 [0.26,0.49]vs 0.29 [0.24, 0.35], p=0.03)和左MPI升高(0.32 [0.29,0.47]vs 0.29 [0.25, 0.35], p=0.02)。合并心输出量无差异(534 [483,596]vs 522 [447, 596], p=0.41)。出生时,55%(6/11)胎儿超声心动图异常的AGA胎儿有RVH和TR,而25%(1/4)的sFGR胎儿有RVH和TR。结论:在这个预期治疗的单绒毛膜双胞胎合并II型和III型sFGR的队列中,注意到较大的双胞胎有几个与血液动力学变化一致的发现,这些变化可能反映了产前时期的心脏负荷。需要进一步评估新生儿和儿童的预后,以确定这些超声结果的长期意义。
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来源期刊
Fetal Diagnosis and Therapy
Fetal Diagnosis and Therapy 医学-妇产科学
CiteScore
4.70
自引率
9.10%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The first journal to focus on the fetus as a patient, ''Fetal Diagnosis and Therapy'' provides a wide range of biomedical specialists with a single source of reports encompassing the common discipline of fetal medicine.
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