Miller Jena, Turan Sifa, Baschat Ahmet A
Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Maryland, Baltimore, MD 21201, USA.
Semin Perinatol. 2008 Aug;32(4):274-80. doi: 10.1053/j.semperi.2008.04.010.
Normal fetal growth is determined by the genetically predetermined growth potential and further modulated by maternal, fetal, placental, and external factors. Fetal growth restriction (FGR) is a failure to reach this potential and is clinically suspected if sonographic estimates of fetal weight, size, or symmetry are abnormal. Integration of fetal anatomy assessment, amniotic fluid dynamics, uterine, umbilical, and fetal middle cerebral artery Doppler is the most effective approach to differentiate potentially manageable placenta-based FGR from aneuploidy, nonaneuploid syndromes, and viral infection. Although placental dysfunction results in a multisystem fetal syndrome with impacts on short- and long-term outcome, only cardiovascular and behavioral responses are helpful to guide surveillance and intervention. Early-onset FGR before 34 weeks gestation is readily recognized but challenging to manage as questions about optimal delivery timing remain unanswered. In contrast, near-term FGR provides less of a management challenge but is often missed as clinical findings are more subtle. Once placenta-based FGR is diagnosed, integrating multivessel Doppler and biophysical profile score provides information on longitudinal progression of placental dysfunction and degree of fetal acidemia, respectively. Choosing appropriate monitoring intervals based on anticipated disease acceleration and intervention when fetal risks exceed neonatal risks are the prevailing current management approaches.
正常胎儿生长由基因预先决定的生长潜力决定,并进一步受到母体、胎儿、胎盘和外部因素的调节。胎儿生长受限(FGR)是指未能达到这种潜力,如果超声估计的胎儿体重、大小或对称性异常,则临床上怀疑存在FGR。整合胎儿解剖结构评估、羊水动力学、子宫、脐动脉和胎儿大脑中动脉多普勒检查是区分潜在可管理的胎盘性FGR与非整倍体、非非整倍体综合征和病毒感染的最有效方法。尽管胎盘功能障碍会导致多系统胎儿综合征,影响短期和长期结局,但只有心血管和行为反应有助于指导监测和干预。妊娠34周前的早发型FGR很容易识别,但由于关于最佳分娩时机的问题仍未得到解答,管理起来具有挑战性。相比之下,近足月FGR带来的管理挑战较小,但由于临床表现更为隐匿,往往容易被漏诊。一旦诊断为胎盘性FGR,整合多血管多普勒检查和生物物理评分分别可提供胎盘功能障碍纵向进展和胎儿酸血症程度的信息。根据预期的疾病进展选择合适的监测间隔,并在胎儿风险超过新生儿风险时进行干预,是目前主要的管理方法。