Malhotra Khushboo, Elayedatt Rinshi Abid, Krishnan Vivek
Department of Fetal Medicine, Amrita Institute of Medical Sciences, Ponekkara, Kochi, Kerala 682041 India.
J Obstet Gynaecol India. 2024 Dec;74(6):523-529. doi: 10.1007/s13224-023-01913-1. Epub 2024 Jan 19.
To report a single tertiary center experience in the management of prenatally diagnosed cases of fetal ascites and their postnatal outcomes.
Prenatally diagnosed fetal ascites cases were retrospectively analyzed from 2015 to 2022 using two-dimensional ultrasound with other investigations as required in a tertiary care center.
Of 126 fetuses with fetal ascites, 70 progressed to hydrops and hence were excluded from the study. Out of the 56 that formed the study group, the median gestational age at presentation was 27.2 weeks (range 15 + 5 to 36 + 4 weeks). A majority (76.8%, 43/56) of ascites had a secondary etiology (secondary ascites) that was identified antenatally (including twin-to-twin transfusion syndrome (TTTS), fetal growth restriction (FGR), fetal anemia, structural cause involving genitourinary, gastrointestinal, cardiovascular system, pulmonary tract and multi-system anomalies), while 23.2% (13/56) were classified as idiopathic ascites where no cause could be determined prenatally. The overall survival rate was 77.4% (24/31) with 41.9% (13/31) needing intervention and 35.5% (11/31) showing spontaneous resolution. 63.6% (7/11) of idiopathic ascites cases had favorable outcomes compared to secondary ascites (17/41, 41.5%).
Fetuses with idiopathic ascites with normal karyotype and negative infection screening demonstrated a higher tendency for spontaneous resolution with a favorable outcome than secondary ascites. However, parents should be informed of the possibility of unexpected rare syndromes/structural abnormalities that may be detected after birth. In cases with secondary ascites, postnatal outcomes could be improved post-intervention. Multidisciplinary team involvement is necessary for the appropriate management and successful outcomes.
报告一家三级医疗中心对产前诊断的胎儿腹水病例的管理经验及其产后结局。
对2015年至2022年在一家三级医疗中心通过二维超声及必要时的其他检查进行产前诊断的胎儿腹水病例进行回顾性分析。
126例有胎儿腹水的胎儿中,70例进展为水肿,因此被排除在研究之外。在组成研究组的56例中,就诊时的中位孕周为27.2周(范围为15⁺⁵至36⁺⁴周)。大多数(76.8%,43/56)腹水有继发病因(继发性腹水),产前已确定(包括双胎输血综合征(TTTS)、胎儿生长受限(FGR)、胎儿贫血、涉及泌尿生殖系统、胃肠道、心血管系统、呼吸道及多系统异常的结构原因),而23.2%(13/56)被归类为特发性腹水,产前无法确定病因。总体生存率为77.4%(24/31),41.9%(13/31)需要干预,35.5%(11/31)显示自发消退。特发性腹水病例中有63.6%(7/11)预后良好,而继发性腹水为(17/41,41.5%)。
核型正常且感染筛查阴性的特发性腹水胎儿比继发性腹水胎儿有更高的自发消退倾向及良好预后。然而,应告知父母出生后可能检测到意外罕见综合征/结构异常的可能性。对于继发性腹水病例,干预后可改善产后结局。多学科团队参与对于恰当管理和成功结局是必要的。