Kasuga Yoshifumi, Fukuma Yuka, Kajikawa Kaoru, Akita Keisuke, Tamai Junko, Tanaka Yuya, Otani Toshimitsu, Fukutake Marie, Ikenoue Satoru, Tanaka Mamoru
Department of Obstetrics and Gynecology, Keio University School of Medicine, 5 Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.
J Clin Med. 2025 Aug 5;14(15):5523. doi: 10.3390/jcm14155523.
: This study aimed to describe the perinatal and neonatal outcomes of chronic abruption oligohydramnios sequence in the Kanto region of Japan. : This survey was conducted at 123 perinatal centers affiliated to this area. Data on the experience of managing chronic abruption oligohydramnios sequence between 1 January 2017, and 31 December 2022, were collected and analyzed. : Among the 82 cases of chronic abruption oligohydramnios sequence that were included in this study, there were seven miscarriages, five artificial abortions, and 70 deliveries beyond 22 gestational weeks (singleton: 68; twin: 2). In 82 patients, vaginal bleeding was the initial symptom of chronic abruption oligohydramnios sequence (88%). The mean gestational duration at the initial symptom onset was 17.3 ± 5.0 weeks. Of the 68 singleton pregnancies delivered after 22 gestational weeks, the mean gestational duration at delivery was 25.2 ± 2.8 weeks. In patients with chronic abruption oligohydramnios sequence, the mean white blood cell count at diagnosis and mean of the maximum white blood cell count during pregnancy were 11,589 ± 2885 and 15,357 ± 4745/μL, respectively; and the mean C-reactive protein at diagnosis and mean of the maximum C-reactive protein during pregnancy were 1.0 ± 1.2 and 2.0 ± 2.1 mg/L, respectively. Chorioamnionitis was identified in 43 patients (63%). All neonates were admitted to the neonatal intensive care unit. Of the 68 singleton neonates, 5 died immediately after birth. : Chronic abruption oligohydramnios sequence is a rare perinatal complication that is possibly associated with infections, such as chorioamnionitis, and linked to adverse perinatal and neonatal outcomes.
本研究旨在描述日本关东地区慢性胎盘早剥羊水过少序列征的围产期和新生儿结局。本调查在该地区所属的123家围产期中心进行。收集并分析了2017年1月1日至2022年12月31日期间管理慢性胎盘早剥羊水过少序列征的经验数据。本研究纳入的82例慢性胎盘早剥羊水过少序列征病例中,有7例流产、5例人工流产以及70例孕22周后分娩(单胎:68例;双胎:2例)。82例患者中,阴道出血是慢性胎盘早剥羊水过少序列征的初始症状(88%)。初始症状出现时的平均孕周为17.3±5.0周。在22周后分娩的68例单胎妊娠中,分娩时的平均孕周为25.2±2.8周。慢性胎盘早剥羊水过少序列征患者诊断时的平均白细胞计数及孕期最高白细胞计数平均值分别为11,589±2885和15,357±4745/μL;诊断时的平均C反应蛋白及孕期最高C反应蛋白平均值分别为1.0±1.2和2.0±2.1mg/L。43例患者(63%)确诊有绒毛膜羊膜炎。所有新生儿均入住新生儿重症监护病房。68例单胎新生儿中,5例出生后即刻死亡。慢性胎盘早剥羊水过少序列征是一种罕见的围产期并发症,可能与绒毛膜羊膜炎等感染有关,并与不良围产期和新生儿结局相关。