Hausman-Kedem Moran, Libzon Stephanie, Fattal Valevski Aviva, Malinger Gustavo, Krajden Haratz Nina, Tokatly Latzer Itay, Blumovich Amit, Roth Jonathan, Constantini Shlomi, Mandel Dror, Ben-Sira Liat, Shiran Shelly I
Pediatric Neurology Institute, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel
Faculty of Medical and Health Sciences, School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Arch Dis Child Fetal Neonatal Ed. 2025 Apr 17;110(3):303-312. doi: 10.1136/archdischild-2024-327243.
To characterise perinatal, clinical and neuroimaging patterns and aetiology of perinatal intracranial haemorrhage (pICH), and to assess potential differences between cases diagnosed antenatally and postnatally.
Prospective, observational, single-centre study of 110 consecutive cases of pICH identified in the fetal or neonatal period or diagnosed with presumed pICH between 2014 and 2023. Prematurity-related cases were excluded. Antenatal and postnatal MRI data were analysed for patterns and mechanisms of haemorrhage and their potential aetiology. Potential associations between pICH with perinatal and clinical risk factors were also explored.
Fifty-nine of the 110 included cases (53.6%) were diagnosed antenatally (termination of pregnancy, n=22), and postnatal data on 81/88 (92%) children were available. Intraventricular haemorrhage (IVH) was the most common haemorrhage type (83/110 (75.5%)) and was more common prenatally (p=0.004). Subpial haemorrhage was exclusively diagnosed postnatally (p<0.001), and it was more commonly detected in primigravida women (p=0.013). The germinal matrix was the most common origin of IVH (n=56, 50.9%) occuring more frequently prenatally (p<0.001), whereas sinus venous thrombosis-related IVH was more commonly detected postnatally (p=0.002). Subdural haemorrhage was associated with haematological abnormalities (p=0.023). Genetic disorders caused 31.9% of the cases (15 of 47 tested cases). Genetic disorders and associated congenital anomalies were more common in the prenatally diagnosed group (p=0.038 and p=0.04, respectively).
The patterns and pathogenesis of pICH appear to be different for prenatally and postnatally diagnosed cases and for types of haemorrhages. Given the important role of genetic factors in prenatal intracranial haemorrhage, next-generation sequencing is indicated in these cases.
描述围产期颅内出血(pICH)的围产期、临床及神经影像学特征和病因,并评估产前和产后诊断病例之间的潜在差异。
对2014年至2023年期间在胎儿期或新生儿期确诊或诊断为疑似pICH的110例连续病例进行前瞻性、观察性单中心研究。排除与早产相关的病例。分析产前和产后MRI数据,以了解出血的模式和机制及其潜在病因。还探讨了pICH与围产期及临床风险因素之间的潜在关联。
110例纳入病例中有59例(53.6%)为产前诊断(终止妊娠,n = 22),81/88例(92%)儿童有产后数据。脑室内出血(IVH)是最常见的出血类型(83/110,75.5%),且在产前更常见(p = 0.004)。软脑膜下出血仅在产后诊断(p < 0.001),且在初产妇中更常见(p = 0.013)。生发基质是IVH最常见的起源(n = 56,50.9%),在产前更频繁发生(p < 0.001),而与静脉窦血栓形成相关的IVH在产后更常见(p = 于0.002)。硬膜下出血与血液学异常有关(p = 0.023)。遗传疾病导致31.9%的病例(47例检测病例中的15例)。遗传疾病及相关先天性异常在产前诊断组中更常见(分别为p = 0.038和p = 0.04)。
产前和产后诊断病例以及不同类型出血的pICH模式和发病机制似乎有所不同。鉴于遗传因素在产前颅内出血中的重要作用,这些病例建议进行下一代测序。