Lee Sun Jin, Kim Jin Kyu, Kim Sun Jun
Department of Pediatrics, Chonbuk National University Medical School, Jeonju, Korea.
Research Institute of Clinical Medicine, Chonbuk National University Medical School, Jeonju, Korea.
Korean J Pediatr. 2018 Dec;61(12):387-391. doi: 10.3345/kjp.2018.06800. Epub 2018 Sep 16.
Subgaleal hemorrhage (SGH) is a rare but potentially fatal condition in newborns; however, few studies have reported on this condition. We aimed to identify the clinical characteristics and prognostic factors of SGH.
We retrospectively reviewed the medical records of 20 neonates diagnosed with SGH between January 2000 and June 2017. Enrolled neonates were clinically diagnosed when they had tender fluctuant scalp swelling that crossed the suture lines.
Among 20 neonates with SGH, 12 were boys and 7 were girls; median hospitalization duration was 9.7±6.9 days. Fourteen neonates (70%) were born via vacuum-assisted vaginal delivery, and 4 via vacuum-assisted cesarean section. Of the neonates enrolled, half of them initially showed unstable vital signs, including apnea, desaturation, and cyanosis. Ten neonates had acidosis and 3 had asphyxia (pH<7.0). Intracranial lesions associated with SGH were observed in 15 neonates (75%), including subdural hemorrhage (50%), subarachnoid hemorrhage (15%), intraventricular hemorrhage (5%), cerebral infarct (15%), skull fracture (30%), and cephalohematoma (20%). Twelve neonates (60%) required transfusion, 5 (25%) had seizures, and 3 (15%) died. Eight neonates (40%) had hyperbilirubinemia (mean total bilirubin, 13.1±7.4). The mean follow-up period was 8.4±7.5 months. At follow-up, 10 neonates (58.8%) were healthy with normal development, whereas 7 (41.2%) had neurological deficits.
The morbidity rate was 41.2% due to severe metabolic acidosis. Anemia, hyperbilirubinemia, low Apgar scores, and subdural hemorrhage did not affect the prognosis. The long-term outcomes of neonates with SGH are generally good. Only arterial blood pH was significantly associated with death.
帽状腱膜下出血(SGH)在新生儿中虽罕见但可能致命;然而,关于这种情况的研究报道较少。我们旨在确定SGH的临床特征和预后因素。
我们回顾性分析了2000年1月至2017年6月期间诊断为SGH的20例新生儿的病历。纳入的新生儿在出现跨越缝线的头皮压痛性波动肿胀时进行临床诊断。
20例SGH新生儿中,12例为男性,7例为女性;中位住院时间为9.7±6.9天。14例新生儿(70%)通过真空辅助阴道分娩出生,4例通过真空辅助剖宫产出生。纳入的新生儿中,一半最初表现出生命体征不稳定,包括呼吸暂停、血氧饱和度下降和发绀。10例新生儿有酸中毒,3例有窒息(pH<7.0)。15例新生儿(75%)观察到与SGH相关的颅内病变,包括硬膜下出血(50%)、蛛网膜下腔出血(15%)、脑室内出血(5%)、脑梗死(15%)、颅骨骨折(30%)和头皮血肿(20%)。12例新生儿(60%)需要输血,5例(25%)有惊厥,3例(15%)死亡。8例新生儿(40%)有高胆红素血症(平均总胆红素,13.1±7.4)。平均随访期为8.4±7.5个月。随访时,1例新生儿(58.8%)健康且发育正常,而7例(41.2%)有神经功能缺损。
由于严重代谢性酸中毒,发病率为41.2%。贫血、高胆红素血症、低阿氏评分和硬膜下出血不影响预后。SGH新生儿的长期预后一般良好。只有动脉血pH与死亡显著相关。