Aziz K, Vickar D B, Sauve R S, Etches P C, Pain K S, Robertson C M
Department of Pediatrics, University of Alberta, Edmonton, Canada.
Pediatrics. 1995 Jun;95(6):837-44.
Adverse neurodevelopmental outcome in premature infants is more common in the presence of certain ultrasonographically detectable intracranial lesions. Present nomenclature and classifications of parenchymal changes in preterm infants of varying gestations have led to some confusion. Descriptive definitions may be clinically useful. Regionalized perinatal and neonatal care enables population-based studies of these lesions and subsequent outcomes.
Two- to 3-year outcomes of neonates weighing 500 through 1249 g born in Alberta to Alberta residents during 1987 through 1990 were reviewed in relation to neonatal cerebral ultrasound lesions. Odds ratios and confidence limits for disability were calculated.
Of 960 live births in this weight group, 669 (70%) survived to 1 year adjusted age; 646 (96.6%) were assessed at follow-up, and 80 (12.4%) of these were disabled: cerebral palsy, 8.7%; vision loss, 2.9%; hearing loss, 1.3%; epilepsy, 0.6%; mental retardation, 4.8%; more than one disability per child, 3.6%; and projected dependent disability, 1.4%. Lesions considered to be predictive of disability on ultrasound (excluding germinal layer hemorrhage) were found in 79 (11.8%), parenchymal lesions in 63 (9.4%) of 1-year survivors: intraventricular hemorrhage (IVH) (n = 59), persistent or transient cerebral ventriculomegaly (n = 50), persistent or transient intraparenchymal periventricular echodensity (n = 29), and cystic periventricular leukomalacia (n = 7). All lesions except isolated IVH were associated with adverse outcome; 37% of disabled children, 61% of multiply disabled children, and all children projected to become dependently disabled had parenchymal lesions with or without IVH. Triple lesions of IVH, cerebral ventriculomegaly, and intraparenchymal periventricular echodensity gave an odds ratio for disability of 50. Transient lesions had significant risk.
This province-based study provides a descriptive scheme of serial neonatal cerebral ultrasound lesions and outcome considered useful for clinicians caring for newborns of lowest gestational ages. The overall incidence of parenchymal lesions was lower than frequently reported. Combinations of lesions were linked to increased incidence, complexity, and severity of childhood disability.
在存在某些超声可检测到的颅内病变的情况下,早产儿出现不良神经发育结局更为常见。目前不同孕周早产儿脑实质变化的命名和分类导致了一些混淆。描述性定义可能具有临床实用性。区域化的围产期和新生儿护理有助于对这些病变及其后续结局进行基于人群的研究。
回顾了1987年至1990年期间在艾伯塔省出生的、体重500至1249克的艾伯塔省居民新生儿的2至3年结局,并与新生儿脑超声病变相关。计算了残疾的比值比和置信区间。
在这个体重组的960例活产中,669例(70%)存活至校正年龄1岁;646例(96.6%)在随访时接受了评估,其中80例(12.4%)有残疾:脑性瘫痪,8.7%;视力丧失,2.9%;听力丧失,1.3%;癫痫,0.6%;智力迟钝,4.8%;每个儿童有不止一种残疾,3.6%;预计为依赖性残疾,1.4%。在79例(11.8%)1岁存活者中发现超声检查时被认为可预测残疾的病变(不包括生发层出血),63例(9.4%)有脑实质病变:脑室内出血(IVH)(n = 59)、持续性或短暂性脑室扩大(n = 50)、持续性或短暂性脑室内周围实质回声增强(n = 29)以及脑室周围白质软化囊性变(n = 7)。除孤立性IVH外,所有病变均与不良结局相关;37%的残疾儿童、61%的多重残疾儿童以及所有预计将成为依赖性残疾的儿童都有伴或不伴IVH的脑实质病变。IVH、脑室扩大和脑室内周围实质回声增强的三联病变导致残疾的比值比为50。短暂性病变有显著风险。
这项基于该省的研究提供了一系列新生儿脑超声病变及其结局的描述性方案,对照顾最低孕周新生儿的临床医生有用。脑实质病变的总体发生率低于经常报道的情况。病变组合与儿童残疾的发生率增加、复杂性和严重程度相关。