Developmental Assessment Unit, Second Department of Pediatrics, National and Kapodistrian University of Athens School of Medicine, P, & A, Kyriakou Children's Hospital, Athens, Greece.
BMC Pediatr. 2014 Feb 12;14:40. doi: 10.1186/1471-2431-14-40.
Although several determinants of global developmental delay (GDD) have been recognized, a significant number of children remain without definitive etiologic diagnosis. The objective of this study was to assess the effect of various prenatal and perinatal factors on the severity and outcome of developmental delay without definitive etiologic yield.
From March 2008 to February 2010, 142 children with developmental quotient (DQ) <70 and without definitive etiologic diagnosis, were included. Prenatal and perinatal risk factors known to be associated with disordered neonatal brain function were identified. Participants underwent a thorough investigation, an individualized habilitation plan was recommended, and the children were followed-up regularly for a period of 2 < years. The effect of prenatal and perinatal risk factors on the severity and outcome of GDD was assessed by regression analysis.
The mean age at enrolment was 31 ± 12 < months, and the mean DQ 52.2 ± 11.4. Prematurity and intrauterine growth restriction (IUGR) were found to be independently associated with lower DQ values. The mean DQ after the 2-year follow-up was 62.5 ± 12.7, and the DQ difference from the enrollment 10.4 ± 8.9 (median 10; range-10 to 42). DQ improvement (defined as a DQ difference?≥?median) was noted in 52.8% of the children. IUGR, low socio-economic status, and poor compliance to habilitation plan were found to be independently associated with poorer developmental outcomes.
Prematurity and IUGR were found to be significantly and independently related to the severity of GDD in cases without definitive etiologic yield. Poorer 2-year developmental outcome was associated with IUGR, low socioeconomic status and non compliance to habilitation plan. Prematurity was a significant determinant of the outcome only in association with the above mentioned factors.
尽管已经确定了一些导致全球发育迟缓(GDD)的因素,但仍有相当数量的儿童无法明确病因诊断。本研究旨在评估各种产前和围产期因素对无明确病因诊断的发育迟缓严重程度和结局的影响。
2008 年 3 月至 2010 年 2 月,纳入了 142 名发育商(DQ)<70 且无明确病因诊断的儿童。确定了与新生儿脑功能障碍相关的已知产前和围产期危险因素。对参与者进行了全面的调查,建议制定个性化的康复计划,并对其进行了为期 2 年以上的定期随访。通过回归分析评估产前和围产期危险因素对 GDD 严重程度和结局的影响。
入组时的平均年龄为 31 ± 12 个月,平均 DQ 为 52.2 ± 11.4。早产和宫内生长受限(IUGR)被发现与较低的 DQ 值独立相关。2 年随访后的平均 DQ 为 62.5 ± 12.7,与入组时的 DQ 差值为 10.4 ± 8.9(中位数为 10;范围-10 至 42)。52.8%的儿童的 DQ 得到改善(定义为 DQ 差值≥中位数)。IUGR、低社会经济地位和康复计划执行不佳与较差的发育结局独立相关。
在无明确病因诊断的情况下,早产和 IUGR 与 GDD 的严重程度显著且独立相关。较差的 2 年发育结局与 IUGR、低社会经济地位和不遵守康复计划相关。早产仅在与上述因素相关时才是结局的重要决定因素。