Kitchen W H, Ryan M M, Rickards A, McDougall A B, Billson F A, Keir E H, Naylor F D
Dev Med Child Neurol. 1980 Apr;22(2):172-88. doi: 10.1111/j.1469-8749.1980.tb04326.x.
A cohort of 169 very low-birthweight infants (800 to 1500g) was followed prospectively to the age of eight years. Information on 159 of the children was available at that age, and for a further five to the age of six years. A comparison group of 67 normal-birthweight children was also followed, but only 43 of these children were seen at the age of eight years. Eight of the very low-birthweight (VLBW) children were attending special schools and 156 attended normal schools: placement of the remaining five was unknown. Of the VLBW children who were adequately assessed, 15.9 per cent were either not reading or were retarded by more than 18 months. Mean VLBW full-scale IQ was 88.8, compared with 98.8 for the normal-birthweight group. A subgroup of 10 VLBW children with birthweights under 1000g had lower mean scores on all three WISC-R scales compared with those with birthweights between 1000 and 1500g. Of the adequately assessed VLBW children, 3.7 per cent had epilepsy, 3.7 per cent had significant sensorineural deafness and 2.4 per cent suffered from cerebral palsy. One or more visual defects were detected in 31.4 per cent of the children, though in only 3.8 per cent was the defect serious. At eight years, growth dimensions for the VLBW children were below the 10th percentile for 11.0 per cent in weight, 16.1 per cent in height and 15.0 per cent in head circumference. Degrees of handicap in the VLBW children were profound in 5.1 per cent, severe in 10.8 per cent and significant in 40.5 per cent: handicap was minimal or absent in the remaining 43.6 per cent. For the normal-birthweight group the percentages were 2.3, 0, 25.6 and 72.1 respectively. The VLBW children with minimal or no handicap were considered to have a satisfactory outcome. This was significantly correlated with the following: gestation over 30 weeks; birthweight over 1199g; no major apnoeic attacks; lowest postnatal weight before six days; return to birth weight before 21 days; peak serum bilirubin not exceeding 255 mumol/litre; and parental social-class between 2 and 5 on the seven-point Congalton Scale.
对169名极低出生体重儿(800至1500克)进行了前瞻性跟踪研究,直至其8岁。在8岁时获取了其中159名儿童的信息,另有5名儿童的信息收集至6岁。还对67名正常出生体重儿童组成的对照组进行了跟踪,但8岁时仅见到其中43名儿童。169名极低出生体重儿中,8名就读于特殊学校,156名就读于普通学校:其余5名儿童的就读情况不明。在经过充分评估的极低出生体重儿中,15.9%的儿童要么不会阅读,要么阅读能力滞后超过18个月。极低出生体重儿的平均全量表智商为88.8,而正常出生体重组为98.8。出生体重低于1000克的10名极低出生体重儿亚组在韦氏儿童智力量表修订版(WISC-R)的所有三个分量表上的平均得分均低于出生体重在1000至1500克之间的儿童。在经过充分评估的极低出生体重儿中,3.7%患有癫痫,3.7%患有严重感音神经性耳聋,2.4%患有脑瘫。31.4%的儿童检测出一种或多种视力缺陷,但只有3.8%的缺陷较为严重。8岁时,极低出生体重儿的生长指标低于第10百分位数的比例为:体重11.0%、身高16.1%、头围15.0%。极低出生体重儿中,5.1%存在严重残疾,10.8%为重度残疾,40.5%为中度残疾:其余43.6%的残疾程度轻微或无残疾。正常出生体重组的相应比例分别为2.3%、0、25.6%和72.1%。残疾程度轻微或无残疾的极低出生体重儿被认为预后良好。这与以下因素显著相关:孕周超过30周;出生体重超过1199克;无严重呼吸暂停发作;出生后6天内最低体重;21天内恢复至出生体重;血清胆红素峰值不超过255微摩尔/升;以及父母在七点康加尔顿量表上的社会阶层为2至5级。