Keith C G, Doyle L W
Division of Paediatrics, Royal Women's Hospital, Carlton, Parkville, Australia.
J Paediatr Child Health. 1995 Apr;31(2):134-6. doi: 10.1111/j.1440-1754.1995.tb00762.x.
To review the incidence and severity of retinopathy of prematurity (ROP) in infants with birthweights 1000-1249 g and 1250-1499 g, to establish whether the upper weight limit for routine ophthalmological examination might safely be lowered.
Prospective cohort study of infants born between 1 January 1977 and 31 December 1992 cared for in the neonatal nurseries at the Royal Women's Hospital, Melbourne. Data were retrieved on 1373 infants who survived their initial hospitalization. They comprised 657 with birthweights 1000-1249 g (group 1) and 716 with birthweights 1250-1499 g (group 2). There were 76 outborn infants in group 1 and 97 in group 2; the remaining infants were all born at the Royal Women's Hospital. Ocular examinations commenced at 2 weeks of age, when possible, and at 2-weekly intervals after that.
In group 1, ROP was detected in 14.6% (96/657) and severe ROP (bilateral stage 3-5) in 5.0% (33/657). Five (0.8%) children required surgical intervention (reaching threshold disease); following surgery, one was legally blind, one had severely impaired vision, and the other three had near-normal vision. Another child was blind; he was born at 28 weeks gestational age with a birthweight of 1170 g, and was transferred to a Level II hospital at 9 weeks chronological age with no detectable retinopathy. He returned 1 year later totally blind with detached retinae (grade 5 ROP). The prevalence of bilateral blindness in this group was 0.3% (2/657). In group 2, ROP was detected in 6.4% (46/716) and severe ROP in 0.8% (6/716). No children required surgery; three were found to be myopic at follow-up but the corrected visual acuity was normal. No children in group 2 were blind. No significant difference was found between the rates of ROP in inborn and outborn infants.
In neonatal units with similar rates of ROP and visual outcome, routine ophthalmological examination in the neonatal nursery of infants weighing more than 1249 g at birth is probably unnecessary.
回顾出生体重在1000 - 1249克和1250 - 1499克的婴儿中早产儿视网膜病变(ROP)的发病率和严重程度,以确定常规眼科检查的体重上限是否可以安全降低。
对1977年1月1日至1992年12月31日在墨尔本皇家妇女医院新生儿重症监护室接受护理的婴儿进行前瞻性队列研究。检索了1373名在首次住院后存活的婴儿的数据。其中657名婴儿出生体重为1000 - 1249克(第1组),716名婴儿出生体重为1250 - 1499克(第2组)。第1组有76名外院出生的婴儿,第2组有97名;其余婴儿均在皇家妇女医院出生。眼部检查尽可能在出生后2周开始,之后每2周进行一次。
在第1组中,检测到ROP的比例为14.6%(96/657),严重ROP(双侧3 - 5期)的比例为5.0%(33/657)。5名(0.8%)儿童需要手术干预(达到阈值病变);手术后,1名儿童法定失明,1名视力严重受损,另外3名视力接近正常。另一名儿童失明;他孕28周出生,出生体重1170克,出生后9周时转至二级医院,当时未检测到视网膜病变。1年后他因视网膜脱离(5期ROP)完全失明。该组双侧失明的患病率为0.3%(2/657)。在第2组中,检测到ROP的比例为6.4%(46/716),严重ROP的比例为0.8%(6/716)。没有儿童需要手术;随访时发现3名儿童近视,但矫正视力正常。第2组中没有儿童失明。在本院出生和外院出生的婴儿中,ROP发生率没有显著差异。
在ROP发生率和视力预后相似的新生儿病房,对出生体重超过1249克的婴儿在新生儿重症监护室进行常规眼科检查可能没有必要。