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首页> 外文期刊>Early human development >Developmental outcome at 18 and 24 months of age in very preterm children: a cohort study from 1996 to 1997.
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Developmental outcome at 18 and 24 months of age in very preterm children: a cohort study from 1996 to 1997.

机译:早产儿在18和24个月大时的发育结局:一项从1996年至1997年的队列研究。

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摘要

OBJECTIVE: To determine the effect of prematurity (gestational age (GA) < 32 weeks) on developmental outcome at the corrected age of 18 and 24 months in a regionally defined, prospective cohort study. STUDY DESIGN: The Leiden Follow-Up Project on Prematurity (LFUPP) includes all live-born infants < 32 weeks GA, born in 1996/1997 in three Dutch health regions (n=266). Mental and psychomotor developmental indices (MDI, PDI) were determined with the Bayley Scales of Infant Development I: > or = -1 S.D.: normal, -2 to -1 S.D.: moderate delay and < -2 S.D.: severe delay. RESULTS: At 18 months 168 (71%) and at 24 months, 151 children (64%) of 235 survivors were assessed. Moderate to severely delayed mental and/or psychomotor development occurred in 40% of the children at both ages. Children lost to follow-up were of lower socioeconomic status and more frequently of non-Dutch origin. Since non-Dutch origin negatively affected the outcome at both test ages, availability of the data of these children would probably have worsened the outcome. Postnatal treatment with dexamethasone was associated with an increased risk of delayed development. Other independent predictors of delayed development were bronchopulmonary dysplasia at 18 months and ethnicity, maternal age at birth, birthweight and gender at 24 months. After adjustment for these other predictors of delayed development, the mean PDI of dexamethasone-treated infants was 16.1 points lower than of non-treated infants at 18 months (p=0.03) and 12.7 points lower at 24 months (p=0.04). CONCLUSIONS: At 18 and 24 months corrected age, 40% of the very prematurely born children had both delayed mental and/or psychomotor development. Treatment with dexamethasone postnatally was a major risk factor for delayed (psychomotor) development.
机译:目的:在区域定义的前瞻性队列研究中,确定早产(胎龄(GA)<32周)在校正后的18和24个月年龄对发育结果的影响。研究设计:莱顿早产儿随访项目(LFUPP)包括所有GA <32周的活产婴儿,出生于1996/1997年的荷兰三个健康地区(n = 266)。心理和心理运动发育指数(MDI,PDI)是根据婴儿发育的Bayley量表I确定的:>或= -1 S.D .:正常; -2至-1 S.D .:中度延迟; <-2 S.D .:重度延迟。结果:在18个月时,有168名(71%)和24个月时,对235名幸存者中的151名儿童(64%)进行了评估。两个年龄段的儿童中,有40%的儿童出现中度至严重延迟的精神和/或精神运动发育。失去随访的儿童的社会经济地位较低,非荷兰裔儿童更为常见。由于非荷兰血统在两个测试年龄均对结果产生负面影响,因此这些儿童的数据可用性可能会使结果恶化。地塞米松的产后治疗与延迟发育的风​​险增加有关。发育迟缓的其他独立预测指标是18个月时的支气管肺发育不良以及24个月时的种族,出生时的母亲年龄,出生体重和性别。在对这些其他延迟发育的预测因素进行调整之后,地塞米松治疗的婴儿在18个月时的平均PDI比未治疗的婴儿低16.1点(p = 0.03),而在24个月时则降低了12.7点(p = 0.04)。结论:在矫正年龄为18和24个月时,40%的早产儿智力和/或精神运动发育均延迟。出生后地塞米松治疗是发育迟缓(精神运动)的主要危险因素。

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