Department of Paediatrics, University of Cambridge, Cambridge, UK.
Section of Neonatal Medicine, Department of Medicine, Chelsea and Westminster Hospital Campus, Imperial College London, London, UK.
Arch Dis Child Fetal Neonatal Ed. 2018 Sep;103(5):F479-F484. doi: 10.1136/archdischild-2016-312535. Epub 2017 Oct 27.
To determine the validity of assessing and recording the neurodevelopmental outcome of very preterm infants during routine clinical follow-up in England.
Children born <30 weeks gestation, attending routine clinical follow-up at post-term ages 20-28 months, were recruited. Data on neurodevelopmental outcomes were recorded by the reviewing clinician in a standardised format in the child's electronic patient record, based on a set of key questions designed to be used without formal training or developmental testing. Using a predefined algorithm, each participant was classified as having 'no', 'mild/moderate' or 'severe' impairment in cognitive, communication and motor domains. All participants also received a research assessment by a single assessor using the Bayley Scales of Infant Development, third edition (Bayley-III). The sensitivity and specificity of routine data in capturing impairment (any Bayley-III score <85) or severe impairment (any Bayley-III score <70) was calculated.
190 children participated. The validity of routine assessments in identifying children with no impairment and no severe impairment was high across all domains (specificities 83.9%-100.0% and 96.6%-100.0%, respectively). However, identification of impairments, particularly in the cognitive (sensitivity 69.7% (55.1%-84.3%)) and communication (sensitivity (53.2% (42.0%-64.5%)) domains, was poor.
Neurodevelopmental status determined during routine clinical assessment lacks adequate sensitivity in cognitive and communication domains. It is uncertain whether this reflects the assessment or/and the recording of findings. As early intervention may improve education and social outcomes, this is an important area for healthcare quality improvement research.
在英格兰,通过常规临床随访评估和记录极早产儿的神经发育结局的有效性。
研究纳入了在足月后 20-28 个月期间接受常规临床随访、胎龄<30 周的儿童。神经发育结局数据由审查临床医生根据一组旨在无需正式培训或发育测试即可使用的关键问题,以标准化格式记录在患儿的电子病历中。使用预定义的算法,每位参与者被分类为在认知、沟通和运动领域具有“无”、“轻度/中度”或“重度”障碍。所有参与者还接受了一位评估者使用贝利婴幼儿发展量表第三版(Bayley-III)进行的研究评估。计算了常规数据捕捉损伤(任何 Bayley-III 评分<85)或严重损伤(任何 Bayley-III 评分<70)的敏感性和特异性。
190 名儿童参与了研究。在所有领域中,常规评估识别无损伤和无严重损伤儿童的有效性均较高(特异性分别为 83.9%-100.0%和 96.6%-100.0%)。然而,损伤的识别,特别是在认知(敏感性 69.7%(55.1%-84.3%))和沟通(敏感性(53.2%(42.0%-64.5%))领域,较差。
常规临床评估中确定的神经发育状况在认知和沟通领域缺乏足够的敏感性。这尚不确定是反映评估还是/和记录结果。由于早期干预可能改善教育和社会结果,因此这是医疗保健质量改进研究的一个重要领域。