Caesar Rebecca, Boyd Roslyn N, Colditz Paul, Cioni Giovani, Ware Robert S, Salthouse Kaye, Doherty Julie, Jackson Maxine, Matthews Leanne, Hurley Tom, Morosini Anthony, Thomas Clare, Camadoo Laxmi, Baer Erica
Faculty of Medicine and Biomedical Science, School of Medicine, The University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre (QCPRRC), South Brisbane, Queensland, Australia Sunshine Coast Hospital and Health Service, Allied Health Women's and Families, Nambour General Hospital, Nambour, Queensland, Australia.
Faculty of Medicine and Biomedical Science, School of Medicine, The University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre (QCPRRC), South Brisbane, Queensland, Australia.
BMJ Open. 2016 Jul 4;6(7):e010726. doi: 10.1136/bmjopen-2015-010726.
Over 80% of very preterm (<32 weeks) and very low birthweight (<1500 g) infants will have either typical development (TD) or mild developmental delay (MDD) in multiple domains. As differentiation between TD and MDD can be difficult, infants with MDD often miss opportunities for intervention. For many clinicians, the ongoing challenge is early detection of MDD without over servicing the population. This study aims to: (1) identify early clinical biomarkers for use in this population to predict and differentiate between TD and MDD at 24 months corrected age. (2) Determine the extent to which family and caregiver factors will contribute to neurodevelopmental and behavioural outcomes.
Participants will be a prospective cohort of 90 infants (<32 weeks and/or <1500 g). Between 34 weeks gestational age and 16 weeks post-term, infants will have a series of 5 neurological, neuromotor, neurobehavioural and perceptual assessments including General Movement Assessment at preterm, writhing and fidgety age. Primary caregivers will complete questionnaires to identify social risk, maternal depression and family strain. Extensive perinatal data will be collected from the medical record. At 24 months, corrected age (c.a) infants will be assessed using standardised tools including the Bayley Scales of Infant and Toddler Development-Third Edition (Bayley III). Longitudinal trajectories of early assessment findings will be examined to determine any predictive relationship with motor and cognitive outcomes at 24 months c.a. Published data of a cohort of Australian children assessed with the Bayley III at 24 months c.a will provide a reference group of term-born controls.
Ethical approval has been obtained from the Queensland Children's Health Services Human Research Ethics Committee (HREC/13/QRCH/66), the University of Queensland (2013001019) and the Sunshine Coast Hospital and Health Service, SC-Research Governance (SSA/13/QNB/66). Publication of all study outcomes will be in peer-reviewed journals.
ACTRN12614000480684; Pre-results.
超过80%的极早产儿(<32周)和极低出生体重儿(<1500克)在多个领域将呈现典型发育(TD)或轻度发育迟缓(MDD)。由于区分TD和MDD可能存在困难,患有MDD的婴儿常常错过干预机会。对于许多临床医生而言,持续面临的挑战是在不过度服务人群的情况下早期发现MDD。本研究旨在:(1)识别适用于该人群的早期临床生物标志物,以预测和区分24个月矫正年龄时的TD和MDD。(2)确定家庭和照料者因素对神经发育和行为结果的影响程度。
参与者将是90名婴儿(<32周和/或<1500克)的前瞻性队列。在孕34周龄至足月后16周期间,婴儿将接受一系列5次神经学、神经运动、神经行为和感知评估,包括早产儿期的全身运动评估、扭动和不安运动评估。主要照料者将完成问卷以确定社会风险、母亲抑郁和家庭压力。将从病历中收集广泛的围产期数据。在24个月矫正年龄时,将使用标准化工具对婴儿进行评估,包括贝利婴幼儿发展量表第三版(Bayley III)。将检查早期评估结果的纵向轨迹,以确定与24个月矫正年龄时的运动和认知结果之间的任何预测关系。一组在24个月矫正年龄时接受Bayley III评估的澳大利亚儿童的已发表数据将提供足月儿对照组的参考群体。
已获得昆士兰儿童健康服务人类研究伦理委员会(HREC/13/QRCH/66)、昆士兰大学(2013001019)以及阳光海岸医院和健康服务中心(SC - 研究治理,SSA/13/QNB/66)的伦理批准。所有研究结果将发表在同行评审期刊上。
ACTRN12614000480684;预结果。