Luke Carly, Mick-Ramsamy Leeann, Bos Arend F, Benfer Katherine A, Bosanquet Margot, Gordon Anya, Williams Hailey, Taifalos Chloe, Smith Maria, Leishman Shaneen, Oakes Ellena, Kentish Megan, McNamara Lynda, Ware Robert S, Boyd Roslyn N
Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, The University of Queensland, Brisbane, Australia; Queensland Paediatric Rehabilitation Service, Children's Health Queensland Hospital and Health Service, Brisbane, Australia.
Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, The University of Queensland, Brisbane, Australia.
Early Hum Dev. 2024 May;192:106004. doi: 10.1016/j.earlhumdev.2024.106004. Epub 2024 Apr 8.
To implement a culturally-adapted screening program aimed to determine the ability of infant motor repertoire to predict early neurodevelopment on the Hammersmith Infant Neurological Examination (HINE) and improve Australian First Nations families' engagement with neonatal screening.
A prospective cohort of 156 infants (55 % male, mean (standard deviation [SD]) gestational age 33.8 (4.6) weeks) with early life risk factors for adverse neurodevelopmental outcomes (ad-NDO) participated in a culturally-adapted screening program. Infant motor repertoire was assessed using Motor Optimality Score-revised (MOS-R), captured over two videos, 11-13 weeks (V1; <14 weeks) and 14-18 weeks (V2; ≥14 weeks) corrected age (CA). At 4-9 months CA neurodevelopment was assessed on the HINE and classified according to age-specific cut-off and optimality scores as; developmentally 'on track' or high chance of either adverse neurodevelopmental outcome (ad-NDO) or cerebral palsy (CP).
Families were highly engaged, 139/148 (94 %) eligible infants completing MOS-R, 136/150 (91 %), HINE and 123 (83 %) both. Lower MOS-R at V2 was associated with reduced HINE scores (β = 1.73, 95 % confidence interval [CI] = 1.03-2.42) and high chance of CP (OR = 2.63, 95%CI = 1.21-5.69) or ad-NDO (OR = 1.38, 95%CI = 1.10-1.74). The MOS-R sub-category 'observed movement patterns' best predicted HINE, infants who score '4' had mean HINE 19.4 points higher than score '1' (95%CI = 12.0-26.9). Receiver-operator curve analyses determined a MOS-R cut-off of <23 was best for identifying mild to severely reduced HINE scores, with diagnostic accuracy 0.69 (sensitivity 0.86, 95%CI 0.76-0.94 and specificity 0.40, 95 % CI 0.25-0.57). A trajectory of improvement on MOS-R (≥2 point increase in MOS-R from 1st to 2nd video) significantly increased odds of scoring optimally on HINE (OR = 5.91, 95%CI 1.16-29.89) and may be a key biomarker of 'on track' development.
Implementation of a culturally-adapted program using evidence-based assessments demonstrates high retention. Infant motor repertoire is associated with HINE scores and the early neurodevelopmental status of developmentally vulnerable First Nations infants.
实施一项经过文化调适的筛查项目,旨在确定婴儿运动技能储备对哈默史密斯婴儿神经学检查(HINE)早期神经发育的预测能力,并提高澳大利亚原住民家庭对新生儿筛查的参与度。
156名有神经发育不良不良结局(ad-NDO)早期生活风险因素的婴儿(55%为男性,平均(标准差[SD])胎龄33.8(4.6)周)的前瞻性队列参与了一项经过文化调适的筛查项目。使用修订后的运动最优性评分(MOS-R)评估婴儿运动技能储备,通过两个视频进行记录,分别在矫正年龄(CA)11 - 13周(V1;<14周)和14 - 18周(V2;≥14周)时拍摄。在矫正年龄4 - 9个月时,根据HINE对神经发育进行评估,并根据特定年龄的临界值和最优性评分分类为:发育“正常”或有神经发育不良不良结局(ad-NDO)或脑瘫(CP)的高风险。
家庭参与度很高,139/148名(94%)符合条件的婴儿完成了MOS-R评估,136/150名(91%)完成了HINE评估,123名(83%)两项评估均完成。V2时较低的MOS-R与较低的HINE评分相关联(β = 1.73,95%置信区间[CI] = 1.03 - 2.42),以及CP(OR = 2.63,95%CI = 1.21 - 5.69)或ad-NDO(OR = 1.38,95%CI = 1.10 - 1.74)的高风险相关。MOS-R子类别“观察到的运动模式”对HINE的预测效果最佳,得分为“4”的婴儿的平均HINE得分比得分为“1”的婴儿高19.4分(95%CI = 12.0 - 26.9)。受试者工作特征曲线分析确定,MOS-R临界值<23最适合识别轻度至重度降低的HINE评分,诊断准确性为0.69(敏感性0.86, 95%CI 0.76 - 0.94,特异性0.40, 95%CI 0.25 - 0.57)。MOS-R的改善轨迹(从第一个视频到第二个视频MOS-R增加≥2分)显著增加了在HINE上获得最优评分的几率(OR = 5.91,95%CI 1.16 - 29.89),并且可能是“正常”发育轨迹的关键生物标志物。
使用循证评估实施经过文化调适的项目显示出高保留率。婴儿运动技能储备与HINE评分以及发育脆弱的原住民婴儿的早期神经发育状况相关。