Department of Pediatrics, Division of Neonatology, University of Virginia, Charlottesville, Virginia.
Department of Pediatrics, Division of Developmental Pediatrics, University of Virginia, Charlottesville, Virginia.
Am J Perinatol. 2022 Oct;29(14):1541-1547. doi: 10.1055/s-0041-1722943. Epub 2021 Feb 3.
Abnormal general movements (GMs) are predictive of later risk of motor impairments in preterm infants. The goals of this study are to (1) describe the implementation of the GM assessment (GMA) in a neonatal intensive care unit (NICU) and (2) investigate the prevalence and evolution of abnormal GMs in very low birth weight (VLBW) infants.
Observational study of GMs in VLBW infants (gestational age [GA] <32 weeks and/or birth weight [BW] <1,500 g) following GMA implementation in a level-IV NICU. All VLBW infants admitted between November 2017 and April 2019 were eligible for the GMA. Infants were excluded if they required high-frequency ventilation or if they could not be unbundled for video acquisition. GMAs were scored weekly by at least 2 GMA-certified providers.
The GMA was performed in 121 VLBW infants with a mean (standard deviation [SD]) GA of 28.3 (2.6) and BW of 1,113 (400 g). Only 28% of infants had normal GMs on initial assessment (32.9 ± 2.7 weeks' GA), while 61 and 11% had poor repertoire and cramped-synchronized GMs, respectively. At NICU discharge (37.6 ± 3.4 weeks corrected GA), 45 and 21% of infants were classified as having poor repertoire and cramped-synchronized GMs, respectively. Most infants with cramped-synchronized GMs on initial assessment had persistent abnormal GMs at discharge. In contrast, only one infant with normal GMs on first assessment developed cramped-synchronized GMs.
Abnormal GMs are common in VLBW infants, including a high prevalence of the more concerning cramped-synchronized movement pattern. The GMA can be successfully performed in VLBW infants. The GMA may be helpful in identifying infants at increased risk of later motor impairments, as well as assisting clinicians, in the stratification of infants who may benefit from additional brain imaging and/or an intensive hospital-based interventions.
· Abnormal GMs are common in VLBW infants.. · Poor repertoire in the most prevalent pattern observed.. · Infants at risk for abnormal motor outcomes can be identified in the NICU..
异常的一般运动(GMs)可预测早产儿日后运动功能受损的风险。本研究的目的是:(1)描述新生儿重症监护病房(NICU)中 GM 评估(GMA)的实施情况;(2)调查极低出生体重(VLBW)婴儿中异常 GMs 的发生率和演变情况。
对 NICU 实施 GMA 后纳入的 VLBW 婴儿(胎龄[GA]<32 周和/或出生体重[BW]<1500g)进行 GMs 的观察性研究。所有 2017 年 11 月至 2019 年 4 月期间入住的 VLBW 婴儿均符合 GMA 条件。如果婴儿需要高频通气或无法拆开进行视频采集,则将其排除在外。每周至少由 2 名 GMA 认证的提供者对 GMA 进行评分。
121 名 VLBW 婴儿接受了 GMA,平均(标准差[SD])GA 为 28.3(2.6),BW 为 1113(400g)。只有 28%的婴儿在初次评估时 GM 正常(GA32.9±2.7 周),而 61%和 11%的婴儿 GM 模式分别为模式差和紧促同步。在 NICU 出院时(校正 GA37.6±3.4 周),45%和 21%的婴儿分别被归类为 GM 模式差和紧促同步。初次评估时 GM 紧促同步的大多数婴儿在出院时 GM 仍异常。相比之下,初次评估 GM 正常的婴儿中只有 1 例出现 GM 紧促同步。
异常 GMs 在 VLBW 婴儿中很常见,包括更常见的紧促同步运动模式的高发生率。GMA 可成功应用于 VLBW 婴儿。GMA 可能有助于识别日后运动功能受损风险较高的婴儿,并协助临床医生对可能受益于额外脑成像和/或强化医院干预的婴儿进行分层。
· VLBW 婴儿中异常 GMs 很常见。
· 观察到最常见的模式为 GM 模式差。
· 在 NICU 中可识别出有异常运动结局风险的婴儿。