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变形性斜头畸形严重程度及新生儿发育迟缓的评估

Assessment of Deformational Plagiocephaly Severity and Neonatal Developmental Delay.

作者信息

Fontana Stefani C, Daniels Debora, Greaves Thomas, Nazir Niaman, Searl Jeff, Andrews Brian T

机构信息

*Department of Plastic Surgery†Department of Hearing and Speech, University of Kansas Medical Center‡Department of Preventive Medicine & Public Health, University of Kansas, Kansas City, KS.

出版信息

J Craniofac Surg. 2016 Nov;27(8):1934-1936. doi: 10.1097/SCS.0000000000003014.

Abstract

Deformational plagiocephaly (DP) in infants has been associated with developmental delay that can last until adolescence. Despite this association and a 5-fold increase in incidence of DP over the past 2 decades, there are currently no guidelines regarding screening for developmental delay or identification of which infants with DP are at the greatest risk of delay. A prospective, nonrandomized study was performed. Infants diagnosed with DP who had no prior intervention were eligible for enrollment. Cranial deformity was measured by cross-cranial measurements using calipers, and developmental delay was measured using the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III). Correlation between cranial deformity and developmental delay was analyzed using a linear regression. Twenty-seven infants, ages 4.0 to 11.0 months (mean = 6.61 months) diagnosed with DP were studied. Developmental delay was observed on the composite language (n = 3 of 27, 11%), and composite motor (n = 5 of 23, 22%) scales, but not the cognitive scale. Severity of cranial deformity did not correlate with scores on any Bayley-III scales (cognitive R = 0.058, P = 0.238; composite language R = 0.03, P = 0.399; composite motor R = 0.0195, P = 0.536). This study demonstrates that severity of cranial deformity cannot be used to predict presence or degree of developmental delay. Craniofacial surgeons should be aware of this risk and consider developmental screening based on clinical suspicion.

摘要

婴儿的变形性斜头畸形(DP)与可能持续至青春期的发育迟缓有关。尽管存在这种关联,且在过去20年中DP的发病率增加了5倍,但目前尚无关于发育迟缓筛查或确定哪些患有DP的婴儿发生发育迟缓风险最高的指南。进行了一项前瞻性、非随机研究。未接受过先前干预且被诊断为DP的婴儿符合入组条件。使用卡尺通过跨颅骨测量来测量颅骨畸形,并使用贝利婴幼儿发展量表第三版(Bayley-III)来测量发育迟缓。使用线性回归分析颅骨畸形与发育迟缓之间的相关性。对27名年龄在4.0至11.0个月(平均=6.61个月)被诊断为DP的婴儿进行了研究。在综合语言量表(27名中有3名,11%)和综合运动量表(23名中有5名,22%)上观察到发育迟缓,但在认知量表上未观察到。颅骨畸形的严重程度与任何Bayley-III量表的得分均无相关性(认知R=0.058,P=0.238;综合语言R=0.03,P=0.399;综合运动R=0.0195,P=0.536)。这项研究表明,颅骨畸形的严重程度不能用于预测发育迟缓的存在或程度。颅面外科医生应意识到这种风险,并根据临床怀疑考虑进行发育筛查。

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