Early Diagnosis of Cerebral Palsy in Preterm Infants with MRI, General Movements and Neurological Exam.

Shipra Jain, Karen Harpster, Stephanie Merhar, Beth Kline-Fath, Mekibib Altaye, Venkata Sita Priyanka Illapani, Colleen Peyton, Nehal A Parikh
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Abstract

Background: The increasing clinical use of combining structural MRI (sMRI) with General Movements Assessment (GMA) or Hammersmith Infant Neurological Exam (HINE) before five months corrected age (CA) for early diagnosis of cerebral palsy (CP) lacks sufficient prognostic data for children with CP, especially those with Gross Motor Function Classification System (GMFCS) I.

Objective: Evaluate the predictive value of sMRI, GMA, and HINE individually and in combination for early CP diagnosis and assess accuracy across varying GMFCS levels in a regional cohort of preterm infants.

Methods: We performed sMRI between 39-44 weeks postmenstrual age and GMA and HINE between 12-18 weeks CA in 395 preterm infants born at ≤32 weeks' gestation across five NICUs in Greater Cincinnati. Brain abnormalities on sMRI included white matter injuries, cortical and deep gray matter lesions, or extensive cerebellar hemorrhage. Absent fidgety movements constituted abnormal GMA; abnormal HINEs were scores <56. The primary outcome was CP diagnosis at 22-26 months CA, classified by the GMFCS. We calculated sensitivity, specificity, positive predictive value, negative predictive value, and likelihood ratios for individual tests and combinations.

Results: Of 338 (86%) infants with complete follow-up, 48 (14.2%) showed sMRI abnormalities, 15 (4.6%) had abnormal GMA, and 69 (20.9%) had abnormal HINE. Thirty-nine children (11.5%) developed CP at age 2, of which 28 had GMFCS level I and 11 had GMFCS >II. The combination of sMRI and GMA achieved 100% specificity but only 22% sensitivity while the combination of abnormal sMRI and HINE demonstrated sensitivity of 32% and specificity of 98% for prediction of CP. Individual or combined tests showed far higher sensitivity (78-100%) for predicting CP in children with GMFCS levels II-V.

Conclusions: The combination of sMRI with GMA or HINE demonstrated high specificity but low sensitivity for early CP diagnosis in a regional cohort of preterm infants. This approach appears effective for early detection of CP levels II-V but not for level I cases, the most prevalent type, underscoring the need for continued developmental follow-up for all very preterm infants and need for more sensitive diagnostic tools for early detection of CP.

Key points: Questions: What is the individual and combined prognostic accuracy of sMRI, GMA, and HINE for early diagnosis of CP in preterm infants?Findings: In our prospective, regional study of preterm infants born at ≤32 weeks' gestation, we found that combining brain abnormalities on sMRI with abnormal GMA achieved 100% specificity but 22% sensitivity for diagnosing CP. Individual or combined tests showed far higher sensitivity (78-100%) for predicting CP in children with GMFCS levels II-V. Both individual and combined tests were poor predictors of GMFCS level I CP, the most common type.Meaning: While sMRI combined with GMA or HINE is effective for diagnosing CP with GMFCS levels II-V, this approach falls short for children with GMFCS level I.

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MRI、全身运动及神经学检查对早产儿脑瘫的早期诊断。
背景:临床上越来越多地使用结构MRI (sMRI)与一般运动评估(GMA)或5个月矫正年龄(CA)前Hammersmith婴儿神经学检查(HINE)相结合的方法来早期诊断脑瘫(CP),但缺乏足够的脑瘫儿童预后数据,特别是那些具有大运动功能分类系统(GMFCS)的儿童。评估sMRI、GMA和HINE单独或联合对早期CP诊断的预测价值,并评估区域早产儿队列中不同GMFCS水平的准确性。方法:我们在大辛辛那提地区的5个新生儿重症监护病房对395名妊娠≤32周的早产儿在经后39-44周进行了sMRI,在12-18周进行了GMA和HINE。sMRI的脑部异常包括白质损伤、皮质和深部灰质病变或广泛的小脑出血。无烦躁运动构成GMA异常;结果:完整随访338例(86%)患儿中,sMRI异常48例(14.2%),GMA异常15例(4.6%),HINE异常69例(20.9%)。39名儿童(11.5%)在2岁时发生CP,其中28名儿童为GMFCS I级,11名儿童为GMFCS bb0 II级。sMRI和GMA联合检测的特异性为100%,但敏感性仅为22%,而异常sMRI和HINE联合检测预测CP的敏感性为32%,特异性为98%。单独或联合检测预测GMFCS水平为II-V的儿童CP的敏感性(78-100%)要高得多。结论:在一个地区早产儿队列中,sMRI联合GMA或HINE对早期CP诊断具有高特异性但低敏感性。该方法似乎对II-V级CP的早期检测有效,但对I级病例(最普遍的类型)无效,强调需要对所有极早产儿进行持续的发育随访,并需要更敏感的早期发现CP的诊断工具。问题:sMRI、GMA和HINE在早期诊断早产儿CP方面的个体和联合预后准确性是什么?研究结果:在我们对妊娠≤32周的早产儿进行的前瞻性、区域性研究中,我们发现将sMRI脑异常与GMA异常相结合诊断CP的特异性为100%,敏感性为22%。单个或联合试验显示,在GMFCS水平为II-V的儿童中,预测CP的敏感性要高得多(78-100%)。单独和联合试验对GMFCS I级CP(最常见的类型)的预测都很差。意义:虽然sMRI联合GMA或HINE对GMFCS水平为II-V的CP有效,但这种方法对GMFCS水平为I的儿童却不足。
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