Novak Iona, Morgan Cathy, Adde Lars, Blackman James, Boyd Roslyn N, Brunstrom-Hernandez Janice, Cioni Giovanni, Damiano Diane, Darrah Johanna, Eliasson Ann-Christin, de Vries Linda S, Einspieler Christa, Fahey Michael, Fehlings Darcy, Ferriero Donna M, Fetters Linda, Fiori Simona, Forssberg Hans, Gordon Andrew M, Greaves Susan, Guzzetta Andrea, Hadders-Algra Mijna, Harbourne Regina, Kakooza-Mwesige Angelina, Karlsson Petra, Krumlinde-Sundholm Lena, Latal Beatrice, Loughran-Fowlds Alison, Maitre Nathalie, McIntyre Sarah, Noritz Garey, Pennington Lindsay, Romeo Domenico M, Shepherd Roberta, Spittle Alicia J, Thornton Marelle, Valentine Jane, Walker Karen, White Robert, Badawi Nadia
Cerebral Palsy Alliance, The University of Sydney, Sydney, Australia.
Norwegian University of Science and Technology, St Olavs University Hospital, Trondheim.
JAMA Pediatr. 2017 Sep 1;171(9):897-907. doi: 10.1001/jamapediatrics.2017.1689.
Cerebral palsy describes the most common physical disability in childhood and occurs in 1 in 500 live births. Historically, the diagnosis has been made between age 12 and 24 months but now can be made before 6 months' corrected age.
To systematically review best available evidence for early, accurate diagnosis of cerebral palsy and to summarize best available evidence about cerebral palsy-specific early intervention that should follow early diagnosis to optimize neuroplasticity and function.
This study systematically searched the literature about early diagnosis of cerebral palsy in MEDLINE (1956-2016), EMBASE (1980-2016), CINAHL (1983-2016), and the Cochrane Library (1988-2016) and by hand searching. Search terms included cerebral palsy, diagnosis, detection, prediction, identification, predictive validity, accuracy, sensitivity, and specificity. The study included systematic reviews with or without meta-analyses, criteria of diagnostic accuracy, and evidence-based clinical guidelines. Findings are reported according to the PRISMA statement, and recommendations are reported according to the Appraisal of Guidelines, Research and Evaluation (AGREE) II instrument.
Six systematic reviews and 2 evidence-based clinical guidelines met inclusion criteria. All included articles had high methodological Quality Assessment of Diagnostic Accuracy Studies (QUADAS) ratings. In infants, clinical signs and symptoms of cerebral palsy emerge and evolve before age 2 years; therefore, a combination of standardized tools should be used to predict risk in conjunction with clinical history. Before 5 months' corrected age, the most predictive tools for detecting risk are term-age magnetic resonance imaging (86%-89% sensitivity), the Prechtl Qualitative Assessment of General Movements (98% sensitivity), and the Hammersmith Infant Neurological Examination (90% sensitivity). After 5 months' corrected age, the most predictive tools for detecting risk are magnetic resonance imaging (86%-89% sensitivity) (where safe and feasible), the Hammersmith Infant Neurological Examination (90% sensitivity), and the Developmental Assessment of Young Children (83% C index). Topography and severity of cerebral palsy are more difficult to ascertain in infancy, and magnetic resonance imaging and the Hammersmith Infant Neurological Examination may be helpful in assisting clinical decisions. In high-income countries, 2 in 3 individuals with cerebral palsy will walk, 3 in 4 will talk, and 1 in 2 will have normal intelligence.
Early diagnosis begins with a medical history and involves using neuroimaging, standardized neurological, and standardized motor assessments that indicate congruent abnormal findings indicative of cerebral palsy. Clinicians should understand the importance of prompt referral to diagnostic-specific early intervention to optimize infant motor and cognitive plasticity, prevent secondary complications, and enhance caregiver well-being.
脑性瘫痪是儿童期最常见的身体残疾,每500例活产儿中就有1例患病。从历史上看,诊断通常在12至24个月龄时做出,但现在可以在矫正年龄6个月之前做出。
系统回顾关于脑性瘫痪早期准确诊断的最佳现有证据,并总结关于脑性瘫痪特异性早期干预的最佳现有证据,这种早期干预应在早期诊断后进行,以优化神经可塑性和功能。
本研究系统检索了MEDLINE(1956 - 2016年)、EMBASE(1980 - 2016年)、CINAHL(1983 - 2016年)和Cochrane图书馆(1988 - 2016年)中关于脑性瘫痪早期诊断的文献,并进行了手工检索。检索词包括脑性瘫痪、诊断、检测、预测、识别、预测效度、准确性、敏感性和特异性。该研究纳入了有或没有Meta分析的系统评价、诊断准确性标准以及循证临床指南。研究结果根据PRISMA声明报告,建议根据指南研究与评价(AGREE)II工具报告。
六项系统评价和两项循证临床指南符合纳入标准。所有纳入文章的诊断准确性研究质量评估(QUADAS)评分都很高。在婴儿中,脑性瘫痪的临床体征和症状在2岁之前出现并演变;因此,应结合临床病史使用标准化工具来预测风险。在矫正年龄5个月之前,检测风险最具预测性的工具是足月年龄磁共振成像(敏感性为86% - 89%)、普雷茨尔全身运动质量评估(敏感性为98%)和哈默史密斯婴儿神经学检查(敏感性为90%)。在矫正年龄5个月之后,检测风险最具预测性的工具是磁共振成像(敏感性为86% - 89%)(在安全可行的情况下)、哈默史密斯婴儿神经学检查(敏感性为90%)和幼儿发育评估(C指数为83%)。脑性瘫痪的部位和严重程度在婴儿期更难确定,磁共振成像和哈默史密斯婴儿神经学检查可能有助于辅助临床决策。在高收入国家,三分之二的脑性瘫痪患者能够行走,四分之三的患者能够说话,二分之一的患者智力正常。
早期诊断始于病史采集,并涉及使用神经影像学、标准化神经学和标准化运动评估,这些评估显示出与脑性瘫痪一致的异常发现。临床医生应理解及时转诊至针对诊断的早期干预的重要性,以优化婴儿的运动和认知可塑性,预防继发性并发症,并提高照顾者的幸福感。