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dc.contributor.authorNovak, Iona
dc.contributor.authorMorgan, Cathy
dc.contributor.authorAdde, Lars
dc.contributor.authorBlackman, James
dc.contributor.authorBoyd, Roslyn
dc.contributor.authorBrunstrom- Hernandez, Janice
dc.contributor.authorCioni, Giovanni
dc.contributor.authorDamiano, Diane
dc.contributor.authorDarrah, Johanna
dc.contributor.authorEliasson, Ann-Christin
dc.contributor.authorde Vries, Linda S.
dc.contributor.authorEinspieler, Christa
dc.contributor.authorFahey, Michael C.
dc.contributor.authorFehlings, Darcy
dc.contributor.authorFerriero, Donna M.
dc.contributor.authorFetters, Linda
dc.contributor.authorFiori, Simona
dc.contributor.authorForssberg, Hans
dc.contributor.authorGordon, Andrew M.
dc.contributor.authorGreaves, Susan
dc.contributor.authorGuzzetta, Andrea
dc.contributor.authorHadders-Algra, Mijna
dc.contributor.authorHarbourne, Regina
dc.contributor.authorKakooza-Mwesige, Angelina
dc.contributor.authorKarlsson, Petra
dc.contributor.authorKrumlinde-Sundholm, Lena
dc.contributor.authorLatal, Beatrice
dc.contributor.authorLougran-Fowlds, Alison
dc.contributor.authorMaitre, Nathalie
dc.contributor.authorMcIntyre, Sarah
dc.contributor.authorNoritz, Garey
dc.contributor.authorPennington, Lindsay
dc.contributor.authorRomeo, Domenico M.
dc.contributor.authorShepherd, Roberta
dc.contributor.authorSpittle, Alicia J.
dc.contributor.authorThornton, Marelle
dc.contributor.authorValentine, Jane
dc.contributor.authorWalker, Karen
dc.contributor.authorWhite, Robert G.
dc.contributor.authorBadawi, Nadia
dc.date.accessioned2018-04-06T12:51:46Z
dc.date.available2018-04-06T12:51:46Z
dc.date.created2017-07-20T09:40:56Z
dc.date.issued2017
dc.identifier.citationJAMA pediatrics. 2017, 171 (9), 897-907.nb_NO
dc.identifier.issn2168-6203
dc.identifier.urihttp://hdl.handle.net/11250/2493075
dc.description.abstractImportance 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. Objectives 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. Evidence Review 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. Findings 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. Conclusions and Relevance 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.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Medical Association (AMA)nb_NO
dc.titleEarly, accurate diagnosis and early intervention in cerebral palsy: Advances in diagnosis and treatmentnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber897-907nb_NO
dc.source.volume171nb_NO
dc.source.journalJAMA pediatricsnb_NO
dc.source.issue9nb_NO
dc.identifier.doi10.1001/jamapediatrics.2017.1689
dc.identifier.cristin1482652
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2017 by American Medical Association (AMA)nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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