Implementation of Early Diagnosis and Intervention Guidelines for Cerebral Palsy in a High-Risk Infant Follow-Up Clinic  Rachel Byrne, PT, Garey Noritz,

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Implementation of Early Diagnosis and Intervention Guidelines for Cerebral Palsy in a High-Risk Infant Follow-Up Clinic  Rachel Byrne, PT, Garey Noritz, MD, Nathalie L. Maitre, MD, PhD  Pediatric Neurology  Volume 76, Pages 66-71 (November 2017) DOI: 10.1016/j.pediatrneurol.2017.08.002 Copyright © 2017 The Authors Terms and Conditions

FIGURE 1 Translation of international guidelines into a clinical practice algorithm in a neonatal intensive care unit follow-up program. Infants referred due to newborn-attributable risks (e.g., neuroimaging findings consistent with neonatal encephalopathy) most frequently start surveillance according to the guidelines at the three- to four-month visits. If they are still hospitalized (e.g., extremely preterm infant with white matter injury and lung disease), the guideline mandated surveillance happens at the bedside with a HINE, a TIMP, and a GMA. Infants referred due to infant-attributable risks start at closest point on the pathway. For example, an infant referred to the program at nine months by their pediatrician due to inability to sit would start with a HINE and a Bayley Scales of Infant and Toddler Development. If an MRI has not yet been performed by the three- to four-month visits when neither sedation nor anesthesia is required, it is deferred until 12 months when anesthesia is no longer required by this particular setting's radiology protocols. During the program, infants are referred to services and subspecialists according to needs and established clinical algorithms. * Select examinations target developmental progression and represent best feasible evidence for specific concern (e.g., Gross Motor Function Measure-66 at 18 months and 30 months when infant walking to begin establishing trajectory, Infant Toddler Sensory Profile for sensory processing concerns, Quality of Upper Extremity Skills Test for arm evaluation in hemiplegia, Receptive Expressive Language Test-3 for speech assessment, etc.). ** Neurological examination after 2-year visit includes Amiel-Tison or other. Bayley III, Bayley Scales of Infant and Toddler Development Third Edition; CBCL, Child Behavior Checklist; CO, cerebral palsy; GMA, General Movements Assessment; HINE, Hammersmith Infant Neurological Examination; TIMP, Test of Infant Motor Performance. (The color version of this figure is available in the online edition.) Pediatric Neurology 2017 76, 66-71DOI: (10.1016/j.pediatrneurol.2017.08.002) Copyright © 2017 The Authors Terms and Conditions

FIGURE 2 Schedule of visits prior (A) and after (B) implementation. The journey in blue represents the schedule before guideline implementation, the red one after. The cognitive, motor, and language domains of the Bayley Scales of Infant and Toddler Development Third edition are administered. Standardized neurological examinations modified from the Amiel-Tison17 are performed at 22 to 26 months on research patients by medical providers trained and certified on an annual basis by a gold-standard per NRN procedures.18 Bayley III, Bayley Scales of Infant and Toddler Development Third Edition; CBCL, Child Behavior Checklist; GMA, General Movements Assessment; HINE, Hammersmith Infant Neurological Examination; NRN neuro, Neonatal Research Network neurological examination; OT, occupational therapist; PT, physical therapist; SLP, speech and language pathologist; TIMP, Test of Infant Motor Performance. (The color version of this figure is available in the online edition.) Pediatric Neurology 2017 76, 66-71DOI: (10.1016/j.pediatrneurol.2017.08.002) Copyright © 2017 The Authors Terms and Conditions

FIGURE 3 Implementation timeline and phases. The initial three phases of the implementation process occurred over the course of 12 months. A consolidation phase with reassessment of strengths and weaknesses offered the opportunity of a new development phase, planning for priorities of the next implementation cycle. Pediatric Neurology 2017 76, 66-71DOI: (10.1016/j.pediatrneurol.2017.08.002) Copyright © 2017 The Authors Terms and Conditions