Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/48099
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dc.contributor.authorConnors R.-
dc.contributor.authorSackett V.-
dc.contributor.authorMachipisa C.-
dc.contributor.authorTan K.-
dc.contributor.authorPharande P.-
dc.contributor.authorZhou L.-
dc.contributor.authorMalhotra A.-
dc.date.accessioned2022-07-11T05:32:58Z-
dc.date.available2022-07-11T05:32:58Z-
dc.date.copyright2022-
dc.date.issued2022-07-08en
dc.identifier.citationBrain Sciences. 12(7) (no pagination), 2022. Article Number: 847. Date of Publication: July 2022.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/48099-
dc.description.abstractBackground: Early diagnosis of cerebral palsy (CP) in high-risk infants is possible at 3-4 months' corrected age (CA) using standardised assessments. Aim(s): To assess the utility of neonatal screening assessments-writhing general movements (GMs) and the Hammersmith Neonatal Neurological Examination (HNNE)-to predict CP/high-risk status at 3-4 months' CA in extremely preterm infants. Method(s): Retrospective cohort study of high-risk preterm infants (born < 29 weeks' gestation and/or birth weight < 1000 g) attending an Early Neurodevelopment Clinic. Data from neonatal assessments were compared with CP/high-risk diagnosis at 3-4 months' CA, fidgety GMs, and Hammersmith Infant Neurological Examinations (HINE) using logistic regression, linear re-gression, and Spearman rank correlation. Result(s): Two hundred and two preterm infants (median gestation age at birth 27.3 (IQR 25.4-28.3) weeks, mean birth weight 870.3 (SD 248.4) grams) were included. A total of 26 (12.8%) infants received early CP/high-risk diagnoses at 3-4 months' CA. A lower gestational age (GA) (OR = 0.78; p = 0.029, 95% CI [0.26, 0.97]) and abnormal writhing GMs (OR 1.56; p = 0.019, 95% CI [1.07, 2.27]) were predictive of CP/high-risk diagnosis. Although after adjustment for sex, GA, birth weight, and growth restriction, GA (aOR = 0.67; p = 0.068, 95% CI [0.44, 1.03]) and writhing GMs (aOR = 1.44; p = 0.087, 95% CI [0.95, 2.20]) were not significant, a strong trend still persisted. The HNNE scores significantly correlated with both the HINE evaluation (rs = 0.43, p < 0.001, 95% CI [0.31, 0.56]) and fidgety GMs (rs = -0.10, p = 0.012, 95% CI [-0.32, -0.04]). Linear regression confirmed the HNNE was highly predictive of the HINE (correlation coefficient 0.82; p < 0.001, 95% CI [0.48, 1.15]). Writhing GMs did not significantly correlate with either fidgety GMs (p = 0.723, 95% CI [-0.12, 0.17]) or the HINE (p = 0.173, 95% CI [-0.24, 0.04]). Conclusion(s): Abnormal writhing GMs in the neonatal period were non-significantly associated with early CP/high-risk diagnoses in extremely preterm infants in a multivariate analysis. Additionally, the HNNE significantly correlated with both fidgety GMs and the HINE.Copyright © 2022 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.publisherMDPI-
dc.relation.ispartofBrain Sciences-
dc.subject.meshbirth weight cerebral palsy early gestational age high risk infant nervous system development neurologic examination newborn pregnancy prematurity-
dc.titleAssessing the Utility of Neonatal Screening Assessments in Early Diagnosis of Cerebral Palsy in Preterm Infants.-
dc.typeArticle-
dc.identifier.affiliationPaediatric - Neonatal (Monash Newborn)-
dc.identifier.affiliationPaediatric - Neurology-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional, or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=https://dx.doi.org/10.3390/brainsci12070847-
dc.publisher.placeSwitzerland-
dc.identifier.institution(Connors, Tan, Zhou, Malhotra) Department of Paediatrics, Monash University, Melbourne, VIC 3800, Australia-
dc.identifier.institution(Sackett, Machipisa) Allied Health Department, Monash Children's Hospital, Melbourne, VIC 3168, Australia-
dc.identifier.institution(Tan, Pharande, Zhou, Malhotra) Monash Newborn, Monash Children's Hospital, Melbourne, VIC 3168, Australia-
dc.identifier.institution(Malhotra) Early Neurodevelopment Clinic, Monash Children's Hospital, 246 Clayton Road, Melbourne, VIC 3168, Australia-
dc.identifier.affiliationmh(Sackett, Machipisa) Allied Health Department, Monash Children's Hospital, Melbourne, VIC 3168, Australia-
dc.identifier.affiliationmh(Tan, Pharande, Zhou, Malhotra) Monash Newborn, Monash Children's Hospital, Melbourne, VIC 3168, Australia-
dc.identifier.affiliationmh(Malhotra) Early Neurodevelopment Clinic, Monash Children's Hospital, 246 Clayton Road, Melbourne, VIC 3168, Australia-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptPaediatric - Neonatal (Monash Newborn)-
crisitem.author.deptHudson Institute - The Ritchie Centre-
crisitem.author.deptPaediatric - Neonatal (Monash Newborn)-
crisitem.author.deptPaediatric - Neonatal (Monash Newborn)-
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