Dianne Creighton
University of Calgary
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Featured researches published by Dianne Creighton.
Archives of Disease in Childhood | 2017
Anne Synnes; Thuy Mai Luu; Paige Church; David S. C. Lee; Michael Vincer; Marilyn Ballantyne; Annette Majnemer; Dianne Creighton; Junmin Yang; Reginald S. Sauve; Saroj Saigal; Prakesh S. Shah; Shoo K. Lee
Objectives Identify determinants of neurodevelopmental outcome in preterm children. Methods Prospective national cohort study of children born between 2009 and 2011 at <29u2005weeks gestational age, admitted to one of 28 Canadian neonatal intensive care units and assessed at a Canadian Neonatal Follow-up Network site at 21u2005months corrected age for cerebral palsy (CP), visual, hearing and developmental status using the Bayley Scales of Infant and Toddler Development-Third Edition (Bayley-III). Stepwise regression analyses evaluated the effect of (1) prenatal and neonatal characteristics, (2) admission severity of illness, (3) major neonatal morbidities, (4) neonatal neuroimaging abnormalities, and (5) site on neurodevelopmental impairment (NDI) (Bayley-III score < 85, any CP, visual or hearing impairment), significant neurodevelopmental impairment (sNDI) (Bayley-III < 70, severe CP, blind or hearing aided and sNDI or death. Results Of the 3700 admissions without severe congenital anomalies, 84% survived to discharge and of the 2340 admissions, 46% (IQR site variation 38%–51%) had a NDI, 17% (11%–23%) had a sNDI, 6.4% (3.1%–8.6%) had CP, 2.6% (2.5%–13.3%) had hearing aids or cochlear implants and 1.6% (0%–3.1%) had a bilateral visual impairment. Bayley-III composite scores of <70 for cognitive, language and motor domains were 3.3%, 10.9% and 6.7%, respectively. Gestational age, sex, outborn, illness severity, bronchopulmonary dysplasia, necrotising enterocolitis, late-onset sepsis, retinopathy of prematurity, abnormal neuroimaging and site were significantly associated with NDI or sNDI. Site variation ORs for NDI, sNDI and sNDI/death ranged from 0.3–4.3, 0.04–3.5 and 0.12–1.96, respectively. Conclusion Most preterm survivors are free of sNDI. The risk factors, including site, associated with neurodevelopmental status suggest opportunities for improving outcomes.
The Journal of Thoracic and Cardiovascular Surgery | 2008
Ruth E. Neufeld; Brenda Clark; Charlene M.T. Robertson; Irina Dinu; Ari R. Joffe; Reg Sauve; Dianne Creighton; Lonnie Zwaigenbaum; David B. Ross; Ivan M. Rebeyka
OBJECTIVESnWe sought to assess the 5-year neurocognition and health of an interprovincial inception cohort undergoing the arterial switch operation for transposition of the great arteries.nnnMETHODSnSixty-nine consecutive neonates had operations from 1996-2003 with full-flow cardiopulmonary bypass and selective deep hypothermic circulatory arrest. Outcomes were recorded at 58 +/- 9 months of age. Univariate and multivariate analyses were used to identify outcome predictors, including surgical subtype and preoperative, operative, and postoperative variables.nnnRESULTSnThere was 1 (1.5%) operative death. Two children were lost to follow-up, and 1 was excluded because of postdischarge meningitis. Outcomes are reported for 65 survivors. Two (3%) children have cerebral palsy, and 7 (11%) have language disorders, 4 of whom also meet the criteria for autism spectrum disorder. Two of the 4 children with autism have an affected older sibling. Of the 61 children without autism, scores approach those of peers, with a full-scale intelligence quotient of 97 +/- 16, a verbal intelligence quotient of 97 +/- 18, a performance intelligence quotient of 96 +/- 15, and a visual-motor integration score of 95 +/- 16. Mothers education, birth gestation or weight, and postoperative plasma lactate values account for 21% to 32% of the variance of these scores. Septostomy adds 7% to the variance of visual-motor integration scores.nnnCONCLUSIONSnMost preschool children do well after surgical correction for transposition of the great arteries, including complex forms. Potentially modifiable variables include high preoperative plasma lactate levels and septostomy. A minority of children were given diagnoses of language disorders, including autism, in which familial factors likely contribute to outcome.
SpringerPlus | 2016
Matt S. Hicks; Reginald S. Sauve; Charlene M.T. Robertson; Ari R. Joffe; Gwen Y. Alton; Dianne Creighton; David B. Ross; Ivan M. Rebeyka
BackgroundDevelopmental and language outcomes at 2xa0years of age of children who had arterial switch operation (ASO) for transposition of the great arteries 2004–2010 are described.MethodsIn this prospective cohort study, 91/98 (93xa0%) children who underwent ASO were assessed at 2xa0years of age with the Bayley Scales of Infant & Toddler Development—3rd Edition. Outcomes were compared by patient and perioperative variables using bivariate and multivariate regression analyses to identify predictors of language delay.ResultsInfants without ventricular septal defect (VSD) (nxa0=xa060) were more likely to be outborn (73 vs 58xa0%, pxa0=xa00.038), require septostomy (80 vs 58xa0%, pxa0=xa00.026), have a shorter cross clamp time (min) (62.7 vs 73.0, pxa0=xa00.019), and a lower day 1 post-operative plasma lactate (mmol/L) (3.9 vs 4.8, pxa0=xa00.010). There were no differences in cognitive, motor and language outcomes based on presence of a VSD. Language delay (<85) of 29xa0% was 1.8 times higher than the normative sample; risk factors for this in multivariate analyses included <12xa0years of maternal education (AOR 19.3, 95xa0% CI 2.5–148.0) and cross-clamp time ≥70xa0min (AOR 14.5, 95xa0% CI 3.1–68.5). Maternal education <12xa0years was associated with lower Language Composite Scores (−20.2, 95xa0% CI −32.3 to −9.1).ConclusionsOutcomes at 2xa0years of age in children who undergo ASO are comparable to the normative sample with the exception of language. There is a risk of language delay for which maternal education and cross-clamp duration are predictors. These findings suggest that focused post-operative early language interventions could be considered.
The Journal of Pediatrics | 2018
Matthew D. Haslam; Sarka Lisonkova; Dianne Creighton; Paige Church; Junmin Yang; Prakesh S. Shah; K.S. Joseph; Anne Synnes; Adele Harrison; Joseph Ting; Zenon Cieslak; Rebecca Sherlock; Wendy Yee; Carlos Fajardo; Khalid Aziz; Jennifer Toye; Zarin Kalapesi; Koravangattu Sankaran; Sibasis Daspal; Molly Seshia; Ruben E. Alvaro; Amit Mukerji; Orlando da Silva; Chuks Nwaesei; Kyong-Soon Lee; Michael Dunn; Brigitte Lemyre; Kimberly Dow; Ermelinda Pelausa; Lajos Kovacs
Objective To assess the impact of variations in the definition of severe neurodevelopmental impairment (NDI) on the incidence of severe NDI and the association with risk factors using the Canadian Neonatal Follow‐Up Network cohort. Study design Literature review of severe NDI definitions and application of these definitions were performed in this database cohort study. Infants born at 23‐28 completed weeks of gestation between 2009 and 2011 (n = 2187) admitted to a Canadian Neonatal Network neonatal intensive care unit and assessed at 21 months corrected age were included. The incidence of severe NDI, aORs, and 95% CIs were calculated to express the relationship between risk factors and severe NDI using the definitions with the highest and the lowest incidence rates of severe NDI. Results The incidence of severe NDI ranged from 3.5% to 14.9% (highest vs lowest rate ratio 4.29; 95% CI 3.37‐5.47). The associations between risk factors and severe NDI varied depending on the definition used. Maternal ethnicity, employment status, antenatal corticosteroid treatment, and gestational age were not associated consistently with severe NDI. Although maternal substance use, sex, score of neonatal acute physiology >20, late‐onset sepsis, bronchopulmonary dysplasia, and brain injury were consistently associated with severe NDI irrespective of definition, the strength of the associations varied. Conclusions The definition of severe NDI significantly influences the incidence and the associations between risk factors and severe NDI. A standardized definition would facilitate site comparisons and scientific communication.
Paediatrics and Child Health | 2018
Dianne Creighton; Selphee Tang; Jill Newman; Leonora Hendson; Reg Sauve
ObjectivenTo evaluate predictive validity and establish cut-off scores on the Bayley-III at age 21 months that best predict Intelligence Quotient (IQ) scores <70 or <80) at 3 years in a high-risk preterm cohort.nnnMethodnBayley-III evaluations at 21 months corrected age and intellectual assessments, primarily with the WPPSI-III, at 3 years corrected age were conducted with 520 infants born less than 29 weeks gestational age or less than 1250 g birth weight. Receiver Operator Characteristic (ROC) curves were used to establish Bayley-III Cognitive Composite cut-off scores that maximized Sensitivity and Specificity in predicting low IQ. Similar analyses were performed using the Language Composite, and a research derived mean Cognitive-Language Composite.nnnResultsnA regression model for the association between 21-month Bayley-III Cognitive Composite and 3-year IQ scores was significant (P<0.0001, Adjusted R2=0.36). The ROC area under the Curve was 0.90 for the Cognitive Composite predicting IQ<70. The cut-off score that maximized Sensitivity and Specificity for predicting 3-year IQ<70 was a Cognitive Composite of <80. The ROC Area under the Curve was 0.80 for Cognitive Composites predicting IQ<80 and a Cognitive Composite cut-off score of <90 maximized Sensitivity and Specificity.nnnConclusionnIn this high-risk preterm cohort, there was a strong association between the Bayley-III Cognitive Composite at 21 months and IQ at 3 years. A Cognitive Composite cut-off score of <80 optimized classification of IQ<70 at 3 years, and a Cognitive Composite cut-off score of <90 optimized classification of IQ<80.
Paediatrics and Child Health | 2010
Abhay Lodha; Je Newman; Dianne Creighton; Amuchou Soraisham; Jl Newman; Selphee Tang; Reg Sauve
Paediatrics and Child Health | 2014
A Lodha; Reginald S. Sauve; Marilyn Ballantyne; Dianne Creighton; A Majnemer
Paediatrics and Child Health | 2014
Marilyn Ballantyne; Reginald S. Sauve; Dianne Creighton; Saroj Saigal; E Asztalos; E Couture; Michael Vincer; A Majnemer; Anne Synnes
Paediatrics and Child Health | 2014
Dianne Creighton; A Lodha; A Majnemer; Paige Church; David S. C. Lee; F Lefebvre
Paediatrics and Child Health | 2012
Su Hasan; Reg Sauve; Dianne Creighton; Selphee Tang; Abhay Lodha