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2.
Arch Dis Child Fetal Neonatal Ed ; 107(1): 87-93, 2022 Jan.
Article En | MEDLINE | ID: mdl-34162693

OBJECTIVES: Health status (HS)/ health-related quality of life measures, completed by self or proxy, are important outcome indicators. Most HS literature on children born preterm includes adolescents and adults with limited data at preschool age. This study aimed to describe parent-reported HS in a large national cohort of extreme preterm children at preschool age and to identify clinical and sociodemographic variables associated with HS. METHODS: Infants born before 29 weeks' gestation between 2009 and 2011 were enrolled in a prospective longitudinal national cohort study through the Canadian Neonatal Network (CNN) and the Canadian Neonatal Follow-Up Network (CNFUN). HS, at 36 months' corrected age (CA), was measured with the Health Status Classification System for Pre-School Children tool completed by parents. Information about HS predictors was extracted from the CNN and CNFUN databases. RESULTS: Of 811 children included, there were 79, 309 and 423 participants in 23-24, 25-26 and 27-28 weeks' gestational age groups, respectively. At 36 months' CA, 78% had a parent-reported health concern, mild in >50% and severe in 7%. Most affected HS attributes were speech (52.1%) and self-care (41.4%). Independent predictors of HS included substance use during pregnancy, infant male sex, Score for Neonatal Acute Physiology-II, bronchopulmonary dysplasia, severe retinopathy of prematurity, caregiver employment and single caregiver. CONCLUSION: Most parents expressed no or mild health concerns for their children at 36 months' CA. Factors associated with health concerns included initial severity of illness, complications of prematurity and social factors.


Health Status , Infant, Extremely Premature/psychology , Parents/psychology , Canada , Child, Preschool , Developmental Disabilities/diagnosis , Female , Follow-Up Studies , Humans , Infant, Newborn , Infant, Premature, Diseases/psychology , Longitudinal Studies , Male , Prospective Studies , Quality of Life , Self Care , Socioeconomic Factors , Speech Disorders/diagnosis
3.
Neurobiol Learn Mem ; 185: 107540, 2021 11.
Article En | MEDLINE | ID: mdl-34673263

Investigations using preclinical models of preterm birth have much contributed, together with human neuropathological studies, for advances in our understanding of preterm brain injury. Here, we evaluated whether the neurodevelopmental and behavioral consequences of preterm birth induced by a non-inflammatory model of preterm birth using mifepristone would differ from those after inflammatory prenatal transient hypoxia-ischemia (TSHI) model. Pregnant Wistar rats were either injected with mifepristone, and pups were delivered on embryonic day 21 (ED21 group), or laparotomized on the 18th day of gestation for 60 min of uterine arteries occlusion. Rat pups were tested postnatally for characterization of developmental milestones and, after weaning, they were behaviorally tested for anxiety and for spatial learning and memory. One month later, brains were processed for quantification of doublecortin (DCX)- and neuropeptide Y (NPY)-immunoreactive cells, and cholinergic varicosities in the hippocampus. ED21 rats did not differ from controls with respect to neonatal developmental milestones, anxiety, learning and memory functions, and neurochemical parameters. Conversely, in TSHI rats the development of neonatal reflexes was delayed, the levels of anxiety were reduced, and spatial learning and memory was impaired; in the hippocampus, the total number of DCX and NPY cells was increased, and the density of cholinergic varicosities was reduced. With these results we suggest that a preterm birth, in a non-inflammatory prenatal environment, does not significantly change neonatal development and adult neurologic outcome. On other hand, prenatal hypoxia and ischemia (inflammation) modifies developmental trajectory, learning and memory, neurogenesis, and NPY GABAergic and cholinergic brain systems.


Hypoxia-Ischemia, Brain/pathology , Infant, Premature, Diseases/physiopathology , Animals , Brain/pathology , Disease Models, Animal , Female , Hippocampus/pathology , Hypoxia-Ischemia, Brain/psychology , Infant, Premature, Diseases/psychology , Male , Mifepristone/pharmacology , Morris Water Maze Test , Open Field Test , Pregnancy , Premature Birth/physiopathology , Rats , Rats, Wistar , Reflex/physiology , Spatial Memory
4.
Ann Surg ; 274(4): e370-e380, 2021 10 01.
Article En | MEDLINE | ID: mdl-34506326

OBJECTIVE: The aim of this study was to determine which initial surgical treatment results in the lowest rate of death or neurodevelopmental impairment (NDI) in premature infants with necrotizing enterocolitis (NEC) or isolated intestinal perforation (IP). SUMMARY BACKGROUND DATA: The impact of initial laparotomy versus peritoneal drainage for NEC or IP on the rate of death or NDI in extremely low birth weight infants is unknown. METHODS: We conducted the largest feasible randomized trial in 20 US centers, comparing initial laparotomy versus peritoneal drainage. The primary outcome was a composite of death or NDI at 18 to 22 months corrected age, analyzed using prespecified frequentist and Bayesian approaches. RESULTS: Of 992 eligible infants, 310 were randomized and 96% had primary outcome assessed. Death or NDI occurred in 69% of infants in the laparotomy group versus 70% with drainage [adjusted relative risk (aRR) 1.0; 95% confidence interval (CI): 0.87-1.14]. A preplanned analysis identified an interaction between preoperative diagnosis and treatment group (P = 0.03). With a preoperative diagnosis of NEC, death or NDI occurred in 69% after laparotomy versus 85% with drainage (aRR 0.81; 95% CI: 0.64-1.04). The Bayesian posterior probability that laparotomy was beneficial (risk difference <0) for a preoperative diagnosis of NEC was 97%. For preoperative diagnosis of IP, death or NDI occurred in 69% after laparotomy versus 63% with drainage (aRR, 1.11; 95% CI: 0.95-1.31); Bayesian probability of benefit with laparotomy = 18%. CONCLUSIONS: There was no overall difference in death or NDI rates at 18 to 22 months corrected age between initial laparotomy versus drainage. However, the preoperative diagnosis of NEC or IP modified the impact of initial treatment.


Drainage , Enterocolitis, Necrotizing/surgery , Infant, Premature, Diseases/surgery , Intestinal Perforation/surgery , Laparotomy , Neurodevelopmental Disorders/epidemiology , Enterocolitis, Necrotizing/mortality , Enterocolitis, Necrotizing/psychology , Feasibility Studies , Female , Humans , Infant, Extremely Low Birth Weight , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/mortality , Infant, Premature, Diseases/psychology , Intestinal Perforation/mortality , Intestinal Perforation/psychology , Male , Neurodevelopmental Disorders/diagnosis , Survival Rate , Treatment Outcome
5.
PLoS One ; 16(6): e0253026, 2021.
Article En | MEDLINE | ID: mdl-34101760

BACKGROUND: Children born preterm, particularly at earlier gestations, are at increased risk for mortality and morbidity, but later health-related quality of life (HRQoL) is less well described. Neurodevelopmental impairment and socio-economic status may also influence HRQoL. Our aim was to describe the HRQoL of a cohort of New Zealand children born very and extremely preterm, and how this is related to neurodevelopmental impairment, gestational age, and socio-economic deprivation. METHODS: Children born <30 weeks' gestation or <1500 g birthweight were assessed at 7 years' corrected age. Caregivers completed the Child Health Questionnaire Parent Form (CHQ-PF50), and the Health Utilities Index Mark 2 (HUI-2). Neurodevelopmental impairment was defined as Wechsler full scale intelligence quotient below -1 standard deviation (SD), Movement Assessment Battery for Children total score ≤15 percentile, cerebral palsy, deafness, or blindness. RESULTS: Data were collected for 127 children, of whom 60 (47%) had neurodevelopmental impairment. Overall, HRQoL was good: mean (SD) CHQ-PF50 physical summary score = 50.8 (11.1), psychosocial summary score = 49.3 (9.1) [normative mean 50 (10)]; HUI-2 dead-healthy scale = 0.92 (0.09) [maximum 1.0]. Neurodevelopmental impairment, lower gestational age, and higher socio-economic deprivation were all associated with reduced HRQoL. However, on multivariable analysis, only intelligence quotient and motor function were associated with psychosocial HRQoL, while intelligence quotient was associated with physical HRQoL. CONCLUSIONS: Most seven-year-old children born very and extremely preterm have good HRQoL. Further improvements will require reduced neurodevelopmental impairment.


Caregivers/statistics & numerical data , Infant, Extremely Premature/psychology , Infant, Premature, Diseases/epidemiology , Quality of Life , Child , Child, Preschool , Cohort Studies , Female , Gestational Age , Humans , Infant , Infant, Extremely Premature/growth & development , Infant, Newborn , Infant, Premature, Diseases/psychology , Male , New Zealand/epidemiology , Pregnancy
6.
Ann Agric Environ Med ; 28(1): 183-188, 2021 Mar 18.
Article En | MEDLINE | ID: mdl-33775086

INTRODUCTION: Premature babies are a special group at risk of persistent brain damage caused by diseases, the most serious of which are cerebral palsy(CP), autism spectrum disorders (ASD) and mental retardation, among others. These conditions may occur concurrently, but appear more often as separate disease syndromes in the same group of at-risk children. Long-term observation of psychomotor development by an interdisciplinary medical team closely cooperating with parents is necessary. It is important to detect the risk of developing these diseases as soon as possible in all development spheres. MATERIAL AND METHODS: The research was conducted to demonstrate the prognostic value of 'red flags' of developmental milestones and the ability to detect early signs of risk of developing CP and ASD in extremely premature babies. In this preliminary study, 42 preterm babies, born after less than 32 weeks pregnancy participated. RESULTS: The occurrence of 'red flags'in the spheres: gross motor, fine motor and cognitive at 9 months was strongly associated with their presence at 24 months. The sensitivity and specificity were: gross motor - 0.91 (95% CI: 0.59, 1.00) and 0.94 (95% CI: 0.79, 0.99); fine motor - 0.83 (95% CI 0.36-1.00) and 1.00 (95% CI: 0.90-1.00); cognitive - 1.00 (0.40, 1.00) and 0.97 (0.86, 1.00). Other spheres had lower sensitivity but high specificity. CONCLUSIONS: The conclusion is that the 'red flags'at the 9 months milestones already predict the normal or developmental delay of premature babies, and predict the risk of CP and ASD. Due to the availability and lack of the need for specialized and costly training, it is worth considering their use in everyday life medical practice.


Infant, Premature, Diseases/diagnosis , Psychomotor Disorders/diagnosis , Child Development , Cognition , Female , Humans , Infant , Infant, Newborn , Infant, Premature/growth & development , Infant, Premature/psychology , Infant, Premature, Diseases/physiopathology , Infant, Premature, Diseases/psychology , Male , Motor Activity , Psychomotor Disorders/physiopathology , Psychomotor Disorders/psychology
7.
Acta Paediatr ; 110(4): 1281-1288, 2021 Apr.
Article En | MEDLINE | ID: mdl-33486835

AIM: To examine how the ongoing COVID-19 pandemic impacts child well-being and family functioning, particularly among children at risk for neurodevelopmental impairments. METHODS: Families of 73 typically developing children, 54 children born very preterm (VPT) and 73 children with congenital heart disease (CHD) from two prospective cohort studies were assessed prior to (mean age: 10.4 [SD: 1.2] years) and during (mean age: 12.8 [SD: 2.0] years) the pandemic, more specifically, in April/May 2020. Child well-being and family functioning were assessed with validated, parent-reported questionnaires and tested with linear mixed models. Group comparison of child distress and parental concerns related to medical implications of COVID-19 and homeschooling, assessed with 5-point Likert scales, was done with Mann-Whitney U tests. RESULTS: Children's psychological well-being and family functioning (both, p < 0.001) decreased significantly during the pandemic, irrespective of group. Children with CHD were reported to be more concerned about becoming infected with SARS-CoV-2 than were others. Child distress due to homeschooling and parents' concerns about children's academic achievements were significantly higher in VPT and CHD children than in typically developing peers (all p < 0.001). CONCLUSION: The COVID-19 pandemic substantially impacts the whole family and leads to additional distress in families with children at risk for neurodevelopmental impairments. These families should receive individualised counselling and assistance from healthcare providers and schools during the pandemic.


COVID-19 , Heart Defects, Congenital/complications , Infant, Premature, Diseases/etiology , Neurodevelopmental Disorders/etiology , Adolescent , Attitude to Health , COVID-19/epidemiology , COVID-19/prevention & control , COVID-19/psychology , Case-Control Studies , Child , Child Health , Cross-Sectional Studies , Family Relations/psychology , Female , Health Surveys , Heart Defects, Congenital/psychology , Humans , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/diagnosis , Infant, Premature, Diseases/psychology , Longitudinal Studies , Male , Mental Health , Neurodevelopmental Disorders/diagnosis , Neurodevelopmental Disorders/epidemiology , Neurodevelopmental Disorders/psychology , Neuropsychological Tests , Pandemics , Physical Distancing , Prospective Studies , Quality of Life , Risk Factors , Stress, Psychological/diagnosis , Stress, Psychological/epidemiology , Stress, Psychological/etiology , Stress, Psychological/psychology , Switzerland/epidemiology
8.
J Pediatr ; 226: 28-35.e3, 2020 11.
Article En | MEDLINE | ID: mdl-32800815

OBJECTIVE: To compare the effect of intervention at low vs high threshold of ventriculomegaly in preterm infants with posthemorrhagic ventricular dilatation on death or severe neurodevelopmental disability. STUDY DESIGN: This multicenter randomized controlled trial reviewed lumbar punctures initiated after either a low threshold (ventricular index of >p97 and anterior horn width of >6 mm) or high threshold (ventricular index of >p97 + 4 mm and anterior horn width of >10 mm). The composite adverse outcome was defined as death or cerebral palsy or Bayley composite cognitive/motor scores <-2 SDs at 24 months corrected age. RESULTS: Outcomes were assessed in 113 of 126 infants. The composite adverse outcome was seen in 20 of 58 infants (35%) in the low threshold group and 28 of 55 (51%) in the high threshold (P = .07). The low threshold intervention was associated with a decreased risk of an adverse outcome after correcting for gestational age, severity of intraventricular hemorrhage, and cerebellar hemorrhage (aOR, 0.24; 95% CI, 0.07-0.87; P = .03). Infants with a favorable outcome had a smaller fronto-occipital horn ratio (crude mean difference, -0.06; 95% CI, -0.09 to -0.03; P < .001) at term-equivalent age. Infants in the low threshold group with a ventriculoperitoneal shunt, had cognitive and motor scores similar to those without (P = .3 for both), whereas in the high threshold group those with a ventriculoperitoneal shunt had significantly lower scores than those without a ventriculoperitoneal shunt (P = .01 and P = .004, respectively). CONCLUSIONS: In a post hoc analysis, earlier intervention was associated with a lower odds of death or severe neurodevelopmental disability in preterm infants with progressive posthemorrhagic ventricular dilatation. TRIAL REGISTRATION: ISRCTN43171322.


Cerebral Hemorrhage/complications , Cerebral Hemorrhage/surgery , Cerebral Ventricles/pathology , Infant, Premature, Diseases/surgery , Neurodevelopmental Disorders/epidemiology , Time-to-Treatment , Cerebral Hemorrhage/psychology , Child, Preschool , Cohort Studies , Dilatation, Pathologic , Female , Humans , Infant , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/psychology , Male , Neurodevelopmental Disorders/diagnosis , Neurodevelopmental Disorders/prevention & control , Spinal Puncture , Ventriculoperitoneal Shunt
9.
Semin Fetal Neonatal Med ; 25(3): 101125, 2020 06.
Article En | MEDLINE | ID: mdl-32540316

Parents and individuals who were born preterm rarely contribute to research study design in order to ensure that outcomes are reported that are of relevance to them. In this article we explore aspects of the measures we use and the lived experiences of three individuals with experience of having a very preterm birth or being very preterm themselves. Their experiences tell us that follow up needs to be more than 2 years, that prematurity needs to be more widely acknowledged in education and that adult services need to consider the consequences of being born early. There are encouraging signs that these important issues are becoming recognised. Individuals designing outcome studies should ensure that these important voices are heard, and their perspectives captured in such studies.


Infant, Premature, Diseases , Patient Reported Outcome Measures , Premature Birth , Research Design , Survivors , Adult , Aftercare/methods , Female , Humans , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/diagnosis , Infant, Premature, Diseases/physiopathology , Infant, Premature, Diseases/psychology , Infant, Premature, Diseases/therapy , Male , Parents/psychology , Pregnancy , Premature Birth/psychology , Professional-Patient Relations , Quality of Life , Survivors/psychology
10.
Pediatrics ; 145(5)2020 05.
Article En | MEDLINE | ID: mdl-32276969

OBJECTIVES: Children born very preterm (VPT) are at an increased risk of developing mental health (MH) disorders. Our aim for this study was to assess rates of MH disorders in children born VPT and term at 13 years of age and stability of MH disorders between ages 7 and 13 years by using a diagnostic measure. METHODS: Participants were from the Victorian Infant Brain Study longitudinal cohort and included 125 children born VPT (<30 weeks' gestational age and/or <1250 g) and 49 children born term (≥37 weeks' gestational age) and their families. Participants were followed-up at both 7 and 13 years, and the Development and Well-Being Assessment was administered to assess for MH disorders. RESULTS: Compared with term peers, 13-year-olds born VPT were more likely to meet criteria for any MH disorder (odds ratio 5.9; 95% confidence interval 1.71-20.03). Anxiety was the most common disorder in both groups (VPT = 14%; term = 4%), whereas attention-deficit/hyperactivity disorder carried the greatest differential elevated risk (odds ratio 5.6; 95% confidence interval 0.71-43.80). Overall rates of MH disorders remained stable between 7 and 13 years, although at an individual level, many participants shifted in or out of diagnostic categories over time. CONCLUSIONS: Children born VPT show higher rates of MH disorders than their term peers, with changing trajectories over time. Findings highlight the importance of early identification and ongoing assessment to support those with MH disorders in this population.


Infant, Extremely Premature/psychology , Infant, Premature, Diseases/psychology , Mental Health/trends , Neurodevelopmental Disorders/psychology , Adolescent , Child , Cohort Studies , Female , Follow-Up Studies , Humans , Infant, Newborn , Infant, Premature, Diseases/diagnosis , Infant, Premature, Diseases/epidemiology , Longitudinal Studies , Male , Neurodevelopmental Disorders/diagnosis , Neurodevelopmental Disorders/epidemiology
11.
Semin Fetal Neonatal Med ; 25(3): 101108, 2020 06.
Article En | MEDLINE | ID: mdl-32284233

Social problems are an important feature of the preterm behavioral phenotype but are diverse and multidimensional. A model of social competence comprised of the three interrelated components of social cognition, social interaction, and social adjustment is useful in conceptualizing these problems. Weaknesses in social cognition in very preterm (VPT) children, although rarely studied, are found on tasks involving interpretation of social cues. Difficulties in social interaction in VPT infants and young children are documented by structured observations of their interactions with adults. Problems in social adjustment are endorsed on parent and teacher ratings of VPT infants and youth and on self-reports of VPT adults. These multiple deficits likely stem from early disruptions in neural development, are related to other consequences of preterm birth, and subject to postnatal environment influences. Further research is needed to more fully account for the effects of VPT birth on the development of social competence.


Emotional Adjustment , Infant, Extremely Premature/psychology , Infant, Premature, Diseases/psychology , Neurodevelopmental Disorders/psychology , Social Cognition , Social Interaction , Social Skills , Adolescent , Adult , Child , Child, Preschool , Humans , Infant , Infant, Extremely Premature/growth & development , Infant, Newborn , Infant, Premature, Diseases/diagnosis , Neurodevelopmental Disorders/diagnosis , Neuropsychological Tests
12.
Pediatrics ; 145(5)2020 05.
Article En | MEDLINE | ID: mdl-32327449

As the technical ability for genetic diagnosis continues to improve, an increasing number of diagnoses are made in infancy or as early as the neonatal period. Many of these diagnoses are known to be associated with developmental delay and intellectual disability, features that would not be clinically detectable at the time of diagnosis. Others may be associated with cognitive impairment, but the incidence and severity are yet to be fully described. These neonates and infants with genetic diagnoses therefore represent an emerging group of patients who are at high risk for neurodevelopmental disabilities. Although there are well-established developmental supports for high-risk infants, particularly preterm infants, after discharge from the NICU, programs specifically for infants with genetic diagnoses are rare. And although previous research has demonstrated the positive effect of early developmental interventions on outcomes among preterm infants, the impact of such supports for infants with genetic disorders who may be born term, remains to be understood. We therefore review the literature regarding existing developmental assessment and intervention approaches for children with genetic disorders, evaluating these in the context of current developmental supports postdischarge for preterm infants. Further research into the role of developmental support programs for early assessment and intervention in high-risk neonates diagnosed with rare genetic disorders is needed.


Developmental Disabilities/psychology , Developmental Disabilities/therapy , Genetic Diseases, Inborn/psychology , Genetic Diseases, Inborn/therapy , Developmental Disabilities/diagnosis , Early Intervention, Educational/methods , Genetic Diseases, Inborn/diagnosis , Humans , Infant, Newborn , Infant, Premature/physiology , Infant, Premature, Diseases/diagnosis , Infant, Premature, Diseases/psychology , Infant, Premature, Diseases/therapy
13.
Acta Paediatr ; 109(1): 45-55, 2020 01.
Article En | MEDLINE | ID: mdl-31350861

AIM: Preterm birth poses concerns in daily functioning and behaviour in childhood, possibly connected to sensory processing disorder. This review aimed to systematically identify assessments, incidence and nature of sensory processing disorder in preterm-born infants and children. METHODS: We searched literature through CINAHL-EBSCOhost, Cochrane, Ovid/PsychINFO, PubMed/Medline, Scopus and Google Scholar, published until November 2018. We included electronically available, peer-reviewed studies of preterm-born children that applied standardised sensory processing assessments. We excluded studies of preterm-born children with major neurodevelopmental impairments. RESULTS: We identified 27 studies of premature children, aged from birth to 9 years 7 months. The assessments represented three versions of Sensory Profile questionnaires and three clinical tests, Test of Sensory Functions in Infants, the Miller Assessment for Preschoolers, and the Sensory Integration and Praxis Test. The studies revealed wide variation of atypical sensory processing: 28%-87% in sensory modulation, 9%-70% in somatosensory processing and 20%-70% in sensory-based motor processing. CONCLUSION: Preterm-born children exhibited elevated risk for sensory processing disorder from infancy into school age. Routine screening of sensory processing, intervention intervals and parental consultations should be considered in ameliorating sensory processing and neurocognitive development. Moreover, a larger body of intervention studies is needed.


Infant, Premature, Diseases/epidemiology , Perception , Somatosensory Disorders/epidemiology , Child , Child, Preschool , Humans , Incidence , Infant , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/psychology
14.
J Pediatr Gastroenterol Nutr ; 70(1): 64-71, 2020 01.
Article En | MEDLINE | ID: mdl-31651669

OBJECTIVE: The impact of pediatric intestinal failure (IF) on neurodevelopment beyond infancy has not been systematically studied. Our aim was to evaluate cognitive and motor impairment and to identify risk factors for adverse outcomes among children with IF. METHODS: We conducted a cross-sectional single-center study at the Helsinki University Children's Hospital. Patients with IF with >60 days of parental nutrition (PN) dependency aged between 3 and 16 years (n = 40) were invited to participate. The cognitive and motor skills were evaluated using validated tests: Wechsler Preschool and Primary Scale of Intelligence, 3rd edition, Wechsler Intelligence Scale for Children, 4th edition, and Movement Assessment Battery for Children, 2nd edition. RESULTS: All the patients attending the study tests (n = 30, males = 24) were included. Their median age, gestational age, and birth weight was 7.5 (range 3-16) years, 35 (interquartile range [IQR] 28-38) weeks and 2238 (IQR 1040-3288) grams, respectively. Median duration of PN was 13 (IQR 5-37) months and 9 patients were currently on PN. Median intelligence quotient was 78 (IQR 65-91) and 10 (35%) patients had an intelligence quotient under 70 (-2 standard deviation). Significant motor impairment was detected in 10 patients (36%) and milder difficulties in 8 (28%). Adverse cognitive outcome was associated with neonatal short bowel syndrome, number of interventions under general anesthesia, and length of inpatient status, whereas adverse motor outcome was associated with prematurity. CONCLUSION: Clinically significant cognitive and motor impairments are alarmingly common among neonatal patients with IF. We recommend early neurodevelopmental follow-up for all children with IF.


Cognition Disorders/etiology , Infant, Premature, Diseases/psychology , Infant, Premature/psychology , Motor Skills Disorders/etiology , Short Bowel Syndrome/psychology , Adolescent , Birth Weight , Child , Child Development , Child, Preschool , Cognition , Cross-Sectional Studies , Female , Gestational Age , Humans , Infant, Newborn , Infant, Premature, Diseases/physiopathology , Intelligence Tests , Male , Motor Skills , Parenteral Nutrition , Risk Factors
15.
Semin Fetal Neonatal Med ; 25(2): 101072, 2020 04.
Article En | MEDLINE | ID: mdl-31879203

This review looks at data on potential associations between intermittent hypoxia (IH) and impaired neurodevelopment in infants and children. In extremely preterm infants (<28 wk gestation), such an association has been established based on a secondary analysis of Canadian Oxygen Trial data. These showed, in 997 infants, that the odds of developing cognitive or language impairment at 18 months corrected age were 3 times higher in infants who were in the highest decile for %time spent with events where pulse oximeter saturation (SpO2) was <80% for ≥1 min during their first 10 postnatal weeks compared to those who had very few such events after birth. In older term and preterm infants, the occurrence of 5 or more events with prolonged apnea and bradycardia during home monitoring was associated with 5 points less on the mental development index of the Bayley-II scales. For older children, associations between sleep-disordered breathing and impaired cognition/academic achievements have also been established, but not consistently, and it remains unclear whether this association is primarily mediated via IH or via sleep deprivation. Animal data show that IH may cause apoptosis particularly in the hippocampus. Although we need to stress that associations cannot prove causality, current evidence provides support for IH to be detected and prevented early. Future studies should focus on IH rather than on apnea/bradycardia.


Hypoxia/complications , Infant, Premature, Diseases , Nervous System Diseases/etiology , Adolescent , Animals , Canada/epidemiology , Child , Child, Preschool , Clinical Trials as Topic/statistics & numerical data , Humans , Hypoxia/congenital , Hypoxia/epidemiology , Hypoxia/therapy , Infant , Infant, Extremely Premature , Infant, Newborn , Infant, Premature, Diseases/epidemiology , Infant, Premature, Diseases/psychology , Infant, Premature, Diseases/therapy , Nervous System Diseases/epidemiology , Nervous System Diseases/prevention & control , Oximetry , Oxygen/therapeutic use , Oxygen Inhalation Therapy/methods , Sleep Apnea Syndromes/complications , Sleep Apnea Syndromes/epidemiology , Sleep Apnea Syndromes/psychology , Sleep Apnea Syndromes/therapy
16.
Neonatal Netw ; 38(2): 88-97, 2019 Mar 01.
Article En | MEDLINE | ID: mdl-31470371

PURPOSE: This study aimed to explore support for mothers and fathers in single-family rooms (SFRs) of a NICU. DESIGN: A qualitative descriptive design was employed. SAMPLE: A convenience sample of 15 parents (nine mothers, six fathers) were recruited from a Level III NICU. METHOD: During their infants' hospitalization, each parent recorded their thoughts and feelings regarding support whenever appropriate over a period of 48 hours using Handy Application to Promote Preterm infant happY-life (HAPPY), an android recording application. RESULTS: Parents felt supported when staff facilitated their learning in a collaborative manner, fostered their optimism, and provided situational assistance. Continuity and consistency of care and presence were important characteristics of supportive nursing care. Though SFRs offered privacy for parents to learn and to be with their infants, the design limited parental access to nursing and medical staff, which sometimes prevented parents from receiving adequate support and partaking in decision making concerning their infants' care.


Emotions , Infant, Premature, Diseases , Parent-Child Relations , Parents/psychology , Patients' Rooms , Professional-Family Relations , Adult , Attitude of Health Personnel , Consumer Behavior , Decision Making, Shared , Female , Humans , Infant, Newborn , Infant, Premature, Diseases/psychology , Infant, Premature, Diseases/therapy , Intensive Care Units, Neonatal/organization & administration , Intensive Care Units, Neonatal/standards , Male , Patients' Rooms/organization & administration , Patients' Rooms/standards , Qualitative Research , Social Support
17.
J Pediatr ; 213: 66-73.e1, 2019 10.
Article En | MEDLINE | ID: mdl-31402139

OBJECTIVE: To increase the understanding of social adjustment and autism spectrum disorder symptoms in adolescents born very preterm by studying the role of emotion recognition and cognitive control processes in the relation between very preterm birth and social adjustment. STUDY DESIGN: A Dutch cohort of 61 very preterm and 61 full-term adolescents aged 13 years participated. Social adjustment was rated by parents, teachers, and adolescents and autism spectrum disorder symptoms by parents. Emotion recognition was assessed with a computerized task including pictures of child faces expressing anger, fear, sadness, and happiness with varying intensity. Cognitive control was assessed using a visuospatial span, antisaccade, and sustained attention to response task. Performance measures derived from these tasks served as indicators of a latent cognitive control construct, which was tested using confirmatory factor analysis. Mediation analyses were conducted with emotion recognition and cognitive control as mediators of the relation between very preterm birth and social problems. RESULTS: Very preterm adolescents showed more parent- and teacher-rated social problems and increased autism spectrum disorder symptomatology than controls. No difference in self-reported social problems was observed. Moreover, very preterm adolescents showed deficits in emotion recognition and cognitive control compared with full-term adolescents. The relation between very preterm birth and parent-rated social problems was significantly mediated by cognitive control but not by emotion recognition. Very preterm birth was associated with a 0.67-SD increase in parent-rated social problems through its negative effect on cognitive control. CONCLUSIONS: The present findings provide strong evidence for a central role of impaired cognitive control in the social problems of adolescents born very preterm.


Autism Spectrum Disorder/psychology , Cognition , Emotions , Infant, Premature, Diseases/psychology , Social Adjustment , Social Behavior , Adolescent , Case-Control Studies , Female , Humans , Infant, Extremely Premature , Infant, Newborn , Male , Netherlands
18.
Early Hum Dev ; 137: 104827, 2019 10.
Article En | MEDLINE | ID: mdl-31374456

AIMS: To determine the impact on families (IOF) of former preterm infants (gestational age < 32 weeks) after posthemorrhagic hydrocephalus requiring shunt (PHH-S), and to identify risk factors of family dysfunction. STUDY DESIGN: 38 preterm infants with PHH-S were matched for gestational age, birthweight, and gender with preterm infants with normal cranial ultrasonography. IOF questionnaire was administered at 5.7 ±â€¯2 years (higher IOF score indicates worse impact). RESULTS: Families of PHH-S children exhibited significantly worse IOF compared to controls in financial (9.2 ±â€¯2.2 vs 5.9 ±â€¯1.4), family-personal (26.6 ±â€¯5.2 vs 20.2 ±â€¯2.8), and disruptive social (21.4 ±â€¯4.9 vs 16.7 ±â€¯3.1) domains (P < 0.001). Multivariate regression incorporating neonatal risk factors revealed an independent effect of parenchymal brain involvement (ß:0.4, P:0.002) and neonatal seizures (ß:0.3, p:0.007) on total IOF. Neurosensory morbidity was significantly higher in the PHH-S group, including cerebral palsy (81.6%), epilepsy (47.4%), problems with vision (63.2%), feeding (39.5%) and hearing (18.4%), chronic health problems (44.7%) and hospital admissions in the last 6 months (44.7%). Worse IOF scores of PHH-S families were associated with socioeconomic status and neurodevelopmental morbidities: cerebral palsy severity, feeding problems, number of neurosurgeries, low cognitive, personal-social, and adaptive scores (P < 0.05). Multivariate analysis indicated an independent contribution from cerebral palsy severity (ß:0.5, p:0.002) and socioeconomic status (ß:-0.4, P: 0.01). CONCLUSIONS: Families of preterm children after PHH-S exhibit significantly worse IOF scores compared to families of preterm peers. Worse IOF is associated with severe hemorrhage, neurodevelopmental morbidities and socioeconomic status. A family centered intervention is warranted after PHH-S.


Cerebral Hemorrhage/epidemiology , Cerebral Palsy/epidemiology , Family Relations , Hydrocephalus/epidemiology , Infant, Premature, Diseases/epidemiology , Infant, Premature/growth & development , Adult , Child, Preschool , Female , Humans , Hydrocephalus/surgery , Infant, Newborn , Infant, Premature/psychology , Infant, Premature, Diseases/psychology , Male , Social Class , Ventriculoperitoneal Shunt
19.
Res Dev Disabil ; 91: 103429, 2019 Aug.
Article En | MEDLINE | ID: mdl-31272067

BACKGROUND: Adequate nutrition is essential for optimal neurodevelopment to preterm infants. Our aim was to evaluate the impact of caloric deprivation on Bayley-III scales performance at 18-24 months of corrected age, in a cohort of preterm infants. METHODS: We prospectively enrolled infants with gestational age <30 weeks and birth weight <1500 g. Apart from a whole cohort analysis, we performed a subgroup analysis between infants received inadequate calories (<85 Kcal/kg/day) during the first two weeks of age, compared to a standard nutrition group. All infants underwent a Bayley-III assessment at 18-24 months of corrected age. RESULTS: From the 63 preterm infants analysed, 25% had caloric deprivation compared to 75% with adequate nutrition. Caloric deprived infants were of lower gestational age and birth weight, and received a lower amount of enteral feeding during the first 14 days of age. There were no differences between the two groups regarding the common neonatal co-morbidities. Caloric deprived infants had significantly lower composite index scores at 18-24 months of corrected age. Caloric deprivation, late onset sepsis, necrotizing enterocolitis, and bronchopulmonary dysplasia were significant risk factors of neurodevelopmental impairment. CONCLUSIONS: Several neonatal factors affect the neurodevelopmental outcome of preterm infants, and nutrition may pose an important role.


Developmental Disabilities/diagnosis , Energy Intake , Food Deprivation , Infant Nutrition Disorders/diagnosis , Infant, Premature, Diseases/diagnosis , Bronchopulmonary Dysplasia/diagnosis , Bronchopulmonary Dysplasia/psychology , Cerebral Intraventricular Hemorrhage/diagnosis , Cerebral Intraventricular Hemorrhage/psychology , Developmental Disabilities/psychology , Female , Follow-Up Studies , Gestational Age , Humans , Infant , Infant Nutrition Disorders/psychology , Infant, Newborn , Infant, Premature, Diseases/psychology , Prospective Studies , Risk Factors
20.
J Pediatr ; 213: 38-45.e3, 2019 10.
Article En | MEDLINE | ID: mdl-31256914

OBJECTIVE: To determine how infant illness and parent demographics are associated with parent health-related quality of life (HRQL) during and 3 months after hospitalization in the neonatal intensive care unit (NICU). We hypothesized that parents of extremely preterm infants would report lower NICU HRQL than other parents, and that all parents would report improved HRQL after discharge. STUDY DESIGN: This prospective study of parent-infant dyads admitted to a level IV NICU for ≥14 days from 2016 to 2017 measured parent HRQL before and 3 months after discharge using the Pediatric Quality of Life Inventory Family Impact Module. Multivariable regression was used to identify risk factors associated with HRQL differences during hospitalization and after discharge. RESULTS: Of the 194 dyads, 167 (86%) completed the study (24% extremely preterm; 53% moderate to late preterm; 22% term). During the NICU hospitalization, parents of extremely preterm infants reported lower adjusted HRQL (-7 points; P = .013) than other parents. After discharge, parents of extremely preterm infants reported higher HRQL compared with their NICU score (+10 points; P = .001). Tracheostomy (-13; P = .006), home oxygen (-6; P = .022), and readmission (-5; P = .037) were associated with lower parent HRQL 3 months after discharge, adjusted for NICU HRQL score. CONCLUSIONS: Parents of extremely preterm infants experienced a greater negative impact on HRQL during the NICU hospitalization and more improvement after discharge than parents of other infants hospitalized in the NICU. Complex home care was associated with lower parent HRQL after discharge. The potential benefit of home discharge should be balanced against the potential negative impact of complex home care.


Hospitalization , Infant, Premature, Diseases/therapy , Intensive Care Units, Neonatal , Parents/psychology , Quality of Life , Adult , Female , Humans , Infant, Extremely Premature , Infant, Newborn , Infant, Premature, Diseases/psychology , Male , Prospective Studies , Young Adult
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