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  1. Article ; Online: Neurodevelopmental outcomes in early childhood for infants born very preterm in countries outside the UK.

    Doyle, Lex W

    Archives of disease in childhood. Fetal and neonatal edition

    2024  Volume 109, Issue 2, Page(s) 117–119

    MeSH term(s) Infant, Newborn ; Infant ; Pregnancy ; Female ; Humans ; Child, Preschool ; Infant, Extremely Premature ; Child Development ; Parturition ; United Kingdom/epidemiology ; Gestational Age ; Neurodevelopmental Disorders/epidemiology
    Language English
    Publishing date 2024-02-19
    Publishing country England
    Document type Editorial
    ZDB-ID 2007331-8
    ISSN 1468-2052 ; 1359-2998
    ISSN (online) 1468-2052
    ISSN 1359-2998
    DOI 10.1136/archdischild-2023-326400
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Antenatal corticosteroids and outcomes into adulthood.

    Doyle, Lex W

    Paediatric and perinatal epidemiology

    2022  Volume 36, Issue 5, Page(s) 640–642

    MeSH term(s) Adrenal Cortex Hormones/adverse effects ; Adult ; Female ; Gestational Age ; Humans ; Infant, Newborn ; Infant, Premature ; Pregnancy ; Premature Birth ; Prenatal Care ; Respiratory Distress Syndrome, Newborn
    Chemical Substances Adrenal Cortex Hormones
    Language English
    Publishing date 2022-08-10
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 639089-4
    ISSN 1365-3016 ; 0269-5022 ; 1353-663X
    ISSN (online) 1365-3016
    ISSN 0269-5022 ; 1353-663X
    DOI 10.1111/ppe.12919
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Postnatal Corticosteroids to Prevent or Treat Bronchopulmonary Dysplasia.

    Doyle, Lex W

    Neonatology

    2021  Volume 118, Issue 2, Page(s) 244–251

    Abstract: Bronchopulmonary dysplasia (BPD) remains a major morbidity for infants born preterm. Postnatal corticosteroids might reduce the risk of developing BPD, or reduce its severity when it occurs, because of their powerful anti-inflammatory effects. However, ... ...

    Abstract Bronchopulmonary dysplasia (BPD) remains a major morbidity for infants born preterm. Postnatal corticosteroids might reduce the risk of developing BPD, or reduce its severity when it occurs, because of their powerful anti-inflammatory effects. However, corticosteroids have adverse effects, including on the developing brain. There have been numerous randomized clinical trials of corticosteroids given via various routes, of varying types, and started at different postnatal ages. There is some evidence that inhaled corticosteroids started earlier in the postnatal period may reduce BPD, but increase mortality. Inhaled corticosteroids started after the first week of age have little effect, but data are sparse. Systemic corticosteroids started in the first week after birth reduce BPD but increase cerebral palsy. Systemic corticosteroids started after the first week of age reduce both BPD and mortality, without evidence of long-term neurological harm. However, no studies have been powered to look for important adverse long-term neurological effects. Of the 2 systemic corticosteroids assessed, most effects relate to dexamethasone and not to hydrocortisone, but hydrocortisone in the first week after birth may reduce mortality, and is worthy of further study. There are limited data directly comparing inhaled versus systemic corticosteroids, with no evidence of superiority of one mode over the other. Corticosteroids instilled into the trachea using surfactant as a vehicle to distribute the drug through the lungs offer promise in preventing BPD. For current clinical practice, systemic corticosteroids should be avoided in the first week of life, and thereafter used only in infants at high risk of BPD.
    MeSH term(s) Administration, Inhalation ; Adrenal Cortex Hormones/therapeutic use ; Bronchopulmonary Dysplasia/drug therapy ; Bronchopulmonary Dysplasia/prevention & control ; Dexamethasone/therapeutic use ; Glucocorticoids/therapeutic use ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Pharmaceutical Preparations
    Chemical Substances Adrenal Cortex Hormones ; Glucocorticoids ; Pharmaceutical Preparations ; Dexamethasone (7S5I7G3JQL)
    Language English
    Publishing date 2021-05-11
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2266911-5
    ISSN 1661-7819 ; 1661-7800
    ISSN (online) 1661-7819
    ISSN 1661-7800
    DOI 10.1159/000515950
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Relationships of Severity of Bronchopulmonary Dysplasia with Adverse Neurodevelopmental Outcomes and Poor Respiratory Function at 7-8 Years of Age.

    Doyle, Lex W / Ranganathan, Sarath / Mainzer, Rheanna M / Cheong, Jeanie L Y

    The Journal of pediatrics

    2024  Volume 269, Page(s) 114005

    Abstract: Objective: To clarify the relationships of 3 definitions of severity of bronchopulmonary dysplasia (BPD) with adverse neurodevelopmental and respiratory outcomes at early school-age.: Study design: Participants comprised 218 consecutive survivors to ... ...

    Abstract Objective: To clarify the relationships of 3 definitions of severity of bronchopulmonary dysplasia (BPD) with adverse neurodevelopmental and respiratory outcomes at early school-age.
    Study design: Participants comprised 218 consecutive survivors to 7-8 years of age born either <28 weeks' gestation or weighing <1000 g in Victoria, Australia, in 2005. BPD was classified as none, grade 1 (mild), grade 2 (moderate), or grade 3 (severe), using 2 commonly accepted definitions: 1) Jobe2001, and 2) Higgins2018, and our own 3) Victorian Infant Collaborative Study (VICS) 2005, adapted from Jensen2019. Outcomes included major neurodevelopmental disability, low IQ and academic achievement, poor motor function, and poor respiratory function as assessed by spirometry. Outcomes for children with each grade of BPD were compared with children with no BPD.
    Results: Of the 218 survivors, 132 (61%) had BPD on Jobe2001 criteria, and 113 (52%) had BPD on both Higgins2018 and VICS2005 criteria. Grade 1 on any criteria was not associated with any adverse neurodevelopmental outcomes. Grade 1 on both Higgins2018 and VICS2005 was associated with reduced spirometry, grade 2 on both Higgins2018 and VICS2005, and grade 3 on all criteria were associated with increased risk for both adverse neurodevelopmental and respiratory outcomes.
    Conclusions: Compared with no BPD, receiving additional oxygen up to 29% but no positive pressure support at 36 weeks' postmenstrual age increased the risk of abnormal respiratory function but not adverse neurodevelopment. Receiving ≥30% oxygen or any positive pressure support at 36 weeks increased the risk of both adverse outcomes.
    Language English
    Publishing date 2024-03-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3102-1
    ISSN 1097-6833 ; 0022-3476
    ISSN (online) 1097-6833
    ISSN 0022-3476
    DOI 10.1016/j.jpeds.2024.114005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Are Neurodevelopmental Outcomes of Infants Born Extremely Preterm Improving Over Time?

    Doyle, Lex W

    Pediatrics

    2018  Volume 141, Issue 5

    MeSH term(s) Developmental Disabilities ; Gestational Age ; Humans ; Infant ; Infant, Extremely Premature ; Infant, Newborn ; Research
    Language English
    Publishing date 2018-04-17
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 207677-9
    ISSN 1098-4275 ; 0031-4005
    ISSN (online) 1098-4275
    ISSN 0031-4005
    DOI 10.1542/peds.2017-4009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The changing face of neonatal intensive care for infants born extremely preterm (<28 weeks' gestation).

    Doyle, Lex W / Darlow, Brian A

    Seminars in perinatology

    2021  Volume 45, Issue 8, Page(s) 151476

    Abstract: Neonatal intensive care for infants born extremely preterm (<28 weeks' gestation) has changed dramatically over the past 60-70 years. From little care being available and few infants surviving in the first half of the 20th century, more intensive care ... ...

    Abstract Neonatal intensive care for infants born extremely preterm (<28 weeks' gestation) has changed dramatically over the past 60-70 years. From little care being available and few infants surviving in the first half of the 20th century, more intensive care and rapidly increasing survival rates followed in the second half, and have continued to rise into the 21st century. However, mistakes were made along the way. The purpose of this article is to recollect some of the pivotal changes in neonatal intensive care of infants born extremely preterm, and the consequences of those changes. Changes in attitudes, the physical environment, staffing, and basic treatments, such as oxygen and assisted ventilation, and evidence-based care are all discussed. Neonatal intensive care will continue to evolve, but in so doing we must learn from past mistakes in order to avoid repeating them.
    MeSH term(s) Female ; Gestational Age ; Humans ; Infant ; Infant, Extremely Premature ; Infant, Newborn ; Infant, Premature, Diseases/therapy ; Intensive Care Units, Neonatal ; Intensive Care, Neonatal ; Parturition ; Pregnancy ; Survival Rate
    Language English
    Publishing date 2021-08-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 752403-1
    ISSN 1558-075X ; 0146-0005
    ISSN (online) 1558-075X
    ISSN 0146-0005
    DOI 10.1016/j.semperi.2021.151476
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Changing outcomes for infants born extremely preterm.

    Doyle, Lex W / Cheong, Jeanie L Y

    Seminars in perinatology

    2021  Volume 45, Issue 8, Page(s) 151475

    MeSH term(s) Female ; Gestational Age ; Humans ; Infant ; Infant, Extremely Premature ; Infant, Newborn ; Parturition ; Pregnancy
    Language English
    Publishing date 2021-08-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 752403-1
    ISSN 1558-075X ; 0146-0005
    ISSN (online) 1558-075X
    ISSN 0146-0005
    DOI 10.1016/j.semperi.2021.151475
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Early developmental intervention programmes provided post hospital discharge to prevent motor and cognitive impairment in preterm infants.

    Orton, Jane / Doyle, Lex W / Tripathi, Tanya / Boyd, Roslyn / Anderson, Peter J / Spittle, Alicia

    The Cochrane database of systematic reviews

    2024  Volume 2, Page(s) CD005495

    Abstract: Background: Infants born preterm are at increased risk of cognitive and motor impairments compared with infants born at term. Early developmental interventions for preterm infants are targeted at the infant or the parent-infant relationship, or both, ... ...

    Abstract Background: Infants born preterm are at increased risk of cognitive and motor impairments compared with infants born at term. Early developmental interventions for preterm infants are targeted at the infant or the parent-infant relationship, or both, and may focus on different aspects of early development. They aim to improve developmental outcomes for these infants, but the long-term benefits remain unclear. This is an update of a Cochrane review first published in 2007 and updated in 2012 and 2015.
    Objectives: Primary objective To assess the effect of early developmental interventions compared with standard care in prevention of motor or cognitive impairment for preterm infants in infancy (zero to < three years), preschool age (three to < five years), and school age (five to < 18 years). Secondary objective To assess the effect of early developmental interventions compared with standard care on motor or cognitive impairment for subgroups of preterm infants, including groups based on gestational age, birthweight, brain injury, timing or focus of intervention and study quality.
    Search methods: We searched CENTRAL, MEDLINE, Embase, CINAHL, PsycINFO and trial registries in July 2023. We cross-referenced relevant literature, including identified trials and existing review articles.
    Selection criteria: Studies included randomised, quasi-randomised controlled trials (RCTs) or cluster-randomised trials of early developmental intervention programmes that began within the first 12 months of life for infants born before 37 weeks' gestational age (GA). Interventions could commence as an inpatient but had to include a post discharge component for inclusion in this review. Outcome measures were not prespecified, other than that they had to assess cognitive outcomes, motor outcomes or both. The control groups in the studies could receive standard care that would normally be provided.
    Data collection and analysis: Data were extracted from the included studies regarding study and participant characteristics, timing and focus of interventions and cognitive and motor outcomes. Meta-analysis using RevMan was carried out to determine the effects of early developmental interventions at each age range: infancy (zero to < three years), preschool age (three to < five years) and school age (five to < 18 years) on cognitive and motor outcomes. Subgroup analyses focused on GA, birthweight, brain injury, time of commencement of the intervention, focus of the intervention and study quality. We used standard methodological procedures expected by Cochrane to collect data and evaluate bias. We used the GRADE approach to assess the certainty of evidence.
    Main results: Forty-four studies met the inclusion criteria (5051 randomly assigned participants). There were 19 new studies identified in this update (600 participants) and a further 17 studies awaiting outcomes. Three previously included studies had new data. There was variability in the focus and intensity of the interventions, participant characteristics, and length of follow-up. All included studies were either single or multicentre trials and the number of participants varied from fewer than 20 to up to 915 in one study. The trials included in this review were mainly undertaken in middle- or high-income countries. The majority of studies commenced in the hospital, with fewer commencing once the infant was home. The focus of the intervention programmes for new included studies was increasingly targeted at both the infant and the parent-infant relationship. The intensity and dosages of interventions varied between studies, which is important when considering the applicability of any programme in a clinical setting. Meta-analysis demonstrated that early developmental intervention may improve cognitive outcomes in infancy (developmental quotient (DQ): standardised mean difference (SMD) 0.27 standard deviations (SDs), 95% confidence interval (CI) 0.15 to 0.40; P < 0.001; 25 studies; 3132 participants, low-certainty evidence), and improves cognitive outcomes at preschool age (intelligence quotient (IQ); SMD 0.39 SD, 95% CI 0.29 to 0.50; P < 0.001; 9 studies; 1524 participants, high-certainty evidence). However, early developmental intervention may not improve cognitive outcomes at school age (IQ: SMD 0.16 SD, 95% CI -0.06 to 0.38; P = 0.15; 6 studies; 1453 participants, low-certainty evidence). Heterogeneity between studies for cognitive outcomes in infancy and preschool age was moderate and at school age was substantial. Regarding motor function, meta-analysis of 23 studies showed that early developmental interventions may improve motor outcomes in infancy (motor scale DQ: SMD 0.12 SD, 95% CI 0.04 to 0.19; P = 0.003; 23 studies; 2737 participants, low-certainty evidence). At preschool age, the intervention probably did not improve motor outcomes (motor scale: SMD 0.08 SD, 95% CI -0.16 to 0.32; P = 0.53; 3 studies; 264 participants, moderate-certainty evidence). The evidence at school age for both continuous (motor scale: SMD -0.06 SD, 95% CI -0.31 to 0.18; P = 0.61; three studies; 265 participants, low-certainty evidence) and dichotomous outcome measures (low score on Movement Assessment Battery for Children (ABC) : RR 1.04, 95% CI 0.82 to 1.32; P = 0.74; 3 studies; 413 participants, low-certainty evidence) suggests that intervention may not improve motor outcome. The main source of bias was performance bias, where there was a lack of blinding of participants and personnel, which was unavoidable in this type of intervention study. Other biases in some studies included attrition bias where the outcome data were incomplete, and inadequate allocation concealment or selection bias. The GRADE assessment identified a lower certainty of evidence in the cognitive and motor outcomes at school age. Cognitive outcomes at preschool age demonstrated a high certainty due to more consistency and a larger treatment effect.
    Authors' conclusions: Early developmental intervention programmes for preterm infants probably improve cognitive and motor outcomes during infancy (low-certainty evidence) while, at preschool age, intervention is shown to improve cognitive outcomes (high-certainty evidence). Considerable heterogeneity exists between studies due to variations in aspects of the intervention programmes, the population and outcome measures utilised. Further research is needed to determine which types of early developmental interventions are most effective in improving cognitive and motor outcomes, and in particular to discern whether there is a longer-term benefit from these programmes.
    MeSH term(s) Infant, Newborn ; Infant ; Child ; Child, Preschool ; Humans ; Adolescent ; Birth Weight ; Patient Discharge ; Infant, Premature ; Cognitive Dysfunction/prevention & control ; Brain Injuries
    Language English
    Publishing date 2024-02-13
    Publishing country England
    Document type Meta-Analysis ; Systematic Review ; Journal Article ; Review
    ISSN 1469-493X
    ISSN (online) 1469-493X
    DOI 10.1002/14651858.CD005495.pub5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Growth of preterm babies after birth.

    Doyle, Lex W

    The Lancet. Global health

    2015  Volume 3, Issue 11, Page(s) e655–6

    MeSH term(s) Anthropometry/methods ; Female ; Humans ; Infant, Premature/growth & development ; Male ; Pregnancy
    Language English
    Publishing date 2015-11
    Publishing country England
    Document type Comment ; Journal Article
    ZDB-ID 2723488-5
    ISSN 2214-109X ; 2214-109X
    ISSN (online) 2214-109X
    ISSN 2214-109X
    DOI 10.1016/S2214-109X(15)00187-4
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  10. Article ; Online: Hypoxemic Episodes and Adverse Neurodevelopmental Outcome in Extremely Preterm Infants.

    Doyle, Lex W

    JAMA

    2015  Volume 314, Issue 6, Page(s) 568–569

    MeSH term(s) Bradycardia ; Female ; Humans ; Hypoxia ; Infant, Extremely Premature ; Male
    Language English
    Publishing date 2015-08-11
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 2958-0
    ISSN 1538-3598 ; 0254-9077 ; 0002-9955 ; 0098-7484
    ISSN (online) 1538-3598
    ISSN 0254-9077 ; 0002-9955 ; 0098-7484
    DOI 10.1001/jama.2015.9136
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