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Change in neurodevelopmental outcomes for extremely premature infants over time: a systematic review and meta-analysis
  1. Joseph W Kaempf1,
  2. Ursula Guillen2,
  3. Jonathan S Litt3,4,5,
  4. John A F Zupancic3,4,
  5. Haresh Kirpalani6,7
  1. 1 Women and Children's Services, Providence Health System, Portland, Oregon, USA
  2. 2 Division of Neonatology, ChristianaCare, Wilmington, Delaware, USA
  3. 3 Department of Neonatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA
  4. 4 Division of Newborn Medicine, Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA
  5. 5 Department of Social and Behavioral Sciences, Harvard TH Chan School of Public Health, Boston, Massachusetts, USA
  6. 6 Emeritus, Division of Neonatology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA
  7. 7 Emeritus, Division of Neonatology, McMaster University, Hamilton, Massachusetts, Canada
  1. Correspondence to Dr Ursula Guillen, Division of Neonatology, ChristianaCare, Wilmington, Delaware, USA; ursula.guillen{at}gmail.com

Abstract

Objective Survival rates of extremely premature infants are rising, but changes in neurodevelopmental impairment (NDI) rates are unclear. Our objective was to perform a systematic review of intrainstitutional variability of NDI over time.

Design Systematic review and meta-analysis.

Data sources Ovid MEDLINE, Embase, PubMed, Cochrane Library and Google Scholar.

Study selection Study eligibility: (1) at least two discrete cohorts of infants born <27 weeks’ gestation or <1000 g birth weight, (2) one cohort born after 1990 and at least one subsequent cohort of similar gestational age, (3) all cohorts cared for within the same Neonatal Intensive Care Unit(s) (NICU) and (4) neurodevelopmental outcomes at 18–36 months corrected age.

Main outcome Change in NDI rates. Quality, validity and bias were assessed using Grading of Recommendations, Assessment, Development, and Evaluation and Quality in Prognosis Studies guidelines.

Results Of 203 publications, 15 were eligible, including 13 229 infants. At the first time point, average NDI rate across study groups weighted by sample size was 41.0% (95% CI 34.0% to 48.0%). The average change in NDI between time points was −3.3% (95% CI −8·8% to 2.2%). For each added week of gestation at birth, the rate of NDI declined by 9.7% (95% CI 6.2% to 13.3%). Most studies exhibited moderate–severe bias in at least one domain, especially attrition rates.

Conclusions When comparing discrete same-centre cohorts over time, there was no significant change in NDI rates in infants born <27 weeks’ gestation or <1000 g. Higher survival rates unaccompanied by improvement in neurodevelopment highlight urgency for renewed focus on the causes of NDI and evidence-based strategies to reduce brain injury.

  • neonatology
  • intensive care units, neonatal

Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

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Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

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Footnotes

  • Twitter @johnzupancic

  • Contributors JK conceptualised and designed the study; designed the data collection instruments; collected data; drafted the initial manuscript; and reviewed and revised the manuscript. UG is the guarantor; conceptualised and designed the study; designed the data collection instruments; collected data; drafted the initial manuscript; and reviewed and revised the manuscript. JL conceptualised and designed the study, carried out the initial analyses, reviewed and revised the manuscript. JZ and HK conceptualised and designed the study; coordinated and supervised data collection; and critically reviewed the manuscript for important intellectual content.

  • Funding JK’s work on this project was supported in part by the Providence Foundation and Providence Women and Children’s Services.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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