Abstract

Background:As clinicians strive to achieve consensus worldwide on how best to diagnose fetal alcohol spectrum disorders (FASD), the most recent FASD diagnosstic systems exhibit convergence and divergence. Applying these systems to a single clinical population illustrates contrasts between them, but validation studies are ultimately required to identify the best system. Currently, only the 4-Digit Code has published comprehensive validation studies.Methods:The 4-Digit Code and Hoyme 2016 FASD systems were applied to the records of 1,392 patients evaluated for FASD at the University of Washington to: 1) Compare the diagnostic criteria and tools used by each system, 2) Compare the prevalence and concordance of diagnostic outcomes and assess measures of validity.Results:Only 38% of patients received concordant diagnoses. The Hoyme criteria rendered half as many diagnoses under the umbrella of FASD (n=558) as the 4-Digit Code (n=1,092) and diagnosed a much higher proportion (53%) as fetal alcohol syndrome/partial fetal alcohol syndrome (FAS/PFAS) than the 4-Digit Code (7%). Key Hoyme factors contributing to discordance included relaxation of facial criteria (40% had the Hoyme FAS face, including patients with confirmed absence of alcohol exposure); setting alcohol exposure thresholds prevented 1/3 with confirmed exposure from receiving FAS/FASD diagnoses; and setting minimum age limits for Alcohol-Related Neurodevelopmental Disorder prevented 79% of alcohol-exposed infants with neurodevelopmental impairment a FASD diagnosis. The Hoyme Lip/Philtrum Guides differ substantively from the 4-Digit Lip-Philtrum Guides and thus are not valid for use with the 4-Digit Code.Conclusions:All FASD diagnostic systems need to publish comprehensive validation studies to identify which is the most accurate, reproducible, and medically valid.

Highlights

  • A systematic review and meta-analysis was conducted to determine the impact of intraoperative goal directed fluid and hemodynamic therapy (GDFHT) in children and postoperative outcome

  • This systematic review and meta-analysis of 23 non randomized and randomized controlled trials (RCT) evidenced that randomized controlled trials concerning the impact on perioperative GDFHT on postoperative outcome in children are lacking

  • RCT using these parameters in GDFHT protocols should be developed to clarify the influence of this therapy on postoperative outcome in children in cardiac and non cardiac surgical pediatric populations

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Summary

Introduction

A systematic review and meta-analysis was conducted to determine the impact of intraoperative goal directed fluid and hemodynamic therapy (GDFHT) in children and postoperative outcome. Methods: Editorial concerning the recent systemetic review and meta-analysis of the impact of intraoperative GDFHT on postoperative outcome in children. Results and Conclusion: This systematic review and meta-analysis of 23 non randomized and randomized controlled trials (RCT) evidenced that randomized controlled trials concerning the impact on perioperative GDFHT on postoperative outcome in children are lacking.

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