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. 2018 Dec 10;14(12):e1007822. doi: 10.1371/journal.pgen.1007822

Table 1. Clinical summary of patients.

Number Percent
Gender
    Male 212 58.6%
    Female 150 41.4%
CDH classification
    Isolated 208 57.5%
    Complex 149 41.2%
    Unknown 5 1.4%
Lesion side
    Left 270 74.6%
    Right 56 15.5%
    Eventration/Morgagni/Agenesis 11 3.0%
    Unknown 25 6.9%
CDH type
    Bochdaleck 294 81.2%
    Other# 22 6.1%
    Unknown 46 12.7%
DHREAMS cohort (n = 283): Time of recruitment
    Neonatal 229 80.9%
    Fetal 9 3.2%
    Child 45 15.9%
Discharge vital status (n = 283)
    Survived 241 85.2%
    Deceased 42 14.8%
Development assessment (n = 283)
    At 2 years follow-up 152 53.7%
    At 5 years follow-up 70 24.7%
    No assessment at either 2 or 5 years 128 45.2%
Additional anomalies in complex cases (n = 149)
    Cardiovascular 66 44.3%
    Neurodevelopmental§ 37 24.8%
    Skeletal 26 17.4%
    Genitourinary 14 9.4%
    Gastrointestinal 13 8.7%

¶ Development assessment at 2 years follow-up include Vineland Adaptive Behavior Assessment (Vineland-II) and/or Bayley Scales of Toddler Development (Bayley-III); tests at 5 years follow-up include Vineland-II and/or Wechsler Preschool and Primary Scale of Intelligence (WPPSI).

§Neurodevelopmental conditions include congenital abnormalities in central nerves system, and developmental delay or neuropsychiatric disorders based on the follow-up developmental evaluations.