Self‐reported respiratory and gastrointestinal outcomes in children with isolated congenital diaphragmatic hernia: A prospective multicentre study

Objective To evaluate medium‐term self‐reported respiratory and gastrointestinal (GI) outcomes in children with congenital diaphragmatic hernia (CDH). Design Self‐reported respiratory and GI outcomes correlated with prenatal severity indicators. Setting Prospective study at three fetal medicine units. Population Families of children prenatally diagnosed with isolated, left‐sided CDH surviving for >1 year. Methods Families received validated questionnaires for GI outcomes (Infant Gastroesophageal Reflux Questionnaire Revised, I‐GERQ‐R, for infants aged 9 years) and respiratory outcomes (preschool respiratory outcome questionnaire, for children aged ≤5 years, or the International Study of Asthma and Allergies in Childhood asthma questionnaire, for children aged 6–8 years or ≥9 years). Prenatal data collected from the medical records included lung size (percentage observed/expected lung‐to‐head ratio, O/E LHR %), liver position, fetal endoluminal tracheal occlusion (FETO) gestational age (GA) at delivery, and perinatal data included birthweight, location, patch repair and respiratory support. Main outcome measures The GI and respiratory scores were correlated with O/E LHR using linear and logistic regression models. Univariate analysis was used to evaluate associations with perinatal variables. Results We obtained 142 responses from 342 families (representing a response rate of 45%). The baseline characteristics of participants and non‐participants were comparable. No correlations between perinatal variables and respiratory or GI scores were identified. Children aged ≤5 years with lower O/E LHR values reported higher respiratory scores (P = 0.0175); this finding was not reported in older children. Overall, the children who underwent FETO (n = 51) had GI (P = 0.290) and respiratory (P = 0.052) scores that were comparable with those of children who were expectantly managed. Conclusions Families and children with prenatally diagnosed CDH reported fewer respiratory symptoms with increasing age. There was no correlation between O/E LHR or the use of FETO and self‐reported outcomes.