Predictors of Post-traumatic stress symptomology in parents of infants with Congenital Heart Disease post-surgery and after four months

J Pediatr Nurs. 2022 Jan-Feb:62:17-22. doi: 10.1016/j.pedn.2021.11.013. Epub 2021 Nov 25.

Abstract

Purpose: To identify predictors of post-traumatic stress symptomology among parents of infants with complex congenital heart defects at hospital discharge and after 4 months.

Design & methods: A secondary analysis utilizing data from a larger RCT performed in three pediatric cardiac centers in North America. Analysis included 158 parent-infant dyads. Generalized Linear Modeling was used to identify predictors of parental post-traumatic symptomology at hospital discharge, and after 4 months. Considered predictors included demographics/SES, illness, and psychosocial parameters.

Results: At discharge, parenting stress, education, and infant's medication number were linked to post-traumatic stress symptomology severity; Parenting stress, education, insurance type, and medications number predicted number of symptoms; Tube-assisted feeding predicted PTSD. At 4 months, parenting stress, ethnicity, and number of ED visits predicted PTSS severity; Parenting stress, ethnicity, and cardiologist visits predicted number of symptoms; Parenting stress, single ventricle physiology, and number of children predicted PTSD.

Conclusions & practical implications: Parental psychosocial factors, additionally to illness and sociodemographic indicators, can potentially risk parents to experience PTSS/PTSD. Nursing and other healthcare professionals can participate in early screening of such factors to determine familial risk.

Trial registration: NCT01941667.

Keywords: Congenital heart defects; Infants; Parents; Post-traumatic stress.

MeSH terms

  • Child
  • Heart Defects, Congenital* / diagnosis
  • Heart Defects, Congenital* / surgery
  • Humans
  • Infant
  • Parenting
  • Parents
  • Stress Disorders, Post-Traumatic* / diagnosis
  • Stress Disorders, Post-Traumatic* / epidemiology

Associated data

  • ClinicalTrials.gov/NCT01941667