Congenital heart disease Congenital heart disease
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
No minimum to 17 Years
Inclusion criteria
Inclusion criteria: Participation in the CardioCare program with informed (verbal) consent on the use of their data for research purposes. Underwent one or more surgical interventions early in life.
Exclusion criteria
Exclusion criteria: Data of patient or legal guardians unable or unwilling to give consent will not be used for research purposes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Long-term outcomes for childrenEndpoint: Long-term outcomes, defined as all data collected on children as part of the CardioCare routine follow-up and stored in the EPR or other relevant databases. This includes metrics on cognitive, social, psychological, and physical functioning, as well as other health-related indicators.2. Impact of illness and hospital treatment on children’s long-term outcomesEndpoint: The relationship between clinical data (e.g., disease characteristics, treatment details, and hospitalization data) and the long-term outcomes of children, derived from EPR data or other databases.3. Impact of illness and treatment on parentsEndpoint: Parent-reported outcomes and other data collected in the context of care provided to children, including psychological, social, and functional metrics for parents, as recorded in the EPR or other relevant sources. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not applicable. | — |
Countries
Netherlands
Contacts
Public ContactA.W. Deutekom
Erasmus MC, Universitair Medisch Centrum Rotterdam
Outcome results
None listed