Q20.0
Conditions
Interventions
Group 1: A retrospective analysis of all neonates who underwent RVOT reconstruction using 12-mm bovine jugular vein conduits or small homografts between January 2005 and December 2020.
Sponsors
Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
1 Days to 4 Weeks
Inclusion criteria
Inclusion criteria: Data analysis of patients who were in treatment from 2005 to 2020
Exclusion criteria
Exclusion criteria: Patients who required reintervention for reasons unrelated to the conduit within the first five years after implantation are excluded. Patients for whom there is insufficient follow-up data or no valid follow-up are also excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is the occurrence of conduit failure, defined as the need for conduit replacement. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include freedom from conduit-related reoperations, long-term overall survival, analysis of the causes of conduit failure, and the maximum duration of conduit use prior to the necessary reoperation | — |
Countries
Germany
Contacts
Public ContactBoulos Asfour
Universitätsklinikum Bonn
Outcome results
None listed