Q25
Conditions
Interventions
Group 1: The study includes newborns and infants with biventricular heart physiology who underwent surgical aortic arch reconstruction between 2014 and 2019.
Sponsors
Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
1 Days to 12 Months
Inclusion criteria
Inclusion criteria: The study includes newborns and infants with biventricular heart physiology who underwent surgical aortic arch reconstruction at the University Hospital Bonn between 2014 and 2019. A prerequisite is the full availability of the relevant preoperative, intraoperative, and postoperative clinical data. Consent to participate in the follow-up study—provided in writing by the individual concerned (if capable of giving consent and =18 years of age) or by their legal guardian/representative (for minors or adults incapable of giving consent). Full availability of preoperative, intraoperative, and postoperative data in the patient records. Documentation of the clinical course.
Exclusion criteria
Exclusion criteria: Refusal by the patient or parents to participate in the study. Patients with incomplete data documentation or a lack of traceability will be excluded. Patients for whom a clear assignment to the respective perfusion strategy is not possible will also be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints are metabolic and renal parameters, specifically intraoperative and postoperative lactate levels, maximum postoperative serum creatinine levels, and urine output within the first 24 hours after surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include the duration of mechanical ventilation, postoperative complications, and early mortality. | — |
Countries
Germany
Contacts
Public ContactBoulos Asfour
Universitätsklinikum Bonn
Outcome results
None listed