Q20 Q21 Q24 Q22 Q23 Q25 Q26 Q27 Q28
Conditions
Interventions
Group 1: Non-interventional observational study in the form of a registry. Routine data are collected and evaluated (longitudinally). No additional diagnostic examinations will be performed.
Sponsors
Deutsches Herzzentrum München
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Minimum age 18 years, patient at one of the participating centers, consent to participate in the study
Exclusion criteria
Exclusion criteria: Failure to meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| (1) Establishment of a registry on heart failure in ACHD ("real world data") (2) Definition of predictors for morbidity and mortality (3) Implementation of measures for long-term improvement of the biopsychosocial situation of ACHD with heart failure or/and abnormal ventricular function (4) Development of hypotheses for prospective multicenter therapy studies | — |
Secondary
| Measure | Time frame |
|---|---|
| - Improve the care of ACHD with heart failure by expanding the previously limited data base, based on older studies that include only small numbers of patients and short observation periods - Increased knowledge through review and improved, more comprehensive documentation of current standards of care. - Generation of evidence-based data on long-term prognosis, treatment regimens, patient safety, quality of care, etc. - Development of measures to improve care (e.g., early detection, targeted interventions, ...) - Development of specific measures for prevention and health promotion in ACHD with heart failure | — |
Countries
Germany
Contacts
Public ContactHarald Kaemmerer
Klinik für angeborene Herzfehler und KinderkardiologieDeutsches Herzzentrum München
Outcome results
None listed