Patients undergoing high and intermediate risk surgery at Heidelberg University Hospital
Conditions
Interventions
Group 1: Prospective single-center observational registry
To implement a clinical database and a corresponding biobank as the basis to predict overall postoperative morbidity and mortality using data
Sponsors
Klinik für Anästhesiologie, Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Planned elective high-risk and intermediate-risk surgery for any indication (Definition Appendix II), 2. Age = 18 years, 3. Ability of subject to understand character and individual consequences of the clinical study and the storage of personal data in the registry, 4. Written informed consent
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hospital mortality | — |
Secondary
| Measure | Time frame |
|---|---|
| Endpoints are included if they can either be derived from routine observations in a semi-structured or structured form or if they are included in the registry as specific study endpoints. Exemplary: Duration of the operation Intraoperative blood loss Histopathological diagnosis pain Heart attack Myocardial Injury After Non-Cardiac Surgery (MINS) Death for any reason Coronary revascularization Acute Respiratory Distress Syndrome Pulmonary embolism Acute kidney damage sepsis Bloodstream infection Superficial, deep infections or infections in the organ space after surgical interventions Postoperative bleeding Anastomotic leakage Ileus of any mechanism Liver failure Re-intervention Redo surgery Length of stay in the intensive care unit Length of hospital stay Overall survival | — |
Countries
Germany
Contacts
Public ContactJan Larmann
Klinik für AnästhesiologieUniversitätsklinikum Heidelberg
Outcome results
None listed