I21
Conditions
Interventions
Group 1: Clinical data of the patients will be extracted from the hospitals information sytsem after their hospital stay. Six weeks after the patients will be contacted to fill out a survey regarding
Sponsors
Martin-Luther-Universität Halle-Wittenberg, Medizinische Fakultät, Institut für Medizinische Epidemiologie, Biometrie und Informatik
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All patients of the cardiological department of one of the participating hospitals who gave informed consent to their data being extracted from the hospital information system and being contacted for further surveys.
Exclusion criteria
Exclusion criteria: patients who did not sign an informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is the diagnosis Acute Myocardial Infarction (ICD-10 I21) in the hospital information system at the end of treatmennt in one of the participating hospitals. The diagnosis is verified by the controlling of the hospital before automated data extraction. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patients of cardiology departments | — |
Countries
Germany
Contacts
Public ContactJanka Massag
Martin-Luther-Universität Halle-Wittenberg; Medizinische Fakultät; Institut für Medizinische Epidemiologie, Biometire und Informatik
Outcome results
None listed