The Marienhaus Group intends to introduce a Clinical Data Repository (CDR). This stores structured and semantically annotated medical data such as diagnoses, findings, medications, laboratory and vital signs, CAVE data from different systems and also makes them available for downstream processes and systems.
The solution is used at the Marienhaus Group sites. In the following, the individual locations are listed according to their affiliation to the individual clients:
Marienhaus Kliniken GmbH
- Marienhaus Klinikum Eifel / Krankenhausstraße 1; D-54634 Bitburg
- Marienhaus Klinikum Eifel / Aloys-Schneider-Straße 37; D-54568 Gerolstein
- St. Josef-Krankenhaus Hermeskeil / Koblenzer Str. 23; D-54411 Hermeskeil
- Marienhaus Klinikum St. Elisabeth Saarlouis / Kapuzinerstraße 4; D-66740 Saarlouis
- Marienhaus Klinikum Hetzelstift Neustadt / Stiftstraße 10; D-67434 Neustadt an der Weinstraße
- Marienhaus Klinikum St. Elisabeth Neuwied / Friedrich-Ebert-Straße 59; D-56564 Neuwied
- Marienhaus Klinikum St. Antonius Waldbreitbach / Margaretha-Flesch-Straße 4; D-56588 Waldbreitbach
- Marienhaus Klinikum im Kreis Ahrweiler / Krankenhaus Maria Hilf / Dahlienweg 3; D-53474 Bad Neuenahr-Ahrweiler
- Marienhaus Klinikum im Kreis Ahrweiler / St. Josef-Krankenhaus / Mühlenstraße 31-35; D-53518 Adenau
Marienhauskliniken im Landkreis Neunkirchen GmbH
- Marienhausklinik St. Josef Kohlhof / Klinikweg 1-4; D-66539 Neunkirchen
- Marienhaus Klinikum St. Wendel - Ottweiler / Am Hirschberg 1a; D-66606 St. Wendel
Marienhaus Klinikum Mainz GmbH
- Marienhaus Klinikum Mainz / An der Goldgrube 11; D-55131 Mainz
Heilig-Geist-Hospital Bingen gGmbH
- Marienhaus Heilig-Geist-Hospital Bingen / Kapuzinerstraße 15-17; D-55411 Bingen am Rhein
The clients intend to introduce a Clinical Data Repository (CDR) as part of the funding under the Hospital Future Act ("KHZG") - Funding Act 6. This stores structured and semantically annotated medical data such as diagnoses, findings, medications, laboratory and vital signs, CAVE data from different systems and also makes them available for downstream processes and systems. To achieve this goal, it is imperative that a CDR supports all necessary communication standards (HL7 v2, FHIR, xDT, etc.) and medical order systems (ICD, OPS, LOINC, SNOMEDCT, etc.).
On the one hand, this will create the necessary and legally prescribed interoperability capability and, on the other hand, it will enable the institutions to build up a complete and quality-assured patient data record and to make it available to all internal and external stakeholders and processes in compliance with data protection and security.