Selected data models

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- 1/23/19 - 1 form, 7 itemgroups, 33 items, 2 languages
Itemgroups: Patient Information, A, B, C, D, E, F
- 2/13/19 - 1 form, 16 itemgroups, 224 items, 1 language
Itemgroups: Pat-Stammdaten, Basisdaten, Einsatztechnische Daten, Notfallgeschehen, Anamnese, Erstbefund, Vormedikation, Vorbehandlung, Erstbefunde Neurologie, Erkrankungen, Messwerte initial, Verletzungen, Verlaufsbeschreibung, Medikation, Reanimation / Tod / Todesfeststellung, Maßnahmen, Übergabe, Einsatzverlauf - Besonderheiten, Übergabe, Bemerkungen
- 2/14/19 - 1 form, 9 itemgroups, 187 items, 1 language
Itemgroups: Basisdaten, Einsatztaktische Daten, Arzt-Arzt-Gespräch, Patientenstatus bei Ankunft / Übernahmestatus, Diagnosen, Verlauf, Maßnahmen/Geräte, Übergabestatus, Ergebnis
- 2/18/19 - 1 form, 13 itemgroups, 168 items, 2 languages
Itemgroups: Stammdaten, Einsatzzeiten, Alamierungsgrund, Höchste Qualifikation Personal, Einsatzort, Patientenstatus, Vermutete Ursache bei Kreislaufstillstand, Krankenhausbehandlung, Notfallgeschehen/ Anamnese/ Erstbefund, Erstbefund, Verlauf, Kernmaßnahmen und Ablauf, Übergabe
- 7/21/18 - 1 form, 14 itemgroups, 61 items, 2 languages
Itemgroups: Aufnahme, Erstuntersuchung/Symptome, Diagnostik, Thrombolyse/Rekanalisation, Verlegung innerhalb 12 h, Behinderung, wenn Verlegung nicht innerhalb von 12 h, Weitere Diagnostik, Risikofaktoren, Therapiemaßnahmen / Frühe Sekundärprävention, Therapie, Komplikationen (nur im Verlauf erworben), Behinderung bei Behandlungsende, Sekundärprophylaxe bei Behandlungsende (einschließlich Empfehlung im Entlassungsbrief), Entlassung
- 7/31/18 - 1 form, 14 itemgroups, 103 items, 2 languages
Itemgroups: Basisdaten, Reanimationsbehandlung, Vermutete Ursache, Einsatzzeiten, Einsatzortbeschreibung, Ärztliche Qualifikation, Erstbefunde nach Kreislaufstillstand, Kernmaßnahmen und Ablauf, Weitere Maßnahmen Technik, Weitere Maßnahmen Medikamente, Defiauswertung, Übergabe, Primäres Reanimationsergebnis, Qualitätsmanagement
- 7/29/18 - 1 form, 9 itemgroups, 55 items, 1 language
Itemgroups: Basisdaten, Koronarangiographie (WV Basis), Aktive Kühlung (WV Basis), Verlauf (WV Basis), Erfassungsstatus (WV), Induktion, Aufrechterhaltung, Wiedererwärmung, Fieberprävention
- 7/29/18 - 1 form, 3 itemgroups, 16 items, 2 languages
Itemgroups: Basisdaten, Verlauf 1. Jahr nach Kreislaufstillstand, Tod
- 7/20/18 - 1 form, 14 itemgroups, 82 items, 2 languages
Itemgroups: Patient information, Aufnahme, Vital signs, Atmung, Glasgow Coma Scale, Pupillen, Blood test, Diagnostics, Volumengabe, Therapy (til Intensive Care), First surgical intervention, Hemostasis Therapy, Medikamentöse Gerinnungstherapie, Further treatment
DGU TraumaRegister® questionnaire; Data are collected prospectively in four consecutive time phases from the site of the accident until discharge from hospital: A) Pre-hospital phase, B) Emergency room and initial surgery, C) Intensive care unit and D) Discharge. The documentation includes detailed information on demographics, injury pattern, comorbidities, pre- and in-hospital management, course on intensive care unit, relevant laboratory findings including data on transfusion and outcome of each individual. The inclusion criterion is admission to hospital via emergency room with subsequent ICU/ICM care or reach the hospital with vital signs and die before admission to ICU. The infrastructure for documentation, data management, and data analysis is provided by AUC - Academy for Trauma Surgery (AUC - Akademie der Unfallchirurgie GmbH), a company affiliated to the German Trauma Society. The scientific leadership is provided by the Committee on Emergency Medicine, Intensive Care and Trauma Management (Sektion NIS) of the German Trauma Society. The participating hospitals submit their data anon-ymously into a central database via a web-based application. Scientific data analysis is approved according to a peer review procedure established by Sektion NIS. TraumaRegister DGU® - Hinweise für die Publikation von Ergebnissen 5 März 2014 Seite 3 von 3 © 2014 TraumaRegister DGU® / AUC GmbH The participating hospitals are primarily located in Germany (90%), but a rising number of hospitals of other countries contribute data as well (at the moment from Austria, Belgium, China, Finland, Luxembourg, Slovenia, Switzerland, The Netherlands, and the United Arab Emirates). Currently, approx. 25,000 cases from more than 600 hospitals are entered into the database per year. Participation in TraumaRegister DGU® is voluntary. For hospitals associated with TraumaNetzwerk DGU®, however, the entry of at least a basic data set is obligatory for reasons of quality assurance. www.traumaregister-dgu.de
- 7/20/18 - 1 form, 8 itemgroups, 37 items, 2 languages
Itemgroups: Aufnahme, Blood test, ROTEM, Hemostasis Therapy, Medikamentöse Gerinnungstherapie, Aufenthaltsdauer/Beatmungstherapie, Therapie, SOFA
DGU TraumaRegister® questionnaire; Data are collected prospectively in four consecutive time phases from the site of the accident until discharge from hospital: A) Pre-hospital phase, B) Emergency room and initial surgery, C) Intensive care unit and D) Discharge. The documentation includes detailed information on demographics, injury pattern, comorbidities, pre- and in-hospital management, course on intensive care unit, relevant laboratory findings including data on transfusion and outcome of each individual. The inclusion criterion is admission to hospital via emergency room with subsequent ICU/ICM care or reach the hospital with vital signs and die before admission to ICU. The infrastructure for documentation, data management, and data analysis is provided by AUC - Academy for Trauma Surgery (AUC - Akademie der Unfallchirurgie GmbH), a company affiliated to the German Trauma Society. The scientific leadership is provided by the Committee on Emergency Medicine, Intensive Care and Trauma Management (Sektion NIS) of the German Trauma Society. The participating hospitals submit their data anon-ymously into a central database via a web-based application. Scientific data analysis is approved according to a peer review procedure established by Sektion NIS. TraumaRegister DGU® - Hinweise für die Publikation von Ergebnissen 5 März 2014 Seite 3 von 3 © 2014 TraumaRegister DGU® / AUC GmbH The participating hospitals are primarily located in Germany (90%), but a rising number of hospitals of other countries contribute data as well (at the moment from Austria, Belgium, China, Finland, Luxembourg, Slovenia, Switzerland, The Netherlands, and the United Arab Emirates). Currently, approx. 25,000 cases from more than 600 hospitals are entered into the database per year. Participation in TraumaRegister DGU® is voluntary. For hospitals associated with TraumaNetzwerk DGU®, however, the entry of at least a basic data set is obligatory for reasons of quality assurance. www.traumaregister-dgu.de
- 7/20/18 - 1 form, 7 itemgroups, 17 items, 2 languages
Itemgroups: Patienten-Identifikation, Patientenalter am Unfalltag, Geschlecht, Unfall-Anamnese, Zuverlegt, Gesundheitszustand vor Unfall, Unfallart
DGU TraumaRegister® questionnaire; Data are collected prospectively in four consecutive time phases from the site of the accident until discharge from hospital: A) Pre-hospital phase, B) Emergency room and initial surgery, C) Intensive care unit and D) Discharge. The documentation includes detailed information on demographics, injury pattern, comorbidities, pre- and in-hospital management, course on intensive care unit, relevant laboratory findings including data on transfusion and outcome of each individual. The inclusion criterion is admission to hospital via emergency room with subsequent ICU/ICM care or reach the hospital with vital signs and die before admission to ICU. The infrastructure for documentation, data management, and data analysis is provided by AUC - Academy for Trauma Surgery (AUC - Akademie der Unfallchirurgie GmbH), a company affiliated to the German Trauma Society. The scientific leadership is provided by the Committee on Emergency Medicine, Intensive Care and Trauma Management (Sektion NIS) of the German Trauma Society. The participating hospitals submit their data anon-ymously into a central database via a web-based application. Scientific data analysis is approved according to a peer review procedure established by Sektion NIS. TraumaRegister DGU® - Hinweise für die Publikation von Ergebnissen 5 März 2014 Seite 3 von 3 © 2014 TraumaRegister DGU® / AUC GmbH The participating hospitals are primarily located in Germany (90%), but a rising number of hospitals of other countries contribute data as well (at the moment from Austria, Belgium, China, Finland, Luxembourg, Slovenia, Switzerland, The Netherlands, and the United Arab Emirates). Currently, approx. 25,000 cases from more than 600 hospitals are entered into the database per year. Participation in TraumaRegister DGU® is voluntary. For hospitals associated with TraumaNetzwerk DGU®, however, the entry of at least a basic data set is obligatory for reasons of quality assurance. www.traumaregister-dgu.de