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German Resuscitation Registry (Reanimationsregister Version 2.0) - Module Telephone CPR (Modul Telefon-CPR)

- 3/18/20 - 1 Formulär, 9 Item-grupper, 17 Dataelement, 2 Språk
Item-grupper: Basic Data, Telephone instructions for CPR, Time end of instructions, Instructions complete, Instructed Ventilation, Used algorithm, Headquarters dispatcher trained, Indication Cardiopulmonary Arrest correct, bystander resuscitation conducted
The German Resuscitation Registry (GRR) (Das Deutsche Reanimationsregister) is a supraregional database for the collection and evaluation of resuscitations in rescue services and clinics, as well as for intraclinical emergency care in Germany. https://www.reanimationsregister.de/downloads/formulare.html The translation of the document from english to german is not an offical translation.

German Rescuitation Registry (Reanimationsregister Version 2.0) - Secondary care max (Weiterversorgung Max)

- 3/18/20 - 1 Formulär, 11 Item-grupper, 135 Dataelement, 2 Språk
Item-grupper: Basic Data, Admittance dates and status, Clinical measures, Temperature management, Temperature management Induction, Temperature management Maintenance, Temperature management Rewarming, Temperature management Fever prevention, Neuroprognostic tests, Result, Acquisition Status
Angaben für die Description: The German Resuscitation Registry (GRR) (Das Deutsche Reanimationsregister) is a supraregional database for the collection and evaluation of resuscitations in rescue services and clinics, as well as for intraclinical emergency care in Germany. https://www.reanimationsregister.de/downloads/formulare.html The translation is not an official translation. The TIMI risk score is part of this form. Morrow, D. A.; Antman, E. M.; Charlesworth, A.; Cairns, R.; Murphy, S. A.; Lemos, J. A. de et al. (2000): TIMI risk score for ST-elevation myocardial infarction: A convenient, bedside, clinical score for risk assessment at presentation: An intravenous nPA for treatment of infarcting myocardium early II trial substudy. In: Circulation 102 (17), S. 2031–2037. The modified Rankin-scale is part of this form. Rankin J. Cerebral vascular accidents in patients over the age of 60: II. Prognosis Scottish Med J. 1957; 2: 200–215. The Cerebral Performance Category is part of this form. Jennett B, Bond M. Assessment of outcome after severe brain damage. Lancet. 1975 Mar 1;1(7905):480-4. The EQ-5D is part of this form. The EuroQol Group. EuroQol—a new facility for the measure-mentofhealth-relatedqualityoflife.HealthPolicy.1990;36:199–208. The SF-12 is part of this form. Ware J, Kosinski M, Keller SD. A 12-item short-form health survey:construction of scales and preliminary tests of reliability and validity. MedCare. 1996;34:220–33.

German Rescuitation Registry (Reanimationsregister Version 2.0) - Further medical care pediatrics (Weiterversorgung Pädiatrie)

- 3/18/20 - 1 Formulär, 7 Item-grupper, 84 Dataelement, 2 Språk
Item-grupper: Basic Data, Admission Status, Temperature management, Clinical Course, Complications, Outcome Data on discharge from acute care, Aquisition Status
The German Resuscitation Registry (GRR) (Das Deutsche Reanimationsregister) is a supraregional database for the collection and evaluation of resuscitations in rescue services and clinics, as well as for intraclinical emergency care in Germany. https://www.reanimationsregister.de/downloads/formulare.html The translation of the document from english to german is not an offical translation.

S.0025_DGU TraumaRegister Outcome Prognosis Thromboembolic Events Point D1 in Time - Outcome Prognosis Thromboembolic Events Point D1 in Time DGU TraumaRegister questionnaire

- 3/19/20 - 1 Formulär, 7 Item-grupper, 11 Dataelement, 2 Språk
Item-grupper: Patient Information, Entlassungs-/Todesdatum, Entlassung/Verlegung, Verlegung in anderes Krankenhaus, Outcome, Todesursache, Klinikrelevante thromboembolische Ereignisse
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

nfdm - Der Notfalldatensatz der eGK

- 10/27/15 - 1 Formulär, 72 Item-grupper, 263 Dataelement, 2 Språk
Item-grupper: Notfalldatensatz, Zusätzliche_Information, Diagnose_1, Identifier_Codiersystem_Diagnose_1, Diagnose_2, Identifier_Codiersystem_Diagnose_2, Diagnose_3, Identifier_Codiersystem_Diagnose_3, Diagnose_4, Identifier_Codiersystem_Diagnose_4, Diagnose_5, Identifier_Codiersystem_Diagnose_5, Diagnose_6, Identifier_Codiersystem_Diagnose_6, Diagnose_7, Identifier_Codiersystem_Diagnose_7, Diagnose_8, Identifier_Codiersystem_Diagnose_8, Diagnose_9, Identifier_Codiersystem_Diagnose_9, Diagnose_10, Identifier_Codiersystem_Diagnose_10, Diagnose_11, Identifier_Codiersystem_Diagnose_11, Diagnose_12, Identifier_Codiersystem_Diagnose_12, Diagnose_13, Identifier_Codiersystem_Diagnose_13, Diagnose_14, Identifier_Codiersystem_Diagnose_14, Diagnose_15, Identifier_Codiersystem_Diagnose_15, Diagnose_16, Identifier_Codiersystem_Diagnose_16, Diagnose_17, Identifier_Codiersystem_Diagnose_17, Diagnose_18, Identifier_Codiersystem_Diagnose_18, Diagnose_19, Identifier_Codiersystem_Diagnose_19, Diagnose_20, Identifier_Codiersystem_Diagnose_20, Allergie_Unverträglichkeiten_1, Allergie_Unverträglichkeiten_2, Allergie_Unverträglichkeiten_3, Allergie_Unverträglichkeiten_4, Allergie_Unverträglichkeiten_5, Allergie_Unverträglichkeiten_6, Allergie_Unverträglichkeiten_7, Allergie_Unverträglichkeiten_8, Allergie_Unverträglichkeiten_9, Allergie_Unverträglichkeiten_10, Behandelnder_Arzt_Institution_1, Behandelnder_Arzt_Institution_2, Behandelnder_Arzt_Institution_3, Einverständniserklärung_Arzt, Zu_benachrichtigende_Person_Institution_1, Zu_benachrichtigende_Person_Institution_2, Zu_benachrichtigende_Person_Institution_3, Versicherter, Besondere_Hinweise, Schwangerschaft, Implantate_1, Implantate_2, Implantate_3, Implantate_4, Implantate_5, Implantate_6, Implantate_7, Implantate_8, Implantate_9, Implantate_10
nfdm of eGK

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