Résultats de recherche - Portail des modèles médicaux de données (portail MDM)

DIVI Kerndatensatz Intensivmedizin 2010 - Entlassung von der Intensivtherapiestation

- 19/03/2020 - 5 Formulaires, 2 Groupes Item, 16 Eléments de données, 1 Langue

Groupes Item: DNR (do not resuscitate) / AND (allowed natural death), Procedures and complications

Kerndatensatz Intensivmedizin 2010 der DIVI und DGAI (nur patientenbezogene Daten, ohne Strukturdaten der Intensivtherapiestation und der Klinik ). Deutsche interdisziplinaere Vereinigung fuer Intensiv und Notfallmedizin DIVI (German interdisciplinary association for intensive and emergeny medical care), http://www.divi.de/images/Dokumente/Empfehlungen/Strukturempfehlungen/2010_KerndatensatzIntensivmedizin.pdf

Entlassung aus dem Krankenhaus

1 Groupe Item 2 Eléments de données

Intensive Care and Outcome: Quality Management Trauma Registry German Society for Trauma Surgery

- 11/05/2016 - 1 Formulaire, 3 Groupes Item, 13 Eléments de données, 2 Langues

Groupes Item: Intensive Care, Outcome, Injuries/Diagnoses

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.

Intensive Care Point C in time DGU TraumaRegister questionnaire

- 27/05/2016 - 1 Formulaire, 5 Groupes Item, 35 Eléments de données, 2 Langues

Groupes Item: Patient information, SOFA, Blood test, Therapy, Hemostasis Therapy

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

Heidelberger Register chronischer Singultus - Primary Visit

- 22/03/2022 - 2 Formulaires, 8 Groupes Item, 118 Eléments de données, 2 Langues

Groupes Item: Demografie und Anamnese bei der Visite, Durchgeführte Diagnostik, Ausführung der Komorbiditäten, Aktuelle Medikation, Pausierung der Medikation, Befund und Beurteilung, Quantifizierung der Symptome, Empfehlungen

Erhebung eines klinischen Datensatzes zum chronischen Singultus (Schluckauf). Durchgeführt durch die Sektion Schmerzmedizin an der Klinik für Anästhesiologie und Intensivmedizin am Universtätsklinikum Heidelberg. Dr. med. Claudia Busch & PD Dr. Jens Keßler

Secondary Visit

6 Groupes Item 84 Eléments de données

Heidelberg Perioperative Deep Data Study – a prospective cohort study - PDMS ICU - Primary data

- 10/01/2022 - 1 Formulaire, 8 Groupes Item, 125 Eléments de données, 1 Langue

Groupes Item: Respiratory system data, Cardiovascular system data, Diagnosis related data, Laboratory values, Medication related data, Medical Scores, Medical device related data, Quantitative data body fluids

HeiPoDD registry will form a clinical database and a corresponding biobank as the basis to predict overall postoperative morbidity and mortality using data-driven, personalized risk prediction from the entirety of available clinical records. Prospective single-center observational registry. DRKS00025924

Heidelberg Perioperative Deep Data Study – a prospective cohort study - DRKS00025924 - Patient monitoring - primary data

- 28/12/2021 - 1 Formulaire, 9 Groupes Item, 242 Eléments de données, 1 Langue

Groupes Item: Height Weight BSA, Respiratory system data, Laboratory data, Medication data, Neurological data, Clinical Scores, Temperature data, Electrocardiography data, Cardiovascular system data

HeiPoDD registry will form a clinical database and a corresponding biobank as the basis to predict overall postoperative morbidity and mortality using data-driven, personalized risk prediction from the entirety of available clinical records. Prospective single-center observational registry. DRKS00025924

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

- 18/03/2020 - 1 Formulaire, 11 Groupes Item, 135 Eléments de données, 2 Langues

Groupes Item: 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.

Registry of Children's Glaucoma, Department of Ophthalmology, University Medical Center Mainz - Examination under anaesthesia (NKU) Form

- 04/06/2018 - 1 Formulaire, 11 Groupes Item, 69 Eléments de données, 1 Langue

Groupes Item: Eye examination under anesthesia, Intraocular Pressure, Eye refractometry, Keratometry, Corneal diameter, Corneal Pachymetry, Anterior eyeball segment, examination fundus, Gonioscopy, Congenital Glaucoma, diagnosis

Form used for the documentation of an eye examination under (general) anesthesia for the Registry of Children's Glaucoma by Department of Ophthalmology, University Medical Center Mainz. ODM derived from original form NKUbogen20161116AS supplied by Center for Ophthalmological Epidemiology and Health Services Research, University Medical Center Mainz

Critical Care case record form (EuSOS)

- 20/09/2021 - 1 Formulaire, 3 Groupes Item, 81 Eléments de données, 1 Langue

Groupes Item: Data describing first hour of admission to critical care, Surgical site, Highest vasoactive drug dose in the first hour following admission

European Surgical Outcomes Study (EuSOS) http://clinicaltrials.gov/show/NCT01203605

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