Search Results - "Zoch, Michéle"

OMOP CDM Can Facilitate Data-Driven Studies for Cancer Prediction: A Systematic Review by Ahmadi, Najia, Peng, Yuan, Wolfien, Markus, Zoch, Michéle, Sedlmayr, Martin

“…The current generation of sequencing technologies has led to significant advances in identifying novel disease-associated mutations and generated large amounts…”
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Assessing the Use of German Claims Data Vocabularies for Research in the Observational Medical Outcomes Partnership Common Data Model: Development and Evaluation Study by Henke, Elisa, Zoch, Michéle, Kallfelz, Michael, Ruhnke, Thomas, Leutner, Liz Annika, Spoden, Melissa, Günster, Christian, Sedlmayr, Martin, Bathelt, Franziska

“…Abstract Background National classifications and terminologies already routinely used for documentation within patient care settings enable the unambiguous…”
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An Extract-Transform-Load Process Design for the Incremental Loading of German Real-World Data Based on FHIR and OMOP CDM: Algorithm Development and Validation by Henke, Elisa, Peng, Yuan, Reinecke, Ines, Zoch, Michéle, Sedlmayr, Martin, Bathelt, Franziska

“…Abstract Background In the Medical Informatics in Research and Care in University Medicine (MIRACUM) consortium, an IT-based clinical trial recruitment support…”
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An ETL-process design for data harmonization to participate in international research with German real-world data based on FHIR and OMOP CDM by Peng, Yuan, Henke, Elisa, Reinecke, Ines, Zoch, Michéle, Sedlmayr, Martin, Bathelt, Franziska

“…•German CDS is defined in HL7 FHIR for better interoperability across university hospitals.•ETL process was developed using SpringBatch to transform German CDS…”
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Conceptual design of a generic data harmonization process for OMOP common data model by Henke, Elisa, Zoch, Michele, Peng, Yuan, Reinecke, Ines, Sedlmayr, Martin, Bathelt, Franziska

“…To gain insight into the real-life care of patients in the healthcare system, data from hospital information systems and insurance systems are required…”
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German Claims Data for Real-World Research: Content Coverage Evaluation in OMOP CDM by Henke, Elisa, Zoch, Michéle, Reinecke, Ines, Spoden, Melissa, Ruhnke, Thomas, Günster, Christian, Sedlmayr, Martin, Bathelt, Franziska

“…Research on real-world data is becoming increasingly important. The current restriction to clinical data in Germany limits the view of the patient. To gain…”
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How to customize common data models for rare diseases: an OMOP-based implementation and lessons learned by Ahmadi, Najia, Zoch, Michele, Guengoeze, Oya, Facchinello, Carlo, Mondorf, Antonia, Stratmann, Katharina, Musleh, Khader, Erasmus, Hans-Peter, Tchertov, Jana, Gebler, Richard, Schaaf, Jannik, Frischen, Lena S, Nasirian, Azadeh, Dai, Jiabin, Henke, Elisa, Tremblay, Douglas, Srisuwananukorn, Andrew, Bornhäuser, Martin, Röllig, Christoph, Eckardt, Jan-Niklas, Middeke, Jan Moritz, Wolfien, Markus, Sedlmayr, Martin

“…Given the geographical sparsity of Rare Diseases (RDs), assembling a cohort is often a challenging task. Common data models (CDM) can harmonize disparate…”
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Ten Topics to Get Started in Medical Informatics Research by Wolfien, Markus, Ahmadi, Najia, Fitzer, Kai, Grummt, Sophia, Heine, Kilian-Ludwig, Jung, Ian-C, Krefting, Dagmar, Kühn, Andreas, Peng, Yuan, Reinecke, Ines, Scheel, Julia, Schmidt, Tobias, Schmücker, Paul, Schüttler, Christina, Waltemath, Dagmar, Zoch, Michele, Sedlmayr, Martin

“…The vast and heterogeneous data being constantly generated in clinics can provide great wealth for patients and research alike. The quickly evolving field of…”
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Secondary use of patient data within decentralized studies using the example of rare diseases in Germany: A data scientist's exploration of process and lessons learned by Zoch, Michele, Gierschner, Christian, Andreeff, Anne-Katrin, Henke, Elisa, Sedlmayr, Martin, Müller, Gabriele, Tippmann, Jenny, Hebestreit, Helge, Choukair, Daniela, Hoffmann, Georg F, Fritz-Kebede, Fleur, Toepfner, Nicole, Berner, Reinhard, Biergans, Stephanie, Verbücheln, Raphael, Schaaf, Jannik, Fleck, Julia, Wirth, Felix Nikolaus, Schepers, Josef, Prasser, Fabian

“…Unlocking the potential of routine medical data for clinical research requires the analysis of data from multiple healthcare institutions. However, according…”
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Predictors of improvement in disease activity in childhood and adolescent Crohn’s disease: an analysis of age, localization, initial severity and drug therapy — data from the Saxon Registry for Inflammatory Bowel Disease in Children in Germany (2000–2014) by Weidner, Jens, Zoch, Michele, Kern, Ivana, Reinecke, Ines, Bathelt, Franziska, Manuwald, Ulf, Peng, Yuan, Henke, Elisa, Rothe, Ulrike, Kugler, Joachim

“…The escalating worldwide prevalence of Crohn’s disease (CD) among children and adolescents, coupled with a trend toward earlier onset, presents significant…”
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A systematic review and meta-regression on international trends in the incidence of ulcerative colitis in children and adolescents associated with socioeconomic and geographic factors by Weidner, Jens, Kern, Ivana, Reinecke, Ines, Bathelt, Franziska, Manuwald, Ulf, Henke, Elisa, Zoch, Michele, Rothe, Ulrike, Kugler, Joachim

“…The incidence of ulcerative colitis (UC) among children and adolescents is rising globally, albeit with notable discrepancies across countries. This systematic…”
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Methods Used in the Development of Common Data Models for Health Data: Scoping Review by Ahmadi, Najia, Zoch, Michele, Kelbert, Patricia, Noll, Richard, Schaaf, Jannik, Wolfien, Markus, Sedlmayr, Martin

“…Common data models (CDMs) are essential tools for data harmonization, which can lead to significant improvements in the health domain. CDMs unite data from…”
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Transition database for rare diseases and its use for clinical documentation by Zoch, Michele, Gierschner, Christian, Gebler, Richard, Leutner, Liz A, Kretschmer, Tanita, Danker, Adrian, Lee-Kirsch, Min Ae, Berner, Reinhard, Sedlmayr, Martin

“…Patients with rare diseases commonly suffer from severe symptoms as well as chronic and sometimes life-threatening effects. Not only the rarity of the diseases…”
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Interdisciplinary care path and potential IT support for people with rare diseases in Germany by Zoch, Michele, Sedlmayr, Brita, Knapp, Andreas, Bathelt, Franziska, Helfer, Sven, Schmitt, Jochen, Sedlmayr, Martin

“…INTRODUCTIONDue to the high variability and, at the same time, rare occurrence of rare diseases, the diagnosis of these patients (approx. 4 million people in…”
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Interdisziplinärer Versorgungspfad und mögliche IT-Unterstützung für Menschen mit Seltenen Erkrankungen in Deutschland by Zoch, Michele, Sedlmayr, Brita, Knapp, Andreas, Bathelt, Franziska, Helfer, Sven, Schmitt, Jochen, Sedlmayr, Martin

“…Durch die hohe Variabilität bei gleichzeitig rarem Auftreten von Seltenen Erkrankungen, gleicht die Diagnosestellung bei Betroffenen (ca. 4 Millionen Menschen…”
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Towards the Improvement of Clinical Guidelines Based on Real World Data by Henke, Elisa, Reinecke, Ines, Zoch, Michele, Sedlmayr, Martin, Bathelt, Franziska

“…Computerized clinical guidelines (CCG) are effective instruments for standardizing, monitoring and optimizing medical treatment processes. Nevertheless, due to…”
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Context-Sensitive Common Data Models for Genetic Rare Diseases - A Concept by Ahmadi, Najia, Zoch, Michele, Sedlmayr, Brita, Schuler, Katharina, Hahn, Waldemar, Sedlmayr, Martin, Wolfien, Markus

“…Current challenges of rare diseases need to involve patients, physicians, and the research community to generate new insights on comprehensive patient cohorts…”
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Development of a Dashboard for Rare Diseases - A Technical Case Report by Leutner, Liz A, Bathelt, Franziska, Sedlmayr, Brita, Sedlmayr, Martin, Zoch, Michele

“…About 30 million people suffer from a rare disease in Europe. Those affected face a variety of problems. These include the lack of information and difficult…”
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