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Studientelegramm 71-2019-3/3
Titel der Studie: 2019 AHA/ACC/HRS Focused Update of the 2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation
Autoren: Calkins et al.
Journal: Circulation
Studientelegramm 72-2019-1/3
Titel der Studie: Cardiovascular Risk Reduction with Icosapent Ethyl for Hypertriglyceridemia
Autoren: Bhatt et al.
Journal: New England Journal of Medicine (NEJM)
Titel der Studie: Effects of Icosapent Ethyl on Total Ischemic Events: From REDUCE-IT
Autoren: Bhatt et al.
Journal: Journal of the American College of Cardiology (JACC)
Studientelegramm 71-2019-2/3
Titel der Studie: FDA adds Boxed Warning for increased risk of death with gout medicine Uloric (febuxostat)
Autoren: U.S. Food and Drug Administration (FDA)
Studientelegramm 68-2019-1/3
Titel der Studie: Association of Adding Aspirin to Warfarin Therapy Without an Apparent Indication With Bleeding and Other Adverse Events
Autoren: Schaefer et al.
Journal: JAMA Internal Medicine
AMBOSS-Inhalte: Therapeutische Antikoagulation - klinische Anwendung, Dual- und Triple-Therapie bei KHK, CHA2DS2VASc-Score (Rechner)
Studientelegramm 66-2019-1/3
Titel der Studie: Assessing the Use of Google Translate for Spanish and Chinese Translations of Emergency Department Discharge Instructions
Autoren: Khoong et al.
Journal: JAMA Internal Medicine
AMBOSS-Kapitel: Anamnese, Versorgung von Geflüchteten und Reiserückkehrern, Verfassen eines Arztbriefes
Studientelegramm 67-2019-2/3
Titel der Studie: The association between heatwaves and risk of hospitalization in Brazil: A nationwide time series study between 2000 and 2015
Autoren: Zhao et al.
Journal: PLOS Medicine
Studientelegramm 67-2019-3/3
Titel der Studie: Evaluation of the Inclusion of Studies Identified by the FDA as Having Falsified Data in the Results of Meta-analyses: The Example of the Apixaban Trials
Autoren: Garmendia et al.
Journal: JAMA Internal Medicine
Studientelegramm 68-2019-3/3
Informationen zu Sotagliflozin (Überblick, Zulassungsinformationen und Produktinformationen)
Herausgeber: European Medicines Agency (EMA)
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