Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Barbara Pfistermeister"'
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0171353 (2017)
PURPOSE:Previous studies suggest an association between use of anticholinergic drugs in elderly patients and cognitive impairment. However, there are still limited data on the association of anticholinergic drug use and cognitive impairment as well a
Externí odkaz:
https://doaj.org/article/1f8c1f858529439f828a9f4eaa0b8bdb
Autor:
Wahram Andrikyan, Lea Jung-Poppe, Anna Altenbuchner, Hagen Fabian Nicolaus, Barbara Pfistermeister, Harald Dormann, Martin F. Fromm, Renke Maas
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 1; Pages: 315
Drug-related problems (DRPs), i.e., adverse drug reactions (ADRs) and medication errors (MEs), constitute a serious threat to the patient’s safety. DRPs are often insufficiently captured by clinical routine documentation, and thus, they frequently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bceb6cb65543628690480713077e0702
https://pubmed.ncbi.nlm.nih.gov/36615115
https://pubmed.ncbi.nlm.nih.gov/36615115
Autor:
Lea Jung-Poppe, Hagen Fabian Nicolaus, Anna Roggenhofer, Anna Altenbuchner, Harald Dormann, Barbara Pfistermeister, Renke Maas
Publikováno v:
Journal of Clinical Medicine. 11:5185
Drug-related problems (DRP, defined as adverse drug events/reactions and medication errors) are a common threat for patient safety. With the aim to aid improved allocation of specialist resources and to improve detection and prevention of DRP, numero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::662e4353e3e32108d9e101171e02dd04
https://doi.org/10.3390/jcm11175185
https://doi.org/10.3390/jcm11175185
Autor:
Hartmut Glaeser, Fabian Müller, Harald Dormann, Andrius Patapovas, Bettina Plank-Kiegele, Barbara Pfistermeister, Anja Sonst, Renke Maas, Thomas Bürkle
Publikováno v:
Notfall + Rettungsmedizin. 19:671-678
The use of cyclooxygenase (COX) inhibitors is increasingly common. Most of them are available for self-medication, either as analgesic or for cardio- and cerebrovascular prevention. We aimed to analyze adverse drug events (ADE) related to COX inhibit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3b66ccc656a31356c0af4018ff65ce5
https://doi.org/10.1007/s10049-016-0184-3
https://doi.org/10.1007/s10049-016-0184-3
Autor:
Thomas Bürkle, Barbara Pfistermeister, Renke Maas, Bettina Plank-Kiegele, Anja Sonst, Harald Dormann, Andrius Patapovas, Florian Meier, Fabian Müller, Oliver Schöffski
Publikováno v:
Pharmacoepidemiology and Drug Safety. 24:176-186
PURPOSE: Several economic evaluations of adverse drug events (ADEs) exist, but the underlying methodology has not been standardized so far. The aim of the study was to combine prospective, intensive pharmacovigilance methods, and standardized account
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90ef0235ce2735b3c29423640b78a3ef
https://doi.org/10.1002/pds.3663
https://doi.org/10.1002/pds.3663
Autor:
Andrius Patapovas, Renke Maas, Thomas Bürkle, Anja Sonst, Barbara Pfistermeister, Nina Hartmann, Fabian Müller, Harald Dormann, Melanie Kirchner, Bettina Plank-Kiegele, Renate Vogler
Publikováno v:
European Journal of Clinical Pharmacology. 70:727-736
Adverse drug events (ADE) and medication errors (ME) are common causes of morbidity in patients presenting at emergency departments (ED). Recognition of ADE as being drug related and prevention of ME are key to enhancing pharmacotherapy safety in ED.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6375faf34a11c16f9ed00098e694a67d
https://doi.org/10.1007/s00228-014-1665-2
https://doi.org/10.1007/s00228-014-1665-2
Autor:
Renke Maas, Andrius Patapovas, Fabian Müller, Anja Sonst, Bettina Plank-Kiegele, Barbara Pfistermeister, Thomas Bürkle, Harald Dormann
Publikováno v:
British Journal of Clinical Pharmacology. 76:56-68
Aims The incidence of clinical events related to medication errors and/or adverse drug reactions reported in the literature varies by a degree that cannot solely be explained by the clinical setting, the varying scrutiny of investigators or varying d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fde033f920cdbdd34cc1e8978881c79
https://doi.org/10.1111/bcp.12189
https://doi.org/10.1111/bcp.12189
Autor:
Harald Dormann, Hans-Ulrich Prokosch, Melanie Kirchner, Barbara Pfistermeister, Bettina Plank-Kiegele, Andrius Patapovas, Renate Vogler, Brita Sedlmayr, Fabian Müller, Renke Maas, Manfred Criegee-Rieck, Anja Sonst, Thomas Bürkle
Publikováno v:
British Journal of Clinical Pharmacology. 76:14-24
Aims The aim was to improve medication safety in an emergency department (ED) by enhancing the integration and presentation of safety information for drug therapy. Methods Based on an evaluation of safety of drug therapy issues in the ED and a review
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2136eafb3d4e336012b81f5da316ec28
https://doi.org/10.1111/bcp.12190
https://doi.org/10.1111/bcp.12190
Autor:
Fabian Müller, Barbara Pfistermeister, Renke Maas, Thomas Bürkle, Harald Dormann, Anja Sonst, Bettina Plank-Kiegele, Andrius Patapovas
Publikováno v:
Methods of information in medicine. 56(4)
Summary Background: Adverse drug events (ADE) involving or not involving medication errors (ME) are common, but frequently remain undetected as such. Presently, the majority of available clinical decision support systems (CDSS) relies mostly on coded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::795ae4bb504c5b8689950748c7356e86
https://pubmed.ncbi.nlm.nih.gov/28451686
https://pubmed.ncbi.nlm.nih.gov/28451686
Autor:
Renke Maas, Brita Sedlmayr, Martin F. Fromm, Barbara Pfistermeister, Ozan Yüksel Tektas, Hans-Ulrich Prokosch, Aleksey Tarkhov, Andrius Patapovas, Johannes Kornhuber, Thomas Bürkle, Gerald Suttner
Publikováno v:
Methods of information in medicine. 55(6)
Summary Background: A well-known problem in current clinical decision support systems (CDSS) is the high number of alerts, which are often medically incorrect or irrelevant. This may lead to the so-called alert fatigue, an over -riding of alerts, inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5866611e63084149a44f2fa3f8c2183
https://pubmed.ncbi.nlm.nih.gov/27782288
https://pubmed.ncbi.nlm.nih.gov/27782288