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Detection and Prevention of Adverse Drug Events: Information Technologies and Human Factors [Kõva köide]

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When someone enters hospital for examination or treatment, is given a doctor's prescription, receives medication from a pharmacist or has his drugs administered by a nurse, he assumes that his health and welfare will benefit from this medical intervention. But the effectiveness of available therapies should also be viewed from the perspective of potentially negative consequences: adverse drug events (ADE). ADEs endanger patients' safety and increase hospital costs, making reduction of preventable ADEs a crucial and challenging public health issue. This book presents papers from the workshop 'Patient Safety through Intelligent Procedures in medication' focusing on the following topics: the identification of ADE and medication errors in hospital settings; the role of human and organizational factors on ADE and medication errors; and information and communication technologies to prevent or correct ADEs and medication errors. The papers in this book are the work of active scientific experts in the field and confront ideas and experiences arising worldwide and in particular from several EU projects directed at resolving ADE problems. Here is an opportunity to find common ways for solving shared difficulties and for making improvements happen.
Preface v
Regis Beuscart
Werner Hackl
Christian Nøhr
Part A. Keynotes on Patient Safety
Measuring Patient Safety: The Need for Prospective Detection of Adverse Events
3(1)
David W. Bates
The Impact of Commercial Electronic Medication Management Systems on Errors and Clinicians' Work in Hospitals
4(2)
Johanna I. Westbrook
Patient Safety Through Intelligent Procedures in Medication: The PSIP Project
6(8)
Regis Beuscart
Peter McNair
Jytte Brender
Human Factors Engineering for Computer-Supported Identification and Prevention of Adverse Drug Events
14(11)
Marie-Catherine Beuscart-Zephir
Christian Nøhr
Decision Support to Avoid Medication Errors --- How Far Have We Come in Denmark and What Are the Present Challenges
25(7)
Annemarie Hellebek
Christianna Marinakis
ReMINE: An Ontology-Based Risk Management Platform
32(11)
Michele Carenini
The EU-ADR Project: Preliminary Results and Perspective
43(7)
Gianluca Trifiro
Annie Fourrier-Reglat
Miriam C.J.M. Sturkenboom
Carlos Diaz Acedo
Johan van der Lei
DebugIT: Building a European Distributed Clinical Data Mining Network to Foster the Fight Against Microbial Diseases
50(13)
Christian Lovis
Teodoro Douglas
Emilie Pasche
Patrick Ruch
Dirk Colaert
Karl Stroetmann
Part B. Detection and Prevention of Adverse Drug Events
Detection of Adverse Drug Events: Proposal of a Data Model
63(12)
Emmanuel Chazard
Beatrice Merlin
Gregoire Ficheur
Jean-Charles Sarfati
Regis Beuscart
Detection of Adverse Drug Events Detection: Data Agregation and Data Mining
75(10)
Emmanuel Chazard
Gregoire Ficheur
Beatrice Merlin
Michael Genin
Cristian Preda
Regis Beuscart
The Expert Explorer: A Tool for Hospital Data Visualization and Adverse Drug Event Rules Validation
85(10)
Adrian Baceanu
Ionut Atasiei
Emmanuel Chazard
Nicolas Leroy
Application of the Apriori Algorithm for Adverse Drug Reaction Detection
95(7)
M.H. Kuo
A.W. Kushniruk
E.M. Borycki
D. Greig
Adverse Drug Events Prevention Rules: Multi-Site Evaluation of Rules from Various Sources
102(10)
Emmanuel Chazard
Gregoire Ficheur
Beatrice Merlin
Elisabeth Serrot
Regis Beuscart
Automatic Indexing in a Drug Information Portal
112(11)
Saoussen Sakji
Catherine Letord
Badisse Dahamna
Ivan Kergourlay
Suzanne Pereira
Michel Joubert
Stefan Darmoni
Implementation of SNOMED CT to the Medicines Database of a General Hospital
123(8)
Francisco J. Farfan Sedano
Marta Terron Cuadrado
Eva M. Garcia Rebolledo
Yolanda Castellanos Clemente
Pablo Serrano Balazote
Angel Gomez Delgado
A Knowledge Engineering Framework Towards Clinical Support for Adverse Drug Event Prevention: The PSIP Approach
131(11)
Vassilis Koutkias
George Stalidis
Ioanna Chouvarda
Katerina Lazou
Vassilis Kilintzis
Nicos Maglaveras
Strategy for Implementation and First Results of Advanced Clinical Decision Support in Hospital Pharmacy Practice
142(7)
A.M.J.W. Scheepers-Hoeks
R.J.E. Grouls
C. Neef
H.H.M. Korsten
Inevitable Components of and Steps for ADE Management Systems: The Need for a Unified Ontological Framework (UOF) and a More Effective Collaboration in Medication Safety
149(10)
Esat N. Eryilmaz
Gul Dundar
Senem Ozgur Sari
Computerised Physician Order Entry (CPOE)
159(6)
Anne Regitze Hartmann Hamilton
Jacob Anhøj
Annemarie Hellebek
Jonas Egebart
Brian Bjørn
Beth Lilja
Part C. Human Factors and Adverse Drug Events
CPOE, Alerts and Workflow: Taking Stock of Ten Years Research at Erasmus MC
165(5)
Jos Aarts
Heleen van der Sijs
Contribution of Human Factors for the Review of Automatically Detected ADE
170(11)
Nicolas Leroy
Michel Luyckx
Philippe Lecocq
Romaric Marcilly
Marie-Catherine Beuscart-Zephir
A Framework for Diagnosing and Identifying Where Technology-Induced Errors Come from
181(7)
E.M. Borycki
A. W. Kushniruk
L. Keay
A. Kuo
Gaming Against Medical Errors: Methods and Results from a Design Game on CPOE
188(9)
Anne Marie Kanstrup
Christian Nøhr
The PSIP Approach to Account for Human Factors in Adverse Drug Events: Preliminary Field Studies
197(9)
Costanza Riccioli
Nicolas Leroy
Sylvia Pelayo
The Problem of Defensive Medicine: Two Italian Surveys
206(17)
Maurizio Catino
Simona Celotti
Subject Index 223(2)
Author Index 225