wow-inequalities/02-data/intermediate/wos_sample/88e330b9b65e602d6d0f77ea4f48aabd-van-stiphout-f.-and/info.yaml

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YAML

abstract: 'Background: Using information technology for medication management is an
opportunity to help physicians to improve the quality of their
documentation and communication and ultimately to improve patient care
and patient safety. Physician education is necessary to take full
advantage of information technology systems. In this trial, we seek to
determine the effectiveness of an intensive educational intervention
compared with the standard approach in improving information
technology-mediated medication management and in reducing potential
adverse drug events in the outpatient clinic.
Methods/Design: We are conducting a multicenter, cluster randomized
controlled trial. The participants are specialists and residents working
in the outpatient clinic of internal medicine, cardiology, pulmonology,
geriatrics, gastroenterology and rheumatology. The intensive educational
intervention is composed of a small-group session and e-learning. The
primary outcome is discrepancies between registered medication (by
physicians) and actually used medication (by patients). The key
secondary outcomes are potential adverse events caused by missed
drug-drug interactions. The primary and key secondary endpoints are
being assessed shortly after the educational intervention is completed.
Sample size will be calculated to ensure sufficient power. A sample size
of 40 physicians per group and 20 patients per physician will ensure a
power of >90 \%, which means we will need a total of 80 physicians and
1,600 patients.
Discussion: We performed an exploratory trial wherein we tested the
recruitment process, e-learning, time schedule, and methods for data
collection, data management and data analysis. Accordingly, we refined
the processes and content: the recruitment strategy was intensified,
extra measures were taken to facilitate smooth conductance of the
e-learning and parts were made optional. First versions of the
procedures for data collection were determined. Data entry and analysis
was further standardized by using the G-standard database in the
telephone questionnaire.'
affiliation: 'van Stiphout, F (Corresponding Author), Univ Med Ctr Utrecht, Dept Internal
Med, Hijmans van den Berghgebouw Kamer 4-21, NL-3508 GA Utrecht, Netherlands.
van Stiphout, F.; ter Braak, E. W. M. T., Univ Med Ctr Utrecht, Dept Internal Med,
NL-3508 GA Utrecht, Netherlands.
van Stiphout, F.; ter Braak, E. W. M. T., Univ Med Ctr Utrecht, Ctr Res \& Dev Educ,
NL-3508 GA Utrecht, Netherlands.
Zwart-van Rijkom, J. E. F.; Egberts, A. C. G., Univ Med Ctr Utrecht, Dept Clin Pharm,
NL-3584 CX Utrecht, Netherlands.
Zwart-van Rijkom, J. E. F.; Egberts, A. C. G., Univ Utrecht, Fac Sci, Utrecht Inst
Pharmaceut Sci, Div Pharmacoepidemiol \& Clin Pharmacol, NL-3508 TB Utrecht, Netherlands.
Aarts, J. E. C. M., Erasmus Univ, Inst Hlth Policy \& Management, Rotterdam, Netherlands.
Aarts, J. E. C. M., SUNY Buffalo, Sch Med \& Biomed Sci, Dept Biomed Informat, Buffalo,
NY 14203 USA.
Koffijberg, H., Univ Med Ctr Utrecht, Julius Ctr, Dept Hlth Technol Assessment,
NL-3508 GA Utrecht, Netherlands.
Klarenbeek-deJonge, E.; Krulder, M., Univ Utrecht, Fac Med, NL-3584 CG Utrecht,
Netherlands.
Roes, K. C. B., Univ Med Ctr Utrecht, Dept Qual \& Patient Safety, NL-3508 GA Utrecht,
Netherlands.'
article-number: '223'
author: van Stiphout, F. and Zwart-van Rijkom, J. E. F. and Aarts, J. E. C. M. and
Koffijberg, H. and Klarenbeek-deJonge, E. and Krulder, M. and Roes, K. C. B. and
Egberts, A. C. G. and ter Braak, E. W. M. T.
author-email: f.vanstiphout@umcutrecht.nl
author_list:
- family: van Stiphout
given: F.
- family: Zwart-van Rijkom
given: J. E. F.
- family: Aarts
given: J. E. C. M.
- family: Koffijberg
given: H.
- family: Klarenbeek-deJonge
given: E.
- family: Krulder
given: M.
- family: Roes
given: K. C. B.
- family: Egberts
given: A. C. G.
- family: ter Braak
given: E. W. M. T.
da: '2023-09-28'
doi: 10.1186/s13063-015-0744-8
eissn: 1745-6215
files: []
journal: TRIALS
keywords: 'Continuing medical education; CPOE; Information technology; Meaningful
use; Medication management; Physicians'
keywords-plus: ADVERSE DRUG EVENTS
language: English
month: MAY 22
number-of-cited-references: '19'
orcid-numbers: 'Egberts, Toine/0000-0003-1758-7779
Aarts, Jos/0000-0002-9787-688X
Roes, Kit/0000-0002-6775-1963
Egberts, Toine/0000-0003-1758-7779
Koffijberg, Hendrik/0000-0002-1753-0652'
papis_id: e135fa57e714732ef7b69bb02db876b1
ref: Vanstiphout2015meducatetrial
researcherid-numbers: 'Egberts, Toine/A-6625-2012
Aarts, Jos/B-4456-2008
Roes, Kit/AAC-4093-2019
Egberts, Toine/K-4579-2019
'
times-cited: '3'
title: 'MEDUCATE trial: effectiveness of an intensive EDUCATional intervention for
IT-mediated MEDication management in the outpatient clinic - study protocol for
a cluster randomized controlled trial'
type: article
unique-id: WOS:000355304300001
usage-count-last-180-days: '0'
usage-count-since-2013: '3'
volume: '16'
web-of-science-categories: Medicine, Research \& Experimental
year: '2015'