“Routine data primarily recorded for reimbursement purposes are increasingly being used on a national level both in pharmacoepidemiological studies and in trigger tools. The aim of this study was to compare the prevalence rates of coded ADEs in hospitals on a transnational level.”
International prevalence of adverse drug events in hospitals: an analysis of routine data from England, Germany, and the USA
J Stausberg
BMC Health Services Research, 2014, 14:125
Read more here.
QIPP stands for Quality, Innovation, Productivity and Prevention. The aim of this initiative is to help health care organisations deliver higher quality care and operate more efficiently and effectively.
Showing posts with label adverse drug events. Show all posts
Showing posts with label adverse drug events. Show all posts
Tuesday, 18 March 2014
Saturday, 16 November 2013
Evaluating adverse drug event reporting in administrative data from emergency departments
"Adverse drug events to outpatient medications were underreported in emergency department administrative data compared to the number of adverse drug events diagnosed and recorded at the point-of-care."
Evaluating adverse drug event reporting in administrative data from emergency departments: a validation study
CM Hohl, L Kuramoto, E Yu, B Rogula, J Stausberg, B Sobolev
BMC Health Services Research, 2013, 13:473
Read more here.
Evaluating adverse drug event reporting in administrative data from emergency departments: a validation study
CM Hohl, L Kuramoto, E Yu, B Rogula, J Stausberg, B Sobolev
BMC Health Services Research, 2013, 13:473
Read more here.
Labels:
accident and emergency,
administrative data,
adverse drug events,
emergency department,
point-of-care,
reporting
Friday, 22 June 2012
Keeping patients safe when they transfer between care providers
"Improving the transfer of information about medicines across all care settings should help to reduce incidents of avoidable harm to patients, improving patient safety and contributing to a reduction in avoidable medicines related admissions and readmissions to hospital."
Keeping patients safe when they transfer between care providers - getting the medicines right
Royal Pharmaceutical Society
June 2012
Read more here.
Keeping patients safe when they transfer between care providers - getting the medicines right
Royal Pharmaceutical Society
June 2012
Read more here.
Labels:
adverse drug events,
discharge planning,
improvement,
integrated care,
medicines,
patient safety,
QIPP,
safety,
transfer
Monday, 3 October 2011
Review of methods used in assessing non-serious adverse drug events in observational studies among type 2 diabetes mellitus patients
"We conclude that the current assessment of adverse drug events is hampered by the choice of methods."
A review of methods used in assessing non-serious adverse drug events in observational studies among type 2 diabetes mellitus patients
L Hakobyan, FM Haaijer-Ruskamp, D de Zeeuw, D Dobre, P Denig
Health and Quality of Life Outcomes, 2011, 9:83
Read more here.
A review of methods used in assessing non-serious adverse drug events in observational studies among type 2 diabetes mellitus patients
L Hakobyan, FM Haaijer-Ruskamp, D de Zeeuw, D Dobre, P Denig
Health and Quality of Life Outcomes, 2011, 9:83
Read more here.
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