A cluster randomized trial evaluating electronic prescribing in an ambulatory care setting

<p>Abstract</p> <p>Background</p> <p>Medication errors, adverse drug events and potential adverse drug events are common and serious in terms of the harms and costs that they impose on the health system and those who use it. Errors resulting in preventable adverse drug...

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Main Authors: Quan Sherman, Dainty Katie N, Zwarenstein Merrick F, Kiss Alex, Adhikari Neill KJ
Format: Article
Language:English
Published: BMC 2007-10-01
Series:Trials
Online Access:http://www.trialsjournal.com/content/8/1/28
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spelling doaj-50d1542b9dfa414b8caa714704700ee42020-11-24T21:56:51ZengBMCTrials1745-62152007-10-01812810.1186/1745-6215-8-28A cluster randomized trial evaluating electronic prescribing in an ambulatory care settingQuan ShermanDainty Katie NZwarenstein Merrick FKiss AlexAdhikari Neill KJ<p>Abstract</p> <p>Background</p> <p>Medication errors, adverse drug events and potential adverse drug events are common and serious in terms of the harms and costs that they impose on the health system and those who use it. Errors resulting in preventable adverse drug events have been shown to occur most often at the stages of ordering and administration. This paper describes the protocol for a pragmatic trial of electronic prescribing to reduce prescription error. The trial was designed to overcome the limitations associated with traditional study design.</p> <p>Design</p> <p>This study was designed as a 65-week, cluster randomized, parallel study.</p> <p>Methods</p> <p>The trial was conducted within ambulatory outpatient clinics in an academic tertiary care centre in Ontario, Canada. The electronic prescribing software for the study is a Canadian electronic prescribing software package which provides physician prescription entry with decision support at the point of care. Using a handheld computer (PDA) the physician selects medications using an error minimising menu-based pick list from a comprehensive drug database, create specific prescription instructions and then transmit the prescription directly and electronically to a participating pharmacy via facsimile or to the physician's printer using local area wireless technology. The unit of allocation and randomization is by 'week', i.e. the system is "on" or "off" according to the randomization scheme and the unit of analysis is the prescription, with adjustment for clustering of patients within practitioners.</p> <p>Discussion</p> <p>This paper describes the protocol for a pragmatic cluster randomized trial of point-of-care electronic prescribing, which was specifically designed to overcome the limitations associated with traditional study design.</p> <p>Trial Registration</p> <p>This trial has been registered with clinicaltrials.gov (ID: NCT00252395)</p> http://www.trialsjournal.com/content/8/1/28
collection DOAJ
language English
format Article
sources DOAJ
author Quan Sherman
Dainty Katie N
Zwarenstein Merrick F
Kiss Alex
Adhikari Neill KJ
spellingShingle Quan Sherman
Dainty Katie N
Zwarenstein Merrick F
Kiss Alex
Adhikari Neill KJ
A cluster randomized trial evaluating electronic prescribing in an ambulatory care setting
Trials
author_facet Quan Sherman
Dainty Katie N
Zwarenstein Merrick F
Kiss Alex
Adhikari Neill KJ
author_sort Quan Sherman
title A cluster randomized trial evaluating electronic prescribing in an ambulatory care setting
title_short A cluster randomized trial evaluating electronic prescribing in an ambulatory care setting
title_full A cluster randomized trial evaluating electronic prescribing in an ambulatory care setting
title_fullStr A cluster randomized trial evaluating electronic prescribing in an ambulatory care setting
title_full_unstemmed A cluster randomized trial evaluating electronic prescribing in an ambulatory care setting
title_sort cluster randomized trial evaluating electronic prescribing in an ambulatory care setting
publisher BMC
series Trials
issn 1745-6215
publishDate 2007-10-01
description <p>Abstract</p> <p>Background</p> <p>Medication errors, adverse drug events and potential adverse drug events are common and serious in terms of the harms and costs that they impose on the health system and those who use it. Errors resulting in preventable adverse drug events have been shown to occur most often at the stages of ordering and administration. This paper describes the protocol for a pragmatic trial of electronic prescribing to reduce prescription error. The trial was designed to overcome the limitations associated with traditional study design.</p> <p>Design</p> <p>This study was designed as a 65-week, cluster randomized, parallel study.</p> <p>Methods</p> <p>The trial was conducted within ambulatory outpatient clinics in an academic tertiary care centre in Ontario, Canada. The electronic prescribing software for the study is a Canadian electronic prescribing software package which provides physician prescription entry with decision support at the point of care. Using a handheld computer (PDA) the physician selects medications using an error minimising menu-based pick list from a comprehensive drug database, create specific prescription instructions and then transmit the prescription directly and electronically to a participating pharmacy via facsimile or to the physician's printer using local area wireless technology. The unit of allocation and randomization is by 'week', i.e. the system is "on" or "off" according to the randomization scheme and the unit of analysis is the prescription, with adjustment for clustering of patients within practitioners.</p> <p>Discussion</p> <p>This paper describes the protocol for a pragmatic cluster randomized trial of point-of-care electronic prescribing, which was specifically designed to overcome the limitations associated with traditional study design.</p> <p>Trial Registration</p> <p>This trial has been registered with clinicaltrials.gov (ID: NCT00252395)</p>
url http://www.trialsjournal.com/content/8/1/28
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