Clinical Trials Directory

Trials / Completed

CompletedNCT00470652

Management of Acute Pain in the Emergency Department

Management of Acute Pain in the Emergency Department:Impact of a Computer-Assisted Support

Status
Completed
Phase
Study type
Observational
Enrollment
631 (actual)
Sponsor
Centre Hospitalier Universitaire Vaudois · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

Oligoanalgesia1 has been widely recognized as an issue in emergency department.The purpose of our study is to assess the impact of the implementation of a computer-assisted support program to improve pain management in our ED.

Detailed description

Inadequate pain management remains a major challenge for health care providers. Despite extensive research on the mechanisms of acute pain, identification of factors leading to poor pain management and development of evidence-based strategies, the transfer of this knowledge into effective clinical practices has been surprisingly slow. Oligoanalgesia1 has been widely recognized as an issue in emergency department (ED) patients. Acute pain is reported by 60-80% of ED inpatients but is frequently undertreated. Overall, an insufficient proportion of patients with acute pain receive any type of analgesia, and pain relief remains unsatisfactory. We showed that the implementation of guidelines improved pain management. However, rotation of the medical \& nursing staff leads to the forgetting of guidelines. The purpose of our study is to assess the impact of the implementation of a computer-assisted support program to improve pain management in our ED.

Conditions

Interventions

TypeNameDescription
DEVICEcomputer-assisted decision supportat the end of the pre-intervention period, the patient flow software was modified to open popup windows automatically when pain intensity was not documented or pain was not reevaluated within the recommended interval. The popup window also detailed appropriate pain treatment guidelines based on the documented pain intensity. In addition, the patient's icon in the flow software changed from black to red when pain intensity was \>4/10. After a 10-day test period, the post-intervention data collection started.

Timeline

Start date
2007-05-01
Completion
2008-09-01
First posted
2007-05-08
Last updated
2009-01-27

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT00470652. Inclusion in this directory is not an endorsement.