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Impact of Medication Reconciliation Intervention on the Rate of Preventable Adverse Drug Events (ADEs) and Healthcare Utilization

Not Applicable
Completed
Conditions
Adverse Drug Events
Interventions
Other: medication reconciliation intervention
Registration Number
NCT02805270
Lead Sponsor
Sultan Qaboos University
Brief Summary

The implementation of a medication reconciliation intervention including: medication reconciliation on admission and discharge, bedside medication counselling and take-home medication list, on the development of adverse drug events within 30 days post discharge as primary outcome. Secondary outcome is the evaluation of its impact on health care resource utilization

Detailed Description

This is a randomized controlled trial in 587 patients randomized to intervention and usual care. The intervention is medication reconciliation on admission and discharge, bedside medication counselling and take-home medication list. Usual care is ward pharmacy practice. The primary outcomes are preventable and potential adverse drug events at 30 days post discharge. The secondary outcome is health care utilization: length of stay, emergency room visits, unplanned hospital visits, readmissions and travel abroad to seek medical attention.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
587
Inclusion Criteria
  • admitted to one of the two medical wards, male and female medical wards.
  • was on at least one medication prior to admission
  • spoke Arabic or English and can be (the patient or care giver) interviewed for medication history
  • stayed in the hospital for at least 24 hours
  • discharged on at least one chronic medication or is at least on one chronic medication even if not prescribed upon discharge
Exclusion Criteria
  • could not be interviewed due to language barrier, impaired cognition or other reasons and did not have a care giver
  • was under specialties other than medical specialties, but was admitted to medical wards because of lack of beds in their respective wards
  • was pregnant
  • was already included in the study at a previous admission
  • left the hospital against medical advice
  • with length of stay of >60 days.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
medication reconciliation interventionmedication reconciliation interventionmedication reconciliation intervention comprises medication reconciliation on admission and discharge, bedside medication counseling and take-home medication list
Primary Outcome Measures
NameTimeMethod
number of potential adverse drug events30 days
number of patients with a preventable adverse drug event30 days
Secondary Outcome Measures
NameTimeMethod
number of emergency room visits30 days
number of patients who traveled abroad to seek second medical opinion30 days
number of hospital readmissions30 days
number of unplanned hospital visits30 days
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