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Clinical Trials/NCT04018781
NCT04018781
Completed
N/A

Eval CONPARMED Haute-Bretagne : Guaranteeing the Continuity of the Care Pathway for the Elderly Patient: Evaluation of a Territorial Approach of Clinical Pharmacy

Rennes University Hospital3 sites in 1 country443 target enrollmentJune 13, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Medication Reconciliation at Discharge
Sponsor
Rennes University Hospital
Enrollment
443
Locations
3
Primary Endpoint
Adverse drug event-related hospital revisits
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

In the context of the ageing of the French population, drug iatrogeny in the elderly is a major public health issue, responsible for approximately 7,500 deaths per year and 3.4% of hospitalizations among patients aged 65 and over.

The interest of the Medication Reconciliation (MR) in reducing medication errors and unintentional discrepancies in prescriptions at transition points in patients' medication care pathways no longer seems to be in doubt both in France and abroad.

On the other hand, the literature on the clinical impact of these drug errors (i. e. occurrence of an adverse drug event (ADE) or readmission rates) is currently limited in France and presents variable results abroad.

Detailed Description

The medication reconciliation implementation mobilizes human resources (pharmacists, pharmacy technician, nurses...) and constitutes an investment for healthcare institutions. However, the resulting improvement in patients' health status (and the potential reduction in ADEs) could reduce their care consumption and thus reduce costs from a healthcare system perspective. We therefore propose to assess the cost-effectiveness of this care strategy. Finally, we will study the impact of the MR deployment on existing professional organizations, both in hospital and between community healthcare professionals and hospital as well as its conditions of implementation.

Registry
clinicaltrials.gov
Start Date
June 13, 2019
End Date
February 13, 2020
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Rennes University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Adverse drug event-related hospital revisits

Time Frame: 30 days after discharge

Rate of adverse drug event-related hospital revisits within 30 days after discharge

Secondary Outcomes

  • General Practitioner consultation(30 days after discharge)
  • All-causes readmissions and/or Emergency Department visits(90 days after discharge)
  • Incremental Cost-Effectiveness Ratio (ICER) at Day 30(30 days after discharge)
  • Incremental Cost-Effectiveness Ratio (ICER) at Day 90(90 days after discharge)
  • Patient reported experience measures(7 days after discharge)
  • Number of Unintended Medication Discrepancies(At admission)
  • Impact of the implementation of the intervention on professional organizations(Before and after the implementation of the intervention in the participating wards)
  • Severity of Unintended Medication Discrepancies(At admission)

Study Sites (3)

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