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Updated: Jun 7, 2026

Direct Drug Delivery to Kidney via the Renal Artery
Published on: April 17, 2021
Access to renal function information to improve pharmaceutical care in direct oral anticoagulant users: a cluster
Imane Badran1, Justine Clarenne1, Céline Mongaret2
1Department of Clinical Pharmacy, Université de Reims Champagne-Ardenne, GRAPP, F-51100, Reims, France.
Insights
Providing community pharmacists with patient renal function data can help optimize direct oral anticoagulant (DOAC) selection and dosage, potentially reducing bleeding risks. This study investigates the impact of this access on bleeding events in DOAC users.
Area of Science:
- Pharmacology and Pharmaceutical Sciences
- Clinical Pharmacy Practice
- Patient Safety and Risk Management
Background:
- Direct oral anticoagulants (DOACs) are crucial for thromboembolic disease management but increase bleeding risk.
- Renal impairment is a significant risk factor for bleeding in DOAC users.
- Community pharmacists often lack access to essential patient renal function data for safe DOAC dispensing.
Purpose of the Study:
- To evaluate the clinical impact of granting community pharmacists systematic access to patients' renal function information.
- To assess if this access optimizes DOAC choice and dosage, thereby reducing bleeding events.
- To determine the feasibility of integrating renal function data access into community pharmacy workflows.
Main Methods:
- A prospective, randomized, cluster, multicenter trial involving 96 community pharmacies.
- 1920 patients will be randomized into an intervention group (access to renal function) and a control group (usual care).
- The primary endpoint is the occurrence of clinically relevant bleeding (major and nonmajor) within three months post-DOAC dispensing.
Main Results:
- This section is to be filled after the study is completed.
Conclusions:
- The study will provide crucial insights into the clinical utility of providing renal function data to community pharmacists.
- Findings may inform best practices for ambulatory pharmaceutical care and enhance patient safety in DOAC therapy.
- The results have the potential to drive significant improvements in medication management and reduce preventable bleeding complications.
Background:
Direct oral anticoagulants (DOACs) are commonly prescribed for the management of thromboembolic diseases and are known to increase the risk of bleeding. Renal impairment is a risk factor for bleeding in DOACs users, making renal function access essential for community pharmacists during the prescription review and dispensing process. However, community pharmacists often have limited access to patients' renal function information. Giving Community Pharmacists full access to the renal function information could help to mitigate this preventable part of the risk of bleeding by optimizing DOACs choice and dosage, thereby helping to reduce the risk of bleeding events. This study aims to assess the impact of providing Community Pharmacists with access to patients' renal function information when dispensing DOACs on the occurrence of clinically relevant bleeding events three months after dispensing.
Methods:
A prospective, comparative, randomized, cluster, multicenter trial involving 96 community pharmacies, allocated into two groups: intervention (systematic access to renal function) and control (usual care). A total of 1920 patients will be included over a 24-month period and followed for 6 months. The primary endpoint is the occurrence of clinically relevant bleeding-major and nonmajor-occurring within three months after DOACs dispensing. Secondary endpoints include detail of pharmacist interventions and an assessment of the feasibility of providing renal function access to Community Pharmacists.
Discussion:
This study will assess the clinical impact of providing Community Pharmacists with access to renal function information. The findings have the potential to inform best practices and drive meaningful changes in ambulatory pharmaceutical care.
Trial Registration:
The trial is registered with ClinicalTrials.gov: NCT06739603, December 17th, 2024. https://clinicaltrials.gov/study/NCT06739603?term=NCT06739603&rank=1 .
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