Effectiveness of a Multidisciplinary Medication Review With Follow-up for Patients Treated With Coumarin Anticoagulants in Primary Care

Medication Therapy Management Clinical Trial

Official title:

Effectiveness of a Multidisciplinary Medication Review With Follow-up for Patients Treated With Coumarin Anticoagulants in Primary Care

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03154489
• Other study ID #: 914913001
• Status: Completed
• Phase: N/A
• Start date: May 22, 2017
• Est. completion date: September 22, 2019

Study information

• Verified date: May 2021
• Source: Universidad San Jorge
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The interdisciplinary collaboration between doctors, nurses and pharmacists, can facilitate the control of patients under treatment with coumarin anticoagulants, increasing their safety and effectiveness. On the other hand, the clinical utility of tools such as pharmacogenetics and the SAME-TT2R2 is unexplored. Based on the foregoing, it seems necessary to study the impact of the Program of medication review with follow-up in collaboration with doctors and nurses in primary care improves the degree of control of the patients under treatment with coumarin anticoagulants. Method: a randomized, controlled study for the main objective. Population and scope of study: Patients on treatment with coumarin anticoagulants with time in therapeutic range (TTR) according to the method of Rosendaal less than 70% in follow-up from primary care in a health area of the Arrabal Health Center (Zaragoza, Spain). Each patient will be followed by a period of 6 months. After this period, patients in the control group (CG) will receive the service of medication review with follow-up for a period of time equivalent (6 months). Intervention: Program of pharmacotherapy follow-up. Variables result: Stability of the INR, drug adherence, intake of vitamin K, knowledge of the patient on the use of acenocoumarol, associated costs, avoided costs, quality of life, satisfaction of patients and professionals involved. Statistical analysis and sample size: 204 patients. Multivariate analysis will be used and cost-effectiveness..

Recruitment information / eligibility

• Status: Completed
• Enrollment: 204
• Est. completion date: September 22, 2019
• Est. primary completion date: January 22, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Submit a TTR less than 70% in the last 6 months.

Exclusion Criteria:

• Not sign the informed consent.

• Present cognitive difficulties for the project.

Related Conditions & MeSH terms

• Anticoagulant
• Community Pharmacy Services
• Drug Utilization Review
• Medication Therapy Management
• Pharmacogenetics

Intervention

Other:
• acenocoumarol
medication review with follow-up in acenocoumarol treatment
• control
group

Locations

Country	Name	City	State
Spain	Centro de Salud Arrabal	Zaragoza

Sponsors (2)

Lead Sponsor	Collaborator
Universidad San Jorge	Roche Diagnostics

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Effectiveness of medication review with follow-up	Compare the effectiveness of medication review with follow-up in collaboration with doctors and nurses of primary care patients in treatment with anticoagulants coumarins against the usual practice used actually. Principally studying INR control of this patients during 6 months.	6 months
Secondary	Quality of life related to health	Evaluate the effect of specific pharmaceutical interventions (medication review with follow-up) aimed at patients in treatment with coumarin anticoagulants within the framework of medication review with follow-up quality of life related to health using validated questionnaires.	6 months
Secondary	Study of patients habits	Evaluate the effect of medication review with follow-up on the adherence of the patient, eating habits in relation to the consumption of vitamin K, and their knowledge about the use of acenocoumarol by using validated questionnaires.	6 months
Secondary	Pharmacogenetic analysis of genes CYP2C9 and VKORC1, ApoE CYP4F2 in each patient	Analyze the clinical utility of the incorporation of additional tools like pharmacogenetic analysis of this four genes (CYP2C9 and VKORC1, ApoE CYP4F2) for clinical decision-making in patients with unstable INR. Thanks to the bibliography is known that these gene affect the individual variability of each patient to the acenocoumarol so is going to be studying patients pharmacogenetics for this four genes.	6 months
Secondary	Satisfaction in primary care professionals	Evaluate the satisfaction of medical prescribers, nurses, patients and community pharmacists with the usefulness of medication review with follow-up realized by a pharmacist with focus groups	6 months
Secondary	Review of clinical guidelines used in primary care	Assess therapeutic appropriateness of coumarins anticoagulants in relation to clinical practice guidelines used actually.	6 months
Secondary	Economic outcomes	Evaluate the effect of specific pharmaceutical interventions (medication review with follow-up) aimed at patients in treatment with coumarin anticoagulants within the framework of medication review with follow-up. The economic outcome is going to be assess by following patients if they have admissions in hospital due to bad INR control or they need some extra visits to doctor. This cost a lot to Health System and if it can be avoided it would save costs.	6 months