Clinical Outcomes of a Collaborative, Home-Based Postdischarge Warfarin Management Service

• Published in: The Annals of pharmacotherapy Vol. 45; no. 3; pp. 325 - 334
• Main Authors: Stafford, Leanne, Peterson, Gregory M, Bereznicki, Luke RE, Jackson, Shane L, Tienen, Ella C van, Angley, Manya T, Bajorek, Beata V, McLachlan, Andrew J, Mullan, Judy R, Misan, Gary MH, Gaetani, Luigi
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA SAGE Publications 01-03-2011; Whitney
• Subjects: Anticoagulants - administration & dosage; Anticoagulants - therapeutic use; Australia; Biological and medical sciences; Cohort Studies; Female; Home Care Services - organization & administration; Humans; International Normalized Ratio; Male; Medical sciences; Patient Discharge; Patient Readmission; Pharmacology. Drug treatments; Prospective Studies; Treatment Outcome; Warfarin - administration & dosage; Warfarin - therapeutic use; Australia; Human; Warfarin; Prognosis; Toxicity; Coumarine derivatives; Anticoagulant; patient discharge; community pharmacy services; Antivitamin K; adverse drug events; Clinical management; At home; International normalized ratio; Drugstore
• ISSN: 1060-0280; 1542-6270
• DOI: 10.1345/aph.1P617

Background:
Warfarin remains a high-risk drug for adverse events, especially following discharge from the hospital. New approaches are needed to minimize the potential for adverse outcomes during this period.
Objective:
To evaluate the clinical outcomes of a collaborative, home-based postdischarge warfarin management service adapted from the Australian Home Medicines Review (HMR) program.
Methods:
In a prospective, nonrandomized controlled cohort study, patients discharged from the hospital and newly initiated on or continuing warfarin therapy received either usual care (UC) or a postdischarge service (PDS) of 2 or 3 home visits by a trained, HMR-accredited pharmacist in their first 8 to 10 days postdischarge. The PDS involved point-of-care international normalized ratio (INR) monitoring, warfarin education, and an HMR, in collaboration with the patient's general practitioner and community pharmacist. The primary outcome measure was the combined incidence of major and minor hemorrhagic events in the 90 days postdischarge. Secondary outcome measures included the incidences of thrombotic events, combined hemorrhagic and thombotic events, unplanned and warfarin-related hospital readmissions, death, INR control, and persistence with therapy al 8 and 90 days postdischarge.
Results:
The PDS (n = 129) was associated with statistically significantly decreased rates of combined major and minor hemorrhagic events to day 90 (5.3% vs 14.7%; p = 0.03) and day 8 (0.9% vs 7.2%; p = 0.01) compared with UC (n = 139). The rate of combined hemorrhagic and thrombotic events to day 90 also decreased (6.4% vs 19.0%; p = 0.008) and persistence with warfarin therapy improved (95.4% vs 83.6%; p = 0.004). No significant differences in readmission and death rates or INR control were demonstrated.
Conclusions:
This study demonstrated the ability of appropriately trained accredited pharmacists working within the Australian HMR framework to reduce adverse events and improve persistence In patients taking warfarin following hospital discharge. Widespread implementation of such a service has the potential to enhance medication safety along the continuum of care. KEY WORDS: adverse drug events, community pharmacy services, international normalized ratio, patient discharge, warfarin.