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Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study

BACKGROUND: Despite the high frequency with which adverse drug events (ADEs) occur in outpatient settings, detailed information regarding these events remains limited. Anticoagulant drugs are associated with increased safety concerns and are commonly involved in outpatient ADEs. We therefore sought...

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Autores principales: Long, Andrea L, Bendz, Lisa, Horvath, Monica M, Cozart, Heidi, Eckstrand, Julie, Whitehurst, Julie, Ferranti, Jeffrey
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843659/
https://www.ncbi.nlm.nih.gov/pubmed/20167114
http://dx.doi.org/10.1186/1477-9560-8-5
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author Long, Andrea L
Bendz, Lisa
Horvath, Monica M
Cozart, Heidi
Eckstrand, Julie
Whitehurst, Julie
Ferranti, Jeffrey
author_facet Long, Andrea L
Bendz, Lisa
Horvath, Monica M
Cozart, Heidi
Eckstrand, Julie
Whitehurst, Julie
Ferranti, Jeffrey
author_sort Long, Andrea L
collection PubMed
description BACKGROUND: Despite the high frequency with which adverse drug events (ADEs) occur in outpatient settings, detailed information regarding these events remains limited. Anticoagulant drugs are associated with increased safety concerns and are commonly involved in outpatient ADEs. We therefore sought to evaluate ambulatory anticoagulation ADEs and the patient population in which they occurred within the Duke University Health System (Durham, NC, USA). METHODS: A retrospective chart review of ambulatory warfarin-related ADEs was conducted. An automated trigger surveillance system identified eligible events in ambulatory patients admitted with an International Normalized Ratio (INR) >3 and administration of vitamin K. Event and patient characteristics were evaluated, and quality/process improvement strategies for ambulatory anticoagulation management are described. RESULTS: A total of 169 events in 167 patients were identified from December 1, 2006-June 30, 2008 and included in the study. A median supratherapeutic INR of 6.1 was noted, and roughly half of all events (52.1%) were associated with a bleed. Nearly 74% of events resulted in a need for fresh frozen plasma; 64.8% of bleeds were classified as major. A total of 59.2% of events were at least partially responsible for hospital admission. Median patient age was 68 y (range 36-95 y) with 24.9% initiating therapy within 3 months prior to the event. Of events with a prior documented patient visit (n = 157), 73.2% were seen at a Duke clinic or hospital within the previous month. Almost 80% of these patients had anticoagulation therapy addressed, but only 60.0% had a follow-up plan documented in the electronic note. CONCLUSIONS: Ambulatory warfarin-related ADEs have significant patient and healthcare utilization consequences in the form of bleeding events and associated hospital admissions. Recommendations for improvement in anticoagulation management include use of information technology to assist monitoring and follow-up documentation, avoid drug interactions, and engage patients in their care.
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spelling pubmed-28436592010-03-23 Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study Long, Andrea L Bendz, Lisa Horvath, Monica M Cozart, Heidi Eckstrand, Julie Whitehurst, Julie Ferranti, Jeffrey Thromb J Original clinical investigation BACKGROUND: Despite the high frequency with which adverse drug events (ADEs) occur in outpatient settings, detailed information regarding these events remains limited. Anticoagulant drugs are associated with increased safety concerns and are commonly involved in outpatient ADEs. We therefore sought to evaluate ambulatory anticoagulation ADEs and the patient population in which they occurred within the Duke University Health System (Durham, NC, USA). METHODS: A retrospective chart review of ambulatory warfarin-related ADEs was conducted. An automated trigger surveillance system identified eligible events in ambulatory patients admitted with an International Normalized Ratio (INR) >3 and administration of vitamin K. Event and patient characteristics were evaluated, and quality/process improvement strategies for ambulatory anticoagulation management are described. RESULTS: A total of 169 events in 167 patients were identified from December 1, 2006-June 30, 2008 and included in the study. A median supratherapeutic INR of 6.1 was noted, and roughly half of all events (52.1%) were associated with a bleed. Nearly 74% of events resulted in a need for fresh frozen plasma; 64.8% of bleeds were classified as major. A total of 59.2% of events were at least partially responsible for hospital admission. Median patient age was 68 y (range 36-95 y) with 24.9% initiating therapy within 3 months prior to the event. Of events with a prior documented patient visit (n = 157), 73.2% were seen at a Duke clinic or hospital within the previous month. Almost 80% of these patients had anticoagulation therapy addressed, but only 60.0% had a follow-up plan documented in the electronic note. CONCLUSIONS: Ambulatory warfarin-related ADEs have significant patient and healthcare utilization consequences in the form of bleeding events and associated hospital admissions. Recommendations for improvement in anticoagulation management include use of information technology to assist monitoring and follow-up documentation, avoid drug interactions, and engage patients in their care. BioMed Central 2010-02-18 /pmc/articles/PMC2843659/ /pubmed/20167114 http://dx.doi.org/10.1186/1477-9560-8-5 Text en Copyright ©2010 Long et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original clinical investigation
Long, Andrea L
Bendz, Lisa
Horvath, Monica M
Cozart, Heidi
Eckstrand, Julie
Whitehurst, Julie
Ferranti, Jeffrey
Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study
title Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study
title_full Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study
title_fullStr Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study
title_full_unstemmed Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study
title_short Characteristics of ambulatory anticoagulant adverse drug events: a descriptive study
title_sort characteristics of ambulatory anticoagulant adverse drug events: a descriptive study
topic Original clinical investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843659/
https://www.ncbi.nlm.nih.gov/pubmed/20167114
http://dx.doi.org/10.1186/1477-9560-8-5
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