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Surveillance of medication use: early identification of poor adherence
BACKGROUND: We sought to measure population-level adherence to antihyperlipidemics, antihypertensives, and oral hypoglycemics, and to develop a model for early identification of subjects at high risk of long-term poor adherence. METHODS: Prescription-filling data for 2 million subjects derived from...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384104/ https://www.ncbi.nlm.nih.gov/pubmed/22101969 http://dx.doi.org/10.1136/amiajnl-2011-000416 |
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author | Jonikas, Magdalena A Mandl, Kenneth D |
author_facet | Jonikas, Magdalena A Mandl, Kenneth D |
author_sort | Jonikas, Magdalena A |
collection | PubMed |
description | BACKGROUND: We sought to measure population-level adherence to antihyperlipidemics, antihypertensives, and oral hypoglycemics, and to develop a model for early identification of subjects at high risk of long-term poor adherence. METHODS: Prescription-filling data for 2 million subjects derived from a payor's insurance claims were used to evaluate adherence to three chronic drugs over 1 year. We relied on patterns of prescription fills, including the length of gaps in medication possession, to measure adherence among subjects and to build models for predicting poor long-term adherence. RESULTS: All prescription fills for a specific drug were sequenced chronologically into drug eras. 61.3% to 66.5% of the prescription patterns contained medication gaps >30 days during the first year of drug use. These interrupted drug eras include long-term discontinuations, where the subject never again filled a prescription for any drug in that category in the dataset, which represent 23.7% to 29.1% of all drug eras. Among the prescription-filling patterns without large medication gaps, 0.8% to 1.3% exhibited long-term poor adherence. Our models identified these subjects as early as 60 days after the first prescription fill, with an area under the curve (AUC) of 0.81. Model performance improved as the predictions were made at later time-points, with AUC values increasing to 0.93 at the 120-day time-point. CONCLUSIONS: Dispensed medication histories (widely available in real time) are useful for alerting providers about poorly adherent patients and those who will be non-adherent several months later. Efforts to use these data in point of care and decision support facilitating patient are warranted. |
format | Online Article Text |
id | pubmed-3384104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BMJ Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33841042012-06-29 Surveillance of medication use: early identification of poor adherence Jonikas, Magdalena A Mandl, Kenneth D J Am Med Inform Assoc Research and Applications BACKGROUND: We sought to measure population-level adherence to antihyperlipidemics, antihypertensives, and oral hypoglycemics, and to develop a model for early identification of subjects at high risk of long-term poor adherence. METHODS: Prescription-filling data for 2 million subjects derived from a payor's insurance claims were used to evaluate adherence to three chronic drugs over 1 year. We relied on patterns of prescription fills, including the length of gaps in medication possession, to measure adherence among subjects and to build models for predicting poor long-term adherence. RESULTS: All prescription fills for a specific drug were sequenced chronologically into drug eras. 61.3% to 66.5% of the prescription patterns contained medication gaps >30 days during the first year of drug use. These interrupted drug eras include long-term discontinuations, where the subject never again filled a prescription for any drug in that category in the dataset, which represent 23.7% to 29.1% of all drug eras. Among the prescription-filling patterns without large medication gaps, 0.8% to 1.3% exhibited long-term poor adherence. Our models identified these subjects as early as 60 days after the first prescription fill, with an area under the curve (AUC) of 0.81. Model performance improved as the predictions were made at later time-points, with AUC values increasing to 0.93 at the 120-day time-point. CONCLUSIONS: Dispensed medication histories (widely available in real time) are useful for alerting providers about poorly adherent patients and those who will be non-adherent several months later. Efforts to use these data in point of care and decision support facilitating patient are warranted. BMJ Group 2011-11-19 2012 /pmc/articles/PMC3384104/ /pubmed/22101969 http://dx.doi.org/10.1136/amiajnl-2011-000416 Text en © 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Research and Applications Jonikas, Magdalena A Mandl, Kenneth D Surveillance of medication use: early identification of poor adherence |
title | Surveillance of medication use: early identification of poor adherence |
title_full | Surveillance of medication use: early identification of poor adherence |
title_fullStr | Surveillance of medication use: early identification of poor adherence |
title_full_unstemmed | Surveillance of medication use: early identification of poor adherence |
title_short | Surveillance of medication use: early identification of poor adherence |
title_sort | surveillance of medication use: early identification of poor adherence |
topic | Research and Applications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384104/ https://www.ncbi.nlm.nih.gov/pubmed/22101969 http://dx.doi.org/10.1136/amiajnl-2011-000416 |
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