Cargando…

Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk

BACKGROUND: Widespread use of statins has improved hypercholesterolemia management, yet a significant proportion of patients remain at risk for cardiovascular (CV) events. Analyses of treatment patterns reveal inadequate intensity and duration of statin therapy among patients with hypercholesterolem...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Iris, Sung, Jennifer, Sanchez, Robert J., Mallya, Usha G., Friedman, Mark, Panaccio, Mary, Koren, Andrew, Neumann, Peter, Menzin, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Managed Care Pharmacy 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397919/
https://www.ncbi.nlm.nih.gov/pubmed/27231796
http://dx.doi.org/10.18553/jmcp.2016.22.6.685
_version_ 1785083984025223168
author Lin, Iris
Sung, Jennifer
Sanchez, Robert J.
Mallya, Usha G.
Friedman, Mark
Panaccio, Mary
Koren, Andrew
Neumann, Peter
Menzin, Joseph
author_facet Lin, Iris
Sung, Jennifer
Sanchez, Robert J.
Mallya, Usha G.
Friedman, Mark
Panaccio, Mary
Koren, Andrew
Neumann, Peter
Menzin, Joseph
author_sort Lin, Iris
collection PubMed
description BACKGROUND: Widespread use of statins has improved hypercholesterolemia management, yet a significant proportion of patients remain at risk for cardiovascular (CV) events. Analyses of treatment patterns reveal inadequate intensity and duration of statin therapy among patients with hypercholesterolemia, and little is known about real-world statin use, specifically in subgroups of patients at high risk for CV events. OBJECTIVE: To examine patterns of statin use and outcomes among patients with high-risk features who newly initiated statin monotherapy. METHODS: Adult patients (aged > 18 years) at high CV risk who received > 1 prescription for statin monotherapy and who had not received lipid-modifying therapy during the previous 12 months were identified from the Truven MarketScan Commercial and Medicare Supplemental databases (from January 2007 to June 2013). Patients with atherosclerotic cardiovascular disease (ASCVD) or diabetes were hierarchically classified into 5 mutually exclusive CV risk categories (listed here in order from highest to lowest risk): (1) recent CV event (subcategorized by hospitalization for acute coronary syndrome [ACS] or other non-ACS CV event within 90 days of index); (2) coronary heart disease (CHD); (3) history of ischemic stroke; (4) peripheral artery disease (PAD); and (5) diabetes. Outcomes of interest included changes in therapy, proportion of days covered (PDC), time to discontinuation, and proportion of patients with ASCVD-related inpatient visit during the follow-up period. Statin therapy was subdivided into high-intensity treatment (atorvastatin 40 mg or 80 mg, rosuvastatin 20 mg or 40 mg, or simvastatin 80 mg) or moderate- to low-intensity treatment (all other statins and statin dosing regimens). Follow-up data were obtained from the index date (statin initiation) until the end of continuous enrollment. RESULTS: A total of 541,221 patients were included in the analysis. The majority of patients were stratified in the diabetes cohort (61.1%), followed in frequency by recent ACS event (15.8%), recent non-ACS CV event (9.9%), PAD (4.7%), CHD (4.4%), and history of ischemic stroke (4.1%). Only 15.0% of the population initiated therapy with a high-intensity statin, and 22.5% of these high-intensity statin initiators switched to a moderate- to low-intensity regimen during the follow-up period. Median time to statin discontinuation was approximately 15 months. Duration of treatment was longer among those who were treated with a high-intensity versus a moderate- to low-intensity statin regimen (21 and 15 months, respectively). The PDC was highest in the recent ACS hospitalization cohort (66.4%) and lowest in the diabetes cohort (55.5%). The PDC was significantly greater among patients who initiated treatment with a high-intensity statin regimen than with a moderate- to low-intensity statin regimen (62.1% vs. 57.5%, respectively; P< 0.001). At 1 year, Kaplan-Meier estimates of the cumulative rates for ASCVD-related hospitalizations ranged from 3.5% (diabetes) to 21.8% (recent ACS hospitalization). CONCLUSIONS: Patients at high risk for CV events are suboptimally dosed with statins, have high rates of discontinuation, and have low rates of adherence. Despite the use of statin therapy, ASCVD-related inpatient visit rates were high, particularly among those patients at highest risk because of a recent ACS hospitalization. Future interventions are required to ensure that high-risk patients are effectively managed to reduce subsequent morbidity and mortality.
format Online
Article
Text
id pubmed-10397919
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Academy of Managed Care Pharmacy
record_format MEDLINE/PubMed
spelling pubmed-103979192023-08-04 Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk Lin, Iris Sung, Jennifer Sanchez, Robert J. Mallya, Usha G. Friedman, Mark Panaccio, Mary Koren, Andrew Neumann, Peter Menzin, Joseph J Manag Care Spec Pharm Research BACKGROUND: Widespread use of statins has improved hypercholesterolemia management, yet a significant proportion of patients remain at risk for cardiovascular (CV) events. Analyses of treatment patterns reveal inadequate intensity and duration of statin therapy among patients with hypercholesterolemia, and little is known about real-world statin use, specifically in subgroups of patients at high risk for CV events. OBJECTIVE: To examine patterns of statin use and outcomes among patients with high-risk features who newly initiated statin monotherapy. METHODS: Adult patients (aged > 18 years) at high CV risk who received > 1 prescription for statin monotherapy and who had not received lipid-modifying therapy during the previous 12 months were identified from the Truven MarketScan Commercial and Medicare Supplemental databases (from January 2007 to June 2013). Patients with atherosclerotic cardiovascular disease (ASCVD) or diabetes were hierarchically classified into 5 mutually exclusive CV risk categories (listed here in order from highest to lowest risk): (1) recent CV event (subcategorized by hospitalization for acute coronary syndrome [ACS] or other non-ACS CV event within 90 days of index); (2) coronary heart disease (CHD); (3) history of ischemic stroke; (4) peripheral artery disease (PAD); and (5) diabetes. Outcomes of interest included changes in therapy, proportion of days covered (PDC), time to discontinuation, and proportion of patients with ASCVD-related inpatient visit during the follow-up period. Statin therapy was subdivided into high-intensity treatment (atorvastatin 40 mg or 80 mg, rosuvastatin 20 mg or 40 mg, or simvastatin 80 mg) or moderate- to low-intensity treatment (all other statins and statin dosing regimens). Follow-up data were obtained from the index date (statin initiation) until the end of continuous enrollment. RESULTS: A total of 541,221 patients were included in the analysis. The majority of patients were stratified in the diabetes cohort (61.1%), followed in frequency by recent ACS event (15.8%), recent non-ACS CV event (9.9%), PAD (4.7%), CHD (4.4%), and history of ischemic stroke (4.1%). Only 15.0% of the population initiated therapy with a high-intensity statin, and 22.5% of these high-intensity statin initiators switched to a moderate- to low-intensity regimen during the follow-up period. Median time to statin discontinuation was approximately 15 months. Duration of treatment was longer among those who were treated with a high-intensity versus a moderate- to low-intensity statin regimen (21 and 15 months, respectively). The PDC was highest in the recent ACS hospitalization cohort (66.4%) and lowest in the diabetes cohort (55.5%). The PDC was significantly greater among patients who initiated treatment with a high-intensity statin regimen than with a moderate- to low-intensity statin regimen (62.1% vs. 57.5%, respectively; P< 0.001). At 1 year, Kaplan-Meier estimates of the cumulative rates for ASCVD-related hospitalizations ranged from 3.5% (diabetes) to 21.8% (recent ACS hospitalization). CONCLUSIONS: Patients at high risk for CV events are suboptimally dosed with statins, have high rates of discontinuation, and have low rates of adherence. Despite the use of statin therapy, ASCVD-related inpatient visit rates were high, particularly among those patients at highest risk because of a recent ACS hospitalization. Future interventions are required to ensure that high-risk patients are effectively managed to reduce subsequent morbidity and mortality. Academy of Managed Care Pharmacy 2016-06 /pmc/articles/PMC10397919/ /pubmed/27231796 http://dx.doi.org/10.18553/jmcp.2016.22.6.685 Text en © 2016, Academy of Managed Care Pharmacy. All rights reserved. https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research
Lin, Iris
Sung, Jennifer
Sanchez, Robert J.
Mallya, Usha G.
Friedman, Mark
Panaccio, Mary
Koren, Andrew
Neumann, Peter
Menzin, Joseph
Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk
title Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk
title_full Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk
title_fullStr Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk
title_full_unstemmed Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk
title_short Patterns of Statin Use in a Real-World Population of Patients at High Cardiovascular Risk
title_sort patterns of statin use in a real-world population of patients at high cardiovascular risk
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397919/
https://www.ncbi.nlm.nih.gov/pubmed/27231796
http://dx.doi.org/10.18553/jmcp.2016.22.6.685
work_keys_str_mv AT liniris patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT sungjennifer patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT sanchezrobertj patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT mallyaushag patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT friedmanmark patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT panacciomary patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT korenandrew patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT neumannpeter patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk
AT menzinjoseph patternsofstatinuseinarealworldpopulationofpatientsathighcardiovascularrisk