Cost-effectiveness and public health benefit of secondary cardiovascular disease prevention from improved adherence using a polypill in the UK

Objective To evaluate the public health and economic benefits of adherence to a fixed-dose combination polypill for the secondary prevention of cardiovascular (CV) events in adults with a history of myocardial infarction (MI) in the UK. Design Markov-model-based cost-effectiveness analysis, informed...

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Veröffentlicht in:BMJ open 2015-01, Vol.5 (5), p.e007111-e007111
Hauptverfasser: Becerra, Virginia, Gracia, Alfredo, Desai, Kamal, Abogunrin, Seye, Brand, Sarah, Chapman, Ruth, García Alonso, Fernando, Fuster, Valentín, Sanz, Ginés
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container_end_page e007111
container_issue 5
container_start_page e007111
container_title BMJ open
container_volume 5
creator Becerra, Virginia
Gracia, Alfredo
Desai, Kamal
Abogunrin, Seye
Brand, Sarah
Chapman, Ruth
García Alonso, Fernando
Fuster, Valentín
Sanz, Ginés
description Objective To evaluate the public health and economic benefits of adherence to a fixed-dose combination polypill for the secondary prevention of cardiovascular (CV) events in adults with a history of myocardial infarction (MI) in the UK. Design Markov-model-based cost-effectiveness analysis, informed by systematic reviews, which identified efficacy, utilities and adherence data inputs. Setting General practice in the UK. Participants Patients with a mean age of 64.7 years, most of whom are men with a recent or non-recent diagnosis of MI and for whom secondary preventive medication is indicated and well tolerated. Intervention Fixed-dose combination polypill (100 mg aspirin, 20 mg atorvastatin and 2.5, 5, or 10 mg ramipril) compared with multiple monotherapy. Primary and secondary outcome measures CV events prevented per 1000 patients; cost per life-year gained; and cost per quality-adjusted life-year (QALY) gained. Results The model estimates that for each 10% increase in adherence, an additional 6.7% fatal and non-fatal CV events can be prevented. In the base case, over 10 years, the polypill would improve adherence by ∼20% and thereby prevent 47 of 323 (15%) fatal and non-fatal CV events per 1000 patients compared with multiple monotherapy, with an incremental cost-effectiveness ratio (ICER) of £8200 per QALY gained. Probabilistic sensitivity analyses for the base-case assumptions showed an 81.5% chance of the polypill being cost-effective at a willingness-to-pay threshold of £20 000 per QALY gained compared with multiple monotherapy. In scenario analyses that varied structural assumptions, ICERs ranged between cost saving and £21 430 per QALY gained. Conclusions Assuming that some 450 000 adults are at risk of MI, a 10 percentage point uptake of the polypill could prevent 3260 CV events and 590 CV deaths over a decade.The polypill appears to be a cost-effective strategy to prevent fatal and non-fatal CV events in the UK.
doi_str_mv 10.1136/bmjopen-2014-007111
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Design Markov-model-based cost-effectiveness analysis, informed by systematic reviews, which identified efficacy, utilities and adherence data inputs. Setting General practice in the UK. Participants Patients with a mean age of 64.7 years, most of whom are men with a recent or non-recent diagnosis of MI and for whom secondary preventive medication is indicated and well tolerated. Intervention Fixed-dose combination polypill (100 mg aspirin, 20 mg atorvastatin and 2.5, 5, or 10 mg ramipril) compared with multiple monotherapy. Primary and secondary outcome measures CV events prevented per 1000 patients; cost per life-year gained; and cost per quality-adjusted life-year (QALY) gained. Results The model estimates that for each 10% increase in adherence, an additional 6.7% fatal and non-fatal CV events can be prevented. In the base case, over 10 years, the polypill would improve adherence by ∼20% and thereby prevent 47 of 323 (15%) fatal and non-fatal CV events per 1000 patients compared with multiple monotherapy, with an incremental cost-effectiveness ratio (ICER) of £8200 per QALY gained. Probabilistic sensitivity analyses for the base-case assumptions showed an 81.5% chance of the polypill being cost-effective at a willingness-to-pay threshold of £20 000 per QALY gained compared with multiple monotherapy. In scenario analyses that varied structural assumptions, ICERs ranged between cost saving and £21 430 per QALY gained. Conclusions Assuming that some 450 000 adults are at risk of MI, a 10 percentage point uptake of the polypill could prevent 3260 CV events and 590 CV deaths over a decade.The polypill appears to be a cost-effective strategy to prevent fatal and non-fatal CV events in the UK.</description><identifier>ISSN: 2044-6055</identifier><identifier>EISSN: 2044-6055</identifier><identifier>DOI: 10.1136/bmjopen-2014-007111</identifier><identifier>PMID: 25991449</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Acute coronary syndromes ; Aged ; Aspirin ; Cardiovascular Agents - economics ; Cardiovascular Agents - therapeutic use ; Cardiovascular disease ; Cardiovascular diseases ; Cardiovascular Diseases - drug therapy ; Cardiovascular Diseases - economics ; Cardiovascular Diseases - prevention &amp; control ; Clinical outcomes ; Cost analysis ; Cost-Benefit Analysis ; Disease prevention ; Drug Therapy, Combination ; Health Economics ; Heart attacks ; Heart failure ; Humans ; Markov Chains ; Medication Adherence - statistics &amp; numerical data ; Models, Economic ; Mortality ; Myocardial infarction ; Polypharmacy ; Population ; Prevention ; Public health ; Public Health - economics ; Sensitivity analysis ; Statins ; Stroke ; Transient ischemic attack</subject><ispartof>BMJ open, 2015-01, Vol.5 (5), p.e007111-e007111</ispartof><rights>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</rights><rights>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.</rights><rights>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 2015 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>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 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b472t-c92afd691a11b07da3c45f7a0bc28c2fc20db66c1da1e24dc5c9a0940731a5043</citedby><cites>FETCH-LOGICAL-b472t-c92afd691a11b07da3c45f7a0bc28c2fc20db66c1da1e24dc5c9a0940731a5043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://bmjopen.bmj.com/content/5/5/e007111.full.pdf$$EPDF$$P50$$Gbmj$$Hfree_for_read</linktopdf><linktohtml>$$Uhttp://bmjopen.bmj.com/content/5/5/e007111.full$$EHTML$$P50$$Gbmj$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27526,27527,27901,27902,53766,53768,77343,77374</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25991449$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Becerra, Virginia</creatorcontrib><creatorcontrib>Gracia, Alfredo</creatorcontrib><creatorcontrib>Desai, Kamal</creatorcontrib><creatorcontrib>Abogunrin, Seye</creatorcontrib><creatorcontrib>Brand, Sarah</creatorcontrib><creatorcontrib>Chapman, Ruth</creatorcontrib><creatorcontrib>García Alonso, Fernando</creatorcontrib><creatorcontrib>Fuster, Valentín</creatorcontrib><creatorcontrib>Sanz, Ginés</creatorcontrib><title>Cost-effectiveness and public health benefit of secondary cardiovascular disease prevention from improved adherence using a polypill in the UK</title><title>BMJ open</title><addtitle>BMJ Open</addtitle><description>Objective To evaluate the public health and economic benefits of adherence to a fixed-dose combination polypill for the secondary prevention of cardiovascular (CV) events in adults with a history of myocardial infarction (MI) in the UK. Design Markov-model-based cost-effectiveness analysis, informed by systematic reviews, which identified efficacy, utilities and adherence data inputs. Setting General practice in the UK. Participants Patients with a mean age of 64.7 years, most of whom are men with a recent or non-recent diagnosis of MI and for whom secondary preventive medication is indicated and well tolerated. Intervention Fixed-dose combination polypill (100 mg aspirin, 20 mg atorvastatin and 2.5, 5, or 10 mg ramipril) compared with multiple monotherapy. Primary and secondary outcome measures CV events prevented per 1000 patients; cost per life-year gained; and cost per quality-adjusted life-year (QALY) gained. Results The model estimates that for each 10% increase in adherence, an additional 6.7% fatal and non-fatal CV events can be prevented. In the base case, over 10 years, the polypill would improve adherence by ∼20% and thereby prevent 47 of 323 (15%) fatal and non-fatal CV events per 1000 patients compared with multiple monotherapy, with an incremental cost-effectiveness ratio (ICER) of £8200 per QALY gained. Probabilistic sensitivity analyses for the base-case assumptions showed an 81.5% chance of the polypill being cost-effective at a willingness-to-pay threshold of £20 000 per QALY gained compared with multiple monotherapy. In scenario analyses that varied structural assumptions, ICERs ranged between cost saving and £21 430 per QALY gained. Conclusions Assuming that some 450 000 adults are at risk of MI, a 10 percentage point uptake of the polypill could prevent 3260 CV events and 590 CV deaths over a decade.The polypill appears to be a cost-effective strategy to prevent fatal and non-fatal CV events in the UK.</description><subject>Acute coronary syndromes</subject><subject>Aged</subject><subject>Aspirin</subject><subject>Cardiovascular Agents - economics</subject><subject>Cardiovascular Agents - therapeutic use</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - drug therapy</subject><subject>Cardiovascular Diseases - economics</subject><subject>Cardiovascular Diseases - prevention &amp; control</subject><subject>Clinical outcomes</subject><subject>Cost analysis</subject><subject>Cost-Benefit Analysis</subject><subject>Disease prevention</subject><subject>Drug Therapy, Combination</subject><subject>Health Economics</subject><subject>Heart attacks</subject><subject>Heart failure</subject><subject>Humans</subject><subject>Markov Chains</subject><subject>Medication Adherence - statistics &amp; numerical data</subject><subject>Models, Economic</subject><subject>Mortality</subject><subject>Myocardial infarction</subject><subject>Polypharmacy</subject><subject>Population</subject><subject>Prevention</subject><subject>Public health</subject><subject>Public Health - economics</subject><subject>Sensitivity analysis</subject><subject>Statins</subject><subject>Stroke</subject><subject>Transient ischemic attack</subject><issn>2044-6055</issn><issn>2044-6055</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>ACMMV</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkc1q3DAUhU1paEKSJygUQTfdOJVkyR5vCmXoHw1kk6zFtXQVa5AlV7IH8hJ55irMNKRdVZsruN853MOpqreMXjHWtB-HaRdnDDWnTNSUdoyxV9UZp0LULZXy9Yv_aXWZ846WJ2QvJX9TnXLZ90yI_qx63Ma81Ggt6sXtMWDOBIIh8zp4p8mI4JeRDGVh3UKiJRl1DAbSA9GQjIt7yHr1kIhxGSEjmRMWn8XFQGyKE3HTnOIeDQEzYsKgkazZhXsCZI7-YXbeExfIMiK5-3lRnVjwGS-P87y6-_rldvu9vr759mP7-boeRMeXWvccrGl7BowNtDPQaCFtB3TQfKO51ZyaoW01M8CQC6Ol7oH2gnYNA0lFc159OviWnBMaXQ5O4NWc3FSiqQhO_b0JblT3ca-EkLwTrBh8OBqk-GvFvKjJZY3eQ8C4ZsXaDRe8axte0Pf_oLu4plDiKdZtZNM0lMpCNQdKp5hzQvt8DKPqqXJ1rFw9Va4OlRfVu5c5njV_Ci7A1QEo6v9y_A0anruH</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Becerra, Virginia</creator><creator>Gracia, Alfredo</creator><creator>Desai, Kamal</creator><creator>Abogunrin, Seye</creator><creator>Brand, Sarah</creator><creator>Chapman, Ruth</creator><creator>García Alonso, Fernando</creator><creator>Fuster, Valentín</creator><creator>Sanz, Ginés</creator><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>Cost-effectiveness and public health benefit of secondary cardiovascular disease prevention from improved adherence using a polypill in the UK</title><author>Becerra, Virginia ; 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numerical data</topic><topic>Models, Economic</topic><topic>Mortality</topic><topic>Myocardial infarction</topic><topic>Polypharmacy</topic><topic>Population</topic><topic>Prevention</topic><topic>Public health</topic><topic>Public Health - economics</topic><topic>Sensitivity analysis</topic><topic>Statins</topic><topic>Stroke</topic><topic>Transient ischemic attack</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Becerra, Virginia</creatorcontrib><creatorcontrib>Gracia, Alfredo</creatorcontrib><creatorcontrib>Desai, Kamal</creatorcontrib><creatorcontrib>Abogunrin, Seye</creatorcontrib><creatorcontrib>Brand, Sarah</creatorcontrib><creatorcontrib>Chapman, Ruth</creatorcontrib><creatorcontrib>García Alonso, Fernando</creatorcontrib><creatorcontrib>Fuster, Valentín</creatorcontrib><creatorcontrib>Sanz, Ginés</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Design Markov-model-based cost-effectiveness analysis, informed by systematic reviews, which identified efficacy, utilities and adherence data inputs. Setting General practice in the UK. Participants Patients with a mean age of 64.7 years, most of whom are men with a recent or non-recent diagnosis of MI and for whom secondary preventive medication is indicated and well tolerated. Intervention Fixed-dose combination polypill (100 mg aspirin, 20 mg atorvastatin and 2.5, 5, or 10 mg ramipril) compared with multiple monotherapy. Primary and secondary outcome measures CV events prevented per 1000 patients; cost per life-year gained; and cost per quality-adjusted life-year (QALY) gained. Results The model estimates that for each 10% increase in adherence, an additional 6.7% fatal and non-fatal CV events can be prevented. In the base case, over 10 years, the polypill would improve adherence by ∼20% and thereby prevent 47 of 323 (15%) fatal and non-fatal CV events per 1000 patients compared with multiple monotherapy, with an incremental cost-effectiveness ratio (ICER) of £8200 per QALY gained. Probabilistic sensitivity analyses for the base-case assumptions showed an 81.5% chance of the polypill being cost-effective at a willingness-to-pay threshold of £20 000 per QALY gained compared with multiple monotherapy. In scenario analyses that varied structural assumptions, ICERs ranged between cost saving and £21 430 per QALY gained. Conclusions Assuming that some 450 000 adults are at risk of MI, a 10 percentage point uptake of the polypill could prevent 3260 CV events and 590 CV deaths over a decade.The polypill appears to be a cost-effective strategy to prevent fatal and non-fatal CV events in the UK.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>25991449</pmid><doi>10.1136/bmjopen-2014-007111</doi><oa>free_for_read</oa></addata></record>
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subjects Acute coronary syndromes
Aged
Aspirin
Cardiovascular Agents - economics
Cardiovascular Agents - therapeutic use
Cardiovascular disease
Cardiovascular diseases
Cardiovascular Diseases - drug therapy
Cardiovascular Diseases - economics
Cardiovascular Diseases - prevention & control
Clinical outcomes
Cost analysis
Cost-Benefit Analysis
Disease prevention
Drug Therapy, Combination
Health Economics
Heart attacks
Heart failure
Humans
Markov Chains
Medication Adherence - statistics & numerical data
Models, Economic
Mortality
Myocardial infarction
Polypharmacy
Population
Prevention
Public health
Public Health - economics
Sensitivity analysis
Statins
Stroke
Transient ischemic attack
title Cost-effectiveness and public health benefit of secondary cardiovascular disease prevention from improved adherence using a polypill in the UK
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