The Cost-effectiveness of Eltrombopag for the Treatment of Immune Thrombocytopenia in the United States
Eltrombopag was evaluated as a second-line treatment for adult chronic immune thrombocytopenia (ITP) in the 2006 Phase III RAISE (Eltrombopag for Management of Chronic Immune Thrombocytopenia) randomized, placebo-controlled trial. More than 80% of patients reached satisfactory platelet counts within...
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description | Eltrombopag was evaluated as a second-line treatment for adult chronic immune thrombocytopenia (ITP) in the 2006 Phase III RAISE (Eltrombopag for Management of Chronic Immune Thrombocytopenia) randomized, placebo-controlled trial. More than 80% of patients reached satisfactory platelet counts within 2 weeks. However, the economic value of eltrombopag as a second-line treatment for ITP remains to be formally assessed. This study aimed to estimate the cost-effectiveness of treating ITP with a comparable thrombopoietin receptor agonist (eltrombopag vs romiplostim).
A Markov model was implemented over a lifetime time horizon to estimate the benefits and costs of each treatment. The model featured 3 health states based on current guidelines: (1) on treatment; (2) treatment failure/discontinuation; and (3) mortality. In line with therapeutic goals in ITP, model patients could experience 3 events: no bleeding, mild/moderate bleeding, or severe bleeding. Data on eltrombopag use were obtained from an open-label extension of previous Phase II/III trials, including RAISE. Romiplostim data were obtained from Phase III trials and an extension study. Lifetime overall survival was extrapolated by using treatment-specific mortality rates derived from severe bleeding and natural mortality rates. The costs of drugs, routine care, bleeding episodes, adverse events, and mortality were represented in the model.
Eltrombopag-treated patients gained 17.58 life years and 14.68 quality-adjusted life years, whereas romiplostim-treated patients gained 17.52 life years and 14.67 quality-adjusted life years. The total lifetime cost of eltrombopag treatment was estimated at $1.58 million versus $2.13 million for romiplostim. Sensitivity analyses supported base case findings. Deterministic sensitivity analysis predicted the greatest sensitivity to the rates of severe bleeding, discontinuation, and natural mortality. Probabilistic sensitivity analysis showed that eltrombopag would be an efficient use of resources at a $50,000 threshold in 52.8% of cases. In all probabilistic iterations, the total cost of eltrombopag treatment was lower than with romiplostim, primarily because of lower drug costs.
Clinical data were applied in an economic analysis, and eltrombopag exhibited economic dominance compared with romiplostim, driven largely by the reduced costs of primary therapy. This model was limited by a lack of specific patient-level data and robust data on the duration of secondary therapy, |
doi_str_mv | 10.1016/j.clinthera.2020.02.020 |
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A Markov model was implemented over a lifetime time horizon to estimate the benefits and costs of each treatment. The model featured 3 health states based on current guidelines: (1) on treatment; (2) treatment failure/discontinuation; and (3) mortality. In line with therapeutic goals in ITP, model patients could experience 3 events: no bleeding, mild/moderate bleeding, or severe bleeding. Data on eltrombopag use were obtained from an open-label extension of previous Phase II/III trials, including RAISE. Romiplostim data were obtained from Phase III trials and an extension study. Lifetime overall survival was extrapolated by using treatment-specific mortality rates derived from severe bleeding and natural mortality rates. The costs of drugs, routine care, bleeding episodes, adverse events, and mortality were represented in the model.
Eltrombopag-treated patients gained 17.58 life years and 14.68 quality-adjusted life years, whereas romiplostim-treated patients gained 17.52 life years and 14.67 quality-adjusted life years. The total lifetime cost of eltrombopag treatment was estimated at $1.58 million versus $2.13 million for romiplostim. Sensitivity analyses supported base case findings. Deterministic sensitivity analysis predicted the greatest sensitivity to the rates of severe bleeding, discontinuation, and natural mortality. Probabilistic sensitivity analysis showed that eltrombopag would be an efficient use of resources at a $50,000 threshold in 52.8% of cases. In all probabilistic iterations, the total cost of eltrombopag treatment was lower than with romiplostim, primarily because of lower drug costs.
Clinical data were applied in an economic analysis, and eltrombopag exhibited economic dominance compared with romiplostim, driven largely by the reduced costs of primary therapy. This model was limited by a lack of specific patient-level data and robust data on the duration of secondary therapy, as well as by the fact that utilization values are likely conservative estimates for routine care use.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2020.02.020</identifier><identifier>PMID: 32199608</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adults ; Benzoates - adverse effects ; Benzoates - economics ; Benzoates - therapeutic use ; Bleeding ; Clinical trials ; Clinical Trials, Phase II as Topic ; Clinical Trials, Phase III as Topic ; Cost analysis ; Cost-Benefit Analysis ; cost-effectiveness ; Costs ; Design ; Economic analysis ; Economic justification ; Electronic health records ; eltrombopag ; Hemorrhage - chemically induced ; Humans ; Hydrazines - adverse effects ; Hydrazines - economics ; Hydrazines - therapeutic use ; Idiopathic thrombocytopenic purpura ; immune thrombocytopenia ; Immunoglobulins ; Immunosuppressive agents ; Markov chains ; Medical records ; Mortality ; Patients ; Platelet Count ; Purpura, Thrombocytopenic, Idiopathic - drug therapy ; Purpura, Thrombocytopenic, Idiopathic - economics ; Pyrazoles - adverse effects ; Pyrazoles - economics ; Pyrazoles - therapeutic use ; Quality of life ; Quality-Adjusted Life Years ; Randomized Controlled Trials as Topic ; Ratios ; Receptors, Fc - therapeutic use ; Receptors, Thrombopoietin - agonists ; Recombinant Fusion Proteins - adverse effects ; Recombinant Fusion Proteins - economics ; Recombinant Fusion Proteins - therapeutic use ; romiplostim ; Sensitivity analysis ; Thrombocytopenia ; Thrombopoietin ; Thrombopoietin - adverse effects ; Thrombopoietin - economics ; Thrombopoietin - therapeutic use ; thrombopoietin receptor agonist ; United States</subject><ispartof>Clinical therapeutics, 2020-05, Vol.42 (5), p.860-872.e8</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><rights>2020. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-a5e3650b7587398104ffca4f090df1e8f85c09795b3132030567dc4ca8a0ea613</citedby><cites>FETCH-LOGICAL-c465t-a5e3650b7587398104ffca4f090df1e8f85c09795b3132030567dc4ca8a0ea613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2425657403?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995,64385,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32199608$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tremblay, Gabriel</creatorcontrib><creatorcontrib>Dolph, Mike</creatorcontrib><creatorcontrib>Roy, Anuja Nidumolu</creatorcontrib><creatorcontrib>Said, Qayyim</creatorcontrib><creatorcontrib>Forsythe, Anna</creatorcontrib><title>The Cost-effectiveness of Eltrombopag for the Treatment of Immune Thrombocytopenia in the United States</title><title>Clinical therapeutics</title><addtitle>Clin Ther</addtitle><description>Eltrombopag was evaluated as a second-line treatment for adult chronic immune thrombocytopenia (ITP) in the 2006 Phase III RAISE (Eltrombopag for Management of Chronic Immune Thrombocytopenia) randomized, placebo-controlled trial. More than 80% of patients reached satisfactory platelet counts within 2 weeks. However, the economic value of eltrombopag as a second-line treatment for ITP remains to be formally assessed. This study aimed to estimate the cost-effectiveness of treating ITP with a comparable thrombopoietin receptor agonist (eltrombopag vs romiplostim).
A Markov model was implemented over a lifetime time horizon to estimate the benefits and costs of each treatment. The model featured 3 health states based on current guidelines: (1) on treatment; (2) treatment failure/discontinuation; and (3) mortality. In line with therapeutic goals in ITP, model patients could experience 3 events: no bleeding, mild/moderate bleeding, or severe bleeding. Data on eltrombopag use were obtained from an open-label extension of previous Phase II/III trials, including RAISE. Romiplostim data were obtained from Phase III trials and an extension study. Lifetime overall survival was extrapolated by using treatment-specific mortality rates derived from severe bleeding and natural mortality rates. The costs of drugs, routine care, bleeding episodes, adverse events, and mortality were represented in the model.
Eltrombopag-treated patients gained 17.58 life years and 14.68 quality-adjusted life years, whereas romiplostim-treated patients gained 17.52 life years and 14.67 quality-adjusted life years. The total lifetime cost of eltrombopag treatment was estimated at $1.58 million versus $2.13 million for romiplostim. Sensitivity analyses supported base case findings. Deterministic sensitivity analysis predicted the greatest sensitivity to the rates of severe bleeding, discontinuation, and natural mortality. Probabilistic sensitivity analysis showed that eltrombopag would be an efficient use of resources at a $50,000 threshold in 52.8% of cases. In all probabilistic iterations, the total cost of eltrombopag treatment was lower than with romiplostim, primarily because of lower drug costs.
Clinical data were applied in an economic analysis, and eltrombopag exhibited economic dominance compared with romiplostim, driven largely by the reduced costs of primary therapy. This model was limited by a lack of specific patient-level data and robust data on the duration of secondary therapy, as well as by the fact that utilization values are likely conservative estimates for routine care use.</description><subject>Adults</subject><subject>Benzoates - adverse effects</subject><subject>Benzoates - economics</subject><subject>Benzoates - therapeutic use</subject><subject>Bleeding</subject><subject>Clinical trials</subject><subject>Clinical Trials, Phase II as Topic</subject><subject>Clinical Trials, Phase III as Topic</subject><subject>Cost analysis</subject><subject>Cost-Benefit Analysis</subject><subject>cost-effectiveness</subject><subject>Costs</subject><subject>Design</subject><subject>Economic analysis</subject><subject>Economic justification</subject><subject>Electronic health records</subject><subject>eltrombopag</subject><subject>Hemorrhage - chemically induced</subject><subject>Humans</subject><subject>Hydrazines - adverse effects</subject><subject>Hydrazines - economics</subject><subject>Hydrazines - therapeutic use</subject><subject>Idiopathic thrombocytopenic purpura</subject><subject>immune thrombocytopenia</subject><subject>Immunoglobulins</subject><subject>Immunosuppressive agents</subject><subject>Markov chains</subject><subject>Medical records</subject><subject>Mortality</subject><subject>Patients</subject><subject>Platelet Count</subject><subject>Purpura, Thrombocytopenic, Idiopathic - drug therapy</subject><subject>Purpura, Thrombocytopenic, Idiopathic - economics</subject><subject>Pyrazoles - adverse effects</subject><subject>Pyrazoles - economics</subject><subject>Pyrazoles - therapeutic use</subject><subject>Quality of life</subject><subject>Quality-Adjusted Life Years</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Ratios</subject><subject>Receptors, Fc - therapeutic use</subject><subject>Receptors, Thrombopoietin - agonists</subject><subject>Recombinant Fusion Proteins - adverse effects</subject><subject>Recombinant Fusion Proteins - economics</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>romiplostim</subject><subject>Sensitivity analysis</subject><subject>Thrombocytopenia</subject><subject>Thrombopoietin</subject><subject>Thrombopoietin - adverse effects</subject><subject>Thrombopoietin - economics</subject><subject>Thrombopoietin - therapeutic use</subject><subject>thrombopoietin receptor agonist</subject><subject>United States</subject><issn>0149-2918</issn><issn>1879-114X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkMFqGzEQhkVoqN2kr5Au9LzuSFrtro7GpE0g0EMcyE3I2pEt45VcSQ7k7SPHia-FgYHhm_mZj5AfFGYUaPtrOzM75_MGo54xYDADVgouyJT2nawpbZ6_kCnQRtZM0n5CvqW0BQAuBftKJpxRKVvop2S93GC1CCnXaC2a7F7QY0pVsNXtLscwrsJerysbYlXSqmVEnUf0-Qjcj-PBl9nmHTOvOezRO105_84-eZdxqB6zzpiuyaXVu4TfP_oVefp9u1zc1Q9__9wv5g-1aVqRay2QtwJWneg7LnsKjbVGNxYkDJZib3thQHZSrDjlDDiIthtMY3SvAXVL-RX5ebq7j-HfAVNW23CIvkQq1jDRiq4BXqjuRJkYUopo1T66UcdXRUEdBautOgtWR8EKWCkomzcf9w-rEYfz3qfRAsxPAJYvXxxGlYxDb3BwsfhVQ3D_DXkDCdOQ1Q</recordid><startdate>202005</startdate><enddate>202005</enddate><creator>Tremblay, Gabriel</creator><creator>Dolph, Mike</creator><creator>Roy, Anuja Nidumolu</creator><creator>Said, Qayyim</creator><creator>Forsythe, Anna</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><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>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>202005</creationdate><title>The Cost-effectiveness of Eltrombopag for the Treatment of Immune Thrombocytopenia in the United States</title><author>Tremblay, Gabriel ; Dolph, Mike ; Roy, Anuja Nidumolu ; Said, Qayyim ; Forsythe, Anna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-a5e3650b7587398104ffca4f090df1e8f85c09795b3132030567dc4ca8a0ea613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adults</topic><topic>Benzoates - adverse effects</topic><topic>Benzoates - economics</topic><topic>Benzoates - therapeutic use</topic><topic>Bleeding</topic><topic>Clinical trials</topic><topic>Clinical Trials, Phase II as Topic</topic><topic>Clinical Trials, Phase III as Topic</topic><topic>Cost analysis</topic><topic>Cost-Benefit Analysis</topic><topic>cost-effectiveness</topic><topic>Costs</topic><topic>Design</topic><topic>Economic analysis</topic><topic>Economic justification</topic><topic>Electronic health records</topic><topic>eltrombopag</topic><topic>Hemorrhage - chemically induced</topic><topic>Humans</topic><topic>Hydrazines - adverse effects</topic><topic>Hydrazines - economics</topic><topic>Hydrazines - therapeutic use</topic><topic>Idiopathic thrombocytopenic purpura</topic><topic>immune thrombocytopenia</topic><topic>Immunoglobulins</topic><topic>Immunosuppressive agents</topic><topic>Markov chains</topic><topic>Medical records</topic><topic>Mortality</topic><topic>Patients</topic><topic>Platelet Count</topic><topic>Purpura, Thrombocytopenic, Idiopathic - drug therapy</topic><topic>Purpura, Thrombocytopenic, Idiopathic - economics</topic><topic>Pyrazoles - adverse effects</topic><topic>Pyrazoles - economics</topic><topic>Pyrazoles - therapeutic use</topic><topic>Quality of life</topic><topic>Quality-Adjusted Life Years</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Ratios</topic><topic>Receptors, Fc - therapeutic use</topic><topic>Receptors, Thrombopoietin - agonists</topic><topic>Recombinant Fusion Proteins - adverse effects</topic><topic>Recombinant Fusion Proteins - economics</topic><topic>Recombinant Fusion Proteins - therapeutic use</topic><topic>romiplostim</topic><topic>Sensitivity analysis</topic><topic>Thrombocytopenia</topic><topic>Thrombopoietin</topic><topic>Thrombopoietin - adverse effects</topic><topic>Thrombopoietin - economics</topic><topic>Thrombopoietin - therapeutic use</topic><topic>thrombopoietin receptor agonist</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tremblay, Gabriel</creatorcontrib><creatorcontrib>Dolph, Mike</creatorcontrib><creatorcontrib>Roy, Anuja Nidumolu</creatorcontrib><creatorcontrib>Said, Qayyim</creatorcontrib><creatorcontrib>Forsythe, Anna</creatorcontrib><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 & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Clinical therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tremblay, Gabriel</au><au>Dolph, Mike</au><au>Roy, Anuja Nidumolu</au><au>Said, Qayyim</au><au>Forsythe, Anna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Cost-effectiveness of Eltrombopag for the Treatment of Immune Thrombocytopenia in the United States</atitle><jtitle>Clinical therapeutics</jtitle><addtitle>Clin Ther</addtitle><date>2020-05</date><risdate>2020</risdate><volume>42</volume><issue>5</issue><spage>860</spage><epage>872.e8</epage><pages>860-872.e8</pages><issn>0149-2918</issn><eissn>1879-114X</eissn><abstract>Eltrombopag was evaluated as a second-line treatment for adult chronic immune thrombocytopenia (ITP) in the 2006 Phase III RAISE (Eltrombopag for Management of Chronic Immune Thrombocytopenia) randomized, placebo-controlled trial. More than 80% of patients reached satisfactory platelet counts within 2 weeks. However, the economic value of eltrombopag as a second-line treatment for ITP remains to be formally assessed. This study aimed to estimate the cost-effectiveness of treating ITP with a comparable thrombopoietin receptor agonist (eltrombopag vs romiplostim).
A Markov model was implemented over a lifetime time horizon to estimate the benefits and costs of each treatment. The model featured 3 health states based on current guidelines: (1) on treatment; (2) treatment failure/discontinuation; and (3) mortality. In line with therapeutic goals in ITP, model patients could experience 3 events: no bleeding, mild/moderate bleeding, or severe bleeding. Data on eltrombopag use were obtained from an open-label extension of previous Phase II/III trials, including RAISE. Romiplostim data were obtained from Phase III trials and an extension study. Lifetime overall survival was extrapolated by using treatment-specific mortality rates derived from severe bleeding and natural mortality rates. The costs of drugs, routine care, bleeding episodes, adverse events, and mortality were represented in the model.
Eltrombopag-treated patients gained 17.58 life years and 14.68 quality-adjusted life years, whereas romiplostim-treated patients gained 17.52 life years and 14.67 quality-adjusted life years. The total lifetime cost of eltrombopag treatment was estimated at $1.58 million versus $2.13 million for romiplostim. Sensitivity analyses supported base case findings. Deterministic sensitivity analysis predicted the greatest sensitivity to the rates of severe bleeding, discontinuation, and natural mortality. Probabilistic sensitivity analysis showed that eltrombopag would be an efficient use of resources at a $50,000 threshold in 52.8% of cases. In all probabilistic iterations, the total cost of eltrombopag treatment was lower than with romiplostim, primarily because of lower drug costs.
Clinical data were applied in an economic analysis, and eltrombopag exhibited economic dominance compared with romiplostim, driven largely by the reduced costs of primary therapy. This model was limited by a lack of specific patient-level data and robust data on the duration of secondary therapy, as well as by the fact that utilization values are likely conservative estimates for routine care use.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32199608</pmid><doi>10.1016/j.clinthera.2020.02.020</doi></addata></record> |
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subjects | Adults Benzoates - adverse effects Benzoates - economics Benzoates - therapeutic use Bleeding Clinical trials Clinical Trials, Phase II as Topic Clinical Trials, Phase III as Topic Cost analysis Cost-Benefit Analysis cost-effectiveness Costs Design Economic analysis Economic justification Electronic health records eltrombopag Hemorrhage - chemically induced Humans Hydrazines - adverse effects Hydrazines - economics Hydrazines - therapeutic use Idiopathic thrombocytopenic purpura immune thrombocytopenia Immunoglobulins Immunosuppressive agents Markov chains Medical records Mortality Patients Platelet Count Purpura, Thrombocytopenic, Idiopathic - drug therapy Purpura, Thrombocytopenic, Idiopathic - economics Pyrazoles - adverse effects Pyrazoles - economics Pyrazoles - therapeutic use Quality of life Quality-Adjusted Life Years Randomized Controlled Trials as Topic Ratios Receptors, Fc - therapeutic use Receptors, Thrombopoietin - agonists Recombinant Fusion Proteins - adverse effects Recombinant Fusion Proteins - economics Recombinant Fusion Proteins - therapeutic use romiplostim Sensitivity analysis Thrombocytopenia Thrombopoietin Thrombopoietin - adverse effects Thrombopoietin - economics Thrombopoietin - therapeutic use thrombopoietin receptor agonist United States |
title | The Cost-effectiveness of Eltrombopag for the Treatment of Immune Thrombocytopenia in the United States |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T07%3A00%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Cost-effectiveness%20of%20Eltrombopag%20for%20the%20Treatment%20of%20Immune%20Thrombocytopenia%20in%20the%20United%20States&rft.jtitle=Clinical%20therapeutics&rft.au=Tremblay,%20Gabriel&rft.date=2020-05&rft.volume=42&rft.issue=5&rft.spage=860&rft.epage=872.e8&rft.pages=860-872.e8&rft.issn=0149-2918&rft.eissn=1879-114X&rft_id=info:doi/10.1016/j.clinthera.2020.02.020&rft_dat=%3Cproquest_cross%3E2425657403%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2425657403&rft_id=info:pmid/32199608&rft_els_id=S0149291820301223&rfr_iscdi=true |