Cost-effectiveness of pharmacy-led versus conventionally delivered antiviral treatment for hepatitis C in patients receiving opioid substitution therapy: An economic evaluation alongside a pragmatic cluster randomised trial
Elimination targets for hepatitis C have been set across the world. In the UK almost 90% of infections are in people who inject drugs. Evidence shows community case-finding is effective at identifying and treating undiagnosed patients. The aim of this analysis was to assess, from a healthcare provid...
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Veröffentlicht in: | The Journal of infection 2022-12, Vol.85 (6), p.676-682 |
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description | Elimination targets for hepatitis C have been set across the world. In the UK almost 90% of infections are in people who inject drugs. Evidence shows community case-finding is effective at identifying and treating undiagnosed patients. The aim of this analysis was to assess, from a healthcare provider perspective, the cost-effectiveness of a new pharmacist-led test and treat pathway for hepatitis C in opioid agonist treatment (OAT) patients attending community pharmacies compared to conventional care.
In a cluster randomised controlled trial, pharmacies were randomised to the pharmacist-led or conventional care pathway. Mean cost per OAT patient and per patient initiating treatment was identified for each pathway. A Markov model tracking disease progression was developed, with a 50-year time horizon and 3·5% time discount rate, to estimate the incremental cost-effectiveness ratio (ICER) per quality-adjusted life-year (QALY) gained and the probability of being cost-effective at a £30,000 per QALY willingness-to-pay threshold. Probabilistic sensitivity analysis was performed for a range of drug discounts, re-infection rates, and model assumptions.
Mean cost per OAT patient (£3,674 vs £1,965) and per patient initiating treatment (£863 vs £404) was higher in the pharmacist-led pathway, due to higher uptake of testing and pharmacist time requirements. Over a 50-year time horizon the ICER per QALY gained was £31,612 at NHS indicative price for treatment (£38,979 for 12 weeks) and 12·1/100 person-years re-infection rate, reducing to £21,027/£10,220/-£501 per QALY gained with 30%/60%/90% drug price discounts and £25,373/£21,738/£14,912 per QALY gained at re-infection rates of 8/5/2 per 100 person-years. At 30%/60%/90% drug discount rates, the pharmacist-led pathway has an 80%/98%/100% probability of being cost-effective.
The pharmacist-led pathway is effective at increasing testing and treatment uptake, with cost-effectiveness being highly dependent on drug price discounts.
Trial funding provided by the Scottish Government, Gilead Sciences, and Bristol-Myers Squibb. |
doi_str_mv | 10.1016/j.jinf.2022.09.021 |
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In a cluster randomised controlled trial, pharmacies were randomised to the pharmacist-led or conventional care pathway. Mean cost per OAT patient and per patient initiating treatment was identified for each pathway. A Markov model tracking disease progression was developed, with a 50-year time horizon and 3·5% time discount rate, to estimate the incremental cost-effectiveness ratio (ICER) per quality-adjusted life-year (QALY) gained and the probability of being cost-effective at a £30,000 per QALY willingness-to-pay threshold. Probabilistic sensitivity analysis was performed for a range of drug discounts, re-infection rates, and model assumptions.
Mean cost per OAT patient (£3,674 vs £1,965) and per patient initiating treatment (£863 vs £404) was higher in the pharmacist-led pathway, due to higher uptake of testing and pharmacist time requirements. Over a 50-year time horizon the ICER per QALY gained was £31,612 at NHS indicative price for treatment (£38,979 for 12 weeks) and 12·1/100 person-years re-infection rate, reducing to £21,027/£10,220/-£501 per QALY gained with 30%/60%/90% drug price discounts and £25,373/£21,738/£14,912 per QALY gained at re-infection rates of 8/5/2 per 100 person-years. At 30%/60%/90% drug discount rates, the pharmacist-led pathway has an 80%/98%/100% probability of being cost-effective.
The pharmacist-led pathway is effective at increasing testing and treatment uptake, with cost-effectiveness being highly dependent on drug price discounts.
Trial funding provided by the Scottish Government, Gilead Sciences, and Bristol-Myers Squibb.</description><identifier>ISSN: 0163-4453</identifier><identifier>EISSN: 1532-2742</identifier><identifier>DOI: 10.1016/j.jinf.2022.09.021</identifier><identifier>PMID: 36170895</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Antiviral Agents - therapeutic use ; Cost-Benefit Analysis ; Hepacivirus ; Hepatitis C - drug therapy ; Humans ; Opiate Substitution Treatment ; Pharmacies ; Pharmacy ; Quality-Adjusted Life Years ; Reinfection</subject><ispartof>The Journal of infection, 2022-12, Vol.85 (6), p.676-682</ispartof><rights>2022</rights><rights>Copyright © 2022. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-cc74b9a041b6f4e3bb5f977f07bb80b7389009d32414587adcf2e45c9441ef203</citedby><cites>FETCH-LOGICAL-c400t-cc74b9a041b6f4e3bb5f977f07bb80b7389009d32414587adcf2e45c9441ef203</cites><orcidid>0000-0002-7811-2091 ; 0000-0002-2164-4476 ; 0000-0003-4772-2388 ; 0000-0002-0840-6254 ; 0000-0002-3141-7496 ; 0000-0002-2266-7303</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jinf.2022.09.021$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36170895$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Myring, G.</creatorcontrib><creatorcontrib>Lim, A.G.</creatorcontrib><creatorcontrib>Hollingworth, W.</creatorcontrib><creatorcontrib>McLeod, H.</creatorcontrib><creatorcontrib>Beer, L.</creatorcontrib><creatorcontrib>Vickerman, P.</creatorcontrib><creatorcontrib>Hickman, M.</creatorcontrib><creatorcontrib>Radley, A.</creatorcontrib><creatorcontrib>Dillon, J.F.</creatorcontrib><title>Cost-effectiveness of pharmacy-led versus conventionally delivered antiviral treatment for hepatitis C in patients receiving opioid substitution therapy: An economic evaluation alongside a pragmatic cluster randomised trial</title><title>The Journal of infection</title><addtitle>J Infect</addtitle><description>Elimination targets for hepatitis C have been set across the world. In the UK almost 90% of infections are in people who inject drugs. Evidence shows community case-finding is effective at identifying and treating undiagnosed patients. The aim of this analysis was to assess, from a healthcare provider perspective, the cost-effectiveness of a new pharmacist-led test and treat pathway for hepatitis C in opioid agonist treatment (OAT) patients attending community pharmacies compared to conventional care.
In a cluster randomised controlled trial, pharmacies were randomised to the pharmacist-led or conventional care pathway. Mean cost per OAT patient and per patient initiating treatment was identified for each pathway. A Markov model tracking disease progression was developed, with a 50-year time horizon and 3·5% time discount rate, to estimate the incremental cost-effectiveness ratio (ICER) per quality-adjusted life-year (QALY) gained and the probability of being cost-effective at a £30,000 per QALY willingness-to-pay threshold. Probabilistic sensitivity analysis was performed for a range of drug discounts, re-infection rates, and model assumptions.
Mean cost per OAT patient (£3,674 vs £1,965) and per patient initiating treatment (£863 vs £404) was higher in the pharmacist-led pathway, due to higher uptake of testing and pharmacist time requirements. Over a 50-year time horizon the ICER per QALY gained was £31,612 at NHS indicative price for treatment (£38,979 for 12 weeks) and 12·1/100 person-years re-infection rate, reducing to £21,027/£10,220/-£501 per QALY gained with 30%/60%/90% drug price discounts and £25,373/£21,738/£14,912 per QALY gained at re-infection rates of 8/5/2 per 100 person-years. At 30%/60%/90% drug discount rates, the pharmacist-led pathway has an 80%/98%/100% probability of being cost-effective.
The pharmacist-led pathway is effective at increasing testing and treatment uptake, with cost-effectiveness being highly dependent on drug price discounts.
Trial funding provided by the Scottish Government, Gilead Sciences, and Bristol-Myers Squibb.</description><subject>Antiviral Agents - therapeutic use</subject><subject>Cost-Benefit Analysis</subject><subject>Hepacivirus</subject><subject>Hepatitis C - drug therapy</subject><subject>Humans</subject><subject>Opiate Substitution Treatment</subject><subject>Pharmacies</subject><subject>Pharmacy</subject><subject>Quality-Adjusted Life Years</subject><subject>Reinfection</subject><issn>0163-4453</issn><issn>1532-2742</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcGO0zAQhiMEYsvCC3BAc-SSYjtOUyMuqwrYlVbiAmfLccatKycOtlOpT8urMKULR06WZ77_93j-qnrL2ZozvvlwXB_95NaCCbFmas0Ef1ateNuIWnRSPK9WBDW1lG1zU73K-cgYU43avKxumg3v2Fa1q-rXLuZSo3Noiz_hhDlDdDAfTBqNPdcBBzhhyksGGycCio-TCeEMAwYSJOobKp58MgFKQlNGgsDFBAecTfHFZ9iBn-ByoVaGhBZJMO0hzj76AfLSZwKXizeUAyYznz_C3QRIb8bRW8CTCYv50zchTvvsBwQDczL7kcoWbFhywQTJTAMpMo1VkjfhdfXCmZDxzdN5W_348vn77r5-_Pb1YXf3WFvJWKmt7WSvDJO83ziJTd-3TnWdY13fb1nfNVtFyxsaIblst50ZrBMoW6uk5OgEa26r91ffOcWfC-aiaQiLIZgJ45K16LiSginWECquqE0x54ROz8mPJp01Z_oSrD7qS7D6EqxmSlOwJHr35L_0Iw7_JH-TJODTFUD65clj0tnSui0OnvZd9BD9__x_A2ZovFs</recordid><startdate>202212</startdate><enddate>202212</enddate><creator>Myring, G.</creator><creator>Lim, A.G.</creator><creator>Hollingworth, W.</creator><creator>McLeod, H.</creator><creator>Beer, L.</creator><creator>Vickerman, P.</creator><creator>Hickman, M.</creator><creator>Radley, A.</creator><creator>Dillon, J.F.</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><orcidid>https://orcid.org/0000-0002-7811-2091</orcidid><orcidid>https://orcid.org/0000-0002-2164-4476</orcidid><orcidid>https://orcid.org/0000-0003-4772-2388</orcidid><orcidid>https://orcid.org/0000-0002-0840-6254</orcidid><orcidid>https://orcid.org/0000-0002-3141-7496</orcidid><orcidid>https://orcid.org/0000-0002-2266-7303</orcidid></search><sort><creationdate>202212</creationdate><title>Cost-effectiveness of pharmacy-led versus conventionally delivered antiviral treatment for hepatitis C in patients receiving opioid substitution therapy: An economic evaluation alongside a pragmatic cluster randomised trial</title><author>Myring, G. ; 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In the UK almost 90% of infections are in people who inject drugs. Evidence shows community case-finding is effective at identifying and treating undiagnosed patients. The aim of this analysis was to assess, from a healthcare provider perspective, the cost-effectiveness of a new pharmacist-led test and treat pathway for hepatitis C in opioid agonist treatment (OAT) patients attending community pharmacies compared to conventional care.
In a cluster randomised controlled trial, pharmacies were randomised to the pharmacist-led or conventional care pathway. Mean cost per OAT patient and per patient initiating treatment was identified for each pathway. A Markov model tracking disease progression was developed, with a 50-year time horizon and 3·5% time discount rate, to estimate the incremental cost-effectiveness ratio (ICER) per quality-adjusted life-year (QALY) gained and the probability of being cost-effective at a £30,000 per QALY willingness-to-pay threshold. Probabilistic sensitivity analysis was performed for a range of drug discounts, re-infection rates, and model assumptions.
Mean cost per OAT patient (£3,674 vs £1,965) and per patient initiating treatment (£863 vs £404) was higher in the pharmacist-led pathway, due to higher uptake of testing and pharmacist time requirements. Over a 50-year time horizon the ICER per QALY gained was £31,612 at NHS indicative price for treatment (£38,979 for 12 weeks) and 12·1/100 person-years re-infection rate, reducing to £21,027/£10,220/-£501 per QALY gained with 30%/60%/90% drug price discounts and £25,373/£21,738/£14,912 per QALY gained at re-infection rates of 8/5/2 per 100 person-years. At 30%/60%/90% drug discount rates, the pharmacist-led pathway has an 80%/98%/100% probability of being cost-effective.
The pharmacist-led pathway is effective at increasing testing and treatment uptake, with cost-effectiveness being highly dependent on drug price discounts.
Trial funding provided by the Scottish Government, Gilead Sciences, and Bristol-Myers Squibb.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>36170895</pmid><doi>10.1016/j.jinf.2022.09.021</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-7811-2091</orcidid><orcidid>https://orcid.org/0000-0002-2164-4476</orcidid><orcidid>https://orcid.org/0000-0003-4772-2388</orcidid><orcidid>https://orcid.org/0000-0002-0840-6254</orcidid><orcidid>https://orcid.org/0000-0002-3141-7496</orcidid><orcidid>https://orcid.org/0000-0002-2266-7303</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antiviral Agents - therapeutic use Cost-Benefit Analysis Hepacivirus Hepatitis C - drug therapy Humans Opiate Substitution Treatment Pharmacies Pharmacy Quality-Adjusted Life Years Reinfection |
title | Cost-effectiveness of pharmacy-led versus conventionally delivered antiviral treatment for hepatitis C in patients receiving opioid substitution therapy: An economic evaluation alongside a pragmatic cluster randomised trial |
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