Hepatitis C virus treatment in people who inject drugs (PWID) in Bangladesh
Given the considerable social marginalization experienced by people who inject drugs (PWID), treatment of hepatitis C virus (HCV) in this population presents unique challenges. This study assessed the feasibility of treating HCV infection with direct-acting antiviral (DAA) medications among PWID rec...
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Veröffentlicht in: | The International journal of drug policy 2019-12, Vol.74, p.69-75 |
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container_title | The International journal of drug policy |
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creator | Rahman, Mustafizur Janjua, Naveed Zafar Shafiq, Tanveer Khan Ibne Chowdhury, Ezazul Islam Sarker, Md. Safiullah Khan, Sharful Islam Reza, Masud Faruque, Mohammad Omar Kabir, Ahmedul Anis, Aslam H. Azim, Tasnim |
description | Given the considerable social marginalization experienced by people who inject drugs (PWID), treatment of hepatitis C virus (HCV) in this population presents unique challenges. This study assessed the feasibility of treating HCV infection with direct-acting antiviral (DAA) medications among PWID receiving harm reduction services from a Drop-in-Center in Dhaka, Bangladesh.
In this prospective study conducted between December 2016 and May 2018, 200 PWID with either recent injecting drug use (i.e., within the previous two months) or a history of injecting drug use and are currently receiving opioid substitution therapy were recruited. Blood was collected to conduct relevant laboratory tests. Eligible PWID who tested positive for HCV RNA (n = 55), were provided daily daclatasvir (60 mg) and sofosbuvir (400 mg) for 12 weeks after which adherence level, sustained virologic response (SVR), and reinfection were assessed.
At baseline, 40% (n = 79) of the 200 participants recruited to the study tested positive for antibodies to HCV and 34% (n = 68) had detectable HCV RNA in their blood. Of 55 eligible PWID who initiated treatment, 93% (n = 51) completed treatment while 87% (n = 48) were available for follow-up SVR assessment, all of whom achieved SVR. Thus, intent-to-treat SVR was 87% and the modified intent-to-treat SVR was 100% with one reinfection (4•2 cases per 100 person–years). Further, 75% (i.e., 41 out of the 55 participants) were at least 90% adherent to therapy.
Our findings strongly suggest that HCV treatment using sofosbuvir+daclatasvir for PWID enrolled in existing harm reduction programs in Bangladesh is feasible but may require additional interventions such as Opioid Substitution Therapy, intense follow up by outreach workers, and services and counselling provided by full time clinicians. |
doi_str_mv | 10.1016/j.drugpo.2019.09.002 |
format | Article |
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In this prospective study conducted between December 2016 and May 2018, 200 PWID with either recent injecting drug use (i.e., within the previous two months) or a history of injecting drug use and are currently receiving opioid substitution therapy were recruited. Blood was collected to conduct relevant laboratory tests. Eligible PWID who tested positive for HCV RNA (n = 55), were provided daily daclatasvir (60 mg) and sofosbuvir (400 mg) for 12 weeks after which adherence level, sustained virologic response (SVR), and reinfection were assessed.
At baseline, 40% (n = 79) of the 200 participants recruited to the study tested positive for antibodies to HCV and 34% (n = 68) had detectable HCV RNA in their blood. Of 55 eligible PWID who initiated treatment, 93% (n = 51) completed treatment while 87% (n = 48) were available for follow-up SVR assessment, all of whom achieved SVR. Thus, intent-to-treat SVR was 87% and the modified intent-to-treat SVR was 100% with one reinfection (4•2 cases per 100 person–years). Further, 75% (i.e., 41 out of the 55 participants) were at least 90% adherent to therapy.
Our findings strongly suggest that HCV treatment using sofosbuvir+daclatasvir for PWID enrolled in existing harm reduction programs in Bangladesh is feasible but may require additional interventions such as Opioid Substitution Therapy, intense follow up by outreach workers, and services and counselling provided by full time clinicians.</description><identifier>ISSN: 0955-3959</identifier><identifier>EISSN: 1873-4758</identifier><identifier>DOI: 10.1016/j.drugpo.2019.09.002</identifier><identifier>PMID: 31542689</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adherence ; Antibodies ; Antiviral drugs ; Blood ; Counseling services ; Direct acting antivirals ; Drop-in centers ; Drug abuse ; Drug policy ; Drug use ; Drugs ; Feasibility ; Harm reduction ; Hepatitis ; Hepatitis C ; Intensive care ; Intensive treatment ; Interferon ; Marginality ; Medical treatment ; Narcotics ; Opioids ; People who inject drugs ; Reinfection ; SVR</subject><ispartof>The International journal of drug policy, 2019-12, Vol.74, p.69-75</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Dec 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-bac75f1a1319b10bff07eb1145562bb19fcbc6b5063a3b25dc348e59b2ff74a23</citedby><cites>FETCH-LOGICAL-c390t-bac75f1a1319b10bff07eb1145562bb19fcbc6b5063a3b25dc348e59b2ff74a23</cites><orcidid>0000-0003-0323-8885 ; 0000-0002-6876-0191 ; 0000-0001-5681-719X ; 0000-0002-7319-1333</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0955395919302452$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27843,27901,27902,30976,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31542689$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rahman, Mustafizur</creatorcontrib><creatorcontrib>Janjua, Naveed Zafar</creatorcontrib><creatorcontrib>Shafiq, Tanveer Khan Ibne</creatorcontrib><creatorcontrib>Chowdhury, Ezazul Islam</creatorcontrib><creatorcontrib>Sarker, Md. Safiullah</creatorcontrib><creatorcontrib>Khan, Sharful Islam</creatorcontrib><creatorcontrib>Reza, Masud</creatorcontrib><creatorcontrib>Faruque, Mohammad Omar</creatorcontrib><creatorcontrib>Kabir, Ahmedul</creatorcontrib><creatorcontrib>Anis, Aslam H.</creatorcontrib><creatorcontrib>Azim, Tasnim</creatorcontrib><title>Hepatitis C virus treatment in people who inject drugs (PWID) in Bangladesh</title><title>The International journal of drug policy</title><addtitle>Int J Drug Policy</addtitle><description>Given the considerable social marginalization experienced by people who inject drugs (PWID), treatment of hepatitis C virus (HCV) in this population presents unique challenges. This study assessed the feasibility of treating HCV infection with direct-acting antiviral (DAA) medications among PWID receiving harm reduction services from a Drop-in-Center in Dhaka, Bangladesh.
In this prospective study conducted between December 2016 and May 2018, 200 PWID with either recent injecting drug use (i.e., within the previous two months) or a history of injecting drug use and are currently receiving opioid substitution therapy were recruited. Blood was collected to conduct relevant laboratory tests. Eligible PWID who tested positive for HCV RNA (n = 55), were provided daily daclatasvir (60 mg) and sofosbuvir (400 mg) for 12 weeks after which adherence level, sustained virologic response (SVR), and reinfection were assessed.
At baseline, 40% (n = 79) of the 200 participants recruited to the study tested positive for antibodies to HCV and 34% (n = 68) had detectable HCV RNA in their blood. Of 55 eligible PWID who initiated treatment, 93% (n = 51) completed treatment while 87% (n = 48) were available for follow-up SVR assessment, all of whom achieved SVR. Thus, intent-to-treat SVR was 87% and the modified intent-to-treat SVR was 100% with one reinfection (4•2 cases per 100 person–years). Further, 75% (i.e., 41 out of the 55 participants) were at least 90% adherent to therapy.
Our findings strongly suggest that HCV treatment using sofosbuvir+daclatasvir for PWID enrolled in existing harm reduction programs in Bangladesh is feasible but may require additional interventions such as Opioid Substitution Therapy, intense follow up by outreach workers, and services and counselling provided by full time clinicians.</description><subject>Adherence</subject><subject>Antibodies</subject><subject>Antiviral drugs</subject><subject>Blood</subject><subject>Counseling services</subject><subject>Direct acting antivirals</subject><subject>Drop-in centers</subject><subject>Drug abuse</subject><subject>Drug policy</subject><subject>Drug use</subject><subject>Drugs</subject><subject>Feasibility</subject><subject>Harm reduction</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Intensive care</subject><subject>Intensive treatment</subject><subject>Interferon</subject><subject>Marginality</subject><subject>Medical treatment</subject><subject>Narcotics</subject><subject>Opioids</subject><subject>People who inject drugs</subject><subject>Reinfection</subject><subject>SVR</subject><issn>0955-3959</issn><issn>1873-4758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><sourceid>7TQ</sourceid><recordid>eNp9kM9r1UAQxxdR7Gv1PxAJeKmHPGf2R5K9CPqstljQg-Jx2d1M2g15SbqbVPrfm_BqDz0UBoaBz8x8-TD2BmGLgMWHdlvH-WocthxQb2Ep4M_YBqtS5LJU1XO2Aa1ULrTSR-w4pRYAJEp8yY4EKsmLSm_Y93Ma7RSmkLJddhvinLIpkp321E9Z6LORhrGj7O_1sEwt-Slbv6bs9Oefiy_vV-Kz7a86W1O6fsVeNLZL9Pq-n7DfX89-7c7zyx_fLnafLnMvNEy5s75UDVoUqB2CaxooySFKpQruHOrGO184BYWwwnFVeyErUtrxpiml5eKEnR7ujnG4mSlNZh-Sp66zPQ1zMpzrAkVRgV7Qd4_Qdphjv6QzXAjJoSrESskD5eOQUqTGjDHsbbwzCGaVbVpzkG1W2QaWgjXH2_vjs9tT_bD03-4CfDwAtNi4DRRN8oF6T3WIi0pTD-HpD_8Az1WQmw</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Rahman, Mustafizur</creator><creator>Janjua, Naveed Zafar</creator><creator>Shafiq, Tanveer Khan Ibne</creator><creator>Chowdhury, Ezazul Islam</creator><creator>Sarker, Md. 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Safiullah</creatorcontrib><creatorcontrib>Khan, Sharful Islam</creatorcontrib><creatorcontrib>Reza, Masud</creatorcontrib><creatorcontrib>Faruque, Mohammad Omar</creatorcontrib><creatorcontrib>Kabir, Ahmedul</creatorcontrib><creatorcontrib>Anis, Aslam H.</creatorcontrib><creatorcontrib>Azim, Tasnim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>PAIS Index</collection><collection>International Bibliography of the Social Sciences (IBSS)</collection><collection>PAIS International</collection><collection>PAIS International (Ovid)</collection><collection>International Bibliography of the Social Sciences</collection><collection>International Bibliography of the Social Sciences</collection><collection>MEDLINE - Academic</collection><jtitle>The International journal of drug policy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rahman, Mustafizur</au><au>Janjua, Naveed Zafar</au><au>Shafiq, Tanveer Khan Ibne</au><au>Chowdhury, Ezazul Islam</au><au>Sarker, Md. Safiullah</au><au>Khan, Sharful Islam</au><au>Reza, Masud</au><au>Faruque, Mohammad Omar</au><au>Kabir, Ahmedul</au><au>Anis, Aslam H.</au><au>Azim, Tasnim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis C virus treatment in people who inject drugs (PWID) in Bangladesh</atitle><jtitle>The International journal of drug policy</jtitle><addtitle>Int J Drug Policy</addtitle><date>2019-12</date><risdate>2019</risdate><volume>74</volume><spage>69</spage><epage>75</epage><pages>69-75</pages><issn>0955-3959</issn><eissn>1873-4758</eissn><abstract>Given the considerable social marginalization experienced by people who inject drugs (PWID), treatment of hepatitis C virus (HCV) in this population presents unique challenges. This study assessed the feasibility of treating HCV infection with direct-acting antiviral (DAA) medications among PWID receiving harm reduction services from a Drop-in-Center in Dhaka, Bangladesh.
In this prospective study conducted between December 2016 and May 2018, 200 PWID with either recent injecting drug use (i.e., within the previous two months) or a history of injecting drug use and are currently receiving opioid substitution therapy were recruited. Blood was collected to conduct relevant laboratory tests. Eligible PWID who tested positive for HCV RNA (n = 55), were provided daily daclatasvir (60 mg) and sofosbuvir (400 mg) for 12 weeks after which adherence level, sustained virologic response (SVR), and reinfection were assessed.
At baseline, 40% (n = 79) of the 200 participants recruited to the study tested positive for antibodies to HCV and 34% (n = 68) had detectable HCV RNA in their blood. Of 55 eligible PWID who initiated treatment, 93% (n = 51) completed treatment while 87% (n = 48) were available for follow-up SVR assessment, all of whom achieved SVR. Thus, intent-to-treat SVR was 87% and the modified intent-to-treat SVR was 100% with one reinfection (4•2 cases per 100 person–years). Further, 75% (i.e., 41 out of the 55 participants) were at least 90% adherent to therapy.
Our findings strongly suggest that HCV treatment using sofosbuvir+daclatasvir for PWID enrolled in existing harm reduction programs in Bangladesh is feasible but may require additional interventions such as Opioid Substitution Therapy, intense follow up by outreach workers, and services and counselling provided by full time clinicians.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31542689</pmid><doi>10.1016/j.drugpo.2019.09.002</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-0323-8885</orcidid><orcidid>https://orcid.org/0000-0002-6876-0191</orcidid><orcidid>https://orcid.org/0000-0001-5681-719X</orcidid><orcidid>https://orcid.org/0000-0002-7319-1333</orcidid></addata></record> |
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source | Applied Social Sciences Index & Abstracts (ASSIA); Elsevier ScienceDirect Journals Complete; PAIS Index |
subjects | Adherence Antibodies Antiviral drugs Blood Counseling services Direct acting antivirals Drop-in centers Drug abuse Drug policy Drug use Drugs Feasibility Harm reduction Hepatitis Hepatitis C Intensive care Intensive treatment Interferon Marginality Medical treatment Narcotics Opioids People who inject drugs Reinfection SVR |
title | Hepatitis C virus treatment in people who inject drugs (PWID) in Bangladesh |
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