Task Shifting for Initiation and Monitoring of Antiretroviral Therapy for HIV-Infected Adults in Uganda: The SHARE Trial
BACKGROUND:With countries moving towards the World Health Organization’s “Treat All” recommendation, there is need to initiate more HIV-infected persons on antiretroviral therapy (ART). In resource-limited settings, task shifting is one approach that can address clinician shortages. SETTING:Uganda M...
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Veröffentlicht in: | Journal of acquired immune deficiency syndromes (1999) 2021-03, Vol.86 (3), p.e71-e79 |
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creator | Sekiziyivu, Brian Arthur Bancroft, Elizabeth Rodriguez, Evelyn M. Sendagala, Samuel Nasirumbi, Muniina Pamela Najjengo, Marjorie Sserunga Kiragga, Agnes N. Musaazi, Joseph Musinguzi, Joshua Sande, Enos Brad, Bartholow Dalal, Shona Byakika-Jayne, Tusiime Kambugu, Andrew |
description | BACKGROUND:With countries moving towards the World Health Organization’s “Treat All” recommendation, there is need to initiate more HIV-infected persons on antiretroviral therapy (ART). In resource-limited settings, task shifting is one approach that can address clinician shortages.
SETTING:Uganda
METHODS:We conducted a randomized controlled trial to test if nurse-initiated and monitored antiretroviral therapy (NIMART) is non-inferior to clinician-initiated and monitored ART (CIMART) in HIV-infected adults in Uganda. Study participants were HIV-infected, ART-naïve, and clinically stable adults. The primary outcome was a composite endpoint of any of the followingall-cause mortality, virological failure, toxicity, and loss to follow up at 12 months post-ART initiation.
RESULTS:Over half of the study cohort (1,760) was female (54.9%). The mean age was 35.1 years (standard deviation 9.51). Five hundred and thirty-three (31.6%) participants experienced the composite endpoint. At 12 months post-ART initiation, NIMART was non-inferior to CIMART. The intention-to-treat site-adjusted risk differences for the composite endpoint were -4.1 (97.5% CI = -9.8 to 0.2) with complete case analysis (CCA) and -3.4 (97.5% CI = -9.1 to 2.5) with multiple imputation analysis (MIA). Per-protocol site-adjusted risk differences were -3.6 (97.5% CI = -10.5 to 0.6) for CCA and -3.1 (-8.8 to 2.8) for MIA. This difference was within hypothesized margins (6%) for non-inferiority.
CONCLUSIONS:Nurses were non-inferior to clinicians for initiation and monitoring of ART. Task shifting to trained nurses is a viable means to increase access to ART. Future studies should evaluate NIMART for other groups (e.g., children, adolescents, and unstable patients). |
doi_str_mv | 10.1097/QAI.0000000000002567 |
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SETTING:Uganda
METHODS:We conducted a randomized controlled trial to test if nurse-initiated and monitored antiretroviral therapy (NIMART) is non-inferior to clinician-initiated and monitored ART (CIMART) in HIV-infected adults in Uganda. Study participants were HIV-infected, ART-naïve, and clinically stable adults. The primary outcome was a composite endpoint of any of the followingall-cause mortality, virological failure, toxicity, and loss to follow up at 12 months post-ART initiation.
RESULTS:Over half of the study cohort (1,760) was female (54.9%). The mean age was 35.1 years (standard deviation 9.51). Five hundred and thirty-three (31.6%) participants experienced the composite endpoint. At 12 months post-ART initiation, NIMART was non-inferior to CIMART. The intention-to-treat site-adjusted risk differences for the composite endpoint were -4.1 (97.5% CI = -9.8 to 0.2) with complete case analysis (CCA) and -3.4 (97.5% CI = -9.1 to 2.5) with multiple imputation analysis (MIA). Per-protocol site-adjusted risk differences were -3.6 (97.5% CI = -10.5 to 0.6) for CCA and -3.1 (-8.8 to 2.8) for MIA. This difference was within hypothesized margins (6%) for non-inferiority.
CONCLUSIONS:Nurses were non-inferior to clinicians for initiation and monitoring of ART. Task shifting to trained nurses is a viable means to increase access to ART. Future studies should evaluate NIMART for other groups (e.g., children, adolescents, and unstable patients).</description><identifier>ISSN: 1525-4135</identifier><identifier>EISSN: 1944-7884</identifier><identifier>DOI: 10.1097/QAI.0000000000002567</identifier><identifier>PMID: 33230029</identifier><language>eng</language><publisher>United States: JAIDS Journal of Acquired Immune Deficiency Syndromes</publisher><subject>Implementation Science</subject><ispartof>Journal of acquired immune deficiency syndromes (1999), 2021-03, Vol.86 (3), p.e71-e79</ispartof><rights>JAIDS Journal of Acquired Immune Deficiency Syndromes</rights><rights>Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright © 2020 Written work prepared by employees of the Federal Government as part of their official duties is, under the U.S. Copyright Act, a “work of the United States Government” for which copyright protection under Title 17 of the United States Code is not available. As such, copyright does not extend to the contributions of employees of the Federal Government.</rights><rights>Written work prepared by employees of the Federal Government as part of their official duties is, under the U.S. Copyright Act, a “work of the United States Government” for which copyright protection under Title 17 of the United States Code is not available. As such, copyright does not extend to the contributions of employees of the Federal Government. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5027-c4b45d4268d3f706bcbc78c3ffe9b16ee1a1da1530c7832352115b863cc2a6cf3</citedby><cites>FETCH-LOGICAL-c5027-c4b45d4268d3f706bcbc78c3ffe9b16ee1a1da1530c7832352115b863cc2a6cf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00126334-202103010-00010$$EHTML$$P50$$Gwolterskluwer$$H</linktohtml><link.rule.ids>230,314,780,784,885,4607,27923,27924,65232</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33230029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sekiziyivu, Brian Arthur</creatorcontrib><creatorcontrib>Bancroft, Elizabeth</creatorcontrib><creatorcontrib>Rodriguez, Evelyn M.</creatorcontrib><creatorcontrib>Sendagala, Samuel</creatorcontrib><creatorcontrib>Nasirumbi, Muniina Pamela</creatorcontrib><creatorcontrib>Najjengo, Marjorie Sserunga</creatorcontrib><creatorcontrib>Kiragga, Agnes N.</creatorcontrib><creatorcontrib>Musaazi, Joseph</creatorcontrib><creatorcontrib>Musinguzi, Joshua</creatorcontrib><creatorcontrib>Sande, Enos</creatorcontrib><creatorcontrib>Brad, Bartholow</creatorcontrib><creatorcontrib>Dalal, Shona</creatorcontrib><creatorcontrib>Byakika-Jayne, Tusiime</creatorcontrib><creatorcontrib>Kambugu, Andrew</creatorcontrib><title>Task Shifting for Initiation and Monitoring of Antiretroviral Therapy for HIV-Infected Adults in Uganda: The SHARE Trial</title><title>Journal of acquired immune deficiency syndromes (1999)</title><addtitle>J Acquir Immune Defic Syndr</addtitle><description>BACKGROUND:With countries moving towards the World Health Organization’s “Treat All” recommendation, there is need to initiate more HIV-infected persons on antiretroviral therapy (ART). In resource-limited settings, task shifting is one approach that can address clinician shortages.
SETTING:Uganda
METHODS:We conducted a randomized controlled trial to test if nurse-initiated and monitored antiretroviral therapy (NIMART) is non-inferior to clinician-initiated and monitored ART (CIMART) in HIV-infected adults in Uganda. Study participants were HIV-infected, ART-naïve, and clinically stable adults. The primary outcome was a composite endpoint of any of the followingall-cause mortality, virological failure, toxicity, and loss to follow up at 12 months post-ART initiation.
RESULTS:Over half of the study cohort (1,760) was female (54.9%). The mean age was 35.1 years (standard deviation 9.51). Five hundred and thirty-three (31.6%) participants experienced the composite endpoint. At 12 months post-ART initiation, NIMART was non-inferior to CIMART. The intention-to-treat site-adjusted risk differences for the composite endpoint were -4.1 (97.5% CI = -9.8 to 0.2) with complete case analysis (CCA) and -3.4 (97.5% CI = -9.1 to 2.5) with multiple imputation analysis (MIA). Per-protocol site-adjusted risk differences were -3.6 (97.5% CI = -10.5 to 0.6) for CCA and -3.1 (-8.8 to 2.8) for MIA. This difference was within hypothesized margins (6%) for non-inferiority.
CONCLUSIONS:Nurses were non-inferior to clinicians for initiation and monitoring of ART. Task shifting to trained nurses is a viable means to increase access to ART. Future studies should evaluate NIMART for other groups (e.g., children, adolescents, and unstable patients).</description><subject>Implementation Science</subject><issn>1525-4135</issn><issn>1944-7884</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkktv1DAUhS0Eog_4Bwh5ySbFryQOC6SoKp1IRah0ytZyHHtimrEH2-nj39fDlKp0Ad74cc93fK1jAN5hdIRRU388b7sj9GSQsqpfgH3cMFbUnLOXeV2SsmCYlnvgIMafCOGKseY12KOU0Ew0--B2KeMVvBitSdatoPEBds4mK5P1Dko3wK8-733YVr2BrUs26BT8tQ1ygstRB7m5-80tuh9F54xWSQ-wHeYpRWgdvFxlF_lpK4UXi_b7CVwGK6c34JWRU9RvH-ZDcPnlZHm8KM6-nXbH7VmhSkTqQrGelQMjFR-oqVHVq17VXFFjdNPjSmss8SBxSVE-zq8qCcZlzyuqFJGVMvQQfN75buZ-rQelXcqNi02waxnuhJdW_F1xdhQrfy1qXjec8Gzw4cEg-F-zjkmsbVR6mqTTfo6CsIphxhinWcp2UhV8jEGbx2swEtvQRA5NPA8tY--ftvgI_UkpC_hOcOOnpEO8muYbHcSo5ZTG_3mzf6D5R5CKUlYQRDCiCKMig3l1D0cYtBQ</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Sekiziyivu, Brian Arthur</creator><creator>Bancroft, Elizabeth</creator><creator>Rodriguez, Evelyn M.</creator><creator>Sendagala, Samuel</creator><creator>Nasirumbi, Muniina Pamela</creator><creator>Najjengo, Marjorie Sserunga</creator><creator>Kiragga, Agnes N.</creator><creator>Musaazi, Joseph</creator><creator>Musinguzi, Joshua</creator><creator>Sande, Enos</creator><creator>Brad, Bartholow</creator><creator>Dalal, Shona</creator><creator>Byakika-Jayne, Tusiime</creator><creator>Kambugu, Andrew</creator><general>JAIDS Journal of Acquired Immune Deficiency Syndromes</general><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210301</creationdate><title>Task Shifting for Initiation and Monitoring of Antiretroviral Therapy for HIV-Infected Adults in Uganda: The SHARE Trial</title><author>Sekiziyivu, Brian Arthur ; Bancroft, Elizabeth ; Rodriguez, Evelyn M. ; Sendagala, Samuel ; Nasirumbi, Muniina Pamela ; Najjengo, Marjorie Sserunga ; Kiragga, Agnes N. ; Musaazi, Joseph ; Musinguzi, Joshua ; Sande, Enos ; Brad, Bartholow ; Dalal, Shona ; Byakika-Jayne, Tusiime ; Kambugu, Andrew</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5027-c4b45d4268d3f706bcbc78c3ffe9b16ee1a1da1530c7832352115b863cc2a6cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Implementation Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sekiziyivu, Brian Arthur</creatorcontrib><creatorcontrib>Bancroft, Elizabeth</creatorcontrib><creatorcontrib>Rodriguez, Evelyn M.</creatorcontrib><creatorcontrib>Sendagala, Samuel</creatorcontrib><creatorcontrib>Nasirumbi, Muniina Pamela</creatorcontrib><creatorcontrib>Najjengo, Marjorie Sserunga</creatorcontrib><creatorcontrib>Kiragga, Agnes N.</creatorcontrib><creatorcontrib>Musaazi, Joseph</creatorcontrib><creatorcontrib>Musinguzi, Joshua</creatorcontrib><creatorcontrib>Sande, Enos</creatorcontrib><creatorcontrib>Brad, Bartholow</creatorcontrib><creatorcontrib>Dalal, Shona</creatorcontrib><creatorcontrib>Byakika-Jayne, Tusiime</creatorcontrib><creatorcontrib>Kambugu, Andrew</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sekiziyivu, Brian Arthur</au><au>Bancroft, Elizabeth</au><au>Rodriguez, Evelyn M.</au><au>Sendagala, Samuel</au><au>Nasirumbi, Muniina Pamela</au><au>Najjengo, Marjorie Sserunga</au><au>Kiragga, Agnes N.</au><au>Musaazi, Joseph</au><au>Musinguzi, Joshua</au><au>Sande, Enos</au><au>Brad, Bartholow</au><au>Dalal, Shona</au><au>Byakika-Jayne, Tusiime</au><au>Kambugu, Andrew</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Task Shifting for Initiation and Monitoring of Antiretroviral Therapy for HIV-Infected Adults in Uganda: The SHARE Trial</atitle><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle><addtitle>J Acquir Immune Defic Syndr</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>86</volume><issue>3</issue><spage>e71</spage><epage>e79</epage><pages>e71-e79</pages><issn>1525-4135</issn><eissn>1944-7884</eissn><abstract>BACKGROUND:With countries moving towards the World Health Organization’s “Treat All” recommendation, there is need to initiate more HIV-infected persons on antiretroviral therapy (ART). In resource-limited settings, task shifting is one approach that can address clinician shortages.
SETTING:Uganda
METHODS:We conducted a randomized controlled trial to test if nurse-initiated and monitored antiretroviral therapy (NIMART) is non-inferior to clinician-initiated and monitored ART (CIMART) in HIV-infected adults in Uganda. Study participants were HIV-infected, ART-naïve, and clinically stable adults. The primary outcome was a composite endpoint of any of the followingall-cause mortality, virological failure, toxicity, and loss to follow up at 12 months post-ART initiation.
RESULTS:Over half of the study cohort (1,760) was female (54.9%). The mean age was 35.1 years (standard deviation 9.51). Five hundred and thirty-three (31.6%) participants experienced the composite endpoint. At 12 months post-ART initiation, NIMART was non-inferior to CIMART. The intention-to-treat site-adjusted risk differences for the composite endpoint were -4.1 (97.5% CI = -9.8 to 0.2) with complete case analysis (CCA) and -3.4 (97.5% CI = -9.1 to 2.5) with multiple imputation analysis (MIA). Per-protocol site-adjusted risk differences were -3.6 (97.5% CI = -10.5 to 0.6) for CCA and -3.1 (-8.8 to 2.8) for MIA. This difference was within hypothesized margins (6%) for non-inferiority.
CONCLUSIONS:Nurses were non-inferior to clinicians for initiation and monitoring of ART. Task shifting to trained nurses is a viable means to increase access to ART. Future studies should evaluate NIMART for other groups (e.g., children, adolescents, and unstable patients).</abstract><cop>United States</cop><pub>JAIDS Journal of Acquired Immune Deficiency Syndromes</pub><pmid>33230029</pmid><doi>10.1097/QAI.0000000000002567</doi><oa>free_for_read</oa></addata></record> |
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title | Task Shifting for Initiation and Monitoring of Antiretroviral Therapy for HIV-Infected Adults in Uganda: The SHARE Trial |
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