Cargando…

Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities

Point-of-care (POC) technologies in resource-limited settings can circumvent challenges of centralized laboratory testing, improving clinical management. However, higher device costs and uncertain indications for use have inhibited scaling up POC modalities. To address this gap, we investigated the...

Descripción completa

Detalles Bibliográficos
Autores principales: Ganesh, Prakash, Heller, Tom, Chione, Boniface, Gumulira, Joe, Gugsa, Salem, Khan, Shaukat, McGovern, Seth, Nhlema, Angellina, Nkhoma, Lyse, Sacks, Jilian A., Trapence, Clement, Tweya, Hannock, Ehrenkranz, Peter, Phiri, Sam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JAIDS Journal of Acquired Immune Deficiency Syndromes 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803448/
https://www.ncbi.nlm.nih.gov/pubmed/33136821
http://dx.doi.org/10.1097/QAI.0000000000002555
_version_ 1783635939543744512
author Ganesh, Prakash
Heller, Tom
Chione, Boniface
Gumulira, Joe
Gugsa, Salem
Khan, Shaukat
McGovern, Seth
Nhlema, Angellina
Nkhoma, Lyse
Sacks, Jilian A.
Trapence, Clement
Tweya, Hannock
Ehrenkranz, Peter
Phiri, Sam
author_facet Ganesh, Prakash
Heller, Tom
Chione, Boniface
Gumulira, Joe
Gugsa, Salem
Khan, Shaukat
McGovern, Seth
Nhlema, Angellina
Nkhoma, Lyse
Sacks, Jilian A.
Trapence, Clement
Tweya, Hannock
Ehrenkranz, Peter
Phiri, Sam
author_sort Ganesh, Prakash
collection PubMed
description Point-of-care (POC) technologies in resource-limited settings can circumvent challenges of centralized laboratory testing, improving clinical management. However, higher device costs and uncertain indications for use have inhibited scaling up POC modalities. To address this gap, we investigated the feasibility and cost of targeted near-POC viral load (VL) testing in 2 large HIV clinics in Lilongwe, Malawi. METHODS: VL testing using GeneXpert was targeted for patients suspected of treatment failure or returning to care after a previously elevated VL (>1000 copies/mL). Descriptive analysis of retrospective clinical and cost data is presented. RESULTS: Two thousand eight hundred thirteen near-POC VL tests were conducted. One thousand five hundred eleven (54%) tests were for patients for whom results and reason for the test were documented: 57% (794/1389) of tests were to confirm a previously high VL, and 33% (462/1389) were due to clinical indications. Sixty-one percent (926/1511) of patients had a high VL, of whom 78% (719/926) had a recorded clinical action: 77% (557/719) switched to second line antiretroviral therapy, and 15% (194/719) were referred for intensive adherence counseling. Eighty-two percent (567/687) of patients received a clinical action on the same day as testing. The “all-in” cost was $33.71 for a valid POC VL test, compared with an international benchmark for a centralized VL test of $28.62. CONCLUSION: Targeted, near-POC VL testing was feasible and consistently enabled prompt clinical action. The difference between the “all-in” cost of near-POC VL and centralized testing of $5.09 could be further reduced in an optimized national program by combining targeted near-POC testing and centralized testing.
format Online
Article
Text
id pubmed-7803448
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher JAIDS Journal of Acquired Immune Deficiency Syndromes
record_format MEDLINE/PubMed
spelling pubmed-78034482021-01-27 Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities Ganesh, Prakash Heller, Tom Chione, Boniface Gumulira, Joe Gugsa, Salem Khan, Shaukat McGovern, Seth Nhlema, Angellina Nkhoma, Lyse Sacks, Jilian A. Trapence, Clement Tweya, Hannock Ehrenkranz, Peter Phiri, Sam J Acquir Immune Defic Syndr Clinical Science Point-of-care (POC) technologies in resource-limited settings can circumvent challenges of centralized laboratory testing, improving clinical management. However, higher device costs and uncertain indications for use have inhibited scaling up POC modalities. To address this gap, we investigated the feasibility and cost of targeted near-POC viral load (VL) testing in 2 large HIV clinics in Lilongwe, Malawi. METHODS: VL testing using GeneXpert was targeted for patients suspected of treatment failure or returning to care after a previously elevated VL (>1000 copies/mL). Descriptive analysis of retrospective clinical and cost data is presented. RESULTS: Two thousand eight hundred thirteen near-POC VL tests were conducted. One thousand five hundred eleven (54%) tests were for patients for whom results and reason for the test were documented: 57% (794/1389) of tests were to confirm a previously high VL, and 33% (462/1389) were due to clinical indications. Sixty-one percent (926/1511) of patients had a high VL, of whom 78% (719/926) had a recorded clinical action: 77% (557/719) switched to second line antiretroviral therapy, and 15% (194/719) were referred for intensive adherence counseling. Eighty-two percent (567/687) of patients received a clinical action on the same day as testing. The “all-in” cost was $33.71 for a valid POC VL test, compared with an international benchmark for a centralized VL test of $28.62. CONCLUSION: Targeted, near-POC VL testing was feasible and consistently enabled prompt clinical action. The difference between the “all-in” cost of near-POC VL and centralized testing of $5.09 could be further reduced in an optimized national program by combining targeted near-POC testing and centralized testing. JAIDS Journal of Acquired Immune Deficiency Syndromes 2021-02-01 2020-10-21 /pmc/articles/PMC7803448/ /pubmed/33136821 http://dx.doi.org/10.1097/QAI.0000000000002555 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Ganesh, Prakash
Heller, Tom
Chione, Boniface
Gumulira, Joe
Gugsa, Salem
Khan, Shaukat
McGovern, Seth
Nhlema, Angellina
Nkhoma, Lyse
Sacks, Jilian A.
Trapence, Clement
Tweya, Hannock
Ehrenkranz, Peter
Phiri, Sam
Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities
title Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities
title_full Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities
title_fullStr Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities
title_full_unstemmed Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities
title_short Near Point-of-Care HIV Viral Load: Targeted Testing at Large Facilities
title_sort near point-of-care hiv viral load: targeted testing at large facilities
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803448/
https://www.ncbi.nlm.nih.gov/pubmed/33136821
http://dx.doi.org/10.1097/QAI.0000000000002555
work_keys_str_mv AT ganeshprakash nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT hellertom nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT chioneboniface nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT gumulirajoe nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT gugsasalem nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT khanshaukat nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT mcgovernseth nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT nhlemaangellina nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT nkhomalyse nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT sacksjiliana nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT trapenceclement nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT tweyahannock nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT ehrenkranzpeter nearpointofcarehivviralloadtargetedtestingatlargefacilities
AT phirisam nearpointofcarehivviralloadtargetedtestingatlargefacilities