A taxonomy of pragmatic measures of HIV preexposure prophylaxis use.
Journal
AIDS (London, England)
ISSN: 1473-5571
Titre abrégé: AIDS
Pays: England
ID NLM: 8710219
Informations de publication
Date de publication:
01 11 2020
01 11 2020
Historique:
entrez:
3
10
2020
pubmed:
4
10
2020
medline:
13
3
2021
Statut:
ppublish
Résumé
As delivery of preexposure prophylaxis (PrEP) becomes an HIV prevention priority in the United States, standard, pragmatic measures of PrEP use are needed to compare and evaluate prevention implementation programs. By using readily available electronic health record data, we describe and compare measures of persistence and retention. Retrospective cohort. Using electronic health record prescription data for patients at a large urban Federally Qualified Health Center from 2015 to 2019, we calculated measures of persistence and retention and compared them to pharmacy claims data, PrEP biomarkers, and HIV outcomes. Total PrEP time was 19.8 months on average. During this period, average adherence by medication prescription ratio (MRxR) was 89%; 77% of patients had an MRxR at least 85% and 90% have an MRxR at least 57%. Over the first 6 months, average proportion of days covered (PDC) at least 85% was 53% and PDC at least 57% was 57%. Prescription fill rates, based on claims data from a pharmacy partner, ranged from 45 to 60%. Using tenofovir-diphosphate as the gold standard, PDC had high sensitivity (97%) but low specificity (≤13%). As a measure of retention, over the first 6 months, 59% of patients had quarterly HIV tests. Total PrEP time is useful measure of overall persistence, while PDC can assess persistence and adherence at a specific time point. Adherence by PDC is more conservative compared with MRxR; both will overestimate true adherence. Retention in care can be measured by quarterly HIV tests. Using consistent terminology and reporting timepoints and adherence thresholds will help reporting and comparing PrEP delivery programs.
Identifiants
pubmed: 33009011
doi: 10.1097/QAD.0000000000002618
pii: 00002030-202011010-00012
pmc: PMC7856306
mid: NIHMS1619090
doi:
Substances chimiques
Anti-HIV Agents
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
1951-1957Subventions
Organisme : NIMH NIH HHS
ID : K23 MH118969
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI117943
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI120700
Pays : United States
Références
PLoS One. 2016 Jun 22;11(6):e0157742
pubmed: 27333000
Ann Epidemiol. 2018 Dec;28(12):841-849
pubmed: 29983236
J Acquir Immune Defic Syndr. 2016 Dec 15;73(5):540-546
pubmed: 27851714
J Int AIDS Soc. 2019 Feb;22(2):e25250
pubmed: 30768762
Sex Transm Dis. 2018 Sep;45(9):e62-e64
pubmed: 29485544
J Acquir Immune Defic Syndr. 2019 Aug 1;81(4):e104-e108
pubmed: 30985557
Value Health. 2008 Jan-Feb;11(1):44-7
pubmed: 18237359
Open Forum Infect Dis. 2018 May 04;5(6):ofy099
pubmed: 29977959
J Manag Care Spec Pharm. 2016 Nov;22(11):1224-1246
pubmed: 27783551
Med Care. 2013 Aug;51(8 Suppl 3):S11-21
pubmed: 23774515
J Int AIDS Soc. 2016 Jun 13;19(1):20903
pubmed: 27302837
AIDS Res Hum Retroviruses. 2013 Feb;29(2):384-90
pubmed: 22935078
AIDS Educ Prev. 2018 Oct;30(5):393-405
pubmed: 30332309
Antimicrob Agents Chemother. 2017 Dec 21;62(1):
pubmed: 29038282
Clin Infect Dis. 2018 Jul 2;67(2):283-287
pubmed: 29506057
J Manag Care Spec Pharm. 2018 Apr;24(4):367-372
pubmed: 29578851
J Acquir Immune Defic Syndr. 2018 Mar 1;77(3):272-278
pubmed: 29210835
Lancet HIV. 2020 Feb;7(2):e113-e120
pubmed: 31784343
AIDS. 2015 Jul 17;29(11):1277-85
pubmed: 26103095