PrEP monitoring and HIV incidence after PrEP initiation in France: 2016-18 nationwide cohort study.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
11 10 2021
Historique:
received: 16 03 2021
accepted: 29 06 2021
pubmed: 23 7 2021
medline: 15 12 2021
entrez: 22 7 2021
Statut: ppublish

Résumé

Clinical trials have demonstrated that oral pre-exposure prophylaxis (PrEP) has high efficacy in preventing HIV transmission. In many countries, HIV testing is recommended prior to PrEP initiation, 1 month after and quarterly thereafter. We assessed the uptake of HIV testing and estimated the incidence of HIV infections after oral PrEP initiation, by using the French national health database (SNDS). A historic cohort study included every adult person who started oral PrEP between 1 January 2016 and 30 June 2018 in France. HIV infection was tracked in the follow-up, from first PrEP dispensation up to 31 December 2018. Factors associated with adherence to HIV testing in PrEP follow-up were analysed using a generalized linear mixed model. PrEP users (9893) were followed for a median duration of 551 days (IQR 350-769). The first HIV test, 1 month after PrEP initiation, was performed by 64% of users. For subsequent tests, this rate exceeded 81% and remained stable over time. HIV testing was lower among PrEP users without prescription refill (OR 0.15; 99% CI 0.12-0.20), but higher if the last prescription was made by a hospital practitioner (OR 2.03; 99% CI 1.69-2.45). Twenty-nine HIV infections were identified, leading to an incidence of 0.19 cases per 100 person-years (99% CI 0.12-0.30). We confirmed good adherence to HIV testing and efficacy of PrEP in users, which should help in decreasing HIV incidence in France. This study also revealed that SNDS could be a powerful automated tool for the epidemiological monitoring of PrEP users.

Sections du résumé

BACKGROUND
Clinical trials have demonstrated that oral pre-exposure prophylaxis (PrEP) has high efficacy in preventing HIV transmission. In many countries, HIV testing is recommended prior to PrEP initiation, 1 month after and quarterly thereafter. We assessed the uptake of HIV testing and estimated the incidence of HIV infections after oral PrEP initiation, by using the French national health database (SNDS).
METHODS
A historic cohort study included every adult person who started oral PrEP between 1 January 2016 and 30 June 2018 in France. HIV infection was tracked in the follow-up, from first PrEP dispensation up to 31 December 2018. Factors associated with adherence to HIV testing in PrEP follow-up were analysed using a generalized linear mixed model.
RESULTS
PrEP users (9893) were followed for a median duration of 551 days (IQR 350-769). The first HIV test, 1 month after PrEP initiation, was performed by 64% of users. For subsequent tests, this rate exceeded 81% and remained stable over time. HIV testing was lower among PrEP users without prescription refill (OR 0.15; 99% CI 0.12-0.20), but higher if the last prescription was made by a hospital practitioner (OR 2.03; 99% CI 1.69-2.45). Twenty-nine HIV infections were identified, leading to an incidence of 0.19 cases per 100 person-years (99% CI 0.12-0.30).
CONCLUSIONS
We confirmed good adherence to HIV testing and efficacy of PrEP in users, which should help in decreasing HIV incidence in France. This study also revealed that SNDS could be a powerful automated tool for the epidemiological monitoring of PrEP users.

Identifiants

pubmed: 34293116
pii: 6325489
doi: 10.1093/jac/dkab263
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3002-3008

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Marc-Florent Tassi (MF)

INSERM U1259, Université de Tours, France.

Emeline Laurent (E)

EA7505, Education Ethique et Santé, Université de Tours, France.
Service d'Information Médicale d'Epidémiologie et d'Economie de la Santé, CHRU de Tours, France.

Guillaume Gras (G)

Coordination Régionale de la lutte contre le VIH, CHRU de Tours, France.
Centre Gratuit d'Information, de Dépistage et de Diagnostic, CHRU de Tours, France.

Florence Lot (F)

Unité VIH-Hépatites B/C-IST, Santé publique France, Saint-Maurice, France.

Francis Barin (F)

INSERM U1259, Université de Tours, France.
Laboratoire de Virologie et CNR VIH-Laboratoire Associé, CHRU de Tours, France.

Sophie Billioti de Gage (SB)

EPI-PHARE Groupement d'Intérêt Scientifique en Epidémiologie des Produits de Santé de l'Agence Nationale de Sécurité de Médicament et de la Caisse Nationale de l'Assurance Maladie, Saint-Denis, France.

Karl Stefic (K)

INSERM U1259, Université de Tours, France.
Laboratoire de Virologie et CNR VIH-Laboratoire Associé, CHRU de Tours, France.

Leslie Grammatico-Guillon (L)

INSERM U1259, Université de Tours, France.
Service d'Information Médicale d'Epidémiologie et d'Economie de la Santé, CHRU de Tours, France.

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