Mother-to-Child HIV Transmission With In Utero Dolutegravir vs. Efavirenz in Botswana.
Adult
Alkynes
/ therapeutic use
Anti-HIV Agents
/ therapeutic use
Anti-Retroviral Agents
/ therapeutic use
Benzoxazines
/ therapeutic use
Botswana
Cyclopropanes
/ therapeutic use
Cytochrome P-450 CYP2B6 Inducers
/ therapeutic use
Cytochrome P-450 CYP2C19 Inhibitors
/ therapeutic use
Cytochrome P-450 CYP2C9 Inhibitors
/ therapeutic use
Cytochrome P-450 CYP3A Inducers
/ therapeutic use
Drug Combinations
Emtricitabine
/ therapeutic use
Female
HIV Infections
/ drug therapy
Heterocyclic Compounds, 3-Ring
/ therapeutic use
Humans
Infectious Disease Transmission, Vertical
/ prevention & control
Mothers
Oxazines
/ therapeutic use
Piperazines
/ therapeutic use
Pregnancy
Pyridones
/ therapeutic use
Reverse Transcriptase Inhibitors
/ therapeutic use
Risk Factors
Tenofovir
/ therapeutic use
Young Adult
Journal
Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005
Informations de publication
Date de publication:
01 07 2020
01 07 2020
Historique:
pubmed:
21
3
2020
medline:
5
1
2021
entrez:
21
3
2020
Statut:
ppublish
Résumé
A large-scale evaluation of mother-to-child transmission (MTCT) with dolutegravir (DTG)-based antiretroviral treatment (ART) has not been conducted previously. Botswana was the first African country to change from efavirenz (EFV)/tenofovir (TDF)/emtricitabine (FTC) to DTG/TDF/FTC first-line ART. From April 2015 to July 2018, the Early Infant Treatment Study offered HIV DNA testing at <96 hours of life. Maternal ART regimen was available for screened infants who could be linked to the separate Tsepamo surveillance study database. We evaluated characteristics of HIV-positive infants, and compared MTCT rates by ART regimen for linked infants. Of 10,622 HIV-exposed infants screened, 42 (0.40%) were HIV-positive. In total, 5064 screened infants could be linked to the surveillance database, including 1235 (24.4%) exposed to DTG/TDF/FTC and 2411 (47.6%) exposed to EFV/TDF/FTC. MTCT was rare when either regimen was started before conception: 0/213 [0.00%, 95% confidence interval (CI): 0.00% to 1.72%] on DTG, 1/1497 (0.07%, 95% CI: 0.00% to 0.37%) on EFV. MTCT was similar for women starting each ART regimen in pregnancy: 8/999 (0.80%, 95% CI: 0.35% to 1.57%) for DTG and 8/883 (0.91%, 95% CI: 0.39% to 1.78%) for EFV (risk difference 0.11%, 95% CI: -0.79% to 1.06%). Most MTCT events (4/8 with DTG, 6/9 with EFV) occurred when ART was started <90 days before delivery. Infants exposed to DTG in utero had lower baseline HIV RNA compared with other HIV-infected infants. In utero MTCT in Botswana remains rare in the DTG era. No significant MTCT differences were observed between DTG/TDF/FTC and EFV/TDF/FTC. Risk was highest for both groups when ART was started in the third trimester.
Sections du résumé
BACKGROUND
A large-scale evaluation of mother-to-child transmission (MTCT) with dolutegravir (DTG)-based antiretroviral treatment (ART) has not been conducted previously.
SETTING
Botswana was the first African country to change from efavirenz (EFV)/tenofovir (TDF)/emtricitabine (FTC) to DTG/TDF/FTC first-line ART.
METHODS
From April 2015 to July 2018, the Early Infant Treatment Study offered HIV DNA testing at <96 hours of life. Maternal ART regimen was available for screened infants who could be linked to the separate Tsepamo surveillance study database. We evaluated characteristics of HIV-positive infants, and compared MTCT rates by ART regimen for linked infants.
RESULTS
Of 10,622 HIV-exposed infants screened, 42 (0.40%) were HIV-positive. In total, 5064 screened infants could be linked to the surveillance database, including 1235 (24.4%) exposed to DTG/TDF/FTC and 2411 (47.6%) exposed to EFV/TDF/FTC. MTCT was rare when either regimen was started before conception: 0/213 [0.00%, 95% confidence interval (CI): 0.00% to 1.72%] on DTG, 1/1497 (0.07%, 95% CI: 0.00% to 0.37%) on EFV. MTCT was similar for women starting each ART regimen in pregnancy: 8/999 (0.80%, 95% CI: 0.35% to 1.57%) for DTG and 8/883 (0.91%, 95% CI: 0.39% to 1.78%) for EFV (risk difference 0.11%, 95% CI: -0.79% to 1.06%). Most MTCT events (4/8 with DTG, 6/9 with EFV) occurred when ART was started <90 days before delivery. Infants exposed to DTG in utero had lower baseline HIV RNA compared with other HIV-infected infants.
CONCLUSION
In utero MTCT in Botswana remains rare in the DTG era. No significant MTCT differences were observed between DTG/TDF/FTC and EFV/TDF/FTC. Risk was highest for both groups when ART was started in the third trimester.
Identifiants
pubmed: 32195745
doi: 10.1097/QAI.0000000000002338
pmc: PMC7293566
mid: NIHMS1575421
pii: 00126334-202007010-00001
doi:
Substances chimiques
Alkynes
0
Anti-HIV Agents
0
Anti-Retroviral Agents
0
Benzoxazines
0
Cyclopropanes
0
Cytochrome P-450 CYP2B6 Inducers
0
Cytochrome P-450 CYP2C19 Inhibitors
0
Cytochrome P-450 CYP2C9 Inhibitors
0
Cytochrome P-450 CYP3A Inducers
0
Drug Combinations
0
Heterocyclic Compounds, 3-Ring
0
Oxazines
0
Piperazines
0
Pyridones
0
Reverse Transcriptase Inhibitors
0
Tenofovir
99YXE507IL
dolutegravir
DKO1W9H7M1
Emtricitabine
G70B4ETF4S
efavirenz
JE6H2O27P8
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
235-241Subventions
Organisme : NIAID NIH HHS
ID : U01 AI114235
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD080471
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI131924
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD095766
Pays : United States
Organisme : NICHD NIH HHS
ID : K23 HD088230
Pays : United States
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