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Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile
OBJECTIVES: To analyze the perinatal outcomes of Perinatally acquired HIV Infection (PHIV) in pregnant women. METHOD: This retrospective cohort study included singleton pregnancies in Women Living with HIV (WLH) between 2006 and 2019. Patient charts were revised, and maternal characteristics, type o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995930/ https://www.ncbi.nlm.nih.gov/pubmed/36870111 http://dx.doi.org/10.1016/j.clinsp.2023.100174 |
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author | Osmundo, Gilmar de Souza da Costa, Rafaela Alkmin Ruocco, Rosa Maria Aveiro Francisco, Rossana Pulcineli Vieira |
author_facet | Osmundo, Gilmar de Souza da Costa, Rafaela Alkmin Ruocco, Rosa Maria Aveiro Francisco, Rossana Pulcineli Vieira |
author_sort | Osmundo, Gilmar de Souza |
collection | PubMed |
description | OBJECTIVES: To analyze the perinatal outcomes of Perinatally acquired HIV Infection (PHIV) in pregnant women. METHOD: This retrospective cohort study included singleton pregnancies in Women Living with HIV (WLH) between 2006 and 2019. Patient charts were revised, and maternal characteristics, type of HIV infection (perinatal vs. behavioral), Antiretroviral Therapy (ART) exposure, and obstetric and neonatal outcomes were assessed. The HIV-related aspects considered were: Viral Load (VL), CD4+ cell count, opportunistic infections, and genotype testing. Laboratory analyses were performed at baseline (first appointment) and 34 weeks of gestation. RESULTS: There were 186 WLH pregnancies, and 54 (29%) patients had PHIV. Patients with PHIV were younger (p < 0.001), had less frequently stable partnerships (p < 0.001), had more commonly serodiscordant partners (p < 0.001), had a longer time on ART (p < 0.001), and had lower rates of undetectable VL at baseline (p = 0.046) and at 34 weeks of gestation (p < 0.001). No association was observed between PHIV and adverse perinatal outcomes. Among patients with PHIV, third trimester anemia was associated with preterm birth (p = 0.039). Genotype testing was available only for 11 patients with PHIV, who presented multiple mutations related to ART resistance. CONCLUSIONS: PHIV did not seem to increase the risk of adverse perinatal outcomes. However, PHIV pregnancies have a higher risk of viral suppression failure and exposure to complex ARTs. |
format | Online Article Text |
id | pubmed-9995930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-99959302023-03-10 Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile Osmundo, Gilmar de Souza da Costa, Rafaela Alkmin Ruocco, Rosa Maria Aveiro Francisco, Rossana Pulcineli Vieira Clinics (Sao Paulo) Original Articles OBJECTIVES: To analyze the perinatal outcomes of Perinatally acquired HIV Infection (PHIV) in pregnant women. METHOD: This retrospective cohort study included singleton pregnancies in Women Living with HIV (WLH) between 2006 and 2019. Patient charts were revised, and maternal characteristics, type of HIV infection (perinatal vs. behavioral), Antiretroviral Therapy (ART) exposure, and obstetric and neonatal outcomes were assessed. The HIV-related aspects considered were: Viral Load (VL), CD4+ cell count, opportunistic infections, and genotype testing. Laboratory analyses were performed at baseline (first appointment) and 34 weeks of gestation. RESULTS: There were 186 WLH pregnancies, and 54 (29%) patients had PHIV. Patients with PHIV were younger (p < 0.001), had less frequently stable partnerships (p < 0.001), had more commonly serodiscordant partners (p < 0.001), had a longer time on ART (p < 0.001), and had lower rates of undetectable VL at baseline (p = 0.046) and at 34 weeks of gestation (p < 0.001). No association was observed between PHIV and adverse perinatal outcomes. Among patients with PHIV, third trimester anemia was associated with preterm birth (p = 0.039). Genotype testing was available only for 11 patients with PHIV, who presented multiple mutations related to ART resistance. CONCLUSIONS: PHIV did not seem to increase the risk of adverse perinatal outcomes. However, PHIV pregnancies have a higher risk of viral suppression failure and exposure to complex ARTs. Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo 2023-03-02 /pmc/articles/PMC9995930/ /pubmed/36870111 http://dx.doi.org/10.1016/j.clinsp.2023.100174 Text en © 2023 HCFMUSP. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Articles Osmundo, Gilmar de Souza da Costa, Rafaela Alkmin Ruocco, Rosa Maria Aveiro Francisco, Rossana Pulcineli Vieira Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile |
title | Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile |
title_full | Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile |
title_fullStr | Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile |
title_full_unstemmed | Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile |
title_short | Pregnancy in women living with perinatally acquired HIV: Perinatal outcomes and drug resistance profile |
title_sort | pregnancy in women living with perinatally acquired hiv: perinatal outcomes and drug resistance profile |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995930/ https://www.ncbi.nlm.nih.gov/pubmed/36870111 http://dx.doi.org/10.1016/j.clinsp.2023.100174 |
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