# The Use of Protease Inhibitors in Pregnancy: Maternal and Fetal Considerations

**Authors:** Elaine Duryea, Fiona Nicholson, Sara Cooper, Scott Roberts, Vanessa Rogers, Donald McIntire, Jeanne Sheffield, Robert Stewart

PMC · DOI: 10.1155/2015/563727 · Infectious Diseases in Obstetrics and Gynecology · 2015-11-05

## TL;DR

This study found that using protease inhibitors during pregnancy does not increase preterm births or small infants in HIV-positive women.

## Contribution

The study clarifies that protease inhibitors do not increase preterm or small-for-gestational-age births in HIV-positive pregnancies.

## Key findings

- Protease inhibitor use was not associated with increased preterm birth rates.
- There was no difference in small-for-gestational-age infants across treatment groups.
- Protease inhibitors were linked to a greater reduction in viral load during pregnancy.

## Abstract

Background. Previous studies examining protease inhibitor use in pregnancy and the rate of preterm and small-for-gestational-age infants have yielded conflicting results. Methods. This was a retrospective study of HIV-infected women who delivered singleton infants at our institution between 1984 and 2014. Women with protease inhibitor use were compared to women on regimens without a protease inhibitor as well as those who received no antepartum antiretroviral therapy. Infants were considered preterm if less than 37 completed weeks of gestation and small-for-gestational-age if less than 10th percentile. Results. During the study period 1,004 pregnancies met inclusion criteria. Of those, 597 received a protease inhibitor as part of their regimen, 230 ART without a protease inhibitor, and 177 no ART. There was no difference in the rate of preterm birth between groups who received ART with or without a protease inhibitor, 14% versus 13%. There was no difference in the rate of small-for-gestational-age infants between the three groups. Use of a protease inhibitor was associated with a greater fall in viral load during pregnancy, p < 0.001. Conclusion. In this population with access to prenatal care and ART, treatment with protease inhibitors was associated with a greater fall in viral load, but not an increase in small or preterm infants.

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** maternal (MESH:D000079262), premature birth (MESH:D047928), infection (MESH:D007239), rash (MESH:D005076), neural tube defects (MESH:D009436), mitochondrial toxicity (MESH:D028361), HIV disease (MESH:D015658),  (MESH:D001724),  (MESH:D011251)
- **Chemicals:** progesterone (MESH:D011374), efavirenz (MESH:C098320), NNRTI (-), nevirapine (MESH:D019829), zidovudine (MESH:D015215), alcohol (MESH:D000438),  (MESH:D011480),  (MESH:D017320)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC4651704/full.md

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Source: https://tomesphere.com/paper/PMC4651704