Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2022 Apr 26.
Published in final edited form as: Obstet Gynecol. 2020 Aug;136(2):427–428. doi: 10.1097/AOG.0000000000004032

In Reply

Mona Prasad 1, George Saade 2, Brenna Hughes 3
PMCID: PMC9040923  NIHMSID: NIHMS1601858  PMID: 32732757

We thank you for your interest in our work.1 We agree that the population we tested may not represent a high-risk group, and that inclusion of the risk factors you mention would have likely increased the prevalence of hepatitis C virus (HCV) in the sampled population. However, the main issue is which population is more representative of the overall U.S. population risk factors. It is interesting that in a critique suggesting that the population in the Maternal-Fetal Medicine Units may be biased, the reference provided was performed in a single hospital that specifically serves the American Indian and Alaska Native population2, a study clearly not representative of the U.S. population as a whole. The fact that we are discussing which population or study result is more representative and the wide variation in prevalence reported in the literature actually argues for an individualized approach rather than a universal one.

Our study was not undertaken to evaluate screening strategies, rather the outcome of interest was mother-to-child transmission of HCV. In the process of identifying a U.S. cohort of HCV-positive pregnant women to evaluate mother-to-child transmission, we amassed screening data on over 106,000 women. This represents the largest and most contemporary cohort of U.S. women evaluated for HCV. We felt compelled to share what we had learned during our years of unselected screening, most notably a low prevalence of women with chronic HCV.

The appropriate strategy for identification of women at risk for mother-to-child transmission of HCV remains unclear, and our findings challenge some recommendations from the Centers for Disease Control and Prevention3, American Association for the Study of Liver Diseases 4, and now U.S. Preventive Services Task Force.5 We offer alternative strategies to identify these women: screening at the time of delivery or postpartum when access to intervention is not limited by the pregnant state, or preferably at preconception so that treatment could be undertaken prior to pregnancy. Strategies targeting pregnant women are likely predicated on the woman’s engagement in the health care system, not necessarily her medical benefit, representing a bigger public health problem than can be addressed herein. We remain hesitant to endorse universal screening during pregnancy without clear evidence that this strategy results in more benefit than harm for pregnant women. The findings of our study demonstrate that majority of patients screened would derive no benefit from this testing.

Footnotes

Financial Disclosure

Mona Prasad disclosed that money was paid to her to from The Ohio State University for reimbursement for travel to and from meetings for work related to this study. Ohio State University was a NICHD-funded MFMU center. She has also received funds from Gilead as a consultant for Medical Advisory Panels in 2019.. Brenna L. Hughes disclosed that she received funds as a scientific advisor for the Merck CMV program (not relevant to the submitted work). The other author did not report any potential conflicts of interest.

Contributor Information

Mona Prasad, Department of Obstetrics and Gynecology of The Ohio State University, Columbus, OH.

George Saade, University of Texas Medical Branch, Galveston, TX.

Brenna Hughes, Brown University, Providence, RI.

References

RESOURCES