About this item:

380 Views | 509 Downloads

Author Notes:

Kathrine R. Tan, Malaria Branch, Center for Global Health, Centers for Disease Control and Prevention, 1600 Clifton Rd. MS A6, Atlanta, GA 30329, USA, Email: ktan@cdc.gov.

KT wrote the protocol, implemented the survey, guided and reviewed the analysis, and wrote the manuscript.

JF contributed to the protocol, reviewed the analysis, and contributed to the manuscript.

MW managed and analyzed the data.

JG contributed to the protocol, guided and reviewed the analysis, and contributed to the manuscript.

All authors read and approved the final manuscript.

The authors declare that they have no competing interests.

The dataset generated are available from the corresponding author on reasonable request.

The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

This study was determined to not require review by the Emory University Institutional Review Board, and was approved by CDC’s Institutional Review Board (Protocol #6752).

Subjects:

Research Funding:

No funding sources.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Infectious Diseases
  • Parasitology
  • Tropical Medicine
  • Malaria
  • Pregnancy
  • Prophylaxis
  • Atovaquone-proguanil
  • UNCOMPLICATED FALCIPARUM-MALARIA
  • WOMEN

A survey on outcomes of accidental atovaquone–proguanil exposure in pregnancy

Tools:

Journal Title:

Malaria Journal

Volume:

Volume 17, Number 1

Publisher:

, Pages 198-198

Type of Work:

Article | Final Publisher PDF

Abstract:

Background: Malaria chemoprophylaxis options in pregnancy are limited, and atovaquone-proguanil (AP) is not recommended because of insufficient safety evidence. An anonymous, internet-based survey was disseminated to describe outcomes of pregnancies accidentally exposed to AP. Outcomes of interest included miscarriage (defined as pregnancy loss before 20 weeks), stillbirth (defined as pregnancy loss at or after 20 weeks), preterm birth or live birth prior to 37 weeks, and the presence of congenital anomalies. Results: A total of 487 women responded and reported on 822 pregnancies. Of the 807 pregnancies with information available on exposure and outcomes, 10 (1.2%) had atovaquone-proguanil exposure, all in the first trimester, and all resulted in term births with no birth defects. Conclusions: Use of an anti-malarial not recommended in pregnancy is likely to occur before the woman knows of her pregnancy. This study adds to the limited evidence of the safety of AP in pregnancy. Further study on use of AP in pregnancy should be a high priority, as an alternative option for the prevention of malaria in pregnancy in non-immune travellers is urgently needed.

Copyright information:

© 2018 The Author(s).

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
Export to EndNote