Exclusion of pregnant and lactating women from COVID-19 vaccine trials: a missed opportunity

Abstract

In the midst of a devastating pandemic with high transmissibility and case fatality, the mRNA COVID-19 vaccine trials represent hope of an end to the global burden of COVID-19 infection, hospital utilization, and death. The efficacy and safety of the vaccines have been demonstrated in adults across a range of demographics, with the exception of those who are pregnant and lactating. This systematic exclusion— common in clinical trials—represents a missed opportunity to protect a group at risk of adverse outcomes in the setting of COVID-19 infection. It has special implications on the healthcare workforce, a majority of whom are women and at high risk of COVID-19 infection. The exclusion of pregnant and lactating women from COVID-19 vaccine trials (Text Box 1) reflects a historic pattern of ‘protection by exclusion’, representing an instance in which the estimated effect of a therapy on mother and child will rely on anecdotal and delayed reports from healthcare settings rather than the monitored setting of a clinical trial. This exclusion is not justified. For example, Pfizer and Moderna excluded pregnant and lactating women from their mRNA COVID-19 vaccine trials with no biological evidence to suggest that the vaccines are teratogenic, and no plausibility that they are transmitted in breast milk. The mRNA vaccines rapidly degenerate after injection in muscle cells, and aside from the post-vaccination immune response that can cause a fever, there is no reason to assume, a priori, that harm will come to pregnant and lactating women enrolled in the trials. The exclusion of pregnant and lactating women from the COVID19 vaccine trials has implications on healthcare workers, who are among the highest risk groups for COVID-19 exposure and infection. As many as three out of four healthcare workers and four out of five nurses are women, and it is estimated that more than 300 000 health care workers in the USA alone are pregnant or immediately postpartum during vaccine implementing. The dual risk posed by COVID-19 to pregnant healthcare professionals—increased workplace exposure and increased risk of adverse outcomes if infected—makes it particularly concerning that the trials failed to include pregnant or lactating individuals. Furthermore, when healthcare workers are infected, they become sources of nosocomial spread thereby posing a risk to patients and to other healthcare workers. The recommendations for use of the COVID-19 Pfizer and Moderna vaccine in pregnant and lactating women now range from avoidance of the vaccine—as recommended by the World Health Organization and some regulatory agencies—to reliance on recipients to make choices guided by their values or their clinicians’ judgement. Some regulatory bodies recommend against pregnancy in the weeks following the vaccine. The rationale for the recommendations of vaccine avoidance in pregnancy, pregnancy avoidance in weeks following vaccination, and decision-making regarding vaccination safety by clinicians in absence of clinical trial data is unclear. Pregnancy and lactation are two distinct biological states that are often conflated in the eligibility criteria of clinical trials. Drugs that may have evidence of teratogenicity in biological studies may not be secreted in breast milk, and drugs secreted in breast milk with harmful effects to baby may not be teratogenic. The grouping of pregnancy and lactation into a single condition that is systematically excluded from clinical trials is often ill-conceived. Indeed, the exclusions of one or both groups of patients from clinical trials is often without justification. For example, pregnant and lactating women were excluded from the COVID-19 hydroxychloroquine and azithromycin trials when these drugs have been used to treat pneumonia, malaria, and lupus in pregnant women and lactating women for several years. The systematic exclusion of pregnant and lactating women from clinical trials, while broadly accepted, does not uphold the ethical principles of justice, beneficence, and autonomy (Figure 1). Results from trials in non-pregnant populations cannot be safely extrapolated to pregnant women due to differences in physiology that influence the pharmacokinetics and pharmacodynamics of drugs. Recommendations for most therapies come with the stipulation that there is no safety or efficacy data to support their use in pregnant or lactating women. The treatment of many conditions during pregnancy or lactation relies on historic drugs for which there is only observational data to confirm safety. This applies to all cardiovascular conditions in pregnant and lactating women; the level of evidence to support treatment recommendations in these women in major guideline documents is almost