Using Brexanolone for Postpartum Depression Must Account for Lactation.
Casey B Rosen-CaroleShinya ItoPublished in: Maternal and child health journal (2021)
On March 19, 2019, Brexanolone (Zulresso ™) was released as the first-ever FDA-approved medication specifically for the treatment of postpartum depression by Sage Therapeutics, Inc. Unfortunately, its use in breastfeeding mothers was not evaluated and is being restricted. An efficacious drug for postpartum depression stands to benefit many families. However, the lack of guidance for breastfeeding patients, and the resultant restrictions on breastfeeding by insurance companies is deeply troubling. Conversely, withholding this medication from a lactating mother is ethically problematic. From a public health perspective, we aim to foster continuous breastfeeding among depressed women while they are being treated for depression. We therefore aim to address concerns about Brexanolone's effects on the breastfed child, as exposed through breastmilk, as well as the impact this medication may have on lactation.
Keyphrases
- depressive symptoms
- public health
- preterm infants
- sleep quality
- dairy cows
- healthcare
- newly diagnosed
- adverse drug
- human milk
- mental health
- small molecule
- ejection fraction
- emergency department
- type diabetes
- low birth weight
- adipose tissue
- patient reported outcomes
- physical activity
- skeletal muscle
- heat stress
- breast cancer risk