Population pharmacokinetic modelling of primaquine exposures in lactating women and breastfed infants.
Thanaporn WattanakulMary Ellen GilderRose McGreadyWarunee HanpithakpongNicholas P J DayNicholas J WhiteFrancois H NostenJoel TarningRichard M HoglundPublished in: Nature communications (2024)
Current guidelines advise against primaquine treatment for breastfeeding mothers to avoid the potential for haemolysis in infants with G6PD deficiency. To predict the haemolytic risk, the amount of drug received from the breast milk and the resulting infant drug exposure need to be characterised. Here, we develop a pharmacokinetic model to describe the drug concentrations in breastfeeding women using venous, capillary, and breast milk data. A mother-to-infant model is developed to mimic the infant feeding pattern and used to predict their drug exposures. Primaquine and carboxyprimaquine exposures in infants are <1% of the exposure in mothers. Therefore, even in infants with the most severe G6PD deficiency variants, it is highly unlikely that standard doses of primaquine (0.25-1 mg base/kg once daily given to the mother for 1-14 days) would cause significant haemolysis. After the neonatal period, primaquine should not be restricted for breastfeeding women (Clinical Trials Registration: NCT01780753).
Keyphrases
- polycystic ovary syndrome
- air pollution
- clinical trial
- preterm infants
- pregnancy outcomes
- drug induced
- cervical cancer screening
- adverse drug
- breast cancer risk
- replacement therapy
- gene expression
- emergency department
- insulin resistance
- genome wide
- copy number
- clinical practice
- adipose tissue
- big data
- risk assessment
- dna methylation
- pregnant women
- combination therapy
- phase iii