Abstract
The objective of this study was to evaluate the contraceptive efficacy and clinical
performance of a Nestorone subdermal implant (NES) in the postpartum period. NES (n
= 100) and Copper T intrauterine device (T-Cu; n = 100) acceptors initiated contraception
at 8 weeks postpartum and were followed at monthly intervals during the first year
and at 3-month intervals thereafter. Pregnancy rates, breastfeeding performance, infant
growth, bleeding pattern, and side effects were assessed. Blood and milk NES concentration
were measured.
No pregnancy occurred in 2195 and 2145 woman-months of NES implant and T-Cu use, respectively.
No effect of NES on lactation and infant growth and no serious adverse events were
observed. Lactational amenorrhea was significantly longer in NES users (353 ± 20 days)
than in T-Cu users (201 ± 11 days). More NES users (55.8%) experienced prolonged bleedings
than did T-Cu users (36.2%). Concentrations of NES in breast milk ranged between 54–135
pmol/liter. The Nestorone implant is a highly effective contraceptive, safe for breastfed
infants because the steroid is inactive by the oral route.
Keywords
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© 2002 Elsevier Science Inc. Published by Elsevier Inc. All rights reserved.