Development of breakthrough bleeding model of combined-oral contraceptives utilizing model-based meta-analysis.

CPT Pharmacometrics Syst Pharmacol

Department of Pharmaceutics, College of Pharmacy, Center for Pharmacometrics and Systems Pharmacology, University of Florida, Orlando, Florida, USA.

Published: November 2024

AI Article Synopsis

  • Breakthrough bleeding (BTB) is a common side effect of hormonal contraceptives, particularly combined oral contraceptives (COCs), and can affect user adherence.
  • A model-based meta-analysis was conducted using data from 25 studies to investigate the dose-response relationship of different progestin/ethinyl estradiol (EE) combinations and their effects on BTB.
  • Results indicate that BTB increases when starting COCs but generally returns to baseline within 3 months, especially at higher EE doses; understanding these relationships can aid in optimizing COC treatment regimens.

Article Abstract

Breakthrough bleeding (BTB) is a common side effect of hormonal contraception and is thought to impact adherence to combined oral contraceptives (COCs) but respective dose-response relationships are not yet fully understood. Therefore, the objective of this model-based meta-analysis (MBMA) was to establish dose-response for COCs containing different progestin/EE combinations using BTB as the pharmacodynamic endpoint. Data from 25 studies containing BTB information of 4 progestins (desogestrel, drospirenone, gestodene, and levonorgestrel) in combination with ethinyl estradiol (EE) at various dose levels was used for this analysis. The results of our MBMA show that BTB is significantly increased upon initiation of COC use but subsides over time. The time needed for BTB to return to baseline depends on the EE dose and differs marginally between progestins during the initial months of use at the same EE dose. BTB typically returns to baseline within 3 months at the highest (30 μg) dose, whereas it can take significantly longer to reestablish a regular bleeding pattern at lower EE doses (15 and 20 μg), irrespective of the progestin used. The dose-response relationships established for BTB across different progestin/EE combinations can now be used to support the selection of optimal COC dosing/treatment regimens and serve as the scientific basis for evaluating the impact of clinically relevant factors, including drug-drug interactions and demographics, on BTB.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578130PMC
http://dx.doi.org/10.1002/psp4.13261DOI Listing

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