Skip to Content
Merck
  • Live birth rates after combined adjuvant therapy in IVF-ICSI cycles: a matched case-control study.

Live birth rates after combined adjuvant therapy in IVF-ICSI cycles: a matched case-control study.

Reproductive biomedicine online (2015-02-14)
C Motteram, B Vollenhoven, N Hope, T Osianlis, L J Rombauts
ABSTRACT

The effectiveness of combined co-treatment with aspirin, doxycycline, prednisolone, with or without oestradiol patches, was investigated on live birth (LBR) rates after fresh and frozen embryo transfers (FET) in IVF and intracytoplasmic sperm injection cycles. Cases (n = 485) and controls (n = 485) were extensively matched in a one-to-one ratio on nine physical and clinical parameters: maternal age, body mass index, smoking status, stimulation cycle number, cumulative dose of FSH, stimulation protocol, insemination method, day of embryo transfer and number of embryos transferred. No significant differences were found in fresh cycles between cases and controls for the pregnancy outcomes analysed, but fewer surplus embryos were available for freezing in the combined adjuvant group. In FET cycles, LBR was lower in the treatment group (OR: 0.49, 95% CI 0.25 to 0.95). The lower LBR in FET cycles seemed to be clustered in patients receiving combined adjuvant treatment without luteal oestradiol (OR 0.37, 95% CI 0.17 to 0.80). No difference was found in LBR between cases and controls when stratified according to the number of previous cycles (<3 or ≥3). There is no benefit of this combined adjuvant strategy in fresh IVF cycles, and possible harm when used in frozen cycles.

MATERIALS
Product Number
Brand
Product Description

Supelco
Prednisolone, VETRANAL®, analytical standard
Sigma-Aldrich
Prednisolone, ≥99%
Sigma-Aldrich
Luteinizing hormone releasing hormone salmon, ≥97% (HPLC)
Supelco
Prednisolone, Pharmaceutical Secondary Standard; Certified Reference Material
Prednisolone, European Pharmacopoeia (EP) Reference Standard
USP
Amoxicillin, United States Pharmacopeia (USP) Reference Standard
Prednisolone for system suitability, European Pharmacopoeia (EP) Reference Standard
Prednisolone, British Pharmacopoeia (BP) Assay Standard
USP
Prednisolone, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Amoxicillin, 95.0-102.0% anhydrous basis
Sigma-Aldrich
Luteinizing hormone releasing hormone, ≥97% (HPLC)
Prednisolone for peak identification, European Pharmacopoeia (EP) Reference Standard