Literature DB >> 28349525

Glucocorticoid supplementation during ovarian stimulation for IVF or ICSI.

Theodoros Kalampokas1, Zabeena Pandian2, Stephen D Keay3, Siladitya Bhattacharya2.   

Abstract

BACKGROUND: Ovarian response to stimulation during in-vitro fertilisation (IVF) and intra-cytoplasmic sperm injection (ICSI) plays an important role in determining live birth rates. Adjuvant treatments during ovarian stimulation that have different modes of action have been used to improve ovarian response to stimulation and outcome of IVF. Glucocorticoids (GCs) are a class of steroid hormones that have been used either alone or in combination with other stimulatory regimens in order to improve folliculogenesis and pregnancy rates. However, considerable uncertainty remains over whether administration of glucocorticoid during ovarian stimulation until oocyte recovery is superior to no glucocorticoid in improving live birth rates in women undergoing IVF/ICSI.
OBJECTIVES: To determine the safety and effectiveness of systemic glucocorticoids during ovarian stimulation for IVF and ICSI cycles. SEARCH
METHODS: We searched the Cochrane Gynaecology and Fertility Group Specialised Register, the Cochrane Central Register of Studies Online (CRSO), MEDLINE, Embase, CINAHL and PsycINFO from inception to 10 October 2016. We handsearched reference lists of articles, trial registers and relevant conference proceedings and contacted researchers in the field. SELECTION CRITERIA: We included randomised controlled trials (RCTs) comparing adjuvant treatment with systemic glucocorticoids during ovarian stimulation for IVF or ICSI cycles versus no adjuvant treatment. DATA COLLECTION AND ANALYSIS: Two review authors independently selected studies, assessed risk of bias and extracted the data. Our primary outcome was live birth. Secondary outcomes included clinical pregnancy, multiple pregnancy, miscarriage, ovarian hyperstimulation syndrome (OHSS) and side-effects. We calculated odds ratios (ORs) with 95% confidence intervals (CIs) and pooled the data using a fixed-effect model. The quality of the evidence was assessed using GRADE methods. MAIN
RESULTS: Four RCTs were included in the review (416 women). The trials compared glucocorticoid supplementation during IVF stimulation versus placebo. Two of the studies had data in a form that we could not enter into analysis, so results include data from only two trials (310) women. For the outcome of live birth, data were available for only 212 women, as the larger study had data available from only one study centre.One of the studies gave inadequate description of randomisation methods, but the other was at low risk of bias in all domains. The evidence was rated as low or very low quality for all outcomes, mainly due to imprecision, with low sample sizes and few events.There was insufficient evidence to determine whether there was any difference between the groups in live birth rate (OR 1.08, 95% CI 0.45 to 2.58; 2 RCTs, n = 212, I2 = 0%, low-quality evidence). Our findings suggest that if the chance of live birth with placebo is assumed to be 15%, the chance following supplementation would be between 7% and 31%. There was no conclusive evidence of a difference in the clinical pregnancy rate (OR 1.69, 95% CI 0.98 to 2.90; 2 RCTs, n = 310, I2 = 0%, low-quality evidence).The evidence suggests that if the chance of clinical pregnancy with placebo is assumed to be 24%, the chance following treatment with glucocorticoid supplementation would be between 23% and 47%. There was also insufficient evidence to determine whether there was any difference between the groups in multiple-pregnancy rate (OR 3.32 , 95% CI 0.12 to 91.60; 1 RCT , n = 20, very low-quality evidence) or miscarriage rate (OR 1.00, 95% CI 0.05 to 18.57; 1 RCT, n = 20, very low-quality evidence). Neither of the studies reported OHSS or side-effects. AUTHORS'
CONCLUSIONS: The safety and effectiveness of glucocorticoid administration in women undergoing controlled ovarian hyperstimulation for IVF/ICSI cycles (until the day of oocyte retrieval) is unclear due to the small number of studies and low event rates. Whilst glucocorticoids possible increase the clinical pregnancy rate, there may be little or no impact on live birth rate. More research is needed.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28349525      PMCID: PMC6464567          DOI: 10.1002/14651858.CD004752.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  7 in total

1.  Assisted reproductive technology: an overview of Cochrane Reviews.

Authors:  Cindy Farquhar; Jane Marjoribanks
Journal:  Cochrane Database Syst Rev       Date:  2018-08-17

Review 2.  Peri-implantation glucocorticoid administration for assisted reproductive technology cycles.

Authors:  Carolien M Boomsma; Mohan S Kamath; Stephen D Keay; Nick S Macklon
Journal:  Cochrane Database Syst Rev       Date:  2022-06-30

3.  Endometrial Immune Profiling: A Method to Design Personalized Care in Assisted Reproductive Medicine.

Authors:  Nathalie Lédée; Marie Petitbarat; Laura Prat-Ellenberg; Géraldine Dray; Guy N Cassuto; Lucie Chevrier; Alaa Kazhalawi; Katia Vezmar; Gerard Chaouat
Journal:  Front Immunol       Date:  2020-06-04       Impact factor: 7.561

4.  Supercritical Fluid Extract of Putranjiva roxburghii Wall. Seeds Mitigates Fertility Impairment in a Zebrafish Model.

Authors:  Acharya Balkrishna; Pradeep Nain; Monali Joshi; Lakshmipathi Khandrika; Anurag Varshney
Journal:  Molecules       Date:  2021-02-15       Impact factor: 4.411

5.  The Endometrial Immune Profiling May Positively Affect the Management of Recurrent Pregnancy Loss.

Authors:  Meryam Cheloufi; Alaa Kazhalawi; Anne Pinton; Mona Rahmati; Lucie Chevrier; Laura Prat-Ellenberg; Anne-Sophie Michel; Geraldine Dray; Arsène Mekinian; Gilles Kayem; Nathalie Lédée
Journal:  Front Immunol       Date:  2021-03-24       Impact factor: 7.561

6.  ERAP, KIR, and HLA-C Profile in Recurrent Implantation Failure.

Authors:  Karolina Piekarska; Paweł Radwan; Agnieszka Tarnowska; Andrzej Wiśniewski; Michał Radwan; Jacek R Wilczyński; Andrzej Malinowski; Izabela Nowak
Journal:  Front Immunol       Date:  2021-10-22       Impact factor: 7.561

7.  Glucocorticoid therapy in assisted reproduction.

Authors:  Yong Jin Kim
Journal:  Clin Exp Reprod Med       Date:  2021-11-30
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.