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Safety and efficacy of low dose hCG for luteal support after triggering ovulation with a GnRH agonist in cases of polyfollicular development.
Eur J Obstet Gynecol Reprod Biol. 2006 May 01; 126(1):87-92.EJ

Abstract

OBJECTIVE

The use of GnRH agonists instead of hCG to trigger ovulation seems to be an effective way to prevent subsequent hCG induced ovarian hyperstimulation in cases of polyfollicular development. But conflicting results are reported on the efficiency of subsequent luteal support using hCG and/or progesterone supplementation.

STUDY DESIGN

We investigated the efficiency and safety of different luteal support regimes in low dose gonadotropin stimulation non-ivf cycles. A risk for an imminent ovarian hyperstimulation was assumed if preovulatory estradiol levels rose up higher than 700 pg/ml and more than 12 intermediate sized follicles (8-14 mm) were observed. Thirty-six women received 0.5mg Triptorelin subcutaneously to trigger the ovulation inducing LH surge. After randomization, luteal support regimes started on day 2 after the Triptorelin administration with injections every second day five times in all. Group (a) received 5 x 1000 IU hCG, group (b) received 5 x 500 IU hCG, and group (c) received 5 x 250 mg progesterone, intramuscularly. The monitoring of the ovulation period and the subsequent luteal phase included sonographic measurement of ovarian diameter and estimation of LH, FSH, estradiol and progesterone levels 10 and 34 h as well as 8 days after Triptorelin administration.

RESULTS

We could prove ovulation in all women and did not find symptoms of ovarian hyperstimulation in any case. Midluteal controls showed extremely low gonadotropins in all groups indicating a long lasting pituitary down regulation after one injection of 0.5 mg Triptorelin. We found high normal sex steroid levels in both hCG groups. The progesterone group displayed a marked luteal phase defect with low levels of progesterone and estradiol in all cases.

CONCLUSION

The use of GnRH agonist in cases of polyfollicular development is capable to induce ovulation without a subsequent ovarian enlargement and/or any sign of hyperstimulation syndrome. Luteal support by low dose hCG does not counteract the benefit of GnRH agonist in preventing an ovarian hyperstimulation syndrome, but seems to remedy at least in part the possible deleterious effects of GnRH agonists on luteal functionality.

Authors+Show Affiliations

IVF-Zentrum Muenster, Hoetteweg 5-7, 48143 Muenster, Germany. b.krause@ivf-muenster.deNo affiliation info available

Pub Type(s)

Journal Article
Randomized Controlled Trial

Language

eng

PubMed ID

16377065

Citation

Krause, B Th, and R Ohlinger. "Safety and Efficacy of Low Dose hCG for Luteal Support After Triggering Ovulation With a GnRH Agonist in Cases of Polyfollicular Development." European Journal of Obstetrics, Gynecology, and Reproductive Biology, vol. 126, no. 1, 2006, pp. 87-92.
Krause BT, Ohlinger R. Safety and efficacy of low dose hCG for luteal support after triggering ovulation with a GnRH agonist in cases of polyfollicular development. Eur J Obstet Gynecol Reprod Biol. 2006;126(1):87-92.
Krause, B. T., & Ohlinger, R. (2006). Safety and efficacy of low dose hCG for luteal support after triggering ovulation with a GnRH agonist in cases of polyfollicular development. European Journal of Obstetrics, Gynecology, and Reproductive Biology, 126(1), 87-92.
Krause BT, Ohlinger R. Safety and Efficacy of Low Dose hCG for Luteal Support After Triggering Ovulation With a GnRH Agonist in Cases of Polyfollicular Development. Eur J Obstet Gynecol Reprod Biol. 2006 May 1;126(1):87-92. PubMed PMID: 16377065.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Safety and efficacy of low dose hCG for luteal support after triggering ovulation with a GnRH agonist in cases of polyfollicular development. AU - Krause,B Th, AU - Ohlinger,R, Y1 - 2005/12/22/ PY - 2005/08/28/received PY - 2005/11/03/revised PY - 2005/11/14/accepted PY - 2005/12/27/pubmed PY - 2006/12/9/medline PY - 2005/12/27/entrez SP - 87 EP - 92 JF - European journal of obstetrics, gynecology, and reproductive biology JO - Eur. J. Obstet. Gynecol. Reprod. Biol. VL - 126 IS - 1 N2 - OBJECTIVE: The use of GnRH agonists instead of hCG to trigger ovulation seems to be an effective way to prevent subsequent hCG induced ovarian hyperstimulation in cases of polyfollicular development. But conflicting results are reported on the efficiency of subsequent luteal support using hCG and/or progesterone supplementation. STUDY DESIGN: We investigated the efficiency and safety of different luteal support regimes in low dose gonadotropin stimulation non-ivf cycles. A risk for an imminent ovarian hyperstimulation was assumed if preovulatory estradiol levels rose up higher than 700 pg/ml and more than 12 intermediate sized follicles (8-14 mm) were observed. Thirty-six women received 0.5mg Triptorelin subcutaneously to trigger the ovulation inducing LH surge. After randomization, luteal support regimes started on day 2 after the Triptorelin administration with injections every second day five times in all. Group (a) received 5 x 1000 IU hCG, group (b) received 5 x 500 IU hCG, and group (c) received 5 x 250 mg progesterone, intramuscularly. The monitoring of the ovulation period and the subsequent luteal phase included sonographic measurement of ovarian diameter and estimation of LH, FSH, estradiol and progesterone levels 10 and 34 h as well as 8 days after Triptorelin administration. RESULTS: We could prove ovulation in all women and did not find symptoms of ovarian hyperstimulation in any case. Midluteal controls showed extremely low gonadotropins in all groups indicating a long lasting pituitary down regulation after one injection of 0.5 mg Triptorelin. We found high normal sex steroid levels in both hCG groups. The progesterone group displayed a marked luteal phase defect with low levels of progesterone and estradiol in all cases. CONCLUSION: The use of GnRH agonist in cases of polyfollicular development is capable to induce ovulation without a subsequent ovarian enlargement and/or any sign of hyperstimulation syndrome. Luteal support by low dose hCG does not counteract the benefit of GnRH agonist in preventing an ovarian hyperstimulation syndrome, but seems to remedy at least in part the possible deleterious effects of GnRH agonists on luteal functionality. SN - 0301-2115 UR - https://www.unboundmedicine.com/medline/citation/16377065/Safety_and_efficacy_of_low_dose_hCG_for_luteal_support_after_triggering_ovulation_with_a_GnRH_agonist_in_cases_of_polyfollicular_development_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0301-2115(05)00640-8 DB - PRIME DP - Unbound Medicine ER -