Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles: multicentre randomised controlled trial

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles : multicentre randomised controlled trial. / Stormlund, Sacha; Sopa, Negjyp; Zedeler, Anne; Bogstad, Jeanette; Prætorius, Lisbeth; Nielsen, Henriette Svarre; Kitlinski, Margaretha Laczna; Skouby, Sven O; Mikkelsen, Anne Lis; Spangmose, Anne Lærke; Jeppesen, Janni Vikkelsø; Khatibi, Ali; la Cour Freiesleben, Nina; Ziebe, Søren; Polyzos, Nikolaos P; Bergh, Christina; Humaidan, Peter; Andersen, Anders Nyboe; Løssl, Kristine; Pinborg, Anja.

In: The BMJ, Vol. 370, m2519, 05.08.2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Stormlund, S, Sopa, N, Zedeler, A, Bogstad, J, Prætorius, L, Nielsen, HS, Kitlinski, ML, Skouby, SO, Mikkelsen, AL, Spangmose, AL, Jeppesen, JV, Khatibi, A, la Cour Freiesleben, N, Ziebe, S, Polyzos, NP, Bergh, C, Humaidan, P, Andersen, AN, Løssl, K & Pinborg, A 2020, 'Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles: multicentre randomised controlled trial', The BMJ, vol. 370, m2519. https://doi.org/10.1136/bmj.m2519

APA

Stormlund, S., Sopa, N., Zedeler, A., Bogstad, J., Prætorius, L., Nielsen, H. S., Kitlinski, M. L., Skouby, S. O., Mikkelsen, A. L., Spangmose, A. L., Jeppesen, J. V., Khatibi, A., la Cour Freiesleben, N., Ziebe, S., Polyzos, N. P., Bergh, C., Humaidan, P., Andersen, A. N., Løssl, K., & Pinborg, A. (2020). Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles: multicentre randomised controlled trial. The BMJ, 370, [m2519]. https://doi.org/10.1136/bmj.m2519

Vancouver

Stormlund S, Sopa N, Zedeler A, Bogstad J, Prætorius L, Nielsen HS et al. Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles: multicentre randomised controlled trial. The BMJ. 2020 Aug 5;370. m2519. https://doi.org/10.1136/bmj.m2519

Author

Stormlund, Sacha ; Sopa, Negjyp ; Zedeler, Anne ; Bogstad, Jeanette ; Prætorius, Lisbeth ; Nielsen, Henriette Svarre ; Kitlinski, Margaretha Laczna ; Skouby, Sven O ; Mikkelsen, Anne Lis ; Spangmose, Anne Lærke ; Jeppesen, Janni Vikkelsø ; Khatibi, Ali ; la Cour Freiesleben, Nina ; Ziebe, Søren ; Polyzos, Nikolaos P ; Bergh, Christina ; Humaidan, Peter ; Andersen, Anders Nyboe ; Løssl, Kristine ; Pinborg, Anja. / Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles : multicentre randomised controlled trial. In: The BMJ. 2020 ; Vol. 370.

Bibtex

@article{2abb3b5150e2482a986d04b48ad62f23,
title = "Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles: multicentre randomised controlled trial",
abstract = "OBJECTIVE: To compare the ongoing pregnancy rate between a freeze-all strategy and a fresh transfer strategy in assisted reproductive technology treatment.DESIGN: Multicentre, randomised controlled superiority trial.SETTING: Outpatient fertility clinics at eight public hospitals in Denmark, Sweden, and Spain.PARTICIPANTS: 460 women aged 18-39 years with regular menstrual cycles starting their first, second, or third treatment cycle of in vitro fertilisation or intracytoplasmic sperm injection.INTERVENTIONS: Women were randomised at baseline on cycle day 2 or 3 to one of two treatment groups: the freeze-all group (elective freezing of all embryos) who received gonadotropin releasing hormone agonist triggering and single frozen-thawed blastocyst transfer in a subsequent modified natural cycle; or the fresh transfer group who received human chorionic gonadotropin triggering and single blastocyst transfer in the fresh cycle. Women in the fresh transfer group with more than 18 follicles larger than 11 mm on the day of triggering had elective freezing of all embryos and postponement of transfer as a safety measure.MAIN OUTCOME MEASURES: The primary outcome was the ongoing pregnancy rate defined as a detectable fetal heart beat after eight weeks of gestation. Secondary outcomes were live birth rate, positive human chorionic gonadotropin rate, time to pregnancy, and pregnancy related, obstetric, and neonatal complications. The primary analysis was performed according to the intention-to-treat principle.RESULTS: Ongoing pregnancy rate did not differ significantly between the freeze-all and fresh transfer groups (27.8% (62/223) v 29.6% (68/230); risk ratio 0.98, 95% confidence interval 0.87 to 1.10, P=0.76). Additionally, no significant difference was found in the live birth rate (27.4% (61/223) for the freeze-all group and 28.7% (66/230) for the fresh transfer group; risk ratio 0.98, 95% confidence interval 0.87 to 1.10, P=0.83). No significant differences between groups were observed for positive human chorionic gonadotropin rate or pregnancy loss, and none of the women had severe ovarian hyperstimulation syndrome; only one hospital admission related to this condition occurred in the fresh transfer group. The risks of pregnancy related, obstetric, and neonatal complications did not differ between the two groups except for a higher mean birth weight after frozen blastocyst transfer and an increased risk of prematurity after fresh blastocyst transfer. Time to pregnancy was longer in the freeze-all group.CONCLUSIONS: In women with regular menstrual cycles, a freeze-all strategy with gonadotropin releasing hormone agonist triggering for final oocyte maturation did not result in higher ongoing pregnancy and live birth rates than a fresh transfer strategy. The findings warrant caution in the indiscriminate application of a freeze-all strategy when no apparent risk of ovarian hyperstimulation syndrome is present.TRIAL REGISTRATION: Clinicaltrials.gov NCT02746562.",
keywords = "Abortion, Spontaneous/epidemiology, Adult, Birth Weight, Blastocyst, Chorionic Gonadotropin/blood, Cryopreservation, Female, Fertilization in Vitro/methods, Humans, Live Birth, Menstrual Cycle, Obstetric Labor Complications/epidemiology, Pregnancy, Pregnancy Rate, Premature Birth/epidemiology, Single Embryo Transfer/methods, Time Factors",
author = "Sacha Stormlund and Negjyp Sopa and Anne Zedeler and Jeanette Bogstad and Lisbeth Pr{\ae}torius and Nielsen, {Henriette Svarre} and Kitlinski, {Margaretha Laczna} and Skouby, {Sven O} and Mikkelsen, {Anne Lis} and Spangmose, {Anne L{\ae}rke} and Jeppesen, {Janni Vikkels{\o}} and Ali Khatibi and {la Cour Freiesleben}, Nina and S{\o}ren Ziebe and Polyzos, {Nikolaos P} and Christina Bergh and Peter Humaidan and Andersen, {Anders Nyboe} and Kristine L{\o}ssl and Anja Pinborg",
note = "{\textcopyright} Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.",
year = "2020",
month = aug,
day = "5",
doi = "10.1136/bmj.m2519",
language = "English",
volume = "370",
journal = "The BMJ",
issn = "0959-8146",
publisher = "BMJ Publishing Group",

}

RIS

TY - JOUR

T1 - Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles

T2 - multicentre randomised controlled trial

AU - Stormlund, Sacha

AU - Sopa, Negjyp

AU - Zedeler, Anne

AU - Bogstad, Jeanette

AU - Prætorius, Lisbeth

AU - Nielsen, Henriette Svarre

AU - Kitlinski, Margaretha Laczna

AU - Skouby, Sven O

AU - Mikkelsen, Anne Lis

AU - Spangmose, Anne Lærke

AU - Jeppesen, Janni Vikkelsø

AU - Khatibi, Ali

AU - la Cour Freiesleben, Nina

AU - Ziebe, Søren

AU - Polyzos, Nikolaos P

AU - Bergh, Christina

AU - Humaidan, Peter

AU - Andersen, Anders Nyboe

AU - Løssl, Kristine

AU - Pinborg, Anja

N1 - © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

PY - 2020/8/5

Y1 - 2020/8/5

N2 - OBJECTIVE: To compare the ongoing pregnancy rate between a freeze-all strategy and a fresh transfer strategy in assisted reproductive technology treatment.DESIGN: Multicentre, randomised controlled superiority trial.SETTING: Outpatient fertility clinics at eight public hospitals in Denmark, Sweden, and Spain.PARTICIPANTS: 460 women aged 18-39 years with regular menstrual cycles starting their first, second, or third treatment cycle of in vitro fertilisation or intracytoplasmic sperm injection.INTERVENTIONS: Women were randomised at baseline on cycle day 2 or 3 to one of two treatment groups: the freeze-all group (elective freezing of all embryos) who received gonadotropin releasing hormone agonist triggering and single frozen-thawed blastocyst transfer in a subsequent modified natural cycle; or the fresh transfer group who received human chorionic gonadotropin triggering and single blastocyst transfer in the fresh cycle. Women in the fresh transfer group with more than 18 follicles larger than 11 mm on the day of triggering had elective freezing of all embryos and postponement of transfer as a safety measure.MAIN OUTCOME MEASURES: The primary outcome was the ongoing pregnancy rate defined as a detectable fetal heart beat after eight weeks of gestation. Secondary outcomes were live birth rate, positive human chorionic gonadotropin rate, time to pregnancy, and pregnancy related, obstetric, and neonatal complications. The primary analysis was performed according to the intention-to-treat principle.RESULTS: Ongoing pregnancy rate did not differ significantly between the freeze-all and fresh transfer groups (27.8% (62/223) v 29.6% (68/230); risk ratio 0.98, 95% confidence interval 0.87 to 1.10, P=0.76). Additionally, no significant difference was found in the live birth rate (27.4% (61/223) for the freeze-all group and 28.7% (66/230) for the fresh transfer group; risk ratio 0.98, 95% confidence interval 0.87 to 1.10, P=0.83). No significant differences between groups were observed for positive human chorionic gonadotropin rate or pregnancy loss, and none of the women had severe ovarian hyperstimulation syndrome; only one hospital admission related to this condition occurred in the fresh transfer group. The risks of pregnancy related, obstetric, and neonatal complications did not differ between the two groups except for a higher mean birth weight after frozen blastocyst transfer and an increased risk of prematurity after fresh blastocyst transfer. Time to pregnancy was longer in the freeze-all group.CONCLUSIONS: In women with regular menstrual cycles, a freeze-all strategy with gonadotropin releasing hormone agonist triggering for final oocyte maturation did not result in higher ongoing pregnancy and live birth rates than a fresh transfer strategy. The findings warrant caution in the indiscriminate application of a freeze-all strategy when no apparent risk of ovarian hyperstimulation syndrome is present.TRIAL REGISTRATION: Clinicaltrials.gov NCT02746562.

AB - OBJECTIVE: To compare the ongoing pregnancy rate between a freeze-all strategy and a fresh transfer strategy in assisted reproductive technology treatment.DESIGN: Multicentre, randomised controlled superiority trial.SETTING: Outpatient fertility clinics at eight public hospitals in Denmark, Sweden, and Spain.PARTICIPANTS: 460 women aged 18-39 years with regular menstrual cycles starting their first, second, or third treatment cycle of in vitro fertilisation or intracytoplasmic sperm injection.INTERVENTIONS: Women were randomised at baseline on cycle day 2 or 3 to one of two treatment groups: the freeze-all group (elective freezing of all embryos) who received gonadotropin releasing hormone agonist triggering and single frozen-thawed blastocyst transfer in a subsequent modified natural cycle; or the fresh transfer group who received human chorionic gonadotropin triggering and single blastocyst transfer in the fresh cycle. Women in the fresh transfer group with more than 18 follicles larger than 11 mm on the day of triggering had elective freezing of all embryos and postponement of transfer as a safety measure.MAIN OUTCOME MEASURES: The primary outcome was the ongoing pregnancy rate defined as a detectable fetal heart beat after eight weeks of gestation. Secondary outcomes were live birth rate, positive human chorionic gonadotropin rate, time to pregnancy, and pregnancy related, obstetric, and neonatal complications. The primary analysis was performed according to the intention-to-treat principle.RESULTS: Ongoing pregnancy rate did not differ significantly between the freeze-all and fresh transfer groups (27.8% (62/223) v 29.6% (68/230); risk ratio 0.98, 95% confidence interval 0.87 to 1.10, P=0.76). Additionally, no significant difference was found in the live birth rate (27.4% (61/223) for the freeze-all group and 28.7% (66/230) for the fresh transfer group; risk ratio 0.98, 95% confidence interval 0.87 to 1.10, P=0.83). No significant differences between groups were observed for positive human chorionic gonadotropin rate or pregnancy loss, and none of the women had severe ovarian hyperstimulation syndrome; only one hospital admission related to this condition occurred in the fresh transfer group. The risks of pregnancy related, obstetric, and neonatal complications did not differ between the two groups except for a higher mean birth weight after frozen blastocyst transfer and an increased risk of prematurity after fresh blastocyst transfer. Time to pregnancy was longer in the freeze-all group.CONCLUSIONS: In women with regular menstrual cycles, a freeze-all strategy with gonadotropin releasing hormone agonist triggering for final oocyte maturation did not result in higher ongoing pregnancy and live birth rates than a fresh transfer strategy. The findings warrant caution in the indiscriminate application of a freeze-all strategy when no apparent risk of ovarian hyperstimulation syndrome is present.TRIAL REGISTRATION: Clinicaltrials.gov NCT02746562.

KW - Abortion, Spontaneous/epidemiology

KW - Adult

KW - Birth Weight

KW - Blastocyst

KW - Chorionic Gonadotropin/blood

KW - Cryopreservation

KW - Female

KW - Fertilization in Vitro/methods

KW - Humans

KW - Live Birth

KW - Menstrual Cycle

KW - Obstetric Labor Complications/epidemiology

KW - Pregnancy

KW - Pregnancy Rate

KW - Premature Birth/epidemiology

KW - Single Embryo Transfer/methods

KW - Time Factors

U2 - 10.1136/bmj.m2519

DO - 10.1136/bmj.m2519

M3 - Journal article

C2 - 32759285

VL - 370

JO - The BMJ

JF - The BMJ

SN - 0959-8146

M1 - m2519

ER -

ID: 251255650