Culture and transfer of human blastocysts increases implantation rates and reduces the need for multiple embryo transfers

被引:522
作者
Gardner, DK
Vella, P
Lane, M
Wagley, L
Schlenker, T
Schoolcraft, WB
机构
[1] Colorado Ctr Reprod Med, Englewood, CO 80110 USA
[2] Monash Univ, Monash Med Ctr, Inst Reprod & Dev, Melbourne, Vic 3004, Australia
基金
澳大利亚研究理事会;
关键词
IVF; blastocyst; viability; embryo culture; defined media;
D O I
10.1016/S0015-0282(97)00438-X
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To determine whether the transfer of blastocysts on day 5, developed in sequential culture media, resulted in an increase in implantation rate compared with embryos transferred on day 3. Design: Comparative study of embryo culture regimes. Setting: Private practice assisted reproductive technology center. Patient(s): Twenty-three patients undergoing routine IVF cycles. Intervention(s): Culture of embryos to day 3 in either standard culture conditions or a serum-free chemically defined medium. One hundred one embryos were subsequently cultured from day 3 to day 5 in a second serum-free medium specifically designed to support development of the blastocyst. Main Outcome Measure(s): Embryo cell number and quality on day 3. Blastocyst development on day 5. Implantation rate (determined by fetal heart) and ongoing pregnancy rate (PR). Result(s): Implantation rates for embryos transferred at the blastocyst stage of development were twice that observed for embryos transferred on day 3, around the eight-cell stage. Significantly more embryos were required for transfer on day 3, compared with day 5, to establish similar PRs. Conclusion(s): Viable human blastocysts can be obtained in sequential culture media the in the absence of coculture and serum. Transfer of blastocysts in IVF will facilitate high PRs while limiting the number of embryos transferred and therefore minimizes the risk of multiple gestation. (C) 1998 by American Society for Reproductive Medicine.
引用
收藏
页码:84 / 88
页数:5
相关论文
共 25 条
[1]   Blastocyst development and birth after in-vitro maturation of human primary oocytes, intracytoplasmic sperm injection and assisted hatching [J].
Barnes, FL ;
Crombie, A ;
Gardner, DK ;
Kausche, A ;
LachamKaplan, O ;
Suikkari, AM ;
Tiglias, J ;
Wood, C ;
Trounson, AO .
HUMAN REPRODUCTION, 1995, 10 (12) :3243-3247
[2]   Culture of preimplantation embryos: Facts and artifacts [J].
Bavister, BD .
HUMAN REPRODUCTION UPDATE, 1995, 1 (02) :91-148
[3]  
BIGGERS JD, 1989, GROWTH FACTORS MAMMA, P19
[4]  
BOLTON VN, 1991, FERTIL STERIL, V55, P830
[5]   BLASTOCYST TRANSFER IN HUMAN IN-VITRO FERTILIZATION - THE USE OF EMBRYO COCULTURE [J].
BONGSO, TA ;
FONG, CY ;
NG, SC ;
RATNAM, SS .
CELL BIOLOGY INTERNATIONAL, 1994, 18 (12) :1181-1189
[6]   BIOLOGIC AND MORPHOLOGIC DEVELOPMENT OF DONATED HUMAN OVA RECOVERED BY NONSURGICAL UTERINE LAVAGE [J].
BUSTER, JE ;
BUSTILLO, M ;
RODI, IA ;
COHEN, SW ;
HAMILTON, M ;
SIMON, JA ;
THORNEYCROFT, IH ;
MARSHALL, JR .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1985, 153 (02) :211-217
[7]  
CHATOT CL, 1989, J REPROD FERTIL, V86, P679, DOI 10.1530/jrf.0.0860679
[8]   DELAYING TRANSFER TO THE 3RD DAY POST-INSEMINATION, TO SELECT NON-ARRESTED EMBRYOS, INCREASES DEVELOPMENT TO THE FETAL HEART STAGE [J].
DAWSON, KJ ;
CONAGHAN, J ;
OSTERA, GR ;
WINSTON, RML ;
HARDY, K .
HUMAN REPRODUCTION, 1995, 10 (01) :177-182
[9]   Environment of the preimplantation human embryo in vivo: Metabolite analysis of oviduct and uterine fluids and metabolism of cumulus cells [J].
Gardner, DK ;
Lane, M ;
Calderon, I ;
Leeton, J .
FERTILITY AND STERILITY, 1996, 65 (02) :349-353
[10]   Culture and selection of viable blastocysts: a feasible proposition for human IVF? [J].
Gardner, DK ;
Lane, M .
HUMAN REPRODUCTION UPDATE, 1997, 3 (04) :367-382