|Year : 2015 | Volume
| Issue : 1 | Page : 54-57
Monochorionic triamniotic triplets following conventional in vitro fertilization and blastocyst transfer
Sumana Gurunath1, Adinarayana Makam2, Sriprada Vinekar3, Reeta H Biliangady1
1 Department of Reproductive Medicine, Cloudnine Hospitals, Malleshwaram, Karnataka, India
2 Department of Fetal Medicine, People Tree Hospitals, Bengaluru, Karnataka, India
3 Department of Gynaecology, Cloudnine Hospitals, Malleshwaram, Karnataka, India
|Date of Submission||29-Jan-2015|
|Date of Decision||11-Mar-2015|
|Date of Acceptance||05-Mar-2015|
|Date of Web Publication||13-Mar-2015|
Department of Reproductive Medicine, Cloudnine Hospitals, Malleshwaram, KarnDepartment of Reproductive Medicine, Cloudnine Hospitals, No. 47, 17th Cross, 11th Main, Malleshwaram, Bengaluru, Karnatakaataka
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Multiple pregnancy in in vitro fertilization (IVF) is on the decline with a reduction in number of embryos transferred. But the risk of monozygotic splitting persists. The risk of monozygotic twinning in women undergoing IVF is reported to be twice that of natural conception, and monochorionic triplets are even rarer at 100 times more than natural conception. We report a case of monochorionic triamniotic (MCTA) triplets following conventional IVF and blastocyst transfer without zona manipulation. This report highlights the possibility of zygotic splitting in IVF in young couples with no family history, in centers with good experience with blastocyst transfer. MCTA triplets carry a high risk of perinatal mortality and morbidity and need multidisciplinary care. Prevention and prediction of zygotic splitting ought to be realized with better reporting and identification of possible risk factors.
Keywords: Blastocyst transfer, in vitro fertilization, monochorionic triamniotic triplet, zygotic splitting
|How to cite this article:|
Gurunath S, Makam A, Vinekar S, Biliangady RH. Monochorionic triamniotic triplets following conventional in vitro fertilization and blastocyst transfer. J Hum Reprod Sci 2015;8:54-7
|How to cite this URL:|
Gurunath S, Makam A, Vinekar S, Biliangady RH. Monochorionic triamniotic triplets following conventional in vitro fertilization and blastocyst transfer. J Hum Reprod Sci [serial online] 2015 [cited 2020 Feb 28];8:54-7. Available from: http://www.jhrsonline.org/text.asp?2015/8/1/54/153131
| Introduction|| |
A significant decline in the incidence of higher order multiple pregnancy has been achieved worldwide with the reduction in the number of embryos transferred during assisted reproduction. Despite this, the prevalence of zygotic splitting and monozygotic multiple pregnancies persists. The risk of monozygotic twinning in women undergoing in vitro fertilization (IVF) is reported to be twice that of natural conception (0.9% vs. 0.4%, respectively). The incidence of monochorionic triplets is even rarer at 0.048%, which is 100 times more than natural conception. 
Various theories have been proposed to explain the increased risk of monozygotic splitting after assisted reproduction. They include advanced maternal age, ovarian stimulation, culture media, prolonged in vitro culture and blastocyst transfer, zona manipulation such as intracytoplasmic sperm injection (ICSI) and assisted hatching. Monochorionic triamniotic (MCTA) triplets are rather uncommon and highly challenging to manage as they are associated with much greater chances of obstetric and perinatal morbidity and mortality. Most of the cases of MCTA triplets reported to date are consequent to some form of zona manipulation either ICSI or assisted laser hatching. To the best of our knowledge, there have been 20 reports of MCTA triplets published in the literature. 11 of these reports are following some form of zona manipulation (ICSI or Assisted hatching) and 8 are following conventional IVF (2 frozen embryo transfer [FET]; 3 day 3 transfer and 3 day 5 transfer) [Table 1].
In this publication, we report a case of MCTA triplets following IVF in a young couple following blastocyst transfer. This is the fourth reported case following blastocyst transfer and conventional IVF.
| Case report|| |
A 29-year-old woman presented with secondary infertility of 3-year duration. The couple was married for 6 years with regular menstrual cycles and normal husband's semen analysis. Her reproductive history included an ectopic pregnancy for which she had undergone the right salpingectomy and a missed miscarriage at 8 weeks pregnancy in the past. She had 4 failed intrauterine insemination cycles and was then planned for IVF in view of tubal factor.
She was started on the standard antagonist protocol and stimulated with 150 iu of recombinant follicle-stimulating hormone (rFSH; Gonal-F, Merck Serono, Geneva, Switzerland) and 75 iu of HMG-HP (Menopur, Ferring Pharmaceuticals, Sweden) daily. GnRH antagonist was started on day 6 of stimulation and administered daily till the day of human chorionic gonadotropin (hCG). Egg retrieval was performed 35 h after administration of 250 ug of recombinant hCG (rhCG; Ovitrelle, Merck Serono) and 16 oocytes were retrieved. The 15 metaphase II oocytes were subjected to conventional IVF since semen parameters were normal. 14 oocytes fertilized and after 5 days of in vitro culture (Vitrolife G1.3, Göteborg, Sweden), 6 blastocysts were obtained. Two top quality blastocysts (4AA, 2AA) were transferred, and 4 were cryopreserved. She received standard luteal support with vaginal progesterone gel (Crinone gel 8%, Merck Serono). A positive beta hCG was obtained 14 days after embryo transfer. Ultrasound performed at 5 weeks of pregnancy showed a single gestational sac. At 7 weeks of gestation, ultrasound revealed MCTA triplets with three yolk sacs and three fetal poles with cardiac activity in each [Figure 1] and [Figure 2]. In view of monochorionic gestation, she was offered fetal reduction by selective cord ligation at 16 weeks. Despite counseling about increased chances of antenatal complications with triplets, the couple chose to continue pregnancy without fetal reduction. She had an uneventful pregnancy till 17 weeks gestation after which she developed preterm premature rupture of membranes and cord prolapse. Her pregnancy was terminated using medical management.
|Figure 1: Three-dimensional scan showing three separate gestational sacs and a single placenta|
Click here to view
| Discussion|| |
This is the fourth reported case of MCTA triplet following conventional IVF and blastocyst transfer without zona manipulation. ,, There are two reported cases following day 3 transfer , and two following FET , [Table 1]. These cases reveal that with the exception of one patient of age 37, most patients were of young age, the average age being 28 years. There was no predilection for any etiology of infertility, drug used, protocol, family history, culture media used. This case report is mainly to highlight that complications such as MCTA triplets can occur in young couples with no family history of twinning and no zona manipulation; in centers with good experience with blastocyst transfer.
There have been various theories proposed to elucidate the reasons for zygotic splitting in such situations. They include anomalies in apoptosis-related remodeling of the inner cell mass during extended culture or excessive growth of the inner cell mass. 
Data from a recent meta-analysis have indicated that the risk of monozygotic twinning following assisted reproductive technology (ART) is 0.9%; which is a 2-fold increase compared to natural conception. Blastocyst transfer is associated with a higher rate of monozygotic twinning at 1.7%.  There are inadequate data regarding the incidence of monozygotic triplet pregnancies. It has been reported to occur in 0.004% of all natural pregnancies.  Though there have been no studies quoting the actual prevalence following IVF, reports range from 10 to 100 times that of natural conception. 
Management of MCTA triplets is highly challenging and needs multidisciplinary care as MCTA triplets are associated with a high chance of miscarriage, preterm birth, low birth weight, twin-twin transfusion syndrome (TTTS), structural abnormalities, and perinatal mortality. TTTS is a major possible complicating factor, the prevalence of which is unknown in triplet.
Selective fetal reduction to twins is an option to improve perinatal outcome. This could be performed by cord occlusion (using ultrasound guided bipolar diathermy or radiofrequency ablation). The potential risks of the procedure include 3-5% chance of pregnancy loss. Couple declined this option understanding the pros and cons.
One of the major goals of IVF, today, is to achieve the birth of a healthy singleton and reduce perinatal morbidity and mortality. Popularizing single embryo transfer has been one of the main interventions to achieve this target. Having said that patients should be counseled that the risk of monozygotic splitting persists. Since zygotic splitting is much more common in ART pregnancies compared to natural conception, efforts must be made to identify the factors which predispose to zygotic splitting. This would assist in the prevention and patient counseling. Patients must be counseled about the higher chances of antenatal and perinatal morbidity and mortality in monozygotic multiple pregnancies.
| References|| |
Dessolle L, Allaoua D, Fréour T, Le Vaillant C, Philippe HJ, Jean M, et al.
Monozygotic triplet pregnancies after single blastocyst transfer: Two cases and literature review. Reprod Biomed Online 2010;21:283-9.
Jain JK, Boostanfar R, Slater CC, Francis MM, Paulson RJ. Monozygotic twins and triplets in association with blastocyst transfer. J Assist Reprod Genet 2004;21:103-7.
Henne MB, Milki AA, Westphal LM. Monochorionic triplet gestation after in vitro
fertilization using donor oocytes: Case report and review. Fertil Steril 2005;83:742-8.
Salat-Baroux J, Alvarez S, Antoine JM. A case of triple monoamniotic pregnancy combined with a bioamniotic twinning after in-vitro
fertilization. Hum Reprod 1994;9:374-5.
Tal R, Fridman D, Grazi RV. Monozygotic triplets and dizygotic twins following transfer of three poor-quality cleavage stage embryos. Case Rep Obstet Gynecol 2012;2012:763057.
Belaisch-Allart J, Elaoufir A, Mayenga JM, Segard L, Bernard JP, Plachot M, et al.
Monozygotic triplet pregnancy following transfer of frozen-thawed embryos. Hum Reprod 1995;10:3064-6.
Faraj R, Evbuomwan I, Sturgiss S, Aird I. Monozygotic triplet pregnancy following egg donation and transfer of single frozen-thawed embryo. Fertil Steril 2008;89:1260.e9-12.
Vitthala S, Gelbaya TA, Brison DR, Fitzgerald CT, Nardo LG. The risk of monozygotic twins after assisted reproductive technology: A systematic review and meta-analysis. Hum Reprod Update 2009;15:45-55.
Imaizumi Y. Perinatal mortality in triplet births in Japan: Time trends and factors influencing mortality. Twin Res 2003;6:1-6.
Yanaihara A, Yorimitsu T, Motoyama H, Watanabe H, Kawamura T. Monozygotic multiple gestation following in vitro
fertilization: Analysis of seven cases from Japan. J Exp Clin Assist Reprod 2007;4:4.
[Figure 1], [Figure 2]