Which is better for mothers and babies: fresh or frozen-thawed blastocyst transfer?

We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines when performing the systematic review and meta-analysis (Additional file  1 ). The articles included compared clinical outcomes between patients undergoing IVF/ICSI cycles with fresh or frozen BT. Studies were excluded if they were duplicate publications, literature reviews or meta-analyses or if they had insufficient data for extraction. We searched the articles published in the PubMed, EMBASE and Cochrane Library databases through May 2020, using the following terms as key words: ‘humans’, ‘embryo*’, ‘cryo*’, ‘frozen’, ‘vitrif*’, ‘freez*’, and ‘fresh’. A comprehensive MEDLINE search strategy is presented in Additional file  2 . Two researchers evaluated the selected studies and extracted the data independently. Any disagreement was resolved by discussion. First, we excluded the obviously ineligible literature by reading the title and abstract and then further read the full texts to identify the studies to be included. The data extracted mainly consisted of the first author, year of publication, study design, sample size, participants, intervention protocol, results, and other characteristics. We assessed the risk of bias of the included studies using RevMan 5.3.0 software and the risk of bias assessment of the Cochrane Collaboration [ 10 ], which assesses the generation of sequence allocation, allocation concealment, blinding, and incomplete outcome data for each trial included in the review. Each study was evaluated as having a high, low, or unclear risk of bias for each item. Any disagreements between the two reviewers were resolved by discussion with the corresponding author. The results of the assessment of risk of bias are shown in Additional file  3 . Publication bias was checked by funnel plot if at least ten studies reported that outcome. Subgroup analysis was done by the design, cryopreservation type, endometrial preparation type, high ovarian response and single BT. Sensitivity analysis was employed to see the effect of single study on the overall estimation. Beyond subgroup analysis, meta-regression for the included studies was conducted to identify factors for heterogeneity. The pregnancy outcomes were as follows: Implantation rate reflected the number of gestational sacs seen per embryo transferred. Pregnancy was identified according to increased serum hCG levels within 10 days after blastocyst transfer. Ongoing pregnancy was defined as pregnancy continuing beyond the 10th gestational week. Clinical pregnancy was considered the presence of a gestational sac with foetal heart activity, as assessed by ultrasound at 7 weeks of gestation. Miscarriage included any pregnancy that did not become an ongoing pregnancy. A multiple pregnancy was defined as a gestation with more than one foetus. The live birth rate was calculated as the number of birthing events per embryo transfer. We recorded the following maternal complications: GDM, pregnancy-induced hypertension (PIH), pre-eclampsia (PE), PTD, PP, PA, PH, and preterm rupture of membrane (PROM). PTD was defined as a liveborn or stillborn infant with a gestational age at birth of at least 28 weeks but less than 37 weeks. Very preterm delivery (VPTD) was defined as a liveborn or stillborn infant with a gestational age at birth of at least 28 weeks but less than 32 weeks. The neonatal outcomes included gestational age at delivery, birth weight, stillbirth, perinatal mortality and neonatal mortality. Large for gestational age (LGA) was defined as a birth weight above the 90th percentile. SGA was defined as birth weight below the 10th percentile. Very small for gestational age (VSGA) was defined as weighing below the 3rd percentile. High birth weight (HBW) was defined as a weight of > 4000 g at birth. Very high birth weight (VHBW) was defined as a weight of > 4500 g at birth. Low birth weight (LBW) was defined as a weight of < 2500 g at birth. Very low birth weight baby (VLBW) was defined as a weight of < 1500 g at birth. We also analysed neonatal malformations (NM), including congenital anomalies, chromosomal aberrations, and different organ system malformations. All statistical analyses were conducted using RevMan software. For the included studies, the results of dichotomous data for each of the studies eligible for meta-analysis were expressed as a risk ratio (RR) with the 95% confidence interval (CI). Although we analysed the data using both fixed effect models and random effect models, the results in the text are only from random effect models due to underlying heterogeneity in the studies. These results were combined for meta-analysis with the use of the Mantel/Haenszel model along with the random effects model. We assessed whether there was sufficient similarity between the eligible studies in regard to their design and clinical characteristics. Statistical heterogeneity was assessed with a chi-squared test and quantified with the I 2 statistic. I 2  > 50% was considered to indicate marked heterogeneity [ 11 ]. p  < 0.05 was considered statistically significant.

A total of 3985 available publications were identified in our search. Of these, 3783 were excluded after reading the title and the abstract. Finally, 54 articles, including 12 randomized controlled trials (RCTs) and 42 nonrandomized controlled trials (NRCTs), were considered eligible by one or both reviewers (Fig.  1 ). Table  1 provides the details of all included studies. Fig. 1 Flowchart showing the study selection process for the meta-analysis Table 1 Characteristics of included studies Author Year Patients Age (fresh/frozen) Numbers of patient (fresh/frozen) Design Duration of trial Outcomes Aflatoonian 2010a [ 12 ] Patients who were classified as high responders 28.1 ± 3.5/27.3 ± 4.4 187/187 Prospective RCT Feb 2007 to Feb 2009 IR, CPR, MR, MPR, OPR Aflatoonian 2010b [ 13 ] Pregnancies after fresh ET vs. FET 29.9 ± 4.7/30.4 ± 4.5 500/200 Prospective RCT Mar 2006 to Mar 2008 MR, LBR, PR, EPR, PTD, LBW, Aghahosseini 2017 [ 14 ] Infertile women with P  ≥ 1.8 ng/dl 32.8 ± 5.8/30.5 ± 4.7 36/36 RCT Jan to Apr 2016 CPR, MR, LBR, PR Ainsworth 2019 [ 15 ] Women who underwent fresh or FET at the Mayo Clinic 33.4 ± 4.4 /32.9 ± 3.6 87/ 49 Retrospective cohort study. 2010 to 2014 PPH, PE, SGA, GDM, PROM, PTD Badalotti 2019 [ 16 ] An assisted reproduction clinic in Brazil No statement 1443/ 486 Retrospective case-control study 2010 to 2019 SGA, PTD, LBW, VLBW Beltrananzola 2019 [ 17 ] Infertile-couples undergoing IVF or IVF-ICSI No statement 1857/ 352 Retrospective cohort study. 1995 to 2015. GDM,hyper, Preterm, Very preterm, Belva 2008 [ 18 ] All pregnancies after transfer of FET No statement 6402/1351 Unmatched cohort study No statement MR, MPR, LBR, OPR, PR, EPR, LBW, Stil Bourdon 2018 [ 19 ] Women with endometriosis infertile 34.3 ± 3.9/34.3 ± 4.1 135/135 Retrospective matched cohort study Oct 2012 to Dec 2014 LBR, MPR, OPR Cavoretto2020 [ 20 ] Women undergoing fresh ET or FET 35.9 ± 3.9/34.9 ± 5.1 164 / 203 Prospective longitudinal study Jan 2016 to Dec 2018 GDM, PTD, PE, SGA, LGA Chen 2016 [ 21 ] Infertile women with PCOS 28.2 ± 3.1/28.1 ± 3.0 762/746 Retrospective matched cohort study Jun 2013 to May 2015 CPR, MR, LBR, OPR, PR, OHSS, PTD, PIH, Stil Coates 2017 [ 22 ] Patients undergoing IVF treatment using preimplantation genetic screening 36.6 (25–42)/ 36.7 (27–42) 88/91 RCT Dec 2013 to Aug 2015 IR, MPR, LBR, OPR Eum 2016 [ 23 ] Women who underwent one or two fresh ET or FET Using a cutoff of 35 years 69/206 Retrospective study Jan 2013 to Dec 2014. IR, CPR, MR, LBR, MPR Fauque 2010 [ 24 ] Women with adequate ovarian function <  36 years No statement Prospective NRCT 2005 to 2007 CPR, MR, LBR, MPR, EPR. Feng 2012 [ 25 ] Women with various infertile causes 31.02 ± 3.69/ 31.60 ± 3.56 604/ 384 Retrospective study Jan 2009 to Dec 2010 IR, CPR, MR, LBR, MPR, EPR, PTD, LBW, Stil, NM Ferraretti 1999 [ 26 ] Patients at risk of OHSS 31.46 ± 2.4/ 31.66 ± 2.8 67/58 Prospective RCT Jan 1996 to Jul 1997 CPR, LBR, PR Ginström 2019 [ 27 ] Singletons born after in Sweden 34.9 ± 5.2 /34.1 ± 4.3 9726/24,365 Retrospective cohort study 2005 to 2015 GDM, PP, PA, PPH, PIH, Healy 2010 [ 28 ] Women with singleton births in Victoria Australia No statement 4058/2045 Retrospective cohort study 1991 to 2004 PP, PA, PH Henningsen 2011 [ 29 ] Singleton born after fresh ET or FET No statement 716/716 Retrospective cohort study 1994 to 2008 LBW Henman 2005 [ 30 ] Patients with three or more usable blastocysts < 38 years 121/156 Prospective study Apr 2000 to Dec 2001 IR, CPR, LBR, MPR Hwang 2019 [ 31 ] Singleton infants born to Massachusetts women who conceived by fresh or FET No statement 12,390/ 2101 Retrospective cohort study. July 2004, to Dec 2013 Preterm, LGA, SGA, LBW, Birth defects Ishihara 2014 [ 32 ] Women undergoing SET Any age 33,559/118866 (5981/27408 singletons) Retrospective study 2008 to 2010 CPR, MR, MPR, EPR, PP, PA, PIH, LGA, SGA, LBW, HBW, Stil Johnson 2019 [ 33 ] Women who underwent an autologous IVF cycle 35.8 (32.8–38.8)/36.3 (33.0–39.8) 1861/ 271 Retrospective cohort study Jan 2000 to Jun 2015 SGA, PA Korosec 2007 [ 34 ] Women undergoing SET < 37 years 65/214 Prospective study Apr 2004 to Jun 2006 CPR Le 2018 [ 35 ] Non-PCOS women undergoing IVF/ICSI Any age 391/391 RCT Jun to Apr 2015 MR, LBR, EPR, GDM, PIH Liu 2019 [ 36 ] Women with 3 and 10 oocytes retrieved underwent fresh or FET < 40 years 495/ 935 Retrospective cohort study Jan 2015 to Jan 2019 CPR, MR, EPR Magdi 2017 [ 37 ] Women with recurrent implantation failure <38 years 90/81 Prospective cohort study Apr 2014 to Oct 2016 IR, CPR, MR, MPR, OPR, PR, Maheshwari 2016 [ 38 ] Singleton births after IVF/ICISI in the UK Any age 95,911/16521 Retrospective cohort study 1991 to2011 PTD, LBW, HBW, NM Martikainen 2001 [ 39 ] Women with at least four good quality embryos No statement 74/74 RCT No statement CPR, MR, LBR, EPR Martikainen 2004 [ 40 ] Women in the first or second treatment cycle when a top-quality embryo is available <36 years 308/311 Retrospective cohort study 2000 to 2002 CPR, MR, MPR, LBR, OPR, EPR Mizrachi 2019 [ 41 ] Women with singleton IVF pregnancies who delivered 33.8 ± 5.5 /32.2 ± 5.2 74/57 Prospective cohort study Dec 2017 to May 2019. GDM, PE, PROM, SGA, LBW Pelkonen 2010 [ 42 ] Women underwent ART with ET leading to birth Any age 3298/1852 Unmatched cohort study 1995 to2006 PP, PA, PH, PTD, LGA, LBW, SGA, Sti Pelkonen 2014 [ 9 ] Women underwent ART with ET leading to singleton births Any age 2942/1830 (Singleton births) Register-based cohort study 1995 to 2006 Major congenital anomalies Pelkonen 2015 [ 43 ] Women underwent ART with ET leading to singleton births Any age 2933/1825 Register-based cohort study 1995 to 2006. PTD, LGA, SGA, LBW, NM Pinborg 2010 [ 44 ] All singletons who according to the Danish IVF Register Any age 10,392/5979 Retrospective cohort study 1995 to 2007 LBW, PTD, Stil, NM Roy 2014 [ 45 ] Infertile patients who underwent fresh ET or FET No statement 1157/645 Retrospective study. Mar2010 to Nov 2011 CPB, MR, LBR, PR, PTD, LBW Serkan 2020 [ 46 ] Infertile patients with various infertility etiology for IVF with fresh ET and sFET 18–42 years 620 /580 Retrospective cross-sectional study Jun 2015 to May 2018 PR, CPR, MR, EPR, LBR Shapiro 2011a [ 47 ] Patients with first-time IVF cycle day 3 FSH < 10 mIU/mL and 8–15 antral follicles <41 years 53/50 RCT No statement IR, CPR, MR, MPR, OPR, PR Shapiro 2011b [ 48 ] Patient must be undergoing her first IVF cycle; cycle day 3 FSH  15 antral follicles No statement 62/60 RCT No statement IR, CPR, MR, MPR, OPR, PR. Shapiro 2013 [ 49 ] Women with SET. 33.8 ± 4.7/33.8 ± 4.7 93/93 Matched cohort study. Dec 2003 to Dec 2011 CPR, MR, MPR, OPR, PR Shavit 2017 [ 6 ] Singletons born after f fresh or FET Any age 1886/1220 Retrospective cohort study Dec 2008 to Dec 2012 CPR, MR, PA, PTD, GDM, PIH, LGA, SGA, LBW, HBW, NM Shih 2008 [ 50 ] Neonatal perinatal statistics unit Australia Any age 3110/2387 Matched cohort study 1978 to 2005 PTD, LBW, NM Vuong 2016 [ 51 ] Non-PCOS infertile couples undergoing IVF/ICSI No statement 391/391 RCT No statement MPR, LBR, MPR, OPR, EPR Vuong 2018 [ 52 ] Non-PCOS infertile women who were undergoing a first or second IVF cycle 3 32 ± 4 /32 ± 4 391/391 RCT No statement IR, CPR, MR, MPR, LBR, OPR, EPR, Walls 2014 [ 53 ] Women with PCOS. Any age 122/179 Retrospective case–control study Mar 2007 to Dec 2012. CPR, MR, LBR, PR Wang 2005 [ 54 ] Infants conceived through ART procedures and born in Australia Any age 7676/3824 Retrospective cohort study 1996 to 2000 LBW. Wei 2019 [ 7 ] Women with regular menstrual cycles undergoing their first cycle of in-vitro fertilization 28.8 (3.0) / 28·8 (3.0) 825/825 RCT Aug 2016, to Jun 2017 R, CPR, MR, MPR, LBR, OPR, PR, EPR, PP, PH, PTD, GDM, PIH, LGA, SGA, NM Wennerholm 1997 [ 55 ] Birth after IVF with cryopreserved–thawed embryos in Sweden 34.0 ± 3.1/ 33.6 ± 3.3 209/209 Matched cohort study Jun1990 to Jul 1995 PH, PTD, GDM, PIH, LBW Wennerholm 2013 [ 56 ] Singletons conceived after FET in Denmark, Norway and Sweden 33.3 ± 4.0/33.7 ± 3.9 42,242/6647 Retrospective cohort study Until Dec 2007 PTD, LGA, SGA, VSGA, LBW, HBW, Wikland 2010 [ 57 ] Children born after vitrified BTor fresh BT 34.7 (22.0–44.0)/35.4 (26.3–45.3) 203/103 Retrospective cohort study Jan 2006 to May 2008 MR, LBR, PR, EPR, PP, PA, GDM, PIH, LGA, SGA, LBW, Wu 2014 [ 58 ] High responder patients diagnosed as primary infertility with more than 15 oocytes retrieved 29.02 ± 2.87/ 29.05 ± 2.48 50/69 Retrospective cohort study Jan to Nov 2012 IR, CPR, MPR, Wu 2019 [ 59 ] Patients with advanced endometriosis undergoing first embryo transfer cycles No statement 255/ 506 Retrospective cohort study Mar 2006 to Mar 2017 IR, CPR, MR, EPR, LBR, PTD, VPTD, LBW, VLBW Xiong 2019 [ 60 ] Women who underwent fresh or frozen ET 33.39 ± 3.75 /34.07 ± 4.14 101/ 179 Retrospective cohort study. Aug 2014 to Jul 2017. PR, IR, CPR, MR, MPR, OPR, LBR, SGA, LGA, Yang 2015 [ 61 ] Patients with P  > 6 nmol/L on the HCG day in IVF/ICSI cycle Between 20 and 40 years 43/42 Retrospective cohort study Mar 2011 to Mar 2012 IR, CPR, LBR, PR, Zhang 2018 [ 62 ] Women with PCOS 28.1 ± 3.1/28.4 ± 2.9 212/250 (singletons) Retrospective cohort study Jun 2013 to Jul 2015 GDM, PE, PTD, LGA, SGA ET Embryo transfer; FET Frozen embryo transfer; IVF In vitro fertilization; ICSI Intracytoplasmic sperm injection; PCOS Polycystic ovary syndrome; RCT Randomized controlled trial; OHSS Ovarian hyper-stimulation syndrome; SET Single embryo transfer; P Progesterone; ART Assisted reproductive technology; IR Implantation rate; PR Pregnancy rate; OPR Ongoing pregnancy rate; EPR Ectopic pregnancy rate; LBR Live birth rate; MR Miscarriage; MPR Multiple pregnancy rate; PH Postpartum haemorrhage; PA Placental abruption; PP Placenta previa; PTD Preterm delivery; VPTD Very preterm delivery; PROM Preterm rupture of membrane; NM Neonatal mortality; PM Perinatal mortality PE Pre-eclampsia; PIH Pregnancy-induced hypertension; LGA Large for gestational age; SGA Small for gestational age; VSGA Very small for gestational age; HBW High birth weight; VHBW Very high birth weight; LBW Low birth weight; VLBW Very low birth weight; Stil Stillbirth; BD Birth defects Flowchart showing the study selection process for the meta-analysis Characteristics of included studies ET Embryo transfer; FET Frozen embryo transfer; IVF In vitro fertilization; ICSI Intracytoplasmic sperm injection; PCOS Polycystic ovary syndrome; RCT Randomized controlled trial; OHSS Ovarian hyper-stimulation syndrome; SET Single embryo transfer; P Progesterone; ART Assisted reproductive technology; IR Implantation rate; PR Pregnancy rate; OPR Ongoing pregnancy rate; EPR Ectopic pregnancy rate; LBR Live birth rate; MR Miscarriage; MPR Multiple pregnancy rate; PH Postpartum haemorrhage; PA Placental abruption; PP Placenta previa; PTD Preterm delivery; VPTD Very preterm delivery; PROM Preterm rupture of membrane; NM Neonatal mortality; PM Perinatal mortality PE Pre-eclampsia; PIH Pregnancy-induced hypertension; LGA Large for gestational age; SGA Small for gestational age; VSGA Very small for gestational age; HBW High birth weight; VHBW Very high birth weight; LBW Low birth weight; VLBW Very low birth weight; Stil Stillbirth; BD Birth defects A total 6 RCT reported that the implantation rate (IR) was lower in the fresh BT group than in the frozen-thawed BT group (RR 0.79, 95% CI 0.70–0.90, P  = 0.0004, heterogeneity: I 2  = 65%) (Fig.  2 ). Compared with frozen-thawed BT, fresh BT was associated with a lower pregnancy rate (PR) according to 6 RCTs (RR 0.83, 95% CI 0.78–0.89, P  < 0.00001, heterogeneity: I 2  = 0%) (Fig.  3 ). Compared with women who underwent frozen-thawed BT, women who underwent fresh BT showed a decreased OPR according to 6 RCTs (RR 0.80, 95% CI 0.75–0.87, P  < 0.00001, heterogeneity: I 2  = 0%) (Fig.  4 ). The clinical pregnancy rate (CPR) was lower in the fresh BT group than in the frozen-thawed BT group according to 7 RCTs (RR 0.86, 95% CI 0.75–1.00, P  = 0.04, heterogeneity: I 2  = 56%) (Fig.  5 ). Six RCTs showed that fresh BT resulted in a significantly higher ectopic pregnancy rate (EPR) than frozen-thawed BT (RR 1.96, 95% CI 1.27–3.01, P  = 0.002, heterogeneity: I 2  = 0%) (Fig.  6 ). The above results indicate that frozen-thawed BT tends to result in higher IR, PR, OPR and CPR and lower EPR. According to the RCTs, the miscarriage rate (MR) (RR 0.86, 95% CI 0.65–1.13, P  = 0.27, heterogeneity: I 2  = 37%), MPR (RR 0.92, 95% CI 0.70–1.21, P  = 0.56, heterogeneity: I 2  = 30%) and LBR (RR 0.92, 95% CI 0.75–1.12, P =  0.41, heterogeneity: I 2  = 87%) showed no statistically significant differences between fresh BT and frozen-thawed BT (Appendix 4) (See Additional file  4 ). Fig. 2 Forest plot of comparison for implantation rate Fig. 3 Forest plot of comparison for pregnancy rate Fig. 4 Forest plot of comparison for ongoing pregnancy rate Fig. 5 Forest plot of comparison for clinical pregnancy rate Fig. 6 Forest plot of comparison for ectopic pregnancy rate Forest plot of comparison for implantation rate Forest plot of comparison for pregnancy rate Forest plot of comparison for ongoing pregnancy rate Forest plot of comparison for clinical pregnancy rate Forest plot of comparison for ectopic pregnancy rate In conclusion, our meta-analysis showed that fresh BT was associated with lower IR, PR, OPR, and CPR and higher EPR than frozen-thawed BT. There were no differences observed in the MR, MPR or LBR between fresh and frozen-thawed BT. To investigate whether fresh BT and frozen-thawed BT have different effects on maternal complications, we compared the incidence of PIH, pre-eclampsia, OHSS, PTD, GDM, PP, PA, PH, and PROM between the two groups. Lower incidences of PIH and pre-eclampsia were observed for fresh BT than for frozen-thawed BT (RR 0.74, 95% CI 0.63–0.87; P  = 0.0002, heterogeneity: I 2  = 57%) (Fig.  7 a). The incidence of GDM showed no statistically significant differences between the two groups (RR 0.94, 95% CI 0.83–1.06; P  = 0.32, heterogeneity: I 2  = 0%) (Fig. 7 b). Women who underwent fresh BT showed an increased risk of PA (RR 1.60, 95% CI 1.26–2.04; P =  0.0001, heterogeneity: I 2  = 0%) (Fig.  8 a). The risk of PP was higher for fresh BT than for frozen-thawed BT (RR 1.64, 95% CI 1.23–2.19; P  = 0.04, heterogeneity: I 2  = 60%) (Fig. 8 b). Compared with the frozen thawed BT group, the fresh group had higher risks of PTD (RR 1.24, 95% CI 1.13–1.36, P  < 0.00001, heterogeneity: I 2  = 73%) (Fig. 8 c) and VPTD (RR 1.27, 95% CI 1.14–1.54, P  = 0.037, heterogeneity: I 2  = 7%) (Appendix 5) (See Additional file 4 ). The incidence of PH (RR 1.00, 95% CI 0.57–1.74; P  = 0.99, heterogeneity: I 2  = 93%) and PROM (RR 1.05, 95% CI 0.77–1.45; P  = 0.74, heterogeneity: I 2  = 0%) did not differ significantly between fresh BT groups and frozen-thawed BT groups (Appendix 5) (See Additional file 4 ). Fig. 7 Forest plot of comparison for ( a ) PIH and pre-eclampsia and ( b ) GDM Fig. 8 Forest plot of comparison for ( a ) placental abruption, ( b ) placenta previa and ( c ) PTD Forest plot of comparison for ( a ) PIH and pre-eclampsia and ( b ) GDM Forest plot of comparison for ( a ) placental abruption, ( b ) placenta previa and ( c ) PTD In summary, the risks of PIH and pre-eclampsia are lower for fresh BT than for frozen-thawed BT, while the risks of PA, PP and PTD for fresh BT are higher than those for frozen-thawed BT. However, the two groups had similar incidences of GDM, PROM and PH. According to 12 studies, the LGA rate of the fresh BT group was lower (RR 0.62, 95% CI 0.57–0.67, P  < 0.00001, heterogeneity: I 2  = 39%) (Fig.  9 a). However, the SGA rate of the fresh BT group was higher than that of the frozen-thawed BT group according to the data from the 23 included studies (RR 1.24, 95% CI 1.13–1.36, P  < 0.00001, heterogeneity: I 2  = 73%) (Fig. 9 b). The RRs of HBW (RR 0.56 95% CI 0.51–0.61, P  < 0.00001, heterogeneity: I 2  = 57%) (Fig.  10 a) and VHBW (RR 0.51, 95% CI 0.36–0.71, P  < 0.0001, heterogeneity: I 2  = 16%) (Appendix 6) (See Additional file 4 ) in the fresh BT group showed an absolute decrease compared with those in the frozen thawed BT group. In contrast, the risks of LBW (RR 1.45, 95% CI 1.34–1.57, P  < 0.00001, heterogeneity: I 2  = 60%) (Fig.  10 b) associated with fresh BT showed an absolute increase when compared with those associated with frozen-thawed BT. No differences in VLBW (RR 0.97, 95% CI 0.55–1.70, P  = 0.92 heterogeneity: I 2  = 96%) were found (Appendix 6) (See Additional file 4 ). In addition, we investigated the differences in stillbirth, perinatal mortality and neonatal mortality between the two groups (Appendix 6) (See Additional file 4 ), and no significant differences were found. Fig. 9 Forest plot of comparison for ( a ) large for gestational age, ( b ) small for gestational age Fig. 10 Forest plot of comparison for ( a ) high birth weight > 4000 g and ( b ) low birth weight  4000 g and ( b ) low birth weight < 2500 g In conclusion, fresh BT tends to lead to SGA and LBW, while frozen-thawed BT has the opposite effect. The stillbirth, perinatal mortality and neonatal mortality risks showed no statistically significant differences between the two groups. From the data we have summarized, the risks of congenital anomalies and chromosomal aberrations of newborns associated with fresh BT showed an absolute increase when compared with frozen-thawed BT (RR 1.09 95% CI 1.02–1.17, P  = 0.009, heterogeneity: I 2  = 0%) (Fig.  11 a). Further inspection of the risk of different organ system malformations in newborns, including malformations in the circulatory system (Fig.  11 b), respiratory system (Fig.  11 c), nervous system (Fig.  11 d), gastrointestinal system, genitourinary system, eyes, ears, face, and musculoskeletal system (Appendix 7) (See Additional file 4 ), revealed no increased risk associated with frozen-thawed BT. The above data indicate that frozen-thawed BT is not a risk factor for neonatal malformations. Fig. 11 Forest plot of comparison for ( a ) congenital anomaly and chromosomal aberrations, ( b ) circulatory. System diseases, ( c ) respiratory system diseases and ( d ) nervous system diseases Forest plot of comparison for ( a ) congenital anomaly and chromosomal aberrations, ( b ) circulatory. System diseases, ( c ) respiratory system diseases and ( d ) nervous system diseases The publication bias could be assessed by using either a funnel plot subjectively and Eggers regression test objectively in Additional file  5 . For this review, funnel plots showed a symmetrical distribution. Egger’s regression test p -value on IR, PR, EPR, PIH &PE, GDM, PTD, LGA and SGA was more than 0.05 and which indicated the absence of publication bias. Egger’s tests yielding statistical evidence of publication bias at a p -value of OPR and CPR less than 0.05. In considering publication bias trim and fill meta-analysis was done. However, based on this analysis, no significant change was seen as compared with the main meta-analysis. Subgroup analysis was performed according to the design of the origin trials, cryopreservation method, endometrial preparation method (See Additional file  6 ). When both RCTs and NRCTs were included, we also reached a similar conclusion of higher IR, PR, OPR for frozen thawed BT, higher EPR for fresh BT, and no differences in CPR, LBR, MR or MPR. When using vitrification for blastocyst cryopreservation in frozen-thawed BT, the trials revealed higher IR, OPR, LGA and lower EPR, SGA for frozen-thawed BT and no differences in PR, CPR, LBR, MR, LBW or stillbirth. Trials adopting the slow-freezing protocol showed higher IR, PR, PIH, pre-eclampsia and LGA and lower LBR, SGA for frozen thawed BT, and no differences in OPR, CPR, MR, EPR, LBW or stillbirth were found. When using the artificial cycle of endometrial preparation in fresh BT, the trials presented higher IR, PR, OPR, PIH and pre-eclampsia, LGA in. for frozen thawed BT and no differences in CPR, LBR, EPR, GDM, PA, PTD, SGA or LBW. The trials using the natural cycle showed higher IR, PR, CPR, and LGA, lower PA for frozen thawed BT and no differences in OPR, LBR, EPR, PIH, pre-eclampsia, GDM or PTD and lower SGA, LBW for frozen thawed BT. Moreover, there were a total of 4 studies analysing women with high ovarian response (See Additional file  7 ). Women with a high ovarian response who underwent frozen-thawed BT showed a higher IR, OPR and CPR and no difference in PR compared to women who underwent fresh BT. We also conducted a separate meta-analysis on single BT (See Additional file  8 ). Women who underwent single BT showed a higher OPR and lower EPR for frozen-thawed BT and no difference in IR, PR or CPR. Sensitivity analysis was done to identify outlier studies. According to the analysis, when performing meta-analysis on PR, Belva 2008 exceeded the upper CI limit so this trial was excluded (Appendix 38) (Additional file  9 ). When performing the remaining meta-analysis, no influential studies were detected so all of the studies were included in the final analysis. Beyond subgroup analysis, meta-regression for the included studies was conducted to identify factors for heterogeneity Meta-regression model in terms of natural cycle on IR, vitrification on PR, natural cycle on CPR, and slow-freezing on EPR was significant ( P  < 0.05) (Additional file  10 ). However, the meta-regression for the remaining results is not statistically significant.

As cryopreservation technology has developed during the past few decades, the proportion of individual undergoing frozen blastocyst transfer (BT) has increased [ 1 ]. There have been concerns about the impact of cryopreservation on pregnancy outcomes, maternal complications and the health of the infant [ 2 ]. A few studies have compared pregnancy outcomes following fresh BT and cryopreserved-thawed BT in patients undergoing in vitro fertilization or intracytoplasmic sperm injection (IVF/ICSI) cycles [ 3 – 5 ]. However, the findings are controversial. A recent meta-analysis supported the hypothesis that single cryopreserved BT might not be a better choice than single fresh BT for patients undergoing IVF/ICSI [ 3 ]. However, another systematic review and meta-analysis suggested that pregnancy outcomes may be improved when frozen-thawed BT is performed [ 4 ]. With regard to maternal complications, Maheshwari et al. showed that frozen-thawed BT was associated with lower risks of postpartum haemorrhage (PH), placental abruption (PA), placenta previa (PP) and preterm delivery (PTD) than fresh BT and that the pregnancies arising from frozen-thawed BT seemed to have lower risks of maternal complications [ 2 ]. Shavit et al. reached the opposite conclusion that frozen-thawed BT may contribute to an increased risk of maternal complications such as preeclampsia and gestational diabetes mellitus (GDM) [ 6 ]. The latest randomized controlled trial reported that the incidence of preeclampsia was higher after frozen-thawed BT than after fresh BT, and the risk of moderate or severe ovarian hyperstimulation syndrome (OHSS) was similar in both groups [ 7 ]. Regarding the neonatal outcomes, an early review demonstrated that there were no significant differences in incidences of perinatal death or low birth weight of infants between fresh BT and frozen-thawed BT [ 8 ]. However, another review suggested that the incidences of small for gestational age (SGA), low birth weight (LBW), and perinatal mortality were lower in women who received frozen thawed BT [ 2 ]. There is growing concern regarding whether children born after frozen thawed BT have higher risks of congenital malformations than those born after fresh BT via IVF/ICSI. A register-based cohort study suggested that the risk for congenital malformation of the children born after frozen thawed BT was not higher than that of children born after fresh BT; in addition, no increased risks regarding the affected organ system were found between the two groups [ 9 ]. Due to limited sample sizes, past meta-analysis conclusions are controversial. With the emergence of new reports, there is an urgent need to perform a meta-analysis to compare the outcomes following fresh BT and frozen-thawed BT to provide guidance for clinical practice. The purpose of this meta-analysis was to examine pregnancy outcomes, maternal complications and neonatal malformations after frozen thawed BT versus those after fresh BT in an IVF/ICSI cycle and assess whether frozen thawed BT is a better choice than fresh BT.

Great advances have been made in cryopreservation culture techniques for embryos since the success of the first pregnancy resulting from frozen-thawed embryo transfer (FET) in 1983 [ 63 ]. This technique has been applied as a supplement to IVF and embryo transfer. FET has been accepted by every centre and has become an essential part of IVF/ICSI treatment. Therefore, the increased use of FET has increased the awareness of the safety of the technique [ 64 ]. This meta-analysis compared the outcomes of fresh BT and frozen-thawed BT in individuals undergoing IVF/ICSI cycles, with comprehensive assessment of the pregnancy outcomes, maternal complications, neonatal outcomes and malformations. Our study showed that frozen BT was associated with increased IR, PR, OPR, CPR, PIH, pre-eclampsia, LGA and HBW. Fresh BT was associated with increased EPR, OHSS, PP, PA, PTB, SGA, LBW, congenital anomalies and chromosomal aberrations in newborns. There were no differences in CPR, MR, MPR, LBR, PH or PROM between the two groups. With respect to pregnancy outcomes, frozen-thawed BT was associated with higher IR, PR, OPR and CPR than fresh BT. There was no difference in MR, MPR, or LBR. Recently, Zeng et al. showed that there was no difference in IR, CPR, MR, or MPR, but an increased LBR was found for fresh BT compared with that of cryopreserved thawed BT [ 3 ]. Roque et al. showed that frozen-thawed BT significantly improved CPR and OPR in patients undergoing IVF/ICSI cycles [ 4 ]. In general, there is more evidence that frozen-thawed BT is associated with better pregnancy outcomes than fresh BT. There may be several reasons, which are described as follows. Embryo implantation is one of the important steps for reproductive success, and implantation failure remains an unsolved problem in the field of IVF/ICSI. The primary cause of failure is the impairment of endometrial receptivity (ER), rather than the embryo itself being responsible for the failure [ 65 ]. A study suggested that impaired ER is more likely to occur in fresh ET cycles after ovarian stimulation than in FET cycles with artificial endometrial preparation. Impaired ER apparently accounted for most implantation failures in the fresh group [ 47 ]. Another explanation for the association of better pregnancy outcomes with frozen BT is that the physical effects of freezing and thawing embryos may filter out weaker embryos and allow only good quality embryos to survive, resulting in better foetal growth [ 50 ]. The incidence of EPR between the two groups varied in different studies. The inconsistent conclusions may be related to differences in the data included. A previous study reported that EPR was higher for frozen thawed BT [ 66 ]. However, our study suggested that frozen thawed BT was related to lower EPR, which is consistent with these studies [ 67 , 68 ]. The reason may be the high gonadotropin levels in ovarian stimulation cycles [ 68 ]. These findings also support the conclusions that a negative effect of ovarian stimulation on endometrial receptivity was reflected by increased EPR rates in the context of fresh BT. From the perspective of maternal complications, our research demonstrated that the risks of PA, PP and PTD are lower for frozen-thawed BT than for fresh BT. In contrast, the risks of PIH and preeclampsia associated with frozen-thawed BT are higher than those associated with fresh BT. Blazquez et al. suggested that FET pregnancies carry a higher risk of PIH and pre-eclampsia than fresh ET pregnancies, possibly indicating that the protocols currently used for endometrial reception of embryos have a deleterious effect on placentation, perhaps due to the long exposure to hormone replacement [ 69 ]. OHSS is an iatrogenic condition resulting from an excessive ovarian response to superovulation medication. According to a previous meta-analysis, no difference was found in OHSS between fresh BT and frozen-thawed BT [ 70 ]. However, the previous data were insufficient. In our studies, 4 trials involving freezing cycles triggered with HCG showed that the risk of OHSS was higher for fresh BT than for frozen-thawed BT. A few recent reviews demonstrated that singleton pregnancies after the transfer of frozen-thawed embryos were associated with lower risks of PTD and VPTD than those after fresh embryo transfer, which is in agreement with our research [ 2 , 71 – 73 ]. A recent meta-analysis showed that spontaneous preterm birth (SPTB) is increased in individuals undergoing IVF/ICSI [ 74 ]. The subgroup sensitivity analysis excluding FET revealed a higher risk of SPTB than that in the general group, supporting the hypothesis of lower prematurity risk in pregnancies from FET [ 74 ]. A recent meta-analysis of cohort studies showed that it is possible that a shift toward FET will determine a reduction in iatrogenic preterm birth. However, the authors advocated caution and further prospective studies to avoid the risk of increasing other negative obstetrics outcomes [ 75 ]. In regard to neonatal outcomes, our study suggested that there were lower risks of SGA and LBW in singleton pregnancies after frozen-thawed BT than in those after fresh BT, which was consistent with the previous meta-analysis [ 2 ]. However, the stillbirth and perinatal mortality and neonatal mortality rates were not significantly different between the two groups. Moreover, with respect to neonatal malformations, there were no differences between fresh BT and frozen-thawed BT. In conclusion, singleton pregnancies after frozen-thawed BT seem to have better neonatal outcomes than those after fresh BT, owing to lower risks of SGA and LBW. The reasons for the association of better neonatal outcomes with frozen BT than with fresh BT are not yet known. Evidence from a recent original study showed that uterine Doppler studies in pregnancies from frozen-thawed blastocysts present an approximately 15% lower uterine artery pulsatility index than those from fresh blastocysts, with a lower risk of SGA in the fresh group than in the frozen group, which is consistent with our conclusion [ 20 ] . In contrast to IVF with fresh embryo transfer, FET is usually performed in minimally stimulated or natural cycles. This lowers the risk of SGA and LBW after FET, which may be attributed to a luteal phase that mirrors the natural cycle, with favourable effects on the endometrium and early implantation [ 72 ]. Another probable explanation is related to the finding that controlled ovarian hyperstimulation (COH) was associated with poorer neonatal outcomes assessed by SGA and LBW in a recent study [ 76 ]. The results favouring frozen thawed BT instead of fresh BT may relate to the adverse effects of COH on ER [ 48 , 77 ]. Therefore, elective cryopreservation of viable embryos could be an alternative to avoid the deleterious effects of COH in embryo endometrium synchrony [ 12 , 47 ]. The major strength of this systematic review is the comprehensive literature search, identifying study subjects from a substantial number of relevant publications; another strength is the many pregnancy outcomes, maternal complications and neonatal outcomes the study evaluated between frozen and fresh BT to explore which method is better for mothers and infants. In addition, we conducted RCT and NRCT meta-analyses separately to improve the quality of evidence. However, the present meta-analysis also has some limitations, one of which was the significant heterogeneity in the pregnancy outcomes in the meta-analysis. We tried to find the source of heterogeneity by performing a subgroup analysis to examine the source of heterogeneity but were not able to identify the source. In addition, the baseline characteristics of patients differed among the included studies, including country, age, smoking status, duration of infertility, type of infertility, endometrial thickness, and cryopreservation type.

In summary, considering the higher IR, PR, OPR, and CPR; lower EPR; and decreased risks of OHSS, PA and PTD, as well as the incidences of SGA and LBW associated with frozen-thawed BT, there is an overall slight preponderance of risks in fresh cycles against frozen. However, frozen-thawed BT also has potential risks, such as LGA, PIH and pre-eclampsia. During the freezing process, there is a trade-off between the risk of pre-eclampsia hypertension and all other higher risks of fresh tranfers. In conclusion, the present review assessed the risks and magnitudes associated with fresh or frozen-thawed transfers, however it could not provide a final answer on the research question in object in the title. Therefore, individualization is required in order to choose the best procedure for each specific case according to the clinical needs.

Additional file 1: Appendix 1. PRISMA checklist. Additional file 2: Appendix 2. Sample search strategy used for PubMed. Additional file 3: Appendix 3. Risk of bias graph. Additional file 4: Appendices 4–7. Supplemental Figures. Additional file 5: Appendices 8–18. Publication bias. Additional file 6: Appendix 19–34. Subgroup analysis. Additional file 7: Appendix 35. Women with high ovarian response. Additional file 8: Appendix 36. Single blastocyst transfer. Additional file 9: Appendix 37–49. Sensitivity analysis. Additional file 10: Appendix 50. Meta regression. Additional file 1: Appendix 1. PRISMA checklist. Additional file 2: Appendix 2. Sample search strategy used for PubMed. Additional file 3: Appendix 3. Risk of bias graph. Additional file 4: Appendices 4–7. Supplemental Figures. Additional file 5: Appendices 8–18. Publication bias. Additional file 6: Appendix 19–34. Subgroup analysis. Additional file 7: Appendix 35. Women with high ovarian response. Additional file 8: Appendix 36. Single blastocyst transfer. Additional file 9: Appendix 37–49. Sensitivity analysis. Additional file 10: Appendix 50. Meta regression.