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Erschienen in: Reproductive Biology and Endocrinology 1/2020

Open Access 01.12.2020 | Research

Number of embryos transferred and diagnosis of preeclampsia

verfasst von: Cynthia K. Sites, Donna Wilson, Dana Bernson, Sheree Boulet, Yujia Zhang

Erschienen in: Reproductive Biology and Endocrinology | Ausgabe 1/2020

Abstract

Background

Multiple births and first pregnancy are associated with higher preeclampsia risk. It is unknown if the transfer of multiple embryos or first embryo transfer with assisted reproductive technology (ART) is also associated with greater preeclampsia risk.

Methods

We performed a retrospective cohort study of IVF clinics and hospitals in Massachusetts. We used linked ART surveillance, birth certificate, and maternal hospitalization discharge data for 21,188 births, considering resident singleton (12,810) and twin (8378) live-births from autologous or donor eggs from 2005 to 2012. We used log binomial and Poisson regression to calculate adjusted relative risks (aRRs) and 95% confidence intervals (CI) for the association between preeclampsia and predictors of preeclampsia. Outcomes were stratified by singleton and twin birth, donor versus autologous cycles, and use of fresh versus cryopreserved embryos.

Results

Considering all singleton births, the transfer of multiple embryos increased the risk of preeclampsia [aRR = 1.10 (95% CI: 1.01–1.19)]. Relative risks were greatest for fresh non-donor cycles [aRR = 1.14 (95% CI: 1.03–1.26)]. Vanishing twin and number of prior ART cycles was not associated with preeclampsia among singleton births [aRR = 1.18 (95% CI: 0.91–1.53)], and aRR = 1.01 (95% CI: 0.96–1.05)], respectively. Considering all twin births, the transfer of > 2 embryos increased the risk of preeclampsia [aRR = 1.09 (95% CI: 1.001–1.19)]. Vanishing triplet and number of prior ART cycles were not associated with preeclampsia among twin births [aRR = 0.93 (95% CI: 0.69–1264), and aRR = 0.98 (CI: 0.95–1.02)], respectively.

Conclusions

Among ART births, the transfer of more than 1 embryo for singleton gestations and more than 2 embryos for twin gestations increased the risk for preeclampsia diagnosis.
Hinweise
Presented at the Annual Meeting of the American Society for Reproductive Medicine, October 28 – November 1, 2017, San Antonio, TX.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
ART
Assisted reproductive technology
aRRs
Adjusted relative risks
CI
Confidence interval
SMART
States Monitoring Assisted Reproductive Technology
CDC
Centers for Disease Control and Prevention
NASS
National Assisted Reproductive Technology Surveillance System
ICD-9-CM
Official system of assigning codes to diagnoses and procedures in the United States
BMI
Body mass index (kg/m2)
SAS
Analytics Software and Solutions

Background

Preeclampsia is defined by the American College of Obstetrics and Gynecology as maternal hypertension with end organ injury after 20 weeks’ gestation [1]. The incidence of preeclampsia is increasing worldwide, with manifestations that include proteinuria, thrombocytopenia, renal insufficiency, impaired liver function, pulmonary edema, visual symptoms, and maternal and fetal mortality [1].
The use of Assisted Reproductive Technology (ART) is reported to increase preeclampsia risk by 16% compared with spontaneous conception [2]. Other risk factors for preeclampsia include advanced maternal age, nulliparity, non-Hispanic Black race/ethnicity, obesity, multiple gestation, egg donor pregnancy, male infant, prior preeclampsia, chronic hypertension, diabetes mellitus, and embryo cryopreservation [1, 3, 4].
The increased rate of preeclampsia among twin births compared with singletons may be due to a larger placental mass or relative placental ischemia in twin gestations compared with singletons [5]. The transfer of multiple embryos often results in twins, but it is unknown if the transfer of multiple embryos increases the risk for preeclampsia.
Vanishing twin, or fetal resorption, is a fetus in a multi-gestation pregnancy that dies in utero, usually early in pregnancy, and is partially or completely reabsorbed [6]. The surviving infant in a vanishing twin ART pregnancy may be small for gestational age [7], or have greater risk for preterm delivery [8, 9] compared to ART pregnancies that were originally singletons. To date, we are unaware of prior reports of the effect of a vanishing twin on preeclampsia risk.
With spontaneous conceptions, the initial pregnancy is at greater risk for preeclampsia compared to subsequent pregnancies, 4.1% vs. 1.7%, which could be related to reduced prior exposure to paternal or fetal antigens in first pregnancies compared to those that follow [10, 11]. We are aware of only one small study considering the risk for preeclampsia in the initial ART cycle versus subsequent ART cycles, showing no difference between groups [12].
We hypothesized that preeclampsia diagnosis would be increased in singleton and twin gestations if more embryos were transferred compared with one embryo for singletons or two embryos for twins, and that the finding of vanishing twin would increase preeclampsia risk. Furthermore, we hypothesized that preeclampsia would be increased in the first ART cycle compared with subsequent ART cycles.

Methods

We used linked data from the States Monitoring ART (SMART) Collaborative, a project whereby the Centers for Disease Control and Prevention (CDC) links data from the National Assisted Reproductive Technology Surveillance System (NASS) to maternal hospital discharge and vital records from State Departments of Health in Connecticut, Massachusetts, and Michigan. Details about this linked data have been described previously [13, 14]. During the time of this analysis, only Massachusetts had all variables necessary for the analysis in hospital discharge data, so data from Connecticut and Michigan were excluded. The linkage rate was 88.5% for Massachusetts from 2005 to 2012.
We included resident births from ART in Massachusetts from 2005 to 2012 at > 20 weeks gestational age. Our study was approved by the Institutional Review Boards of the CDC and the Massachusetts Department of Public Health, and was deemed exempt by the Institutional Review Board at Baystate Medical Center.
We compared demographic and clinical characteristics of singleton and twin births, stratified by cycle type (autologous vs. donor egg, and fresh vs. cryopreserved embryo). Demographic and clinical variables were obtained from the NASS database (gravidity, parity, body mass index [BMI] at the start of the ART cycle, embryo transfer type, number of pregnancy sacs seen by initial ultrasound), birth certificates (number of infants born, gestational age, infant sex, mother’s age and race/ethnicity), and maternal hospital discharge information. Cells with n < 5 in tables were suppressed to protect confidentiality, per CDC and MA State Department of Health requirements.
We used ICD-9-CM codes from maternal hospital discharge information to identify the diagnosis of preeclampsia without and with severe features (642.40–642.54, and 642.50–642.5), pregestational diabetes (648.00), gestational diabetes (648.8), chronic hypertension (401.90) and gestational hypertension (642.0–642.04). An additional variable to identify women diagnosed with both preeclampsia and preterm (< 37 weeks) delivery was created by combining preeclampsia and preterm delivery information, as described previously [4]. We could not determine when the diagnosis of preeclampsia was made during gestation in this database.
Vanishing twin or vanishing triplet was identified if the number of fetal heartbeats by ultrasound at 6–8 weeks estimated gestational age was greater than the number of infants born [6]. If early ultrasound information was missing, cases were excluded (0.5% of singletons and 0.4% of twin births). The number of records dropped from the models due to missing data was low (< 1% for singleton births and < 2% for twin births). Maternal demographic variables were missing in < 1% of records, with the exception of maternal BMI, which was missing in 47% of cases. Mothers of twins were included only once in the analysis.
Chi-square and Fisher’s exact tests were used for bivariate comparisons. Continuous variables were compared with unpaired t-tests. We used log binomial and Poisson regression to calculate associations between preeclampsia and possible predictors (number of embryos transferred, finding of a vanishing twin or triplet, or prior ART cycles), stratified by singleton and twin birth and accounting for correlated responses of women with more than one record. Approximately 3% of singleton births had more than one record [15].
Results were calculated for all births and stratified by use of autologous vs. donor eggs and fresh vs. cryopreserved embryos due to heterogeneity of relationships between preeclampsia and predictors by cycle type. Covariates in the models were gravidity, infant sex, mother’s age, non-white race, maternal diabetes, and maternal hypertension. Two-tailed probabilities of < 0.05 were considered as significant. All analyses were conducted using SAS (SAS Institute, Cary, NC, USA).

Results

Maternal demographic and clinical characteristics are presented in Table 1. Our sample of 21,188 births from ART (12,810 singleton and 8378 twin) included a majority of patients who were nulliparous and Non-Hispanic White. Women having donor egg cycles were older than those having non-donor egg cycles.
Table 1
Demographic and clinical characteristics of singleton and twin births by oocyte source and embryo type
Characteristic N (%)
Singleton Birth
Twin Birth
Autologous
Donor
Autologous
Donor
Fresh (N = 10,137)
Cryopreserved (N = 1557)
Fresh (N = 861)
Cryopreserved (N = 363)
Fresh (N = 6742)
Cryopreserved (N = 809)
Fresh (N = 855)
Cryopreserved (N = 142)
Age, years (mean ± S.D.)
35.3 (4.1)
35.1 (3.9)
41.9 (4.4)
42.4 (4.4)
34.6 (3.8)
34.4 (3.8)
41.3 (4.8)
43.1 (4.1)
Infant sex: Male
5257 (51.9)
802 (51.5)
438 (50.9)
180 (49.6)
3435 (51.0)
429 (53.0)
433 (50.6)
75 (52.8)
Gravida = 1
4638 (45.8)
488 (31.4)
377 (44.1)
81 (22.5)
3263 (48.4)
305 (38.0)
373 (43.8)
38 (26.8)
Parity = 0
6834 (67.8)
784 (50.8)
627 (73.7)
187 (53.1)
4657 (69.5)
477 (59.9)
603 (71.4)
74 (52.1)
Body Mass Index (kg/m2)
  < 18.5
129 (2.4)
25 (3.1)
8 (1.9)
< 5
98 (2.7)
6 (1.4)
10 (2.7)
< 5
 18.5–24.9
3245 (59.1)
454 (56.2)
273 (63.3)
92 (55.8)
2092 (58.9)
256 (58.5)
246 (66.5)
38 (63.3)
 25–25.9
1260 (22.9)
203 (25.1)
96 (22.3)
44 (44 (26.7)
798 (22.5)
106 (24.2)
88 (23.8)
12 (20.0)
  > 30
859 (15.6)
126 (15.6)
54 (12.5)
27 (16.4)
567 (16.0)
70 (16.0)
26 (7.0)
8 (13.3)
 Missing (N)
4644
749
430
198
3187
371
495
82
Race/Ethnicity
 White, non-Hispanic
8428 (83.3)
1280 (82.2)
732 (85.3)
318 (87.6)
5641 (83.9)
671 (83.6)
765 (89.9)
114 (80.3)
 Black, non-Hispanic
327 (3.2)
65 (4.2)
26 (3.0)
10 (2.8)
182 (2.7)
36 (4.5)
20 (2.4)
6 (4.2)
 Hispanic
406 (4.0)
66 (4.2)
36 (4.2)
14 (3.9)
292 (4.3)
46 (5.7)
26 (3.1)
< 5
 American Indian
90 (0.9)
12 (0.8)
< 5
< 5
68 (1.0)
7 (0.9)
6 (0.7)
< 5
 Asian/Pacific Islander
869 (8.6)
134 (8.6)
57 (6.6)
20 (5.5)
542 (8.1)
43 (5.4)
34 (4.0)
20 (14.1)
Chronic hypertension
113 (1.1)
25 (1.6)
23 (2.7)
7 (1.9)
102 (1.5)
6 (0.7)
30 (3.5)
6 (4.2)
Gestational Hypertension
476 (4.7)
93 (6.0)
63 (7.3)
39 (10.7)
465 (6.9)
86 (10.6)
88 (10.3)
8 (5.6)
Diabetes
92 (0.9)
16 (1.0)
5 (0.6)
< 5
48 (0.7)
< 5
< 5
< 5
Gestational Diabetes
746 (7.4)
123 (7.9)
80 (9.3)
31 (8.5)
665 (9.9)
60 (7.4)
98 (11.5)
26 (18.3)
Infertility Diagnosis
 Tubal
819 (8.1)
135 (8.7)
8 (0.9)
6 (1.7)
472 (7.0)
85 (10.5)
6 (0.7)
< 5
 Ovulatory dysfunction
849 (6.6)
155 (10.0)
17 (2.0)
20 (5.5)
619 (9.2)
95 (11.7)
34 (4.0)
10 (7.0)
 Diminished ovarian reserve
455 (4.5)
25 (1.6)
404 (46.9)
140 (38.6)
220 (3.3)
6 (0.7)
372 (43.5)
52 (36.6)
 Endometriosis
415 (4.1)
61 (3.9)
11 (1.3)
< 5
273 (4.1)
34 (4.2)
14 (1.6)
6 (4.2)
 Uterine
116 (1.1)
19 (1.2)
< 5
< 5
70 (1.0)
6 (0.7)
< 5
< 5
 Male only
2441 (24.1)
382 (24.5)
18 (2.1)
< 5
1610 (23.9)
198 (24.5)
36 (4.2)
< 5
 Other
879 (8.7)
116 (7.5)
137 (15.9)
81 (22.3)
572 (8.5)
74 (9.2)
163 (19.1)
34 (23.9)
 Unknown
2532 (25.0)
388 (24.9)
54 (6.3)
25 (6.9)
1847 (27.4)
205 (25.3)
66 (7.7)
10 (7.0)
 Multiple female w/o male
512 (5.1)
98 (6.3)
88 (10.2)
40 (11.0)
317 (4.7)
24 (3.0)
76 (8.9)
14 (10.0)
 Multiple female + male
1119 (11.0)
178 (11.4)
122 (14.2)
40 (11.0)
742 (11.0)
82 (10.1)
86 (10.1)
8 (5.6)
Cells with N < 5 were suppressed to protect confidentiality
Table 2 depicts the frequencies of preeclampsia and of preeclampsia occurring with preterm delivery in each group, along with preeclampsia predictors (number of embryos transferred, number of prior ART cycles, and vanishing twin or triplet). In non-donor cycles, women having cryopreserved transfers were more likely to be diagnosed with preeclampsia or preeclampsia occurring with preterm delivery compared with those having fresh transfers. Overall, the mean number of embryos transferred was similar between groups. Women having prior ART cycles were more likely to have cryopreserved transfers compared to fresh transfers. Vanishing twins or triplets occurred in approximately 7% of cycles.
Table 2
Predictors of preeclampsia in singleton and twin births by oocyte source and embryo type
 
Singleton Birth
Twin Birth
Autologous
Donor
Autologous
Donor
Variable N (%)
Fresh (N=10137)
Cryopreserved (N=1557)
Fresh (N=861)
Cryopreserved (N=363)
Fresh (N=6742)
Cryopreserved (N=809)
Fresh (N=855)
Cryopreserved (N=142)
Preeclampsia
468 (4.6)
114 (7.3)
105 (12.2)
32 (8.8)
1148 (17.0)
172 (21.3)
230 (26.9)
42 (29.6)
Preeclampsia with preterm delivery
168 (1.7)
41 (2.6)
37 (4.3)
14 (3.9)
832 (12.3)
129 (16.0)
166 (19.4)
34 (23.9)
# of embryos transferred
 1
2006 (19.8)
453 (29.1)
152 (17.7)
99 (27.3)
70 (1.0)
22 (2.7)
<5
<5
 2
5614 (55.4)
802 (51.5)
674 (78.3)
212 (58.4)
4744 (70.4)
559 (69.1)
806 (94.3)
104 (73.4)
 3+
2517 (24.8)
302 (19.4)
35 (4.1)
52 (14.3)
1928 (28.6)
228 (28.2)
45 (5.3)
34 (23.9)
# embryos transferred (mean ± S.D.)
2.2 (1.0)
2.0 (0.8)
1.9 (0.5)
1.9 (0.7)
2.4 (0.9)
2.4 (0.8)
2.1 (0.3)
2.3 (0.6)
# prior ART cycles
 0
5240 (51.7)
249 (16.0)
362 (42.0)
43 (11.9)
3464 (51.4)
107 (13.2)
340 (39.8)
12 (8.5)
 1+
4896 (48.3)
13.8 (84.0)
499 (58.0)
320 (88.2)
3278 (48.6)
702 (86.8)
515 (60.2)
130 (91.6)
Vanishing twin/triplet
864 (8.5)
88 (5.8)
82 (9.6)
26 (7.4)
395 (5.9)
32 (4.1)
13 (1.5)
10 (7.3)
The results of the adjusted binomial and Poisson regression models for preeclampsia among singletons is shown in Table 3. Considering all singleton births, with the transfer of each additional embryo beyond 1, the risk of preeclampsia increased by 10%. Among births from fresh autologous embryos, number of embryos transferred was associated with preeclampsia [adjusted risk ratio (aRR) = 1.14 (95% confidence interval (CI): 1.03–1.26)]. Among singleton births from fresh donor egg transfer, preeclampsia risks were increased for those who had a prior ART cycle vs. a first ART cycle [aRR = 1.07 (95% CI: 1.001–1.14]. Preeclampsia was not associated with vanishing twin [aRR = 1.18 (95% CI: 0.91–1.53)], or with having a prior ART cycle when all singleton cycle types were considered together [aRR = 1.01 (95% CI: 0.96–1.05)].
Table 3
Adjusteda multivariable log binomial and Poisson regression models: single birth preeclampsia relative risk
 
All cycles N=12,810
Fresh Autologous N=10,110
Cryopreserved Autologous N=1,502
Fresh Donor N=849
Cryopreserved Donor N=349
aRR (CI)
p value
aRR (CI)
p value
aRR (CI)
p value
aRR (CI)
p value
aRR (CI)
p value
# embryos transferred (continuous)
1.10 (1.01, 1.19)
0.045
1.14 (1.03, 1.26)
0.018
1.14 (0.90, 1.44)
0.309
0.80 (0.56, 1.15)
0.222
0.90 (0.58, 1.39)
0.628
# prior ART cycles (continuous)
1.01 (0.96, 1.05)
0.724
0.99 (0.92, 1.05)
0.659
0.96 (0.86, 1.08)
0.495
1.07 (1.001, 1.14)
0.038
0.98 (0.87, 1.11)
0.742
Vanishing twin (yes vs. no)
1.18 (0.91, 1.53)
0.268
1.03 (0.72, 1.44)
0.911
1.62 (0.84, 3.14)
0.236
1.35 (0.79, 2.33)
0.277
1.31 (0.40, 4.32)
0.697
acontrolling for cycle type (all cycles model only), gravida, infant sex, mother's age, non-White race, diabetes and hypertension
Referent values:
Total embryos: Continuous
Prior ART: Continuous
Vanishing twin: No
Cycle type: Fresh non-donor
Gravida: Continuous
Infant sex: Male
Mother's age: Continuous
Non-White race: White
Diabetes: No
Hypertension: No
The results of the adjusted binomial and Poisson regression model for preeclampsia among twin births is shown in Table 4. Considering all cycles, with each additional embryo transferred greater than 2, the risk of preeclampsia increased by 9%. However, there was no association with the finding of a vanishing triplet [aRR = 0.93 (95% CI: 0.69–1.26)]. History of prior ART cycles had no effect on preeclampsia diagnosis among twin gestations considered together or as separate groups.
Table 4
Adjusteda multivariable log binomial and Poisson regression models: twin birth preeclampsia relative risk
 
All cycles N=8,378
Fresh Autologous N=6,650
Cryopreserved Autologous N=753
Fresh Donor N=841
Cryopreserved Donor N=134
aRR (CI)
p value
aRR (CI)
p value
aRR (CI)
p value
aRR (CI)
p value
aRR (CI)
p value
# embryos transferred (continuous)
1.09 (1.001, 1.19)
0.040
1.07 (0.98, 1.17)
0.137
1.03 (0.84, 1.28)
0.722
0.58 (0.24, 1.41)
0.232
1.49 (0.69, 3.19)
0.300
# prior ART cycles (continuous)
0.98 (0.95, 1.02)
0.406
0.99 (0.96, 1.02)
0.701
1.13 (0.99, 1.28)
0.062
0.97 (0.89, 1.06)
0.548
1.01 (0.89, 1.16)
0.854
Vanishing triplet (yes vs. no)
0.93 (0.69, 1.26)
0.639
0.93 (0.78, 1.11)
0.453
0.86 (0.32, 2.31)
0.766
1.53 (0.42, 5.52)
0.519
0.28 (0.01, 7.76)
0.451
acontrolling for cycle type (all cycles model only), gravida, infant sex, mother's age, non-White race, diabetes and hypertension
Referent values:
Total embryos: Continuous
Prior ART: Continuous
Vanishing twin: No
Cycle type: Fresh non-donor
Gravida: Continuous
Infant sex: Male
Mother's age: Continuous
Non-White race: White
Diabetes: No
Hypertension: No

Discussion

We report that the transfer of > 1 embryo with singleton gestations and > 2 embryos with twin gestations increased the risk of preeclampsia diagnosis. The transfer of multiple embryos may result in multiple implantations with an increased placental mass, or relative placental ischemia, which could increase preeclampsia risk [5]. However, we did not find that the presence of a vanishing twin or triplet by early ultrasound increased the risk of preeclampsia, which may be related to the definition of vanishing twin, which requires fetal cardiac activity by ultrasound [6]. We hypothesized that women having their first ART cycle would have greater risk of preeclampsia than those having subsequent cycles due to reduced exposure to new paternal or fetal antigens, but our data did not support this.
It is biologically plausible that early implantations that do not progress to viability with fetal cardiac activity could increase preeclampsia risk. One theory of preeclampsia development involves greater genetic or immune incompatibility between mother and fetuses in dichorionic twin gestations compared to monochorionic twin or singleton gestations [16]. Maternal natural killer cells may interact with paternal human leukocyte antigens, with a cytotoxic T-cell response leading to the development of preeclampsia [17, 18]. In twin gestations, women are exposed to a greater number of fetal antigens compared to women with singleton gestations, with the possibility of triggering a greater immune response, increasing the development of preeclampsia. Our database was unable to identify early gestational sacs (implantations) before viability was confirmed by ultrasound, which may have contributed to increased preeclampsia risk when multiple embryos were transferred.
An effect of vanishing twin on early placentation has been reported previously. Specifically, the surviving infant of a vanishing twin ART pregnancy is reported to be smaller for gestational age [7], and be more likely to deliver preterm [8, 9] compared with ART gestations that were originally singletons. In addition, the later that the vanishing twin occurred in gestation, the greater the risk for the singleton survivor to have a birthweight < 2500 g [7]. Furthermore, preterm and extremely preterm delivery were increased with singleton survivors, especially with late vanishing twin pregnancies [9]. In our study, we compared fetal heartbeats by ultrasound early in gestation to number of infants born, and were unable to determine specifically when the vanishing twin or triplet occurred in gestation after viability was confirmed.
The incidence of vanishing twin/triplet is reported to occur in 50% of pregnancies that have at least three gestational sacs initially, and in 36% of pregnancies with two gestational sacs initially [19]. Among ART conceptions, it may occur in 12–30% of conceptions [20]. Our 7% overall incidence of vanishing twin with ART was somewhat lower than 12–30%, possibly due to the trend toward elective single embryo transfer in recent years in Massachusetts.
We found that cryopreserved autologous embryo transfer with singleton birth resulted in a 1.59-fold increase in preeclampsia compared to fresh transfer with singleton birth. During this time period in Massachusetts, endometrial preparation for cryopreserved embryo transfers was usually “artificial” or with hormone replacement therapy rather than by natural corpus luteum hormone production or by “natural” cycle. A recent study reported an association between the absence of a corpus luteum, as would be seen with artificial or hormone replacement therapy, and higher rates of preeclampsia, compared to natural cycle frozen embryo transfer [21]. It is possible that our finding of a higher incidence of preeclampsia diagnosis with cryopreserved autologous transfers compared to fresh transfers is related to absence of a corpus luteum with these cryopreserved embryo transfers [22]. Our finding of similar rates of preeclampsia in cryopreserved and fresh embryo transfers following donor egg cycles, where no corpora lutea were likely present in either type of cycle, support this hypothesis. Our database did not include information about endometrial preparation, so we cannot confirm this finding.
Our finding that the first embryo transfer did not increase preeclampsia risk compared to subsequent embryo transfers is similar to a smaller study of 364 patients that reported no differences in preeclampsia rates between those who conceived following the first embryo transfer and those who conceived after two or more transfers [12]. Our finding of a small increased risk for preeclampsia in singleton fresh donor egg gestations following subsequent embryo transfer compared to first embryo transfer was unexpected. Although we adjusted for maternal age and other known confounders, there could be residual confounding, or this finding may have been due to chance.
Our study had several strengths as well as a few limitations. We considered a large database, with high linkage of all ART cases to hospital and vital records of infant deliveries in a single state. We controlled for multiple confounders of preeclampsia diagnosis in the multivariable models. Nearly all pregnancies had early ultrasounds to detect fetal heart beats, with < 1% excluded for missing early ultrasounds. However, we were unable to determine in which trimester the vanishing twin/triplet occurred in our study, and were unable to determine if a gestational sac was present without cardiac activity by ultrasound. The definition of prior ART cycles included cycles with a prior embryo transfer, but could not determine whether these prior cycles were fresh or cryopreserved-thawed. In addition, we had no information about history of preeclampsia in prior pregnancies, and we assume that the birth certificate estimate of gestational age accurately reflects the known gestational age based on the date of embryo transfer. Finally, there may be ICD-9-CM coding errors for diagnosis of preeclampsia among different providers. Women with a diagnosis of chronic hypertension (642.7) or gestational hypertension (642.0–642.04) may have been classified as having preeclampsia, but we considered these diagnoses and controlled for them in our analysis as coded.

Conclusions

The policy of single embryo transfer, in addition to its known reduction in multiple births and prematurity, may also reduce preeclampsia risk. Given the increased trend toward performing cryopreserved embryo transfers, it is relevant that we did not find that transferring more cryopreserved embryos was correlated to preeclampsia diagnosis. Understanding how increasing single embryo transfer, in addition to its known reduction in multiple births and prematurity, may also reduce the risk for preeclampsia, is important for patient and provider awareness and care delivery policies.

Acknowledgements

Not applicable.
Approved by the IRB of the MA Department of Public Health and by the Center for Disease Control and Prevention. Deemed exempt by the IRB at Baystate Medical Center. No patient consent was required for this retrospective cohort study.
All authors have reviewed the manuscript and consent for publication.

Competing interests

None.
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Literatur
1.
Zurück zum Zitat American College of Obstetricians and Gynecologists, Task Force on Hypertension in Pregnancy. Hypertension in pregnancy. Report of the American College of Obstetricians and Gynecologists’ Task Force on Hypertension in Pregnancy. Obstet Gynecol. 2013;122:1122–31.CrossRef American College of Obstetricians and Gynecologists, Task Force on Hypertension in Pregnancy. Hypertension in pregnancy. Report of the American College of Obstetricians and Gynecologists’ Task Force on Hypertension in Pregnancy. Obstet Gynecol. 2013;122:1122–31.CrossRef
2.
Zurück zum Zitat Opdahl S, Henningsen AA, Tiitinen A, Bergh C, Pinborg A, Romundstad PR, et al. Risk of hypertensive disorders in pregnancies following assisted reproductive technology: a cohort study from the CoNARTaS group. Hum Reprod. 2015;30:1724–31.CrossRef Opdahl S, Henningsen AA, Tiitinen A, Bergh C, Pinborg A, Romundstad PR, et al. Risk of hypertensive disorders in pregnancies following assisted reproductive technology: a cohort study from the CoNARTaS group. Hum Reprod. 2015;30:1724–31.CrossRef
3.
Zurück zum Zitat Barsky M, St. Marie P, Rahil T, Markenson GR, Sites CK. Are perinatal outcomes affected by blastocyst vitrification and warming? Am J Obstet Gynecol. 2016;215:603e1–5.CrossRef Barsky M, St. Marie P, Rahil T, Markenson GR, Sites CK. Are perinatal outcomes affected by blastocyst vitrification and warming? Am J Obstet Gynecol. 2016;215:603e1–5.CrossRef
4.
Zurück zum Zitat Sites CK, Wilson MS, Barsky M, Bernson D, Bernstein IM, Boulet S, Zhang Y. Embryo cryopreservation and preeclampsia risk. Fertil Steril. 2017;108:784–90.CrossRef Sites CK, Wilson MS, Barsky M, Bernson D, Bernstein IM, Boulet S, Zhang Y. Embryo cryopreservation and preeclampsia risk. Fertil Steril. 2017;108:784–90.CrossRef
5.
Zurück zum Zitat Bdolah Y, Lam C, Rajakumar A, Shivalingappa V, Mutter W, Sachs BP, et al. Twin pregnancy and the risk of preeclampsia: bigger placenta or relative ischemia? Am J Obstet Gynecol. 2008;198:428.e1–6.CrossRef Bdolah Y, Lam C, Rajakumar A, Shivalingappa V, Mutter W, Sachs BP, et al. Twin pregnancy and the risk of preeclampsia: bigger placenta or relative ischemia? Am J Obstet Gynecol. 2008;198:428.e1–6.CrossRef
6.
Zurück zum Zitat Magnus MC, Ghaderi S, Morken N-H, Magnus P, Romundstad LB, Skjaerven R, et al. Vanishing twin syndrome among ART singletons and pregnancy outcomes. Hum Reprod. 2017;32:2298–304.CrossRef Magnus MC, Ghaderi S, Morken N-H, Magnus P, Romundstad LB, Skjaerven R, et al. Vanishing twin syndrome among ART singletons and pregnancy outcomes. Hum Reprod. 2017;32:2298–304.CrossRef
7.
Zurück zum Zitat Pinborg A, Lidegaard O, Freiesleben NI, Andersen AN. Vanishing twins: a predictor of small-for-gestational age in IVF singletons. Hum Reprod. 2007;22:2707–14.CrossRef Pinborg A, Lidegaard O, Freiesleben NI, Andersen AN. Vanishing twins: a predictor of small-for-gestational age in IVF singletons. Hum Reprod. 2007;22:2707–14.CrossRef
8.
Zurück zum Zitat Luke B, Stern JE, Kotelchuck M, Declercq ER, Hornstein MD, Gopal D, et al. Adverse pregnancy outcomes after in vitro fertilization: effect of number of embryos transferred and plurality at conception. Fertil Steril. 2015;104:79–86.CrossRef Luke B, Stern JE, Kotelchuck M, Declercq ER, Hornstein MD, Gopal D, et al. Adverse pregnancy outcomes after in vitro fertilization: effect of number of embryos transferred and plurality at conception. Fertil Steril. 2015;104:79–86.CrossRef
9.
Zurück zum Zitat Zhou L, Gao X, Wu Y, Zhang Z. Analysis of pregnancy outcomes for survivors of the vanishing twin syndrome after in vitro fertilization and embryo transfer. Eur J Obstet Gynecol Reprod Biol. 2016;203:35–9.CrossRef Zhou L, Gao X, Wu Y, Zhang Z. Analysis of pregnancy outcomes for survivors of the vanishing twin syndrome after in vitro fertilization and embryo transfer. Eur J Obstet Gynecol Reprod Biol. 2016;203:35–9.CrossRef
10.
Zurück zum Zitat Hernandez-Diaz S, Toh S, Cnattingius S. Risk of pre-eclampsia in first and subsequent pregnancies: prospective cohort study. BMJ. 2009;338:b2255.CrossRef Hernandez-Diaz S, Toh S, Cnattingius S. Risk of pre-eclampsia in first and subsequent pregnancies: prospective cohort study. BMJ. 2009;338:b2255.CrossRef
11.
Zurück zum Zitat Einarsson JI, Sangi-Haghpeykar H, Gardner MO. Sperm exposure and development of preeclampsia. Am J Obstet Gynecol. 2003;188(5):1241–3.CrossRef Einarsson JI, Sangi-Haghpeykar H, Gardner MO. Sperm exposure and development of preeclampsia. Am J Obstet Gynecol. 2003;188(5):1241–3.CrossRef
12.
Zurück zum Zitat Tsoumpou I, Mohamed AM, Tower C, Roberts SA, Nardo LG. Failed IVF cycles and the risk of subsequent preeclampsia or fetal growth restriction: a case-control exploratory study. Fertil Steril. 2011;95:973–8.CrossRef Tsoumpou I, Mohamed AM, Tower C, Roberts SA, Nardo LG. Failed IVF cycles and the risk of subsequent preeclampsia or fetal growth restriction: a case-control exploratory study. Fertil Steril. 2011;95:973–8.CrossRef
13.
Zurück zum Zitat Mneimneh AS, Boulet SL, Sunderam S, Zhang Y, Jameson DJ, Crawford S, et al. States monitoring assisted reproductive technology (SMART) collaborative: data collection, linkage, dissemination, and use. J Women's Health (Larchmt). 2013;22:571–7.CrossRef Mneimneh AS, Boulet SL, Sunderam S, Zhang Y, Jameson DJ, Crawford S, et al. States monitoring assisted reproductive technology (SMART) collaborative: data collection, linkage, dissemination, and use. J Women's Health (Larchmt). 2013;22:571–7.CrossRef
14.
Zurück zum Zitat Zhang Y, Cohen B, Macaluso M, Zhang Z, Durant T, Nannini A. Probabilistic linkage of assisted reproductive technology information with vital records, Massachusetts 1997-2000. Matern Child Health J. 2012;16:1703–8.CrossRef Zhang Y, Cohen B, Macaluso M, Zhang Z, Durant T, Nannini A. Probabilistic linkage of assisted reproductive technology information with vital records, Massachusetts 1997-2000. Matern Child Health J. 2012;16:1703–8.CrossRef
15.
Zurück zum Zitat Robbins AS, Chao SY, Fonseca VP. What’s the relative risk? A method to directly estimate risk ratios in cohort studies of common outcomes. Ann Epidemiol. 2002;12:452–4.CrossRef Robbins AS, Chao SY, Fonseca VP. What’s the relative risk? A method to directly estimate risk ratios in cohort studies of common outcomes. Ann Epidemiol. 2002;12:452–4.CrossRef
16.
Zurück zum Zitat Sparks TN, Cheng YW, Phan N, Caughey AB. Does risk of preeclampsia differ by twin chorionicity? J Matern Fetal Neonatal Med. 2013;26(13):1273–7.CrossRef Sparks TN, Cheng YW, Phan N, Caughey AB. Does risk of preeclampsia differ by twin chorionicity? J Matern Fetal Neonatal Med. 2013;26(13):1273–7.CrossRef
17.
Zurück zum Zitat Stevenson AC, Davison BCC, Say B, et al. Contribution of fetal/maternal incompatibility to aetiology of pre-eclamptic toxaemia. Lancet. 1971;2:1286–9.CrossRef Stevenson AC, Davison BCC, Say B, et al. Contribution of fetal/maternal incompatibility to aetiology of pre-eclamptic toxaemia. Lancet. 1971;2:1286–9.CrossRef
18.
Zurück zum Zitat De Groot CJ, van der Mast BJ, Visser W, et al. Preeclampsia is associated with increased cytotoxic T-cell capacity to paternal antigens. Am J Obstet Gynecol. 2010;203:496.e1–6.CrossRef De Groot CJ, van der Mast BJ, Visser W, et al. Preeclampsia is associated with increased cytotoxic T-cell capacity to paternal antigens. Am J Obstet Gynecol. 2010;203:496.e1–6.CrossRef
19.
Zurück zum Zitat Dickey RP, Taylor SN, Lu PY, Sarton BM, Storment JM, Rye PH, et al. Spontaneous reduction of multiple pregnancy: incidence and effect on outcome. Am J Obstet Gynecol. 2002;186:77–83.CrossRef Dickey RP, Taylor SN, Lu PY, Sarton BM, Storment JM, Rye PH, et al. Spontaneous reduction of multiple pregnancy: incidence and effect on outcome. Am J Obstet Gynecol. 2002;186:77–83.CrossRef
20.
Zurück zum Zitat Gjerris AC, Tabor A, Loft A, Christiansen M, Pinborg A. First trimester prenatal screening among women pregnant after IVF/ICSI. Hum Reprod Update. 2012;18:350–9.CrossRef Gjerris AC, Tabor A, Loft A, Christiansen M, Pinborg A. First trimester prenatal screening among women pregnant after IVF/ICSI. Hum Reprod Update. 2012;18:350–9.CrossRef
21.
Zurück zum Zitat Von Versen-Hoynck F, Schaub AM, Chi YY, et al. Increased preeclampsia risk and reduced aortic compliance with in vitro fertilization cycles in the absence of a corpus luteum. Hypertension. 2019;73:640–9.CrossRef Von Versen-Hoynck F, Schaub AM, Chi YY, et al. Increased preeclampsia risk and reduced aortic compliance with in vitro fertilization cycles in the absence of a corpus luteum. Hypertension. 2019;73:640–9.CrossRef
22.
Zurück zum Zitat Orvieto R, Kirshenbaum M, Gleicher N. Is embryo cropreservation causing macrosomia—and what else? Front Endocrinol. 2020;11:1–6.CrossRef Orvieto R, Kirshenbaum M, Gleicher N. Is embryo cropreservation causing macrosomia—and what else? Front Endocrinol. 2020;11:1–6.CrossRef
Metadaten
Titel
Number of embryos transferred and diagnosis of preeclampsia
verfasst von
Cynthia K. Sites
Donna Wilson
Dana Bernson
Sheree Boulet
Yujia Zhang
Publikationsdatum
01.12.2020
Verlag
BioMed Central
Erschienen in
Reproductive Biology and Endocrinology / Ausgabe 1/2020
Elektronische ISSN: 1477-7827
DOI
https://doi.org/10.1186/s12958-020-00627-7

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