Mortality and major morbidities in very preterm infants born from assisted conception or naturally conceived: results of the area-based ACTION study

Births after Assisted Conception (AC) have increased in the last decades in industrialized countries, currently accounting for over 1% of all livebirths in the USA, nearly 2% in Italy and UK, and up to 6% in other European countries [1‐3]. As a consequence, concerns have been raised about possible increased risks of adverse pregnancy and infant outcomes, in particular after the use of assisted reproductive technologies (ART) that involve gamete manipulation outside the reproductive systems. Multiple pregnancy, placenta praevia, antepartum haemorrhage, incompetent cervix, pregnancy-induced hypertension, preterm birth, low birth weight, foetal growth restriction, birth defects, caesarean delivery, and admission of newborn babies to neonatal intensive care unit (NICU) have been reported [4‐7]. Risks appear to be higher in single compared to multiple births [8, 9]. Open issues still remain, mainly related to the potential confounding effects of maternal sociodemographic characteristics and lifestyles, the possibility of spontaneous reduction in case of multifoetal pregnancy, the effect of infertility “per se” and of the different technical approaches adopted [4].

Most of the adverse neonatal outcomes after AC are linked to the increased risk of prematurity. When the analysis was restricted to infants born before 32 weeks gestation (Very Preterm Infants, VPI) or with birth weight <1500 g (Very Low Birth Weight Infants, VLBWI), no excess mortality and morbidity linked to AC was found [10‐15]; nor there was an increased emotional burden in mothers after AC during the neonatal period [16]. However, with the exception of one area-based [12] and one multi-centre hospital based [10] studies, most of the evidence is derived from retrospective single-centre investigations [11, 13‐16].

In this study we used the data of a large area-based prospective cohort study aiming at comparing the neonatal outcomes of AC- and naturally conceived VPI, separately for singletons and multiples.

One hundred and thirty one mothers (4.9%) were excluded because mode of conception was unknown (Figure 1). AC was employed in 163 of the remaining 2529 mothers (6.4%). Details about the technique used were available for 113 births: in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) was used in 68% of them. The overall frequency of multiple births was 16.1% (n = 407): 73.0% (n = 119) in AC group and 12.2% (n = 288) in non-AC group. Liveborn infants were 2934 (314 following AC, 10.7%); 27.7% of them were multiples (n = 812), and 72.3% were singletons (n = 2122).

AC use was significantly more frequent when mothers were older and more educated, and less frequent in foreign mothers and after previous births (Table 1). No statistically significant differences in pregnancy complications, GA distribution and administration of antenatal steroids were found between non-AC and AC pregnancies. Twin, triplet and quadruplet births were more frequent following AC. Mothers with AC pregnancies were more likely to have a spontaneous onset of labour, be delivered in a tertiary centre, and have a caesarean section.

Infants’ characteristics and outcomes by plurality and mode of conception are shown in Table 2. Females were more frequent among AC singletons. Frequencies of mechanical ventilation, PDA, and BPD were lower in AC compared to non-AC multiples. A shorter length of hospitalization was observed in surviving AC multiples.

In multivariable analyses (Table 3), the aOR point estimates for hospital mortality and survival without major morbidities were 1.60 and 0.75 respectively in singletons, and 0.79 and 1.30 in multiples. The associations were not significant as all the CIs included unity. However, the statistical power estimates were low, ranging from 0.23 for mortality and 0.13 for survival without major morbidities in singletons, and 0.13 and 0.25 for the two outcomes, respectively, in multiples. We cannot therefore exclude that a much larger study might have led to statistically significant results.

Similar non-significant differences were found for the other morbidity outcomes in singletons, although in some cases the aOR point estimates were well above 2 (severe IVH) or below 0.5 (sepsis/meningitis). Among multiples, however, statistically significant lower risks for PDA (aOR 0.64, CI 0.45-0.90) and BPD (aOR 0.41, CI 0.20-0.87) were found, while for NEC the decreased risk (aOR 0.44, CI 0.19-1.02) was at borderline significance. The association between AC and PDA in multiples remained statistically significant after adjustment for mechanical ventilation (aOR 0.68, CI 0.48-0.97), and that with BPD did not change after controlling for ventilation or PDA, (aORs 0.42, CI 0.20-0.85, and 0.39, CI 0.18-0.84, respectively).

In this area-based cohort of very preterm infants we could not demonstrate clear differences in mortality and survival without major morbidities between naturally and AC-conceived babies.

To some extent our findings are comparable to those of previous studies in very preterm or VLBWI. Stewart et al. [10] studied 1473 VLBWI, and found no difference in cranial ultrasound abnormalities between naturally conceived babies and those born after ART or use of fertility therapy. In multiple VLBWI Hashimoto et al. [11] found no difference in mortality, BPD, and the combined outcome mortality or BDP between naturally conceived babies and those conceived following fertility treatment. In a large population of VLBWI, Schimmel et al. [12] found no difference in mortality, respiratory distress syndrome, PDA, NEC, IVH, BPD, and congenital malformations between babies born after IVF (n = 1396) and those naturally conceived (n = 6765). Messerschmidt et al. [13] compared 195 VLBWI born after IVF with 1228 naturally conceived VLBWI, and found no difference in mortality, short term pulmonary morbidity, severe cerebral morbidity and frequency of SGA babies. Shah et al. [14] compared the neonatal outcome of 137 multiple infants ≤32 weeks GA born after ART with that of 233 naturally conceived multiple babies with similar GA, and found no difference in outcome defined as a combination of death, grade 3/4 IVH or periventricular leukomalacia, ROP stage >2, and chronic lung disease. Picaud et al. [15] reported survival without severe morbidity in 612 infants <33 weeks GA: 81 were born following ART and 521 were naturally conceived. Using a composite morbidity index based on the occurrence of NEC, IVH grade ≥3, periventricular leukomalacia, and BPD, these authors found that survival without severe morbidity was higher in ART infants.

Most of the unfavourable neonatal outcomes reported when also moderate/late preterm and term infants are included in the study populations are probably the consequence of the shift of GA distribution toward lower values; this shift is predominantly related to the higher frequency of multiplicity, but it was observed also in single pregnancies [4, 8, 27‐29]. Causes of infertility, in adjunct to and independently from factors related to the reproductive technology itself, may also contribute to the unfavorable outcomes associated with AC [30]. However, when only very preterm or very low birth weight infants are considered, the effect of multiplicity on gestational age does not apply, and both AC- and naturally conceived infants are exposed to the adverse influence of very early birth and immaturity of organs. Additionally, AC pregnancies may benefit from the better prenatal and perinatal care associated with medically assisted reproduction, including earlier contact with the obstetric services and more careful monitoring of mother and foetus conditions [15, 31]. It is also possible that pre-pregnancy health and lifestyles of mothers determined to conceive and ultimately accessing AC services are more favourable than in naturally conceiving women and able to promote better perinatal outcomes [32].

Indeed in our study women using AC, although older than those who conceived naturally, did not seem to have increased rates of pregnancy inflammation/infection or disorders of placentation that have been linked with different patterns of placental pathologies and foetal/neonatal outcomes [19, 33, 34]. They were also more likely to be Italian and to have a higher education, and therefore have access to the information and contacts that facilitate healthier lifestyles and better health care.

We found that, compared to non-AC peers, AC multiples had a lower risk of BPD, and this result persisted after adjustment for PDA and mechanical ventilation, two possible antecedents of BPD. Previous studies reported inconclusive results about BPD. Schimmel et al. found no difference in risk of chronic lung disease in single and multiple VLBWI according to mode of conception [12], while Picaud et al. reported a lower BPD rates in infants <29 weeks gestation born after ART [15]. In contrast, Shah et al. found higher rates of BPD in ART preterm multiples less than 33 weeks gestation compared to naturally conceived peers [14].

These results are not directly comparable with ours because of differences in study design (centre-based rather than area-based) or eligibility criteria (birth weight rather than gestational age). Other studies including both preterm and at-term twins found better perinatal outcomes in ART- than in naturally conceived infants [31, 35]. Most unlikely these differences can be causally linked to specific ART treatment effect. As already discussed, better pre-pregnancy health and perinatal care associated with medically assisted reproduction may result in offspring with more favourable clinical conditions.

This study has limitations. As in most studies focusing on the special populations of very preterm or very low birth weight infants (about 1-1.5% of total births), sample size may be not large enough to detect the neonatal outcomes associated with AC. Also, we were not able to separately investigate the risks of the different AC technologies, particularly those involving manipulation of gametes outside the reproductive system, such as IVF and ICSI. Nevertheless, the worse outcome in AC than in non-AC singletons suggested by our findings, and the reverse trend in multiple babies, is in agreement with the worse outcomes in AC-conceived singletons reported in recent meta-analyses [29, 36].

The strengths of this study are the area-based prospective design, thus averting selection biases caused by a centre-based approach. Additionally, and unlike most previous studies, recruitment was based on GA, which prevented the bias arising when the birth weight criterion is employed to study the relationship between antenatal and perinatal factors and neonatal outcomes.

In our population of newborn infants <32 weeks GA, although a lower risk of some short-term outcomes, such as PDA and BPD, was found in AC-multiples, we could not demonstrate the presence or absence of different risks of mortality and survival without major morbidities in AC compared to non-AC conceived babies. A final conclusion about differences of outcomes in VPI born from assisted conception or naturally conceived cannot therefore be reached. Although some of our results may be of interest and suggest clues for clinical interpretations, larger and more powered studies are needed before confidently exclude the effects of AC on the short term outcomes of very preterm infants. To this end, this study can serve as a suitable pilot investigation.