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Intrapartum exposure to synthetic oxytocin, maternal BMI, and neurodevelopmental outcomes in children within the ECHO consortium

Abstract

Background

Synthetic oxytocin (sOT) is frequently administered during parturition. Studies have raised concerns that fetal exposure to sOT may be associated with altered brain development and risk of neurodevelopmental disorders. In a large and diverse sample of children with data about intrapartum sOT exposure and subsequent diagnoses of two prevalent neurodevelopmental disorders, i.e., attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD), we tested the following hypotheses: (1) Intrapartum sOT exposure is associated with increased odds of child ADHD or ASD; (2) associations differ across sex; (3) associations between intrapartum sOT exposure and ADHD or ASD are accentuated in offspring of mothers with pre-pregnancy obesity.

Methods

The study sample comprised 12,503 participants from 44 cohort sites included in the Environmental Influences on Child Health Outcomes (ECHO) consortium. Mixed-effects logistic regression analyses were used to estimate the association between intrapartum sOT exposure and offspring ADHD or ASD (in separate models). Maternal obesity (pre-pregnancy BMI ≥ 30 kg/m2) and child sex were evaluated for effect modification.

Results

Intrapartum sOT exposure was present in 48% of participants. sOT exposure was not associated with increased odds of ASD (adjusted odds ratio [aOR] 0.86; 95% confidence interval [CI], 0.71–1.03) or ADHD (aOR 0.89; 95% CI, 0.76–1.04). Associations did not differ by child sex. Among mothers with pre-pregnancy obesity, sOT exposure was associated with lower odds of offspring ADHD (aOR 0.72; 95% CI, 0.55–0.96). No association was found among mothers without obesity (aOR 0.97; 95% CI, 0.80–1.18).

Conclusions

In a large, diverse sample, we found no evidence of an association between intrapartum exposure to sOT and odds of ADHD or ASD in either male or female offspring. Contrary to our hypothesis, among mothers with pre-pregnancy obesity, sOT exposure was associated with lower odds of child ADHD diagnosis.

Background

For over 50 years, synthetic oxytocin (sOT), an exogenous neuropeptide and uterine stimulant (trade names Pitocin® and Syntocinon®), typically administered to the pregnant individual by intravenous infusion, has been increasingly used as a first line approach to induce and/or augment labor by stimulating uterine contractions [1,2,3,4,5,6]. Administration of sOT as a single agent for labor induction and/or augmentation assists in the expulsion of the fetus in the setting of childbirth complications [7] and may minimize risk of instrumental deliveries [8]. However, despite the increasing frequency with which sOT is administered to pregnant women [9,10,11], only a few large studies have characterized the relationship of intrapartum sOT and child neurodevelopmental outcome. One of the largest studies (n = 1.5 million), based on a national cohort of Scandinavian children, found an approximately 20% increased risk of attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) associated with sOT exposure. However, authors were reassured regarding clinical use of sOT as confounder adjustment attenuated this association [12].

Child neurodevelopmental outcomes following intrapartum sOT exposure have not been studied in large samples of children born in the United States (US) [13, 14], where obstetric medical practices may differ from those of other countries [15]. Among existing studies, some report associations between sOT exposure and ADHD and/or ASD [13, 14, 16,17,18,19], some report mixed results [20,21,22,23,24,25], and some report no associations [12, 26,27,28,29]. Preclinical models provide evidence of potential neuroprotective effects of endogenous oxytocin; however, if pulsatile uterine contractions are excessively prolonged by treatment with exogenous sOT, uteroplacental perfusion can be reduced to an extent sufficient to alter brain development [30]. Thus, a greater understanding is needed regarding the relationship of fetal intrapartum exposure to sOT and the risk(s) of child neurodevelopmental outcomes.

ADHD and ASD are among the most prevalent neurodevelopmental disorders with poorly understood etiology. ADHD, a disorder characterized by symptoms of inattention, distractibility, impulsivity, hyperactivity and behavioral dysregulation [31], affects almost 10% of US children [32, 33]. ASD, characterized by deficits in social interaction and social communications with restricted or repetitive patterns of behavior and interests [34], affects 1 in 36 [35] eight-year-old US children [36]. ADHD and ASD demonstrate high diagnostic comorbidity [37], and represent the two most prevalent developmental disabilities among children aged 3 to 17 years in the US and other high-income countries [38, 39]. In addition, the unique constellation of behavioral characteristics typified by children diagnosed with ADHD and/or ASD have long posed significant burdens within the familial and educational settings [40,41,42,43]. Importantly, the steadily rising prevalence of both ADHD and ASD impel an urgent need to identify modifiable risk factors [44,45,46,47,48]. The poorly understood etiology, comorbidity, and prevalence of ADHD and ASD prompted our examination of the association between intrapartum sOT exposure and these specific neurodevelopmental conditions.

Because females and males differ with respect to neurodevelopmental vulnerability [17, 49] and males experience increased risk of both ADHD and ASD [50], we evaluated sex differences in the associations between sOT and neurodevelopmental outcomes. In addition, because mothers with obesity exhibit poor uterine contractility as compared to non-obese mothers, and therefore often require sOT induction to facilitate labor (50–53), we evaluated maternal pre-pregnancy obesity (e.g. BMI) as a potential effect measure modifier [51]. Here we tested three hypotheses: (1) Intrapartum exposure to sOT is associated with increased odds of child ADHD or ASD; (2) associations differ across sex; (3) associations between intrapartum sOT exposure and ADHD or ASD would be accentuated in offspring of mothers with pre-pregnancy obesity.

Methods

Data source

We used data from a large consortium, the Environmental influences on Child Health Outcomes (ECHO) program, to evaluate the association between intrapartum sOT and offspring ADHD and ASD. The ECHO program is a consortium of longitudinal cohort studies established by the National Institutes of Health (NIH) to examine the impacts of various exposures – chemical, biological, physical, and social – in relation to child health and development [52]. Specifically, ECHO research focuses on childbirth and perinatal outcomes, respiratory illness, obesity, neurodevelopment, and overall wellness, relying on a protocol of harmonized derived variables among cohort sites [53,54,55]. The study protocol was approved by the cohort-specific and/or the single ECHO Institutional Review Boards. Written informed consent was obtained for ECHO Cohort Data Collection Protocol participation and for participation in specific cohorts.

The study population included 12,503 biological mother/child pairs enrolled in 44 ECHO cohorts. The 44 cohorts included two ASD-enriched studies, six cohorts enrolling children from neonatal intensive care units (NICU), and thirty-six general population cohorts (See Additional File 1 Table S1 and Table S2). ASD-enriched studies included children originally enrolled as part of a case-control study of ASD, developmental delays, and typical development as well as a cohort enrolling younger siblings of children with ASD. NICU cohorts enrolled directly from NICUs. General population cohorts consisted of pregnancy and early-childhood studies evaluating other child health outcomes, including birth outcomes, growth and development, asthma, and overall wellbeing. Inclusion criteria for the study were (1) singleton births; (2) data available on child ADHD and ASD diagnoses, and (3) data on maternal administration of sOT during labor or delivery. For families with more than one child enrolled in the ECHO cohort, one sibling was randomly selected to be included in this study. We restricted inclusion to those cohorts with available data on at least 20 mother/child dyads. The decision-logic for inclusion and exclusion of cohorts and participants is displayed in Additional File 1 Fig. S1. We identified 1073 ADHD cases and 851 ASD cases in our study population.

Synthetic oxytocin administration

Synthetic oxytocin use during childbirth (yes vs. no) was ascertained from either medical record abstraction or self-report by the mother. Regarding forms of terminology used to search the ECHO platform to identify relevant data included for harmonization of extant and new data (related to intrapartum sOT use), the following terms were included: sOT, Oxytocin, Pitocin, Syntocinon, uterotonic, uterine stimulant, stimulation, induction, induce, augmentation, augment. Terminology on the ECHO forms were oxytocin and Pitocin. Use of sOT for each mother-child pair was ascertained based on a prioritization of available information for use in the following order: (1) documentation of sOT administration during labor and delivery in maternal medical records, (2) documentation of labor induction or augmentation in maternal medical records, (3) documentation of labor induction or augmentation in childbirth medical records, and (4) maternal self-report of having been administered sOT.

ADHD and ASD

We defined ADHD and ASD based on caregiver report of physician-diagnosed disorders. Caregivers were asked whether a doctor or other health care provider had ever informed them that their child has or had Attention Deficit Disorder (ADD) or Attention Deficit /Hyperactivity Disorder (ADHD) for an ADHD diagnosis, and/or ASD Spectrum Disorder (ASD), Asperger’s Disorder or Pervasive Developmental Disorder (PDD) for an ASD diagnosis. In some cohorts, ASD diagnosis was obtained by utilizing several clinical sources, including established gold-standard diagnostic instruments, such as the Autism Diagnostic Observation Schedule [56] or a diagnosis extracted from medical records.

Covariates

Self-reported maternal races were defined as American Indian/Alaskan Native, Asian, Black, Native Hawaiian or Pacific Islander, White, Other Race, and Multiple Races. Mother’s highest education was categorized as high school degree or equivalent or less; some college with no degree; and bachelor’s degree and above. Child characteristics include caregiver-reported child race, childbirth year (< 2005; 2006–2010; 2011–2015; 2016–2022), and child sex assigned at birth (male or female).

Maternal age at the time of delivery was determined from demographic questionnaires and maternal medical records. Preterm birth (yes/no), defined as birth prior to 37 weeks gestation, was based on available reports for gestational age.

Gestational age at birth in completed weeks was obtained through abstraction of maternal or child medical records or through parent-report. For medical record abstraction, an accepted hierarchy [57, 58] was employed to ascertain the most accurate measure for estimating the due date: dating based on embryo placement following in vitro fertilization or dating based on artificial insemination, obstetrical estimate from first trimester ultrasound; obstetrical estimated from ultrasound taken in the second trimester with fetal biparietal diameter dating within 2 weeks of sure last menstrual period (LMP); ultrasound taken in the second trimester with unsure or no LMP date; report from obstetrical medical record reporting “consensus” estimated date of delivery with no ultrasound documented during first and second trimester; obstetrical estimate from LMP only; neonatal estimate of gestational age at birth obtained from child medical records; estimated from cohort research encounter; reported by mother; and estimated on cohort-provided estimated date of delivery without further description.

Large for gestational age (LGA), defined as child birthweight-for-gestational age and sex > 90th percentile (percentiles derived from the International Fetal and Newborn Growth Consortium for the 21st Century [INTERGROWTH-21]) [59] was calculated. Pre-pregnancy obesity was defined as a body mass index (BMI)  30 kg/m2 according to accepted definitions [35]. Pre-pregnancy BMI was obtained using measured or self-reported height and weight between 12 months prior to conception through the first trimester. Gestational diabetes mellitus (GDM) was defined as new-onset diabetes during pregnancy based on self-report or as indicated in maternal medical records.

Statistical analysis

We compared the distribution of demographic characteristics and medical conditions between women who received sOT during labor and delivery and those who did not using Pearson chi-square tests. Using mixed-effects logistic models (“glmer” function from the “lme4” R package), we calculated unadjusted and covariate-adjusted odds ratios (aORs) and corresponding 95% confidence intervals (CI) to estimate associations between sOT use during childbirth and risk of ADHD or ASD in the offspring. Models were fitted with maximum likelihood estimators. Wald 95% CIs were constructed, and P-values were derived from the Wald z-test. In multivariable analyses, we adjusted for child race, ethnicity, sex, child’s birth year, gestational age and LGA status at birth, maternal age at delivery, and highest maternal education level. Maternal obesity prior to pregnancy and GDM were added to the adjusted model as covariates independently and in tandem. Models were fitted with random effects for individual cohorts to account for clustering within cohort. Based on a priori hypotheses that there would be variation by child sex and maternal pre-pregnancy obesity, fully adjusted models for both ADHD and ASD were stratified to examine for differences by strata. We evaluated effect modification by sex and by maternal pre-pregnancy obesity using product terms, sOT x sex, and sOT x maternal pre-pregnancy obesity. For all analyses, the criterion for statistical significance was P < 0.05, without adjustment for multiple comparisons.

Imputation was performed for missing data using multiple imputation by chained equations from the “mice” R package [60]. The results were pooled after 25 imputations with a maximum of 10 iterations. The imputation models included our variables of interest with cohort type (general population, NICU, or ASD-enriched) and individual cohort membership as classification variables. Regression estimates from the imputed datasets were pooled together using Rubin’s rule.

In a set of sensitivity analyses, we explored potential cohort effects by assessing whether observed associations between the sOT use and odds of ADHD or ASD differed after removing individual cohorts and/or cohort types based on specific enrollment criteria (e.g. ASD-enriched, NICU, and general population cohorts). All analyses were performed using the R statistical software package, version 4.1.0 (R Foundation for Statistical Computing, Vienna, Austria).

Results

Associations between participant characteristics and sOT exposure

Forty-eight percent of study participants were exposed to sOT. Table 1 shows socio-demographic characteristics of the sample by sOT exposure status. Maternal age at delivery and child sex assigned at birth were similar in sOT exposed mothers compared with those not exposed. Mean child age at diagnosis for ADHD was 7.10 in the sOT exposed group vs. 6.81 in the non-exposed group. Mean child age at diagnosis for ASD was 3.0 in the sOT exposed group, vs. 3.86 in the non-exposed group. Children exposed to sOT were more likely to be Hispanic (24.5% vs. 20.5%), and less likely to be White (56.7% vs. 60.9%) and born preterm (9.1% vs. 20.2%). Exposed mothers were more likely to have pre-pregnancy obesity (28.8% vs. 26.7%) and GDM (9.0% vs. 7.2%) compared with those not exposed.

Table 1 Characteristics of children and mothers according to sOT exposure status, ECHO study (N = 12,503)

Associations between sOT exposure and attention deficit hyperactivity disorder

As shown in Table 2, the adjusted association between sOT exposure and ADHD was not significant in the pooled sample (aOR 0.89; 95% CI, 0.76, 1.04). In analysis stratified by child sex, the odds ratios were not statistically significant in either male (aOR 0.89; 95% CI, 0.73, 1.07) or female offspring (aOR 0.91; 95% CI, 0.69, 1.19) (P = 0.83).

Table 2 Unadjusted and adjusted odds ratios for associations between sOT use and reported attention deficit/hyperactivity disorder (ADHD) diagnosis

Associations between sOT exposure and autism spectrum disorder

The unadjusted and adjusted ORs of associations between sOT exposure during labor and delivery and ASD diagnosis are shown in Table 3. After adjusting for confounders, the aOR was 0.86 (95% CI, 0.71, 1.03) for the associations between ASD diagnosis and sOT exposure. Odds ratios were similar in male (aOR 0.81; 95% CI, 0.65, 1.01) and female offspring (aOR 0.97; 95% CI, 0.68, 1.39) (P = 0.42).

Table 3 Unadjusted and adjusted odds ratios for associations between sOT use and reported autism spectrum disorder (ASD) diagnosis

Effect modification by maternal obesity status

Participant clusters grouped by maternal pre-pregnancy obesity status are shown in Table 4. In analyses adjusted for potential confounders, the interaction between sOT and maternal pre-pregnancy obesity was statistically significant for ADHD (P = 0.03) but was not statistically significant for ASD (P = 0.37). Forest plots depicting analysis of the association of sOT and ADHD, stratified by maternal obesity status, are presented in Fig. 1. Among mothers who were obese prior to pregnancy, sOT was associated with lower odds of ADHD (aOR 0.72 95% CI, 0.55, 0.96); this association was not found among children of mothers who were not obese before pregnancy (aOR 0.97; 95% CI, 0.80, 1.18).

Table 4 Participant clusters by pre-pregnancy obesity status
Fig. 1
figure 1

Analysis of the association of sOT and ADHD, stratified by maternal pre-pregnancy obesity. Adjusted associations between sOT exposure and attention deficit hyperactivity disorder (ADHD) stratified by obesity before pregnancy. Adjusted for maternal age at delivery, highest maternal education level, child race, ethnicity, and sex, gestational age and large for gestational age at birth, child birth year, and gestational diabetes mellitus; ASD, autism spectrum disorder; CI, confidence interval; NICU, neonatal intensive care units; OR, odds ratio; sOT, synthetic Oxytocin. ASD-enriched cohorts: n = 828. NICU cohorts: n = 878. Other cohorts: n = 10,797

Overall, we did not observe significant heterogeneity in cohort-specific and cohort type-specific effect estimates for the associations between intrapartum sOT exposure and child ADHD and ASD. There was no meaningful change in effect estimates after removing each cohort and after restricting to each cohort type (NICU, ASD-enriched, general population) (Fig. 1 and Additional File 1 Figs. S2-S4).

Discussion

In a multi-site, diverse cohort, in which 48% of mothers were administered sOT during childbirth, we found no evidence of an association between intrapartum exposure to sOT and odds of ADHD or ASD in either male or female offspring. Contrary to our hypothesis, among mothers with pre-pregnancy obesity, sOT was associated with lower odds of child ADHD diagnosis.

Our finding that intrapartum sOT exposure was not associated with adverse neurodevelopmental outcomes in the offspring is consistent with findings from several prior studies [12, 20,21,22,23,24,25,26,27,28]. In contrast to some of these prior studies and current results, preclinical studies suggest that sOT exposure might disrupt fetal neurodevelopment [61, 62] via cellular mechanisms such as epigenetic triggering [2, 63,64,65], oxytocin receptor alterations [6], DNA damage and cellular death [66, 67], complex signaling pathways [19], and transgenerational hormonal imprinting [68, 69]. Biologically plausible mechanisms that could link fetal exposure to intrapartum sOT with ADHD or ASD include excessive uterine contractility leading to decreased uteroplacental perfusion and fetal hypoxemia [18, 70,71,72,73,74,75,76], and especially at high cumulative doses [17] and transplacental transfer of sOT [77, 78] resulting in sOT-induced oxytocinergic signaling in the developing brain, the importance of which is suggested by the role that oxytocinergic signaling plays in the development of social behaviors that are characteristically impaired in ASD [79]. Exogenous sOT differs from the human endogenous oxytocin hormone [6, 80], and rodents exposed to sOT demonstrate altered behavioral presentations consistent with psychiatric phenotypes [81], pervasive developmental conditions [69], and enduring male specific neuroendocrine impairments, including dysfunctional cortical connectivity [71].

To our knowledge, the interaction of maternal obesity and intrapartum sOT exposure in relation to offspring neurodevelopmental outcomes has not previously been investigated. Recent reports suggest maternal weight gain and pre-pregnancy BMI may contribute to child ASD outcomes [82, 83]. Maternal obesity can lead to poor uterine contractility [84, 85], and thus impede the progression of labor and increase the likelihood of sOT exposure and exposure to higher cumulative doses of sOT [86,87,88,89]. Given these reports, we explored a potential joint effect between sOT exposure and maternal pre-pregnancy BMI on offspring neurodevelopmental outcomes in our study. Our finding that sOT was associated with lower odds of ADHD among offspring of mothers with pre-pregnancy obesity might be explained, at least in part, by confounding by indication, whereby mothers with obesity, and diminished uterine contractility, were more likely to be delivered promptly by C-section after an initial, possibly non-productive induction using sOT, thereby mitigating fetal exposure to the intense stress of labor that is typically involved during sOT exposure [90, 91]. This may also explain our observed trend of more frequent sOT childbirth intervention among mothers with pre-pregnancy obesity.

It also is plausible that in obese mothers, sOT augmentation and/or induction of labor may reduce the risk of a prolonged second stage of labor and potentially mitigate the impact of stress to the vulnerable fetal brain. Additionally, it seems possible that this exposure could mechanistically mimic the neuroprotective effect of endogenous oxytocin, as has been reported in preclinical models [92, 93].

Although our study’s findings did not confirm an association between intrapartum exposure to sOT and subsequent onset of child ADHD or ASD, the well documented routinization of sOT utilization during childbirth leaves us curious about the potential influence of this exposure on child neurodevelopmental outcomes. Synthetic oxytocin is in widespread use in the United States and globally [4, 6]. Labor induction and augmentation with sOT is one of the most prevalent clinical interventions in modern obstetric practice [86, 94]. In specific circumstances in which spontaneous labor has not begun, e.g., as pregnancies at term gestations with vertex, non-anomalous, singleton fetuses, induction of labor with sOT as compared to expectant management provides significant maternal (reduced maternal mortality, lower Cesarean delivery rate) and neonatal (reduced rate of neonatal death and meconium aspiration syndrome) benefits compared to expectant management [95,96,97]. Among pharmacologic agents used for labor induction and augmentation, sOT is by far the most frequently used. Furthermore, maternal obesity, and GDM are associated with higher doses of sOT during childbirth intervention [98].

For labor induction and/or augmentation, and for the management of the third stage of labor, US professional associations and the WHO recommend sOT as the uterotonic agent of choice [99,100,101]. This medical agent is administered intravenously, via infusion pump to provide a precise infusion rate which is adjusted based on the uterine activity (frequency and strength of contraction), fetal heart rate, and progress of labor [102]. In patients who achieve a desirable labor pattern and progress, there is no consensus about whether the sOT dose should be discontinued or continued, and consequently, sOT dosage tends to vary across birthing facilities [102]. Based on medical indication and local practices, initial sOT dosage varies from 0.5 to 6 milliunits/minute and the maximum dose varies between 16 and 64 milliunits/minute. Per this protocol, sOT is administered continuously until which point uterine contractions are deemed inefficient to reliably expel the fetus, and labor is declared a “failure to progress,” warranting a Cesarean Sects. [62, 103].

Strengths and limitations

A chief limitation of our study was our lack of information on indications for childbirth intervention with sOT (specifically, the clinical indication for labor induction or augmentation), length of labor, mode of delivery (e.g. vaginal or C-section), and sOT dosage administered to laboring mothers during offspring delivery. We defined sOT exposure as a binary category, so we were unable to assess a potential dose-response association, or threshold effects. Findings from a study by Soltys et al. (17) are consistent with the concept that the strength and direction of the relationship of sOT and ASD varies across a range of sOT doses; specifically, low dose/short duration sOT exposure was associated with a statistically non-significant decrease in the odds of ASD, moderate dose/duration was associated with a non-significant increase in odds of ASD, and high dose/long duration exposure was associated with an increase in odds of ASD among male offspring. Our use of binary exposure limited the opportunity to assess such dose-dependent associations, leaving us questioning a potential dose-response influence on our results.

Given the limitations of the current study, and the fact that the main non-null finding was unexpected, replication of our analyses in other cohorts with clinical data related to indication for and dosage of intrapartum sOT is needed before drawing conclusions about associations between intrapartum sOT exposure and neurodevelopmental outcomes in the offspring.

Another potential limitation of our study is that child diagnoses of ADHD or ASD were based on parent report of physician diagnosis, rather than a rigorous assessment by clinicians with expertise in diagnosing these specific neurodevelopmental conditions, which could have led to misclassification regarding our outcomes.

Despite these limitations, our study had some notable strengths including a large, diverse, multi-site study cohort, which allowed us to derive precise estimates of associations, adjust for confounders, and explore effect measure modification by maternal pre-pregnancy obesity. Secondly, this was the first known endeavor which assessed the interaction between intrapartum sOT exposure and maternal BMI on child neurodevelopmental outcomes.

Conclusions

In a sample from the ECHO cohort, we found no evidence of an association between intrapartum sOT exposure and ADHD and ASD in the offspring. Instead, we observed an unexpected association between intrapartum sOT exposure and decreased odds of child ADHD among women with pre-pregnancy obesity. We observed use of intrapartum sOT in nearly half our sample, and more frequently among mothers with pre-pregnancy obesity. The unknown complexities, and under-investigated mechanisms and pathways of intrapartum sOT as weighed against the sensitivity of the still developing fetal brain provides a robust opportunity for future exploration regarding this early exposure.

Data availability

Select de-identified data from the ECHO Program are available through NICHD’s Data and Specimen Hub (DASH). Information on study data not available on DASH, such as some Indigenous datasets, can be found on the ECHO study DASH webpage.

Abbreviations

ADHD:

Attention deficit hyperactivity disorder

aOR:

Adjusted odds ratio

ASD:

Autism spectrum disorder

BMI:

Body mass index

CI:

Confidence Interval

ECHO:

Environmental influences on Child Health Outcomes

GDM:

Gestational diabetes mellitus

INTERGROWTH-21:

International Fetal and Newborn Growth Consortium for the 21st Century

ICD:

International Classification of Disease

LGA:

Large for gestational age

NICU:

Neonatal intensive care units

sOT:

Synthetic oxytocin

References

  1. Perry RL, Satin AJ, Barth WH, Valtier S, Cody JT, Hankins GD. The pharmacokinetics of oxytocin as they apply to labor induction. Am J Obstet Gynecol. 1996;174(5):1590–93.

    Article  CAS  PubMed  Google Scholar 

  2. Kenkel W, Perkeybile A-M, Yee J, Pournajafi-Nazarloo H, Lillard T, Ferguson E, et al. Behavioral and epigenetic consequences of oxytocin treatment at birth. Sci Adv. 2019;5(5):eaav2244.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Laughon SK, Branch DW, Beaver J, Zhang J. Changes in labor patterns over 50 years. Am J Obstet Gynecol. 2012;206(5):e4191–9.

    Article  Google Scholar 

  4. Talati C, Carvalho JCA, Luca A, Balki M. The effect of intermittent oxytocin pretreatment on oxytocin-induced contractility of human myometrium in vitro. Anesth Analg. 2019;128(4):671–78.

    Article  CAS  PubMed  Google Scholar 

  5. Oscarsson ME, Amer-Wåhlin I, Rydhstroem H, Källén K. Outcome in obstetric care related to oxytocin use. A population-based study. Acta Obstet Gynecol Scand. 2006;85(9):1094–8.

    Article  PubMed  Google Scholar 

  6. Carter CS, Kenkel WM, MacLean EL, Wilson SR, Perkeybile AM, Yee JR, et al. Is oxytocin nature’s medicine? Pharmacol Rev. 2020;72(4):829–61.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Clapp MA, James KE, Bates SV, Kaimal AJ. Patient and hospital factors associated with unexpected newborn complications among term neonates in US hospitals. JAMA Netw Open. 2020;3(2):e1919498.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Hinshaw K, Simpson S, Cummings S, Hildreth A, Thornton J. A randomised controlled trial of early versus delayed oxytocin augmentation to treat primary dysfunctional labour in nulliparous women. Brit J Obstet Gynecol. 2008;115(10):1289–95. discussion 95 – 6.

    Article  CAS  Google Scholar 

  9. Mirzabagi E, Deepak NN, Koski A, Tripathi V. Uterotonic use during childbirth in uttar pradesh: accounts from community members and health providers. Midwifery. 2013;29(8):902–10.

    Article  PubMed  Google Scholar 

  10. Zhang J, Laughon SK, Branch DW. Oxytocin regimen for labor augmentation, labor progression, and perinatal outcomes. Obstet Gynecol. 2012;119(2):381–82.

    Article  CAS  Google Scholar 

  11. Harris JC, Carter CS. Therapeutic interventions with oxytocin: current status and concerns. J Am Acad Child Adolesc Psychiatry. 2013;52(10):998–1000.

    Article  PubMed  Google Scholar 

  12. Stokholm L, Juhl M, Talge NM, Gissler M, Obel C, Strandberg-Larsen K. Obstetric oxytocin exposure and ADHD and ASD among Danish and Finnish children. Int J Epidemiol. 2021;50(2):446–56.

    Article  PubMed  Google Scholar 

  13. Kurth L, Davalos D. Prenatal exposure to synthetic oxytocin: risk to neurodevelopment? J Prenat Perinat Psychol Health. 2012;27(1):3.

    Google Scholar 

  14. Kurth L, Haussmann R. Perinatal pitocin as an early ADHD biomarker: neurodevelopmental risk? J Atten Disord. 2011;15(5):423–31.

    Article  PubMed  Google Scholar 

  15. Tikkanen R, Gunja M, Fitzgerald M, Zephyrin L. Maternal mortality and maternity care in the United States compated to 10 other developed countries. Commonw Fund; 2020:1–17.

  16. Smallwood M, Sareen A, Baker E, Hannusch R, Kwessi E, Williams T. Increased risk of autism development in children whose mothers experienced birth complications or received labor and delivery drugs. ASN Neuro. 2016;8(4):1759091416659742.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Soltys SM, Scherbel JR, Kurian JR, Diebold T, Wilson T, Hedden L, et al. An association of intrapartum synthetic oxytocin dosing and the odds of developing autism. Autism. 2020;24(6):1400–10.

    Article  PubMed  PubMed Central  Google Scholar 

  18. García-Alcón A, González-Peñas J, Weckx E, Penzol MJ, Gurriarán X, Costas J, et al. Oxytocin exposure in labor and its relationship with cognitive impairment and the genetic architecture of autism. J Autism Dev Disord. 2022;53(1):66–79.

    Article  PubMed  Google Scholar 

  19. Torres G, Mourad M, Leheste JR. Perspectives of pitocin administration on behavioral outcomes in the pediatric population: recent insights and future implications. Heliyon. 2020;6(5):e04047.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Lønfeldt NN, Verhulst FC, Strandberg-Larsen K, Plessen KJ, Lebowitz ER. Assessing risk of neurodevelopmental disorders after birth with oxytocin: a systematic review and meta-analysis. Psychol Med. 2019;49(6):881–90.

    Article  PubMed  Google Scholar 

  21. Hertz-Picciotto I, Schmidt RJ, Krakowiak P. Understanding environmental contributions to autism: causal concepts and the state of science. Autism Res. 2018;11(4):554–86.

    Article  PubMed  Google Scholar 

  22. Monks DT, Palanisamy A, Oxytocin. At birth and beyond. A systematic review of the long-term effects of peripartum oxytocin. Anaesthesia. 2021;76(11):1526–37.

    Article  CAS  PubMed  Google Scholar 

  23. Saade GR, Sibai BM, Silver R. Induction or augmentation of labor and autism. JAMA Pediatr. 2014;168(2):190–1.

    Article  PubMed  Google Scholar 

  24. Wang C, Geng H, Liu W, Zhang G. Prenatal, perinatal, and postnatal factors associated with autism: a meta-analysis. Med (Baltim). 2017;96(18):e6696.

    Article  CAS  Google Scholar 

  25. Gardener H, Spiegelman D, Buka SL. Perinatal and neonatal risk factors for autism: a comprehensive meta-analysis. Pediatrics. 2011;128(2):344–55.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Guastella AJ, Cooper MN, White CR, White MK, Pennell CE, Whitehouse AJ. Does perinatal exposure to exogenous oxytocin influence child behavioural problems and autistic-like behaviours to 20 years of age? J Child Psychol Psychiatry. 2018;59(12):1323–32.

    Article  PubMed  Google Scholar 

  27. Henriksen L, Wu CS, Secher NJ, Obel C, Juhl M. Medical augmentation of labor and the risk of ADHD in offspring: a population-based study. Pediatrics. 2015;135(3):e672–7.

    Article  PubMed  Google Scholar 

  28. Oberg AS, D’Onofrio BM, Rickert ME, Hernandez-Diaz S, Ecker JL, Almqvist C, et al. Association of labor induction with offspring risk of autism spectrum disorders. JAMA Pediatr. 2016;170(9):e160965–65.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Wiggs KK, Rickert ME, Hernandez-Diaz S, Bateman BT, Almqvist C, Larsson H, et al. A family-based study of the association between labor induction and offspring attention-deficit hyperactivity disorder and low academic achievement. Behav Genet. 2017;47(4):383–93.

    Article  PubMed  Google Scholar 

  30. Miranda A, Sousa N. Maternal hormonal milieu influence on fetal brain development. Brain Behav. 2018;8(2):e00920.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Singh A, Yeh CJ, Verma N, Das AK. Overview of attention deficit hyperactivity disorder in young children. Health Psychol Res. 2015;3(2):2115.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Xu G, Strathearn L, Liu B, Yang B, Bao W. Twenty-year trends in diagnosed attention-deficit/hyperactivity disorder among US children and adolescents, 1997–2016. JAMA Netw Open. 2018;1(4):e181471.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Xu G, Strathearn L, Liu B, O’Brien M, Kopelman TG, Zhu J, et al. Prevalence and treatment patterns of autism spectrum disorder in the United States, 2016. JAMA Pediatr. 2019;173(2):153–59.

    Article  PubMed  Google Scholar 

  34. Crespi BJ. Autism as a disorder of high intelligence. Front Neurosci. 2016;10:300.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Flegal KM, Kit BK, Orpana H, Graubard BI. Association of all-cause mortality with overweight and obesity using standard body mass index categories: a systematic review and meta-analysis. JAMA. 2013;309(1):71–82.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Maenner MJ, Shaw KA, Bakian AV, Bilder DA, Durkin MS, Esler A, et al. Prevalence and characteristics of autism spectrum disorder among children aged 8 years - autism and developmental disabilities monitoring network, 11 sites, United States, 2018. Morbidity Mortal Wkly Rep Surveillance Summaries (Washington D C : 2002). 2021;70(11):1–16.

    Google Scholar 

  37. Hours C, Recasens C, Baleyte JM. ASD and ADHD comorbidity: what are we talking about? Front Psychiatry. 2022;13:837424.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Dalsgaard S, Thorsteinsson E, Trabjerg BB, Schullehner J, Plana-Ripoll O, Brikell I, et al. Incidence rates and cumulative incidences of the full spectrum of diagnosed mental disorders in childhood and adolescence. JAMA Psychiatry. 2020;77(2):155–64.

    Article  PubMed  Google Scholar 

  39. Zablotsky B, Black LI, Maenner MJ, Schieve LA, Danielson ML, Bitsko RH et al. Prevalence and trends of developmental disabilities among children in the United States: 2009–2017. Pediatrics. 2019;144(4).

  40. Flenik TMN, Bara TS, Cordeiro ML. Family functioning and emotional aspects of children with autism spectrum disorder in southern Brazil. J Autism Dev Disord. 2022;53(6):2306–13.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Picardi A, Gigantesco A, Tarolla E, Stoppioni V, Cerbo R, Cremonte M, et al. Parental burden and its correlates in families of children with autism spectrum disorder: a multicentre study with two comparison groups. Clin Pract Epidemiol Ment Health. 2018;14:143–76.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Rosello B, Berenguer C, Baixauli I, Colomer C, Miranda A. ADHD symptoms and learning behaviors in children with ASD without intellectual disability. A mediation analysis of executive functions. PLoS ONE. 2018;13(11):e0207286.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Usami M. Functional consequences of attention-deficit hyperactivity disorder on children and their families. Psychiatry Clin Neurosci. 2016;70(8):303–17.

    Article  PubMed  Google Scholar 

  44. Leitner Y. The co-occurrence of autism and attention deficit hyperactivity disorder in children–what do we know? Front. Hum Neurosci. 2014;8:268.

    Google Scholar 

  45. Goldstein RF, Abell SK, Ranasinha S, Misso M, Boyle JA, Black MH, et al. Association of gestational weight gain with maternal and infant outcomes: a systematic review and meta-analysis. JAMA. 2017;317(21):2207–25.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Rao PA, Landa RJ. Association between severity of behavioral phenotype and comorbid attention deficit hyperactivity disorder symptoms in children with autism spectrum disorders. Autism. 2014;18(3):272–80.

    Article  PubMed  Google Scholar 

  47. Akinbami LJ, Liu X, Pastor PN, Reuben CA. Attention deficit hyperactivity disorder among children aged 5–17 years in the United States, 1998–2009. NCHS Data Brief. 2011(70):1–8.

  48. Baio J, Wiggins L, Christensen DL, Maenner MJ, Daniels J, Warren Z, et al. Prevalence of autism spectrum disorder among children aged 8 years - autism and developmental disabilities monitoring network, 11 sites, United States, 2014. MMWR Surveill Summ. 2018;67(6):1–23.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Weisman O, Agerbo E, Carter CS, Harris JC, Uldbjerg N, Henriksen TB, et al. Oxytocin-augmented labor and risk for autism in males. Behav Brain Res. 2015;284:207–12.

    Article  CAS  PubMed  Google Scholar 

  50. Wang S, Wang B, Drury V, Drake S, Sun N, Alkhairo H, et al. Rare x-linked variants carry predominantly male risk in autism, tourette syndrome, and ADHD. Nat Commun. 2023;14(1):8077.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Ellis JA, Brown CM, Barger B, Carlson NS. Influence of maternal obesity on labor induction: a systematic review and meta-analysis. J Midwifery Womens Health. 2019;64(1):55–67.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Jacobson LP, Lau B, Catellier D, Parker CB. An environmental influences on Child Health outcomes viewpoint of data analysis centers for collaborative study designs. Curr Opin Pediatr. 2018;30(2):269–75.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Hertz-Picciotto I, Korrick SA, Ladd-Acosta C, Karagas MR, Lyall K, Schmidt RJ, et al. Maternal tobacco smoking and offspring autism spectrum disorder or traits in ECHO cohorts. Autism Res. 2022;15(3):551–69.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Schantz SL, Eskenazi B, Buckley JP, Braun JM, Sprowles JN, Bennett DH, et al. A framework for assessing the impact of chemical exposures on neurodevelopment in ECHO: opportunities and challenges. Environ Res. 2020;188:109709.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Volk HE, Perera F, Braun JM, Kingsley SL, Gray K, Buckley J, et al. Prenatal air pollution exposure and neurodevelopment: a review and blueprint for a harmonized approach within ECHO. Environ Res. 2021;196:110320.

    Article  CAS  PubMed  Google Scholar 

  56. Lord C, Risi S, Lambrecht L, Cook EH Jr., Leventhal BL, DiLavore PC, et al. The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord. 2000;30(3):205–23.

    Article  CAS  PubMed  Google Scholar 

  57. National Center for Health Statistics, US Department of Health and Human Services, Centers for Disease Control and Prevention. Updated 2003. Accessed at: https://www.cdc.gov/nchs/data/dvs/GuidetoCompleteFacilityWks.pdf. Accessed on 2024 January 1.

  58. Committee opinion 700. Methods for estimating the due date. Obstet Gynecol. 2017;129(5):e150–54.

    Article  Google Scholar 

  59. Dighe MK, Frederick IO, Andersen HF, Gravett MG, Abbott SE, Carter AA, et al. Implementation of the intergrowth-21st project in the United States. BJOG. 2013;120(Suppl 2):123–8.

    Article  PubMed  Google Scholar 

  60. van Buuren S, Groothuis-Oudshoorn K, Mice. Multivariate imputation by chained equations in R. J Stat Softw. 2011;45(3):1–67.

    Article  Google Scholar 

  61. Uvnas-Moberg K, Ekstrom-Bergstrom A, Berg M, Buckley S, Pajalic Z, Hadjigeorgiou E, et al. Maternal plasma levels of oxytocin during physiological childbirth - a systematic review with implications for uterine contractions and central actions of oxytocin. BMC Pregnancy Childbirth. 2019;19(1):285.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Daly D, Minnie KCS, Blignaut A, Blix E, Vika Nilsen AB, Dencker A, et al. How much synthetic oxytocin is infused during labour? A review and analysis of regimens used in 12 countries. PLoS ONE. 2020;15(7):e0227941.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Nigg JT. Toward an emerging paradigm for understanding attention-deficit/hyperactivity disorder and other neurodevelopmental, mental, and behavioral disorders: environmental risks and epigenetic associations. JAMA Pediatr. 2018;172(7):619–21.

    Article  PubMed  PubMed Central  Google Scholar 

  64. Andari E, Nishitani S, Kaundinya G, Caceres GA, Morrier MJ, Ousley O, et al. Epigenetic modification of the oxytocin receptor gene: implications for autism symptom severity and brain functional connectivity. Neuropsychopharmacology. 2020;45(7):1150–58.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Perera F, Herbstman J. Prenatal environmental exposures, epigenetics, and disease. Reprod Toxicol. 2011;31(3):363–73.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Leffa DD, Daumann F, Damiani AP, Afonso AC, Santos MA, Pedro TH, et al. DNA damage after chronic oxytocin administration in rats: a safety yellow light? Metab. Brain Dis. 2017;32(1):51–5.

    Article  CAS  Google Scholar 

  67. Hirayama T, Hiraoka Y, Kitamura E, Miyazaki S, Horie K, Fukuda T, et al. Oxytocin induced labor causes region and sex-specific transient oligodendrocyte cell death in neonatal mouse brain. J Obstet Gynaecol Res. 2020;46(1):66–78.

    Article  CAS  PubMed  Google Scholar 

  68. Csaba G. Transgenerational effects of perinatal hormonal imprinting. Transgenerational epigenetics: Elsevier; 2014. pp. 255–67.

    Google Scholar 

  69. Hashemi F, Tekes K, Laufer R, Szegi P, Tóthfalusi L, Csaba G. Effect of a single neonatal oxytocin treatment (hormonal imprinting) on the biogenic amine level of the adult rat brain: could oxytocin-induced labor cause pervasive developmental diseases? Reprod. Sci. 2013;20(10):1255–63.

    CAS  Google Scholar 

  70. Sato M, Noguchi J, Mashima M, Tanaka H, Hata T. 3d power doppler ultrasound assessment of placental perfusion during uterine contraction in labor. Placenta. 2016;45:32–6.

    Article  PubMed  Google Scholar 

  71. Palanisamy A, Giri T, Jiang J, Bice A, Quirk JD, Conyers SB et al. In utero exposure to transient ischemia-hypoxemia promotes long-term neurodevelopmental abnormalities in male rat offspring. JCI Insight. 2020;5(10).

  72. Palanisamy A, Lopez J, Frolova A, Macones G, Cahill AG. Association between uterine tachysystole during the last hour of labor and cord blood lactate in parturients at term gestation. Am J Perinatol. 2019;36(11):1171–78.

    Article  PubMed  Google Scholar 

  73. Crane JM, Young DC, Butt KD, Bennett KA, Hutchens D. Excessive uterine activity accompanying induced labor. Obstet Gynecol. 2001;97(6):926–31.

    CAS  PubMed  Google Scholar 

  74. Heuser CC, Knight S, Esplin MS, Eller AG, Holmgren CM, Manuck TA, et al. Tachysystole in term labor: incidence, risk factors, outcomes, and effect on fetal heart tracings. Am J Obstet Gynecol. 2013;209(1):e321–6.

    Article  Google Scholar 

  75. Kunz MK, Loftus RJ, Nichols AA. Incidence of uterine tachysystole in women induced with oxytocin. J Obstet Gynecol Neonatal Nurs. 2013;42(1):12–8.

    Article  PubMed  Google Scholar 

  76. Walter MH, Abele H, Plappert CF. The role of oxytocin and the effect of stress during childbirth: neurobiological basics and implications for mother and child. Front Endocrinol (Lausanne). 2021;12:742236.

    Article  PubMed  Google Scholar 

  77. Malek A, Blann E, Mattison DR. Human placental transport of oxytocin. J Matern Fetal Med. 1996;5(5):245–55.

    CAS  PubMed  Google Scholar 

  78. Nathan NO, Hedegaard M, Karlsson G, Knudsen LE, Mathiesen L. Intrapartum transfer of oxytocin across the human placenta: an ex vivo perfusion experiment. Placenta. 2021;112:105–10.

    Article  CAS  PubMed  Google Scholar 

  79. Froemke RC, Young LJ. Oxytocin, neural plasticity, and social behavior. Annu Rev Neurosci. 2021;44:359–81.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  80. Bell AF, Erickson EN, Carter CS. Beyond labor: the role of natural and synthetic oxytocin in the transition to motherhood. J Midwifery Womens Health. 2014;59(1):35–42. quiz 108.

    Article  PubMed  PubMed Central  Google Scholar 

  81. Palanisamy A, Kannappan R, Xu Z, Martino A, Friese MB, Boyd JD, et al. Oxytocin alters cell fate selection of rat neural progenitor cells in vitro. PLoS ONE. 2018;13(1):e0191160.

    Article  PubMed  PubMed Central  Google Scholar 

  82. Matias SL, Pearl M, Lyall K, Croen LA, Kral TVE, Fallin D, et al. Maternal prepregnancy weight and gestational weight gain in association with autism and developmental disorders in offspring. Obes (Silver Spring). 2021;29(9):1554–64.

    Article  Google Scholar 

  83. Windham GC, Anderson M, Lyall K, Daniels JL, Kral TVE, Croen LA, et al. Maternal pre-pregnancy body mass index and gestational weight gain in relation to autism spectrum disorder and other developmental disorders in offspring. Autism Res. 2019;12(2):316–27.

    Article  PubMed  Google Scholar 

  84. Maeder AB, Vonderheid SC, Park CG, Bell AF, McFarlin BL, Vincent C, et al. Titration of intravenous oxytocin infusion for postdates induction of labor across body mass index groups. J Obstetric Gynecologic Neonatal Nurs. 2017;46(4):494–507.

    Article  Google Scholar 

  85. Zhang J, Bricker L, Wray S, Quenby S. Poor uterine contractility in obese women. BJOG. 2007;114(3):343–48.

    Article  CAS  PubMed  Google Scholar 

  86. Kernberg A, Caughey AB. Augmentation of labor: a review of oxytocin augmentation and active management of labor. Obstet Gynecol Clin North Am. 2017;44(4):593–600.

    Article  PubMed  Google Scholar 

  87. Carlson NS, Corwin EJ, Lowe NK. Oxytocin augmentation in spontaneously laboring, nulliparous women: multilevel assessment of maternal BMI and oxytocin dose. Biol Res Nurs. 2017;19(4):382–92.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  88. Lassiter JR, Holliday N, Lewis DF, Mulekar M, Abshire J, Brocato B. Induction of labor with an unfavorable cervix: how does BMI affect success? J Maternal-Fetal Neonatal Med. 2016;29(18):3000–02.

    Article  Google Scholar 

  89. Mackeen AD, Durie D, Lin M, Huls C, Packard R, Sciscione A. Effect of obesity on labor inductions with foley plus oxytocin versus oxytocin alone [37m]. Obstet Gynecol. 2017;129(5):S142.

    Article  Google Scholar 

  90. Alan S, Akca E, Senoglu A, Gozuyesil E, Surucu SG. The use of oxytocin by healthcare professionals during labor. Yonago Acta Med. 2020;63(3):214–22.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  91. Litorp H, Sunny AK, Kc A. Augmentation of labor with oxytocin and its association with delivery outcomes: a large-scale cohort study in 12 public hospitals in Nepal. Acta Obstet Gynecol Scand. 2021;100(4):684–93.

    Article  CAS  PubMed  Google Scholar 

  92. Leuner B, Caponiti JM, Gould E. Oxytocin stimulates adult neurogenesis even under conditions of stress and elevated glucocorticoids. Hippocampus. 2012;22(4):861–8.

    Article  CAS  PubMed  Google Scholar 

  93. Panaitescu AM, Isac S, Pavel B, Ilie AS, Ceanga M, Totan A, et al. Oxytocin reduces seizure burden and hippocampal injury in a rat model of perinatal asphyxia. Acta Endocrinol (Buchar). 2018;14(3):315–19.

    Article  CAS  PubMed  Google Scholar 

  94. Zhang J, Branch DW, Ramirez MM, Laughon SK, Reddy U, Hoffman M, et al. Oxytocin regimen for labor augmentation, labor progression, and perinatal outcomes. Obstet Gynecol. 2011;118(2 Pt 1):249–56.

    Article  PubMed  PubMed Central  Google Scholar 

  95. Darney BG, Snowden JM, Cheng YW, Jacob L, Nicholson JM, Kaimal A, et al. Elective induction of labor at term compared with expectant management: maternal and neonatal outcomes. Obstet Gynecol. 2013;122(4):761–9.

    Article  PubMed  PubMed Central  Google Scholar 

  96. Keulen JK, Bruinsma A, Kortekaas JC, van Dillen J, Bossuyt PM, Oudijk MA, et al. Induction of labour at 41 weeks versus expectant management until 42 weeks (index): Multicentre, randomised non-inferiority trial. BMJ. 2019;364:l344.

    Article  PubMed  PubMed Central  Google Scholar 

  97. Knight HE, Cromwell DA, Gurol-Urganci I, Harron K, van der Meulen JH, Smith GCS. Perinatal mortality associated with induction of labour versus expectant management in nulliparous women aged 35 years or over: an English national cohort study. PLoS Med. 2017;14(11):e1002425.

    Article  PubMed  PubMed Central  Google Scholar 

  98. Reinl EL, Goodwin ZA, Raghuraman N, Lee GY, Jo EY, Gezahegn BM, et al. Novel oxytocin receptor variants in laboring women requiring high doses of oxytocin. Am J Obstet Gynecol. 2017;217(2):214. e1-14 e8.

    Article  PubMed Central  Google Scholar 

  99. Practice bulletin no. 183: Postpartum hemorrhage. Obstet Gynecol. 2017;130(4):e168–86.

    Article  Google Scholar 

  100. September ACNMU. 2017. Accessed at: http://www.midwife.org/acnm/files/ACNMLibraryData/UPLOADFILENAME/000000000310/AMTSL-PS-FINAL-10-10-17.pdf. Accessed on 2024 January 1.

  101. World Health Organization. WHO recommendations for the prevention and treatment of postpartum haemorrhage. Geneva; 2012.

  102. Jiang D, Yang Y, Zhang X, Nie X. Continued versus discontinued oxytocin after the active phase of labor: an updated systematic review and meta-analysis. PLoS ONE. 2022;17(5):e0267461.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  103. American College of Obstetricians Gynecologists, Society for Maternal-Fetal Medicine, Caughey AB, Cahill AG, Guise JM, Rouse DJ. Safe prevention of the primary cesarean delivery. Am J Obstet Gynecol. 2014;210(3):179–93.

    Article  Google Scholar 

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Acknowledgements

We wish to posthumously thank our colleague Li-Ching Lee, PhD whose input and insightful contributions to this endeavor were invaluable. We also thank C. Sue Carter, Ph.D. for her contributions.

The authors want to thank our ECHO colleagues; the medical, nursing, and program staff; and the children and families participating in the ECHO cohorts. We also acknowledge the contribution of the following ECHO program collaborators: ECHO Components—Coordinating Center: Duke Clinical Research Institute, Durham, North Carolina: Smith PB, Newby KL; Data Analysis Center: Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland: Jacobson LP; Research Triangle Institute, Durham, North Carolina: Parker CB; Research Triangle Institute, Durham, North Carolina: Catellier DJ; Person-Reported Outcomes Core: Northwestern University, Evanston, Illinois: Gershon R, Cella D; ECHO Awardees and Cohorts— Albert Einstein College of Medicine, Bronx, New York: Aschner J; Cincinnati Children’s Hospital Medical Center, Cincinnati, OH: Merhar S; Children’s Hospital and Clinic Minneapolis, MN: Lampland A; Icahn School of Medicine at Mount Sinai, New York, NY: Teitelbaum S; Cohen Children’s Medical Center, Northwell Health, New Hyde Park, NY: Stroustrup A; University of Buffalo, Jacobson School of Medicine and Biomedical Sciences, Buffalo, NY: Reynolds A; University of Florida, College of Medicine, Jacksonville, FL: Hudak M; University of Rochester Medical Center, Rochester, NY: Pryhuber G; Vanderbilt Children’s Hospital, Nashville, TN: Moore P; Wake Forest University School of Medicine, Winston Salem, NC: Washburn L; Massachusetts General Hospital, Boston, MA: Camargo C; Boston Children’s Hospital, Boston, MA: Mansbach J; Children’s Hospital of Philadelphia, Philadelphia, PA: Spergel J; Norton Children’s Hospital, Louisville, KY: Stevenson M; Phoenix Children’s Hospital, Phoenix AZ: Bauer C; Memorial Hospital of Rhode Island, Providence RI: Deoni S; Avera Health Rapid City, Rapid City, SD: Elliott A; Kaiser Permanente Northern California Division of Research, Oakland, CA: Ferrara A; University of Wisconsin, Madison WI: Gern J; Marshfield Clinic Research Institute, Marshfield, WI: Seroogy C: Bendixsen C; University of California Davis Mind Institute, Sacramento, CA: Hertz-Picciotto I, Restrepo B; University of Pittsburgh, Pittsburgh, PA: Hipwell A; Geisel School of Medicine at Dartmouth, Lebanon, NH: Karagas M; University of Washington, Department of Environmental and Occupational Health Sciences, Seattle, WA: Karr C; University of Tennessee Health Science Center, Memphis, TN: Mason A; Seattle Children’s Research Institute, Seattle, WA: Sathyanarayana S; Women & Infants Hospital of Rhode Island, Providence RI, Lester B; Children’s Mercy, Kansas City, MO: Carter B; Emory University, Atlanta, GA: Marsit C; Helen DeVos Children’s Hospital, Grand Rapids, MI: Pastyrnak S; Kapiolani Medical Center for Women and Children, Providence, RI: Neal C; Los Angeles Biomedical Research Institute at Harbour-UCLA Medical Center, Los Angeles CA: Smith L; Wake Forest University School of Medicine, Winston Salem, NC: Helderman J; Prevention Science Institute, University of Oregon, Eugene, OR: Leve L; George Washington University, Washington, DC: Ganiban J; Pennsylvania State University, University Park, PA; Neiderhiser J; Brigham and Women’s Hospital, Boston, MA: Weiss S; Boston University Medical Center, Boston, MA: O’Connor G; Kaiser Permanente, Southern California, San Diego, CA: Zeiger R; Washington University of St. Louis, St Louis, MO: Bacharier L; Pennsylvania State University, University Park, PA: Lyall K; Johns Hopkins Bloomberg School of Public Health Kennedy Krieger Institute, Baltimore, MD: Landa R; University of California, UC Davis Medical Center Mind Institute, Sacramento, CA: Ozonoff, S; University of Rochester Medical Center Rochester, NY: O’Connor T; University of Pittsburgh Medical Center, Magee Women’s Hospital, Pittsburgh, PA: Simhan H; Baystate Children’s Hospital, Springfield, MA : Vaidya R; Beaumont Health Medical Center, Royal Oak, MI: Obeid R; Boston Children’s Hospital, Boston, MA: Rollins C; East Carolina University Brody School of Medicine, Greenville, NC: Bear K; Michigan State University College of Human Medicine, East Lansing, MI: Lenski, M; University of Chicago, Chicago IL: Msall M; University of Massachusetts Medical School, Worcester, MA: Frazier J; Wake Forest Baptist Health (Atrium Health), Winston Salem, NC: Washburn, L; Yale School of Medicine, New Haven, CT: Montgomery A; Michigan State University, East Lansing, MI: Kerver J; Henry Ford Health System, Detroit, MI: Barone, C; Michigan Department of Health and Human Services, Lansing, MI: McKane, P; Michigan State University, East Lansing, MI: Paneth N; University of Michigan, Ann Arbor, MI: Elliott, M; Columbia University Medical Center, New York, NY: Herbstman J; University of Illinois, Beckman Institute, Urbana, IL: Schantz S; University of California, San Francisco:, San Francisco, CA: Woodruff T; University of Utah, Salt Lake City, UT: Stanford J; Icahn School of Medicine at Mount Sinai, New York, NY: Wright R; George Mason University, Fairfax, VA: Huddleston K; New York University School of Medicine, Karr C; Trasande L; University of California, San Francisco, San Francisco CA: Bush N; University of Minnesota, Minneapolis, MN: Nguyen R; University of Rochester Medical Center: Rochester, NY: Barrett E; Emory University, Atlanta, GA: Carlson-Smith, N.

Funding

Research reported in this publication was supported by the Environmental influences on Child Health Outcomes (ECHO) program, Office of the Director, National Institutes of Health, under Award Numbers U2COD023375 (Coordinating Center), U24OD023382 (Data Analysis Center, Jacobson), U24OD023319 (PRO Core), UH3OD023248 (Dabelea), UH3OD023318 (Dunlop), UH3OD023348 (O’Shea), The following grants supported colleagues who contributed to this research but are not authors. These contributors are listed in the acknowledgments. UH3OD023320, UH3OD023253, UH3OD023313, UH3OD023279, UH3OD023289, UH3OD023282, UH3OD023365, UH3OD023244, UH3OD023275, UH3OD023271, UH3OD023347, UH3OD023389, UH3OD023268, UH3OD023342, UH3OD023349, UH3OD023285, UH3OD023290, UH3OD023272, UH3OD023249, UH3OD023337, UH3OD023305. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

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LK conceptualized and designed the study, drafted original manuscript. TMO critically reviewed and revised original manuscript draft. IB critically reviewed and revised manuscript. ALD critically reviewed and revised manuscript. LC critically reviewed and revised manuscript. GW critically reviewed and revised manuscript. TH and MLC collected and analyzed data, reviewed and revised the article critically for important intellectual content. SE developed study design, coordinated data analysis, and reviewed and revised the article critically for important intellectual content. AP critically reviewed and revised manuscript. MM supervised data collection and data analysis process and reviewed and revised the article critically for important intellectual content. DW critically reviewed and revised manuscript. MG critically reviewed and revised manuscript. DD critically reviewed and revised original manuscript draft. All authors read and approved the final manuscript.

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Correspondence to Lisa Kurth.

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Kurth, L., O’Shea, T.M., Burd, I. et al. Intrapartum exposure to synthetic oxytocin, maternal BMI, and neurodevelopmental outcomes in children within the ECHO consortium. J Neurodevelop Disord 16, 26 (2024). https://doi.org/10.1186/s11689-024-09540-1

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