- 1Department of Paediatrics, Mercy Hospital for Women, Melbourne, VIC, Australia
- 2Heart Research Group, Murdoch Children’s Research Institute, Melbourne, VIC, Australia
- 3Department of Paediatrics, The University of Melbourne, Melbourne, VIC, Australia
Preterm infants are more likely to be born with congenital anomalies than those who are born at full-term. Conversely, neonates born with congenital anomalies are also more likely to be born preterm than those without congenital anomalies. Moreover, the comorbid impact of prematurity and congenital anomalies is more than cumulative. Multiple common factors increase the risk of brain injury and neurodevelopmental impairment in both preterm babies and those born with congenital anomalies. These include prolonged hospital length of stay, feeding difficulties, nutritional deficits, pain exposure and administration of medications including sedatives and analgesics. Congenital heart disease provides a well-studied example of the impact of comorbid disease with prematurity. Impaired brain growth and maturity is well described in the third trimester in this population; the immature brain is subsequently more vulnerable to further injury. There is a colinear relationship between degree of prematurity and outcome both in terms of mortality and neurological morbidity. Both prematurity and relative brain immaturity independently increase the risk of subsequent neurodevelopmental impairment in infants with CHD. Non-cardiac surgery also poses a greater risk to preterm infants despite the expectation of normal in utero brain growth. Esophageal atresia, diaphragmatic hernia and abdominal wall defects provide examples of congenital anomalies which have been shown to have poorer neurodevelopmental outcomes in the face of prematurity, with associated increased surgical complexity, higher relative cumulative doses of medications, longer hospital and intensive care stay and increased rates of feeding difficulties, compared with infants who experience either prematurity or congenital anomalies alone.
Introduction
Congenital anomalies which require surgery during the neonatal period predispose infants to brain injury and subsequent neurodevelopmental impairment, including both cardiac and non-cardiac lesions (Snookes et al., 2010; Walker et al., 2012; Gaynor et al., 2015; Gunn et al., 2016a; Stolwijk et al., 2016; Moran et al., 2019). Contributing factors include the underlying anomaly and associated genetic contributors, the fetal environment before birth, intensive care exposure and the perioperative period including medications and the environment, surgery and anesthesia, prolonged hospitalization and the impact on the family and caregivers. Neonates born preterm are also prone to increased rates of brain injury and impaired neurodevelopment (van Bel et al., 2019; Cheong et al., 2021); this risk is markedly amplified with the frequent co-existence of prematurity and congenital anomalies, which is the focus of this review (Figure 1).
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/880891/fphys-13-880891-HTML-r1/image_m/fphys-13-880891-g001.jpg)
FIGURE 1. Disrupted brain development and brain injury in context of cumulative insults and risk factors subsequent developmental delay and neurodevelopmental impairment.
Brain Injury in Preterm Infants
The fetal and preterm brain is vulnerable to injury throughout the third trimester, regardless of in utero or ex utero status. The impaired in utero environment may compromise brain growth and development due to placental dysfunction, uterine dysfunction, maternal ill health, infection, or injury (Ophelders et al., 2020). The preterm delivery of a fetus is usually due to one or more of these reasons. Conversely, an abnormality in the fetus can also lead to both preterm delivery and/or impaired brain growth and development. As such, preterm infants are vulnerable to brain injury and impaired development both due to the reasons for their prematurity, but also as a consequence of preterm delivery itself. Brain development is programmed throughout the third trimester, regardless of whether the fetus or neonate is in utero or ex utero (Buss et al., 2012). As such, the vulnerability of the brain to insult is likely to lead to a similar pattern of injury regardless of whether the baby is yet born. It is thus helpful to consider the fetal and neonatal brain on a continuum of growth and development with the same vulnerabilities and protective strategies in the face of hypoxia, ischemia, infection, toxins and over- or under-stimulation.
The more preterm an infant is at birth, the higher the risk of brain injury, such that every extra day in utero is of benefit in minimizing events leading to injury, as long as both the in utero environment and the fetus themself is healthy (Ophelders et al., 2020; Cheong et al., 2021). The typical pattern of brain injury experienced by preterm neonates is well described and includes intraventricular hemorrhage, venous infarction, periventricular echogenicity and leukomalacia, post-hemorrhagic ventricular dilatation, and hypoxic ischemic injury (Inder et al., 2021; Ortinau and Neil, 2015). However, only the more severe lesions evident on neuroimaging translate into longer term outcomes, with environmental factors exerting a greater influence on outcomes over time, especially in those with milder brain injury on imaging (Jansen et al., 2021). Furthermore, developmental delay in the preschool years does not necessarily portend later neurodevelopmental impairment in later years, particularly in the absence of neurosensory impairment or motor disability such as cerebral palsy (Hack et al., 2005).
Prematurity and Congenital Anomalies
Prematurity and congenital anomalies frequently co-exist. In New York, congenital malformations were twice as likely in the preterm population and 3.5 times more likely in very preterm infants, for all systems other than pulmonary disease (Kase and Visintainer, 2007). Further, nationwide analysis of more than one million births confirmed these findings of a strong association between prematurity and congenital malformations (Egbe et al., 2015).
In 2015–2016, in Victoria, Australia, 1 in 22 pregnancies had a congenital anomaly, most commonly chromosomal anomalies, followed by urogenital, cardiac, musculoskeletal and nervous system problems (CCOPPM, 2018). Population level data confirmed that preterm infants were more likely than full-term infants to be born with a congenital malformation. Moreover, infants with congenital anomalies were 3 times more likely to be born preterm than those without. Furthermore, regardless of gestation, small for gestational age (SGA) was more common in infants with congenital anomalies and, regardless of gestation, congenital anomalies were more common in infants born SGA.
Neurodevelopmental Delay Following Neonatal Surgery
Anomalies which require surgical management in the newborn period inevitably increase the risk of brain injury and subsequent neurodevelopmental impairment. Stolwijk et al. reported cognitive and motor developmental delay in 23% of patients in a systematic review of 1- to 2-year outcomes using the Bayley Scales of Infant and Toddler Development (Stolwijk et al., 2016). Delays were most prominent for the children with congenital diaphragmatic hernia, generally the most unwell group of anomalies requiring non-cardiac surgery, and therefore the most vulnerable to brain injury. Similarly, the DAISy study reported reduced Bayley Scales on all domains amongst infants who had either cardiac or non-cardiac surgery in the first 90 days of life, at both 1 and 3 years of age (Walker et al., 2015).
Risk of Brain Injury in Neonates Requiring Surgery
There are multiple potential contributors to brain injury in infants requiring neonatal surgery, beyond the direct impact of congenital anomalies, including: hypoxia and ischemia related to the underlying condition; vulnerability due to comorbid genetic anomalies; pain, sedation and analgesia; surgery and anesthesia; prolonged hospitalization; the altered family environment and impact on parental mental health, as well as parent-infant attachment (Govindaswamy et al., 2020; Diffin et al., 2016).
The literature regarding the impact of anesthesia on the neonatal brain is rapidly expanding. Whilst retrospective studies of infants have raised some concerns about anesthetic toxicity in the developing brain, prospective research has been somewhat reassuring. The GAS trial taught us that 40 min of general anesthesia for the repair of inguinal hernias in boys did not impact on measured 2- or 5-year neurodevelopmental outcomes, compared to those who received a spinal anesthetic (Davidson et al., 2016; McCann et al., 2019). A Canadian population-based study also showed no increased risk of adverse child development on school entry for children who had undergone surgery compared with sibling-matched pairs (O'Leary et al., 2019). However, that study intentionally excluded children with neurodevelopmental impairment. Of course, anesthesia and surgery occur for a few hours amongst what is often many weeks spent in the neonatal intensive care unit (NICU) for babies with congenital anomalies.
While clinical studies to date have largely focused on the impact of anesthesia on healthy infants, much pre-clinical research should lead us to interpret these findings with caution (Ben-Ari, 2002). Many anesthetic and sedative agents are GABA antagonists and have been shown to be neurotoxic in neonates (Andropoulos, 2018; Gascoigne et al., 2021). It also follows that the variability of development of GABA synapses may also further be altered by other neuronal disruptions such as prematurity. GABA is excitatory in the newborn brain, becoming inhibitory as chloride co-transporters mature, most importantly KCC2. Extensive animal research has identified the potentially toxic effects of a mismatch between GABA- and glutamate-mediated inhibition and excitation, which may occur with altered maturation of chloride co-transporters. Ben-Ari proposed that ‘the shift of GABA actions is a developmentally regulated function that signals the shift from a genetically determined programme to one that takes neuronal and environmental factors into account’.
Minimal human research exits regarding the impact of anesthesia on neonates who have already experienced some degree of brain compromise and in those requiring multiple operations over the first weeks of life. The extended peri-operative period and intensive care stay clearly exposes infants to ongoing risks beyond the surgery and anesthesia itself. For example, exposure to opiates both in utero and during preterm care has impacts on brain growth and later neurodevelopmental profile (Ranger et al., 2015; Zwicker et al., 2016; Steinbauer et al., 2021; Walhovd et al., 2007). Moreover, exposure to pain itself during the preterm course has an impact on thalamic development and longer-term neurodevelopment (Duerden et al., 2018; Schneider et al., 2018).
Functional deficits may also emerge through limits to prone positioning in the NICU following thoracic or abdominal surgery. The development of feeding disorders is also frequently experienced by neonates due to the balance of adverse oral experiences such as regular suctioning or severe gastro-esophageal reflux disease (Ferguson, 2017). The physical impact of impairment on normal nutritional intake for infants who are dependent on parenteral nutrition, or those with excessive caloric requirements due to underlying disease, also has the potential to impact both physical and brain development.
The risks to neonates undergoing surgery for congenital anomalies are demonstrated through imaging studies showing increased rates of brain injury and deviation from normal growth and development patterns. Moran et al. reported the post-operative MRI findings of 39 neonates with congenital diaphragmatic hernia, esophageal atresia or abdominal wall defects, who were subsequently assessed at 2 years of age (Moran et al., 2019). Compared with gender and gestational-age matched controls, infants requiring surgery had smaller brains on quantitative measures, were 10 times more likely to have white matter signal abnormalities and 6 times more likely to have delayed gyral maturation. The group who underwent surgery for congenital anomalies also had lower mean scores than controls in all three domains of the Bayley Scales at 2 years.
Stolwijk et al. performed MRI brain scans post-operatively in 101 infants, of whom 32 were born prematurely (Stolwijk et al., 2017). MRI abnormalities were found in 75% pre-term and 58% full-term infants. In the pre-term group, most abnormalities were parenchymal and included white matter lesions, punctate cerebellar lesions, thalamic infarction and periventricular hemorrhagic infarction. Prematurity and the type of congenital anomaly were most predictive of brain injury.
Surgery and Prematurity
Congenital anomalies have long been known to be an independent risk factor for neonatal morbidity in infants born prematurely (Linhart et al., 2000). In an outcome study of 5- and 8-year-olds with abdominal wall defects, infants born before 37 weeks gestation performed worse on every test compared with term-born infants at both 5 and 8 years (Burnett et al., 2018). In infants with congenital diaphragmatic hernia, lower gestational age was an independent risk factor for impaired language and motor development at 2 years but had an ongoing impact on full-scale intelligence quotient (FSIQ) and processing speed even at 8 years (Gunn-Charlton et al., 2019). For infants born with esophageal atresia, the acute impact of comorbid prematurity is substantial, including pre-operative respiratory compromise, delayed repair and gastrostomy formation, increased risk of surgical complications, oral aversion and feeding difficulties, length of stay as well as potential comorbid lesions including cardiac anomalies (Hunt et al., 2016). In 32.2-year-olds with esophageal atresia, infants with a Bayley score more than 1 standard deviation below the test normative mean at 2 years were, on average, 3 weeks more premature, 1 kg lighter at birth and had more than twice the hospital length of stay, compared with infants with a 2-year Bayley score in the normal range (Gunn et al., 2016b). However, by school-age the impact of prematurity was overcome by other contributing illness-related and environmental factors (Burnett et al., 2021).
If surgery itself (as well as the condition leading to surgery) is a risk to term-born neonates, then the additive impact of prematurity is potentially cumulative. Hunt et al. reported the 8-year-old outcomes of three cohorts of extremely preterm infants who underwent a surgical procedure during their NICU admission (Hunt et al., 2018). They found that rates of neurosensory disability were more than 4-fold higher in children who had undergone surgery (33%) compared with those who didn’t (10%). Surgery in those infants would most likely have been for conditions such as necrotizing enterocolitis or a patent ductus arteriosus ligation rather than for management of a congenital anomaly per se.
Walsh et al. specifically excluded congenital anomalies from a group of preterm infants less than 30 weeks gestation included in a study comparing MRI at term-equivalent age and 2-year outcome between those who did and did not receive surgery and anesthesia (Walsh et al., 2021). A relationship was found between exposure to surgery (with a dose effect of time) and relative reductions in white matter and deep gray matter volume. At 2 years, surgical exposure was associated with lower cognitive and motor scores and there remained a dose effect of surgical time, even when controlling for the MRI findings, suggesting that more complex microstructural factors are at play beyond brain growth. Gano et al. also described adverse neurodevelopmental outcomes in preterm infants born before 33 weeks who underwent two or more surgeries during the preterm period, with 20-point lower FSIQ at school age compared with children had not undergone surgery (Gano et al., 2015).
Most major neonatal surgery is time-critical such that pre-operative MRI is very challenging to obtain. Those researchers who have managed to obtain such images are subject to extreme bias as the more complex or unwell infants are least likely to have been able to access the MRI scanner prior to surgery. Fetal imaging would be the obvious solution to exploring brain growth prior to non-cardiac surgery but has not yet been widely explored to date.
Brain Injury in Congenital Heart Disease
Congenital heart disease (CHD) makes up the largest cohort of infants with congenital anomalies requiring neonatal surgery and has provided a helpful model to understand the impact of impaired fetal development on the growing brain. Fortunately, cardiac anomalies often have a slightly longer window of opportunity to allow pre-operative imaging than non-cardiac surgical anomalies. Furthermore, there is an extensive literature exploring fetal MRI in this population.
Fetal and Neonatal Brain Development With CHD
Many studies using both ultrasound and MRI have now shown reductions in brain growth during the second and third trimester in fetuses with CHD, the variance from normal fetal brains of which becomes more pronounced through pregnancy (Limperopoulos et al., 2010; Ortinau et al., 2019). Early neonatal MRI confirms that brain abnormalities include delayed myelination patterns, impaired white matter microstructural development, abnormal brain metabolism, abnormal cortical folding and reductions in brain volumes (Beca et al., 2013; Ortinau et al., 2013; Ortinau et al., 2012; Miller et al., 2007; Licht et al., 2009). These findings are not specific to the cardiac diagnosis but are seen in infants with right and left heart obstruction, suggesting the impact is related more closely to chronic cerebral hypoxia rather than altered cerebral blood flow per se. This potential link has been confirmed by MRI studies linking cerebral oxygenation with impaired growth in fetuses with CHD (Sun et al., 2015). Gestational age and chronicity of hypoxia affect the fetal response, which most commonly includes cerebral vasodilation (Ortinau and Shimony, 2020).
It is likely that hypoxic injury in the third trimester has a similar effect on brain development to that seen in preterm infant brains. It is therefore not surprising that the pattern of injury seen in term newborns with CHD is remarkably similar that of term-corrected preterm brains. In particular, MRI studies have shown that periventricular punctuate white matter injury is very common in both populations, although the more extensive patterns of periventricular leukomalacia seen historically, and still occasionally contemporaneously, in preterm infants, are seen less commonly in CHD (Beca et al., 2013; Ortinau and Neil, 2015; Guo et al., 2019). Intriguingly, the long-term motor development trajectory varies somewhat between the two groups, with lower rates of cerebral palsy in CHD, except where later cerebrovascular accidents have occurred. However, the pattern of attentional problems into school age is very similar between the groups (Claessens et al., 2018; O'Shea et al., 2013). The differences are most likely impacted by chronicity of illness and subsequent brain impacts, especially low cardiac output syndrome and stroke.
Given the impaired fetal pattern of brain development in CHD, it follows that the brains of newborns born with CHD are more immature than their healthy counterparts (Beca et al., 2013; Licht et al., 2009). Furthermore, the brains of neonates showing evidence of immaturity relative to their gestational age on pre-operative scans, have higher rates of injury detected on post-operative MRI scans and, perhaps more importantly, are more likely to exhibit subsequent developmental delay (Beca et al., 2013; Andropoulos et al., 2014).
Prematurity and Brain Injury in CHD
As with non-cardiac congenital anomalies, neonates with CHD are more likely than those without CHD to be born preterm and/or SGA and preterm infants are more likely to be born with CHD than those who reach full-term. Lower gestational age is a strong predictor of brain injury (encompassing a range of patterns of anomalies on neuroimaging) and neurodevelopmental impairment in CHD, even in early term-born infants. A study of 971 consecutive neonates with critical CHD was stratified by gestational age and adjusted for severity of lesion, against a reference group of neonates born at 39–40 weeks gestation. The risk of cerebral injury increased 2-fold in the 37–39 week gestation group; 8-fold in the 34–37 week gestation group and 25-fold in infants less than 34 weeks gestation at birth (Costello et al., 2010). In the Hearts and Minds Study of babies over 36 weeks at birth with critical CHD, on multivariable analysis of 2-year outcomes, the lowest developmental quotients on the Bayley Scales related to intrinsic patient factors including reduced gestational age at birth, single ventricle physiology with pulmonary obstruction and the need for repeat surgery (Gunn et al., 2016a). Ortinau et al. demonstrated that CHD does not increase the risk of intraventricular hemorrhage over that of gestation-associated risk (Ortinau et al., 2018), but Bell et al. showed that preterm neonates cared for in a cardiac intensive care unit are 3.2 times more likely to display acute neurological events (including cerebral hemorrhage or white matter injury) compared with older patients (Bell et al., 2019).
There has been much debate regarding optimal timing of surgery for infants born prematurely with critical CHD (Curzon et al., 2008; Hickey et al., 2012; Chu et al., 2017). Intentionally delayed surgery, beyond the best-practice timing for a given cardiac lesion, allows for organ growth and maturity, potential nutritional benefits, fall in pulmonary vascular resistance, improvement in immune competence and safe operative scheduling. Conversely, the risks of delaying surgery include the secondary effects of unrepaired CHD including hypoxemia, increased pulmonary blood flow, systemic pulmonary artery pressures, ductal steal, intensive care morbidity and the overall cost of care. Studies have shown that elective delayed surgery in preterm infants increases the risk of mortality, white matter injury on MRI and secondary morbidities such as infection, apnea, and necrotizing enterocolitis, whereas intentional delays reduce the risk of intracerebral hemorrhage, renal dysfunction and coagulopathy. These difficult decisions regarding competing clinical interests will continue to be made at an institutional level, weighing up risk and benefit for individual patients. However, it is clear than in most centers, a collaborative approach in care between cardiac intensive care, cardiology and neonatology is likely to lead to the best outcomes for preterm infants with CHD (Krishnamurthy et al., 2013).
Conclusion
Both critical CHD and non-cardiac congenital anomalies which require neonatal surgery, increase the risk of brain injury and subsequent neurodevelopmental impairment compared with healthy infants. MRI patterns of impairment suggest different mechanisms are at play between the two surgical groups, with myelination delay more prominent in the cardiac group and gyral maturation delays more common in the non-cardiac group. However, both types of lesions place the neonate at risk of further brain injury throughout their peri-operative and intensive care course. The additive burden of prematurity is complex but combines the vulnerable states of both prematurity and relative immaturity such that an increased risk of brain injury and subsequent neurodevelopmental impairment is inevitable.
Many studies (including my own) have attempted to simplify and homogenize research findings, by excluding preterm infants from explorations of congenital anomalies on injury and outcome, when in fact this is exactly the group who needs the most attention. Rather than excluding infants with anomalies from studies of preterm neurodevelopment and preterm infants from studies of congenital anomalies, future studies should focus specifically on minimizing risk to preterm infants with comorbid congenital anomalies. This could include health-service research exploring the multidisciplinary team requirements to merge best practices across clinical craft groups with a patient-centered focus. Studies of the impact of developmental care practices in preterm infants could be extended into the surgical and cardiac environment. Further studies should provide gestation-based dosing for commonly used anesthetic and analgesic agents. Follow-up programs should incorporate later preterm infants than historically included, to allow for the potentially additive impact of surgical complexity.
A more concerted focus on these high-risk infants should obviate the increased risk of impairment through improvements in patient-centered, developmentally appropriate care, which carefully balances pain management, nutritional support and brain-protective strategies from fetal or neonatal diagnosis to childhood and beyond.
Author Contributions
JG-C was the sole contributing author of this manuscript.
Conflict of Interest
The handling editor [RWH] declared a past co-authorship with the author.
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
Andropoulos D. B., Ahmad H. B., Haq T., Brady K., Stayer S. A., Meador M. R., et al. (2014). The Association between Brain Injury, Perioperative Anesthetic Exposure, and 12-month Neurodevelopmental Outcomes after Neonatal Cardiac Surgery: a Retrospective Cohort Study. Paediatr. Anaesth. 24, 266–274. doi:10.1111/pan.12350
Andropoulos D. B. (2018). Effect of Anesthesia on the Developing Brain: Infant and Fetus. Fetal Diagn. Ther. 43, 1–11. doi:10.1159/000475928
Beca J., Gunn J. K., Coleman L., Hope A., Reed P. W., Hunt R. W., et al. (2013). New white Matter Brain Injury after Infant Heart Surgery Is Associated with Diagnostic Group and the Use of Circulatory Arrest. Circulation 127, 971–979. doi:10.1161/circulationaha.112.001089
Bell J. L., Saenz L., Domnina Y., Baust T., Panigrahy A., Bell M. J., et al. (2019). Acute Neurologic Injury in Children Admitted to the Cardiac Intensive Care Unit. Ann. Thorac. Surg. 107, 1831–1837. doi:10.1016/j.athoracsur.2018.12.027
Ben-Ari Y. (2002). Excitatory Actions of Gaba during Development: the Nature of the Nurture. Nat. Rev. Neurosci. 3, 728–739. doi:10.1038/nrn920
Burnett A. C., Gunn J. K., Hutchinson E. A., Moran M. M., Kelly L. M., Sevil U. C., et al. (2018). Cognition and Behaviour in Children with Congenital Abdominal wall Defects. Early Hum. Develop. 116, 47–52. doi:10.1016/j.earlhumdev.2017.11.002
Burnett A. C., Gunn-Charlton J. K., Malarbi S., Hutchinson E., Tan T. Y., Teague W. J., et al. (2021). Cognitive, Academic, and Behavioral Functioning in School-Aged Children Born with Esophageal Atresia. J. Pediatr. Surg. 56, 1737–1744. doi:10.1016/j.jpedsurg.2021.01.014
Buss C., Entringer S., Wadhwa P. D. (2012). Fetal Programming of Brain Development: Intrauterine Stress and Susceptibility to Psychopathology. Sci. Signal. 5, pt7. doi:10.1126/scisignal.2003406
CCOPPM (2018). Victorian Congenital Anomalies Register 2018, Congenital Anomalies in Victoria 2015–2016. Melbourne: Safer Care Victoria.
Cheong J. L. Y., Olsen J. E., Lee K. J., Spittle A. J., Opie G. F., Clark M., et al. (2021). Temporal Trends in Neurodevelopmental Outcomes to 2 Years after Extremely Preterm Birth. JAMA Pediatr. 175, 1035–1042. doi:10.1001/jamapediatrics.2021.2052
Chu P. Y., Li J. S., Kosinski A. S., Hornik C. P., Hill K. D. (2017). Congenital Heart Disease in Premature Infants 25-32 Weeks' Gestational Age. J. Pediatr. 181, 37–41. doi:10.1016/j.jpeds.2016.10.033
Claessens N. H. P., Algra S. O., Ouwehand T. L., Jansen N. J. G., Schappin R., Haas F., et al. (2018). Perioperative Neonatal Brain Injury Is Associated with Worse School‐age Neurodevelopment in Children with Critical Congenital Heart Disease. Dev. Med. Child. Neurol. 60, 1052–1058. doi:10.1111/dmcn.13747
Costello J. M., Polito A., Brown D. W., Mcelrath T. F., Graham D. A., Thiagarajan R. R., et al. (2010). Birth before 39 Weeks' Gestation Is Associated with Worse Outcomes in Neonates with Heart Disease. Pediatrics 126, 277–284. doi:10.1542/peds.2009-3640
Curzon C. L., Milford-Beland S., Li J. S., O'Brien S. M., Jacobs J. P., Jacobs M. L., et al. (2008). Cardiac Surgery in Infants with Low Birth Weight Is Associated with Increased Mortality: Analysis of the Society of Thoracic Surgeons Congenital Heart Database. J. Thorac. Cardiovasc. Surg. 135, 546–551. doi:10.1016/j.jtcvs.2007.09.068
Davidson A. J., Disma N., De Graaff J. C., Withington D. E., Dorris L., Bell G., et al. (2016). Neurodevelopmental Outcome at 2 Years of Age after General Anaesthesia and Awake-Regional Anaesthesia in Infancy (GAS): an International Multicentre, Randomised Controlled Trial. The Lancet 387, 239–250. doi:10.1016/s0140-6736(15)00608-x
Diffin J., Spence K., Naranian T., Badawi N., Johnston L. (2016). Stress and Distress in Parents of Neonates Admitted to the Neonatal Intensive Care Unit for Cardiac Surgery. Early Hum. Develop. 103, 101–107. doi:10.1016/j.earlhumdev.2016.08.002
Duerden E. G., Grunau R. E., Guo T., Foong J., Pearson A., Au-Young S., et al. (2018). Early Procedural Pain Is Associated with Regionally-specific Alterations in Thalamic Development in Preterm Neonates. J. Neurosci. 38, 878–886. doi:10.1523/jneurosci.0867-17.2017
Egbe A., Uppu S., Lee S., Stroustrup A., Ho D., Srivastava S. (2015). Congenital Malformations in the Newborn Population: a Population Study and Analysis of the Effect of Sex and Prematurity. Pediatr. Neonatal. 56, 25–30. doi:10.1016/j.pedneo.2014.03.010
Ferguson E. A. (2017). The Development of Feeding in Infants with Oesophageal Atresia between Birth and Nine Months of Age. Melbourne: The University of Melbourne
Gano D., Andersen S. K., Glass H. C., Rogers E. E., Glidden D. V., Barkovich A. J., et al. (2015). Impaired Cognitive Performance in Premature Newborns with Two or More Surgeries Prior to Term-Equivalent Age. Pediatr. Res. 78, 323–329. doi:10.1038/pr.2015.106
Gascoigne D. A., Serdyukova N. A., Aksenov D. P. (2021). Early Development of the GABAergic System and the Associated Risks of Neonatal Anesthesia. Int. J. Mol. Sci. 22. doi:10.3390/ijms222312951
Gaynor J. W., Stopp C., Wypij D., Andropoulos D. B., Atallah J., Atz A. M., et al. (2015). Neurodevelopmental Outcomes after Cardiac Surgery in Infancy. Pediatrics 135, 816–825. doi:10.1542/peds.2014-3825
Govindaswamy P., Laing S., Waters D., Walker K., Spence K., Badawi N. (2020). Stressors of Parents of Infants Undergoing Neonatal Surgery for Major Non‐cardiac Congenital Anomalies in a Surgical Neonatal Intensive Care Unit. J. Paediatr. Child. Health 56, 512–520. doi:10.1111/jpc.14673
Gunn J. K., Beca J., Hunt R. W., Goldsworthy M., Brizard C. P., Finucane K., et al. (2016a). Perioperative Risk Factors for Impaired Neurodevelopment after Cardiac Surgery in Early Infancy. Arch. Dis. Child. 101, 1010–1016. doi:10.1136/archdischild-2015-309449
Gunn J. K., Greaves S., Hutchinson E. A., Kelly L. M., Moran M. M., Chisholm A. K., et al. (2016b). P-18: Two Year Neurodevelopmental Outcome Following Neonatal Repair of Oesophageal Atresia. Dis. Esophagus 29, 293–294. doi:10.1093/dote/29.3.293b
Gunn-Charlton J. K., Burnett A. C., Malarbi S., Moran M. M., Hutchinson E. A., Greaves S., et al. (2019). Neonatal Neuroimaging after Repair of Congenital Diaphragmatic Hernia and Long-Term Neurodevelopmental Outcome. World Jnl Ped Surg. 2, e000037. doi:10.1136/wjps-2019-000037
Guo T., Chau V., Peyvandi S., Latal B., Mcquillen P. S., Knirsch W., et al. (2019). White Matter Injury in Term Neonates with Congenital Heart Diseases: Topology & Comparison with Preterm Newborns. Neuroimage 185, 742–749. doi:10.1016/j.neuroimage.2018.06.004
Hack M., Taylor H. G., Drotar D., Schluchter M., Cartar L., Wilson-Costello D., et al. (2005). Poor Predictive Validity of the Bayley Scales of Infant Development for Cognitive Function of Extremely Low Birth Weight Children at School Age. Pediatrics 116, 333–341. doi:10.1542/peds.2005-0173
Hickey E. J., Nosikova Y., Zhang H., Caldarone C. A., Benson L., Redington A., et al. (2012). Very Low-Birth-Weight Infants with Congenital Cardiac Lesions: Is There merit in Delaying Intervention to Permit Growth and Maturation? J. Thorac. Cardiovasc. Surg. 143, 126–136. doi:10.1016/j.jtcvs.2011.09.008
Hunt R. W., Hickey L. M., Burnett A. C., Anderson P. J., Cheong J. L. Y., Doyle L. W., et al. (2018). Early Surgery and Neurodevelopmental Outcomes of Children Born Extremely Preterm. Arch. Dis. Child. Fetal Neonatal. Ed. 103, F227–F232. doi:10.1136/archdischild-2017-313161
Hunt R. W., Perkins E. J., King S. (2016). Peri-operative Management of Neonates with Oesophageal Atresia and Tracheo-Oesophageal Fistula. Paediatric Respir. Rev. 19, 3–9. doi:10.1016/j.prrv.2016.01.002
Inder T. E., De Vries L. S., Ferriero D. M., Grant P. E., Ment L. R., Miller S. P., et al. (2021). Neuroimaging of the Preterm Brain: Review and Recommendations. J. Pediatr. 237, 276–287. doi:10.1016/j.jpeds.2021.06.014
Jansen L., Van Steenis A., Van Den Berg-Huysmans A. A., Wiggers-De Bruine S. T., Rijken M., De Vries L. S., et al. (2021). Associations between Neonatal Magnetic Resonance Imaging and Short- and Long-Term Neurodevelopmental Outcomes in a Longitudinal Cohort of Very Preterm Children. J. Pediatr. 234, 46–53. doi:10.1016/j.jpeds.2021.02.005
Kase J. S., Visintainer P. (2007). The Relationship between Congenital Malformations and Preterm Birth. J. Perinat Med. 35, 538–542. doi:10.1515/JPM.2007.132
Krishnamurthy G., Ratner V., Bacha E. (2013). Neonatal Cardiac Care, a Perspective. Semin. Thorac. Cardiovasc. Surg. Pediatr. Card. Surg. Annu. 16, 21–31. doi:10.1053/j.pcsu.2013.01.007
Licht D. J., Shera D. M., Clancy R. R., Wernovsky G., Montenegro L. M., Nicolson S. C., et al. (2009). Brain Maturation Is Delayed in Infants with Complex Congenital Heart Defects. J. Thorac. Cardiovasc. Surg. 137, 529–537. doi:10.1016/j.jtcvs.2008.10.025
Limperopoulos C., Tworetzky W., Mcelhinney D. B., Newburger J. W., Brown D. W., Robertson R. L., et al. (2010). Brain Volume and Metabolism in Fetuses with Congenital Heart Disease. Circulation 121, 26–33. doi:10.1161/circulationaha.109.865568
Linhart Y., Bashiri A., Maymon E., Shoham-Vardi I., Furman B., Vardi H., et al. (2000). Congenital Anomalies Are an Independent Risk Factor for Neonatal Morbidity and Perinatal Mortality in Preterm Birth. Eur. J. Obstet. Gynecol. Reprod. Biol. 90, 43–49. doi:10.1016/s0301-2115(99)00196-7
Mccann M. E., De Graaff J. C., Dorris L., Disma N., Withington D., Bell G., et al. (2019). Neurodevelopmental Outcome at 5 Years of Age after General Anaesthesia or Awake-Regional Anaesthesia in Infancy (GAS): an International, Multicentre, Randomised, Controlled Equivalence Trial. The Lancet 393, 664–677. doi:10.1016/s0140-6736(18)32485-1
Miller S. P., Mcquillen P. S., Hamrick S., Xu D., Glidden D. V., Charlton N., et al. (2007). Abnormal Brain Development in Newborns with Congenital Heart Disease. N. Engl. J. Med. 357, 1928–1938. doi:10.1056/nejmoa067393
Moran M. M., Gunn-Charlton J. K., Walsh J. M., Cheong J. L. Y., Anderson P. J., Doyle L. W., et al. (2019). Associations of Neonatal Noncardiac Surgery with Brain Structure and Neurodevelopment: A Prospective Case-Control Study. J. Pediatr. 212, 93–101. doi:10.1016/j.jpeds.2019.05.050
O'Leary J. D., Janus M., Duku E., Wijeysundera D. N., To T., Li P., et al. (2019). Influence of Surgical Procedures and General Anesthesia on Child Development before Primary School Entry Among Matched Sibling Pairs. JAMA Pediatr. 173, 29–36. doi:10.1001/jamapediatrics.2018.3662
O'Shea T. M., Downey L. C., Kuban K. K. C. (2013). Extreme Prematurity and Attention Deficit: Epidemiology and Prevention. Front. Hum. Neurosci. 7, 578. doi:10.3389/fnhum.2013.00578
Ophelders D. R. M. G., Gussenhoven R., Klein L., Jellema R. K., Westerlaken R. J. J., Hütten M. C., et al. (2020). Preterm Brain Injury, Antenatal Triggers, and Therapeutics: Timing Is Key. Cells, 9. doi:10.3390/cells9081871
Ortinau C., Alexopoulos D., Dierker D., Van Essen D., Beca J., Inder T. (2013). Cortical Folding Is Altered before Surgery in Infants with Congenital Heart Disease. J. Pediatr. 163, 1507–1510. doi:10.1016/j.jpeds.2013.06.045
Ortinau C., Beca J., Lambeth J., Ferdman B., Alexopoulos D., Shimony J. S., et al. (2012). Regional Alterations in Cerebral Growth Exist Preoperatively in Infants with Congenital Heart Disease. J. Thorac. Cardiovasc. Surg. 143, 1264–1270. doi:10.1016/j.jtcvs.2011.10.039
Ortinau C. M., Anadkat J. S., Smyser C. D., Eghtesady P. (2018). Intraventricular Hemorrhage in Moderate to Severe Congenital Heart Disease. Pediatr. Crit. Care Med. 19, 56–63. doi:10.1097/pcc.0000000000001374
Ortinau C. M., Rollins C. K., Gholipour A., Yun H. J., Marshall M., Gagoski B., et al. (2019). Early-Emerging Sulcal Patterns Are Atypical in Fetuses with Congenital Heart Disease. Cereb. Cortex 29, 3605–3616. doi:10.1093/cercor/bhy235
Ortinau C. M., Shimony J. S. (2020). The Congenital Heart Disease Brain: Prenatal Considerations for Perioperative Neurocritical Care. Pediatr. Neurol. 108, 23–30. doi:10.1016/j.pediatrneurol.2020.01.002
Ortinau C., Neil J. (2015). The Neuroanatomy of Prematurity: normal Brain Development and the Impact of Preterm Birth. Clin. Anat. 28, 168–183. doi:10.1002/ca.22430
Ranger M., Zwicker J. G., Chau C. M. Y., Park M. T. M., Chakravarthy M. M., Poskitt K., et al. (2015). Neonatal Pain and Infection Relate to Smaller Cerebellum in Very Preterm Children at School Age. J. Pediatr. 167, 292–298. doi:10.1016/j.jpeds.2015.04.055
Schneider J., Duerden E. G., Guo T., Ng K., Hagmann P., Bickle Graz M., et al. (2018). Procedural Pain and Oral Glucose in Preterm Neonates: Brain Development and Sex-specific Effects. Pain 159, 515–525. doi:10.1097/j.pain.0000000000001123
Snookes S. H., Gunn J. K., Eldridge B. J., Donath S. M., Hunt R. W., Galea M. P., et al. (2010). A Systematic Review of Motor and Cognitive Outcomes after Early Surgery for Congenital Heart Disease. Pediatrics 125, e818–e827. doi:10.1542/peds.2009-1959
Steinbauer P., Deindl P., Fuiko R., Unterasinger L., Cardona F., Wagner M., et al. (2021). Long-term Impact of Systematic Pain and Sedation Management on Cognitive, Motor, and Behavioral Outcomes of Extremely Preterm Infants at Preschool Age. Pediatr. Res. 89, 540–548. doi:10.1038/s41390-020-0979-2
Stolwijk L. J., Lemmers P. M., Harmsen M., Groenendaal F., De Vries L. S., Van Der Zee D. C., et al. (2016). Neurodevelopmental Outcomes after Neonatal Surgery for Major Noncardiac Anomalies. Pediatrics 137, e20151728. doi:10.1542/peds.2015-1728
Stolwijk L. J., Keunen K., De Vries L. S., Groenendaal F., Van Der Zee D. C., Van Herwaarden M. Y. A., et al. (2017). Neonatal Surgery for Noncardiac Congenital Anomalies: Neonates at Risk of Brain Injury. J. Pediatr. 182, 335–341. doi:10.1016/j.jpeds.2016.11.080
Sun L., Macgowan C. K., Sled J. G., Yoo S.-J., Manlhiot C., Porayette P., et al. (2015). Reduced Fetal Cerebral Oxygen Consumption Is Associated with Smaller Brain Size in Fetuses with Congenital Heart Disease. Circulation 131, 1313–1323. doi:10.1161/circulationaha.114.013051
Van Bel F., Vaes J., Groenendaal F. (2019). Prevention, Reduction and Repair of Brain Injury of the Preterm Infant. Front. Physiol. 10, 181. doi:10.3389/fphys.2019.00181
Walhovd K. B., Moe V., Slinning K., Due-Tønnessen P., Bjørnerud A., Dale A. M., et al. (2007). Volumetric Cerebral Characteristics of Children Exposed to Opiates and Other Substances In Utero. Neuroimage 36, 1331–1344. doi:10.1016/j.neuroimage.2007.03.070
Walker K., Badawi N., Halliday R., Stewart J., Sholler G. F., Winlaw D. S., et al. (2012). Early Developmental Outcomes Following Major Noncardiac and Cardiac Surgery in Term Infants: a Population-Based Study. J. Pediatr. 161, 748–752. doi:10.1016/j.jpeds.2012.03.044
Walker K., Loughran-Fowlds A., Halliday R., Holland A. J., Stewart J., Sholler G. F., et al. (2015). Developmental Outcomes at 3 Years of Age Following Major Non-cardiac and Cardiac Surgery in Term Infants: A Population-Based Study. J. Paediatr. Child. Health 51, 1221–1225. doi:10.1111/jpc.12943
Walsh B. H., Paul R. A., Inder T. E., Shimony J. S., Smyser C. D., Rogers C. E. (2021). Surgery Requiring General Anesthesia in Preterm Infants Is Associated with Altered Brain Volumes at Term Equivalent Age and Neurodevelopmental Impairment. Pediatr. Res. 89, 1200–1207. doi:10.1038/s41390-020-1030-3
Keywords: prematurity, congenital anomaly, neonate, brain injury, neurodevelopment
Citation: Gunn-Charlton JK (2022) Impact of Comorbid Prematurity and Congenital Anomalies: A Review. Front. Physiol. 13:880891. doi: 10.3389/fphys.2022.880891
Received: 22 February 2022; Accepted: 11 April 2022;
Published: 01 July 2022.
Edited by:
Rod W. Hunt, Monash University, AustraliaReviewed by:
Christopher G. Wilson, Loma Linda University, United StatesMatthew J. Fogarty, Mayo Clinic, United States
Copyright © 2022 Gunn-Charlton. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Julia K. Gunn-Charlton, julia.charlton@mcri.edu.au