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Article

Resuscitation with an Intact Cord Enhances Pulmonary Vasodilation and Ventilation with Reduction in Systemic Oxygen Exposure and Oxygen Load in an Asphyxiated Preterm Ovine Model

by
Praveen Chandrasekharan
1,*,
Sylvia Gugino
1,
Justin Helman
1,
Carmon Koenigsknecht
1,
Lori Nielsen
1,
Nicole Bradley
1,
Jayasree Nair
1,
Vikash Agrawal
2,
Mausma Bawa
1,
Andreina Mari
1,
Munmun Rawat
1 and
Satyan Lakshminrusimha
3
1
Department of Pediatrics, Jacobs School of Medicine & Biomedical Sciences, University at Buffalo, Buffalo, NY 14260, USA
2
Department of Pediatrics, Loma Linda University, Loma Linda, CA 92350, USA
3
Department of Pediatrics, Division of Neonatology, University of California Davis School of Medicine, Sacramento, CA 95817, USA
*
Author to whom correspondence should be addressed.
Children 2021, 8(4), 307; https://0-doi-org.brum.beds.ac.uk/10.3390/children8040307
Submission received: 1 April 2021 / Revised: 13 April 2021 / Accepted: 15 April 2021 / Published: 17 April 2021
(This article belongs to the Special Issue Neonatal Resuscitation with Placental Circulation Intact)
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Versions Notes

Abstract

:
(1) Background: Optimal initial oxygen (O2) concentration in preterm neonates is controversial. Our objectives were to compare the effect of delayed cord clamping with ventilation (DCCV) to early cord clamping followed by ventilation (ECCV) on O2 exposure, gas exchange, and hemodynamics in an asphyxiated preterm ovine model. (2) Methods: Asphyxiated preterm lambs (127–128 d) with heart rate <90 bpm were randomly assigned to DCCV or ECCV. In DCCV, positive pressure ventilation (PPV) was initiated with 30–60% O2 and titrated based on preductal saturations (SpO2) with an intact cord for 5 min, followed by clamping. In ECCV, the cord was clamped, and PPV was initiated. (3) Results: Fifteen asphyxiated preterm lambs were randomized to DCCV (N = 7) or ECCV (N = 8). The inspired O2 (40 ± 20% vs. 60 ± 20%, p < 0.05) and oxygen load (520 (IQR 414–530) vs. 775 (IQR 623–868), p-0.03) in the DCCV group were significantly lower than ECCV. Arterial oxygenation and carbon dioxide (PaCO2) levels were significantly lower and peak pulmonary blood flow was higher with DCCV. (4) Conclusion: In asphyxiated preterm lambs, resuscitation with an intact cord decreased O2 exposure load improved ventilation with an increase in peak pulmonary blood flow in the first 5 min.

Graphical Abstract

1. Introduction

In the delivery room, a depressed preterm neonate often needs positive pressure ventilation (PPV) with supplemental oxygen [1]. In a surfactant deficient state complicated by birth asphyxia, the current recommendations to start ventilation with 21–30% oxygen (O2) may not achieve target saturations (SpO2) [2,3,4]. Inability to achieve target SpO2 by 5 min is associated with poor outcomes in preterm infants. Birth asphyxia could increase pulmonary vascular resistance (PVR) and impair pulmonary vascular transition at birth. In a subgroup analysis of the Targeted Oxygen in the Resuscitation of Preterm Infants and their Developmental Outcomes (To2rpido) trial by Oei et al. <28-week gestation preterm infants resuscitated with 21% O2 had higher mortality due to respiratory failure, compared to 100% O2 [5]. Previously, we have shown that ventilation with 100% O2 (but not 21%), led to a decrease in PVR and increased systemic to pulmonary pressure gradient in preterm lambs [6]. Such impaired pulmonary vascular transition at birth could explain the higher mortality demonstrated by Oei et al. in <28-week infants resuscitated with 21% oxygen [5]. Although 100% O2 exposure in preterm lambs was associated with improved pulmonary blood flow and preductal SpO2, it also led to supraphysiological arterial oxygenation (PaO2) that could lead to hyperoxic injury [6]. With concerns of hyperoxia, higher oxidative injury, the use of 100% O2 is not recommended [2,3].
The feasibility of delaying the clamping of the cord and its benefits have been studied extensively [1,7,8,9,10,11,12,13,14,15]. However, optimal oxygenation during delayed cord claming (DCC) and ventilation is not known. Ventilation with an intact cord has been shown to improve cardiovascular transition in both translational animal models and human newborns [10,11,12,13,15,16,17,18,19,20,21,22,23,24]. It has been recently reported that the preductal SpO2 in neonates who had an intact cord was higher compared to the recommended SpO2 ranges obtained following early cord clamping (ECC) [13,16,22].
Currently, there are no concrete recommendations to delay the clamping of the cord and provide positive pressure ventilation in a depressed preterm neonate [2,3]. We conducted this pilot study to understand the effect of ventilation and supplemental oxygen with an intact cord using an asphyxiated preterm ovine model to address this knowledge gap. We aimed to study the effect of supplementing oxygen with and without an intact cord in the setting of perinatal acidosis, on preductal SpO2, oxygenation, ventilation, and hemodynamic parameters in the first 5 min of resuscitation.

2. Materials and Methods

The study was approved by the Institutional Animal Care and Use Committee, University of Buffalo, Buffalo New York, USA and followed the ARRIVE guidelines. Time-dated ewes (127–128 d, gestation), approximately equivalent in lung maturity to preterm neonate ≈28-week gestation were used in this study. The ewes did not receive antenatal steroids. After an overnight fast, the ewes were anesthetized, a caesarean section was performed, and fetal lambs were partially exteriorized. These fetal lambs were instrumented while in placental circulation as described previously [6]. Instrumentation included placement of the right jugular and carotid lines for access, pressure monitoring, and blood draws. A left carotid artery probe was placed to monitor blood flows. The left pulmonary artery probe and ductal arteriosus probe were placed to monitor blood flows. The lambs were intubated, and the lung fluid was drained by gravity.
Asphyxia was induced by umbilical cord occlusion until the heart rate (HR) reached <90 bpm. Once the target HR was achieved, the fetus was randomized to early cord clamping and ventilation (ECCV) or delayed cord clamping and ventilation (DCCV) for 5 min. Our primary objective was to achieve a composite outcome of HR ≥100 bpm and SpO2 ≥80% by 5 min. For this reason, in DCCV, the cord was clamped only after 5 min unless the fetus had a drop in HR <60 bpm and ventilation continued. To simulate a real-life clinical scenario, the initial supplemental oxygen (O2) concentration was between 30–60% in both groups and not changed during the first 2 min of PPV. After 2 min, the O2 concentration was adjusted based on the neonatal resuscitation program (NRP) recommended target preductal SpO2. The titration of O2 was proportional to the difference between observed SpO2 and target SpO2 and was performed every min. In order to obtain an accurate and continuous recording of preductal SpO2, two preductal probes (on the tongue and the right upper limb) were placed.
Oxygen load (OL) was calculated using the following formula, OL = (VT × FiO2)/kg, where VT is tidal volume and FiO2 is a fraction of inspired oxygen. Total OL was calculated using the summation of breaths for 5 min as defined previously [25].
In a depressed, asphyxiated and surfactant-deficient preterm lamb with HR < 90 bpm, our primary objective was to evaluate if titrating supplemental O2 with (DCCV) and without an intact cord (ECCV) would lead to a higher rate of success in achieving target saturations as recommended by neonatal resuscitation program (NRP). The secondary objectives were to assess gas exchange and systemic and pulmonary hemodynamics along with oxygen load in the first 5 min of resuscitation.
Parametric data are presented as mean and standard deviation and analyzed by ANOVA. Non-parametric data are presented as median and interquartile range and analyzed by the Kruskal-Wallis test. The significance was set at a probability of less than five percent.

3. Results

Fifteen preterm lambs were randomized to DCCV (N-7) and ECCV (N-8). The characteristics are shown in Table 1 and were similar.
The asphyxiated preterm model had perinatal acidosis as shown in Table 1, which improved significantly with DCCV (7.02 ± 0.08) compared to ECCV (6.96 ± 0.13). The difference in pH was statistically significant throughout the first 5 min of PPV (p = 0.02). The HR improved in both groups by 5 min—DCCV (180 ± 20 bpm) and ECCV (188 ± 30 bpm). The mean blood pressures in both groups by 5 min were similar (DCCV (40 ± 10 mmHg) and ECCV (44 ± 15 mmHg)).

3.1. Oxygenation

A higher percentage of lambs achieved preductal saturation targets in the DCCV group (75%) in the first 5 min compared to ECCV (60%). However, this result was not statistically significant (p-0.065). Preductal SpO2 was significantly higher in the DCCV group compared to ECCV (p-0.01) (Figure 1).
The required oxygen concentration to achieve these target SpO2 were significantly higher in the ECCV group compared to the DCCV group (Figure 2).
Oxygen load (OL)—as mentioned previously, OL was calculated using the tidal volume (TV) per kg in the first 5 min. The average TV in ECCV and DCCV were 6.0 ± 1.5 mL/kg and 6.0 ± 2.3 mL/kg, respectively. The OL with DCCV (520 (414–530) mLO2/kg) was significantly lower compared to ECCV (775 (630–867) mLO2/kg) (p = 0.03) as shown in Figure 3.
Arterial oxygenation (PaO2)—despite the lower percentage of SpO2 targets with ECCV, the PaO2 was significantly higher (95 ± 65 mmHg) compared to DCCV (38 ± 9 mmHg, p-0.007) (Figure 4). The variability in arterial oxygenation with DCCV was minimal compared to ECCV, as shown by the standard deviations in Figure 4. The PaO2/FiO2 ratio at 5 min of PPV was 98 ± 50 in the DCCV group and 135 ± 87 mmHg in the ECCV group (p-0.4).

3.2. Ventilation

As mentioned previously, despite similar TV and ventilation rates in both groups in the first 5 min, the arterial carbon dioxide (PaCO2) levels were significantly lower with DCCV compared to ECCV (Figure 5).

3.3. Hemodynamics

Pulmonary blood flow—the peak left pulmonary blood flows (PBF) were significantly higher in the DCCV group compared to ECCV (Figure 6).
Carotid blood flow—the peak left carotid blood flow (CBF) was not different between the two groups as shown in Figure 7.

4. Discussion

In a depressed preterm neonate with HRs between 60–90 bpm, lower supplemental O2, as currently recommended by NRP, may not achieve the pre-specified target SpO2 or sustain pulmonary vasodilation. An alternative strategy is to ventilate with an intact cord and higher concentrations of supplemental O2, especially in the setting of perinatal acidosis. Perinatal acidosis increases PVR. Low FiO2 may not increase alveolar oxygen adequately to induce pulmonary vasodilation in preterm infants with high PVR. A combination of increased FiO2 and resuscitation with an intact cord results in “transient alveolar hyperoxia” without systemic hyperoxia due to “buffering” of PaO2 by umbilical venous return (Figure 4 and Figure 8). Such “differential oxygenation” may be an effective concept for the resuscitation of depressed preterm infants that do not show spontaneous respiratory activity. The second advantage of resuscitation with an intact cord is “dual-site” gas exchange enabling CO2 elimination in both the lungs and placenta.
In our pilot study, we tested our concept of “differential oxygenation” and “dual-site gas exchange” in a surfactant-deficient asphyxiated preterm lamb. We assessed the success of achieving target preductal saturation, gas exchange, and hemodynamics during ventilation with an intact cord as compared to the current standard of early cord clamping followed by resuscitation.
Arterial PaCO2 levels were significantly lower in the DCCV group despite similar inflation pressures, tidal volumes, and ventilator rates (Figure 5). We speculate the contribution of placental gas exchange during resuscitation with an intact cord for this decrease. More efficient ventilation leads to earlier normalization of pH with DCCV. Early normalization of PaCO2 increases pulmonary blood flow and avoids cerebral hyperemia.
The success in achieving the target preductal SpO2 in asphyxiated preterm lambs was similar in DCCV (75%) compared to ECCV (60%) lambs, although DCCV lambs required significantly lower FiO2. Previous clinical studies have shown improved SpO2 in the first few minutes after birth with an intact cord compared to immediate cord clamping [16,18,22]. Recently, the preductal SpO2 curves in spontaneous breathing term infants with an intact cord for a min were developed by Padilla-Sánchez et al. These curves show increased SpO2 compared to immediate cord clamping, as shown in a study published by Dawson et al. [13].
Our study’s striking feature was that the arterial oxygenation was much lower with decreased variability (as observed by lower standard deviations) in the DCCV group compared to the ECCV in the first 5 min. We speculate that the mixing of higher PO2 pulmonary venous return with lower PO2 in the umbilical venous return in the atrium, reduces systemic oxygenation as evidenced by lower PaO2/FiO2 ratios in the DCCV lambs. We speculate that, with a mix of PO2 from the placenta and lungs, these term babies would have had lower PaO2 compared to infants breathing with their umbilical cord cut despite higher SpO2.
Despite lower PaO2 in DCCV, the SpO2 was significantly higher compared to ECCV. We speculate that the better SpO2 reading in the DCCV lambs is due to two factors: better perfusion and prevention of a rightward shift in hemoglobin oxygen dissociation curve due to the rapid correction of acidosis. Asphyxia with combined respiratory and metabolic acidosis shifts the hemoglobin-oxygen dissociation curve leading to lower SpO2 for a given PaO2. We speculate that with better ventilation (lower PaCO2) and higher pH in the DCCV group, SpO2 values were higher despite lower PaO2 levels in DCCV compared to ECCV [26]. By 5 min, the highest PaO2 in DCCV was 38 ± 9 mmHg compared to ECCV, where it was 96 ± 65 mmHg. In a study, involving term neonates, Kapadia et al. have shown that perinatal acidemia and post-resuscitation hyperoxemia (defined as an initial PaO2 of >100 mmHg) were associated with a higher incidence of hypoxic ischemic encephalopathy [27]. It is prudent to avoid high systemic PaO2 and PaCO2 values in asphyxiated preterm infants to limit cerebral hyperemia and oxidative reperfusion injury. Such injury can also predispose infants to intraventricular hemorrhage (IVH) in preterm neonates [28,29].
The oxygen exposure in the DCCV group was also much lower compared to the ECCV group. Hyperoxia in the delivery room is associated with an inflammatory response in the brain and the heart [30,31,32,33,34]. In a study involving an ovine model, hyperoxic resuscitation after fetal asphyxia led to the cerebral inflammatory response [34]. Secondary to the immature antioxidant response, oxidative injury in preterm infants can modify DNA methylation patterns, thus affecting gene expressions [35]. Lorente-Pozo et al. studied the effect of OL in preterm infants <32 weeks who were resuscitated with supplemental O2 on DNA methylome [25]. The study concluded that OL during resuscitation altered DNA methylome that could potentially alter genes related to cell cycle progression, oxidative stress, and DNA repair [25]. In this study, the median OL during stabilization was 644 mLO2/kg, and >500 mLO2/kg could alter the methylation pattern. In our study, the OL in the first 5 min of resuscitation was 520 mLO2/kg and was significantly lower than ECCV, which had an OL of 775 mLO2/kg. In this asphyxiated model, the decreased OL observed in the DCCV group can decrease oxidative injury.
The significant improvement in peak left pulmonary blood flow observed in the DCCV was similar to a previous study by Bhatt et al. in a preterm non-asphyxiated ovine model [19]. The increase in PBF could possibly be secondary to stable hemodynamics, better pH with lower PaCO2 in the DCCV group. Arterial oxygenation plays a great role in pulmonary vascular transition. Although the change point (PaO2 value) for pulmonary vascular transition in an asphyxiated preterm neonate/model remains unknown, we have previously shown that in a non-asphyxiated preterm model, a PaO2 of 31 ± 0.7 mmHg led to a drop in PVR [36]. In our study, we speculate that despite the lower PaO2 observed in the arterial blood, higher alveolar PAO2 helped overcome hypoxic pulmonary vasoconstriction and an improvement in pulmonary vascular transition in the DCCV group [26]. Custer et al. have shown that alveolar hypoxia could worsen hypoxic pulmonary vasoconstriction leading to a redistribution of pulmonary blood flow in a newborn ovine model [37]. Moreover, acidosis exacerbates hypoxic pulmonary vasoconstriction and better pH in DCCV could have ameliorated this effect, thus, leading to improved pulmonary vascular transition compared to ECCV.
Our study had some limitations. The data presented here are only for the first 5 min to compare the parameters while ventilating with and without an intact cord. We did not perform a sample size/power calculation for this pilot study. We did not collect markers of oxidative stress injury and used OL as a surrogate. The study was done in a controlled setting with multiple experienced personnel and may not be the case in real-life scenarios. Species differences do exist, but this asphyxiated preterm model with surfactant-deficient lungs has been widely used to study gas exchange and hemodynamics in the setting of placental transfusion. Since this was a pilot study and the recommended initial supplemental oxygen range by International Liaison Committee on Resuscitation is 30–60%, we chose random initial oxygen concentration with an average initial O2 concentration within the specified range. The distribution was similar in both ECCV and DCCV groups as shown in Figure 2.

5. Conclusions

In this pilot study, in an asphyxiated preterm ovine model with perinatal metabolic acidosis, ventilation with an intact cord for 5 min (DCCV), decreased oxygen exposure, decreased oxygen load, with improved ventilation, while increasing peak pulmonary blood flow compared to immediate clamping of the cord and ventilation (ECCV). In the future, we intend to study the effect of DCCV with low (30–60%) and high (60–100%) oxygen exposure and its effect on oxidative injury and its impact on pulmonary and systemic hemodynamics. Clinical trials evaluating the resuscitation of extremely preterm infants with an intact cord at different concentrations of supplemental oxygen are warranted.

Author Contributions

Conceptualization, P.C. and S.L.; methodology, all authors.; software, P.C., S.G., J.H., C.K.; validation, P.C., S.G., J.H., N.B., C.K., L.N., J.N., V.A., M.B., A.M., M.R., S.L.; formal analysis, P.C., S.G., J.H., C.K.; writing—original draft preparation, P.C., S.L.; writing—review and editing, P.C., S.G., J.H., N.B., C.K., L.N., J.N., V.A., M.B., A.M., M.R., S.L.; funding acquisition, P.C., S.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by NICHD, grant number R03HD096510 (PC), RO1 HD072929 (SL) and NHLBI-K12 HL138052 (PC).

Institutional Review Board Statement

The study was approved by the State University of New York at Buffalo, IACUC ID–PED10085N. All studies were conducted as per IACUC/ARRIVE guidelines.

Informed Consent Statement

Not applicable.

Conflicts of Interest

Satyan Lakshminrusimha is a member of the Neonatal Resuscitation Program Steering Committee of the American Academy of Pediatrics (AAP). The opinions expressed in this manuscript are the author’s own and do not reflect the official position of the AAP. All other authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data, in the writing of the manuscript, or in the decision to publish the results.

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Children 08 00307 g001 550
Figure 1. Preductal SpO2 are shown on the y-axis and the events or duration of positive pressure ventilation (PPV) on the x-axis. The data are represented as average and standard deviation. The SpO2 between ECCV (early cord clamping followed by ventilation) and DCCV (delayed cord clamping with ventilation) was significantly different (* p < 0.05 by ANOVA).
Figure 1. Preductal SpO2 are shown on the y-axis and the events or duration of positive pressure ventilation (PPV) on the x-axis. The data are represented as average and standard deviation. The SpO2 between ECCV (early cord clamping followed by ventilation) and DCCV (delayed cord clamping with ventilation) was significantly different (* p < 0.05 by ANOVA).
Children 08 00307 g001
Children 08 00307 g002 550
Figure 2. Fraction of inspired oxygen (FiO2) is shown on the y-axis and the events or duration of PPV on the x-axis. The data are represented as average and standard deviation. The difference between ECCV and DCCV was significantly different (* p < 0.05 by ANOVA).
Figure 2. Fraction of inspired oxygen (FiO2) is shown on the y-axis and the events or duration of PPV on the x-axis. The data are represented as average and standard deviation. The difference between ECCV and DCCV was significantly different (* p < 0.05 by ANOVA).
Children 08 00307 g002
Children 08 00307 g003 550
Figure 3. The oxygen load (OL) in milliliters of oxygen per kilogram is shown on the y-axis. The box and whiskers plot shows a significantly higher OL with ECCV compared to DCCV. OL in ECCV was significantly higher compared to DCCV (* p < 0.05 by Kruskal-Wallis test).
Figure 3. The oxygen load (OL) in milliliters of oxygen per kilogram is shown on the y-axis. The box and whiskers plot shows a significantly higher OL with ECCV compared to DCCV. OL in ECCV was significantly higher compared to DCCV (* p < 0.05 by Kruskal-Wallis test).
Children 08 00307 g003
Children 08 00307 g004 550
Figure 4. The PaO2 in mm Hg is shown on the y-axis and the events or duration of PPV on the x-axis. The PaO2 was significantly lower in DCCV (* p < 0.05 by ANOVA).
Figure 4. The PaO2 in mm Hg is shown on the y-axis and the events or duration of PPV on the x-axis. The PaO2 was significantly lower in DCCV (* p < 0.05 by ANOVA).
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Children 08 00307 g005 550
Figure 5. The arterial carbon dioxide (PaCO2 in mmHg) is shown on the y-axis and the events on the x-axis. The PaCO2 was significantly lower in DCCV compared to ECCV. (* p < 0.05 by ANOVA).
Figure 5. The arterial carbon dioxide (PaCO2 in mmHg) is shown on the y-axis and the events on the x-axis. The PaCO2 was significantly lower in DCCV compared to ECCV. (* p < 0.05 by ANOVA).
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Children 08 00307 g006 550
Figure 6. The left peak PBF is shown on the y-axis and the events on the x-axis. The PBF was significantly higher with DCCV compared to ECCV (* p < 0.05 by ANOVA).
Figure 6. The left peak PBF is shown on the y-axis and the events on the x-axis. The PBF was significantly higher with DCCV compared to ECCV (* p < 0.05 by ANOVA).
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Children 08 00307 g007 550
Figure 7. The left peak CBF is shown on the y-axis and the events or duration of PPV on the x-axis.
Figure 7. The left peak CBF is shown on the y-axis and the events or duration of PPV on the x-axis.
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Children 08 00307 g008 550
Figure 8. The benefits of delayed cord clamping and ventilation (DCCV) for 5 min in a lamb model of preterm asphyxia. With positive pressure ventilation and an intact cord, there was a mixing of lower umbilical vein oxygen tension (UVPO2) with higher pulmonary venous oxygen tension (PVO2) leading to overall systemic lower oxygen tension (PaO2)—“differential oxygenation” with alveolar hyperoxia but systemic normoxia. With the placenta and lungs simultaneously acting as organs of gas exchange, the arterial carbon dioxide (PaCO2) was lower (“dual-site gas exchange”). Copyright Satyan Lakshminrusimha.
Figure 8. The benefits of delayed cord clamping and ventilation (DCCV) for 5 min in a lamb model of preterm asphyxia. With positive pressure ventilation and an intact cord, there was a mixing of lower umbilical vein oxygen tension (UVPO2) with higher pulmonary venous oxygen tension (PVO2) leading to overall systemic lower oxygen tension (PaO2)—“differential oxygenation” with alveolar hyperoxia but systemic normoxia. With the placenta and lungs simultaneously acting as organs of gas exchange, the arterial carbon dioxide (PaCO2) was lower (“dual-site gas exchange”). Copyright Satyan Lakshminrusimha.
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Table
Table 1. Characteristics of preterm lambs.
Table 1. Characteristics of preterm lambs.
CharacteristicsECC + V (N = 8)DCC + V (N = 7)
Gestational age (days)127 ± 0.52128 ± 0.84
Female (N)43
Birth weight (kg)3.3 ± 0.633.3 ± 0.70
Born by multiplicity (N)Twin–6Twin–4
Heart rate at asphyxia (bpm)88 ± 886 ± 10
Mean blood pressure at asphyxia (mmHg)36 ± 834 ± 10
pH before resuscitation7.04 ± 0.087.0 ± 0.08
PaCO2 before resuscitation( mmHg)90 ± 25101 ± 23
PaO2 before resuscitation (mmHg)14 ± 615 ± 11
Data presented as numbers or as average and standard deviation. ECC—early cord clamping, DCC—delayed cord clamping, V—ventilation. PaCO2—arterial carbon dioxide, PaO2—arterial oxygenation.
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Chandrasekharan, P.; Gugino, S.; Helman, J.; Koenigsknecht, C.; Nielsen, L.; Bradley, N.; Nair, J.; Agrawal, V.; Bawa, M.; Mari, A.; et al. Resuscitation with an Intact Cord Enhances Pulmonary Vasodilation and Ventilation with Reduction in Systemic Oxygen Exposure and Oxygen Load in an Asphyxiated Preterm Ovine Model. Children 2021, 8, 307. https://0-doi-org.brum.beds.ac.uk/10.3390/children8040307

AMA Style

Chandrasekharan P, Gugino S, Helman J, Koenigsknecht C, Nielsen L, Bradley N, Nair J, Agrawal V, Bawa M, Mari A, et al. Resuscitation with an Intact Cord Enhances Pulmonary Vasodilation and Ventilation with Reduction in Systemic Oxygen Exposure and Oxygen Load in an Asphyxiated Preterm Ovine Model. Children. 2021; 8(4):307. https://0-doi-org.brum.beds.ac.uk/10.3390/children8040307

Chicago/Turabian Style

Chandrasekharan, Praveen, Sylvia Gugino, Justin Helman, Carmon Koenigsknecht, Lori Nielsen, Nicole Bradley, Jayasree Nair, Vikash Agrawal, Mausma Bawa, Andreina Mari, and et al. 2021. "Resuscitation with an Intact Cord Enhances Pulmonary Vasodilation and Ventilation with Reduction in Systemic Oxygen Exposure and Oxygen Load in an Asphyxiated Preterm Ovine Model" Children 8, no. 4: 307. https://0-doi-org.brum.beds.ac.uk/10.3390/children8040307

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