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Factors associated with renal oxygen extraction in mechanically ventilated children after the Norwood operation: insights from high fidelity haemodynamic data

Published online by Cambridge University Press:  24 May 2024

Rohit S. Loomba Open the ORCID record for Rohit S. Loomba [Opens in a new window] ,
Enrique G. Villarreal Open the ORCID record for Enrique G. Villarreal [Opens in a new window] ,
Juan S. Farias Open the ORCID record for Juan S. Farias [Opens in a new window] ,
Saul Flores Open the ORCID record for Saul Flores [Opens in a new window]  and
Joshua Wong Open the ORCID record for Joshua Wong [Opens in a new window]
Rohit S. Loomba
Affiliation:
Advocate Children’s Hospital, Chicago, IL, USA Rosalind Franklin University of Medicine and Science, Chicago, IL, USA
Enrique G. Villarreal*
Affiliation:
Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Monterrey, NL, Mexico
Juan S. Farias
Affiliation:
Children’s Mercy Hospital, Kansas City, MO, USA
Saul Flores
Affiliation:
Texas Children’s Hospital, Baylor College of Medicine, Houston, TX, USA
Joshua Wong
Affiliation:
Advocate Children’s Hospital, Chicago, IL, USA
*
Corresponding author: E. G. Villarreal; Email: quique_villarreal93@hotmail.com
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Abstract

Background:

Maintaining the adequacy of systemic oxygen delivery is of utmost importance, particularly in critically ill children. Renal oxygen extraction can be utilised as metric of the balance between systemic oxygen delivery and oxygen consumption. The primary aim of this study was to determine what clinical factors are associated with renal oxygen extraction in children after Norwood procedure.

Methods:

Mechanically ventilated children who underwent Norwood procedure from 1 September, 2022 to 1 March, 2023 were identified as these patients had data collected and stored with high fidelity by the T3 software. Data regarding haemodynamic values, fluid balance, and airway pressure were collected and analysed using Bayesian regression to determine the association of the individual metrics with renal oxygen extraction.

Results:

A total of 27,270 datapoints were included in the final analyses. The resulting top two models explained had nearly 80% probability of being true and explained over 90% of the variance in renal oxygen extraction. The coefficients for each variable retained in the best were −1.70 for milrinone, −19.05 for epinephrine, 0.129 for mean airway pressure, −0.063 for mean arterial pressure, 0.111 for central venous pressure, 0.093 for arterial saturation, 0.006 for heart rate, −0.025 for respiratory rate, 0.366 for systemic vascular resistance, and −0.032 for systemic blood flow.

Conclusion:

Increased milrinone, epinephrine, mean arterial pressure, and systemic blood flow were associated with decreased (improved) renal oxygen extraction, while increased mean airway pressure, central venous pressure, arterial saturation, and systemic vascular resistance were associated with increased (worsened) renal oxygen extraction.

Keywords

Paediatric critical carerenal oxygen extractionNorwood operationBayesian regressionhaemodynamic factors
Type
Original Article
Information
Cardiology in the Young , First View , pp. 1 - 6
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Copyright
© The Author(s), 2024. Published by Cambridge University Press

Parallel circulation represents a unique circulatory physiology in which the systemic saturation is dependent on a weighted average of the systemic and pulmonary venous saturations. The weights for this average depend on the relative proportion of blood flow going to the pulmonary and systemic circulations. This ratio of pulmonary and systemic blood flow is further dependent on the relative resistances in these two beds. Reference Magoon, Makhija and Jangid1–Reference Nelson, Schwartz and Chang3

Optimal management of children with parallel circulation, particularly after the Norwood operation, requires a thorough understanding of the nuances of the circulation and understanding of how the circulation is impacted by various clinical interventions. Data on the impact of clinical interventions on the physiology itself are limited. More detailed understanding of these impacts could better help improve the management of the children.

Oxygen extraction reflects the balance between oxygen delivery and oxygen consumption, or in other words, the adequacy of systemic oxygen delivery. Increased oxygen extraction has been demonstrated to increase morbidity and mortality, with oxygen extraction of 30–40 being as a period of increased risk of morbidity, such as impaired neurodevelopment, acute kidney injury, hepatic insufficiency, necrotising enterocolitis, and cardiac arrest increase. Reference Joffe, Al Aklabi and Bhattacharya4–Reference Sheikholeslami, Dyson and Villarreal22

The primary aim of this study was to utilise high fidelity data to characterise the association of various clinical parameters and renal oxygen extraction in children with parallel circulation after the Norwood operation.

Methods

Study design

This study protocol was approved by the institutional review board. It is in concordance with the Helsinki Declaration. This study was a single-centre, retrospective study aimed to characterise the association between various clinical parameters and renal oxygen extraction. The resulting model and the ability to predict the renal oxygen extraction were not necessarily the main aim of this study, but rather to demonstrate the relationship between the independent variables and renal oxygen extraction.

Variables of interest

The variables of interest collected were as follows: central venous pressure, heart rate, respiratory rate, mean arterial blood pressure, arterial saturation by pulse oximetry, renal near infrared spectroscopy, peak airway pressure, mean airway pressure, positive end expiratory pressure, body temperature, fluid balance, epinephrine dose, norepinephrine dose, dopamine dose, dobutamine dose, vasopressin dose, nitroprusside dose, and nicardipine dose. Patient weight and gestational age were also collected.

All the data except for vasoactive doses were collected from the T3 software. T3 is software designed to integrate multiple data streams in real time in clinical settings. The data from all the streams can then be displayed by the software in a user-defined fashion. Additionally, T3 also estimates the venous saturation and then displays the probability of the venous saturation being under 30, 40, or 50% in a metric known as the index of inadequate delivery of oxygen. The T3 software collects data from the available streams at an interval of 5 s, thus offering high temporal resolution.

Central venous pressures were obtained by use of femoral lines terminating in the inferior caval vein. Line placement was confirmed by radiographs.

Renal near infrared spectroscopy values were collected. Near infrared spectroscopy values were obtained using the Casmed ForeSight Elite tissue oximeter.

Vasoactive doses were collected manually through the electronic medical record as charted. It is local practice to document every time an infusion dose has been changed and at regular intervals. Doses of all vasoactive infusions were collected for each timepoint at which the data from T3 were collected.

Fluid balance was collected manually through the electronic medical record as charted. It is local practice to update fluid balance hourly. Fluid balance for each timepoint at which T3 data were collected was collected as the fluid balance for the hour prior to that timepoint.

Some values were also calculated. Renal oxygen extraction was calculated as ((arterial saturation by pulse oximetry – renal near infrared spectroscopy)/(arterial saturation by pulse oximetry)) × 100. Thus, if the arterial saturation were 80 and the renal near infrared spectroscopy value was 60, the renal oxygen extraction ratio would be 25. Oxygen consumption in ml/min was estimated using the LaFarge equation. Systemic blood flow was calculated by dividing the estimated oxygen consumption by the arteriovenous oxygen content difference. The renal near infrared spectroscopy value was used for this. Systemic vascular resistance was then calculated using the following equations: (mean arterial blood pressure – central venous pressure)/systemic blood flow.

Patient inclusion

Neonates with functionally univentricular hearts who underwent a Norwood operation were eligible for inclusion in this study. Data must have been collected and available for patients in T3 for patients to be included in this study. T3 was implemented locally on 1 September 1, 2022 and a final inclusion date of 1 March, 2023 was utilised. Only data while patients were intubated and mechanically ventilated were included as this allowed for airway pressures to be quantified. Data were available at five second intervals for patients with T3 data. Datapoints were included in the final analyses only if there was a central venous pressure and airway pressures available at that specific timepoint.

Statistical analyses

The primary statistical aim of the analyses was to model renal oxygen extraction ratio using the other collected data in order to quantitatively assess the association of the various parameters with renal oxygen extraction ratio. This was done utilising a Bayesian linear regression. Renal oxygen extraction ratio was the dependent variable, and the following independent variables were included: central venous pressure, heart rate, respiratory rate, mean arterial blood pressure, arterial saturation by pulse oximetry, mean airway pressure, body temperature, fluid balance, epinephrine dose, norepinephrine dose, dopamine dose, dobutamine dose, vasopressin dose, nitroprusside dose, nicardipine dose, estimated systemic blood flow, and estimated systemic vascular resistance. The Jeffreys–Zellner–Siow prior was utilised. The top 10 most likely models were evaluated.

Bayesian statistics were utilised rather than frequentist regressions for several reasons. The details of these are beyond the scope of this manuscript but in general Bayesian statistics allows for generating a distribution for all point estimates. This allows for the quantification of the probability of specific outcomes and models describing the outcomes. Bayesian models have also been demonstrated to be more well-fitted and reproducible.

Statistical analyses were conducted using JASP Version 0.16 (University of Amsterdam, Amsterdam, Netherlands). P-values are not presented as Bayesian statistical tools, and no frequentist statistical tools were utilised.

Results

Cohort information (Table 1)

A total of 27,270 datapoints were included in the final analyses. These were collected from nine patients over a total of 1,338 patient hours (55.7 days). As per the inclusion criteria for retaining datapoints in the final analyses, central venous pressure and airway pressures must have been available for the data for a timepoint to be included. It is important that the sample size here is 27,270 as the analyses are done on a datapoint level and not on an individual patient level.

Table 1. Descriptive data regarding cohort

Average gestational age was 38 weeks with 2 patients being premature. Average patient age at the time of the Norwood operation was 20 days. This was due to two patients getting their Norwood done closer to 2 months of life following a hybrid procedure. When these two patients are excluded, the mean age at time of Norwood was 2 days. Of the nine patients for whom data were collected, two had an identified genetic anomaly.

Regarding vasoactive agents, epinephrine was utilised during 91% of the timepoints at which data were collected, dopamine during 14.5%, milrinone during 24.8%, and nitroprusside during 3.8%, and vasopressin 0.3%. Norepinephrine, dobutamine, and nicardipine were not utilised in any of the patients during the study period.

Regression analyses (Table 2)

The most probable model had a probability of 71.5% and an R2 value of 0.932. The R2 value indicated that 93.2% of the variability in renal oxygen extraction ratio could be explained by the model and it’s included variables.

Table 2. Association of variables with change in renal oxygen extraction

a Only variable with significant associations are included in the table.

The most probable model retained the following independent variables: milrinone, mean airway pressure, mean arterial pressure, central venous pressure, arterial saturation by pulse oximetry, heart rate, respiratory rate, systemic vascular resistance, and systemic blood flow.

The coefficients for each variable retained in the best were as follows: −1.70 for milrinone, −19.05 for epinephrine, 0.129 for mean airway pressure, −0.063 for mean arterial pressure, 0.111 for central venous pressure, 0.093 for arterial saturation by pulse oximetry, 0.006 for heart rate, −0.025 for respiratory rate, 0.366 for systemic vascular resistance, and −0.032 for systemic blood flow.

Correlation was present in this analysis between independent variables such as milrinone and systemic vascular resistance, milrinone and systemic blood flow.

To put the above in a more clinically relevant context, a 0.5 mcg/kg/min increase of milrinone is associated with a 0.85 decrease in renal oxygen extraction, a 0.01 mcg/kg/min increase of epinephrine is associated with a 0.19 decrease in renal oxygen extraction, a 1 cmH20 increase in mean airway pressure was associated with a 0.12 increase in renal oxygen extraction, a 5 mmHg increase in mean arterial pressure was associated with a 0.31 decrease in renal oxygen extraction, a 1 cmH20 increase in central venous pressure was associated with a 0.11 increase in renal oxygen extraction, a 5 increase in arterial saturation by pulse oximetry was associated with a 0.46 increase in renal oxygen extraction, a 10 beat per minute increase in heart rate was associated with a 0.06 increase in renal oxygen extraction, a 5 Woods units increase in systemic vascular resistance was associated with a 1.83 increase in renal oxygen extraction, and a 1 l/min increase in systemic blood flow was associated with a 0.03 decrease in renal oxygen extraction.

Thus, increased milrinone, epinephrine, mean arterial pressure, and systemic blood flow were associated with decreased (improved) renal oxygen extraction, while increased mean airway pressure, central venous pressure, arterial saturation by pulse oximetry, and systemic vascular resistance were associated with increased (worsened) renal oxygen extraction.

The second most probable model had a probability of 10.9% and an R2 value of 0.931. Thus, the two most probable models had a total probability of 82.4%; thus, these two models were able to explain a majority of the data, accounting for 93% of the variance in renal oxygen extraction. The second most probable model was similar to the most probable model except for the addition of temperature as a retained variable.

Discussion

The current study demonstrates factors that were statistically significantly associated with renal oxygen extraction in mechanically ventilated children with parallel circulation after the Norwood operation. Renal oxygen extraction improved with increases in milrinone, epinephrine, mean arterial pressure, and systemic blood flow while renal oxygen worsened with increasing mean airway pressure, arterial saturation by pulse oximetry, and systemic vascular resistance. Of equal note is that other vasoactive agents such as dopamine, vasopressin, and nicardipine did not demonstrate any statistically significant effect on renal oxygen extraction.

While statistical significance was demonstrated for the above-mentioned variables, milrinone and systemic vascular resistance seemed to be the most clinically significant. The subjective review of the change in the variable needed to modify renal oxygen extraction was most clinically possible. For instance, a 1 change in renal oxygen extraction would require a 15 mmHg change in mean arterial pressure which in a neonate is an unlikely clinical change to experience.

Oxygen extraction can be evaluated regionally using near infrared spectroscopy as a surrogate for venous saturation. The correlation between near infrared spectroscopy and underlying venous saturations has been demonstrated. Reference Loomba, Rausa and Sheikholeslami23 More importantly, an independent association between regional near infrared spectroscopy values and morbidity and mortality has been demonstrated. Reference Li, Van Arsdell and Zhang24–Reference Dabal, Rhodes, Borasino, Law, Robert and Alten28 Use of superior or inferior caval vein saturations, or analogously, cerebral or renal near infrared spectroscopy seems reasonable according to findings of published data, despite anecdotally perpetuated superiority of the superior caval vein saturation or cerebral near infrared spectroscopy. Reference Law, Benscoter and Borasino27,Reference Dabal, Rhodes, Borasino, Law, Robert and Alten28

Parallel circulation is a unique circulation in which the systemic venous blood and pulmonary venous blood mix. Thus, the systemic arterial saturation becomes a weighted average of the systemic venous and pulmonary venous saturation with the weights of each being dictated by the relative amount of pulmonary and systemic blood flow. The systemic and pulmonary blood flow have a unique relationship in that cardiac output is the sum of these two individual flows and a change in either must be met by a change of equal magnitude but opposite direction in the other circulation if total cardiac output remains constant. This delicate balance of saturations and flows between the pulmonary and systemic circulations puts children with parallel circulation at greater risk of experiencing inadequacy of systemic oxygen delivery. Reference Magoon, Makhija and Jangid1 The findings of this study seem to demonstrate that increased systemic oxygen delivery seems to largely be mediated by increase in systemic blood flow and decreased systemic vascular resistance.

A growing body of data has helped lend valuable insight into the factors that help mediate this balance and subsequently decrease the risk of morbidity and mortality, particularly in parallel circulation. Reference Savorgnan, Loomba and Flores14,Reference Patel, Weld and Flores29–Reference O’Blenes, Roy, Konstantinov, Bohn and Van Arsdell70 The current data add to the present data with the benefit of high temporal resolution of collected data. This is particularly beneficial in characterising the associations with changes in vasoactive medication doses. Data regarding dose-dependent changes in haemodynamics in the setting of CHD is lacking, nonetheless in the setting of parallel circulation. Reference Li, Zhang and Holtby46,Reference Hendon, Kane and Golem71,Reference Loomba and Flores72 Characterisation of vasoactive support has largely been done based on the vasoactive-inotrope score which assigns relatively arbitrary coefficients to the dosage of vasoactive medications to result in a score which has subsequently been demonstrated to correlate with morbidity and mortality. This more vasoactive support worse outcome approach doesn’t directly reflect haemodynamic changes. A scoring system in which coefficients are based on haemodynamic changes associated with vasoactive medications could be much more telling and have a more pragmatic impact on bedside vasoactive titration.

The adequacy of systemic oxygen delivery represents the relative balance between oxygen delivery and oxygen consumption. Reference Dhillon, Yu, Zhang, Cai and Li73 Systemic oxygen delivery is the product of cardiac output and oxygen content. Cardiac output further breaks down into the quotient of oxygen consumption and the arteriovenous oxygen content difference, while oxygen content is a function of haemoglobin, arterial saturation, and partial pressure of oxygen. Reference Loomba, Lion and Flores74,Reference Loomba75 With this in mind, it becomes apparent why conventionally monitored haemodynamic parameters may not reflect systemic oxygen delivery as they do not actually directly influence them. Reference Li, Zhang and Holtby9,Reference Li, Zhang and McCrindle20 Additionally, monitored pressures are a product of flow and resistance and resistance cannot be quantified in any meaningful way, nonetheless on a second-to-second base. Thus, whether a change in arterial pressure, for instance, is due to an increase in cardiac output or system vascular resistance cannot be easily delineated. This, however, is of utmost importance if arterial pressure is to be used to guide clinical care as increased blood pressure driven by increased cardiac output may help improve systemic oxygen delivery while increased blood pressure driven by increased systemic vascular resistance may actually decrease systemic oxygen delivery.

The current data serve as a proof of concept that high fidelity haemodynamic monitoring tools such as T3 can be used to help more clearly characterise the effects of various clinical factors, including vasoactive medications in vivo. This is important as much of the current understanding of such effects vastly originates from ex vivo studies or animal studies. Ex vivo studies lack the ability to replicate in vivo feedback mechanism while animal studies may not be generalisable to humans due to differences between species. Even human in vivo data from specific subsets of patients may not be generalisable to all humans. But leveraging large, high fidelity sets from multiple institutions in a manner done in the current study may help characterise in vivo effects of vasoactive medications in specific patient populations.

The novel application of high-fidelity haemodynamic data is one strength of this study. Additionally, factors such as vasoactive medication doses and fluid balance which aren’t captured by the T3 system were manually collected in high fidelity to be combined with the T3 dataset, allowing for additional insight. The characterisation of effects was done at a time point level, which led to a robust sample size of underlying data. Additionally, the use of baseline values with subsequent time points allowed for some characterisation of the effect of time with the principles of causal-mediated analysis. Additionally, the high temporal resolution of data further sides to this. The incorporation of fluid balance, airway pressures, multiple haemodynamic variables, and multiple vasoactive medications help make the variable specific effect estimates more convincing. The use of Bayesian statistics is also a strength of this study as it allowed for quantifying the probabilities of the dependent and independent variables as well as allowed for comparison of multiple models to help determine which model was most helpful. The high probability of the data being explained by the top two models and the high degree of similarity between these two models (second most probable model included all the same instrument variables as the most likely and included the addition of only a single variable) speak to the strength of the resulting models. The selection of a very specific patient population may have also contributed to the ability for models to be quite predictive.

The study is not without its limitations. Some vasoactive medications, specifically nicardipine, could not be well characterised due to the relatively short duration they were utilised during the study period. As this is a single centre study generalisability may be limited. For instance, centres who utilise routine postoperative alpha blockade or differing cardiopulmonary bypass strategies may see slightly different effects of specific vasoactive medications. The overall physiologic implications should be less variable. The local practice of using specific vasoactive medications also affects the generalisation of this data. For instance, the institution in the current study does not utilise norepinephrine or nicardipine as much as other centres may and may utilise dopamine more often than other centres may. Additionally, cerebral near infrared spectroscopy data were not available during this monitoring period for technical reasons.

Conclusion

In children with parallel circulation immediately following the Norwood operation, increased milrinone, increased epinephrine, mean arterial pressure, and systemic blood flow were associated with decreased (improved) renal oxygen extraction, while increased mean airway pressure, central venous pressure, arterial saturation by pulse oximetry, and systemic vascular resistance were associated with increased (worsened) renal oxygen extraction.

Acknowledgements

None.

Financial support

None.

Author contribution

RSL, SF and EGV contributed to the study conception and design. Material preparation, data collection, and analysis were performed by JW and RSL. The first draft of the manuscript was written by JSF and JW. SF and EGV commented on previous versions of the manuscript. All authors read and approved the final manuscript. Reviewing and editing was done by EGV.

Competing interests

None.

Ethical standard

The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national guidelines on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008.

Statement of human rights

The study have been approved by the appropriate institutional ethics committee and have been performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards.

Data transparency

All data and materials, as well as software application, support our published claims and comply with field standards.

References

Magoon, R, Makhija, N, Jangid, SK. Balancing a single-ventricle circulation: ‘physiology to therapy’. Indian J Thorac Cardiovasc Surg 2020; 36: 159–162.CrossRefGoogle ScholarPubMed
Lawrenson, J, Eyskens, B, Vlasselaers, D, Gewillig, M. Manipulating parallel circuits: the perioperative management of patients with complex congenital cardiac disease. Cardiol Young 2003; 13: 316–322.CrossRefGoogle ScholarPubMed
Nelson, DP, Schwartz, SM, Chang, AC. Neonatal physiology of the functionally univentricular heart. Cardiol Young 2004; 14: 52–60.CrossRefGoogle ScholarPubMed
Joffe, R, Al Aklabi, M, Bhattacharya, S, et al. Cardiac surgery-associated kidney injury in children and renal oximetry. Pediatr Crit Care Med 2018; 19: 839–845.CrossRefGoogle ScholarPubMed
Scott, JP, Hoffman, GM. Near-infrared spectroscopy: exposing the dark (venous) side of the circulation. Paediatr Anaesth 2014; 24: 74–88.CrossRefGoogle ScholarPubMed
Dorum, BA, Ozkan, H, Cetinkaya, M, Koksal, N. Regional oxygen saturation and acute kidney injury in premature infants. Pediatr Int 2021; 63: 290–294.CrossRefGoogle ScholarPubMed
Verhagen, EA, Van Braeckel, KN, van der Veere, CN, et al. Cerebral oxygenation is associated with neurodevelopmental outcome of preterm children at age 2 to 3 years. Dev Med Child Neurol 2015; 57: 449–455.CrossRefGoogle ScholarPubMed
Tewari, Kumar VV, Kurup, A, Daryani, HA, Saxena, A. Impact of cerebral oxygen saturation monitoring on short-term neurodevelopmental outcomes in neonates with encephalopathy - a prospective Cohort study. Curr Pediatr Rev 2022; 18: 301–317.CrossRefGoogle ScholarPubMed
Li, J, Zhang, G, Holtby, H, et al. The influence of systemic hemodynamics and oxygen transport on cerebral oxygen saturation in neonates after the Norwood procedure. J Thorac Cardiovasc Surg 2008; 135: 83–90.CrossRefGoogle ScholarPubMed
Kussman, BD, Wypij, D, Laussen, PC, et al. Relationship of intraoperative cerebral oxygen saturation to neurodevelopmental outcome and brain magnetic resonance imaging at 1 year of age in infants undergoing biventricular repair. Circulation 2010; 122: 245–254.CrossRefGoogle ScholarPubMed
Hoffman, GM, Mussatto, KA, Brosig, CL, et al. Systemic venous oxygen saturation after the Norwood procedure and childhood neurodevelopmental outcome. J Thorac Cardiovasc Surg 2005; 130: 1094–1100.CrossRefGoogle ScholarPubMed
Takano, H, Matsuda, H, Kadoba, K, et al. Monitoring of hepatic venous oxygen saturation for predicting acute liver dysfunction after Fontan operations. J Thorac Cardiovasc Surg 1994; 108: 700–708.CrossRefGoogle ScholarPubMed
Loomba, RS, Dyamenahalli, U, Savorgnan, F, et al. Association of immediate postoperative hemodynamic and laboratory values in predicting Norwood admission outcomes. Pediatr Cardiol 2022.CrossRefGoogle ScholarPubMed
Savorgnan, F, Loomba, RS, Flores, S, et al. Descriptors of failed extubation in Norwood patients using physiologic data streaming. Pediatr Cardiol 2022; 44: 396–403.CrossRefGoogle ScholarPubMed
Palleri, E, Wackernagel, D, Wester, T, Bartocci, M. Low splanchnic oxygenation and risk for necrotizing enterocolitis in extremely preterm newborns. J Pediatr Gastroenterol Nutr 2020; 71: 401–406.CrossRefGoogle ScholarPubMed
Ozkan, H, Cetinkaya, M, Dorum, BA, Koksal, N. Mesenteric tissue oxygenation status on the development of necrotizing enterocolitis. Turk J Pediatr 2021; 63: 811–817.CrossRefGoogle ScholarPubMed
Tweddell, JS, Ghanayem, NS, Mussatto, KA, et al. Mixed venous oxygen saturation monitoring after stage 1 palliation for hypoplastic left heart syndrome. Ann Thorac Surg 2007; 84: 1301–1310.CrossRefGoogle ScholarPubMed
van der Heide, M, Hulscher, JBF, Bos, AF, Kooi, EMW. Near-infrared spectroscopy as a diagnostic tool for necrotizing enterocolitis in preterm infants. Pediatr Res 2021; 90: 148–155.CrossRefGoogle ScholarPubMed
Tweddell, JS, Hoffman, GM, Fedderly, RT, et al. Patients at risk for low systemic oxygen delivery after the Norwood procedure. Ann Thorac Surg 2000; 69: 1893–1899.CrossRefGoogle ScholarPubMed
Li, J, Zhang, G, McCrindle, BW, et al. Profiles of hemodynamics and oxygen transport derived by using continuous measured oxygen consumption after the Norwood procedure. J Thorac Cardiovasc Surg 2007; 133: 441–448.CrossRefGoogle ScholarPubMed
Hoffman, GM, Ghanayem, NS, Kampine, JM, et al. Venous saturation and the anaerobic threshold in neonates after the Norwood procedure for hypoplastic left heart syndrome. Ann Thorac Surg 2000; 70: 1515–1520.CrossRefGoogle ScholarPubMed
Sheikholeslami, D, Dyson, AE, Villarreal, EG, et al. Venous blood gases in pediatric patients: a lost art? Minerva Pediatr (Torino) 2021; 74: 789–794.Google ScholarPubMed
Loomba, RS, Rausa, J, Sheikholeslami, D, et al. Correlation of near-infrared spectroscopy oximetry and corresponding venous oxygen saturations in children with congenital heart disease. Pediatr Cardiol 2021; 43: 197–206.CrossRefGoogle ScholarPubMed
Li, J, Van Arsdell, GS, Zhang, G, et al. Assessment of the relationship between cerebral and splanchnic oxygen saturations measured by near-infrared spectroscopy and direct measurements of systemic haemodynamic variables and oxygen transport after the Norwood procedure. Heart 2006; 92: 1678–1685.CrossRefGoogle ScholarPubMed
Ghanayem, NS, Hoffman, GM. Near infrared spectroscopy as a hemodynamic monitor in critical illness. Pediatr Crit Care Med 2016; 17: S201–206.CrossRefGoogle ScholarPubMed
Hoffman, GM, Ghanayem, NS, Scott, JP, Tweddell, JS, Mitchell, ME, Mussatto, KA. Postoperative cerebral and somatic near-infrared spectroscopy saturations and outcome in hypoplastic left heart syndrome. Ann Thorac Surg 2017; 103: 1527–1535.CrossRefGoogle ScholarPubMed
Law, MA, Benscoter, AL, Borasino, S, et al. Inferior and superior vena cava saturation monitoring after neonatal cardiac surgery. Pediatr Crit Care Med 2022; 23: e347–e355.CrossRefGoogle ScholarPubMed
Dabal, RJ, Rhodes, LA, Borasino, S, Law, MA, Robert, SM, Alten, JA. Inferior vena cava oxygen saturation monitoring after the Norwood procedure. Ann Thorac Surg 2013; 95: 2114–2120.CrossRefGoogle ScholarPubMed
Patel, RD, Weld, J, Flores, S, et al. The acute effect of packed red blood cell transfusion in mechanically ventilated children after the norwood operation. Pediatr Cardiol 2021; 43: 401–406.CrossRefGoogle ScholarPubMed
Thomas, L, Flores, S, Wong, J, Loomba, R. Acute effects of hypoxic gas admixtures on pulmonary blood flow and regional oxygenation in children awaiting Norwood palliation. Cureus 2019; 11: e5693.Google ScholarPubMed
Loomba, RS, Culichia, C, Schulz, K, et al. Acute effects of vasopressin arginine infusion in children with congenital heart disease: higher blood pressure does not equal improved systemic oxygen delivery. Pediatr Cardiol 2021; 42: 1792–1798.CrossRefGoogle Scholar
Bronicki, RAA, Savorgnan, S, Flores, F, et al. The acute impact of vasopressin on hemodynamics and tissue oxygenation following the norwood procedure. JTCVS open 2022; 22: 217–224.Google Scholar
Lee, B, Villarreal, EG, Mossad, EB, et al. Alpha-blockade during congenital heart surgery admissions: analysis from national database. Cardiol Young 2021: 1–7.Google ScholarPubMed
Loomba, RS, Villarreal, EG, Dhargalkar, J, et al. The effect of dexmedetomidine on renal function after surgery: a systematic review and meta-analysis. J Clin Pharm Ther 2022; 47: 287–297.CrossRefGoogle ScholarPubMed
Loomba, RS, Dorsey, V, Villarreal, EG, Flores, S. The effect of milrinone on hemodynamic and gas exchange parameters in children. Cardiol Young 2020; 30: 55–61.CrossRefGoogle ScholarPubMed
Villarreal, EG, Aiello, S, Evey, LW, Flores, S, Loomba, RS. Effects of inhaled nitric oxide on haemodynamics and gas exchange in children after having undergone cardiac surgery utilising cardiopulmonary bypass. Cardiol Young 2020; 30: 1151–1156.CrossRefGoogle ScholarPubMed
Farias, JS, Villarreal, EG, Flores, S, et al. Effects of vasopressin infusion after pediatric cardiac surgery: a meta-analysis. Pediatr Cardiol 2021; 42: 225–233.CrossRefGoogle ScholarPubMed
Loomba, RS, Gray, SB, Flores, S. Hemodynamic effects of ketamine in children with congenital heart disease and/or pulmonary hypertension. Congenit Heart Dis 2018; 13: 646–654.CrossRefGoogle ScholarPubMed
Savorgnan, F, Flores, S, Loomba, RS, et al. Hemodynamic response to calcium chloride boluses in single-ventricle patients with parallel circulation. Pediatr Cardiol 2021; 43: 554–560.Google ScholarPubMed
Savorgnan, F, Flores, S, Loomba, RS, Acosta, S. Hemodynamic response to fluid boluses in patients with single-ventricle parallel circulation. Pediatr Cardiol 2022; 43: 1784–1791.Google ScholarPubMed
Bronicki, RA, Flores, S, Loomba, RS, et al. Impact of corticosteroids on cardiopulmonary bypass induced inflammation in children: a meta-analysis. Ann Thorac Surg 2021; 112: 1363–1370.CrossRefGoogle ScholarPubMed
Loomba, RS, Rausa, J, Farias, JS, et al. Impact of medical interventions and comorbidities on norwood admission for patients with hypoplastic left heart syndrome. Pediatr Cardiol 2022; 43: 267–278.CrossRefGoogle ScholarPubMed
Loomba, RS, Abdulkarim, M, Bronicki, RA, Villarreal, EG, Flores, S. Impact of sodium bicarbonate therapy on hemodynamic parameters in infants: a meta-analysis. J Matern Fetal Neonatal Med 2022; 35: 2324–2330.CrossRefGoogle Scholar
Wong, J, Loomba, RS, Evey, L, Bronicki, RA, Flores, S. Postoperative inhaled nitric oxide does not decrease length of stay in pediatric cardiac surgery admissions. Pediatr Cardiol 2019; 40: 1559–1568.CrossRefGoogle Scholar
Savorgnan, F, Bhat, PN, Checchia, PA, et al. RBC transfusion induced ST segment variability following the Norwood procedure. Crit Care Explor 2021; 3: e0417.CrossRefGoogle ScholarPubMed
Li, J, Zhang, G, Holtby, H, et al. Adverse effects of dopamine on systemic hemodynamic status and oxygen transport in neonates after the Norwood procedure. J Am Coll Cardiol 2006; 48: 1859–1864.CrossRefGoogle ScholarPubMed
Hoffman, GM, Tweddell, JS, Ghanayem, NS, et al. Alteration of the critical arteriovenous oxygen saturation relationship by sustained afterload reduction after the Norwood procedure. J Thorac Cardiovasc Surg 2004; 127: 738–745.CrossRefGoogle ScholarPubMed
Blackwood, J, Joffe, AR, Robertson, CM, et al. Association of hemoglobin and transfusion with outcome after operations for hypoplastic left heart. Ann Thorac Surg 2010; 89: 1378–1384.e2.CrossRefGoogle ScholarPubMed
Jobes, DR, Nicolson, SC, Steven, JM, Miller, M, Jacobs, ML, Norwood, WI Jr. Carbon dioxide prevents pulmonary overcirculation in hypoplastic left heart syndrome. Ann Thorac Surg 1992; 54: 150–151.CrossRefGoogle ScholarPubMed
Keidan, I, Mishaly, D, Berkenstadt, H, Perel, A. Combining low inspired oxygen and carbon dioxide during mechanical ventilation for the Norwood procedure. Paediatr Anaesth 2003; 13: 58–62.CrossRefGoogle ScholarPubMed
Photiadis, J, Hubler, M, Sinzobahamvya, N, et al. Does size matter? Larger Blalock-taussig shunt in the modified Norwood operation correlates with better hemodynamics. Eur J Cardiothorac Surg 2005; 28: 56–60.CrossRefGoogle ScholarPubMed
Maher, KO, Pizarro, C, Gidding, SS, et al. Hemodynamic profile after the Norwood procedure with right ventricle to pulmonary artery conduit. Circulation 2003; 108: 782–784.CrossRefGoogle ScholarPubMed
Shime, N, Hashimoto, S, Hiramatsu, N, Oka, T, Kageyama, K, Tanaka, Y. Hypoxic gas therapy using nitrogen in the preoperative management of neonates with hypoplastic left heart syndrome. Pediatr Crit Care Med 2000; 1: 38–41.CrossRefGoogle ScholarPubMed
Hoffman, GM, Scott, JP, Ghanayem, NS, et al. Identification of time-dependent risks of hemodynamic states after Stage 1 Norwood palliation. Ann Thorac Surg 2020; 109: 155–162.CrossRefGoogle ScholarPubMed
Corsini, C, Migliavacca, F, Hsia, T-Y, Pennati, G. The influence of systemic-to-pulmonary arterial shunts and peripheral vasculatures in univentricular circulations: focus on coronary perfusion and aortic arch hemodynamics through computational multi-domain modeling. J Biomech 2018; 79: 97–104.CrossRefGoogle ScholarPubMed
Hoffman, GM, Neibler, RA, Scott, JP, et al. Interventions associated with treatment of low cardiac output following stage I norwood palliation. Ann Thorac Surg 2020 111: 1620–1627.Google Scholar
Mroczek, T, Malota, Z, Wojcik, E, Nawrat, Z, Skalski, J. Norwood with right ventricle-to-pulmonary artery conduit is more effective than Norwood with Blalock-Taussig shunt for hypoplastic left heart syndrome: mathematic modeling of hemodynamics. Eur J Cardiothorac Surg 2011; 40: 1412–1417.Google ScholarPubMed
Photiadis, J, Sinzobahamvya, N, Fink, C, et al. Optimal pulmonary to systemic blood flow ratio for best hemodynamic status and outcome early after Norwood operation. Eur J Cardiothorac Surg 2006; 29: 551–556.CrossRefGoogle ScholarPubMed
Loomba, RS, Villarreal, EG, Farias, JS, Flores, S. Predicting intensive care unit length of stay and inpatient mortality after the Norwood procedure: the search for the holy grail. Eur J Cardiothorac Surg 2022; 62: 188.CrossRefGoogle ScholarPubMed
Eagam, M, Loomba, RS, Pelech, AN, Tweddell, JS, Kirkpatrick, E. Predicting the need for neoaortic arch intervention in infants with hypoplastic left heart syndrome through the Glenn procedure. Pediatr Cardiol 2017; 38: 70–76.CrossRefGoogle ScholarPubMed
De Oliveira, NC, Ashburn, DA, Khalid, F, et al. Prevention of early sudden circulatory collapse after the Norwood operation. Circulation 2004; 110: II133–138.CrossRefGoogle ScholarPubMed
Karikari, Y, Abdulkarim, M, Li, Y, Loomba, RS, Zimmerman, F, Husayni, T. The progress and significance of QRS duration by electrocardiography in hypoplastic left heart syndrome. Pediatr Cardiol 2020; 41: 141–148.CrossRefGoogle ScholarPubMed
Bradley, SM, Atz, AM, Simsic, JM. Redefining the impact of oxygen and hyperventilation after the Norwood procedure. J Thorac Cardiovasc Surg 2004; 127: 473–480.CrossRefGoogle ScholarPubMed
Malec, E, Januszewska, K, Kolcz, J, Mroczek, T. Right ventricle-to-pulmonary artery shunt versus modified Blalock-Taussig shunt in the Norwood procedure for hypoplastic left heart syndrome - influence on early and late haemodynamic status. Eur J Cardiothorac Surg 2003; 23: 728–733.CrossRefGoogle ScholarPubMed
Taeed, R, Schwartz, SM, Pearl, JM, et al. Unrecognized pulmonary venous desaturation early after Norwood palliation confounds Gp: Gs assessment and compromises oxygen delivery. Circulation 2001; 103: 2699–2704.CrossRefGoogle ScholarPubMed
Burton, GL, Kaufman, J, Goot, BH, da Cruz, EM. The use of arginine vasopressin in neonates following the Norwood procedure. Cardiol Young 2011; 21: 536–544.CrossRefGoogle ScholarPubMed
Abbas, U, Flores, S, Wong, J, Loomba, R. Use of hypoxic gas admixture (Subambient) prior to norwood and its impact on the Norwood hospitalization. EC Cardiol 2019; 6: 926–932.Google Scholar
Bove, EL, Migliavacca, F, de Leval, MR, et al. Use of mathematic modeling to compare and predict hemodynamic effects of the modified Blalock-Taussig and right ventricle-pulmonary artery shunts for hypoplastic left heart syndrome. J Thorac Cardiovasc Surg 2008; 136: 312–320 e312.CrossRefGoogle ScholarPubMed
Chowdhury, SM, Graham, EM, Atz, AM, Bradley, SM, Kavarana, MN, Butts, RJ. Validation of a simple score to determine risk of hospital mortality after the Norwood procedure. Semin Thorac Cardiovasc Surg 2016; 28: 425–433.CrossRefGoogle ScholarPubMed
O’Blenes, SB, Roy, N, Konstantinov, I, Bohn, D, Van Arsdell, GS. Vasopressin reversal of phenoxybenzamine-induced hypotension after the Norwood procedure. J Thorac Cardiovasc Surg 2002; 123: 1012–1013.CrossRefGoogle ScholarPubMed
Hendon, E, Kane, J, Golem, GM, et al. Acute effects of vasoactive medications in patients with parallel circulation awaiting hybrid or Norwood procedure. Ann Pediatr Cardiol 2022; 15: 34–40.Google ScholarPubMed
Loomba, RS, Flores, S. Use of vasoactive agents in postoperative pediatric cardiac patients: insights from a national database. Congenit Heart Dis 2019; 14: 1176–1184.CrossRefGoogle ScholarPubMed
Dhillon, S, Yu, X, Zhang, G, Cai, S, Li, J. Clinical hemodynamic parameters do not accurately reflect systemic oxygen transport in neonates after the Norwood procedure. Congenit Heart Dis 2015; 10: 234–239.CrossRefGoogle Scholar
Loomba, R, Lion, R, Flores, S. Oxygen Delivery: A Conceptual Approach Using Cardiac Output, Oxygen Content, and Vascular Principles. Heart University, Cincinnati, 2021.Google Scholar
Loomba, RS. The oximetric approach to clinical care. Pediatr Cardiol 2023; 44: 960–961.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Descriptive data regarding cohort

Figure 1

Table 2. Association of variables with change in renal oxygen extraction