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Dead space ratio as a tool in nitric oxide weaning: a study in pulmonary hypertensive disease

Published online by Cambridge University Press:  09 December 2021

Alvaro D. Garcia
Affiliation:
Pediatric Critical Care Department, Pediatric Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
Wei Liu
Affiliation:
Department of Quantitative Health Sciences, Cleveland Clinic Foundation, Cleveland, OH, USA
Hemant Agarwal
Affiliation:
Pediatric Critical Care Department, Pediatric Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
William J. Hanna*
Affiliation:
Pediatric Critical Care Department, Pediatric Institute, Cleveland Clinic Foundation, Cleveland, OH, USA
*
Author for correspondence: W. J. Hanna, Pediatric Critical Care Department, Pediatric Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, M14, Cleveland, OH 44121, USA. Tel: 2162134513. E-mail: hannaw@ccf.org
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Abstract

Objectives:

To describe the association between successful weaning of inhaled nitric oxide and trends in dead space ratio during such weans in patients empirically initiated on nitric oxide therapy out of concern of pulmonary hypertensive crisis.

Patients:

Children in a cardiac intensive care unit initiated on inhaled nitric oxide out of clinical concern for pulmonary hypertensive crisis retrospectively over 2 years.

Measurements and Main Results:

Twenty-seven patients were included, and nitric oxide was successfully discontinued in 23/27. These patients exhibited decreases in dead space ratio (0.18 versus 0.11, p = 0.047) during nitric oxide weaning, and with no changes in dead space ratio between pre- and post-nitric oxide initiation (p = 0.88) and discontinuation (p = 0.63) phases. These successful patients had a median age of 10 months [4.0, 57.0] and had a pre-existent diagnosis of CHD in 6/23 and pulmonary hypertension in 2/23. Those who failed nitric oxide discontinuation trended with a higher dead space ratio at presentation (0.24 versus 0.10), were more likely to carry a prior diagnosis of pulmonary hypertension (50% versus 8.7%), and had longer mechanical ventilation days (5 versus 12).

Conclusions:

Patients empirically placed on nitric oxide out of concern of pulmonary hypertensive crisis and successfully weaned off showed unchanged or decreased dead space ratio throughout the initiation to discontinuation phases of nitric oxide therapy. Trends in dead space ratio may aid in determining true need for nitric oxide and facilitate effective weaning. Further studies are needed to directly compare trends between success and failure groups.

Type
Original Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Background

During a pulmonary hypertensive crisis, acute elevations in pulmonary vascular resistance trigger ventricular dysfunction and a low cardiac output state which can be lethal when not recognised and treated early.Reference Hopkins, Bull, Haworth, de Leval and Stark1Reference Oishi and Fineman3 Inhaled nitric oxide, a selective pulmonary vasodilator, has been shown to effectively reverse this process in many patients, and is currently used as a first-line agent in children with known or suspected pulmonary hypertensive crises.Reference Pepke-Zaba, Higenbottam, Dinh-Xuan, Stone and Wallwork4Reference Rimensberger, Spahr-Schopfer and Berner10

In acutely deteriorating patients however, reliably diagnosing a decompensation as a pulmonary hypertensive crisis and recognising the need for and response to nitric oxide remains an ongoing challenge at the bedside. In patients who have been empirically started on inhaled nitric oxide, titration is often is dictated by institution-based guidelines that include arbitrary time-based weaning strategies and/or changes in biomarkers such as PaO2 that lack strong physiologic justification as surrogates for changes in pulmonary blood flow.Reference Di Genova, Sperling and Gionfriddo11,Reference Schindler, Bohn, Bryan, Cutz and Rabinovitch12 The increasing implementation of stewardship programmes’ in centres using inhaled nitric oxide may reflect the extent of this problem.Reference Di Genova, Sperling and Gionfriddo11

Of existing biomarkers that reflect changes in pulmonary blood flow, use of the dead space ratio has a strong physiologic basis and has shown some promise in the existing literature. Measured using the Enghoff modification of the Bohr equation ((PaC02 − PeCO2)/PaC02), the dead space ratio and its derivatives have been used for the last 30 years in the paediatric population.Reference Arnold, Thompson and Arnold13 Available literature includes its use as a prognostic indicator in patients with compromised pulmonary blood flow such as congenital diaphragmatic hernia or with Fontan circulation, and as a tool in evaluating for ECMO decannulation readiness, reflecting increases in pulmonary blood flow as a surrogate for increased native cardiac output.Reference Arnold, Thompson and Benjamin14Reference Naruke, Inomata and Imai18

Changes in dead space ratio, as a reflection of changes in pulmonary blood flow, may thus prove novel as an effective bedside tool in guiding the appropriate initiation and titration of inhaled nitric oxide in patients with suspected pulmonary hypertension. We thus seek to describe trends in dead space ratio during initiation and weaning phases of inhaled nitric oxide in patients placed on it out of concern of pulmonary hypertensive crisis.

Methods

Patients and settings

This single centre retrospective cohort study was approved by the Institutional Review Board of Cleveland Clinic. We included children admitted to the PICU between January 2018 and June 2020 who were started on inhaled nitric oxide out of clinical concern for pulmonary hypertensive crisis and had documented continuous capnography and arterial blood gas data at time points of ≥20 ppm and ≤5 ppm nitric oxide during weaning.

Study procedures

The database of patients initiated on inhaled nitric oxide was obtained from the Respiratory Therapy Department. Charts were individually reviewed, and we included the patients that met the eligibility criteria. Dead space ratio was calculated using the Enghoff modification of the Bohr equation (Vd/Vt= (PaC02 − PetCO2)/PaCO2). iNOmax® was used for iNO delivery. Servo-i® and Servo-U® mechanical ventilators with in-line ETCO2 monitoring and GE® E-mini-CO2 modules were used for continuous wave capnography measurements.

Data collection

In addition to arterial CO2 and ETCO2, relevant demographic data were collected, including age, gender, cardiac anatomy, presence of co-morbidities, and chromosomal defects. Additional variables collected included vasoactive infusion score, minute ventilation, oxygenation index, and hours on iNO.

Determination of pulmonary hypertensive crisis

After identification of the patients that were started on inhaled nitric oxide from the database, we excluded the patients that had been started on inhaled nitric oxide for other reasons besides clinicians concerns of pulmonary hypertensive crisis. This criterion was taken based on the documentation in the patient’s chart. Patients included in the study were started on inhaled nitric oxide either in the PICU or the cardiac OR and subsequently transferred to the PICU and had either documented history of pulmonary hypertension or had cardiac lesions with risk of developing a pulmonary hypertensive crisis.

Determination of success or failure to wean from inhaled nitric oxide

Failure to wean from inhaled nitric oxide was defined as reinitiating it within 72 hours of discontinuation.

Statistical analysis

Continuous variables were described using medians and interquartile ranges; categorical variables were described using counts and percentages. Between-group comparisons of demographic and clinical characteristics by inhaled nitric oxide success were assessed by using Wilcoxon rank sum test for continuous data and Fisher’s exact test for categorical data, as appropriate. Dead space ratios, as well as FiO2, vasoactive infusion score, oxygenation index, and minute ventilation, in different time points of inhaled nitric oxide procedure were compared by Wilcoxon signed rank test. Pearson’s correlation coefficient was used to explore associations between dead space ratio and vasoactive infusion scores and oxygenation indexes.

All analyses were performed on a complete case basis; subjects with missing data on particular variables were only excluded for analyses in which those variables were used. All tests were two-tailed and performed at a significance level of 0.05. SAS 9.4 software (SAS Institute, Cary, NC, USA) was used for all analyses.

Results

Patient demographics and characteristics

Table 1 shows demographic and clinic characteristics of the success and failure groups. In total, 27 patients were included (see Fig 1), of which 23 (85%) were in the success group and 5 (15%) in the failure group. Patients in the success group had a median age of 10 months [4.0, 57], had pre-existing CHD in 9/23 (39%), and had a pre-existent diagnosis of pulmonary hypertension in 2/23 (8.7%). Dead space ratio before inhaled nitric oxide initiation was 0.1 [0.06, 0.27] in this group, with 9/23 (39%) initiated on additional pulmonary vasodilators during the weaning process, and with a median total time on inhaled nitric oxide of 53.0 hours [26.0, 121.0]. Patients in the failure group had a median age of 10.5 months [2, 29.5], had pre-existing CHD in 2/4 (50%), had a pre-existent diagnosis of pulmonary hypertension in 2/4 (50%), had a dead space ratio before inhaled nitric oxide initiation of 0.24 [0.15, 0.37], with 3/4 (75%) initiated on additional pulmonary vasodilators during weaning, and with a median time on iNO of 74.0 hours [65.3, 80.5].

Figure 1. Inclusion and exclusion criteria.

Figure 2. Dead space ratio success to wean group.

Table 1. Characteristics by overall success and failure of iNO therapy wean

p-values: b = Wilcoxon rank sum test; d = Fisher’s exact test.

Primary analysis

Given the small sample size of the failure group (Supplemental Data, Figure 1), further quantitative analysis focused upon trends in dead space within the success group. In this group, the median dead space ratio after initiation of inhaled nitric oxide (>20 ppm) was 0.18 [0.09, 0.27] and prior to inhaled nitric oxide discontinuation (<5 ppm) decreased to 0.11 [0.060, 0.22], p = 0.043 (Figure 2). No significant differences were noted between dead space ratio pre- and post-inhaled nitric oxide initiation (p = 0.88) and pre- and post-inhaled nitric oxide discontinuation (p = 0.63). The PaO2 after initiation (>20 ppm) was 82 mmHg [40, 157], and prior discontinuation was 90 mmHg [47, 129], p = 0.34. Vasoactive infusion score after initiation (>20 ppm) and prior to discontinuation (<5 ppm) were 12 [7.5, 17] and 8 [5.3, 8.5], respectively (p < 0.001).

Secondary analysis

Using alternative outcome measures of changes in vasoactive infusion score and changes in oxygenation index in all subjects (N = 27), no significant correlation was found between changes in dead space ratio and changes in vasoactive infusion score (r = −0.23, p = 0.25) or oxygenation index (r = 0.30, p = 0.16) during the weaning process.

Discussion

In this retrospective review, we studied the utility of dead space ratio trends as a novel tool in predicting ongoing need for inhaled nitric oxide in patients with clinical concern for pulmonary hypertensive crisis. For those successfully weaned off, we found that dead space ratio decreased during the weaning process and that no significant differences in dead space ratio existed between pre- and post-inhaled nitric oxide initiation and pre- and post-inhaled nitric oxide discontinuation phases. These results suggest that trends in dead space ratio, as a surrogate for changes in pulmonary blood flow, may aid in determining true need for inhaled nitric oxide and facilitate effective inhaled nitric oxide weaning using a physiologically based and target-driven approach.

Continuous waveform capnography has been recognised as a powerful tool in assessing changes in pulmonary blood flow and hence as a surrogate of left ventricular cardiac output.Reference Young, Marik, Sibole, Grooms and Levitov19 Most notably, it has been incorporated into AHA resuscitation guidelines as a marker of adequate cardiopulmonary resuscitation and a reflection of return of spontaneous circulation.Reference Pokorná, Necas, Kratochvíl, Skripský, Andrlík and Franek20Reference Davis, Johns and Olvera23 In isolation, however, end-tidal capnography (ETCO2), being one component of the dead space equation, may not be an accurate reflection of pulmonary blood flow, given that changes in minute ventilation may also affect its result. Incorporating changes between alveolar and arterial C02 content as a more accurate surrogate for changes in pulmonary blood flow, an early proof-of-concept study by Askrog investigated changes in arterial-alveolar C02 difference (ΔC02) among healthy post-operative adult patients following a 1L rapid infusion IV bolus. Directly measured mean pulmonary artery pressures immediately increased by 5 mm Hg, and a clear inverse linear relationship was found between mean pulmonary artery pressures and ΔC02.Reference Askrog24 A more recent study by Chauhan and Deb found that use of alveolar functional fraction (ETCO2/PaCO2) can accurately reflect changes in the ratio pulmonary to systemic blood flow (Qp:Qs) in those CHD patients with intracardiac shunting, data validated by comparing this metric to direct catheterisation measurements of Qp:Qs (r = 0.83, p < 0.0001).Reference Chauhan and Deb25

To date, dead space ratio using the modified Bohr equation has been studied extensively in patients as a prognosticator in acute lung injury, and it has been recently highlighted in patients with single ventricle physiology.Reference Kallet, Zhuo, Ho, Lipnick, Gomez and Matthay26 Shostak et alReference Shostak, Schiller and Merzbach27 described that in patients with Fontan physiology (a population with potentially compromised pulmonary blood flow) and those with increased dead space values had higher morbidity, with increased duration of mechanical ventilation, severity of illness, and ICU length of stay. Likewise, Cigarroa et alReference Cigarroa, van den Bosch and Tang28 described that in patients following bidirectional cavo-pulmonary anastomosis, a dead space more than 0.28 upon ICU admission increased the risk of requiring reintervention or death during admission. Little focus has been placed on its primary use as a surrogate for changes in pulmonary blood flow in conditions such as an acute pulmonary hypertensive crisis. In many pulmonary hypertension-related inhaled nitric oxide protocols, biomarkers with less physiologic plausibility such as PaO2 are commonly used to help guide weans of inhaled nitric oxide.Reference Todd Tzanetos, Housley, Barr, May and Landers29,Reference Aly, Sahni and Wung30 To this point, Schindler et alReference Schindler, Bohn, Bryan, Cutz and Rabinovitch12 described the clinical characteristics of 15 children during acute pulmonary hypertensive crises using invasive monitoring, finding that only 1/15 patients exhibited hypoxaemia in the midst of these episodes, with that 1 patient having an intracardiac shunt. While the gold standard in monitoring for real-time changes in pulmonary blood flow may involve pulmonary artery catheters, their placement is often technically challenging in the paediatric population and has a higher risk of bleeding during removal, in addition to their inability to assess hemodynamic data in the face of intracardiac shunting, a condition that many children with pulmonary hypertension exhibit.Reference Cigarroa, Lange, Williams, Bedotto and Hillis31Reference Flori, Johnson, Hanley and Fineman33 The need for non-invasive, readily available, and accurate markers of pulmonary blood flow remain an ongoing need in this population.

Comparing those patients failing inhaled nitric oxide discontinuation in our cohort to the success group, a trend appears of a higher dead space ratio prior to inhaled nitric oxide initiation, along with increased pre-existing documentation of a pulmonary hypertension diagnosis, longer times on inhaled nitric oxide, higher FiO2 need after inhaled nitric oxide discontinuation, and longer need for mechanical ventilation. This higher dead space ratio may thus serve as a prognostic marker of pulmonary HTN disease severity, although reaching further conclusions on this failure group and its trends requires a larger population.

Limitations

One of the main limitations of our study was the low number of patients in the inhaled nitric oxide failure group, which hindered our ability to quantitatively compare the success and failure to wean groups. In addition, the outcome variable of success/failure was dependent on physician’s clinical judgment to reinitiate inhaled nitric oxide without including supportive echocardiographic or catheterisation-based hemodynamic data, data not consistently available within our studied population. Using the alternative outcome measures of changes in vasoactive infusion score or oxygenation index during nitric oxide weaning, no significant correlations were found between decreases in dead space ratio and decreases in these variables. While this may reflect limitations in dead space ratio as a tool in weaning inhaled nitric oxide, it must also be recognised that the vasoactive infusion score as an outcome measure may be influenced by other hemodynamic perturbations not related to pulmonary hypertension and that worsening oxygenation both may not be a primary manifestation of worsening pulmonary hypertension and may also be influenced by other primary pulmonary pathology.Reference Schindler, Bohn, Bryan, Cutz and Rabinovitch12

An additional limitation in our analysis is that in the success to wean group, 9/23 (39%) were started on an additional pulmonary vasodilator during the weaning process. However, it should be mentioned that the question of our study is centred more on the relationship of dead space ratio changes and inhaled nitric oxide weaning per se, independently of the use of additional vasodilators during this weaning process. With this in mind, we reviewed the dead space ratio trends in the remaining 14 patients without finding significant changes (0.25–0.17, p = 0.25) in this group. Another limitation of our study involves not including the presence of ETT leak as a variable in the analysis of dead space ratio. In our unit, it is standard of care to use cuffed ETT, but we acknowledge that in patients with ETT leak, the calculated dead space ratio may be falsely overestimated.

Conclusions

Children empirically placed on inhaled nitric oxide out of concern of pulmonary hypertensive crisis and then successfully weaned off exhibited an unchanged or decreased dead space ratio throughout the initiation to discontinuation phases of inhaled nitric oxide therapy, suggesting that trends in dead space ratio may aid in determining true need for inhaled nitric oxide and facilitate effective weaning. Further studies with both larger sample sizes and thoughtful outcome measures are needed to directly compare trends between success and failure groups.

Supplementary material

To view supplementary material for this article, please visit https://doi.org/10.1017/S1047951121004662

Acknowledgements

None.

Conflicts of Interest

None.

Author Contribution

ADG: Literature search, Study design, Data collection, Analysis of data, Manuscript preparation, Review of manuscript. WL: Statistical method development, Analysis of data. HA: Study design, Review of Manuscript. WJH: Study design, Analysis of data, Review of manuscript.

References

Hopkins, RA, Bull, C, Haworth, SG, de Leval, MR, Stark, J. Pulmonary hypertensive crises following surgery for congenital heart defects in young children. Eur J Cardiothorac Surg 1991; 5: 628634.CrossRefGoogle ScholarPubMed
Abman, SH, Hansmann, G, Archer, SL, et al. Pediatric pulmonary hypertension: guidelines from the American Heart Association and American Thoracic Society. Circulation 2015; 132: 20372099.CrossRefGoogle ScholarPubMed
Oishi, P, Fineman, JR. Pulmonary hypertension. Pediatr Crit Care Med 2016; 17: S140S145.CrossRefGoogle ScholarPubMed
Pepke-Zaba, J, Higenbottam, TW, Dinh-Xuan, AT, Stone, D, Wallwork, J. Inhaled nitric oxide as a cause of selective pulmonary vasodilatation in pulmonary hypertension. Lancet 1991; 338: 11731174.CrossRefGoogle ScholarPubMed
Frostell, C, Fratacci, MD, Wain, JC, Jones, R, Zapol, WM. Inhaled nitric oxide. A selective pulmonary vasodilator reversing hypoxic pulmonary vasoconstriction. Circulation 1991; 83: 20382047.CrossRefGoogle ScholarPubMed
Journois, D, Pouard, P, Mauriat, P, Malhère, T, Vouhé, P, Safran, D. Inhaled nitric oxide as a therapy for pulmonary hypertension after operations for congenital heart defects. J Thorac Cardiovasc Surg 1994; 107: 11291135.CrossRefGoogle ScholarPubMed
Miller, OI, Tang, SF, Keech, A, Pigott, NB, Beller, E, Celermajer, DS. Inhaled nitric oxide and prevention of pulmonary hypertension after congenital heart surgery: a randomised double-blind study. Lancet 2000; 356: 14641469.CrossRefGoogle ScholarPubMed
Barr, FE, Macrae, D. Inhaled nitric oxide and related therapies. Pediatr Crit Care Med 2010; 11: S30S36.CrossRefGoogle ScholarPubMed
Morris, K, Beghetti, M, Petros, A, Adatia, I, Bohn, D. Comparison of hyperventilation and inhaled nitric oxide for pulmonary hypertension after repair of congenital heart disease. Crit Care Med 2000; 28: 29742978.CrossRefGoogle ScholarPubMed
Rimensberger, PC, Spahr-Schopfer, I, Berner, M, et al. Inhaled nitric oxide versus aerosolized iloprost in secondary pulmonary hypertension in children with congenital heart disease: vasodilator capacity and cellular mechanisms. Circulation 2001; 103: 544548.CrossRefGoogle ScholarPubMed
Di Genova, T, Sperling, C, Gionfriddo, A, et al. A stewardship program to optimize the use of inhaled nitric oxide in pediatric critical care. Qual Manag Health Care 2018; 27: 7480.CrossRefGoogle ScholarPubMed
Schindler, MB, Bohn, DJ, Bryan, AC, Cutz, E, Rabinovitch, M. Increased respiratory system resistance and bronchial smooth muscle hypertrophy in children with acute postoperative pulmonary hypertension. Am J Respir Crit Care Med 1995; 152: 13471352.CrossRefGoogle ScholarPubMed
Arnold, JH, Thompson, JE, Arnold, LW. Single breath CO2 analysis: description and validation of a method. Crit Care Med 1996; 24: 96102.CrossRefGoogle ScholarPubMed
Arnold, JH, Thompson, JE, Benjamin, PK. Respiratory deadspace measurements in neonates during extracorporeal membrane oxygenation. Crit Care Med 1993; 21: 18951900.CrossRefGoogle ScholarPubMed
Arnold, JH, Bower, LK, Thompson, JE. Respiratory deadspace measurements in neonates with congenital diaphragmatic hernia. Crit Care Med 1995; 23: 371375.CrossRefGoogle ScholarPubMed
Bhalla, AK, Belani, S, Leung, D, Newth, CJ, Khemani, RG. Higher dead space is associated with increased mortality in critically ill children. Crit Care Med 2015; 43: 24392445.CrossRefGoogle ScholarPubMed
Devor, RL, Kang, P, Wellnitz, C, Nigro, JJ, Velez, DA, Willis, BC. Pulmonary dead space fraction and extubation success in children after cardiac surgery. Pediatr Crit Care Med 2018; 19: 301309.CrossRefGoogle ScholarPubMed
Naruke, T, Inomata, T, Imai, H, et al. End-tidal carbon dioxide concentration can estimate the appropriate timing for weaning off from extracorporeal membrane oxygenation for refractory circulatory failure. Int Heart J 2010; 51: 116120.CrossRefGoogle ScholarPubMed
Young, A, Marik, PE, Sibole, S, Grooms, D, Levitov, A. Changes in end-tidal carbon dioxide and volumetric carbon dioxide as predictors of volume responsiveness in hemodynamically unstable patients. J Cardiothorac Vasc Anesth 2013; 27: 681684.CrossRefGoogle ScholarPubMed
Pokorná, M, Necas, E, Kratochvíl, J, Skripský, R, Andrlík, M, Franek, O. A sudden increase in partial pressure end-tidal carbon dioxide (P(ET)CO(2)) at the moment of return of spontaneous circulation. J Emerg Med 2010; 38: 614621.CrossRefGoogle ScholarPubMed
Levine, RL, Wayne, MA, Miller, CC. End-tidal carbon dioxide and outcome of out-of-hospital cardiac arrest. N Engl J Med 1997; 337: 301306.CrossRefGoogle ScholarPubMed
Panchal, AR, Berg, KM, Hirsch, KG, et al. 2019 American Heart Association focused update on advanced cardiovascular life support: use of advanced airways, vasopressors, and extracorporeal cardiopulmonary resuscitation during cardiac arrest: an update to the American Heart Association Guidelines for cardiopulmonary resuscitation and emergency cardiovascular care. Circulation 2019; 140: e881e894.Google Scholar
Davis, JS, Johns, JA, Olvera, DJ, et al. Vital sign patterns before shock-related cardiopulmonary arrest. Resuscitation 2019; 139: 337342.CrossRefGoogle ScholarPubMed
Askrog, V. Changes in (a-A)CO2 difference and pulmonary artery pressure in anesthetized man. J Appl Physiol 1966; 21: 12991305.CrossRefGoogle Scholar
Chauhan, JC, Deb, R. Relationship between pulmonary-to-systemic-blood-flow ratio (Qp:Qs) based on cardiac catheterization and indices derived from simultaneously measured end tidal CO. Pediatr Cardiol 2019; 40: 182187.CrossRefGoogle Scholar
Kallet, RH, Zhuo, H, Ho, K, Lipnick, MS, Gomez, A, Matthay, MA. Lung injury etiology and other factors influencing the relationship between dead-space fraction and mortality in ARDS. Respir Care 2017; 62: 12411248.CrossRefGoogle ScholarPubMed
Shostak, E, Schiller, O, Merzbach, A, et al. Alveolar dead-space fraction and arterial saturation predict postoperative course in Fontan patients. Pediatr Crit Care Med 2020; 21: e200e206.CrossRefGoogle ScholarPubMed
Cigarroa, CL, van den Bosch, SJ, Tang, X, et al. Measurement of dead space fraction upon ICU admission predicts length of stay and clinical outcomes following bidirectional cavopulmonary anastomosis. Pediatr Crit Care Med 2018; 19: 2331.CrossRefGoogle ScholarPubMed
Todd Tzanetos, DR, Housley, JJ, Barr, FE, May, WL, Landers, CD. Implementation of an inhaled nitric oxide protocol decreases direct cost associated with its use. Respir Care 2015; 60: 644650.CrossRefGoogle ScholarPubMed
Aly, H, Sahni, R, Wung, J-T. Weaning strategy with inhaled nitric oxide treatment in persistent pulmonary hypertension of the newborn. Arch Dis Child Fetal Neonatal Ed 1997; 76: F118F122.CrossRefGoogle ScholarPubMed
Cigarroa, RG, Lange, RA, Williams, RH, Bedotto, JB, Hillis, LD. Underestimation of cardiac output by thermodilution in patients with tricuspid regurgitation. Am J Med 1989; 86: 417420.CrossRefGoogle ScholarPubMed
Perkin, RM, Anas, N. Pulmonary artery catheters. Pediatr Crit Care Med 2011; 12: S12S20.CrossRefGoogle ScholarPubMed
Flori, HR, Johnson, LD, Hanley, FL, Fineman, JR. Transthoracic intracardiac catheters in pediatric patients recovering from congenital heart defect surgery: associated complications and outcomes. Crit Care Med 2000; 28: 29973001.CrossRefGoogle ScholarPubMed
Figure 0

Figure 1. Inclusion and exclusion criteria.

Figure 1

Figure 2. Dead space ratio success to wean group.

Figure 2

Table 1. Characteristics by overall success and failure of iNO therapy wean

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