Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-18T04:40:20.922Z Has data issue: false hasContentIssue false

Near-infrared spectroscopy after high-risk congenital heart surgery in the paediatric intensive care unit

Published online by Cambridge University Press:  13 February 2014

Lyvonne N. Tume*
Affiliation:
Department of PICU, Alder Hey Children’s NHS Foundation Trust and Department, Liverpool, United Kingdom School of Health, The University of Central Lancashire, Preston, United Kingdom
Philip Arnold
Affiliation:
Department of Translational Medicine, Alder Hey Children’s NHS Foundation Trust, University of Liverpool, Liverpool, United Kingdom
*
Correspondence to: L. N. Tume, Senior Research Fellow of PICU, Department of PICU, Alder Hey Children’s NHS Foundation Trust and Department, Eaton Road, Liverpool L12 2AP, United Kingdom. Tel:+44 151 282 4588; Fax:+44 151 252 5771; E-mails: [email protected]; [email protected]

Abstract

Objective: To establish whether the use of near-infrared spectroscopy is potentially beneficial in high-risk cardiac infants in United Kingdom paediatric intensive care units. Design: A prospective observational pilot study. Setting: An intensive care unit in North West England. Patients: A total of 10 infants after congenital heart surgery, five with biventricular repairs and five with single-ventricle physiology undergoing palliation. Interventions: Cerebral and somatic near-infrared spectroscopy monitoring for 24 hours post-operatively in the intensive care unit. Measurement and main results: Overall, there was no strong correlation between cerebral near-infrared spectroscopy and mixed venous oxygen saturation (r=0.48). At individual time points, the correlation was only strong (r=0.74) 1 hour after admission. The correlation was stronger for the biventricular patients (r=0.68) than single-ventricle infants (r=0.31). A strong inverse correlation was demonstrated between cerebral near-infrared spectroscopy and serum lactate at 3 of the 5 post-operative time points (1, 4, and 12 hours: r=−0.76, −0.72, and −0.69). The correlation was stronger when the cerebral near-infrared spectroscopy was <60%. For cerebral near-infrared spectroscopy <60%, the inverse correlation with lactate was r=−0.82 compared with those cerebral near-infrared spectroscopy >60%, which was r=−0.50. No correlations could be demonstrated between (average) somatic near-infrared spectroscopy and serum lactate (r=−0.13, n=110) or mixed venous oxygen saturation and serum lactate. There was one infant who suffered a cardiopulmonary arrest, and the cerebral near-infrared spectroscopy showed a consistent 43 minute decline before the event. Conclusions: We found that cerebral near-infrared spectroscopy is potentially beneficial as a non-invasive, continuously displayed value and is feasible to use on cost-constrained (National Health Service) cardiac intensive care units in children following heart surgery.

Type
Original Articles
Copyright
© Cambridge University Press 2014 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Durandy, Y, Rubatti, M, Couturier, R. Near infrared spectroscopy during pediatric cardiac surgery: errors and pitfalls. Perfusion 2011; 26: 441446.CrossRefGoogle Scholar
2. Ghanayem, N, Mitchell, M, Tweddell, J, Hoffman, G. Monitoring the brain before, during and after cardiac surgery to improve long-term neurodevelopmental outcomes. Cardiol Young 2006; 16: S103S109.Google Scholar
3. Booth, E, Dukatz, C, Ausman, J, Wider, M. Cerebral and somatic venous oximetry in adults and infants. Surg Neurol Int 2010; 1: 75.Google Scholar
4. Phelps, H, Mahle, W, Kim, D, et al. Postoperative cerebral oxygenation in hypoplastic left heart syndrome after the Norwood procedure. Ann Thorac Surg 2009; 87: 1490.CrossRefGoogle Scholar
5. Hoffman, G, Brosig, C, Mussatto, K, Tweddell, J, Ghanayem, N. Perioperative cerebral oxygen saturation in neonates with hypoplastic left heart syndrome and childhood neurodevelopmental outcome. J Thorac Cardiovasc Surg 2013; 146: 11531164.Google Scholar
6. Hirsch, J, Charpie, J, Ohye, R, Gurney, J. Near-infrared spectroscopy: what we know and what we need to know – a systematic review of the congenital heart disease literature. J Thorac Cardiovasc Surg 2009; 137: 154159.CrossRefGoogle Scholar
7. Arnold, D, Burns, C, Adhikari, N, Kho, M, Meade, M, Cook, D. The design and interpretation of pilot trials in clinical research in critical care. Crit Care Med 2009; 37: S69S74.CrossRefGoogle ScholarPubMed
8. Plowman, S, Smith, D. Exercise Physiology for Health, Fitness and Performance, 2nd edn. Lippincott, Williams and Wilkins, Baltimore, USA, 2008: 156.Google Scholar
9. Li, J, Zhang, G, Holtby, HM, et al. Inclusion of oxygen consumption improves the accuracy of arterial and venous oxygen saturation interpretation after the Norwood procedure. J Thorac Cardiovasc Surg 2006; 131: 10991107.CrossRefGoogle ScholarPubMed
10. Chakravarti, S, Mittnacht, A, Katz, J, Nguyen, K, Joashi, U, Srivastava, S. Multisite near-infrared spectroscopy predicts elevated blood lactate level in children after cardiac surgery. J Cardiothorac Vasc Anesth 2009; 23: 663667.CrossRefGoogle ScholarPubMed
11. MacLeod, DB, Ikeda, K, Keifer, J, Moretti, E. Validation of the CAS adult cerebral oximeter during hypoxia in healthy volunteers. Anesth Analg, 102S: S-162.Google Scholar
12. Toet, M, Flinterman, A, van der Laar, I. Cerebral oxygen saturation and electrical brain activity before, during and up to 36 hours after arterial switch procedure in neonates without pre-existing brain damage: its relationship to neurodevelopmental outcome. Exp Brain Res 2005; 165: 343350.CrossRefGoogle ScholarPubMed
13. Kane, J. Near-infrared spectroscopy monitors: a novel tool for patient safety in the intensive care unit. J Patient Safety 2009; 5: 2931.CrossRefGoogle Scholar
14. Maher, K, Phelps, H, Krishbom, P. Near infrared spectroscopy changes with pericardial tamponade. Ped Crit Care Med 2009; 10: e13e15.CrossRefGoogle Scholar
15. Morris, K, McShane, P, Stickley, J, Parslow, R. The relationship between blood lactate concentration, the Pediatric Index of Mortality 2 (PIM2) and mortality in pediatric intensive care. Intensive Care Medicine 2012; 38: 20422046.CrossRefGoogle Scholar
16. Basaran, M, Sever, K, Kafali, E, et al. Serum lactate level has prognostic significance after pediatric cardiac surgery. J Cardiothorac Vasc Anesth 2006; 20: 4347.CrossRefGoogle Scholar
17. Hoffman, G, Ghanayem, N, Kampine, J. Venous saturation and the anaerobic threshold in neonates after the Norwood procedure for hypoplastic left heart syndrome. Ann Thorac Surg 2000; 70: 15151521.CrossRefGoogle ScholarPubMed
18. Kasnitz, P, Druger, G, Yorra, F, Simmons, D. Mixed venous oxygen tension and hyperlactataemia: survival in severe cardiopulmonary disease. JAMA 1976; 236: 570574.CrossRefGoogle ScholarPubMed
19. Rashkin, M, Bosken, C, Baughman, R. Oxygen delivery in critically ill patients – relationship to blood lactate and survival. Chest 1985; 87: 580584.CrossRefGoogle ScholarPubMed
20. Meastiz, M, Rackow, E, Kaufman, B. Relationship of oxygen delivery and mixed venous oxygen saturation to lactic acidosis in patients with sepsis and acute myocardial infarction. Critical Care Med 1988; 16: 655659.Google Scholar
21. 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: 8390.CrossRefGoogle ScholarPubMed
22. Hoffman, G, Stuth, E, Jacquiss, R, et al. Changes in cerebral and somatic oxygenation during stage 1 palliation of hypoplastic left heart syndrome using continuous regional cerebral perfusion. J Thorac Cardiovasc Surg 2004; 127: 223233.CrossRefGoogle ScholarPubMed
23. Johnson, B, Hoffman, G, Tweddell, J, et al. Near-infrared spectroscopy in neonates before palliation of hypoplastic left heart syndrome. Ann Thorac Surg. 2009; 87: 571579.Google Scholar
24. Dodge-Khatami, J, Gottschalk, U, Eulenburg, C, et al. Prognostic value of perioperative near-infrared spectroscopy during neonatal and infant congenital heart surgery for adverse in-hospital clinical events. World J Pediatr Congenit Heart Surg 2012; 3: 221228.CrossRefGoogle ScholarPubMed
25. Hovarth, R, Shore, S, Schultz, S, Rosenkranz, E, Cousins, M, Ricci, M. Cerebral and somatic oxygen saturation decrease after delayed sternal closure in children after cardiac surgery. J Thoracic Cardiovascular Surgery 2010; 139: 894900.Google Scholar
26. Marimón, GA, Dockery, WK, Sheridan, MJ, Agarwal, S. Near-infrared spectroscopy cerebral and somatic (renal) oxygen saturation correlation to continuous venous oxygen saturation via intravenous oximetry catheter. J Crit Care 2012; 27: 314.e13314.e18.CrossRefGoogle ScholarPubMed
27. McQuillen, P, Nishimoto, M, Bottrell, C, et al. Regional and central venous oxygen saturation monitoring following pediatric cardiac surgery: concordance and association with clinical variables. Pediatr Crit Care Med 2007; 8: 154160.CrossRefGoogle ScholarPubMed
28. Moreno, G, Pilán, M, Manara, C, et al. Regional venous oxygen saturation versus mixed venous saturation after paediatric cardiac surgery. Acta Anaesthesiol Scand 2013; 57: 373379.Google Scholar
29. Ricci, Z, Garisto, C, Favia, I, et al. Cerebral NIRS as a marker of superior vena cava oxygen saturation in neonates with congenital heart disease. Paediatr Anaesth 2010; 20: 10401045.Google Scholar
30. Tortoriello, T, Stayer, S, Mott, A, et al. A noninvasive estimation using near-infrared spectroscopy by cerebral oximetry in pediatric cardiac surgery patients. Pediatr Anesth 2005; 15: 495503.Google Scholar
31. Zulueta, J, Vida, V, Perisinotto, E, et al. The role of intraoperative regional oxygen saturation using near infrared spectroscopy in the prediction of low output syndrome after pediatric heart surgery. J Card Surg 2013; 28: 446452.CrossRefGoogle ScholarPubMed
32. Bhalala, U, Nishisaki, A, McQueen, D, et al. Change in regional (somatic) near-infrared spectroscopy is not a useful indicator of clinically detectable low cardiac output in children after surgery for congenital heart defects. Pediatr Crit Care Med 2012; 13: 529534.Google Scholar
33. Colasacco, C, Worthen, M, Peterson, B, Lamberti, J, Spear, R. Near-infrared spectroscopy monitoring to predict postoperative renal insufficiency following repair of congenital heart disease. World J Pediatr Congenit Heart Surg 2011; 2: 536540.CrossRefGoogle ScholarPubMed
34. Hazle, M, Gajarski, R, Aiyagari, R, et al. Urinary biomarkers and renal near-infrared spectroscopy predict intensive care unit outcomes after cardiac surgery in infants younger than 6 months of age. J Thorac Cardiovasc Surg 2013; 146: 861867.el.CrossRefGoogle Scholar
35. Kaufman, J, Almodovar, M, Zuk, J, Friesen, R. Correlation of abdominal site near-infrared spectroscopy with gastric tonometry in infants following surgery for congenital heart disease. Pediatr Crit Care Med 2008; 9: 6268.CrossRefGoogle ScholarPubMed
36. Owens, G, King, K, Gurney, J, Charpie, J. Low renal oximetry correlates with acute kidney injury after infant heart surgery. Pediatr Cardiol 2011; 32: 183188.CrossRefGoogle Scholar
37. Schultz, G, Weiss, M, Bauersfeld, U. Liver tissue oxygenation as measured by near-infrared spectroscopy in the critically ill child in correlation with central venous oxygen saturation. Intensive Care Med 2002; 28: 184189.CrossRefGoogle Scholar