Présentation par Mano DESFOUR sous la direction du Docteur Nicolas COURTIN exposant la littérature sur l’utilisation du NIRS (near Infrared-reflected spectroscopy) en périopératoire.

Le résumé de la présentation sous format pdf.

NIRS-peroperatoire-topo-01_2024

Et le diaporama

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Références:

  1. Bickler P., Feiner J., Rollins M. Factors affecting the performance of 5 cerebral oximeters during hypoxia in healthy volunteers Anesth Analg 2013 ; 117 : 813-823
  2. Murkin J.M., Arango M. Near-infrared spectroscopy as an index of brain and tissue oxygenation Br J Anaesth 2009 ; 103 (Suppl. 1) : i3-i13
  3. Laurent Delaunay, Florence Plantet. NIRS cérébrale en peropératoire : est ce utile ? Le praticien en anesthésie réanimation. Volume 24, numéro 2, pages 98-107 (avril 2020)
  4. McCormick P.W., Stewart M., Goetting M.G., Balakrishnan G. Regional cerebrovascular oxygen saturation measured by optical spectroscopy in humans Stroke 1991 ; 22 : 596-602
  5. G Nollert, T Shin’oka, R A Jonas. Near-infrared spectrophotometry of the brain in cardiovascular surgery. J Thorac Cardiovasc Surg 1998; 46:167-75
  6. M. Heringlake, C. Garbers, J. H. Kabler et coll., « Preoperative cerebral oxygen saturation and clinical outcomes in cardiac surgery », Anesthesiology, vol. 114, no 1 (2011), p. 58-69
  7. Yao FS, Yao D, Jin J. Age and gender differences in cerebral oxygen saturations. Paper presented at: the Annual Meeting of the American Society of Anesthesiologists; October 23-27, 2004; Las
    Vegas, Nevada. Anesthesiology. 2004;101:A193
  8. Kishi K, Kawaguchi M, Yoshitani K, Nagahata T, Furuya H. Influence of patient variables and sensor location on regional cerebral oxygen saturation measured by INVOS 4100 near-infrared
    spectrophotometers. J Neurosurg Anesthesiol. 2003;15:302-306.
  9. Davie S.N., Grocott H.P. Impact of extracranial contamination on regional cerebral oxygen saturation: a comparison of three cerebral oximetry technologies Anesthesiology 2012 ; 116 :
    834-840
  10. Greenberg S., Shear T., Murphy G. Extracranial contamination of NIRS devices Anesth Analg 2017 ; 124 : 356-358
  11. Sun X., Ellis J., Corso P., Hill P., Chen F., Lindsay J. Skin pigmentation interferes with the clinical measurement of regional cerebral oxygen saturation Br J Anaesth 2015 ; 114 : 276-280
  12. Madsen P., Skak C., Rasmussen A., Secher N.H. Interference of cerebral near-infrared oximetry in patients with icterus Anesth Analg 2000 ; 90 : 489-493
  13. G. Schwarz, G. Litscher, R. Kleinert et R. Jobstmann, « Cerebral oximetry in dead subjects », Journal of Neurosurgical Anesthesiology, vol. 8, no 3 (1996), p. 189-193H. L. Edmonds Jr., «
    Monitoring during cardiopulmonary bypass », Dans : A. Koht, T. Sloan et J. R. Toleikis, éd., Dans : Neuromonitoring for the Anesthesiologist and Other Health Care Providers, 2e éd., New York
    (New York), Springer, 2017, p. 617-624
  14. O. Tatli, O. Bekar, M. Imamoglu et coll., « Cerebral Oximetry as an Auxiliary Diagnostic Tool in the Diagnosis of Brian Death », Transplantation Proceedings, vol. 49 (2017), p. 1702-1707.
  15. H. Maeda, K. Fukita, S. Oritani, K. Ishida et B. L. Zhu, « Evaluation of postmortem oxymetry with reference to the causes of death », Forensic Science International, vol. 87, no 3 (1997), p. 201-
    210
  16. Harvey L. Edmonds Jr., Ph. D. Détection et correction des déséquilibres de l’oxygène cérébral. Applications du moniteur d’oxymétrie cérébrale et somatique INVOSMC en chirurgie et en soins
    intensifs. Guide de poche pour le clinicien. Medtronic, 2019
  17. K. Kobayashi, T. Kitamura, S. Kohira et coll., « Factors associated with a low initial cerebral oxygen saturation value in patients undergoing cardiac surgery », The International Journal of Artificial
    Organs, vol. 20, no 2 (2017), p. 110-116.
  18. A J. Gregory, M. A. Hatem, K. Yee et H. P. Grocott, « Optimal placement of cerebral oximeter monitors to avoid the frontal sinus as determined by computed tomography », Journal of
    Cardiothoracic and Vascular Anesthesia, vol 30, n°1 (2016), p. 127-133.
  19. B. Bongiorno. Prevention of secondary cerebral injury of systemic origin : physiological concepts and nursing practice. Méd. Intensive Réa (2019) 28:408-413
  20. A. Denault, A. Deschamps, J. Murkin. Le monitorage par oxymétrie cérébrale en anesthésiologie. Anesthésiologie – Conférences scientifiques, volume 7, numéro 2. 2008
  21. PG Chassot. Précis d’anesthésie cardiaque 2010 (MAJ 2017). Chapitre 6 : le monitorage en anesthésie cardiaque, mesure de l’oxygénation tissulaire
  22. S. Y. Kim, D. W. Chae, Y.-M. Chun et coll., « Modelling of the effect of end-tidal no carbon dioxide on cerebral oxygen saturation in beach chair position under general anaesthesia », Basic &
    Clinical Pharmacology & Toxicology, vol. 119, 1 (2016), p. 85-92
  23. W. L. Lanier, « Cerebral perfusion: err on the side of caution », Bulletin d’information de l’APSF, vol. 24, no 1 (2009), p. 1-3
  24. X. Sun, J. Ellis, P. J. Corso et coll., « Mortality predicted by preinduction cerebral oxygen saturation after cardiac operation », The Annals of Thoracic Surgery, vol. 98, no 1 (2014), p. 91-96
  25. Albaladejo P. La pression artérielle : encore et toujours un monitorage important en périopératoire MAPAR 2013 ; 113-118 Ferraris A, Jacquet-Lagreze M, Fellahi JL. Four-wavelength near-infrared peripheral oximetry in cardiac surgery patients: a comparison between EQUANOX and O3. J Clin Monit Comput. 2018;32:253–9.
  26. Mashour GA, Moore LE, Lele AV, Robicsek SA, Gelb AW. Perioperative care of patients at high risk for stroke during or after non-cardiac, non-neurologic surgery: consensus statement from the
    Society for Neuroscience in Anesthesiology and Critical Care*. J Neurosurg Anesthesiol 2014;26:273–85)
  27. Jan Bucerius, Jan F Gummert, Michael A Borger, Sebastian Metz, Volkmar Falk, Friedrich W Mohr. Stroke after cardiac surgery: a risk factor analysis of 16,184 consecutive adult patients – The
    Annals of Thoracic Surgery n.d. (accessed December 24, 2016)
  28. Newman M.F., Mathew J.P., Grocott H.P., Mackensen G.B., Monk T., Welsh-Bohmer K.A., et al. Central nervous system injury associated with cardiac surgery Lancet. 2006 ; 368 : 694-703
  29. Relander K., Hietanen M., Rantanen K., Saastamoinen K-P., Soinne L., Ramo J., et al. Postoperative cognitive change after cardiac surgery predicts long-term cognitive outcome. Brain
    Behav. (2020) 10:e01750. 10.1002/brb3.1750
  30. Tony Vu and Julian A. An Update on Postoperative Cognitive Dysfunction Following Cardiac Surgery. Front Psychiatry. 2022; 13: 884907
  31. Murkin JM, Adams SJ, Novick RJ, Quantz M, Bainbridge D, Iglesias I, et al. Monitoring brain oxygen saturation during coronary bypass surgery: a randomized, prospective study. Anesth
    Analg 2007; 104: 51-8
  32. Denault A., Deschamps A., Murkin J.M. A proposed algorithm for the intraoperative use of cerebral near-infrared spectros- copy Semin Cardiothorac Vasc Anesth 2007 ; 11 : 274-281
  33. Deschamps A., Hall R., Grocott H., Mazer C.D., Choi P.T., Turgeon A.F., et al. for the Canadian Perioperative Anesthesia Clinical Trials Group: Cerebral oximetry monitoring to maintain normal
    cerebral oxygen saturation during high-risk cardiac surgery: a randomized controlled feasibility trial Anesthesiology 2016 ; 124 : 826-83
  34. Rogers CA, Stoica S, Ellis L, et al.. Randomized trial of near-infrared spectroscopy for personalized optimization of cerebral tissue oxygenation during cardiac surgery. BJA: British Journal of
    Anaesthesia 2017 10.1093/bja/aex182
  35. Serraino G., Murphy G. Effects of cerebral near-infrared spectroscopy on the outcome of patients undergoing cardiac surgery: a systematic review of randomised trials BMJ Open 2017 ; 7 :
    e016613
  36. Vohra HA, Modi A, Ohri SK. Does use of intra-operative cerebral regional oxygen saturation monitoring during cardiac surgery lead to improved clinical outcomes? Interact Cardiovasc
    Thorac Surg 2009;9:318-22
  37. Colak Z., Borojevic M., Bogovic A., Ivancan V., Biocina B., Majeric-Kogler V.. Influence of intraoperative cerebral oximetry monitoring on neurocognitive function after coronary artery
    bypass surgery: a randomized, prospective study. Eur J Cardiothor Surg. (2015) 47:447–54. 10.1093/ejcts/ezu193
  38. Kara I., Erkin A., Sacli H., Demirtas M., Percin B., Diler MS., et al. The effects of near-infrared spectroscopy on the neurocognitive functions in the patients undergoing coronary artery bypass
    grafting with asymptomatic carotid artery disease: a randomized prospective study. Ann Thorac Cardiovasc Surg. (2015) 21:544–50. 10.5761/atcs.oa.15-00118
  39. Zorrilla-Vaca A., Healy R., Grant MC., Joshi B., Rivera-Lara L., Brown C., et al. Intraoperative cerebral oximetry-based management for optimizing perioperative outcomes: a meta-analysis of
    randomized controlled trials. Can J Anesth. (2018) 65:529–42.
  40. Slater T., Stanik-Hutt J., Davidson P.. Cerebral perfusion monitoring in adult patients following cardiac surgery: an observational study. Contemp Nurse. (2017) 53:669–80
  41. Charles W. Hogue, M.D.; Annabelle Levine, M.D.; Aaron Hudson, M.D.; Choy Lewis, M.D. Clinical Applications of Near-infrared Spectroscopy Monitoring in Cardiovascular Surgery. Anesthesiology
    May 2021, Vol. 134, 784–791
  42. Brott T.G., Hobson R.W., Howard G., Roubin G.S., Clark W.M., et al. CREST Investigators. Stenting versus endarterectomy for treatment of carotid-artery stenosis N Engl J Med 2010 ; 363 : 11-23
  43. Fontaine M, Cannesson M, Lehot J-J. Anesthésie pour endartériectomie carotidienne. EMC (Elsevier Masson SAS, Paris), Anesthésie-Réanimation, 36-586-A-10, 2016
  44. Samra S.K., Dy E.A., Welch K., Dorje P., Zelenock G.B., Stanley J.C. Evaluation of a cerebral oximeter as a monitor of cerebral ischemia during carotid endarterectomy Anesthesiology 2000 ; 93 : 964e70
  45. Stilo F, Spinelli F, Martelli E, Pipitó N, Barillà D, De Caridi G, et al. The sensibility and specificity of cerebral oximetry, measured by INVOS – 4100, in patients undergoing carotid endarterectomy
    compared with awake testing. Minerva Anestesiol. 2012;78:1126–35 Moritz S., Kasprzak P., Arlt M., Taeger K., Metz C. Accuracy of cerebral monitoring in detecting cerebral ischemia during ca- rotid endarterectomy: a comparison of transcranial doppler sonography, near-infrared spectroscopy, stump pressure, and somatosensory evoked potentials Anesthesiology 2007 ; 107 : 563e9
  46. Luís Duarte-Gamas, António Pereira-Neves, Joel Sousa, Bernardo Sousa-Pinto, João Rocha-Neves. The Diagnostic Accuracy of Intra-Operative Near Infrared Spectroscopy in Carotid Artery
    Endarterectomy Under Regional Anaesthesia: Systematic Review and Meta-Analysis. Eur J Vasc Endovasc Surg. 2021 Oct;62(4):522-531
  47. Pedrini L, Magnoni F, Sensi L, et al. Is Near-Infrared Spectroscopy a Reliable Method to Evaluate Clamping Ischemia during Carotid Surgery?[J]. Stroke Res Treat, 2012,2012:156975
  48. Pennekamp C.W., Immink R.V., den Ruijter H.M., Kappelle L.J., Bots M.L., Buhre W.F., et al. Nearinfrared spectroscopy to indicate selective shunt use during carotid endarterectomy Eur J Vasc Endovasc Surg 2013 ; 46 : 397e403
  49. Zogogiannis ID, Iatrou CA, Lazarides MK, et al. Evaluation of an intraoperative algorithm based on near-infrared refracted spectroscopy monitoring, in the intraoperative decision for shunt placement, in patients undergoing carotid endarterectomy. Middle East J Anaesthesiol. 2011;21(3):367–373
  50. Mayer RC, Bingley J, Westcott MJ, Deshpande A, Davies MJ, Lovelock ME, et al. Intraoperative neurological changes in 1665 regional anaesthetic carotid endarterectomies predicts postoperative stroke. ANZ J Surg 2007;77:49–53
  51. Évaluation médico-économique de la surveillance par oxymétrie cérébrale (INVOS™) en peropératoire lors d’endartériectomies carotidiennes. Essai EMOCAR (2010-2017). Investigateur Principal : Dr Yann Le Teurnier, CHU de Nantes. Non publiée
  52. Pohl A., Cullen D.J. Cerebral ischemia during shoulder surgery in the upright position: a case series J Clin Anesth 2005 ; 17 : 463-469
  53. Bhatti, M. T. & Enneking, F. K. Visual loss and ophthalmoplegia after shoulder surgery. Anesth. Analg. 96, 899–902, table of contents (2003)
  54. Villevielle T., Delaunay L., Gentili M., Benhamou D. Chirurgie arthroscopique de l’épaule et complications ischémiques cérébrale Ann Fr Anesth Reanim 2012 ; 31 : 914-918
  55. Friedman D.J., Parnes N.Z., Zimmer Z., Higgins L.D., Warner J.J. Prevalence of cerebrovascular events during shoulder surgery and association with patient position Orthopedics 2009 ; 32 (4) :
    256
  56. Salazar D, Hazel A, Tauchen AJ, Sears BW, Marra G: Neurocognitive deficits and cerebral desaturation during shoulder arthroscopy with patient in beach-chair position: A review of the current literature. Am J Orthop (Belle Mead NJ) 2016;45:63-68
  57. Moraine JJ, Berre J, Melot C, et al. Is cerebral perfusion pressure a major determinant of cerebral blood flow during head elevation in comatose patients with severe intracranial lesions? J Neurosurg 2000;92:606-14
  58. Murphy GS, Szokol JW, Marymont JH, et al.: Cerebral oxygen desaturation events assessed by near-infrared spectroscopy during shoulder arthroscopy in the beach chair and lateral decubitus positions. Anesth Analg 2010;111:496-505
  59. Cullen D.J., Kirby R.R. Beach chair position may decrease cerebral perfusion. Catastrophic outcomes have occurred APSF Newsl 2007 ; 22 (2) : 25-27
  60. Papadonikolakis A., Wiesler E.R., Olimpio M.A., Poehling G.G. Avoiding catastrophic complications of stroke and death related to shoulder surgery in the sitting position Arthroscopy 2008 ; 24 : 481-482
  61. Soeding P.F., Wang J., Hoy G., Jarman P., Phillips H., Marks P., et al. The effect of the sitting upright or ‘beachchair’ position on cerebral blood flow during anaesthesia for shoulder surgery Anaesth Intensive Care 2011 ; 39 : 1-9
  62. K. Ramesh, M. Yusuf, N. Makaram, R. Milton, A. Mathew, and M. Srinivasan. Safety and CostEffectiveness of Interscalene Brachial Plexus Block With Sedation in Reverse Total Shoulder Replacement. Cureus. 2021 Mar; 13(3): e14106.
  63. C Pereira, C Pinto, CGaio Lima and M Soares. Brachial plexus block under dexmedetomidine sedation for shoulder arthroscopy. Reg Anesth Pain Med 2021 ; 70 (Suppl1) : A1–A127
  64. Gelber P.E., Reina F., Caceres E., Monllau J.C. A comparison of risk between the lateral decubitus and the beach-chair position when establishing an anteroinferior shoulder portal: a cadaveric study Arthroscopy 2007 ; 23 : 522-528
  65. Dane H. Salazar, William J. Davis, Nezih Ziroğlu, and Nickolas G. Garbis. Cerebral Desaturation Events During Shoulder Arthroscopy in the Beach Chair Position. J Am Acad Orthop Surg Glob Res Rev. 2019 Aug; 3(8): e007
  66. Lee JH, Min KT, Chun YM, Kim EJ, Choi SH. Effects of beach chair position and induced hypotension on cérébral oxygen saturation in patients undergoing arthroscopic shoulder surgery. Arthroscopy 2011;27:889-94.
  67. Delaunay L., Souron C., Lafosse L. Intérêt de la saturation tissulaire cérébrale en oxygène en chirurgie de l’épaule en position assise. Congrès Sfar : (2011). R399 Moerman A., De Hert S., Jacobs T., De Wilde L., Wouters P. Cerebral oxygen desaturation during beach chair position Eur J Anaesthesiol 2012 ; 29 : 82-87
  68. Aguirre J., Etzensperger F., Brada M., Guzzella S., Saporito A., Blumenthal S., et al. The beach chair position for shoulder surgery in intravenous general anesthesia and controlled hypotension: impact on cerebral oxygenation, cerebral blood flow and neurobehavioral outcome J Clin Anest 2019 ; 53 : 40-48
  69. Cox R.M., Jamgochian G.C., Nicholson K., Wong J.C., Namdari S., Abboud J.A. The effectiveness of cerebral oxygenation monitoring during arthroscopic shoulder surgery in the beach chair position: a randomized blinded study J Shoulder Elbow Surg 2018 ; 27 : 692-700
  70. Murphy GS, Szokol JW, Avram MJ, et al.: Effect of ventilation on cerebral oxygenation in patients undergoing surgery in the beach chair position: A randomized controlled trial. Br J Anaesth 2014;113:618-627
  71. Casati A, Fanelli G, Pietropaoli P, et coll. Continuous monitoring of cerebral oxygen saturation in elderly patients undergoing major abdominal surgery minimizes brain exposure to potential hypoxia. Anesth Analg. 2005;101:740-747
  72. Fellahi J.L., Portran P. In cerebral oximetry: do we trust? Anesthesiology 2016 ; 125 : 818
  73. Slater J.P., Guarino T., Stack J., et al. Cerebral oxygen desaturation predicts cognitive decline and longer hospital stay after cardiac surgery Ann Thorac Surg 2009 ; 87 : 36-45
  74. Drummond J.C., Patel P.M. The lower limit of autoregulation: time to revise our thinking? Anesthesiology 1997 ; 86 : 1431-1433
  75. Brady K., Lee J., Kibler K., Smielewski P., Czosnyka M., Easley R.B., et al. Continuous time-domain analysis of cerebrovascular autoregulation using near-infrared spectroscopy Stroke 2007 ; 38 : 2818-2825
  76. Brady K., Joshi B., Zweifel C., Smielewski P., Czosnyka M., Easley R.B., et al. Real-time continuous monitoring of cerebral blood flow autoregulation using near-infrared spectroscopy in patients undergoing cardiopulmonary bypass Stroke 2010 ; 41 : 1951-1956
  77. Joshi B, Ono M, Brown C, et al. Predicting the limits of cerebral autoregulation during cardioplumonary bypass. Anesth Analg 2012; 114:503-10
  78. Hori D., Brown C., Ono M., Rappold T., Sieber F., Gottschalk A., et al. Arterial pressure above the upper cerebral autoregulation limit during cardiopulmonary bypass is associated with postoperative delirium Br J Anaesth 2014 ; 113 : 1009-1017
  79. Jeanette Tas, Nick Eleveld, Melisa Borg, Kirsten D. J. Bos et al. Cerebral Autoregulation Assessment Using the Near Infrared Spectroscopy ‘NIRS-Only’ High Frequency Methodology in Critically Ill Patients: A Prospective Cross-Sectional Study. Cells. 2022 Jul; 11(14): 2254