Noninvasive detection of alarming intracranial pressure changes by auditory monitoring in early management of brain injury: a prospective invasive versus noninvasive study

Fabrice Giraudet, François Longeras, Aurélien Mulliez, Aurélie Thalamy, Bruno Pereira, Paul Avan, Laurent Sakka, Fabrice Giraudet, François Longeras, Aurélien Mulliez, Aurélie Thalamy, Bruno Pereira, Paul Avan, Laurent Sakka

Abstract

Background: In brain-injured patients intracranial pressure (ICP) is monitored invasively by a ventricular or intraparenchymal transducer. The procedure requires specific expertise and exposes the patient to complications such as malposition, hemorrhage or infection. As inner-ear fluid compartments are connected to the cerebrospinal fluid space, ICP changes elicit subtle changes in the physiology of the inner ear. Notably, we previously demonstrated that the phase of cochlear microphonic potential (CM) generated by sound stimuli rotates with ICP. The aim of our study was to validate the monitoring of CM as a noninvasive method to follow ICP.

Methods: Non-invasive measure of CM-phase was compared to ICP recorded invasively in a prospective series of patients with acute brain injury managed in a neuro-intensive care unit. The study focused on patients with varying ICP and normal middle-ear function.

Results: In the 24 patients with less than 4 days of endotracheal ventilation and whose ICP fluctuated (50-hour data), we demonstrated close correlation between CM-phase rotation and ICP (average 1.26 degrees/mmHg). As a binary classifier, CM phase changes of 7-10 degrees signaled 7.5-mmHg ICP increases with a sensitivity of 83% and 19% fallout.

Conclusion: Reference methods to measure ICP require the surgical placement of a pressure transducer. Noninvasive CM-based monitoring of ICP might be beneficial to early management of brain-injured patients with initially preserved consciousness and to the diagnosis of neurological conditions, whenever invasive monitoring cannot be performed.

Trial registration: ClinicalTrials.gov NCT01685476 , registered on 30 August 2012.

Keywords: Cochlear electrophysiology; Intracranial pressure; Noninvasive monitoring.

Figures

Fig. 1
Fig. 1
Characteristics of intracranial pressure (ICP) events and their tracking by cochlear microphonic potential (CM). a Size of ICP events in mmHg. b Duration of ICP events in minutes. c Pearson correlation coefficients (R) describing the CM-phase-to-ICP linear relationship, vertically aligned for every individual ear (stars), with the 95% confidence interval for each of them (bars)
Fig. 2
Fig. 2
Examples of individual time courses of ICP (red, mmHg) and CM phase (blue, degrees). Vertical range: 20 mmHg for ICP in all diagrams; adjusted according to the CM-phase-to-ICP slope, for CM phase (also see Fig. 3a). In every panel labeled from a-i, patient numbers (#n, upper right corners) match those in Fig. 1c, left column. Dashed lines: intervals of time during which data collection was interrupted by a nursing procedure
Fig. 3
Fig. 3
Statistical analysis of cochlear microphonic potential (CM) monitoring outcomes. a linear fits of individual CM-phase to intracranial pressure (ICP) relationships. b Pearson R coefficients against age. c-d Receiver operating characteristic plots of true positive vs fallout of binary classifications based upon a 5-mmHg increase in ICP (c) and a 5-mmHg decrease in ICP (d)

References

    1. Miller JD, Stanek A, Langfitt TW. Concepts of cerebral perfusion pressure and vascular compression during intracranial hypertension. Prog Brain Res. 1972;35:411–32. doi: 10.1016/S0079-6123(08)60102-8.
    1. Czosnyka M, Pickard JD. Monitoring and interpretation of intracranial pressure. J Neurol Neurosurg Psychiatry. 2004;75(6):813–21. doi: 10.1136/jnnp.2003.033126.
    1. Guillaume J, Janny P. Continuous intracranial manometry; importance of the method and first results. Rev Neurol (Paris) 1951;84(2):131–42.
    1. Chesnut R, Videtta W, Vespa P, Le Roux P. Participants in the International Multidisciplinary Consensus Conference on Multimodality M. Intracranial pressure monitoring: fundamental considerations and rationale for monitoring. Neurocrit Care. 2014;21(Suppl 2):S64–84. doi: 10.1007/s12028-014-0048-y.
    1. Le Roux P, Menon DK, Citerio G, Vespa P, Bader MK, Brophy G, Diringer MN, Stocchetti N, Videtta W, Armonda R, et al. The International Multidisciplinary Consensus Conference on Multimodality Monitoring in Neurocritical Care: a list of recommendations and additional conclusions: a statement for healthcare professionals from the Neurocritical Care Society and the European Society of Intensive Care Medicine. Neurocrit Care. 2014;21(Suppl 2):S282–296. doi: 10.1007/s12028-014-0077-6.
    1. Buki B, Avan P, Lemaire JJ, Dordain M, Chazal J, Ribari O. Otoacoustic emissions: a new tool for monitoring intracranial pressure changes through stapes displacements. Hear Res. 1996;94(1-2):125–39. doi: 10.1016/0378-5955(96)00015-9.
    1. Avan P, Buki B, Maat B, Dordain M, Wit HP. Middle ear influence on otoacoustic emissions. I: noninvasive investigation of the human transmission apparatus and comparison with model results. Hear Res. 2000;140(1-2):189–201. doi: 10.1016/S0378-5955(99)00201-4.
    1. Traboulsi R, Avan P. Transmission of infrasonic pressure waves from cerebrospinal to intralabyrinthine fluids through the human cochlear aqueduct: Non-invasive measurements with otoacoustic emissions. Hear Res. 2007;233(1-2):30–9. doi: 10.1016/j.heares.2007.06.012.
    1. Buki B, Giraudet F, Avan P. Non-invasive measurements of intralabyrinthine pressure changes by electrocochleography and otoacoustic emissions. Hear Res. 2009;251(1-2):51–9. doi: 10.1016/j.heares.2009.02.004.
    1. Minto CF, Schnider TW, Gregg KM, Henthorn TK, Shafer SL. Using the time of maximum effect site concentration to combine pharmacokinetics and pharmacodynamics. Anesthesiology. 2003;99(2):324–33. doi: 10.1097/00000542-200308000-00014.
    1. Avan P, Buki B, Petit C. Auditory distortions: origins and functions. Physiol Rev. 2013;93(4):1563–619. doi: 10.1152/physrev.00029.2012.
    1. Hamill-Ruth RJ, Ruth RA. Evaluation of audiologic impairment in critically ill patients: results of a screening protocol. Crit Care Med. 2003;31(9):2271–7. doi: 10.1097/.
    1. Cavaliere F, Masieri S, Liberini L, Proietti R, Magalini SI. Tympanometry for middle-ear effusion in unconscious ICU patients. Eur J Anaesthesiol. 1992;9(1):71–5.
    1. Kashif FM, Verghese GC, Novak V, Czosnyka M, Heldt T. Model-based noninvasive estimation of intracranial pressure from cerebral blood flow velocity and arterial pressure. Sci Transl Med. 2012;4(129):129ra144. doi: 10.1126/scitranslmed.3003249.
    1. Probst R. Electrocochleography: using extratympanic or transtympanic methods? ORL J Otorhinolaryngol Relat Spec. 1983;45(6):322–9. doi: 10.1159/000275662.
    1. Popovic D, Khoo M, Lee S. Noninvasive monitoring of intracranial pressure. Recent Patents Biomed Eng. 2009;2:165–179. doi: 10.2174/1874764710902030165.
    1. Firsching R, Muller C, Pauli SU, Voellger B, Rohl FW, Behrens-Baumann W. Noninvasive assessment of intracranial pressure with venous ophthalmodynamometry. Clinical article. J Neurosurg. 2011;115(2):371–4. doi: 10.3171/2011.3.JNS101275.
    1. Ragauskas A, Matijosaitis V, Zakelis R, Petrikonis K, Rastenyte D, Piper I, Daubaris G. Clinical assessment of noninvasive intracranial pressure absolute value measurement method. Neurology. 2012;78(21):1684–91. doi: 10.1212/WNL.0b013e3182574f50.
    1. Gelabert-Gonzalez M, Ginesta-Galan V, Sernamito-Garcia R, Allut AG, Bandin-Dieguez J, Rumbo RM. The Camino intracranial pressure device in clinical practice. Assessment in a 1000 cases. Acta Neurochir (Wien) 2006;148(4):435–41. doi: 10.1007/s00701-005-0683-3.
    1. Raboel PH, Bartek J, Jr, Andresen M, Bellander BM, Romner B. Intracranial pressure monitoring: invasive versus non-invasive methods - a review. Crit Care Res Pract. 2012;2012:950393.

Source: PubMed

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