Literature DB >> 29415172

Reply: Response to 'Minimally conscious state or cortically mediated state?'

Lionel Naccache1,2,3,4.   

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Year:  2018        PMID: 29415172      PMCID: PMC5888962          DOI: 10.1093/brain/awy026

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


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Sir, I read with interest the letter by Bayne and colleagues (2018) on my recent reinterpretation of the minimally conscious state (MCS) as a cortically mediated state (CMS). In their letter, Bayne et al. agreed on my demonstration of MCS being rather a CMS, and on the necessity to create a new classification combining behavioural and functional brain-imaging criteria, but they disagreed on adopting this new CMS label based on several concerns (Naccache, 2017; Bayne ). First, they raised the issue that criteria used to label the MCS “also inform us with certainty that the patient is still alive, but no-one would suggest that the MCS should be relabelled the ‘Still Alive State’”. Here, Bayne et al. missed a crucial point that I could have framed more explicitly: the label that we attribute to a given patient corresponds to the richer state we were able to observe with certitude when examining this patient. So, when we say that a patient is in an MCS, we also imply that we couldn’t find reliable evidence in favour of a richer state. Thus describing a patient as being in an MCS also means that there is no evidence that this patient is in a conscious exit-MCS. Likewise diagnosing a patient as being in a vegetative state (VS) also implies that there is no evidence that the patient is in an MCS, even if vegetative functions that are preserved in VS are also obviously preserved in MCS patients. Similarly, stating that a patient is in a CMS means that he/she expresses complex behaviours which necessarily recruit cortical networks (contrarily to what we observe in the behaviour of a VS patient), but without any additional certitude about the conscious versus unconscious type of these cortically-mediated behaviours. Indeed, many cortically mediated behaviours and cognitive processes do occur unconsciously, both during conscious and unconscious states. So the CMS label keeps its relevance to differentiate close but distinct states, in difference with a useless label such as the ‘Still Alive State’ common to all categories at stake. Second, Bayne et al. worried about the absence of EMCS in the new classification I proposed. I reassure them: patients who are in a behavioural EMCS fall, in this proposed new classification, in the conscious 4b category given that functional communication enables to be sure of the existence of subjective reports. Actually, this point was mentioned in my article: ‘At the top of this classification, the label 4b corresponds to the current exit-MCS label’. Bayne et al. then discussed the utility of such a CMS valid label for care-givers and relatives of patients who: ‘are not interested in whether the patient’s behaviours are cortically mediated; instead, they want to know whether these behaviours are accompanied by experiences (and if so, what those experiences are like)’. I fully agree with the premises of this point. But when confronted with these complex situations of patients showing rich behaviours but unable to engage in functional communication, we have no choice but to face and to address this complexity. To do so, our first duty deals with clarity: using words that we can explain and define. I doubt ‘minimally conscious’ is a clear expression, pending the question of what is ‘minimal’ here, and pending the absence of consensus about the definition of ‘consciousness’ (see below). The use of an ambiguous wording opens many misunderstandings. Moreover, my experience with families and caregivers leads me not to underestimate their great ability to understand the following core principle when clearly explained to them: organized patterns of cortical activity (such as the ones translating into cortically mediated behaviours) are mandatory for conscious states, but this necessary condition is not sufficient. As mentioned above, some complex cortically mediated behaviours can occur in unconscious patients. As I wrote: “Once we redefine the MCS as a CMS, rather than a direct and univocal evidence of conscious processing (conscious but ‘minimal’), these problems and misunderstandings should be addressed more easily. This could be a clear starting point to then explain the much less clear issue of consciousness in the concerned patient”. Please note, that my proposed classification does not avoid addressing the central issue of consciousness, but tries to address it on firm and clear grounds. Finally, Bayne et al. questioned the self-reportability definition of consciousness I adopted. This refers to a rich, longstanding, philosophical psychological and scientific debate that is clearly out of the scope of this concise response. However, I would like to emphasize the following three points. First, self-reportability is consensual (an individual able to self-report is consensually defined as being conscious), whereas the ‘aware without self-reportability but still conscious state’ proposed by Bayne et al. is much looser. At the extreme, disentangling conscious from unconscious non self-reported experiences may turn out to be impossible to test (and maybe even to define) within the Bayne et al. perspective, and may finally resemble to the irrelevant ‘Still Alive State’ they mentioned. One risk inherent to this posture consists precisely in throwing ‘the baby [here, the psychological importance of subjective reports in consciousness] out with the bathwater [motivated by the search of an exhaustive definition of consciousness]’. In other terms, when Bayne et al. qualify my view on consciousness as being ‘conservative’ by sticking to reportability, I consider their statement as a compliment: being conservative means here taking conscious subjective thoughts seriously and rigorously. No need to mention that dignity of patients is not affected by the clinical label used to describe him/her. Second, and contrarily to the apparent claims of Bayne et al., reportability can be probed in ‘infants, brain-damaged patients and non-human animals’. For instance, Cowey and Stoerig (1995) magistrally designed a blindsight-inspired visual paradigm enabling the probing of subjective perceptual reports in macaque monkeys. Similarly, subjective reports can be explored in aphasic patients, in paralysed or non-communicating patients (Bekinschtein ), or even in the mute disconnected right hemisphere of a split-brain patient (Gazzaniga ) using innovative behavioural or physiological methods. In the same vein, once a neural signature of conscious access is defined (Sergent ), one can look for it, and find it, in 5-month-old young infants (Kouider ), in non-communicating patients (Bekinschtein ), or in non-human primates (Uhrig ), in order to reveal the functionality of this core mechanism of reportability. A reportability definition of consciousness may therefore be psychologically much richer than intuitively thought, and cover a much larger perimeter of situations than expected. Third, I agree on the multidimensional view of consciousness proposed by Bayne and his colleagues (Bayne ), but from a different perspective. Pragmatically, we recently showed that probing conscious processing in patients through the manipulation of several (rather than only one) cognitive dimensions within the same EEG protocol enabled us to increase diagnostic sensitivity (Sergent ). Conceptually, the multidimensional view of consciousness is not incompatible with the existence of one core process showing an ‘all-or-none’ property (reportability present or absent), combined with multiple other components (e.g. language, episodic memory, executive functions, etc.) the functionality of which would contribute to a taxonomy of various conscious states. Such a multidimensional view of patients can be derived from the global workspace theory of consciousness (Dehaene and Naccache, 2001). Therefore, adopting a multidimensional view on consciousness (Bayne ) does not preclude the ability to differentiate between various conscious and non-conscious fine-grained states based on presence/absence of self-reportability in behavioural and brain imaging data. As a conclusion, this diversity of conceptual views on consciousness further strengthens the importance of building and explaining our clinical diagnoses on firm grounds, and to describe fairly what is observed with certitude. Reinterpreting MCS as CMS could contribute to this clarification, as well as our respective calls for a new classification combining behavioural evidence with functional brain-imaging data. This perspective could open a dialectic and progressive improvement in the way we describe, understand, name, explain, and ultimately try to cure, patients affected with disorders of consciousness.
  12 in total

1.  Can electromyography objectively detect voluntary movement in disorders of consciousness?

Authors:  T A Bekinschtein; M R Coleman; J Niklison; J D Pickard; F F Manes
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-12-20       Impact factor: 10.154

2.  Neural signature of the conscious processing of auditory regularities.

Authors:  Tristan A Bekinschtein; Stanislas Dehaene; Benjamin Rohaut; François Tadel; Laurent Cohen; Lionel Naccache
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-21       Impact factor: 11.205

Review 3.  Are There Levels of Consciousness?

Authors:  Tim Bayne; Jakob Hohwy; Adrian M Owen
Journal:  Trends Cogn Sci       Date:  2016-04-18       Impact factor: 20.229

Review 4.  Reforming the taxonomy in disorders of consciousness.

Authors:  Tim Bayne; Jakob Hohwy; Adrian M Owen
Journal:  Ann Neurol       Date:  2017-12-04       Impact factor: 10.422

5.  Response to 'Minimally conscious state or cortically mediated state?'

Authors:  Tim Bayne; Jakob Hohwy; Adrian M Owen
Journal:  Brain       Date:  2018-04-01       Impact factor: 13.501

6.  Blindsight in monkeys.

Authors:  A Cowey; P Stoerig
Journal:  Nature       Date:  1995-01-19       Impact factor: 49.962

7.  A neural marker of perceptual consciousness in infants.

Authors:  Sid Kouider; Carsten Stahlhut; Sofie V Gelskov; Leonardo S Barbosa; Michel Dutat; Vincent de Gardelle; Anne Christophe; Stanislas Dehaene; Ghislaine Dehaene-Lambertz
Journal:  Science       Date:  2013-04-19       Impact factor: 47.728

8.  Towards a cognitive neuroscience of consciousness: basic evidence and a workspace framework.

Authors:  S Dehaene; L Naccache
Journal:  Cognition       Date:  2001-04

9.  A hierarchy of responses to auditory regularities in the macaque brain.

Authors:  Lynn Uhrig; Stanislas Dehaene; Béchir Jarraya
Journal:  J Neurosci       Date:  2014-01-22       Impact factor: 6.167

10.  Multidimensional cognitive evaluation of patients with disorders of consciousness using EEG: A proof of concept study.

Authors:  Claire Sergent; Frédéric Faugeras; Benjamin Rohaut; Fabien Perrin; Mélanie Valente; Catherine Tallon-Baudry; Laurent Cohen; Lionel Naccache
Journal:  Neuroimage Clin       Date:  2016-12-10       Impact factor: 4.881

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  4 in total

Review 1.  Why and how access consciousness can account for phenomenal consciousness.

Authors:  Lionel Naccache
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-09-19       Impact factor: 6.237

Review 2.  Challenges for theories of consciousness: seeing or knowing, the missing ingredient and how to deal with panpsychism.

Authors:  Victor A F Lamme
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-09-19       Impact factor: 6.237

3.  Habituation of auditory startle reflex is a new sign of minimally conscious state.

Authors:  Bertrand Hermann; Amina Ben Salah; Vincent Perlbarg; Mélanie Valente; Nadya Pyatigorskaya; Marie-Odile Habert; Federico Raimondo; Johan Stender; Damien Galanaud; Aurélie Kas; Louis Puybasset; Pauline Perez; Jacobo D Sitt; Benjamin Rohaut; Lionel Naccache
Journal:  Brain       Date:  2020-07-01       Impact factor: 13.501

Review 4.  Brainstem dysfunction in critically ill patients.

Authors:  Sarah Benghanem; Aurélien Mazeraud; Eric Azabou; Vibol Chhor; Cassia Righy Shinotsuka; Jan Claassen; Benjamin Rohaut; Tarek Sharshar
Journal:  Crit Care       Date:  2020-01-06       Impact factor: 9.097

  4 in total

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