J Neurocrit Care.  2019 Jun;12(1):37-45. 10.18700/jnc.190080.

Clinical and neuroimaging determinants of minimally conscious and persistent vegetative states after acute stroke

Affiliations
  • 1Department of Neurology, Ege University Medical School Hospital, Izmir, Turkey. emre.kumral@ege.edu.tr

Abstract

BACKGROUND
Patients with persistent vegetative state (PVS) show no evidence of awareness of self or their environment, and those with minimally conscious state (MCS) have severely impaired consciousness with minimal but definite behavioral evidence of self or environmental awareness after stroke. Neuroimaging and clinical characteristics separating these two close consciousness states after stroke were insufficiently studied.
METHODS
We conducted a hospital-based cohort study of all patients with stroke (2011 to 2017) who underwent 3T magnetic resonance imaging and consciousness assessment after 3 months of inclusion. Univariate and multivariate regression analyses were used to estimate the relative risk of neuroimaging markers for differentiation of PVS and MCS.
RESULTS
Of 3,600 eligible subjects, 323 patients (0.09%) had PVS and 93 (0.02%) had MCS (mean age, 62.25±13.4 years). Higher stroke volume was strongly associated with PVS compared to MCS (odds ratio [OR], 0.99; 95% confidence interval [CI], 0.98 to 1.00; P=0.001). On univariate analysis, cingulate gyrus (OR, 2.7; 95% CI, 1.62 to 4.36; P=0.001) and corpus callosum (OR, 2.1; 95% CI, 1.28 to 3.44; P=0.003) involvement was significantly associated with PVS. However, on multivariate analysis, only cingulate gyrus involvement was independently associated with PVS (OR, 2.2; 95% CI, 1.33 to 3.72; P=0.002).
CONCLUSION
Our results indicate that PVS and MCS are different consciousness states according to clinical and neuroimaging findings. To predict outcome, cognitive performance of these patients should be well questioned after stroke.

Keyword

Minimally conscious state; Persistent vegetative state; Ischemic stroke; Hemorrhagic stroke; Cognition disorders; Outcome

MeSH Terms

Cognition Disorders
Cohort Studies
Consciousness
Corpus Callosum
Gyrus Cinguli
Humans
Magnetic Resonance Imaging
Multivariate Analysis
Neuroimaging*
Persistent Vegetative State*
Stroke Volume
Stroke*

Reference

References

1. Edelman GM, Tononi GA. A universe of consciousness: how matter becomes imagination. New York (NY): Basic Books;2000.
2. Plum F. Coma and related global disturbances of the human conscious state. In : Peters A, Jones EG, editors. Cerebral cortex. Vol. 9. Boston (MA): Springer;1991. p. 359–425.
3. Posner JB, Saper CB, Schiff ND, Plum F. Approach to management of the unconscious patient. In : Posner JB, Saper CB, Schiff ND, Plum F, editors. Plum and Posner's diagnosis of stupor and coma. 4th ed. London (UK): Oxford University Press;2007. p. 309–30.
4. Jennett B, Plum F. Persistent vegetative state after brain damage. A syndrome in search of a name. Lancet. 1972; 1:734–7.
5. Giacino JT, Ashwal S, Childs N, Cranford R, Jennett B, Katz DI, et al. The minimally conscious state: definition and diagnostic criteria. Neurology. 2002; 58:349–53.
Article
6. Schiemanck SK, Kwakkel G, Post MW, Prevo AJ. Predictive value of ischemic lesion volume assessed with magnetic resonance imaging for neurological deficits and functional outcome poststroke: a critical review of the literature. Neurorehabil Neural Repair. 2006; 20:492–502.
Article
7. Heldner MR, Zubler C, Mattle HP, Schroth G, Weck A, Mono ML, et al. National Institutes of Health Stroke Scale score and vessel occlusion in 2152 patients with acute ischemic stroke. Stroke. 2013; 44:1153–7.
Article
8. Poisson SN, Nguyen-Huynh MN, Johnston SC, Furie KL, Lev MH, Smith WS. Intracranial large vessel occlusion as a predictor of decline in functional status after transient ischemic attack. Stroke. 2011; 42:44–7.
Article
9. Lövblad KO, Baird AE, Schlaug G, Benfield A, Siewert B, Voetsch B, et al. Ischemic lesion volumes in acute stroke by diffusion-weighted magnetic resonance imaging correlate with clinical outcome. Ann Neurol. 1997; 42:164–70.
10. Johnston KC, Connors AF Jr, Wagner DP, Knaus WA, Wang X, Haley EC Jr. A predictive risk model for outcomes of ischemic stroke. Stroke. 2000; 31:448–55.
Article
11. Mijajlović MD, Pavlović A, Brainin M, Heiss WD, Quinn TJ, Ihle-Hansen HB, et al. Post-stroke dementia: a comprehensive review. BMC Med. 2017; 15:11.
12. Kumral E, Ozkaya B, Sagduyu A, Sirin H, Vardarli E, Pehlivan M. The Ege Stroke Registry: a hospital-based study in the Aegean region, Izmir, Turkey. Analysis of 2,000 stroke patients. Cerebrovasc Dis. 1998; 8:278–88.
13. Wilson JT, Hareendran A, Grant M, Baird T, Schulz UG, Muir KW, et al. Improving the assessment of outcomes in stroke: use of a structured interview to assign grades on the modified Rankin Scale. Stroke. 2002; 33:2243–6.
14. Goldstein LB, Bertels C, Davis JN. Interrater reliability of the NIH stroke scale. Arch Neurol. 1989; 46:660–2.
Article
15. Teasdale G, Knill-Jones R, van der Sande J. Observer variability in assessing impaired consciousness and coma. J Neurol Neurosurg Psychiatry. 1978; 41:603–10.
Article
16. Adams HP Jr, Davis PH, Leira EC, Chang KC, Bendixen BH, Clarke WR, et al. Baseline NIH Stroke Scale score strongly predicts outcome after stroke: a report of the Trial of Org 10172 in Acute Stroke Treatment (TOAST). Neurology. 1999; 53:126–31.
Article
17. Multi-Society Task Force on PVS. Medical aspects of the persistent vegetative state (1). N Engl J Med. 1994; 330:1499–508.
18. Multi-Society Task Force on PVS. Medical aspects of the persistent vegetative state (2). N Engl J Med. 1994; 330:1572–9.
19. Wardlaw JM, Smith EE, Biessels GJ, Cordonnier C, Fazekas F, Frayne R, et al. Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration. Lancet Neurol. 2013; 12:822–38.
Article
20. Fazekas F, Niederkorn K, Schmidt R, Offenbacher H, Horner S, Bertha G, et al. White matter signal abnormalities in normal individuals: correlation with carotid ultrasonography, cerebral blood flow measurements, and cerebrovascular risk factors. Stroke. 1988; 19:1285–8.
Article
21. Cordonnier C, Potter GM, Jackson CA, Doubal F, Keir S, Sudlow CL, et al. Improving interrater agreement about brain microbleeds: development of the Brain Observer MicroBleed Scale (BOMBS). Stroke. 2009; 40:94–9.
22. Schnakers C, Vanhaudenhuyse A, Giacino J, Ventura M, Boly M, Majerus S, et al. Diagnostic accuracy of the vegetative and minimally conscious state: clinical consensus versus standardized neurobehavioral assessment. BMC Neurol. 2009; 9:35.
Article
23. Childs NL, Mercer WN. Brief report: late improvement in consciousness after post-traumatic vegetative state. N Engl J Med. 1996; 334:24–5.
24. Kampfl A, Schmutzhard E, Franz G, Pfausler B, Haring HP, Ulmer H, et al. Prediction of recovery from post-traumatic vegetative state with cerebral magnetic-resonance imaging. Lancet. 1998; 351:1763–7.
Article
25. Laureys S, Owen AM, Schiff ND. Brain function in coma, vegetative state, and related disorders. Lancet Neurol. 2004; 3:537–46.
Article
26. Thomalla G, Hartmann F, Juettler E, Singer OC, Lehnhardt FG, Köhrmann M, et al. Prediction of malignant middle cerebral artery infarction by magnetic resonance imaging within 6 hours of symptom onset: a prospective multicenter observational study. Ann Neurol. 2010; 68:435–45.
Article
27. Mega MS, Cohenour RC. Akinetic mutism: disconnection of frontal-subcortical circuits. Neuropsychiatry Neuropsychol Behav Neurol. 1997; 10:254–9.
28. Katz DI, Alexander MP, Mandell AM. Dementia following strokes in the mesencephalon and diencephalon. Arch Neurol. 1987; 44:1127–33.
Article
29. van Domburg PH, ten Donkelaar HJ, Notermans SL. Akinetic mutism with bithalamic infarction. Neurophysiological correlates. J Neurol Sci. 1996; 139:58–65.
Article
30. Giacino JT, Kalmar K. Diagnostic and prognostic guidelines for the vegetative and minimally conscious states. Neuropsychol Rehabil. 2005; 15:166–74.
31. Wei JW, Heeley EL, Wang JG, Huang Y, Wong LK, Li Z, et al. Comparison of recovery patterns and prognostic indicators for ischemic and hemorrhagic stroke in China: the ChinaQUEST (QUality Evaluation of Stroke Care and Treatment) Registry study. Stroke. 2010; 41:1877–83.
32. Németh G, Hegedüs K, Molnár L. Akinetic mutism associated with bicingular lesions: clinicopathological and functional anatomical correlates. Eur Arch Psychiatry Neurol Sci. 1988; 237:218–22.
33. Qin P, Di H, Liu Y, Yu S, Gong Q, Duncan N, et al. Anterior cingulate activity and the self in disorders of consciousness. Hum Brain Mapp. 2010; 31:1993–2002.
Article
34. Laureys S, Schiff ND. Coma and consciousness: paradigms (re)framed by neuroimaging. Neuroimage. 2012; 61:478–91.
Article
35. Gosseries O, Di H, Laureys S, Boly M. Measuring consciousness in severely damaged brains. Annu Rev Neurosci. 2014; 37:457–78.
Article
36. Giacino JT, Fins JJ, Laureys S, Schiff ND. Disorders of consciousness after acquired brain injury: the state of the science. Nat Rev Neurol. 2014; 10:99–114.
Article
37. Go RC, Todorov AB, Elston RC, Constantinidis J. The malignancy of dementias. Ann Neurol. 1978; 3:559–61.
Article
38. Barba R, Morin MD, Cemillán C, Delgado C, Domingo J, Del Ser T. Previous and incident dementia as risk factors for mortality in stroke patients. Stroke. 2002; 33:1993–8.
Article
39. Béjot Y, Rouaud O, Jacquin A, Osseby GV, Durier J, Manckoundia P, et al. Stroke in the very old: incidence, risk factors, clinical features, outcomes and access to resources: a 22-year population-based study. Cerebrovasc Dis. 2010; 29:111–21.
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