Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2007;38:3172-3174
Published online before print October 25, 2007, doi: 10.1161/STROKEAHA.107.489096
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
38/12/3172    most recent
STROKEAHA.107.489096v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Becker, E.
Right arrow Articles by Karnath, H.-O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Becker, E.
Right arrow Articles by Karnath, H.-O.
Related Collections
Right arrow Acute Stroke Syndromes
Right arrow Behavioral Changes and Stroke

(Stroke. 2007;38:3172.)
© 2007 American Heart Association, Inc.


Original Contributions

Incidence of Visual Extinction After Left Versus Right Hemisphere Stroke

Elisabeth Becker, MS Hans-Otto Karnath, MD, PhD

From Section Neuropsychology, Center of Neurology, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.

Correspondence to Prof Hans-Otto Karnath, MD, PhD, Center of Neurology, University of Tübingen, Hoppe-Seyler-Str.3, D-72076 Tübingen, Germany. E-mail Karnath{at}uni-tuebingen.de


*    Abstract
up arrowTop
*Abstract
down arrowIntroduction
down arrowPatients and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Background and Purpose— Generally it is accepted that spatial neglect occurs predominantly after stroke of the human right hemisphere. In contrast, it remained controversial whether extinction follows the same hemispheric asymmetry. The opinion prevails that the laterality of visual extinction is not as pronounced as it is for spatial neglect.

Methods— To directly compare the incidence of the 2 disorders within the same sample, spatial neglect and visual extinction were investigated during a 1-year period in 83 consecutively admitted patients with unilateral right or left hemisphere stroke.

Results— The incidence of visual extinction and of spatial neglect was not significantly different, neither after left hemisphere (2.4% neglect; 4.9% extinction) nor after right hemisphere (26.2% neglect; 24.3% extinction) stroke.

Conclusions— Visual extinction seems to be as asymmetrically associated with the human right hemisphere as is spatial neglect.


Key Words: brain damage • clinical neurology • cognitive impairment • human • neuropsychology • spatial neglect • visual extinction


*    Introduction
up arrowTop
up arrowAbstract
*Introduction
down arrowPatients and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Spatial neglect is a lateralized disorder with a characteristic failure to explore or react to stimuli presented in contralesional space.1 Visual extinction, however, is a failure to detect a contralesional target in the presence of a competing ipsilesional stimulus. In contrast to neglect, extinction is apparent only when 2 stimuli compete for the subject’s attention.

Generally it is accepted that spatial neglect occurs predominantly after disruption of the human right hemisphere.2–9 The disorder seems to be as asymmetrically represented in the right hemisphere, as are language functions in the human left hemisphere. In contrast, it remained controversial whether extinction follows the same hemispheric asymmetry as spatial neglect. In the literature, the opinion prevails that the laterality of visual extinction is not as pronounced as it is for spatial neglect. It has been suggested that the association with damage of the right hemisphere is much weaker in visual extinction than in spatial neglect.10–14

However, the empirical basis underlying this assumption is weak. Whereas the asymmetrical representation has been frequently demonstrated for spatial neglect, to our knowledge only very few studies investigated hemispheric lateralization for visual extinction by comparing directly right-side and left-side stroke patients.4,15 Moreover, their results remained controversial. Although Odgen15 found a preponderance of extinction after left brain damage (16% with left versus 6% with right brain damage), Stone et al4 reported the opposite pattern (2% after left versus 23% after right brain damage). The controversial results could be attributable to the fact that the studies included patients with different etiologies (tumor/stroke) or used different clinical methods/cut-off scores for evaluation.

The present study aimed to reinvestigate the question whether visual extinction follows the same hemispheric asymmetry as spatial neglect by comparing the incidence of both disorders—visual extinction and spatial neglect—in a prospective 1-year study assessing a group of acute stroke patients with unilateral left-side or right-side lesions.


*    Patients and Methods
up arrowTop
up arrowAbstract
up arrowIntroduction
*Patients and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
During a 1-year period, all patients admitted to the Center of Neurology at Tübingen University with acute unilateral right or unilateral left hemispheric brain lesion caused by first-ever stroke were clinically tested for spatial neglect and for visual extinction. Brain lesions were documented by MRI or by spiral computed tomography in all subjects. Patients with bilateral brain lesions, pathological cerebral atrophy, former strokes, patients with tumors, as well as patients in whom imaging revealed no lesion were excluded. Moreover, 11 patients with unilateral right brain damage (RBD) and 14 with left brain damage (LBD) had to be excluded because of poststroke complications inducing coma, death, or marked reduction in vigilance that did not allow the neuropsychological investigation outlined here. The remaining 1-year sample of patients with unilateral LBD or RBD comprised 93 subjects. Clinical and demographic data of these patients are given in the Table.


View this table:
[in this window]
[in a new window]

 
Table. Demographic and Clinical Data of the Patients With LBD or RBD

The patients were systematically assessed for spatial neglect using the "Bells Test,"16 which has been shown to be a sensitive measure for the exploration deficit of patients with spatial neglect.17 It consists of a horizontally oriented 21x29.7-cm sheet of paper with a total of 35 targets (bells) amid 40 distractors, distributed in 7 columns over the whole page. Three of the 7 columns (=15 targets) are on the left side, 1 is in the middle, and 3 are on the right (=15 targets). Patients are asked to cancel all of the targets. More than 5 target omissions located on the contralesional side were taken to indicate neglect. Visual extinction was investigated with the usual neurological confrontation technique, ie, by using slight wiggling of the index finger(s) in the left or right visual half field. Ten unilateral left or right visual field stimuli were randomly presented with 10 bilateral stimuli. Patients were classified as showing visual extinction when they reported at least 90% of the left or right stimuli on each side correctly, but failed to indicate the contralesional stimulus during bilateral stimulation in >50% of trails. In patients with visual field defects (assessed using standardized neurological confrontation technique), unilateral and bilateral stimuli were presented in the intact visual field. Aphasia was investigated using a bedside examination that evaluated spontaneous speech, auditory and reading comprehension, picture naming, reading, and oral repetition.18 Neuropsychological examination was performed on average 2.9 days after stroke (SD=2.7). All subjects gave their informed consent to participate in the study, which has been performed in accordance with the ethical standards stated in the 1964 Declaration of Helsinki.


*    Results
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowPatients and Methods
*Results
down arrowDiscussion
down arrowReferences
 
In the sample of 93 investigated patients, 42 (45.2%) had RBD and 51 (54.8%) LBD. From the patients with LBD, 10 could not be assessed for spatial neglect and for visual extinction because of severe global aphasia. Thus, 42 patients with RBD and 41 with LBD could be formally tested.

The Figure illustrates that the frequency of spatial neglect was very similar to the frequency of visual extinction in the 2 patient groups. In the 42 patients with RBD, 11 showed spatial neglect and 9 patients visual extinction. The difference in frequency for spatial neglect and for visual extinction was not significantly different ({chi}2df=1=0.2, P=0.6). In the patients with LBD, only 1 (2.4%) of the patients had spatial neglect and 2 (4.9%) had visual extinction. Again, the difference in frequency for spatial neglect and for visual extinction was not significant ({chi}2df=1=0.27; P=0.58).


Figure 1489096
View larger version (8K):
[in this window]
[in a new window]

 
Figure. Frequency of spatial neglect and of visual extinction after unilateral LBD or RBD.

In the group of RBD patients, only 4 subjects exhibited both spatial neglect and visual extinction. In the group of LBD patients, spatial neglect and visual extinction were not observed in combination.


*    Discussion
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowPatients and Methods
up arrowResults
*Discussion
down arrowReferences
 
Our study aimed to investigate the incidence of visual extinction and of spatial neglect after RBD versus LBD within the same patient sample. Neither in the LBD nor in the RBD group did we find significant differences in incidence for visual extinction compared with spatial neglect.

The question thus arises whether visual extinction and spatial neglect represent the same or distinct phenomena. In the literature the terms "extinction" and "spatial neglect" have been19,20 and still are used21–23 interchangeably, reflecting these authors’ view of seeing no or only little difference between the 2 disorders. Very similarly, other studies described extinction as a mild form of neglect.24–26 Our present observation that the frequencies of spatial neglect and of visual extinction are comparable after left as well as after right hemisphere damage could be taken as an argument in favor of the view that the 2 disorders are manifestations of the same phenomenon.

However, whereas we found comparable frequencies for both disorders in the 2 patient groups, only half of the sample with RBD and none of the sample with LBD showed visual extinction and spatial neglect in combination. Stroke patients presenting either one or the other disorder have frequently been described in previous studies.12,14,15,27–29 The observation of a double dissociation of the 2 phenomena has led to a suggestion contrasting the view outlined here, namely to the suggestion of distinct anatomo-functional systems underlying both extinction and neglect.11–13,30 Supporting anatomical evidence for this latter view derived from a recent study comparing the typical lesion location in patients with visual extinction and in patients with spatial neglect.31 The authors observed closely related but anatomically distinct areas of brain damage in the 2 groups. In the patients with visual extinction, the center of lesion overlap was found more caudally and dorsally in the temporo-parietal junction.

In summary, our present results clearly revealed that the incidence of visual extinction and of spatial neglect was not significantly different, neither with LBD nor with RBD. We thus conclude that visual extinction is as asymmetrically associated with the human right hemisphere as is spatial neglect.


*    Acknowledgments
 
The authors are grateful to Monika Fruhmann Berger, Marc Himmelbach, Leif Johannsen, Inga Liepelt, Rebekka Pross, and Regine Zopf for their support with the neuropsychological testing of the patients.

Sources of Funding

This work was supported by the Bundesministerium für Bildung und Forschung (BMBF-Verbundprojekt "Räumliche Orientierung" 01GW0641) and the Deutsche Forschungsgemeinschaft (SFB 550-A4).

Disclosures

None.

Received March 23, 2007; revision received April 18, 2007; accepted May 8, 2007.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowPatients and Methods
up arrowResults
up arrowDiscussion
*References
 
1. Karnath H-O, Zihl J. Disorders of spatial orientation. In: Brandt T, Caplan LR, Dichgans J, Diener HC, Kennard C, eds. Neurological disorders: course and treatment. San Diego, CA: Academic Press; 2003: 277–286.

2. Gainotti G, Messerli P, Tissot R. Qualitative analysis of unilateral spatial neglect in relation to laterality of cerebral lesions. J Neurol Neurosurg Psych. 1972; 35: 545–550.[Abstract/Free Full Text]

3. Denes G, Semenza C, Stoppa E, Lis A. Unilateral spatial neglect and recovery from hemiplegia. Brain. 1982; 105: 543–552.[Abstract/Free Full Text]

4. Stone SP, Halligan PW, Greenwood RJ. The incidence of neglect phenomena and related disorders in patients with an acute right or left hemispheric stroke. Age Ageing. 1993; 22: 46–52.[Abstract/Free Full Text]

5. Heilman KM, Watson RT, Valenstein E. Neglect: Clinical and anatomic aspects. In: Feinberg TE, Farah MJ, eds. Behavioral Neurology and Neuropsychology. New York: Mc Graw-Hill; 1997: 309–318.

6. Pedersen PM, Jorgensen HS, Nakayama H, Raaschou HO, Olsen TS. Hemineglect in acute stroke- incidence and prognostic implications. Am J Phys Med Rehabil. 1997; 76: 122–127.[CrossRef][Medline] [Order article via Infotrieve]

7. Bisiach E. Unilateral Neglect and Related Disorders. In: Denes G, Pizzamiglio L, eds. Handbook of Clinical and Experimental Neuropsychology. Hove, UK: Psychology Press; 1999: 479–495.

8. Bowen A, Mc Kenna K, Tallis RC. Reasons for variability in the reported rate of occurrence of unilateral spatial neglect after stroke. Stroke. 1999; 30: 1196–1202.[Abstract/Free Full Text]

9. Ringman JM, Saver JL, Wolson RF, Clarke WR, Adams HP. Frequency, risk factors, anatomy, and course of unilateral neglect in an acute stroke cohort. Neurology. 2004; 63: 468–474.[Abstract/Free Full Text]

10. De Renzi E, Gentilini M, Pattacini F. Auditory extinction following hemisphere damage. Neuropsychologia. 1984; 22: 733–744.[CrossRef][Medline] [Order article via Infotrieve]

11. Bisiach E. Extinction and neglect: same or different? In: Paillard J, ed. Brain and Space. Oxford: Oxford University Press; 1991: 251–257.

12. Vallar G, Rusconi ML, Bignamini L, Geminiani G, Prani D. Anatomical correlates of visual and tactile extinction in humans: a clinical CT scan study. J Neurol Neurosurg Psychiatry. 1994; 57: 464–470.[Abstract/Free Full Text]

13. Milner AD. Neglect, extinction, and the cortical streams of visual processing. In: Thier P, Karnath H-O, eds. Parietal Lobe Contributions to Orientation in 3D Space. Heidelberg: Springer; 1997: 3–22.

14. Cocchini G, Cubelli R, Della Sala S, Beschin N. Neglect without extinction. Cortex. 1999; 35: 285–313.[Medline] [Order article via Infotrieve]

15. Odgen JA. Anterior-posterior interhemispheric differences in the loci of lesions producing visual hemineglect. Brain Cognition. 1985; 4: 59–75.[CrossRef][Medline] [Order article via Infotrieve]

16. Gauthier L, Dehaut F, Joanette Y. The bells test: a quantitative and qualitative test for visual neglect. Int J Clin Neuropsychol. 1989; 11: 49–54.

17. Ferber S, Karnath H-O. How to assess spatial neglect-line bissection or cancellation tasks? J Clin Exper Neuropsych. 2001; 23: 599–607.

18. Weniger D. Aphasie. In: Karnath H-O, Hartje W, Ziegler W, eds. Kognitive Neurologie. Stuttgart: Thieme; 2006: 48–64.

19. Heilman KM, Valenstein E. Auditory neglect in man. Arch Neurol. 1972; 26: 32–35.[Abstract/Free Full Text]

20. Watson RT, Heilman KM, Cauthern JC, King FA. Neglect after cingulotomy. Neurology. 1973; 23: 1003–1007.[Free Full Text]

21. Manes F, Paradiso S, Springer JA, Lamberty G, Robinson RG. Neglect after right insular cortex infarction. Stroke. 1999; 30: 946–948.[Abstract/Free Full Text]

22. Hilgetag CC, Théoret H, Pascual-Leone A. Enhanced visuo-spatial attention ipsilateral to rTMS-induced, virtual lesions’ of human parietal cortex. Nat Neurosci. 2001; 4: 953–957.[CrossRef][Medline] [Order article via Infotrieve]

23. Corbetta M, Shulman GL. Control of goal-directed and stimulus driven attention in the brain. Nat Rev Neurosci. 2002; 3: 201–215.[Medline] [Order article via Infotrieve]

24. Denny-Brown D, Banquer BQ. Amorphosynthesis from left parietal lesions. Arch Neurol Psych. 1954; 71: 302–313.

25. Kinsbourne M. Lateral interactions in the brain. In: Kinsbourne M, Smith WL, eds. Hemisphere Disconnection and Cerebral Function. Springfield, IL: Thomas; 1974: 239–259.

26. Heilman KM, Watson RT. Mechanisms underlying the unilateral neglect syndrome. In: Weinstein EA, Friedland RP, eds. Hemi-Inattention and Hemisphere Specialisation, New York: Raven Press; 1977: 93–106.

27. Hier DB, Mondlock J, Caplan LR. Behavioural abnormalities after right hemisphere stroke. Neurology. 1983; 33: 337–344.[Abstract/Free Full Text]

28. Barbieri C, De Renzi E. Patterns of neglect dissociation. Behav Neurol. 1989; 2: 13–24.[Medline] [Order article via Infotrieve]

29. Vallar G, Perani D. The anatomy of spatial neglect in humans. In: Jeannerod M, ed. Neurophysiological and Neuropsychological Aspects of Spatial Neglect. Amsterdam: Elsevier; 1987: 235–258.

30. Milner AD. Cerebral correlates of visual awareness. Neuropsychologia. 1995; 33: 1117–1130.[CrossRef][Medline] [Order article via Infotrieve]

31. Karnath H-O, Himmelbach M, Küker W. The cortical substrates of visual extinction. Neuroreport. 2003; 14: 437–442.[CrossRef][Medline] [Order article via Infotrieve]




This article has been cited by other articles:


Home page
Cereb CortexHome page
H.-O. Karnath, C. Rorden, and L. F. Ticini
Damage to White Matter Fiber Tracts in Acute Spatial Neglect
Cereb Cortex, October 1, 2009; 19(10): 2331 - 2337.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
B. Davis, J. Christie, and C. Rorden
Temporal Order Judgments Activate Temporal Parietal Junction
J. Neurosci., March 11, 2009; 29(10): 3182 - 3188.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
38/12/3172    most recent
STROKEAHA.107.489096v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Becker, E.
Right arrow Articles by Karnath, H.-O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Becker, E.
Right arrow Articles by Karnath, H.-O.
Related Collections
Right arrow Acute Stroke Syndromes
Right arrow Behavioral Changes and Stroke