Literature DB >> 30877695

Conjugate Eye Deviation in Unilateral Lateral Medullary Infarction.

Julian Teufel1,2, Michael Strupp1,2, Jennifer Linn3, Roger Kalla4, Katharina Feil1,5.   

Abstract

BACKGROUND AND
PURPOSE: The initial diagnosis of medullary infarction can be challenging since CT and even MRI results in the very acute phase are often negative.
METHODS: A retrospective, observer-blinded study of horizontal conjugate eye deviation was performed in 1) 50 consecutive patients [age 58±15 years (mean±SD), 74% male, National Institutes of Health Stroke Scale 2±1] with acute unilateral lateral medullary infarction as seen in MRI (infarction group), 2) 54 patients with transient brainstem symptoms [transient ischemic attack of brainstem (TIA) group; age 69±16 years, 59% male], and 3) 53 patients (age 59±20 years, 49% male) with diagnoses other than stroke (control group).
RESULTS: Conjugate eye deviation was found in all patients in the infarction group [n=47 (94%) with ipsilesional deviation and n=3 (6%) with contralesional deviation] compared to 41% (n=22) in the brainstem TIA group and 15% (n=8) in the control group (p<0.0001). Within all groups mean deviation and range were similar for both sides (to the right vs. to the left side 26.6°±12.3 vs. 26.1°±12.3 in the infarction group, 10.5°±5.8 vs. 8.4°±6.3 in the brainstem TIA group and 4.5°±3.2 vs. 7.5°±3.2 in the control group). The extent of eye deviation was significantly greater in the infarction group (p<0.05).
CONCLUSIONS: All patients with MRI-demonstrated unilateral medullary infarction showed conjugate eye deviation. Therefore, conjugate eye deviation in patients with suspected acute lateral medullary infarction is a helpful sensitive sign for supporting the diagnosis, particularly if the deviation is >20°.
Copyright © 2019 Korean Neurological Association.

Entities:  

Keywords:  cerebral stroke; dorsolateral medullary syndrome; eye motility disorders; neurological examination; orthoptics; transient ischemic attack

Year:  2019        PMID: 30877695      PMCID: PMC6444143          DOI: 10.3988/jcn.2019.15.2.228

Source DB:  PubMed          Journal:  J Clin Neurol        ISSN: 1738-6586            Impact factor:   3.077


INTRODUCTION

Ischemic brainstem strokes constitute 10% of all ischemic brain strokes with medullary infarction, thus accounting for 7% of all brainstem strokes. Making the initial diagnosis can frequently be challenging due to large variations in the extent of clinical manifestations. CT results are commonly negative in ischemic brainstem stroke.1 Moreover, 30% of patients with clinical diagnoses of brainstem stroke have false-negative diffusion-weighted imaging (DWI) findings, especially within the first 72 hours after symptom onset.2 Horizontal conjugate eye deviation as a tonic displacement of both eyes away from the midline toward one side is a well-known phenomenon in unilateral infra- and supratentorial central lesions. Partial and forced conjugate eye deviations are found in 6% and 27% of the patients, respectively, more frequently in right hemispheric stroke.34 Conjugate eye deviation has also been described in lesions affecting the vestibular system.567 However, the exact role of conjugate eye deviations in brainstem lesions remains less clear, and their usefulness in diagnosis remains to be systematically examined. The aim of this retrospective observer-blinded study was to determine the frequency and extent of horizontal conjugate eye deviation in the initial imaging in patients with acute unilateral lateral medullary infarction compared to patients with transient brainstem symptoms and patients with diagnoses other than stroke.

METHODS

We analyzed the clinical and imaging data of consecutive patients treated in our neurological department. Patients and controls were excluded if no appropriate evaluation of the eyes was possible due to technical reasons, which resulted in a dropout rate of about 10% for screened patients and controls. The patient group with MRI-demonstrated infarction in the lateral medulla was compared to a brainstem transient ischemic attack (TIA) group consisting of patients with transient neurological brainstem symptoms and no evidence of infarction in MRI, and to a control group consisting of patients with normal CT/MRI findings and diagnoses other than stroke. The imaging data were analyzed by an experienced neuroradiologist who was blinded to the diagnosis and evaluated an anonymized set of single CT/ MRI slices on which only the eyes were seen. The eye deviation angle was analyzed with GeoGebra software (version 4.2; https://www.geogebra.org) (Fig. 1) and measured in angular degrees between the midline and equator of the lens. The mean value of deviation of both eyes was used for further analysis. We classified the deviations into mild (1–10°), moderate (11–20°), and severe (>20°).
Fig. 1

CT and MRI scan of patients. A: CT scan of a middle-aged patient with right dorsolateral medulla infarction, which was later demonstrated in MRI (eye deviation angle α of 47° on the right side and 38° on the left side), with the eyes closed. B: MRI scan of a middle-aged patient with right dorsolateral medulla infarction (eye deviation angle β of 37° on the right side and 35° on the left side), with the eyes closed.

Statistical analysis was performed using GraphPad Prism (GraphPad Software, La Jolla, CA, USA). One-way ANOVA (for nonparametric values) was performed to compare the mean values of conjugate eye deviation in the three groups. Differences were considered significant if p<0.05. This study was approved by the Local Ethics Committee and was performed in accordance with their ethical standards (project number 18-055).

RESULTS

Three groups of patients were examined and compared in terms of conjugate eye deviation as determined by CT or MRI. Fifty patients with MRI-demonstrated unilateral lateral medullary infarction (infarction group) were identified during the study period [age 58±15 years (mean±SD), 74% male, National Institutes of Health Stroke Scale (NIHSS) 2±1; for further details see Table 1]. An initial CT scan was obtained for 43 patients (35 within 1 day after symptom onset, 5 on days 1–5, and 3 on days 5–10), with no infarctions identified; initial MRI was performed in the other 7 patients (5 within 1 day and 2 within 5 days). A purely medullary infarction was found in 31 patients (19 right-sided and 12 left-sided), and 19 patients had an additional ipsilateral cerebellar infarction (8 right-sided and 11 left-sided).
Table 1

Clinical characteristics of the patient group

Case no.SexAge (years)Onset to first imaging (days)Vascular risk factorsStroke lesion localizationEtiologyNIHSS at admissionEye deviation (side)Eye deviation (side)Conjugate eye deviation (side, mean for both eyes)Conjugate eye deviation to lesioned side
SideFurther localization
1M541NoneRCardioembolic3R31°R25°R28.0°Yes
2F720HyperlipidemiaROther determined cause: dissection3R38°R33°R35.4°Yes
3M571HypertensionRLarge-vessel disease1R24°R18°R21.3°Yes
4M551NoneRPlus ipsilateral cerebellumUndetermined1R35°R34°R34.5°Yes
5M6911Hypertension, hyperlipidemia, smokerLLarge-vessel diseaseRRR2.5°No
6M751Hypertension, diabetesLUndetermined2L10°L21°L15.4°Yes
7M770Hypertension, diabetes, hyperlipidemia, family historyLCardioembolic4L16°L19°L17.7°Yes
8M561Hypertension, diabetes, hyperlipidemiaLPlus ipsilateral cerebellumLarge-vessel disease3L21°L31°L26.0°Yes
9M440HypertensionLPlus ipsilateral cerebellumUndetermined1L31°L24°L27.7°Yes
10M480Hypertension, diabetes, hyperlipidemia, smoker, family historyRSmall-vessel disease1R38°R31°R34.4°Yes
11M400Hyperlipidemia, smokerRUndetermined2R47°R45°R46.0°Yes
12M710Hypertension, smokerLLarge-vessel disease2L45°L46°L43.8°Yes
13F881HypertensionRPlus ipsilateral cerebellumLarge-vessel disease1R27°R21°R23.9°Yes
14M530Hypertension, diabetes, smokerRLarge-vessel disease1R26°R22°R24.2°Yes
15F816SmokerRLarge-vessel disease1R16°RR9.6°Yes
16F571Hypertension, hyperlipidemia, smokerRLarge-vessel disease1R40°R31°R35.6°Yes
17M690Hypertension, hyperlipidemiaLUndetermined2L13°LL10.4°Yes
18M6514Hypertension, hyperlipidemia, family historyLOther determined cause: dissection2LL27°L17.3°Yes
19F740Hypertension, hyperlipidemiaRPlus ipsilateral cerebellumUndetermined3R40°R36°R38.3°Yes
20F500SmokerRPlus ipsilateral cerebellumUndetermined2R49°R40°R44.3°Yes
21F460HypertensionLPlus ipsilateral cerebellumOther determined cause: dissection2L28°L41°L34.8°Yes
22M760Hypertension, diabetes, hyperlipidemiaRUndetermined3RRR5.7°Yes
23M421Hypertension, diabetes, hyperlipidemia, smokerLCardioembolic0LL26°L24.4°Yes
24F401Smoker, family historyRPlus ipsilateral cerebellumUndetermined2R40°R31°R35.1°Yes
25M490HypertensionLPlus ipsilateral cerebellumCardioembolic1R10°LL9.3°Yes
26M830HypertensionRCardioembolic2R37°R34°R35.5°Yes
27M690Hypertension, diabetes, hyperlipidemiaLUndetermined2L38°L43°L40.5°Yes
28M362NoneROther determined cause: dissection2R34°R27°R30.3°Yes
29M571Hypertension, diabetesRPlus ipsilateral cerebellumLarge-vessel disease1R33°R30°R31.7°Yes
30M710NoneRLarge-vessel disease1R37°R33°R34.8°Yes
31F510Hypertension, diabetes, smokerLPlus ipsilateral cerebellumLarge-vessel disease2R43°R17°R29.8°No
32M752HypertensionLPlus ipsilateral cerebellumCardioembolic3L33°L26°L14.4°Yes
33M621SmokerLPlus ipsilateral cerebellumLarge-vessel disease1L21°L27°L24.0°Yes
34M595HypertensionLPlus ipsilateral cerebellumOther determined cause: dissection4L11°LL7.8°Yes
35M480Hypertension, hyperlipidemiaRLarge-vessel disease1R39°R22°R30.6°Yes
36M391Hypertension, diabetesLPlus ipsilateral cerebellumOther determined cause: dissection2L23°L29°L26.2°Yes
37M742Hypertension, diabetes, hyperlipidemiaLPlus ipsilateral cerebellumLarge-vessel disease0R13°R13°R13.0°No
38M681Hypertension, hyperlipidemia, smokerRLarge-vessel disease1RRR1.6°Yes
39M471Hypertension, hyperlipidemia, smokerLOther determined cause: dissection2L46°L41°L43.4°Yes
40M530Hypertension, hyperlipidemia, smokerROther determined cause: dissection4RRR5.4°Yes
41F511HypertensionLLarge-vessel disease4L31°L35°L33.3°Yes
42M651NoneRLarge-vessel disease3R30°R36°R33.0°Yes
43M6710Hypertension, hyperlipidemiaRSmall-vessel disease2R29°R22°R25.3°Yes
44F253SmokerROther determined cause: dissection2R19°RR12.7°Yes
45F362NoneLOther determined cause: dissection1L26°L33°L29.8°Yes
46M664HypertensionRPlus ipsilateral cerebellumLarge-vessel disease4R38°R32°R35.0°Yes
47F311NoneROther determined cause: dissection1R39°R36°R37.7°Yes
48M570Hypertension, hyperlipidemia, smokerRLarge-vessel disease4R35°R22°R28.2°Yes
49M450Hypertension, diabetes, hyperlipidemia, family historyRPlus ipsilateral cerebellumLarge-vessel disease2R38°R37°R37.5°Yes
50M710Hypertension, diabetesLSmall-vessel disease2L36°L32°L33.8°Yes

F: female, L: left, M: male, NIHSS: National Institutes of Health Stroke Scale, R: right.

Ipsilateral conjugate eye deviation to the side of the lesion was found in 47 (94%) of those in the infarction group, while the other 3 (6%) patients showed conjugate eye deviation contralateral to the lesion (3°, 4°, and 25°; all left-sided). Mean deviation and extent were similar to the right (26.6°±12.3) and to the left (26.1°±10.6). The deviation was severe in 68% (21 to the right and 13 to the left), while 7 patients had moderate (2 and 5 respectively) and 9 mild deviation (5 and 4 respectively). The group was compared to 54 patients in the brainstem TIA group (age 69±16 years, 59% male, NIHSS 1.4±0.7). Conjugate eye deviation was present in 41% of those in this group (13 on the right side and 9 on the left side). Mean deviation was 10.5±5.8° to the right and 8.4±6.3° to the left. The deviation was mild in 61% (8 to the right and 4 to the left), while 8 patients had moderate (5 and 3 respectively) and 2 severe deviation (0 and 2 respectively). Other eye deviations observed were single-eye deviation (n=8) and disconjugate deviation (n=23). The control group consisted of 53 patients (age 59±19 years, 49% male, NIHSS 0.7±1.3): 8 with benign paroxysmal positional vertigo, 6 with acute vestibular syndrome, 6 with epilepsy, 7 with functional disorders, and 26 with other conditions. Conjugate eye deviation was observed in 15% (n=8), while 15% (n=8) had disconjugate eye deviation and 17% (n=9) had single-eye deviation. The conjugate eye deviation was 4.5°±3.2 to the right and 7.5°±3.2 to the left side, and all cases were classified as mild (5 and 3 respectively). The incidence of conjugate eye deviation was significantly higher in both the infarction and the brainstem TIA groups compared to the control group (p<0.001) (Fig. 2). In addition, the deviation was more severe in the infarction group, whereas the control group showed only mild deviations of ≤10°. Furthermore, eye deviations other than conjugate eye deviation were observed in the brainstem TIA and the control groupss. Therefore, there were significant intergroup differences regarding the incidence of conjugate eye deviations as well as in their severity and extent (all p<0.05).
Fig. 2

Overview of study results. A: Results of conjugate eye deviation in the three compared groups (lateral medullary infarction, demonstrated in MRI; brainstem TIA group; and control group). B: Comparison of mean of conjugate eye deviation. *In MRI, purely medullary infarction was found in 31 patients (19 right-sided, 12 left-sided); 19 patients had an additional ipsilateral cerebellar infarction (8 right-sided, 11 left-sided). NIHSS: National Institutes of Health Stroke Scale, TIA: transient ischemic attack of brainstem.

The main findings of this study, which performed the first standardized workup of eye deviation in such a large group of patients, are described below. Firstly, all of the infarction patients had conjugate eye deviation, compared to 42% of those in the brainstem TIA group and 15% in the control group. Secondly, the extent of the eye deviation was significantly higher in the patient group than in the control group. Therefore, looking at the eye position in the initial imaging may give the neurologist and radiologist an indication for a diagnosis of posterior circulation stroke. Furthermore, in patients with suspected acute lateral medullary infarction conjugate eye deviation could be a helpful sign and support the diagnosis, particularly if the deviation is >20°. The above findings are in line with those of a previous investigation in patients with Wallenberg syndrome using videooculography that found conjugate eye deviation toward the lesioned side in 91% of patients when the eyes were closed.8 This phenomenon can be used to reveal conjugate eye deviation in clinical examination with only a low prevalence of 6% which has been reported in 130 patients with lateral medullary infarction.9 The presumed mechanism behind the phenomenon of conjugate eye deviations is a lesion within the olivary projections to the contralateral vestibulocerebellum.10 Approximately one-third (38%) of our patients had an additional ipsilateral cerebellar infarct. Radiographic conjugate eye deviation was described in 37% of 35 patients with acute cerebellar infarction, mostly contralateral to the lesion, particularly among patients with infarction of the PICA territory including the flocculonodular lobe and/or vermis.11 In another case series of 19 patients with acute vestibular syndrome, radiographic conjugate eye deviation was reportedly present in most of those patients (with 2 patients excluded from the further analysis), of whom 11 had central lesions (10 with stroke and 1 with multiple sclerosis) and 6 had peripheral vestibulopathies (all vestibular neuritis).7 However, although the range of conjugate eye deviation was higher in patients with central lesions, those authors were not able to discriminate between central and peripheral lesions.7 In contrast, in our larger cohort comparing only acute lateral medullary infarction to brainstem TIA patients and control subjects we were able to demonstrate that the occurrence of conjugate eye deviation is helpful in diagnosing acute lateral medullary infarction, particularly if the conjugate eye deviation is >20°. Thirdly, three of the present patients had contralateral conjugate eye deviation. There has been only one case report on a patient with upper medial medullary infarction and contralateral conjugate eye deviation.12 Those authors attributed the contralateral eye deviation to a synergic mechanism involving the nucleus prepositus hypoglossi, the inferior olivary nucleus, flocculus, and vestibular nucleus. Fourthly, 42% of the current brainstem TIA patients showed conjugate eye deviation, which could be best explained by transient brainstem dysfunction. Since 30% of patients have false-negative DWI imaging in the very acute stage,2 some of these patients still could have an infarction. The clinical implication of finding conjugate eye deviation in patients with suspected brainstem TIA is that they should be followed up after 48–72 h. This study has several limitations. Firstly, it has a retrospective design. Secondly, the frequency of eye deviation in other brainstem and cerebellar infarctions as well as in the subgroup of acute vestibular syndrome (and especially peripheral lesions) was not examined. Thirdly, since the patients did not receive any specific instructions, it cannot be ruled out that some of them had their eyes open during the scan or accidentally moved their eyes horizontally, which may have biased the analysis and reduced both the number of patients with eye deviation and the extent of eye deviation. Fourthly, the possibility of clinical overlap between the brainstem TIA and control groups also cannot be ruled out. In conclusion, this study shows that conjugate eye deviation observed in initial imaging can guide the clinician toward a diagnosis of lateral medullary infarction. This is highly relevant from a clinical point of view, because CT is the most commonly used imaging modality in patients with acute brainstem stroke, and it normally does not allow the diagnosis of an acute brainstem infarction within the first hours; however, the present study has revealed that eye deviation may allow such a diagnosis.
  3 in total

1.  Ocular Lateral Deviation in Severe Gait Imbalance Pointing to Lateral Medullary Stroke.

Authors:  Maritta Spiegelberg; Corinne Morel; Jürg-Hans Beer; Annette Dietmaier; Alexander A Tarnutzer
Journal:  Neurohospitalist       Date:  2021-03-24

2.  Isolated axial lateropulsion caused by an acute lateral medullary infarction involving the dorsal spinocerebellar tract: A case report.

Authors:  Marco Sparaco; Maria Carmela Addonizio; Giancarlo Apice; Giuseppina Cafasso; Amedeo D'Alessio; Gabriella Di Iasi; Carmine Franco Muccio
Journal:  Brain Circ       Date:  2022-09-21

3.  Ocular lateral deviation with brief removal of visual fixation differentiates central from peripheral vestibular syndrome.

Authors:  Jorge C Kattah; Shervin Badihian; John H Pula; Alexander A Tarnutzer; David E Newman-Toker; David S Zee
Journal:  J Neurol       Date:  2020-07-28       Impact factor: 6.682

  3 in total

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