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Late ophthalmological assessment of patients with subarachnoid hemorrhage and clipping of cerebral aneurysm

  • Clinical Article
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Abstract

Purpose

To estimate prospectively late ocular manifestations in patients after aneurysmal subarachnoid hemorrhage (SAH) treated with aneurysm clipping.

Methods

Forty-six patients (12 men and 34 women), 23–69 years of age, were included in this study. A conventional ophthalmological examination, visual evoked potentials (VEPs), and static perimetry were performed on all patients. The mean interval between the onset of SAH and the aforementioned examination was 1.9 ± 1.3 years (range 0.5-5 years). The following were compared between patients with affected and non-affected visual fields as well as between those with normal and abnormal VEPs: sex, age, time from SAH to surgery, Hunt and Hess scale, Glasgow Coma Scale, Glasgow Outcome Scale, grading of SAH according to the Fisher scale, and the size and site of aneurysm.

Results

Visual field defects were found in 23 patients (50%). In all of these patients, both eyes were affected. The most frequent type of visual field defects were: constricted field (47.8%), multiple peripheral foci (26.1%), and superior field defect (17.4%). There was no significant relationship between the analyzed factors and the occurrence of visual field defects, although statistical significance was almost observed in respect to the Fisher scale (p = 0.055).

Deterioration in VEPs was observed in nine patients (19.6%). In the group of patients with abnormal VEPs, the time from onset of SAH to surgery was 2.6 ± 1.8 days, whereas in the group of patients with normal VEPs this time amounted to 6.4 ± 2.4 days (p = 0.02). In patients with no changes in VEPs, the mean Fisher score was significantly higher than in the group with abnormal VEPs (2.8 ± 0.6 vs 2.0 ± 0.4 respectively, p = 0.04).

Conclusion

Visual field defects and VEP deterioration are frequent late ocular manifestations of SAH treated with aneurysm clipping. Damage to the visual pathway correlates with the severity of SAH and timing of aneurysmal surgery.

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Acknowledgments

This study was supported by Polish Ministry of Science and Higher Education grant N 403 040 32/2157.

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Correspondence to Iwona Obuchowska.

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Comment

Patients with SAH have more visual problems than we may recognize as other neurological sequelae may steal the attention initially. But, after the initial recovery, visual problems may disturb daily activities and this has not been well studied in detail in the long run. The current paper shows that visual field defects are quite common after SAH and clipping of aneurysms, but the effects of each can not be separated. We do not know the visual state well enough before the ictus. The paper also addresses the importance of gentle dissection under high magnification of the operating microscope in slack brain using modern neuroanesthesia, preferably without the use of retractors to avoid iatrogenic brain and nerve damage.

There are biases concerning the examination of the patients affecting the results. In cases of constricted visual fields and normal appearing optic nerve heads, you should take into consideration the huge effect of learning: in some patients the first visual field examination is worse than the later ones and these results should be evaluated carefully. Even though you have a commonly accepted automated perimeter and the examination is performed according to a strict standard methodology, many patients cannot cope with the automated static perimetry as it may be too exhaustive for them, with negative effects on the results. In patients with severe visual field defects, kinetic perimetry by a skilled perimetrist should be performed.

Elina Koskela

Kirsi Setälä

Mika Niemelä

Juha Hernesniemi

Helsinki, Finland

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Obuchowska, I., Turek, G., Mariak, Z. et al. Late ophthalmological assessment of patients with subarachnoid hemorrhage and clipping of cerebral aneurysm. Acta Neurochir 153, 2127–2136 (2011). https://doi.org/10.1007/s00701-011-1161-8

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  • DOI: https://doi.org/10.1007/s00701-011-1161-8

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