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CASE REPORT |
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Year : 2018 | Volume
: 66
| Issue : 5 | Page : 712-714 |
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Fluvoxamine-induced intracranial hypertension in a 10-year-old boy
Hemalini Samant, Preetam Samant
Department of Pediatric Ophthalmology, Sir J. J. Hospital and Grant Medical College, Mumbai, Maharashtra, India
Date of Submission | 07-Sep-2017 |
Date of Acceptance | 05-Mar-2018 |
Date of Web Publication | 20-Apr-2018 |
Correspondence Address: Dr. Hemalini Samant The Eye Associates, 3/4 Jain Towers, 6th Floor, 17 Mathew Road, Mumbai - 400 004, Maharashtra India
Source of Support: None, Conflict of Interest: None | Check |
DOI: 10.4103/ijo.IJO_833_17
Drug-induced intracranial hypertension is a well-established entity. We report a rare case of intracranial hypertension with papilledema in a 10-year-old boy following use of fluvoxamine, a selective serotonin reuptake inhibitor. On discontinuing the drug, the papilledema resolved over 4 months without any residual visual anomalies. To the best of our knowledge, this is the first report of fluvoxamine-induced intracranial hypertension with papilledema.
Keywords: Benign intracranial hypertension, fluvoxamine, papilledema
How to cite this article: Samant H, Samant P. Fluvoxamine-induced intracranial hypertension in a 10-year-old boy. Indian J Ophthalmol 2018;66:712-4 |
Intracranial hypertension in prepubertal children differs significantly from adult and postpubertal intracranial hypertension. Some of the differences are an equal sex distribution, less frequent obesity, more frequent ocular motility defects, and greater incidence of medical conditions compared with adult patients.[1] Drug-induced intracranial hypertension has been known to occur with isotretinoin, lithium, and tetracycline derivatives.[2] Selective serotonin reuptake inhibitors (SSRIs) which have become the first-line drugs for treating depression in the young due to their favorable side effect profile [3] have been rarely implicated in the development of intracranial hypertension.[4],[5]
Fluvoxamine is an SSRI approved for the use of obsessive-compulsive disorders (OCD) in children.[6] We report a rare case of fluvoxamine-induced intracranial hypertension in a young boy with OCD.
Case Report | | |
A 10-year-old boy, averagely built and nourished, complained of seeing black spots in front of his right eye for a few days without headache. His vision with spectacles was 20/40 in the right eye and 20/32 in the left eye. Anterior segment was normal, and dilated fundus evaluation revealed bilateral moderate optic disc edema [Figure 1]a and [Figure 1]b. The disc and peripapillary edema was confirmed and quantified using optical coherence tomography [Figure 2]a, and visual fields showed an enlarged physiological blind spot [Figure 3]. Subsequently, the patient underwent a magnetic resonance imaging and magnetic resonance venography which were both normal. A lumbar puncture was done which revealed raised intracranial pressure (300 mmH2O) with normal cellularity and chemistry results. Based on these findings, a diagnosis of intracranial hypertension with papilledema was made. | Figure 1: (a and b) Papilledema at presentation, (c and d) resolving papilledema at 2-week follow-up, and (e and f) resolved edema with temporal disc pallor at 4 months
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| Figure 2: (a) Retinal nerve fiber layer edema at presentation, (b) resolving edema at 2 weeks, and (c) resolved edema at 4 months
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| Figure 3: (a and b) Enlarged blind spot on visual field analysis in the right and left eye
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On further questioning, the mother reported that her son was on oral fluvoxamine (100 mg/day) that was initiated by psychiatrist for OCD 2 years back. In view of the possible drug-induced intracranial hypertension, fluvoxamine was discontinued immediately, and the patient was started on oral acetazolamide. Within 2 weeks, the papilledema had started resolving [Figure 1]c and [Figure 1]d and [Figure 2]b and by 4 months had completely resolved [Figure 1]e and [Figure 1]f and [Figure 2]c. There was mild temporal disc pallor with normal visual acuity, visual fields, and color vision.
Discussion | | |
Drug-induced intracranial hypertension is well established,[2] but SSRIs leading to papilledema has been very rarely reported.[4],[5] Lithium used previously for treating various psychiatric disorders was known to lead to this complication more frequently.[7] Hutcheon reported a case of a 7-year-old patient who developed bilateral papilledema while taking sertraline hydrochloride, an SSRI, for an anxiety disorder.[5] Mirtazapine, another antidepressant thought to have similar mechanism of action like SSRIs, has also been reported to cause intracranial hypertension.[4] However, to the best of our knowledge, fluvoxamine use has never been associated with intracranial hypertension in the past.
SSRIs have been shown to be associated with intracranial hemorrhage with papilledema within first 30 days of initiation, especially if administered with oral nonsteroidal anti-inflammatory drugs.[8] In experimental animal models, SSRIs have been shown to cause reduction in cranial blood flow with resultant hypoxia and cerebral edema.[9],[10],[11] These mechanisms may be responsible for intracranial hypertension in our patient. However, it was interesting that papilledema developed after 2 years of fluvoxamine use. It is possible that prolonged administration of the drug may have caused a cumulative effect which may have resulted in subsequent papilledema.
Conclusion | | |
In conclusion, we report a very rare case of SSRI-induced intracranial hypertension in a child that resolved promptly on withdrawing fluvoxamine. It may be prudent for psychiatrists to have an ophthalmology consultation for their patients on SSRIs to understand whether this is indeed rare or underreported. In addition, patients may also be warned to get ophthalmic consultation if they experience blurred vision or dark spots.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Acknowledgment
We acknowledge the assistance by Dr. Sabyasachi Sengupta from Sengupta's Research Academy in manuscript preparation.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3]
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