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Optic Neuritis

para>Never use oral prednisone alone as the primary treatment because this may increase the risk for recurrent ON (3)[A]. ‚  
Pediatric Considerations

  • No systematic study defining high-dose corticosteroids in children with ON have been conducted.

    • Consensus recommends: 3 to 5 days of IV methylprednisolone (4 to 30 mg/kg per day), followed by a 2 to 4 week taper of oral steroids (6)[C]

  • Optic disc swelling and bilateral disease are more common in children as is severe loss of visual acuity (20/200 or worse).

  • Consider infectious and postinfectious causes of optic nerve impairment.

‚  

ISSUES FOR REFERRAL


Referral to a neurologist and/or ophthalmologist ‚  

ONGOING CARE


FOLLOW-UP RECOMMENDATIONS


Patient Monitoring
Monthly follow-up to monitor visual changes and steroid side effects ‚  

PATIENT EDUCATION


  • Provide reassurance about recovery of vision.
  • If the disease is believed to be secondary to demyelinating disease, patient should be informed of the risk of developing MS.
  • For patient education materials favorably reviewed on this topic, contact:
    • National Eye Institute, Information Officer, Department of Health and Human Services, 9000 Rockville Pike, Bethesda, MD 20892, 301-496-5248
    • North American Neuro-Ophthalmology Society (NANOS), 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416, 952-646-2037, fax: 952-545-6073, http://www.nanosweb.org/i4a/pages/index.cfm?pageid=3280

PROGNOSIS


  • Orbital pain usually resolves within 1 week.
  • Visual acuity
    • Rapid spontaneous improvement at 2 to 3 weeks and continues for several months (may be faster with IV corticosteroids)
    • Often returns to normal or near-normal levels (20/40 or better) within 1 year (90 " “95%), even after near blindness
  • Other visual disturbances (e.g., contrast sensitivity, stereopsis) often persist after acuity returns to normal.
  • Recurrence risk of 35% within 10 years: 14% affected eye, 12% contralateral, 9% bilateral; recurrence is higher in MS patients (48%).
  • ON is associated with an increased risk of developing MS; 35% risk at 7 years, 58% at 15 years (7)[A]:
    • Brain MRI helps to predict risk:
      • 0 lesions: 16%
      • 1 to 2 lesions: 37%
      • 3+ lesions: 51%
  • Poor prognostic factors:
    • Absence of pain
    • Low initial visual acuity
    • Involvement of intracanalicular optic nerve
  • Children with bilateral visual loss have a better prognosis than adults.

COMPLICATIONS


Permanent loss of vision ‚  

REFERENCES


11 Vedula ‚  SS, Brodney-Folse ‚  S, Gal ‚  RL, et al. Corticosteroids for treating optic neuritis. Cochrane Database Syst Rev.  2007;(1):CD001430.22 Keltner ‚  JL, Johnson ‚  CA, Cello ‚  KE, et al. Visual field profile of optic neuritis: a final follow-up report from the optic neuritis treatment trial from baseline through 15 years. Arch Ophthalmol.  2010;128(3):330 " “337.33 Simsek ‚  I, Erdem ‚  H, Pay ‚  S, et al. Optic neuritis occurring with anti-tumour necrosis factor alpha therapy. Ann Rheum Dis.  2007;66(9):1255 " “1258.44 Gleicher ‚  NB, ed. Principles and Practice of Medical Therapy in Pregnancy. 3rd ed. Norwalk, CT: Appleton & Lange; 1998:1396 " “1399.55 Galetta ‚  SL. The controlled high risk Avonex multiple sclerosis trial (CHAMPS Study). J Neuroophthalmol.  2001;21(4):292 " “295.66 Bonhomme ‚  GR, Mitchell ‚  EB. Treatment of pediatric optic neuritis. Curr Treat Options Neurol.  2012;14(1):93 " “102.77 Optic Neuritis Study Group. Visual function 15 years after optic neuritis: a final follow-up report from the Optic Neuritis Treatment Trial. Ophthalmology.  2008;115(6):1079.e5 " “1082.e5.88 Kaufman ‚  DI, Trobe ‚  JD, Eggenberger ‚  ER, et al. Practice parameter: the role of corticosteroids in the management of acute monosymptomatic optic neuritis. Report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology.  2000;54(11):2039 " “2044.99 Arnold ‚  AC. Evolving management of optic neuritis and multiple sclerosis. Am J Ophthalmol.  2005;139(6):1101 " “1108.1010 Balcer ‚  LJ. Clinical practice. Optic neuritis. N Engl J Med.  2006;354(12):1273 " “1280.

SEE ALSO


Multiple Sclerosis ‚  

CODES


ICD10


  • H46.9 Unspecified optic neuritis
  • H46.00 Optic papillitis, unspecified eye
  • H46.10 Retrobulbar neuritis, unspecified eye
  • H46.3 Toxic optic neuropathy
  • H46.13 Retrobulbar neuritis, bilateral
  • H46.2 Nutritional optic neuropathy
  • H46.8 Other optic neuritis
  • H46.12 Retrobulbar neuritis, left eye
  • H46.11 Retrobulbar neuritis, right eye
  • H46.03 Optic papillitis, bilateral
  • H46.01 Optic papillitis, right eye
  • G36.0 Neuromyelitis optica [Devic]
  • H46.02 Optic papillitis, left eye

ICD9


  • 377.30 Optic neuritis, unspecified
  • 377.31 Optic papillitis
  • 377.32 Retrobulbar neuritis (acute)
  • 377.34 Toxic optic neuropathy
  • 341.0 Neuromyelitis optica
  • 377.39 Other optic neuritis

SNOMED


  • 66760008 Optic neuritis (disorder)
  • 73221001 Optic papillitis (disorder)
  • 230507009 Retrobulbar neuritis (disorder)
  • 26125006 Toxic optic neuropathy
  • 25044007 neuromyelitis optica (disorder)

CLINICAL PEARLS


  • MRI is the procedure of choice for determining relative risk and possible therapy for MS prevention.
  • The ONTT showed that high-dose IV methylprednisolone followed by oral prednisone accelerated visual recovery but did not improve the 6-month or 1-year visual outcome compared with placebo, whereas treatment with oral prednisone alone did not improve the outcome and was associated with an increased rate of recurrence of ON (1,2,8)[A],(9)[B],(10)[C].
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