Nonarteritic anterior ischemic optic neuropathy (NAION) has been reported after various intraocular procedures, including extracapsular cataract extraction by nuclear expression or phacoemulsification, intracapsular cataract extraction, and secondary intraocular lens implantation or exchange (1-9). NAION may occur in the immediate postoperative period with spikes in intraocular pressure, as originally described by Hayreh (2), or weeks to months postoperatively (1-4). Although the mechanism underlying delayed NAION cases is undetermined, there is substantial evidence supporting a causal relationship to the surgery. We previously determined the incidence of delayed NAION after cataract extraction to be slightly greater than 1 in 2000 surgeries, substantially higher than expected based on the estimated annual incidence of spontaneously occurring NAION of 2.3 to 10.3 of 100,000 (5,10,11). Additionally, by analyzing the temporal relationship of 18 cases (17 subjects) of NAION occurring within 1 year of anterior segment surgery, we found a significant association between NAION and intraocular surgery. All cases occurred within the first 19 postoperative weeks and none during the remainder of the first postoperative year, contrasting with a more uniform distribution to be expected were the association coincidental (1). In this study, we compare the prevalence of NAION risk factors in a sub-group of the previously reported patient sample of 17 subjects with postoperative NAION (1) to a similarly aged control group with spontaneous NAION.
By reviewing the medical records of patients with NAION diagnosed between January 1, 1993 and December 31, 1999, 11 patients (six male, five female; mean age 75 years, range 64 to 85 years) were identified as having NAION develop within 30 days of intracapsular or extracapsular cataract extraction, secondary intraocular lens placement, or intraocular lens exchange (postoperative NAION group). A similarly aged control group consisting of 37 patients (19 male, 18 female; mean age 71 years, range 50 to 87 years) with spontaneously occurring NAION was randomly selected from the same medical record database (spontaneous NAION group). The diagnosis of NAION was based on the following criteria: (1) acute decrease in vision; (2) nerve fiber layer defect on visual field testing; (3) relative afferent pupillary defect; (4) observed optic nerve edema or segmental pallor, if acute visual loss occurred 6 weeks or longer before examination; and (5) an appropriate evaluation had been performed to exclude alternative causes.
The number of subjects with hypertension, diabetes mellitus, hypercholesterolemia, tobacco use, and cup-to-disc ratio of 0.2 or less in the affected and fellow eyes was obtained for both the postoperative and spontaneous NAION groups. The Fisher exact test was used to assess differences between groups.
Table 1 summarizes the results of the 11 patients (12 eyes) in the study group. Four (36%) were the immediate type, occurring within 24 hours of surgery, and seven (64%) were of the delayed type. Extensive detail and analysis regarding the times of onset has been previously published (1). Table 2 summarizes the NAION risk factors for the postoperative and spontaneous NAION groups. The prevalence of hypertension and small cup-to-disc ratio was significantly lower in the postoperative NAION group than in the spontaneous NAION group. The prevalence of hypertension among the seven patients with delayed postoperative NAION was lower than in the spontaneous NAION group (43% vs. 68%), but the difference was not statistically significant (P = 0.24). The occurrence of a small cup-to-disc ratio in the affected eye of the patients with delayed postoperative NAION was statistically lower than in the eyes of the spontaneous NAION group (57% vs. 94%; P = 0.028). The prevalence of diabetes mellitus, hypercholesterolemia, and tobacco use was similar in the two groups.
When the prevalence of NAION risk factors was compared between patients with postoperative NAION and a control group of similarly aged patients with spontaneous NAION, the prevalence of hypertension and small cup-to-disc ratio was notably lower in patients with postoperative NAION. This finding suggests that persons who have larger cup-to-disc ratios are also at risk for postoperative NAION.
Although the exact mechanism has not been established, NAION is thought to be caused by microvascular hypoperfusion of the posterior ciliary arteries. NAION occurring during the first 24 hours after surgery has been reported to be associated with high intraocular pressures (1,2). Elevation in intraocular pressure likely impedes the blood flow to the optic nerve head, resulting in infarction. Although cases of immediate postoperative NAION have been reported without a documented elevation in intraocular pressure, transient increases in intraocular pressure during the operative and perioperative periods in these patients may have occurred. In support of the association between increased intraocular pressure and immediate postoperative NAION was the finding that of four patients with the immediate type of postoperative NAION in our study, three had documented intraocular pressure measurements of 45 mm Hg or higher.
The causal relationship between the delayed type of postoperative NAION and intraocular surgery is less clear. One possible mechanism may be posterior pole edema related to surgical compression of optic nerve microvasculature. Optic disc edema has been observed preceding the onset of visual symptoms of NAION (12-14). Also, the occurrence of optic nerve edema without visual dysfunction has been reported weeks to months after cataract extraction (15,16). In patients with tenuous blood perfusion of the optic nerve head, minimal edema, possibly subclinical, may result in NAION weeks to months after surgery. This phenomenon could also explain why 45% of postoperative NAION cases in this series occurred in patients who lacked a small cup-to-disc ratio. Interstitial edema may cause crowding of nerve fibers and microvasculature.
Potential limitations of our study include selection bias and its retrospective nature. Some differences between the study and control groups may have been influenced by differences in referral base between patients with post-operative and spontaneous NAION. Because of the low incidence of postoperative NAION, an adequately controlled prospective study would be difficult.
1. McCulley TJ, Lam BL, Feuer WJ. Nonarteritic Anterior Ischemic Optic Neuropathy and Surgery of the Anterior Segment: Temporal Relationship Analysis. Am J Ophthalmol.
2. Hayreh SS. Anterior ischemic optic neuropathy. IV. Occurrence after cataract extraction. Arch Ophthalmol.
3. Carroll FD. Optic nerve complications of cataract extraction. Trans Am Acad Ophthalmol Otolaryngol.
4. Reese AB, Carroll FD. Optic neuritis following cataract extraction. Am J Ophthalmol.
5. McCulley TJ, Lam BL, Feuer WJ. Incidence of Nonarteritic Anterior Ischemic Optic Neuropathy Associated with Cataract Extraction. Ophthalmology.
6. Townes CD, Moran CT, Pfingst HA. Complications of cataract surgery. Trans Am Acad Ophthalmol.
7. Michaels DD, Zugsmith GS. Optic neuropathy following cataract extraction. Ann Ophthalmol.
8. Serrano LA, Behrens MM, Carroll FD. Postcataract extraction ischemic optic neuropathy. Arch Ophthalmol.
9. Spedick MJ, Tomsak RL. Ischemic optic neuropathy following secondary intraocular lens implantation. J Clin Neuroophthalmol.
10. Johnson LN, Arnold AC. Incidence of nonarteritic and arteritic anterior ischemic optic neuropathy. Population-based study in the state of Missouri and Los Angeles County, California. J Neuroophthalmol.
11. Hattenhauer MG, Leavitt JA, Hodge DO, et al. Incidence of nonarteritic anterior ischemic optic neuropathy. Am J Ophthalmol.
12. Boghen DR, Glaser JS. Ischaemic optic neuropathy: The clinical profile and natural history. Brain.
13. Borchert M, Lessell S. Progressive and recurrent nonarteritic anterior ischemic optic neuropathy. Am J Ophthalmol.
14. Hayreh SS. Anterior ischemic optic neuropathy: V. Optic disc edema an early sign. Arch Ophthalmol.
15. Gass JD, Norton EW. Cystoid macular edema and papilledema following cataract extraction: a fluorescein fundoscopic and angiographic study. Arch Ophthalmol.
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16. Slavin ML, Lopinto RJ, Prywes AS, Rosen DA. Optic disc edema with aphakic cystoid maculopathy masquerading as ischemic optic neuropathy. J Clin Neuroophthalmol.