Table 3. Summary of studies evaluating secondary prevention of NAION in the fellow eye.
Author, year (reference) | § Level of evidence | Number of patients | Type of study | Treatment (dose) | Frequency of NAION in the fellow eye | p value |
---|---|---|---|---|---|---|
Beck, 1997 (7) | III | 153 treated 278 untreated | Retrospective | Aspirin | At 2 years: 7% of treated,15% of untreated At 5 years: 17% of treated, 20% of untreated | p=0.22 |
Kupersmith, 1997 (57) | III | 57 treated 43 untreated | Retrospective | Aspirin (65-1300 mg) | At 2 years: 17.5% of 57 treated, 53.5% of 16 untreated | p=0.01 |
Salomon, 1999 (76) | III | 36 treated 16 untreated | Retrospective | Aspirin (100 - 325 mg) | 22.2% of 36 treated, 50% of 16 untreated | N/A |
IONDT, 2002 (70) | III | At baseline: 87 treated 237 untreated After baseline: 86 treated 131 untreated | Retrospective* | Aspirin |
** Aspirin at baseline: 20% of 87 treated, 13% of 237 untreated *** Aspirin after baseline:15% of 86 treated, 15% of 131 untreated |
p=0.25 p=0.65 |
Although the IONDT was a prospective trial to evaluate optic nerve sheath decompression, it was not a prospective trial to evaluate aspirin therapy. Aspirin data are observational only.
Reported starting regular aspirin use at least 1 month before onset of symptoms at baseline visit.
Responded positively to ‘started regular use’ of aspirin on at least one study visit after baseline.