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. Author manuscript; available in PMC: 2011 Jun 1.
Published in final edited form as: Ophthalmology. 2010 Apr 28;117(6):1064–1077.e35. doi: 10.1016/j.ophtha.2010.02.031

Table 17.

Cardiovascular Events According to Antiplatelet Trialists’ Collaboration* through 1 and 2 Years

Through 1 Yr
Through 2 Yrs
ShamN=130 Ranibizumab N=375 Triamcinolone N=186 ShamN=130 Ranibizumab N=375 Triamcinolone N=186
Nonfatal myocardial infarction, No. (%) 3 (2%) 1 (<1%) 2 (1%) 4 (3%) 5 (1%) 5 (3%)
Nonfatal cerebrovascular accident—ischemic or hemorrhagic (or unknown), No. (%) 5 (4%) 3 (1%) 1 (1%) 8 (6%) 6 (2%) 3 (2%)
Vascular death (from any potential vascular or unknown cause§), No. (%) 4 (3%) 7 (2%) 2 (1%) 6 (5%) 8 (2%) 4 (2%)
Any ATC cardiovascular event, No. (%) 10 (8%) 11 (3%) 5 (3%) 15 (12%) 19 (5%) 12 (6%)

ATC = Antiplatelet Trialists’ Collaboration.

*

Collaborative overview of randomised trials of antiplatelet therapy—I: Prevention of death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients. Antiplatelet Trialists’ Collaboration. BMJ 1994;308:81-106.

One participant had a nonfatal myocardial infarction and a nonfatal stroke and 1 participant had a nonfatal myocardial infarction and a subsequent vascular death through 1 year; an additional participant had a nonfatal stroke and a subsequent vascular death through 2 years. Multiple events are counted once in the any ATC cardiovascular event row.

N = number of study participants. Study participants with 2 study eyes are assigned to the non-sham group. Multiple events within a study participant are only counted once per event.

§

Four of the 6 vascular deaths in the sham group, 1 of the 8 vascular deaths in the ranibizumab group, and 1 of the 4 vascular deaths in the triamcinolone group were from an unknown cause.