TY - JOUR
T1 - Immediate intraocular pressure changes following intravitreal injections of triamcinolone, pegaptanib, and bevacizumab
AU - Bakri, S. J.
AU - Pulido, J. S.
AU - McCannel, C. A.
AU - Hodge, D. O.
AU - Diehl, N.
AU - Hillemeier, J.
PY - 2009/1
Y1 - 2009/1
N2 - Purpose: To assess the intraocular pressure (IOP) changes, within the first 30 min after intravitreal injection of 0.1 ml (4 mg) triamcinolone, 0.09 ml (0.3 mg) pegaptanib, and 0.05 ml (1.25 mg) bevacizumab. Methods: Records of patients who received intravitreal triamcinolone, pegaptanib, and bevacizumab and who had their IOP measured post-injection were reviewed. Results: A total of 212 injections were performed (76 bevacizumab in 63 patients, 42 triamcinolone in 41 patients, 94 pegaptanib in 74 patients). At 10 min, over 87% of eyes receiving each drug had an IOP of less than 35 mmHg. Three of the 42 eyes receiving intravitreal triamcinolone were treated with IOP-lowering drops for pressures of 44, 46, and 60 mmHg. No patients treated with intravitreal bevacizumab or pegaptanib received IOP-lowering drops. The number of eyes in each injection group that had an IOP rise >10 mmHg within 30 min after injection was 27.6% of eyes receiving bevacizumab, 33.3% of eyes receiving triamcinolone, and 36.2% of eyes receiving pegaptanib. At 10 min, eyes with glaucoma were less likely to have an IOP<35 mmHg, but this difference became less marked with time. Conclusion: In our series, most patients receiving intravitreal injections did not require IOP-lowering drops after injection, and none required a paracentesis.
AB - Purpose: To assess the intraocular pressure (IOP) changes, within the first 30 min after intravitreal injection of 0.1 ml (4 mg) triamcinolone, 0.09 ml (0.3 mg) pegaptanib, and 0.05 ml (1.25 mg) bevacizumab. Methods: Records of patients who received intravitreal triamcinolone, pegaptanib, and bevacizumab and who had their IOP measured post-injection were reviewed. Results: A total of 212 injections were performed (76 bevacizumab in 63 patients, 42 triamcinolone in 41 patients, 94 pegaptanib in 74 patients). At 10 min, over 87% of eyes receiving each drug had an IOP of less than 35 mmHg. Three of the 42 eyes receiving intravitreal triamcinolone were treated with IOP-lowering drops for pressures of 44, 46, and 60 mmHg. No patients treated with intravitreal bevacizumab or pegaptanib received IOP-lowering drops. The number of eyes in each injection group that had an IOP rise >10 mmHg within 30 min after injection was 27.6% of eyes receiving bevacizumab, 33.3% of eyes receiving triamcinolone, and 36.2% of eyes receiving pegaptanib. At 10 min, eyes with glaucoma were less likely to have an IOP<35 mmHg, but this difference became less marked with time. Conclusion: In our series, most patients receiving intravitreal injections did not require IOP-lowering drops after injection, and none required a paracentesis.
KW - Bevacizumab
KW - Eye
KW - Intraocular pressure
KW - Intravitreal
KW - Pegaptanib
KW - Triamcinolone
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U2 - 10.1038/sj.eye.6702938
DO - 10.1038/sj.eye.6702938
M3 - Article
C2 - 17693999
AN - SCOPUS:58249105827
SN - 0950-222X
VL - 23
SP - 181
EP - 185
JO - Eye
JF - Eye
IS - 1
ER -