Short-Term Intraocular Pressure Trends Following Intravitreal Pegaptanib (Macugen) Injection

Department of Ophthalmology and Visual Science, University of Chicago, Chicago, Illinois, USA.
American Journal of Ophthalmology (Impact Factor: 3.87). 02/2006; 141(1):200-1. DOI: 10.1016/j.ajo.2005.07.053
Source: PubMed


To report the changes and trends in intraocular pressures (IOP) following intravitreal injection of Pegaptanib (Macugen) for the treatment of exudative age-related macular degeneration.
Retrospective chart review.
Review of 79 patients who underwent 122 consecutive Pegaptanib injections. Analysis of the short-term effect of Pegaptanib injections on IOP was performed.
Baseline mean IOP was 15.73 +/- 3.41 mm Hg (mean +/- standard deviation) with a range of 9 to 27 mm Hg. Postinjection mean IOP was 24.47 +/- 6.29 mm Hg with a range of 8 to 36 mm Hg. Mean IOP change from baseline to roughly 30 minutes after Pegaptanib injection was 8.74 +/- 7.23 mm Hg. At the 5- to 7-day follow-up visit, IOP had normalized.
Pegaptanib injection in this limited series seems to be safe from an IOP standpoint in the short-term. IOP monitoring postinjection may not be necessary.

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    • "According to earlier publications on pegaptanib injections and their effect on IOP, anterior chamber paracentesis has not been used as part of the routine procedure (Hariprasad et al. 2006; Bakri et al. 2007; Frenkel et al. 2007). "
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    ABSTRACT: To investigate how prophylactic anterior chamber paracentesis affects the intraocular pressure (IOP) after intravitreal pegaptanib injections. In this prospective study, 41 eyes of 41 patients receiving intravitreal pegaptanib injections were randomly assigned either to receive anterior chamber paracentesis prior to the injection (Group A, 20 patients, n = 35 injections) or not (Group B, 21 patients, n = 38 injections). IOP was measured before the pegaptanib injection (T0) and 2 min (T1), 30 min (T2) and 1 week (T3) after the injection. A four-point scale was used to evaluate the subjective pain experienced during the procedure. The mean IOP at T1 was 15.3 ± 7.5 mmHg in group A and 47.1 ± 24.1 mmHg in group B (difference -31.85 mmHg, 95% Confidence interval -40.13 to -23.56; p < 0.0001). In 45% of the injections without paracentesis, IOP was higher than 50 mmHg 2 min after the pegaptanib injection. No significant difference in IOP was observed at T0, T2 and T3 between the two study groups. The mean pain scores did not differ significantly (0.97 in group A versus 1.32 in group B; p = 0.08). The results suggest that prophylactic anterior chamber paracentesis helps to prevent the high postoperative IOP spike without causing patients any additional pain.
    Acta ophthalmologica 04/2010; 90(3):254-8. DOI:10.1111/j.1755-3768.2010.01904.x · 2.84 Impact Factor
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    • "In phase III, most of the undesirable effects were attributed to injection procedures. Following intravitreous Pegaptanib injection a mild increase of intraocular pressure was observed (Hariprasad et al 2006). Consequently, the FDA recommends tonometry within 30 minutes following injection and biomicroscopy between two and seven days subsequent to the injection. "
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    ABSTRACT: Age-related macular degeneration (AMD) is the main cause of loss of sight in the world and is characterized by neovascularization of the macula. The factors producing choroidal vascularization involve various growth factors, including the vascular endothelial growth factor (VEGF(165)). In this context, the systematic evolution of ligands by exponential enrichment (SELEX) became a tool for developing new therapeutic agents for AMD treatment. The SELEX is a combinatorial oligonucleotide library-based in vitro selection approach in which DNA or RNA molecules (aptamers) are identified by their ability to bind their targets with high affinity and specificity. Recently, the use of the SELEX technique was extended to isolate oligonucleotide ligands for a wide range of proteins of clinical importance. For instance, Pegaptanib sodium, a 28-nucleotide polyethylene glycol RNA aptamer that selectively binds to VEGF(165) and inhibits angiogenesis, was approved by the Food and Drug Administration for the treatment of wet AMD, thereby providing significant benefits to a great number of patients with minimal adverse effects.
    Clinical ophthalmology (Auckland, N.Z.) 01/2008; 1(4):393-402.
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    ABSTRACT: Purpose: To report the trends in intraocular pressures (IOP) following intravitreal injection of ranibizumab (Lucentis) for the treatment of exudative age-related macular degeneration. Methods: Study of 33 patients who underwent 33 consecutive ranibizumab injections. Analysis of the short-term effect of ranibizumab injections on IOP and correlation with age, gender, pseudophakia, history of glaucoma, refractive error, and previous intravitreal injections was performed. Results: Baseline IOP was 16.03 ± 3.396 mm Hg (mean ± standard deviation) with a median of 16 mm Hg and a range of 10 to 23 mm Hg. Immediate post-injection IOP was 34.787 ± 9.08 mm Hg with a median of 34 mm Hg and a range of 10 to 56 mm Hg. All IOP measurements were below 25 mm Hg within 45 minutes of intravitreal injection. Baseline IOP, age, gender, history of glaucoma, refractive error, and previous intravitreal injections were of no predictive value in determining post-injection IOP. Patients who were phakic versus pseudophakic may have a slight correlation of having a higher IOP after injection. Conclusions: IOP returned to below 25 mm Hg in all patients within 45 minutes after ranibizumab injection. Post-injection IOP cannot be predicted by age, gender, baseline IOP, history of glaucoma, number of previous intravitreal injections, or refractive error. Phakia may have some correlation to increased post-injection IOP but more research is needed.
    Clinical and Refractive Optometry 01/2008; 19(4).
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