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dc.contributor.authorKemp, A.
dc.contributor.authorPreen, D.
dc.contributor.authorMorlet, Nigel
dc.contributor.authorClark, Antony
dc.contributor.authorMcAllister, I.
dc.contributor.authorBriffa, T.
dc.contributor.authorSanfilippo, F.
dc.contributor.authorNg, Jonathon
dc.contributor.authorMcKnight, C.
dc.contributor.authorReynolds, W.
dc.contributor.authorGilles, M.
dc.date.accessioned2017-01-30T12:28:01Z
dc.date.available2017-01-30T12:28:01Z
dc.date.created2013-05-06T20:00:22Z
dc.date.issued2013
dc.identifier.citationKemp, A and Preen, David and Morlet, Nigel and Clark, Antony and McAllister, Ian and Briffa, Thomas and Sanfilippo, Frank and Ng, Jonathon and McKnight, Charlotte and Reynolds, Wayne and Gilles, Mark. 2013. Myocardial infarction after intravitreal vascular endothelial growth factor inhibitors: a whole population study. Retina: The Journal of retinal and vitreous diseases 33 (5): pp. 920-927.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/21879
dc.identifier.doi10.1097/IAE.0b013e318276e07b
dc.description.abstract

Purpose: To determine the risk of thromboembolic and gastrointestinal bleeding events in the 12 months after injections of bevacizumab or ranibizumab compared with photodynamic therapy and a non-treated community sample.Methods: Hospital and death records were examined for 1,267 patients treated with vascular endothelial growth factor inhibitor and 399 patients treated with photodynamic therapy attending Western Australian eye clinics from 2002 to 2008, and 1,763 community controls, aged =50 years. Hospital records from 1995 to 2009 were analyzed for history of myocardial infarction (MI), stroke, and gastrointestinal bleeding before treatment. Records were searched for evidence of these events in the 12 months after treatment.Results: The 12-month MI rate was higher for vascular endothelial growth factor inhibitor patients than photodynamic therapy patients and the community group (1.9/100 vs. 0.8 and 0.7, respectively). No differences were observed between patients treated with bevacizumab and ranibizumab. The adjusted MI rate was 2.3 times greater than the community group (95% confidence interval, 1.2–4.5) and photodynamic therapy rate (95% confidence interval, 0.7–7.7). The 12-month MI risk did not increase with the number of injections administered (hazard ratio, 0.9; 95% confidence interval, 0.5–1.5). Stroke and gastrointestinal bleeding did not differ between any exposure groups.Conclusion: Although all the adverse events examined were rare, patients treated with vascular endothelial growth factor inhibitors were significantly more likely to experience fatal or nonfatal MI than the community group. This increased risk may be related to the underlying age-related macular degeneration or vascular endothelial growth factor inhibitor use itself.

dc.publisherLippincott, Wliiams & Wilkins
dc.subjectstroke
dc.subjectranibizumab
dc.subjectthromboembolic and gastrointestinal bleeding events
dc.subjectphotodynamic therapy
dc.subjectbevacizumab
dc.subjectmyocardial infarction (MI)
dc.subjectgastrointestinal bleeding
dc.subjectvascular endothelial growth factor inhibitor
dc.titleMyocardial infarction after intravitreal vascular endothelial growth factor inhibitors: a whole population study
dc.typeJournal Article
dcterms.source.volume33
dcterms.source.number5
dcterms.source.startPage920
dcterms.source.endPage927
dcterms.source.issn0275-004X
dcterms.source.titleRetina: The Journal of retinal and vitreous diseases
curtin.department
curtin.accessStatusFulltext not available


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