2012
DOI: 10.1111/j.1755-3768.2009.01841.x
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Intravitreal bevacizumab alone versus in combination with photodynamic therapy for the treatment of neovascular maculopathy in patients aged 50 years or older: 1‐year results of a prospective clinical study

Abstract: ABSTRACT.Purpose: To compare the outcomes of treatment with intravitreal bevacizumab alone (BEVA group) or in combination with photodynamic therapy (PDT) (COMB group), in patients aged at least 50 years with neovascular maculopathy. Methods: Forty-one patients with neovascular age-related macular degeneration (AMD) (n = 31) or polypoidal choroidal vasculopathy (PCV) (n = 10) were randomized to either the BEVA group (n = 18) or the COMB group (n = 23). A total of three intravitreal bevacizumab injections (1.25 … Show more

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Cited by 32 publications
(34 citation statements)
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“…30 A single clinical trial in neovascular AMD and PCV was graded as level II, but, because only 10 of the randomized patients had PCV, this effectively constitutes level III evidence for this indication. 76 The remaining articles were considered to be level III evidence, together with the collective unpublished experience and expertise of the panel.…”
Section: Resultsmentioning
confidence: 99%
“…30 A single clinical trial in neovascular AMD and PCV was graded as level II, but, because only 10 of the randomized patients had PCV, this effectively constitutes level III evidence for this indication. 76 The remaining articles were considered to be level III evidence, together with the collective unpublished experience and expertise of the panel.…”
Section: Resultsmentioning
confidence: 99%
“…There are fewer studies assessing the efficacy of bevacizumab, and most of them have short follow up duration or were not performed on treatment naïve patients [164,165,166,167,168,169,170,171]. In a retrospective case control study, Cho et al .…”
Section: Treatmentmentioning
confidence: 99%
“…Combination of all groups showed a mean gain of VA of 5.7 letters at week 12 and 5.3 letters at week 52 ( P < 0.0001) [20, 22]. Ocular AEs of aflibercept included conjunctival hemorrhage (38.2%, 5.6%), retinal hemorrhage (14.0%, 11.3%), subjective visual loss (13.4%, 6.3%), vitreous detachment (11.5%, 7.3%), and eye pain (9.6%, 11.4%) at the end of the study [20, 23]. …”
Section: Previously Established Therapiesmentioning
confidence: 99%