TY - JOUR
T1 - Behandling af neovaskulaer aldersrelateret maculadegeneration med intravitreal vaskulaer endotelial vaekstfaktor-haemmer--sekundaerpublikation
AU - Larsen, Michael
AU - Sander, Birgit
AU - Villumsen, Jørgen Ebbe
AU - Haamann, Per H
AU - la Cour, Morten
AU - Lund-Andersen, Henrik
AU - VEGF Inhibition Study in Ocular Neovascularization Clinical Trial Group
PY - 2005/8/29
Y1 - 2005/8/29
N2 - Subfoveal neovascularization is the most frequent cause of severe visual loss in patients with age-related macular degeneration (AMD). Pharmacologic inhibition of vascular endothelial growth factor (VEGF) is a new principle of treatment of this condition. The effects of intravitreal pegaptanib administered every sixth week for 48 weeks in three different dosages were examined in a prospective, double-masked, randomised trial against subconjunctival sham injection with change in visual acuity as the outcome parameter in 1,186 patients with subfoveal neovacularization in AMD. 70% of the patients treated with pegaptanib avoided moderate visual loss, compared to only 55% of the control group (p < 0.001 for 0.3 mg pegaptanib versus the control group, p < 0.001 for 1.0 mg and p = 0,03 for 3.0 mg). The improved visual prognosis was detectable beginning six weeks after the first injection (p < 0.002). Adverse events included endophthalmitis (1.3% of patients), traumatic lens damage (0.7%), retinal detachment (0.6%) and severe visual loss in one patient (0.1%). Intravitreal pegaptanib improves the visual prognosis in neovascular AMD. The long-term effect and safety of the treatment are not known.
AB - Subfoveal neovascularization is the most frequent cause of severe visual loss in patients with age-related macular degeneration (AMD). Pharmacologic inhibition of vascular endothelial growth factor (VEGF) is a new principle of treatment of this condition. The effects of intravitreal pegaptanib administered every sixth week for 48 weeks in three different dosages were examined in a prospective, double-masked, randomised trial against subconjunctival sham injection with change in visual acuity as the outcome parameter in 1,186 patients with subfoveal neovacularization in AMD. 70% of the patients treated with pegaptanib avoided moderate visual loss, compared to only 55% of the control group (p < 0.001 for 0.3 mg pegaptanib versus the control group, p < 0.001 for 1.0 mg and p = 0,03 for 3.0 mg). The improved visual prognosis was detectable beginning six weeks after the first injection (p < 0.002). Adverse events included endophthalmitis (1.3% of patients), traumatic lens damage (0.7%), retinal detachment (0.6%) and severe visual loss in one patient (0.1%). Intravitreal pegaptanib improves the visual prognosis in neovascular AMD. The long-term effect and safety of the treatment are not known.
KW - Aged
KW - Aged, 80 and over
KW - Angiogenesis Inhibitors/administration & dosage
KW - Aptamers, Nucleotide
KW - Choroidal Neovascularization/drug therapy
KW - Female
KW - Fluorescein Angiography
KW - Humans
KW - Injections
KW - Macular Degeneration/drug therapy
KW - Male
KW - Middle Aged
KW - Oligonucleotides/administration & dosage
KW - Photochemotherapy
KW - Treatment Outcome
KW - Vascular Endothelial Growth Factors/antagonists & inhibitors
KW - Visual Acuity
KW - Vitreous Body/drug effects
M3 - Tidsskriftartikel
C2 - 16138974
SN - 0041-5782
VL - 167
SP - 3301
EP - 3305
JO - Ugeskrift for Laeger
JF - Ugeskrift for Laeger
IS - 35
ER -