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Intravitreal pegaptanib combined with diode laser therapy for stage 3+ retinopathy of prematurity in zone I and posterior zone II
R. Autrata, I. Krejcírová, K. Senková, M. Holoušová, Z. Doležel, I. Borek,
Jazyk angličtina Země Itálie
Typ dokumentu srovnávací studie, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
PubMed
22669848
DOI
10.5301/ejo.5000166
Knihovny.cz E-zdroje
- MeSH
- aptamery nukleotidové aplikace a dávkování MeSH
- gestační stáří MeSH
- inhibitory angiogeneze aplikace a dávkování MeSH
- injekce intravitreální MeSH
- kombinovaná terapie MeSH
- kryoterapie MeSH
- laserová koagulace MeSH
- lasery polovodičové terapeutické užití MeSH
- lidé MeSH
- následné studie MeSH
- neovaskularizace sítnice prevence a kontrola MeSH
- novorozenec s extrémně nízkou porodní hmotností MeSH
- novorozenec MeSH
- prospektivní studie MeSH
- retinální cévy patologie MeSH
- retinopatie nedonošených klasifikace farmakoterapie chirurgie terapie MeSH
- vaskulární endoteliální růstový faktor A antagonisté a inhibitory MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- novorozenec MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- srovnávací studie MeSH
PURPOSE: To investigate efficacy of intravitreal injection of pegaptanib and laser photocoagulation for treatment of stage 3+ retinopathy of prematurity (ROP) affecting zone I and posterior zone II, and to compare the results in terms of regression, development of peripheral retinal vessels, and final structural outcome with conventional laser photocoagulation or combined with cryotherapy. METHODS: In a prospective comparative study, 152 eyes with zone I, II posterior ROP 3+ (76 premature rabies), from 2009 to 2011, were included. Patients were randomly assigned to receive intravitreal pegaptanib (Macugen® 0.3 mg = 0.02 mL, Pfizer) with conventional diode laser photocoagulation in group 1 (68 eyes of 34 infants) or only laser therapy combined with cryotherapy in group 2 (84 eyes of 42 infants), bilaterally. The primary outcome of treatment success was defined as absence of recurrence of stage 3+ ROP. The mean follow-up after treatment was 19.3 months in group 1 and 21.5 months in group 2. RESULTS: Final favorable anatomic outcome and stable regression of ROP at last control examination was noted in 89.7% of eyes in group 1 and 60.8 % of eyes in group 2. Regression of plus disease and peripheral retinal vessels development appeared significantly more rapidly in group 1. No recurrence of neovascularization (stage 3+ ROP) was identified in 85.4% of patients in group 1 and 50% of patients in group 2. CONCLUSIONS: Results of this study support the administration of intravitreal pegaptanib as useful therapy in the management of stage 3+ ROP.
Citace poskytuje Crossref.org
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