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Delayed resolution of vitreomacular traction syndrome following intravitreal injection of ocriplasmin

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Resumo:Introduction: Ocriplasmin is the first pharmacological treatment option approved for the treatment of vitreomacular traction (VMT), including those associated with macular holes. Resolution of vitreomacular adhesion is typically observed within 28 days of intravitreal ocriplasmin injection with the vast majority of patients experiencing vitreomacular release within the first 7 days of treatment. Methods: We report two cases of symptomatic VMT, in which we observed delayed VMT release after intravitreal ocriplasmin. Results: One month after treatment, there was only partial release of VMT in both cases. Complete VMT resolution was achieved in 4 and 2 months, respectively, following intravitreal ocriplasmin injection. Conclusions: Our case reports shows that favorable results can be observed long after the 28 days established to achieve the final outcome of ocriplasmin treatment, and this may have been facilitated by the initial release of VMT by ocriplasmin. The description of the present case reports adds to the literature suggesting that longer observation may be needed after intravitreal ocriplasmin.
Autores principais:Moreira, Jorge
Outros Autores:Teixeira, Carla; Gonçalves, Rita; Coelho, Pedro; Maio, Tiago
Assunto:Comunicações Curtas e Imagens em Oftalmologia
Ano:2017
País:Portugal
Tipo de documento:relatório
Tipo de acesso:acesso aberto
Instituição associada:Sociedade Portuguesa de Oftalmologia
Idioma:inglês
Origem:Revista Sociedade Portuguesa de Oftalmologia
Descrição
Resumo:Introduction: Ocriplasmin is the first pharmacological treatment option approved for the treatment of vitreomacular traction (VMT), including those associated with macular holes. Resolution of vitreomacular adhesion is typically observed within 28 days of intravitreal ocriplasmin injection with the vast majority of patients experiencing vitreomacular release within the first 7 days of treatment. Methods: We report two cases of symptomatic VMT, in which we observed delayed VMT release after intravitreal ocriplasmin. Results: One month after treatment, there was only partial release of VMT in both cases. Complete VMT resolution was achieved in 4 and 2 months, respectively, following intravitreal ocriplasmin injection. Conclusions: Our case reports shows that favorable results can be observed long after the 28 days established to achieve the final outcome of ocriplasmin treatment, and this may have been facilitated by the initial release of VMT by ocriplasmin. The description of the present case reports adds to the literature suggesting that longer observation may be needed after intravitreal ocriplasmin.