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Two-step versus 1-step subretinal injection to compare subretinal drug delivery: a randomised study protocol.
Simunovic, Matthew P; Shao, Emily H; Osaadon, Perach; Sasongko, Muhammad Bayu; Too, Lay Khoon.
Afiliação
  • Simunovic MP; Save Sight Institute, University of Sydney, Sydney, New South Wales, Australia matthew.simunovic@sydney.edu.au.
  • Shao EH; Retinal Unit, Sydney Eye Hospital, Sydney, New South Wales, Australia.
  • Osaadon P; Retinal Unit, Sydney Eye Hospital, Sydney, New South Wales, Australia.
  • Sasongko MB; Retinal Unit, Sydney Eye Hospital, Sydney, New South Wales, Australia.
  • Too LK; Retinal Unit, Sydney Eye Hospital, Sydney, New South Wales, Australia.
BMJ Open ; 11(12): e049976, 2021 12 15.
Article em En | MEDLINE | ID: mdl-34911710
ABSTRACT

INTRODUCTION:

There is increasing interest in subretinal injections as a surgical procedure, largely as a result of emerging treatments for ocular diseases which necessitate this manoeuvre. However, surgical variables in the efficacy of such treatments have to date been largely overlooked and the proportion of drug which reaches the intended compartment of the subretinal space remains unknown. Our aims are twofold first, to determine the proportion of subretinally injected medication retained following surgical delivery and second, to compare two different techniques of injection ('1-step' vs '2-step').

METHODS:

We outline a randomised controlled trial of subretinal injection of alteplase following vitrectomy for the management of submacular haemorrhage secondary to age-related macular degeneration. Patients will be randomised to receive either 1-step injection, where the therapeutic solution simultaneously defines the surgical plane or 2-step injection, where the surgical plane is first identified with balanced salt solution prior to injection of subretinal alteplase, as outlined below. Sodium fluorescein will be used as an optical label to track drug reflux into the vitreous cavity using quantitative protocols established in our laboratory. All patients will undergo fluid air exchange at the completion of surgery, with injection of bevacizumab 1.25 mg and 20% sulfahexafluoride gas as the vitreous substitute (both of which may help improve outcomes). Alteplase, sodium fluorescein and bevacizumab will all be used for off-label indications in the trial. ETHICS AND DISSEMINATION Ethical approval has been obtained from the South Eastern Sydney Local Health District's Human Research Ethics Committee (HREC 17/092). The results of this trial will be disseminated in peer-reviewed proceedings (associated with conference presentation) and in scholarly journals. TRIAL REGISTRATION NUMBER ACTRN12619001121156.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemorragia Retiniana / Degeneração Macular Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemorragia Retiniana / Degeneração Macular Idioma: En Ano de publicação: 2021 Tipo de documento: Article