Background/objectives Retinopathy of prematurity (ROP) is a potentially blinding disease of immature retinal vasculature. ROP regresses in majority of the cases and very few go on to develop ROP needing treatment. Fundus fluorescein angiography (FFA) is the gold standard technique to study retinal vasculature. The present study was undertaken with the objective to identify the FFA findings associated with the progression of ROP. Subject/methods Prospective single centre study in a tertiary care hospital of 99 eyes of 50 preterm babies. Fundus fluorescein angiography (FFA) was performed in all babies using RetCam 3 at the first detection of ROP. The babies were followed up for the progression of ROP. The FFA predictors for the progression of ROP were evaluated using the Mann-Whitney U test and Fisher's test. Results Thirty-eight eyes were Type 1 ROP at initial presentation and were lasered. Amongst the rest, 24 eyes showed features of stage 3 ROP with intense leakage on FFA and were designated as FFA-treatable ROP and were also lasered. Amongst the rest of the 37 eyes, the disease progression was seen in 13 eyes and the disease regression was seen in 24 eyes. The baseline FFA findings associated with the progression of ROP were delayed retinal arterial perfusion (p = 0.037) and popcorn lesions (p = 0.042). The post hoc analysis was done using a validated FFA scoring system. Conclusions FFA may be added in the classification of ROP and delayed retinal arterial perfusion and popcorn lesions on FFA may predict the progression of ROP.
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Flinders Med Ctr, Dept Ophthalmol, Div Surg, Adelaide, Australia
Royal Adelaide Hosp, Dept Ophthalmol, Port Rd, Adelaide, SA 5000, AustraliaRoyal Adelaide Hosp, Dept Ophthalmol, Adelaide, Australia
Kvopka, Michael
Chan, Wengonn
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Royal Adelaide Hosp, Dept Ophthalmol, Adelaide, Australia
Univ Adelaide, Discipline Ophthalmol & Visual Sci, Adelaide, AustraliaRoyal Adelaide Hosp, Dept Ophthalmol, Adelaide, Australia
Chan, Wengonn
Lake, Stewart R.
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Univ Adelaide, Machine Learning Div, Ophthalm Res Lab, Adelaide, AustraliaRoyal Adelaide Hosp, Dept Ophthalmol, Adelaide, Australia
Lake, Stewart R.
Durkin, Shane
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机构:Royal Adelaide Hosp, Dept Ophthalmol, Adelaide, Australia
Durkin, Shane
Taranath, Deepa
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Univ Adelaide, Machine Learning Div, Ophthalm Res Lab, Adelaide, AustraliaRoyal Adelaide Hosp, Dept Ophthalmol, Adelaide, Australia
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Weill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USAWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
Patel, Samir N.
Klufas, Michael A.
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Weill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USAWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
Klufas, Michael A.
Ryan, Michael C.
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Oregon Hlth & Sci Univ, Dept Ophthalmol, Casey Eye Inst, Portland, OR 97201 USAWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
Ryan, Michael C.
Jonas, Karyn E.
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Weill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USAWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
Jonas, Karyn E.
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Ostmo, Susan
Ana Martinez-Castellanos, Maria
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Asociac Evitar Ceguera Mexico, Mexico City, DF, MexicoWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
Ana Martinez-Castellanos, Maria
Berrocal, Audina M.
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Bascom Palmer Eye Inst, Dept Ophthalmol, Miami, FL 33136 USAWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
Berrocal, Audina M.
Chiang, Michael F.
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Oregon Hlth & Sci Univ, Dept Ophthalmol, Casey Eye Inst, Portland, OR 97201 USA
Oregon Hlth & Sci Univ, Dept Med Informat & Clin Epidemiol, Portland, OR 97201 USAWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
Chiang, Michael F.
Chan, R. V. Paul
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Weill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USAWeill Cornell Med Coll, Dept Ophthalmol, New York, NY 10021 USA