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Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6, 2017년, pp.488 - 491.e1   SCIE
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Retinal vascular changes in preterm infants: heart and lung diseases and plus disease

Arriola-Lopez, Andrea Elizabeth    (Retina Department, Asociación para Evitar la Ceguera en México, Hospital “Luis Sánchez Bulnes”, Mexico City   ); Martinez-Perez, M. Elena    (Department of Computer Science, Institute of Research in Applied Mathematics and Systems, Universidad Nacional Autónoma de Mexico, Mexico City   ); Martinez-Castellanos, Maria Ana    (Retina Department, Asociación para Evitar la Ceguera en México, Hospital “Luis Sánchez Bulnes”, Mexico City  );
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    Purpose To report the retinal vascular features of preterm infants with congenital heart disease (CHD), lung disease (pulmonary hypertension [PH] and bronchopulmonary dysplasia [BPD]), and ROP with plus disease to determine whether these disease entities are distinguishable on the basis of retinal vessel morphology. Methods The medical records of preterm infants with CHD, lung disease, and ROP with plus disease were reviewed retrospectively. Qualitative vascular findings were validated using computer-based software to analyze 25 representative images, each corresponding to one infant's eye. The images were organized into five groups, based on clinical information. Vessel diameter (d) and tortuosity index (TI) were measured. Results A total of 106 infants (mean gestational age, 30.5 ± 2.22 weeks) were initially included. Ophthalmologic evaluation of preterm infants with CHD and lung diseases showed vascular tortuosity without vasodilation at the posterior pole as well as in the periphery. Quantitative analysis showed that venular diameter was significantly increased in the plus disease group ( P = 0.0022) compared to other groups. There was significantly less tortuosity in both arterioles and venules in BPD ( P P = 0.0453) compared with plus group. Conclusions The patterns of retinal vascular tortuosity observed in preterm infants may be unique to different systemic congestive conditions and could have therapeutic implications.


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