Pueyo Victoria, González Inmaculada, Altemir Irene, Pérez Teresa, Gómez Galadriel, Prieto Esther, Oros Daniel
Ophthalmology Department, Hospital Universitario Miguel Servet, Zaragoza, Spain; Instituto Aragonés de Ciencias de la Salud, Zaragoza, Spain.
Ophthalmology Department, Hospital Universitario Miguel Servet, Zaragoza, Spain; Instituto Aragonés de Ciencias de la Salud, Zaragoza, Spain.
Am J Ophthalmol. 2015 Apr;159(4):797-802. doi: 10.1016/j.ajo.2014.12.015. Epub 2014 Dec 20.
To assess retinal morphology changes in patients born at different stages of prematurity, accounting for the presence or absence of retinopathy of prematurity (ROP) and comorbidity, using spectral-domain optical coherence tomography (SD OCT).
Retrospective cohort study.
Preterm and term infants underwent an ophthalmologic assessment (best-corrected visual acuity, stereoacuity, cycloplegic refraction and funduscopy). Retinal layers were imaged, segmented, and measured by SD-OCT. In total 114 full term controls and 60 preterm children, classified as late preterm (32-36 weeks gestational age), early preterm (<32 weeks of gestational age) without ROP, and early preterm with previously treated ROP, were included in the study.
No retinal structure differences were observed in preterm infants with no treated ROP compared to term infants. Early preterm infants with previous treated ROP had decreased retinal nerve fiber layer (RNFL) thickness in the superior and nasal quadrants, increased RNFL in the temporal quadrant, and a thinner ganglion cell and inner plexiform layer complex (GCL-IPL). Low birthweight percentile was associated with increased foveal thickness and ganglion cell damage (RNFL and GCL-IPL) independent of gestational age. Among all the coexisting events, inflammation and hypoxia were correlated with more severe detrimental effects.
In the absence of treated ROP, prematurity was not associated with disturbed retinal structure. Severe ROP and low birthweight were related to neuronal and axonal damage in the inner retinal layers. Detailed comorbidity should be reviewed when evaluating preterm infants.
使用频域光学相干断层扫描(SD OCT)评估不同早产阶段出生的患者的视网膜形态变化,同时考虑早产儿视网膜病变(ROP)的存在与否及合并症情况。
回顾性队列研究。
对早产儿和足月儿进行眼科评估(最佳矫正视力、立体视锐度、睫状肌麻痹验光和眼底镜检查)。通过SD - OCT对视网膜各层进行成像、分割和测量。本研究共纳入114名足月儿作为对照,以及60名早产儿,这些早产儿分为晚期早产儿(胎龄32 - 36周)、无ROP的早期早产儿(胎龄<32周)和曾接受ROP治疗的早期早产儿。
未接受ROP治疗的早产儿与足月儿相比,未观察到视网膜结构差异。曾接受ROP治疗的早期早产儿,其视网膜神经纤维层(RNFL)在上象限和鼻侧象限厚度降低,颞侧象限RNFL增厚,神经节细胞和内丛状层复合体(GCL - IPL)变薄。低出生体重百分位数与黄斑厚度增加及神经节细胞损伤(RNFL和GCL - IPL)相关,且独立于胎龄。在所有并存事件中,炎症和缺氧与更严重的有害影响相关。
在未接受ROP治疗的情况下,早产与视网膜结构紊乱无关。严重的ROP和低出生体重与视网膜内层的神经元和轴突损伤有关。评估早产儿时应详细审查合并症情况。